WO1992007852A1 - Biphenylalkyl xanthine compounds for treatment of cardiovascular disorders - Google Patents

Biphenylalkyl xanthine compounds for treatment of cardiovascular disorders Download PDF

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Publication number
WO1992007852A1
WO1992007852A1 PCT/US1991/007426 US9107426W WO9207852A1 WO 1992007852 A1 WO1992007852 A1 WO 1992007852A1 US 9107426 W US9107426 W US 9107426W WO 9207852 A1 WO9207852 A1 WO 9207852A1
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Prior art keywords
methyl
biphenyl
tetrazol
purine
dihydro
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PCT/US1991/007426
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French (fr)
Inventor
Philippe R. Bovy
Joe T. Collins
Timothy S. Chamberlain
Brian K. Gheng
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G.D. Searle & Co.
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Publication of WO1992007852A1 publication Critical patent/WO1992007852A1/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems

Definitions

  • Non-peptidic biphenylalkyl xanthine compounds are described for use in treatment of cardiovascular disorders such as hypertension and congestive heart failure.
  • angiotensin II antagonist compounds having a biphenylmethyl moiety attached to the N-7 or N-9 position of the xanthine ring.
  • Angiotensin II is a potent vasoconstrictor agent and also produces other physiological effects such as promoting aldosterone secretion, promoting sodium and fluid retention, inhibiting renin secretion, increasing sympathetic nervous system activity, increasing vasopressin secretion, causing positive cardiac inotropic effect and modulating other hormonal systems.
  • antagonizing angiotensin II at its receptors is a viable approach to inhibit the renin-angiotensin system, given the pivotal role of this octapeptide which mediates the actions of the renin-angiotensin system through interaction with various tissue receptors.
  • angiotensin II antagonists most of which are peptidic in nature .
  • Such peptidic compounds are of limited use due to their lack of oral bioavailability or their short duration of action.
  • commercially-available peptidic angiotensin II antagonists e.g., Saralasin
  • Non-peptidic compounds with angiotensin II antagonist properties are known.
  • the sodium salt of 2-n-butyl-4-chloro-1-(2-chlorobenzyl)imidazole-5- acetic acid has specific competitive angiotensin II antagonist activity as shown in a series of binding experiments, functional assays and in vivo tests [P. C. Wong et al, J. Pharmacol. Exp. Ther., 247 (1), 1-7 (1988)].
  • the sodium salt of 2-sbutyl-4-choloro-1-(2- nitrobenzyl)imidazole-5-acetic acid has specific
  • biphenylmethyl substituted imidazoles as antagonists to the angiotensin II receptor.
  • EP No. 323,841 published 12 July 1989, describes four classes of angiotensin II antagonists, namely, biphenylmethylpyrroles,
  • U.S. Patent No. 4,880,804 to Carini et al describes a family of
  • biphenylmethylbenzimidazole compounds as angiotensin II receptor blockers for use in treatment of hypertension and congestive heart failure.
  • imidazo[4,5-d]pyridazines were synthesized including the compound 4,7-bisethylmercapto-1-ethylimidazo[4,5- d]pyridazine [R. N. Castle et al, J . Org. Chem., 23, 1534- 1538 (1958)].
  • a family of ⁇ - dialkylaminoalkylaminoimidazo[4,5-d]pyridazines was synthesized including, typically, the compound 4- (3- dimethylaminopropylamino)-7-chloro-1-(tetrahydro-2'- pyranyl)imidazo[4,5-d]pyridazine [N. R. Patel et al,
  • 4,722,929 describes 2-aryl-imidazo-pyridazine compounds for use as cardiotonics, including a benzyloxy-substituted 2- phenyl-4-chloro-imidazo[4,5-d] pyridazine.
  • Alkylated xanthine compounds are known for example, 1,3, 7, 8-alkyl-substituted xanthine compounds have been prepared by crotyl bromide alkylation of theophylline at the C 8 position of the theophylline nucleus to provide, specifically, 1,3,7-trimethyl-8-crotyl-xanthine [J. Donat et al, Chim . Ber., 92, 1500-1503 (1959)]. Also, xanthines have been selectively alkylated by various benzylic halides.
  • a xanthine compound having a biphenylmethyl substitutent at the N 7 position namely 7- [[(1,1'-biphenyl)-4-ylJmethyl]-3,7-dihydro-1H-purine-2,6- dione, has been prepared.
  • This compound was made to show regioselective alkylation of the xanthine nucleus [L.G. Marzilli et al, J. Am. Chem. Soc., 97(12), 3351- 3358 (1975)].
  • Theophylline, theobromine and other alkylated xanthines derivatives have been used for many years in various pharmaceutical applications, including the
  • U.S. Patent No. 4,061,753 describes certain alkylated xanthines, such as 7- ⁇ -ethoxybenzyl)theophylline, for use in treatment of dermal inflammation, such as psoriasis.
  • a class of biphenylalkyl xanthine compounds useful in treating circulatory disorders, particularly cardiovascular disorders, is defined by Formula I:
  • m is a number selected from one to four, inclusive; wherein the dotted line between seven- and eight-positions and the eight- and nine-positions represents optionally a double bond; wherein each of X 1 and X 2 is independently selected from oxygen atom and sulfur atom; wherein each of R 0 and R 1 is independently selected from hydrido, alkyl, hydroxyalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, aroylalkyl,
  • alkylalkoxyalkyl alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, alkenyl, cycloalkenyl, aralkoxycarbonyl, alkynyl, cyanoalkyl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, mercaptoalkyl, mercaptocarbonylalkyl,
  • mercaptothiocarbonylalkyl alkylthiocarbonylalkyl, alkylthiothiocarbonylalkyl, arylthiocarbonylalkyl, arylthiothiocarbonylalkyl, aralkylthiocarbonylalkyl, alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
  • arylsulfonyl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and radicals of the formula
  • X is oxygen atom or sulfur atom with z being a number selected from one to four, inclusive; wherein each of R 12 and R 13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R 12 and R 13 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein each of R 2 through R 11 is independently selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl. cycloalkyl, cycloalkylalkyl, cycloalkylhaloalky
  • cycloalkylcarbonyl formyl, alkoxy, aralkyl
  • aralkylhaloalkyl aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
  • alkylcarbonyloxyalkyl alkoxycarbonylalkyl
  • alkylthiothiocarbonyl alkylthiothiocarbonyl, alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl,
  • alkylsulfonyl aralkylsulfinyl, aralkylsulfonyl,
  • arylsulfinyl arylsulfonyl
  • phthalimido phthalimidoalkyl
  • heteroaryl heteroarylalkyl
  • phthalimidoalkyl heteroaryl
  • heteroarylalkyl cycloheteroalkyl
  • each of said heteroaryl- and cyclohetero-containing groups has one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R 2 through R 11 may be further independently selected from amino and amido radicals of the formula
  • X is oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R 14 through R 26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
  • cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R 14 and R 15 taken together, R 16 and R 17 taken together, R 18 and R 19 taken together, R 21 and R 22 taken together and R 23 and R 24 taken together may each form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; and wherein each of R 3 through R 11 may be further
  • n is a number selected from zero through three, inclusive, and wherein A is an acidic group selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties;
  • Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R 1 through R 26 , Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, alkynyl, aralkyl, hydroxyalkyl, haloalkyl, halo, oxo, alkoxy, aryloxy, aralkoxy, aralkylthio, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, aryl, aroyl, cycloalkenyl, cyano, cyanoamino, nitro, alkylcarbonyloxy, alk
  • aralkoxycarbonyl carboxyl, mercapto, mercaptocarbonyl, alkylthio, arylthio, alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, aralkylsulfinyl,
  • aralkylsulfonyl arylsulfinyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amino and amido radicals of the formula
  • R 27 through R 31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, DR 32 and
  • D is selected from oxygen atom and sulfur atom and R 32 is selected from hydrido, alkyl, cycloalkyl,
  • R 27 , R 28 , R 29 , R 30 , R 31 , R 33 and R 34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, alkylsulfinyl, alkylsulfonyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl,
  • R 27 , R 28 , R 29 , R 30 , R 31 , R 33 and R 34 is further independently selected from amino and amido radicals of the formula
  • X is oxygen atom or sulfur atom
  • the optionally-present double bond at the N 7 or N 8 positions within the five-membered ring-portion of the xanthine ring of Formula I it is intended that no more than one such double bond may be present. That is, only one of the N 7 or N 8 atoms may have a double bond at one time. It is also intended that when the N 7 atom has a double bond in the rings the depicted biphenylalkyl portion of Formula I must be attached at the other N 9 atom. When the N 9 atom has a double bond within the ring, the biphenylalkyl portion of Formula I is attached at the N 7 atom such as depicted in Formula II, below.
  • a preferred class of compounds consists of those compounds of Formula I within a sub-set of compounds of Formula II:
  • each of R 0 and R 1 is independently selected from hydrido, alkyl, hydroxyalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, mercaptoalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, alkylsulfonyl, aralkylsulfonyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amido radicals of the formula
  • X is oxygen atom or sulfur atom with r being a number selected from one or two; wherein each of R 12 and R 13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; with the proviso that R 0 and R 1 cannot simultaneously be hydrido; wherein R 2 is selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
  • cycloalkylhaloalkyl cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
  • alkylcarbonyloxyalkyl alkoxycarbonylalkyl
  • alkylthiothiocarbonyl alkylthiothiocarbonyl, alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl,
  • alkylsulfonyl aralkylsulfinyl, aralkylsulfonyl,
  • arylsulfinyl arylsulfonyl
  • phthalimido phthalimidoalkyl
  • heteroaryl heteroarylalkyl
  • phthalimidoalkyl heteroaryl
  • heteroarylalkyl cycloheteroalkyl
  • each of said heteroaryl- and cycloheteroalkyl- containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R 2 through R 11 may be further independently selected from amino and amido radicals of the formula
  • X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R 14 through R 26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
  • each of R 3 through R 11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
  • cycloalkynyl cyano, nitro, carboxyl, alkylcarbonyloxy, mercaptocarbonyl, mercaptothiocarbonyl, alkoxycarbonyloxy, alkylthio, alkylthiocarbonyl, alkylcarbonylthio,
  • alkylthiocarbonyloxy alkylthiocarbonylthio
  • X is oxygen atom or sulfur atom
  • R 3 through R 11 may be further selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R 3 through R 11 may be further
  • n is a number selected from zero through three, inclusive; wherein A is an acidic group selected from acids containing one or more atoms selected from oxygen, sulfur, phosphorus and nitrogen atoms, and wherein said acidic group is selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl,
  • cycloalkylalkyl alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R 1 through R 26 , Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, haloalkyl, oxo, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, mercaptocarbonyl, alkylthio and alkylthiocarbonyl, and amino and amido radicals of the formula wherein X is oxygen atom or
  • D is selected from oxygen atom and sulfur atom
  • R 32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl
  • each of R 27 , R 28 , R 29 , R 30 , R 31 , R 33 and R 34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl,
  • haloalkylsulfonyl aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
  • Compounds of Formula I and Formula II would be useful in treating a variety of circulatory disorders. including cardiovascular disorders, such as hypertension, congestive heart failure and arteriosclerosis, and to treat other disorders such as glaucoma. Treatment subjects would include mammalian subjects, particularly human subjects, afflicted by or susceptible to circulatory disorders.
  • compounds of Formula I and Formula II may be used in combination with other drugs, such as a diuretic, to treat hypertension.
  • compounds of Formula I and Formula II may be used in combination with other drugs, such as a diuretic, to treat hypertension.
  • compounds of Formula I and Formula II may be used in combination with other drugs, such as a diuretic, to treat hypertension.
  • Formula I and Formula II could be used in conjunction with certain surgical procedures.
  • these compounds could be used to prevent post-angioplasty re-stenosis.
  • Compounds of Formula I and Formula II are therapeutically effective in treatment of cardiovascular disorders by acting as antagonists to, or blockers of, the angiotensin II (All) receptor.
  • Compounds of Formula I and Formula II would be therapeutically effective in treatment of the above-mentioned circulatory and cardiovascular disorders or would be precursors to, or prodrugs of, therapeutically- effective compounds.
  • acidic group selected to contain at least one acidic hydrogen atom is intended to embrace chemical groups which, when attached to any of the R 3 through R 11 positions of Formula I and Formula II, confers acidic character to the compounds of Formula I and Formula II.
  • acidic character means proton-donor capability, that is, the capacity of the compounds of Formula I and Formula II to be a proton donor in the presence of a proton-receiving substance such as water.
  • the acidic group should be selected to have proton-donor capability such that the product
  • compounds of Formula I and Formula II has a pK a in a range from about one to about twelve. More typically, the
  • Formula I and Formula II compounds would have a pK a in a range from about two to about seven.
  • An example of an acidic group containing at least one acidic hydrogen atom is carboxyl group (-COOH). Where n is zero and A is -COOH, in the -Y n A moiety, such carboxyl group would be attached directly to one of the R 3 through R 11 positions.
  • the Formula I and Formula II compounds may have one -Y n A moiety attached at one of the R 3 through R 11 positions, or may have a plurality of such -Y n A moieties attached at more than one of the R 3 through R 11 positions, up to a maximum of nine such -Y n A moieties.
  • acidic groups other than carboxyl group selectable to contain at least one acidic hydrogen atom. Such other acidic groups may be collectively referred to as
  • bioisosteres of carboxylie acid or referred to as “acidic bioisosteres”. Specific examples of such acidic
  • a more preferred class of compounds consists of those compounds of Formula II wherein m is one; wherein each of X 1 and X 2 is independently selected from oxygen atom and sulfur atom; wherein each of R 0 and R 1 is
  • alkyl independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
  • alkylcarbonyloxyalkyl alkenyl, cycloalkenyl, alkynyl and cycloalkynyl; wherein R 2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
  • cycloalkylhaloalkyl cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, araxkoxycarbonylalkyl,
  • aralkylcarbonyloxyalkyl alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio,
  • alkylsulfonyl aralkylsulfinyl, aralkylsulfonyl,
  • arylsulfinyl arylsulfonyl
  • phthalimido phthalimidoalkyl
  • heteroaryl heteroarylalkyl
  • phthalimidoalkyl heteroaryl
  • heteroarylalkyl cycloheteroalkyl
  • each of said heteroaryl- and cycloheteroalkyl- containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein R 2 may be further selected from amino and amido radicals of the formula
  • X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R 14 through R 26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
  • each of R 3 through R 11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
  • haloalkyl cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl,
  • alkoxycarbonyl alkenyl, cycloalkenyl, alkynyl, cyano. nitro, carboxyl, alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylthio, arylthio, aralkylthio, mercapto, alkylsulfonyl, aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula
  • R 3 through R 11 may be further selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R 3 through R 11 may be further
  • n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
  • each W is independently selected from oxygen atom, sulfur atom and NR 39 ; wherein each of R 35 , R 36 , R 37 , R 38 and R 39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl,
  • each of R 35 , R 36 , R 37 and R 39 may be further independently selected from amino radical of the formula wherein each of R 40 and R 41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R 40 and R 41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially
  • R 40 and R 41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; wherein each of R 36 and R 37 may be further independently selected from hydroxy, alkoxy, alkylthio, aryloxy, arylthio, aralkylthio and aralkoxy; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which heterocyclic ring contains at least one hetero atom selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R 3 through R 11 or may be attached at any two adjacent positions selected
  • alkylthiocarbonyl alkylthiocarbonyl, and amino and amido radicals of the formula
  • X is selected from oxygen atom and sulfur atom
  • R 27 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl and DR 32 and wherein D is selected from oxygen atom and sulfur atom;
  • R 32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R 27 , R 28 , R 29 , R 30 , R 31 , R 33 and R 34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl,
  • alkoxyalkyl alkanoyl, alkoxycarbonyl, carboxyl,
  • An even more preferred class of compounds consists of those compounds of Formula II wherein m is one; wherein each of X 1 and X 2 is selected from oxygen atom and sulfur atom; wherein each of R 0 and R 1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl and alkynyl with the proviso that R 0 and R 1 cannot simultaneously be hydrido; wherein R 2 is selected from alkyl, hydroxyalky
  • cycloalkylhaloalkyl cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
  • alkylcarbonyloxyalkyl alkoxycarbonylalkyl
  • mercaptocarbonyl mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl,
  • each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R 2 through R 11 may be further independently selected from amino and amido radicals of the formula
  • X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R 14 through R 26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
  • each of R 3 through R 11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
  • haloalkyl cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl,
  • n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
  • each W is independently selected from oxygen atom, sulfur atom and NR 39 ; wherein each of R 35 , R 38 and R 39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl,
  • each of R 35 and R 39 may be further independently selected from amino radical of the formula wherein each of R 40 and R 41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R 40 and R 41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms, and which heterocyclic group may be saturated or partially
  • R 40 and R 41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of
  • carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which
  • heterocyclic ring may be attached at a single position selected from R 3 through R 11 or may be attached at any two adjacent positions selected from R 3 through R 11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups;
  • Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; wherein each of R 1 through R 26 , R 35 and R 38 through R 41 , Y and A independently may be substituted at any substitutable position with one or more groups selected from alkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and
  • Formula II consists of those compounds wherein m is one; wherein each of X 1 and X 2 is independently selected from oxygen atom and sulfur atom; wherein each of R 0 and R 1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
  • R 2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
  • cycloalkylhaloalkyl cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy,
  • alkoxyalkyl alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl,
  • cycloalkylalkylthio phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl,
  • each of said heteroaryl- and cycloheteroalkyl- containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R 2 through R 11 may be further independently selected from amino and amido radicals of the formula
  • X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R 14 through R 26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
  • each of R 3 through R 11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
  • haloalkyl cycloalkyl, alkoxy, phenalkyl, phenyl, benzoyl, phenoxy, phenalkyloxy, alkoxyalkyl, alkylcarbonyl,
  • n is a number selected from zero through two, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
  • each W is independently selected from oxygen atom, sulfur atom and NR 39 ; wherein each of R 35 , R 38 and R 39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl, phenyl and benzyl; wherein each of R 35 and R 39 may be further independently selected from amino radical of the formula wherein each of R 40 and R 41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, benzyl and phenyl; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which
  • heterocyclic ring unsaturated, and which heterocyclic ring may be attached at a single position selected from R 3 through R 11 or may be attached at any two adjacent positions selected from R 3 through R 11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups;
  • Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, phenyl, phenalkyl and aralkyl; wherein each of R 1 through R 26 , R 35 and R 38 through R 41 , Y and A and independently may be substituted at any
  • alkylsulfonyl haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
  • An even more highly preferred class of compounds consists of those compounds of Formula II wherein m is one; wherein each of X 1 and X 2 is independently selected from oxygen atom and sulfur atom; wherein R 0 and R 1 is
  • alkyl independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
  • R 2 is selected from alkyl, aminoalkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
  • cycloalkylhaloalkyl cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy,
  • alkoxyalkyl acetyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
  • alkoxycarbonyloxy alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl
  • aralkylcarbonyloxyalkyl phthalimido, phthalimidoalkyl, imidazoalkyl, tetrazole, tetrazolealkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, and amino and amido radicals of the formula
  • X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R 14 through R 26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
  • each of R 3 through R 11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
  • R 3 through R 11 may be further haloalkyl, alkoxy, phenyl, benzoyl, phenoxy, alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R 3 through R 11 may be further
  • CONHOC 2 H 5 CONHCF 3 , OH, CH 2 OH, C 2 H 4 OH, OPO 3 H 2 , OSO 3 H ,
  • each of R 42 , R 43 and R 44 is independently selected from H, Cl, CN, NO 2 , CF 3, C 2 F 5 , C 3 F 7 , CHF 2 , CH 2 F, CO 2 CH 3 , CO 2 C 2 H 5 , SO 2 CH 3 SO 2 CF 3 and SO 2 C 5 F 5 ;
  • Z is selected from O, S, NR 45 and CH 2 ;
  • R 45 is selected from hydrido, CH 3 and CH 2 C 6 H 5; and wherein said acidic moiety may be a heterocyclic acidic group attached at any two adjacent positions of R 3 through R 11 so as to form a fused ring system with one of the phenyl rings of the biphenyl moiety of Formula II, said biphenyl fused ring system selected from
  • esters, amides and salts of said acidic moieties or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
  • a class of compounds of particular interest consists of those compounds of Formula II wherein m is one; wherein each of X 1 and X 2 is independently selected from oxygen atom and sulfur atom; wherein each of R 0 and R 1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert- butyl, n-pentyl, isopentyl, neopentyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclopropylmethyl, cyclopropylethyl, cyclohexylmethyl, alkoxycarbonylalkyl,
  • each of R 3 through R 11 is hydrido with the proviso that at least one of R 5 , R 6 , R 8 and R 9 is an acidic group selected from CO 2 H, SH, PO 3 H 2 , SO 3 H,
  • each of R 42 and R 43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
  • a class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein each of X 1 and X 2 is independently selected from oxygen atom and sulfur atom; wherein R 0 and R 1 is
  • n-propyl independently selected from hydrido, methyl, ethyl. n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert- butyl, 4-methylbutyl, n-pentyl, neopentyl,
  • R 2 is selected from ethyl, n-propyl, isopropyl,
  • R 3 through R 11 is hydrido with the proviso that at least one of R 5 , R 6 , R 8 and R 9 is an acidic group selected from CO 2 H, SH, PO 3 H 2 , SO 3 H, CONHNH 2 , CONHNHSO 2 CF 3 , OH,
  • each of R 42 and R 43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
  • a class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein each of X 1 and X 2 is independently selected from oxygen atom and sulfur atom; wherein each of R 0 and R 1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tertbutyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexl, cyclohexylmethyl, methoxycarbonyl- methyl, methoxycarbonylethyl, 4-hydroxy-butyl, 2- hydroxyethyl and 3-hydroxypropyl; wherein R 2 is selected from ethyl, n-propyl, is
  • a class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein X 1 is an oxygen atom and X 2 is a sulfur atom;
  • each of R 0 and R 1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexl, cyclohexylmethyl, methoxycarbonylmethyl, methoxycarbonylethyl, 4-hydroxy- butyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R 2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, ne
  • R 3 , R 4 , R 6 , R 7 , R 8 , R 10 and R 11 is hydrido; wherein one of R 5 and R 9 is hydrido and the other of R 5 and R 9 is an acidic group selected from CO 2 H and
  • a class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein X 1 is an oxygen atom and X 2 is an oxygen atom;
  • each of R 0 and R 1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexl, cyclohexylmethyl, methoxycarbonylmethyl, methoxycarbonylethyl, 4-hydroxy- butyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R 2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, ne
  • R 3 , R 4 , R 6 , R 7 , R 8 , R 10 and R 11 is hydrido; wherein one of R 5 and R 9 is hydrido and the other of R 5 and R 9 is an acidic group selected from CO 2 H and
  • hydroxido denotes a single hydrogen atom (H). This hydrido group may be attached, for example, to a oxygen atom to form a hydroxyl group; or, as another example, two hydrido groups may be attached to a carbon atom to form a -CH 2 - group.
  • alkyl is used, either alone or within other terms such as
  • alkyl embraces linear or branched radicals having one to about twenty carbon atoms or, preferably, one to about twelve carbon atoms. More preferred alkyl radicals are “lower alkyl” radicals having one to about ten carbon atoms. Most preferred are lower alkyl radicals having one to about five carbon atoms.
  • cycloalkyl embraces cyclic radicals having three to about ten ring carbon atoms, preferably three to about six carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
  • haloalkyl embraces radicals wherein any one or more of the alkyl carbon atoms is substituted with one or more halo groups, preferably selected from bromo, chloro and fluoro.
  • haloalkyl preferably selected from bromo, chloro and fluoro.
  • haloalkyl preferably selected from bromo, chloro and fluoro.
  • a monohaloalkyl group for example, may have either a bromo, a chloro, or a fluoro atom within the group.
  • Dihaloalkyl and polyhaloalkyl groups may be substituted with two or more of the same halo groups, or may have a combination of different halo groups.
  • a dihaloalkyl group may have two fluoro atoms, such as difluoromethyl and difluorobutyl groups, or two chloro atoms, such as a dichloromethyl group, or one fluoro atom and one chloro atom, such as a fluoro-chloromethyl group.
  • Examples of a polyhaloalkyl are trifluoromethyl, 1,1-difluoroethyl, 2,2,2-trifluoroethyl, perfluoroethyl and 2,2,3,3- tetrafluoropropyl groups.
  • difluoroalkyl embraces alkyl groups having two fluoro atoms substituted on any one or two of the alkyl group carbon atoms.
  • alkylol and hydroxyalkyl embrace linear or branched alkyl groups having one to about ten carbon atoms any one of which may be substituted with one or more hydroxyl groups.
  • alkenyl embraces linear or branched radicals having two to about twenty carbon atoms, preferably three to about ten carbon atoms, and containing at least one carbon-carbon double bond, which carbon-carbon double bond may have either cis or trans geometry within the alkenyl moiety.
  • alkynyl embraces linear or branched radicals having two to about twenty carbon atoms, preferably two to about ten carbon atoms, and containing at least one carbon-carbon triple bond.
  • cycloalkenyl embraces cyclic radicals having three to about ten ring carbon atoms including one or more double bonds involving adjacent ring carbons.
  • alkoxy and alkoxyalkyl embrace linear or branched oxy-containing radicals each having alkyl portions of one to about ten carbon atoms, such as methoxy group.
  • alkoxyalkyl also embraces alkyl radicals having two or more alkoxy groups attached to the alkyl radical, that is, to form monoalkoxyalkyl and dialkoxyalkyl groups.
  • alkoxy or “alkoxyalkyl” radicals may be further substituted with one or more halo atoms, such as fluoro, chloro or bromo, to provide haloalkoxy or haloalkoxyalkyl groups.
  • alkylthio embraces radicals containing a linear or branched alkyl group, of one to about ten carbon atoms attached to a divalent sulfur atom, such as a methythio group.
  • Preferred aryl groups are those consisting of one, two, or three benzene rings.
  • aryl embraces aromatic radicals such as phenyl, naphthyl and biphenyl.
  • aralkyl embraces aryl-substituted alkyl radicals such as benzyl, diphenylmethyl, triphenylmethyl, phenyl- ethyl, phenylbutyl and diphenylethyl.
  • benzyl and phenylmethyl are interchangeable.
  • aryloxy and arylthio denote radical respectively, aryl groups having an oxygen or sulfur atom through which the radical is attached to a nucleus, examples of which are phenoxy and phenylthio.
  • sulfinyl and sulfonyl denotes respectively divalent radicals SO and SO 2 .
  • aralkoxy alone or within another term, embraces an aryl group attached to an alkoxy group to form, for example, benzyloxy.
  • acyl denotes a radical provided by the residue after removal of hydroxyl from an organic acid, examples of such radical being acetyl and benzoyl.
  • “Lower alkanoyl” is an example of a more prefered sub-class of acyl.
  • amido denotes a radical consisting of nitrogen atom attached to a carbonyl group, which radical may be further substituted in the manner described herein.
  • the amido radical can be attached to the nucleus of a compound of the invention through the carbonyl moiety or through the nitrogen atom of the amido radical.
  • alkenylalkyl denotes a radical having a double-bond unsaturation site between two carbons, and which radical may consist of only two carbons or may be further substituted with alkyl groups which may optionally contain additional double-bond unsaturation.
  • heteroaryl embraces aromatic ring systems containing one or two hetero atoms selected from oxygen, nitrogen and sulfur in a ring system having five or six ring members, examples of which are thienyl, furanyl, pyridinyl, thiazolyl, pyrimidyl and isoxazolyl. Such heteroaryl may be attached as a
  • heteroaryl may be attached through a ring nitrogen atom as long as
  • radicals are those containing from one to about ten carbon atoms.
  • alkyl groups are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, methylbutyl, dimethylbutyl and neopentyl.
  • Typical alkenyl and alkynyl groups may have one unsaturated bond, such as an allyl group, or may have a plurality of unsaturated bonds, with such plurality of bonds either adjacent, such as allene-type structures, or in conjugation, or separated by several saturated carbons.
  • R 0 and R 1 substituents which are each attached to a nitrogen atom of the xanthine ring, it is preferred that certain selections of radicals for R 0 and R 1 be avoided.
  • Radicals which should preferably be avoided are alkyl, alkenyl and alkynyl moieties having a halo, hydroxy, alkoxy or double bond or triple bond attached to the alpha carbon of the moiety, that is, the carbon attached to a nitrogen atom of the xanthine ring.
  • Angiotensin II is a potent vasoconstrictor and participates in the formation of aldosterone which regulates sodium and water balance in mammals.
  • compounds of Formulas I and II are therapeutically useful in methods for treating hypertension by administering to a hypertensive patient a therapeutically-effective amount of a compound of Formula I or II.
  • hypertensive patient means, in this context, a mammalian subject suffering from or afflicted by the effects of hypertension or susceptible to a hyperten- sive condition if not treated to prevent or control such hypertension.
  • pharmaceutically- acceptable salts embraces salts commonly used to form alkali metal salts and to form addition salts of free acids or free bases.
  • the nature of the salt is not critical, provided that it is pharmaceutically-acceptable. Suitable pharmaceutically-acceptable acid addition salts of
  • compounds of Formulas I and II may be prepared from an inorganic acid or from an organic acid.
  • inorganic acids are hydrochloric, hydrobromic, hydroiodic, nitric, carbonic, sulfuric and phosphoric acid.
  • organic acids may be selected from aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic and sulfonic classes of organic acids, example of which are formic, acetic, propionic, succinic, glycolic, gluconic, lactic, malic, tartaric, citric, ascorbic, glucuronic, maleic, fumaric, pyruvic, aspartic, glutamic, benzoic, anthranilic, p-hydroxybenzoic, salicyclic, phenylacetic, mandelic, embonic (pamoic), methansulfonic, ethanesulfonic, 2-hydroxyethanesulfonic, pantothenic, benzenesulfonic, toluenesulfonic, sulfanilic, mesylic, cyclohexylaminosulfonic, stearic, algenic,
  • Suitable pharmaceutically-acceptable base addition salts of compounds of Formulas I and II include metallic salts made from aluminium, calcium, lithium, magnesium, potassium, sodium and zinc or organic salts made from N,N'- dibenzylethylenediamine, chloroprocaine, choline,

Abstract

A class of non-peptidic biphenylalkyl xanthine compounds is described for use in treatment of cardiovascular disorders. Compounds of particular interest are angiotensin II antagonists of formula (I) wherein each of X?1 and X2¿ is independently selected from oxygen atom and sulfur atom; wherein m is one; wherein each of R?0 and R1¿ is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, methoxycarbonylmethyl, methoxycarbonylethyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, 2-cyclohexylethyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3 through R11 is hydrido with the proviso that at lest one of R?5, R6, R8 and R9¿ is an acidic group selected from CO¿2?H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3, OH, NHSO2CH3, NHSO2CF3, NHCOCF3, CONHSO2C6H5, CONHOH, CONHOCH3, CONHSO2CH3 and tetrazole; or a tautomer thereof or a pharmaceutically-acceptable salt thereof. These compounds are particularly useful in treatment or control of hypertension and congestive heart failure.

Description

BIPHENYLALKYL XANTHINE COMPOUNDS FOR TREATMENT OF CARDIOVASCULAR DISORDERS
Field of the Invention
Non-peptidic biphenylalkyl xanthine compounds are described for use in treatment of cardiovascular disorders such as hypertension and congestive heart failure. Of particular interest are angiotensin II antagonist compounds having a biphenylmethyl moiety attached to the N-7 or N-9 position of the xanthine ring.
Background of the Invention The renin-angiotensin system is one of the hormonal mechanisms involved in regulation of
pressure/volume homeostasis and in expression of
hypertension. Activation of the renin-angiotensin cascade begins with renin secretion from the juxtaglomerular apparatus of the kidney and culminates in the formation of angiotensin II, an octapeptide which is the primary active species of this system. Angiotensin II is a potent vasoconstrictor agent and also produces other physiological effects such as promoting aldosterone secretion, promoting sodium and fluid retention, inhibiting renin secretion, increasing sympathetic nervous system activity, increasing vasopressin secretion, causing positive cardiac inotropic effect and modulating other hormonal systems. Previous studies have shown that antagonizing angiotensin II at its receptors is a viable approach to inhibit the renin-angiotensin system, given the pivotal role of this octapeptide which mediates the actions of the renin-angiotensin system through interaction with various tissue receptors. There are several known angiotensin II antagonists, most of which are peptidic in nature . Such peptidic compounds are of limited use due to their lack of oral bioavailability or their short duration of action. Also, commercially-available peptidic angiotensin II antagonists (e.g., Saralasin) have a significant residual agonist activity which further limit their therapeutic application.
Non-peptidic compounds with angiotensin II antagonist properties are known. For example, the sodium salt of 2-n-butyl-4-chloro-1-(2-chlorobenzyl)imidazole-5- acetic acid has specific competitive angiotensin II antagonist activity as shown in a series of binding experiments, functional assays and in vivo tests [P. C. Wong et al, J. Pharmacol. Exp. Ther., 247 (1), 1-7 (1988)]. Also, the sodium salt of 2-sbutyl-4-choloro-1-(2- nitrobenzyl)imidazole-5-acetic acid has specific
competitive angiotensin II antagonist activity as shown in a series of binding experiments, functional assays and in vivo tests [A. T. Chiu et al, European J. Pharmacol., 157, 3121 (1988)]. A family of 1-benzylimidazole-5-acetate derivatives has been shown to have competitive angiotensin II antagonist properties [A. T. Chiu et al, J. Pharmacol. Exp. Ther., 250 (3) , 867-874 (1989)]. U.S. Patent No.
4,816,463 to Blankey et al describes a family of 4,5,6,7- tetrahydro-1H-imidazo(4,5-c)-tetrahydro-pyridine
derivatives useful as antihypertensives, some of which are reported to antagonize the binding of labelled angiotensin II to rat adrenal receptor preparation and thus cause a significant decrease in mean arterial blood pressure in conscious hypertensive rats. EP No. 253,310, published 20 January 1988, describes a series of aralkyl imidazole compounds, including in particular a family of
biphenylmethyl substituted imidazoles, as antagonists to the angiotensin II receptor. EP No. 323,841, published 12 July 1989, describes four classes of angiotensin II antagonists, namely, biphenylmethylpyrroles,
biphenylmethylpyrazoles, biphenylmethyl-1,2,3-triazoles and biphenylmethyl 4-substituted-4H-1,2,4-triazoles, including the compound 3,5-dibutyl-4-[(2'-carboxybiphenyl-4- yl)methyl]-4H-1,2,4-triazole. U.S. Patent No. 4,880,804 to Carini et al describes a family of
biphenylmethylbenzimidazole compounds as angiotensin II receptor blockers for use in treatment of hypertension and congestive heart failure.
Several families of imidazo-pyridazine derivatives have been synthesized. For example, alkaline hydrolysis of 1,2,5-thiadiazole-3,4-dicarboxylic acid bishydrazide followed by a cyclization step in the presence of formic acid produced 4,7-dihydroxy- and 4,7- dichloro[4,5-d]pyridazine derivatives [I. Sekikawa,
J. Heterocyclic Chem., 6, 129-130 (1969)]. Also synthesis of imidazo-pyridazine nucleoside analogues has been described. For example, ring closure of an imidazole nucleoside produced the compound 1- (β-D- ribofuranosyl)imidazo[4,5-d]pyridazine-4,7-dione [C.
Tapiero et al, J. of Carbohydrates Nucleoside s Nncleotides,3(3), 191-195 (1976)]. In a study of chemical modification of antibiotic nucleosides, the compound 1-(2,3,5-tri-O- benzoyl-β-D-ribofuranosyl)imidazo-[4,5-d]pyridazine- 4,7(5H,7H)dione was synthesized [P.D. Cook et al, J.
Heterocyclic Chem., 15, 1 (1978)]. A series of substituted imidazo(4,5-d)pyridazines has been studied for
pharmacological properties [G. G. Ferguson et al, J. Pharm. Sci., 59(11), 1584-1586 (1970)]. A family of 4-substituted imidazo[4,5-d]pyridazines, including several 4-amino- and 4-alkylamino-1-benzyl-7-chloroimidazo[4,5-d]pyridazines, has been prepared for antitumor evaluation [J.A. Carbon, J. Am. Chem. Soc., 80, 6083-6088 (1958)]. In view of the antitumor activity of 5-amino-7-hydroxy-v- triazolo[d]pyrimidine, several 4,7-disubstituted
imidazo[4,5-d]pyridazines were synthesized including the compound 4,7-bisethylmercapto-1-ethylimidazo[4,5- d]pyridazine [R. N. Castle et al, J . Org. Chem., 23, 1534- 1538 (1958)]. Based on the antimalarial activity of certain quinoline derivatives, a family of ω- dialkylaminoalkylaminoimidazo[4,5-d]pyridazines was synthesized including, typically, the compound 4- (3- dimethylaminopropylamino)-7-chloro-1-(tetrahydro-2'- pyranyl)imidazo[4,5-d]pyridazine [N. R. Patel et al,
J. Heterocyclic Chem., 5, 13-24 (1968)].
Certain imidazo-pyridazine compounds have been described for treatment of cardiovascular disorders. For example, EP #184,738, published 18 June 1986, describes a family of 2-naphthyl-substituted imidazo [4, 5-d]pyridazin-4- on compounds having antithrombotic, cardiotonic and hypotensive properties. Japanese Patent #065,202,
published 18 March 1987, describes a family of imidazo heterocyclic carbostyril derivatives useful as cardiotonic, hypotensive and antiinflammatory agents. U.S. Patent No. 4,656,171 describes certain 2-phenyl-imidazo-pyridazines for use as cardiotonics, including a benzyloxy-substituted 2-phenyl-imidazole[4,5-c]pyridazine. U.S. Patent No.
4,722,929 describes 2-aryl-imidazo-pyridazine compounds for use as cardiotonics, including a benzyloxy-substituted 2- phenyl-4-chloro-imidazo[4,5-d] pyridazine.
Alkylated xanthine compounds are known for example, 1,3, 7, 8-alkyl-substituted xanthine compounds have been prepared by crotyl bromide alkylation of theophylline at the C8 position of the theophylline nucleus to provide, specifically, 1,3,7-trimethyl-8-crotyl-xanthine [J. Donat et al, Chim . Ber., 92, 1500-1503 (1959)]. Also, xanthines have been selectively alkylated by various benzylic halides. Specifically, a xanthine compound having a biphenylmethyl substitutent at the N7 position, namely 7- [[(1,1'-biphenyl)-4-ylJmethyl]-3,7-dihydro-1H-purine-2,6- dione, has been prepared. This compound was made to show regioselective alkylation of the xanthine nucleus [L.G. Marzilli et al, J. Am. Chem. Soc., 97(12), 3351- 3358 (1975)]. Theophylline, theobromine and other alkylated xanthines derivatives have been used for many years in various pharmaceutical applications, including the
treatment of certain cardiac conditions and as diuretics. For example. East German Patent No. 39,142 published 25 May 1965 describes certain alkylated or alkoxylated xanthines for use as heart and circulatory activators. French Patent Document No. 3586M published 8 November 1965 describes 7- (paradimethylaminobenzyl)-1,3-dimethylxanthine for use in treatment of dyspnea and asthma, and for use as a
cardiotonic and as a coronary vasodilator. U.S. Patent No. 4,061,753 describes certain alkylated xanthines, such as 7- α-ethoxybenzyl)theophylline, for use in treatment of dermal inflammation, such as psoriasis.
DESCRIPTION OF THE INVENTION A class of biphenylalkyl xanthine compounds useful in treating circulatory disorders, particularly cardiovascular disorders, is defined by Formula I:
(I)
Figure imgf000007_0001
wherein m is a number selected from one to four, inclusive; wherein the dotted line between seven- and eight-positions and the eight- and nine-positions represents optionally a double bond; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, aroylalkyl,
alkylalkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, alkenyl, cycloalkenyl, aralkoxycarbonyl, alkynyl, cyanoalkyl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, mercaptoalkyl, mercaptocarbonylalkyl,
mercaptothiocarbonylalkyl, alkylthiocarbonylalkyl, alkylthiothiocarbonylalkyl, arylthiocarbonylalkyl, arylthiothiocarbonylalkyl, aralkylthiocarbonylalkyl, alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl,
arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and radicals of the formula
Figure imgf000008_0001
wherein X is oxygen atom or sulfur atom with z being a number selected from one to four, inclusive; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R12 and R13 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein each of R2 through R11 is independently selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl. cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl,
cycloalkylcarbonyl, formyl, alkoxy, aralkyl,
aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio,
cycloalkylalkylthio, alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio,
alkylthiothiocarbonyl, alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl,
arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, alkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl,
arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl,
cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cyclohetero-containing groups has one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further independently selected from amino and amido radicals of the formula
Figure imgf000009_0001
wherein X is oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
monoalkylamino, dialkylamino, hydroxyalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R14 and R15 taken together, R16 and R17 taken together, R18 and R19 taken together, R21 and R22 taken together and R23 and R24 taken together may each form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; and wherein each of R3 through R11 may be further
independently selected from hydroxy and acidic moieties of the formula -YnA wherein n is a number selected from zero through three, inclusive, and wherein A is an acidic group selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties;
wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, alkynyl, aralkyl, hydroxyalkyl, haloalkyl, halo, oxo, alkoxy, aryloxy, aralkoxy, aralkylthio, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, aryl, aroyl, cycloalkenyl, cyano, cyanoamino, nitro, alkylcarbonyloxy, alkoxycarbonyloxy, alkylcarbonyl, alkoxycarbonyl,
aralkoxycarbonyl, carboxyl, mercapto, mercaptocarbonyl, alkylthio, arylthio, alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, aralkylsulfinyl,
aralkylsulfonyl, arylsulfinyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amino and amido radicals of the formula
Figure imgf000011_0001
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, DR32 and
Figure imgf000011_0002
wherein D is selected from oxygen atom and sulfur atom and R32 is selected from hydrido, alkyl, cycloalkyl,
cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, alkylsulfinyl, alkylsulfonyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl,
haloalkylsulfonyl, aralkyl and aryl, and wherein each of R27, R28, R29, R30, R31, R33 and R34 is further independently selected from amino and amido radicals of the formula
Figure imgf000012_0001
wherein X is oxygen atom or sulfur atom;
wherein each of R35, R36, R37, R38, R39 and R40 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl,
haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl, and wherein each of R28 and R29 taken together and each of R30 and R31 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially
unsaturated; with the proviso that R0, R1, and R2 cannot all
simultaneously be hydrido; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
With regard to the optionally-present double bond at the N7 or N8 positions within the five-membered ring-portion of the xanthine ring of Formula I, it is intended that no more than one such double bond may be present. That is, only one of the N7 or N8 atoms may have a double bond at one time. It is also intended that when the N7 atom has a double bond in the rings the depicted biphenylalkyl portion of Formula I must be attached at the other N9 atom. When the N9 atom has a double bond within the ring, the biphenylalkyl portion of Formula I is attached at the N7 atom such as depicted in Formula II, below.
A preferred class of compounds consists of those compounds of Formula I within a sub-set of compounds of Formula II:
Figure imgf000013_0001
wherein m is one; wherein each of X1 and X2 is
independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, mercaptoalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, alkylsulfonyl, aralkylsulfonyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amido radicals of the formula
Figure imgf000013_0002
wherein X is oxygen atom or sulfur atom with r being a number selected from one or two; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio,
cycloalkylalkylthio, alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio,
alkylthiothiocarbonyl, alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl,
arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, aralkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl,
arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl,
cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl- containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further independently selected from amino and amido radicals of the formula
Figure imgf000015_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
monoalkylamino, dialkylamino, hydroxyalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
haloalkyl, cycloalkyl, cycloalkylalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl,
cycloalkynyl, cyano, nitro, carboxyl, alkylcarbonyloxy, mercaptocarbonyl, mercaptothiocarbonyl, alkoxycarbonyloxy, alkylthio, alkylthiocarbonyl, alkylcarbonylthio,
alkylthiocarbonyloxy, alkylthiocarbonylthio,
alkylthiothiocarbonyl, arylthio, arylthiocarbonyl,
arylcarbonylthio, arylthiocarbonyloxy,
arylthiothiocarbonyl, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, aralkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfonyl,
aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula 14
Figure imgf000016_0001
wherein X is oxygen atom or sulfur atom;
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is an acidic group selected from acids containing one or more atoms selected from oxygen, sulfur, phosphorus and nitrogen atoms, and wherein said acidic group is selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl,
cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, haloalkyl, oxo, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, mercaptocarbonyl, alkylthio and alkylthiocarbonyl, and amino and amido radicals of the formula
Figure imgf000017_0001
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, and DR32 and
Figure imgf000017_0002
wherein D is selected from oxygen atom and sulfur atom, and R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl,
alkoxycarbonyl, carboxyl, haloalkylsulfinyl,
haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
Compounds within the foregoing classes of
Formula I and II are believed to be structurally novel when the definitions of compounds within each class are
qualified by the proviso language which excludes known compounds. All of the compounds of Formula I and II without the proviso language are believed novel for use in pharmaceutical applications, more particularly, for use in treatment of circulatory disorders.
Compounds of Formula I and Formula II would be useful in treating a variety of circulatory disorders. including cardiovascular disorders, such as hypertension, congestive heart failure and arteriosclerosis, and to treat other disorders such as glaucoma. Treatment subjects would include mammalian subjects, particularly human subjects, afflicted by or susceptible to circulatory disorders.
These compounds would also be useful as adjunctive
therapies. For example, compounds of Formula I and Formula II may be used in combination with other drugs, such as a diuretic, to treat hypertension. Also, compounds of
Formula I and Formula II could be used in conjunction with certain surgical procedures. For example, these compounds could be used to prevent post-angioplasty re-stenosis.
Compounds of Formula I and Formula II are therapeutically effective in treatment of cardiovascular disorders by acting as antagonists to, or blockers of, the angiotensin II (All) receptor. Compounds of Formula I and Formula II would be therapeutically effective in treatment of the above-mentioned circulatory and cardiovascular disorders or would be precursors to, or prodrugs of, therapeutically- effective compounds.
The phrase "acidic group selected to contain at least one acidic hydrogen atom", as used to define the -YnA moiety, is intended to embrace chemical groups which, when attached to any of the R3 through R11 positions of Formula I and Formula II, confers acidic character to the compounds of Formula I and Formula II. "Acidic character" means proton-donor capability, that is, the capacity of the compounds of Formula I and Formula II to be a proton donor in the presence of a proton-receiving substance such as water. Typically, the acidic group should be selected to have proton-donor capability such that the product
compounds of Formula I and Formula II has a pKa in a range from about one to about twelve. More typically, the
Formula I and Formula II compounds would have a pKa in a range from about two to about seven. An example of an acidic group containing at least one acidic hydrogen atom is carboxyl group (-COOH). Where n is zero and A is -COOH, in the -YnA moiety, such carboxyl group would be attached directly to one of the R3 through R11 positions. The Formula I and Formula II compounds may have one -YnA moiety attached at one of the R3 through R11 positions, or may have a plurality of such -YnA moieties attached at more than one of the R3 through R11 positions, up to a maximum of nine such -YnA moieties. There are many examples of acidic groups other than carboxyl group, selectable to contain at least one acidic hydrogen atom. Such other acidic groups may be collectively referred to as
"bioisosteres of carboxylie acid" or referred to as "acidic bioisosteres". Specific examples of such acidic
bioisosteres are described hereinafter. Compounds of
Formula I and Formula II having the -YnA moiety attached at one of positions R5, R6, R8 and R9 would be expected to have preferred properties, while attachment at R5 or R9 would be more preferred. A more preferred class of compounds consists of those compounds of Formula II wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is
independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl and cycloalkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, araxkoxycarbonylalkyl,
aralkylcarbonyloxyalkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio,
aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl,
arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl,
cycloheteroalkylalkyl and cycloheteroalklylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl- containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein R2 may be further selected from amino and amido radicals of the formula
Figure imgf000020_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
monoalkylamino, dialkylamino, hydroxyalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl,
alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano. nitro, carboxyl, alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylthio, arylthio, aralkylthio, mercapto, alkylsulfonyl, aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula
Figure imgf000021_0001
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000021_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R36, R37, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl,
cycloalkyl, cycloalkylalkyl, aryl and aralkyl; wherein each of R35, R36, R37 and R39 may be further independently selected from amino radical of the formula
Figure imgf000022_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 and R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially
unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; wherein each of R36 and R37 may be further independently selected from hydroxy, alkoxy, alkylthio, aryloxy, arylthio, aralkylthio and aralkoxy; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which heterocyclic ring contains at least one hetero atom selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; and wherein any of the foregoing R1 through R26 and R35 through R41, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl,
hydroxyalkyl, halo, oxo, haloalkyl, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, mercaptocarbonyl, alkylthio and
alkylthiocarbonyl, and amino and amido radicals of the formula
Figure imgf000023_0001
wherein X is selected from oxygen atom and sulfur atom; wherein R27 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl and DR32 and
Figure imgf000023_0002
wherein D is selected from oxygen atom and sulfur atom;
wherein R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl,
alkoxyalkyl, alkanoyl, alkoxycarbonyl, carboxyl,
haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof. An even more preferred class of compounds consists of those compounds of Formula II wherein m is one; wherein each of X1 and X2 is selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl and alkynyl with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl,
arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further independently selected from amino and amido radicals of the formula
Figure imgf000025_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
monoalkylamino, dialkylamino, hydroxyalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl,
alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, alkylthio, aralkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000025_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl,
cycloalkylalkyl, aryl and aralkyl; wherein each of R35 and R39 may be further independently selected from amino radical of the formula
Figure imgf000026_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 and R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms, and which heterocyclic group may be saturated or partially
unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of
carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which
heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and A independently may be substituted at any substitutable position with one or more groups selected from alkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof. A highly preferred class of compounds within
Formula II consists of those compounds wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl and alkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy,
alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl,
carboxyalkyl, alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl, mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio,
cycloalkylalkylthio, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl,
cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl- containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further independently selected from amino and amido radicals of the formula
Figure imgf000028_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
haloalkyl, cycloalkyl, alkoxy, phenalkyl, phenyl, benzoyl, phenoxy, phenalkyloxy, alkoxyalkyl, alkylcarbonyl,
alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through two, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000029_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl, phenyl and benzyl; wherein each of R35 and R39 may be further independently selected from amino radical of the formula
Figure imgf000029_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, benzyl and phenyl; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially
unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, phenyl, phenalkyl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and A and independently may be substituted at any
substitutable position with one or more groups selected from alkyl, cycloalkyl, cycloalkylalkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro,
alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof. An even more highly preferred class of compounds consists of those compounds of Formula II wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is
independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl and alkynyl; where R2 is selected from alkyl, aminoalkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy,
alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, mercaptoalkyl, mercaptocarbonyl,
alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl,
aralkylcarbonyloxyalkyl, phthalimido, phthalimidoalkyl, imidazoalkyl, tetrazole, tetrazolealkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, and amino and amido radicals of the formula
Figure imgf000031_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino,
hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo,
haloalkyl, alkoxy, phenyl, benzoyl, phenoxy, alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties consisting of CO2H, CO2CH3, SH, CH2SH, C2H4SH, PO3H2, NHSO2CF3,
NHSO2C6F5, SO3H, CONHNH2, CONHNHSO2CF3, CONHOCH3,
CONHOC2H5, CONHCF3, OH, CH2OH, C2H4OH, OPO3H2, OSO3H ,
Figure imgf000032_0001
wherein each of R42, R43 and R44 is independently selected from H, Cl, CN, NO2, CF3, C2F5, C3F7, CHF2, CH2F, CO2CH3, CO2C2H5, SO2CH3 SO2CF3 and SO2C5F5; wherein Z is selected from O, S, NR45 and CH2; wherein R45 is selected from hydrido, CH3 and CH2C6H5; and wherein said acidic moiety may be a heterocyclic acidic group attached at any two adjacent positions of R3 through R11 so as to form a fused ring system with one of the phenyl rings of the biphenyl moiety of Formula II, said biphenyl fused ring system selected from
Figure imgf000033_0001
and the esters, amides and salts of said acidic moieties; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
A class of compounds of particular interest consists of those compounds of Formula II wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert- butyl, n-pentyl, isopentyl, neopentyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclopropylmethyl, cyclopropylethyl, cyclohexylmethyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, buten-2-yl, 3-butenyl, butyn-2-yl, butyn-3-yl, haloloweralkyl and hydroxyloweralkyl; wherein R2 is selected from methyl, ethyl, n-propyl, isopropyl, n- butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, isopentyl, neopentyl, phenyl, cyclohexyl, cyclohexylmethyl, CH3CH=CH-CH2, SC3H7, cyclohex-3-en-1-yl, SC4H9,
CH2S , CH3CH=CH, CH2=CH-CH2, CH3CH2CH2CH=CH-, amino,
Figure imgf000034_0002
alkoxy, aminomethyl, aminoethyl, aminopropyl, CH2OCOCH3, CH2CI, CH2OCH3, CH2OCH(CH3)2, CH2CO2H, CH(CH3)CO2H,
-CH2OCOCH2CH2 -CH2CH2CH2CO2H, -CH2CH2F, -CH2CH2CH2F,
Figure imgf000034_0003
-CH2ONO2, -CH2SH, -CH2O > CF3, CH2OH, hydroxyalkyl,
Figure imgf000034_0004
halo, 1-oxo-2-phenylethyl, 2-cyclohexylethyl,
3-cyclohexylpropyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexanoyl, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl and
difluoromethyl; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H,
CONHNH2, CONHNHSO2CF3, OH,
Figure imgf000034_0001
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
A class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is
independently selected from hydrido, methyl, ethyl. n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert- butyl, 4-methylbutyl, n-pentyl, neopentyl,
cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl,
methoxycarbonylmethyl, methoxycarbonylethyl, 4- hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein
R2 is selected from ethyl, n-propyl, isopropyl,
n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, 2-phenylethyl, 2-cyclohexylethyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3- butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3, OH,
Figure imgf000035_0001
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
A class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tertbutyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexl, cyclohexylmethyl, methoxycarbonyl- methyl, methoxycarbonylethyl, 4-hydroxy-butyl, 2- hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3- butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000036_0001
N or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
A class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein X1 is an oxygen atom and X2 is a sulfur atom;
wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexl, cyclohexylmethyl, methoxycarbonylmethyl, methoxycarbonylethyl, 4-hydroxy- butyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2-phenylethyl, 3-phenylpropyl,
cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000037_0001
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
A class of compounds of more particular interest consists of those compounds of Formula II wherein m is one; wherein X1 is an oxygen atom and X2 is an oxygen atom;
wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexl, cyclohexylmethyl, methoxycarbonylmethyl, methoxycarbonylethyl, 4-hydroxy- butyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2-phenylethyl, 3-phenylpropyl,
cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000037_0002
or a tautomer thereof or a pharmaceutically-acceptable salt thereof. The term "hydrido" denotes a single hydrogen atom (H). This hydrido group may be attached, for example, to a oxygen atom to form a hydroxyl group; or, as another example, two hydrido groups may be attached to a carbon atom to form a -CH2- group. Where the term "alkyl" is used, either alone or within other terms such as
"haloalkyl" and "hydroxyalkyl", the term "alkyl" embraces linear or branched radicals having one to about twenty carbon atoms or, preferably, one to about twelve carbon atoms. More preferred alkyl radicals are "lower alkyl" radicals having one to about ten carbon atoms. Most preferred are lower alkyl radicals having one to about five carbon atoms. The term "cycloalkyl" embraces cyclic radicals having three to about ten ring carbon atoms, preferably three to about six carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. The term "haloalkyl" embraces radicals wherein any one or more of the alkyl carbon atoms is substituted with one or more halo groups, preferably selected from bromo, chloro and fluoro. Specifically embraced by the term "haloalkyl" are monohaloalkyl, dihaloalkyl and polyhaloalkyl groups. A monohaloalkyl group, for example, may have either a bromo, a chloro, or a fluoro atom within the group. Dihaloalkyl and polyhaloalkyl groups may be substituted with two or more of the same halo groups, or may have a combination of different halo groups. A dihaloalkyl group, for example, may have two fluoro atoms, such as difluoromethyl and difluorobutyl groups, or two chloro atoms, such as a dichloromethyl group, or one fluoro atom and one chloro atom, such as a fluoro-chloromethyl group. Examples of a polyhaloalkyl are trifluoromethyl, 1,1-difluoroethyl, 2,2,2-trifluoroethyl, perfluoroethyl and 2,2,3,3- tetrafluoropropyl groups. The term "difluoroalkyl" embraces alkyl groups having two fluoro atoms substituted on any one or two of the alkyl group carbon atoms. The terms "alkylol" and "hydroxyalkyl" embrace linear or branched alkyl groups having one to about ten carbon atoms any one of which may be substituted with one or more hydroxyl groups. The term "alkenyl" embraces linear or branched radicals having two to about twenty carbon atoms, preferably three to about ten carbon atoms, and containing at least one carbon-carbon double bond, which carbon-carbon double bond may have either cis or trans geometry within the alkenyl moiety. The term "alkynyl" embraces linear or branched radicals having two to about twenty carbon atoms, preferably two to about ten carbon atoms, and containing at least one carbon-carbon triple bond. The term
"cycloalkenyl" embraces cyclic radicals having three to about ten ring carbon atoms including one or more double bonds involving adjacent ring carbons. The terms "alkoxy" and "alkoxyalkyl" embrace linear or branched oxy-containing radicals each having alkyl portions of one to about ten carbon atoms, such as methoxy group. The term
"alkoxyalkyl" also embraces alkyl radicals having two or more alkoxy groups attached to the alkyl radical, that is, to form monoalkoxyalkyl and dialkoxyalkyl groups. The
"alkoxy" or "alkoxyalkyl" radicals may be further substituted with one or more halo atoms, such as fluoro, chloro or bromo, to provide haloalkoxy or haloalkoxyalkyl groups. The term "alkylthio" embraces radicals containing a linear or branched alkyl group, of one to about ten carbon atoms attached to a divalent sulfur atom, such as a methythio group. Preferred aryl groups are those consisting of one, two, or three benzene rings. The term "aryl" embraces aromatic radicals such as phenyl, naphthyl and biphenyl. The term "aralkyl" embraces aryl-substituted alkyl radicals such as benzyl, diphenylmethyl, triphenylmethyl, phenyl- ethyl, phenylbutyl and diphenylethyl. The terms "benzyl" and "phenylmethyl" are interchangeable. The terms
"aryloxy" and "arylthio" denote radical respectively, aryl groups having an oxygen or sulfur atom through which the radical is attached to a nucleus, examples of which are phenoxy and phenylthio. The terms "sulfinyl" and "sulfonyl", whether used alone or linked to other terms, denotes respectively divalent radicals SO and SO2 . The term "aralkoxy", alone or within another term, embraces an aryl group attached to an alkoxy group to form, for example, benzyloxy. The term "acyl" whether used alone, or within a term such as acyloxy, denotes a radical provided by the residue after removal of hydroxyl from an organic acid, examples of such radical being acetyl and benzoyl. "Lower alkanoyl" is an example of a more prefered sub-class of acyl. The term "amido" denotes a radical consisting of nitrogen atom attached to a carbonyl group, which radical may be further substituted in the manner described herein. The amido radical can be attached to the nucleus of a compound of the invention through the carbonyl moiety or through the nitrogen atom of the amido radical. The term "alkenylalkyl" denotes a radical having a double-bond unsaturation site between two carbons, and which radical may consist of only two carbons or may be further substituted with alkyl groups which may optionally contain additional double-bond unsaturation. The term "heteroaryl" embraces aromatic ring systems containing one or two hetero atoms selected from oxygen, nitrogen and sulfur in a ring system having five or six ring members, examples of which are thienyl, furanyl, pyridinyl, thiazolyl, pyrimidyl and isoxazolyl. Such heteroaryl may be attached as a
substituent through a carbon atom of the heteroaryl ring system, or may be attached through a carbon atom of a moiety substituted on a heteroaryl ring-member carbon atom, for example, through the methylene substituent of
imidazolemethyl moiety. Also, such heteroaryl may be attached through a ring nitrogen atom as long as
aromaticity of the heteroaryl moiety is preserved after attachment. For any of the foregoing defined radicals, preferred radicals are those containing from one to about ten carbon atoms. Specific examples of alkyl groups are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, methylbutyl, dimethylbutyl and neopentyl. Typical alkenyl and alkynyl groups may have one unsaturated bond, such as an allyl group, or may have a plurality of unsaturated bonds, with such plurality of bonds either adjacent, such as allene-type structures, or in conjugation, or separated by several saturated carbons. For the R0 and R1 substituents which are each attached to a nitrogen atom of the xanthine ring, it is preferred that certain selections of radicals for R0 and R1 be avoided. Radicals which should preferably be avoided are alkyl, alkenyl and alkynyl moieties having a halo, hydroxy, alkoxy or double bond or triple bond attached to the alpha carbon of the moiety, that is, the carbon attached to a nitrogen atom of the xanthine ring.
Compounds of Formulas I and II have been found to inhibit the action of angiotensin II in mammals.
Angiotensin II is a potent vasoconstrictor and participates in the formation of aldosterone which regulates sodium and water balance in mammals. Thus, compounds of Formulas I and II are therapeutically useful in methods for treating hypertension by administering to a hypertensive patient a therapeutically-effective amount of a compound of Formula I or II. The phrase "hypertensive patient" means, in this context, a mammalian subject suffering from or afflicted by the effects of hypertension or susceptible to a hyperten- sive condition if not treated to prevent or control such hypertension.
Also included in the family of compounds of Formulas I and II are isomeric forms including
diastereoisomers, regioisomers and the pharmaceutically- acceptable salts thereof. The term "pharmaceutically- acceptable salts" embraces salts commonly used to form alkali metal salts and to form addition salts of free acids or free bases. The nature of the salt is not critical, provided that it is pharmaceutically-acceptable. Suitable pharmaceutically-acceptable acid addition salts of
compounds of Formulas I and II may be prepared from an inorganic acid or from an organic acid. Examples of such inorganic acids are hydrochloric, hydrobromic, hydroiodic, nitric, carbonic, sulfuric and phosphoric acid.
Appropriate organic acids may be selected from aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic and sulfonic classes of organic acids, example of which are formic, acetic, propionic, succinic, glycolic, gluconic, lactic, malic, tartaric, citric, ascorbic, glucuronic, maleic, fumaric, pyruvic, aspartic, glutamic, benzoic, anthranilic, p-hydroxybenzoic, salicyclic, phenylacetic, mandelic, embonic (pamoic), methansulfonic, ethanesulfonic, 2-hydroxyethanesulfonic, pantothenic, benzenesulfonic, toluenesulfonic, sulfanilic, mesylic, cyclohexylaminosulfonic, stearic, algenic,
β-hydroxybutyric, malonic, galactaric and galacturonic acid. Suitable pharmaceutically-acceptable base addition salts of compounds of Formulas I and II include metallic salts made from aluminium, calcium, lithium, magnesium, potassium, sodium and zinc or organic salts made from N,N'- dibenzylethylenediamine, chloroprocaine, choline,
diethanolamine, ethylenediamine, meglumine (N-methylglucamine) and procaine. All of these salts may be prepared by conventional means from the corresponding compound of Formula I or II by reacting, for example, the appropriate acid or base with the compound of Formula I or II. A family of specific compounds of particular interest within Formula I and Formula II consists of the following compounds:
8-butyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-ρropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-cycloρroρylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-ethyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biρhenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-methyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-isopropyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isoρropyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8 -neopentyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-proρyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8 -neopentyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-neopentyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl] -1H-purine-2, 6- dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3, 7-dihydro-1-methyl-7- [ [2'- (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione;
8-propyl-3, 7-dihydro-1, 3-dimethyl-7- [ [2 '- (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-propyl-3, 7-dihydro-1-methyl-3-propyl-7- [ [2 '- (1H-tetrazol-
5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione; 8-propyl-3, 7-dihydro-1-methyl-3-isobutyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6 - dione;
8-propyl-3, 7-dihydro-1-methyl-3-phenyl-7- [ [2 '- (1H-tetrazol- 5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-propyl-3, 7-dihydro-1-methyl-3-cyclopropylmethyl-7- [ [2 ' -
(1H-tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-
2, 6-dione;
8-propyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2, 6-dione;
8-ethyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-(iphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2, 6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-p-urine-2,6-dione; 8-methyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-isopropyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isoproρyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]met4yl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-neopentyl-3, 7-dihydro-1-methyl-3-ethyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-neopentyl-3, 7-dihydro-1-methyl-3-propyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-neopentyl-3, 7-dihydro-1-methyl-3-isobutyl-7- [ [2 ' - (1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methyl-3)cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-neopentyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-diethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1,3-diethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purinee2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-ρhenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-pentyl-3, 7-dihydro-1, 3-diethyl-7- [ [2 ' - (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-ethyl-3, 7-dihydro 1-ethyl-3-methyl-7- [ [2'- (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione;
8-ethyl-3, 7-dihydro-1, 3-diethyl-7- [ [2 '- (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione;
8-ethyl-3, 7-dihydro-1-ethyl-3-isobutyl-7- [ [2 '- (1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethy1-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1'-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-methyl-3, 7-dihydro-1, 3-diethyl-7- [ [2'- (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-ddone; 8-methyl-3, 7-dihydro-1-ethyl-3-propyl-7- [ [2 ' - (1H-tetrazol-
5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-methyl-3, 7-dihydro-1-ethyl-3-isobutyl-7- [ [2 ' - (1H- tetrazdl-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1,3-diethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-ylt(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1,3-diethyl-7-[[2'-(1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-propyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-isoρropyl-3, 7-dihydro-1-ethyl-3-isobutyl-7- [ [2 '- (1H- tetrazol-5-yl)(1,1'-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-isopropyl-3, 7-dihydro-1-ethyl-3-methoxyethyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopyntyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3, 7-dihydro-1-ethyl-3-methyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6 - dione;
8-neopentyl-3,7-dihydro-1,3-diethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetr-zol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-cycloρropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1,3-diρropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-propyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-proρyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yllmethyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-diine; 8-ethyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1Hhtetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethy1-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-methyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydrop1,3-dipropyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-isopropyl-3, 7-dihydro-1, 3-dipropyl-7- [ [2' - (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-isopropyl-3, 7-dihydro-1-propyl-3-phenyl-7-[ [2 ' - (1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-iso ropyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-l-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-neopentyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-propyl-3-carbomlthoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-diisobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-butyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-[ [2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1,3-diisobutyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydr3-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[(2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-y1)(1,1'-biphenyl)-4-y1]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1,3-diisobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl 3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1,3-diisobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethy1-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-ethyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3, 7-dihydro-1, 3-diisobutyl-7- [ [2 '- (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione;
8-methyl-3, 7-dihydro-1-isobutyl-3-phenyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H- urine-2, 6- dione;
8-methyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1,3-diisobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-
(1H-tetraz-l-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3, 7-dihydro-1-isobutyl-7- [ [2 '- (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-isopropyl-3, 7-dihydro-1-isobutyl-3-methyl-7- [ [2 '- (1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1,3-diisobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-isopropyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neoρentyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1,3-diisobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2 ' - (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-butyl-3, 7-dihydro-1-phenyl-3-methyl-7- [ [2 '- (1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-diphenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-3-phenyl-7-[[2 ' -(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-propyl-3, 7-dihydro-1-phenyl-3-propyl-7- [ [2 ' - (1H-tetrazol-
5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-propyl-3, 7-dihydro-1, 3-diphenyl-7- [ [2 '- (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-propyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-y1]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-diphenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-ρhenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3, 7-dihydro-1-phenyl-7- [ [2'- (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-methyl-7- [ [2 '- (1H-tetrazol-
5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-propyl-7- [ [2 ' - (1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1,3-diphenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-ethyl-3,7-dihydro-1-phenyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3, 7-dihydro-1-phenyl-3-methoxyethyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-ethyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(-,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1,3-diphenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione; 8-cyclohexyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1,3-diphenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1,3-diphenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-isopropyl-3, 7-dihydro-1-phenyl-3-phenyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6 - dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dion ;
8-isopropyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3, 7-dihydro-1-phenyl-3-carbomethoxymethyl-7-
[ [2 '- (1H-tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H- purine-2, 6-dione;
8-neopentyl-3, 7-dihydro-1-phenyl-7- [ [2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1,3-diphenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2, - dione; 8-neopentyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7- [[2'-(1H-petrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)
4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione; 8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5 yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)- 4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-cycloρropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3, 7-dihydro-1-cyclopropylmethyl-3-methyl-7- [ [2 ' -
(1H-tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-
2, 6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-71[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-bichenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3- methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl] -1H-purine-2, 6-dione; 8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-yiphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1,3-dicyclopropylmethyl-7-[[2 ' -(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-p-rine-2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purin -
2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-pentyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-methoxyethy1-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8- entyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2 '-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-ethyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-n-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-isopropyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethy--3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-neopentyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl] 1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-propyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxyaethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione; 8-ethyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dιone;
8-methyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7-
[[2'- 1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-
(1H-tet-azol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yi]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-isopropyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-meth1xyethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyll-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1,3-dimethoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2, 6-dione;
8-neopentyl-3, 7-dihydro-1-methoxyethyl-3-phenylethyl-7-
[ [2 '- (1H-tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-neoρentyl-3, 7-dihydro-1-methoxyethyl-3-methoxyethyl-7-
[ [2 ' - (1H-tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H- purine-2, 6-dione; 8-neopentyl-3,7-dihydro-1-methoxyethyl-3- carbomethoxymethyl-7-[ [2 ' - (1H-tetrazol-5-yl) (1, 1 '- biphenyl) -4-yl]methyl] -1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl -1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7-
[[2'-(1Hetetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione; 8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-r-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione; 8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)- 4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1Hepurine- 2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2*- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethy1-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethy1-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)- 4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-ethyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'-(1H- tetraz1l-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3- phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3- methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7- [[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihy ro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)- 4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3- methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione; 8-neopentyl-3,7-dihydro-1,3-dicarbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-buty1-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-buty1-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dirydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-1-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-methyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-isopropyl-3, 7-dihydro-1-methyl-7- [ [2 ' - (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione;
8-isopropyl-3, 7-dihydro-1-ethyl-7- [ [2 '- (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione;
8-isopropyl-3, 7-dihydro-1-propyl-7- [ [2 ' - (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione; 8-isopropyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2, one;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-btphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-butyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-proρyl-3-methyl-7-[[2'-(1H-tetrazol-
5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H-tetrazol-
5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-m-thyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-methyl-7-[ [2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3, 7-dihydro-1-carbomethoxymethyl-3-methyl-7- [ [2 ' -
(1H-tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine- 2, 6-dione; 8-ethyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)51,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2' -(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphen yl]-1H-purine-2, 6-dione;
8-methyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dionn; 8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3, 7-dihydro-1-propyl-3-methyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-cyclohexyl-3, 7-dihydro-1-isobutyl-3-methyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2, - dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-neopentyl-3, 7-dihydro-1-propyl-3-methyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)o1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-buty1-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-butyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-ethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-isobutyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenyl-3-ethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-pentyl-3,7-dihydro-1-propyl-3-ethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenyl-3-ethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-ethyl- , 7-dihydro-1-phenyl-3-ethyl-7- [ [2 ' - (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-ethyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3, -dihydro-1-methyl-3-ethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-ethyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-methyl-3, 7-dihydro-1-isobutyl-3-ethyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-methyl-3, 7-dihydro-1-phenyl-3-ethyl-7- [ [2 '- (1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1-propyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3, 7-dihydro-1-phenyl-3-ethyl-7- [ [2 '- (1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-ethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3, 7-dihydro-1-methyl-3-ethyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-isopropyl-3, 7-dihydro-1-propyl-3-ethyl-7- [ [2 '- (1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione; 8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]mtthyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-ethyl-7-[[2' (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-ethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-ethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-ethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-propyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyle-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3, 7-dihydro-1-ethyl-3-proρyl-7- [ [2 '- (1H-tetrazol- 5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-pentyl-3, 7-dihydro-1-isobutyl-3-propyl-7- [ [2 '- (1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3, 7-dihydro-3-propyl-7- [ [2 ' - (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-ethyl-3, 7-dihydro-1-methyl-3-propyl-7- [ [2 '- (1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione 8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-proρyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-methyl-3, 7-dihydro-1-isobutyl-3-propyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione; 8-methyl-3, 7-dihydro-1-phenyl-3-propyl-7- [ [2 ' - (1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purne-2,6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,-6- dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3, 7-dihydro-1-phenylethyl-3-propyl-7- [ [2 '- (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione; 8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazolr5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-neopentyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-propyl-7-
[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3lpropyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-propyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-butyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro 3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione; 8-propyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl -4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-methyl-3, 7-dihydro-1-ethyl-3-isobutyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-methyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-cyclohexyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-yyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-isopropyl-3, 7-dihydro-1-methyl-3-isobutyl-7- [ [2'- (1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isoproρyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-isopropyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-el]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1,3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-isobutyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-isobutyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione; 8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-isobutyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3, 7-dihydro-1-isobutyl-3-phenyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-propyl-3, 7-dihydro-1, 3-phenyl-7- [ [2 ' - (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]mthyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1,3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl]-1H-purine-2, 6-dione;
8-ethyl-3, 7-dihydr3-1-methyl-3-phenyl-7- [ [2 '- (1H-tetrazol- 5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-ethyl-3, 7-dihydro-1-ethyl-3-phenyl-7- [ [2 '- (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-ethy1l3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1,3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6 dione; 8-methyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1,3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6- ione;
8-methyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1,3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isoproρyl-3,7-dihydro-1,3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-isopropyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neop ntyl-3,7-dihydro-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1,3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-butyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-buphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione; 8-propyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihndro-1-isobutyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-pentyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]-ethyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione; 8-methyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3 7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)- 4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-cyclohexyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]mtthyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)- 4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-5-7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-isopropyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-cyclopropylmethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- diote;
8-neopentyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-cyclopropylmethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-propyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-cyclopropylmethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-cyclopropylmethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-cyclopropylmethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-cyclopropylmethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3- cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-
4-yl]methyl]-1H-purine-2,6-dione; 8-butyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]meth l]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-propyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-l-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-y1)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-ρhenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]m-thyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-methyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6 - dione;
8-methyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl-methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3, 7-dihydro-1-methoxyethyl-3-phenylethyl-7- [ [2 ' -
(1H-tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-
2, 6-dione;
8-methyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-di-ydro-1-methoxyethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3- phenylethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2 ' -(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-phenylethyl-7- tetrazol-5-yl)(1,1'-bipheny l]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-phenylethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-phenylethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-phenylethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-phenylethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3-phenylethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3-phenylethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-butyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2 6-dione;
8-butyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-propyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2 ' -(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-pur ne-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-cyclopropyImethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine--,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3, 7-dihydro-1-phenyl-3-methoxyethyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-methyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-phe yl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-methyl-3, 7-dihydro-1-carbomethoxymethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1;-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3- methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-carbomethoxymethyl-3- methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-isopropyl-3, 7-dihydro-1-phenyl-3-methoxyethyl-7- [ [2 ' - (1H- tetrazol-5-yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6 - dione; 8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-carbomethoxymethyl-3- methoxyethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-3-methoxyethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-propyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-methoxyethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-methoxyethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-cyclopropylmethyl-3-methoxyethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-methoxyethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-carbomethoxymethyl-3- methoxyethyl-7- [ [2 ' - (1H-tetrazol-5-yl) (1, 1 ' -biphenyl) -4- yl]methyl] -1H-purine-2, 6-dione; 8-butyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-meyhyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7-
[[2 '-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3, 7-dihydro-1-ethyl-3-carbomethoxymethyl-7- [ [2 ' - (1H-tetrazol-5-yl) (1, 1' -biphenyl) -4-yl]methyl] -1H-purine-
2, 6-dione; 8-propyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-cyclopropylmethyl-3-carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-ethyl-3-carbomethoxymeth l-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-pentyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione; 8-pentyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- teyrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-ethyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-ethyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-ethyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-ethyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-ethyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-methyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-methyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-methyl-3,7-dihydro-1-cyclopropylmethyl-3-carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-methyl-3,7-dihydro-1-methoxyethyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-cyclohexyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-phenylethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methoxyethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-isopropyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-isopropyl-3,7-dihydro-1-cyclopropylmethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl- 7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-isopropyl-3,7-dihydro-1-methoxyethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dioee;
8-neopentyl-3,7-dihydro-3-carbomethoxymethyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-neopentyl-3,7-dihydro-1-methyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-ethyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-propyl-3-carbomethoxymethyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-isobutyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenyl-3-carbomethoxymethyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3, 7-dihydro-1-cyclopropylmethyl-3
carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-phenylethyl-3-carbomethoxymethyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-neopentyl-3,7-dihydro-1-methoxyethyl-3- carbomethoxymethyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 4'-[[8-propyl-1,2,3,6-tetrahydro-3-(methyl)-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-propyl-1,2,3,6-tetrahydro-3-(propyl)-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-propyl-1,2,3,6-tetrahydro-1-methyl-3-2,6-dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-propyl-1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-propyl-1,2,3,6-tetrahydro-1-methyl-3-propyl-2,6- dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylie acid;
4'-[[8-propyl-1,2,3,6-tetrahydro-1-propyl-2,6-dioxo-7H- purin-7-yl]methyl] [1, 1 ' -biphenyl-2-carboxylic acid;
4 '- [ [8-propyl-1, 2, 3, 6-tetrahydro-1-propyl-3-methyl-2, 6- dioxo-7H-purin-7-yl]methyl] [1, 1 ' -biphenyl-2-carboxylic acid;
4'-[[8-propyl-1,2,3,6-tetrahydro-1,3-dipropyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-3-(methyl)-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-3-(propyl)-2,6-dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-1-methyl-3-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylie acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-1-methyl-3-propyl-2,6- dioxo-7H-purin-7-yl]methyl] [1, 1 ' -biphenyl-2-carboxylic acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-1-propyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-1-propyl-3-methyl-2,6- dioxo-7H-purie-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-butyl-1,2,3,6-tetrahydro-1,3-dipropyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid; 4'-[[8-pentyl-1,2,3,6-tetrahydro-3-(methyl)-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-pentyl-1,2,3,6-tetrahydro-3-(propyl)-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-pentyl-1,2,3,6-tetrahydro-1-methyl-3-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-pentyl-1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-pentyl-1,2,3,6-tetrahydro-1-methyl-3-propyl-2,6- dioxo-7H-purin-7-yl]methyl][1, '-biphenyl-2-carboxylic acid;
4'-[[8-pentyl-1,2,3,6-tetrahydro-1-propyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-pentyl-1,2,3,6-tetrahydro-1-propyl-3-methyl-2,6- dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-pentyl-1,2,3,6-tetrahydro-1,3-dipropyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-3-(methyl)-2,6-dioxo- 7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-3-(propyl)-2,6-dioxo- 7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-1-methyl-3-2,6-dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-1,3-dimethyl-2,6- dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-1-methyl-3-propyl-2,6- dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-1-propyl-2,6-dioxo-7H- purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-1-propyl-3-methyl-2,6- dioxo-7H-purin-7-yl]methyl][1,1'-bipheny1-2-carboxylie acid; 4'-[[8-cyclohexyl-1,2,3,6-tetrahydro-1,3-dipropyl-2,6- dioxo-7H-purin-7-yl]methyl][1,1'-biphenyl-2-carboxylic acid;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-buty1-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyL-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-buty1-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-butyl-3, 7-dihydro-3-propyl-7- [ [2' - (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-butyl-3, 7-dihydro-1-propyl-7- [ [2 ' - (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-butyl-3, 7-dihydro-1-methyl-7- [ [2 ' - (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl)-6-oxo-2-thioxo-1H-purine;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-buty1-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-butyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-thione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-thione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-cyclohexyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1 1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-cyclohexyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl- 7-[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione; 8-cyclohexyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-thione;
8-cyclohexyl-3, 7-dihydro-1-methyl-3- (cyclopropyl-methyl) -7- [ [2 '- (1H-tetrazol- -yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H- purine-2, 6-thione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-cyclohexyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-lH-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-
[ [2 ' - (1H-tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H- purine-2, 6-dione; 8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methhl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-pentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-pentyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione; 8-pentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-pentyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-thione;
8-pentyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-thione; 8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(propen-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-bi henyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3- methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(propen-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-(buten-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3- methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-
[[2'-y1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-IH- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H- tetrazol-5-yl )(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3- methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7- [[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-(buten-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7- [[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl7methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-thione;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-
1H-purine;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-propyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine; 8-propyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-propyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione; 8-propyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-propyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-propyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione; and 8-propyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione.
A family of compounds of more particular interest within Formula II consists of the following compounds:
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methye]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-r,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl ) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5 yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]y1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-
1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione; 8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-cyclohexyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3, 7-dihydro-3-propyl-7-[ [2 ' - (1H-tetrazol-5- yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-cyclohexyl-3, 7-dihydro-1-propyl-7- [ [2 ' - (1H-tetrazol-5- yl) (1, 1 '-biphenyl) -4-yl]methyl] -1H-purine-2, 6-dione;
8-cyclohexyl-3, 7-dihydro-1-methyl-7- [ [2 ' - (1H-tetrazol-5- yl) (1, 1 ' -biphenyl) -4-yl]methyl] -6-oxo-2-thioxo-1H-purine; 8-cyclohexyl-3, 7-dihydro-1-methyl-7- [ [2 ' - (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-puriny-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine
2,6-dione;
8-cyclohexyl-3,7-dihydro-1-(2-hydroxyethyl)-l-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-thione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-thione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-cyclohexyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1,3-dimethyl-7d[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol- 5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-pentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-pentyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-l-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-pentyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(propen-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2, 6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione; 8-(propen-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-l-yl)-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(propen-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-
5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-l-yl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione; 8-(buten-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-
7-[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-l-yl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione; 8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H- purine;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-propyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-1-(3-hydroxyproρyl)-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3, 7-dihydro-1- (2-carbomethoxy-ethyl) -3-methyl-7- [ [2' - (1H-tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6- dione;
8-propyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-(1H- tetrazol-5-yl) (1, 1 ' -biphenyl) -4-yl]methyl] -1H-purine-2, 6 - dione;
8-propyl-3, 7-dihydro-1-propyl-3-methyl-7- [ [2 ' - (1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-proρyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-propyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-propyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(lH-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione; and
8-propyy-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione.
A family of compounds of even more particular interest within Formula II consists of the following
compounds: 8-(buten-2-yl)-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine; and
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione. GENERAL SYNTHETIC PROCEDURES
The compounds of the invention can be synthesized in accordance to the following procedures which are modeled upon a subset of biphenylmethyl carboxylic acid or
biphenylmethyl tetrazole compounds of the family of compounds of Formula II. The reactions are performed in a solvent appropriate to the reagent and material employed and suitable to the transformation being performed. Some of the steps will involve reagents and substrates with functionality that will require protection. For the synthetic description and examples which follow, abbreviations which have been used have the following meanings:
CHCl 3 = chloroform
DMF = dimethylformamide
DMSO = dimethylsulf oxide
g = gram
MeOH = methanol
min = minute
h = hour
mol = mole
mmol = millimole
mw = molecular weight
TIC = thin layer chromatography
Trt = trityl
AIBN = 2, 2 ' -azobisisobutyronitrile
KtBuO = potassium t-butoxide
Other abbreviations may be explained in the text. A. Synthesis of the xanthine nuclei.
A versatile general synthesis of the purines involves cyclization of the appropriate 4,5-diaminouracil to complete the purine ring. The cyclization of the appropriate aromatic diamine can be accomplished with a rather large number of reagents, ring closure of the purine ring can occur by the action of numerous reagents and the appropriate
4,5-diaminopyrimidine. The method of preparation of a
4,5-diaminopyrimidine followed by cyclization to give a purine is referred to as the Traube synthesis, since Wilhelm Traube was responsible for most of the early work. The starting 1,3-dialkyl-4,5-diaminouracil 4 have been prepared from N,N'-dialkylureas 1 and cyanoacetic acid. The condensation between N,N'-dialkylureas 1 and cyanoacetic acid to give the 1,3-dialkyl-4-aminourocil 2 is best performed by heating at a temperature between 30° and 80°C equimolecular amounts of the starting materials in the presence of two equivalents of acetic anhydride in acetic acid as solvent for several hours.
The formation of the 1,3-dialkyl-4-aminouracile 2 can also be catalyzed by a base such as sodium ethoxyde in a wet solvent such as ethanol. In the latter case, the reaction is normally brought about at reflux temperature of ethanol for 10-30 hours. Usually when R0 and R1 have not the same value, a mixture of isomeric 1,3-dialkyl-aminouracile 2 is formed. The two isomeric compounds may be present in any ratio depending upon the nature of the R1, R2 substituants (J. H. Speer et al., J. Am . Chem. Soc., 75, 114-115, 1953). The aminouracile compounds can be converted to the corresponding 1,3-dialkyl-5-nitroso-4-aminouracile 3.
derivative by treatment of the uracile with an inorganic nitrite salt in a solvent or mixture of solvents such as water, alcohol, acetic acid, dimethylformamide or dioxane. The reaction is preferably performed at a temperature between 0°C and room temperature. The nitrosoaminouracile derivative 3 can be reduced to the 4,5-diamino uracile 4 with the help of hydrogen in the presence of a hydrogenation catalyst such as Raney nickel, platinum or palladium on charcoal, with metals such as iron, tin or zinc in the presence of an acid, with salt such as iron (II) sulfate, tin (II) chloride or with sodium dithionite or sodium hyposulfite in a solvent such as water, water/ethanol, methanol, glacial acetic acid, ethyl acetate or dimethylformamide at temperatures between 0°C and 50°C but preferably at a temperature around room temperature.
The subsequent cyclocondensation reaction toward the 1,3,8-trisubstituted xanthine 5 is carried out by heating at elevated temperatures, between 110° and 300°C, a mixture of one part of diaminouracile 4 wwith about four parts of a carboxylic acid of formula R-CO2H (wherein R is the
substituant to be introduced at the 8 position of the
resulting xanthine). The reaction last for a period of time between 30 min and 48 hrs, depending on the temperature at which it is performed.
The preparation of xanthine 6 (Scheme 2) which is substituted with an hydride group on the N-l nitrogen, follows essentially the same procedure as described above in scheme 1 with the notable exception that the cyclization of a monoalkyl urea 7 to the aminouracile is better performed in the presence of a base, such as sodium ethoxide in an inert solvent such as ethanol. Advantageously, the reaction mixture is heated for several hours, if required to reflux under an inert anhydrous atmosphere to complete the reaction.
Another route to trialkylxanthine nuclei 5 is derived from the method reported by J. Donat and E. Carstens
(Cham . Bar., 92, 1500-1504, 1959). The treatment of
theophylline 8 with crotylbromide afford in modest yield
8-crotylitheophylline 9. The reaction is carried out with crotylbromide on chloride as the alkylating agent,
advantageously in a solvent or mixture of solvents such as methylene chloride, dioxane, water or dimethylformamide in the presence of a base such as an hydroxyde or a carbonate salt of an alkali, triethylamine or sodium hydride, preferably at temperatures between room temperature and 50°C. The double bond in 9 can be reduced to a single bond (as in 10),
preferably with hydrogen in the presence of a hydrogenation catalyst such as Raney Nickel, platinum or palladium on charcoal in a solvent such as ethanol, methanol, ethylacetate or acetic acid at temperatures ranging between 0°C and 50°C.
B. Synthesis of biphenyltetrazoly l derivatives
In Scheme 4, a biphenylcarboxylic acid ester 11 is converted to the cyanoderivative 12 by a method described by J. A. Krynitsky et al [org. Synth. Coll., 3, 698 (1955)] and J. Cason [Org. Synth. Coll., 3, 169 (1955)]. The acid obtained by saponification of ester 11 is transformed into the acid chloride which in turn is converted into the primary carboxamide eventually dehydrated to cyano derivative 12. The cyano derivative 12 is reacted by a 1,3-dipolar cycloaddition with trialkyltin azide to produce the corresponding tetrazole 13 as described by K. Sisido et al [J . organomgtal. Chem., 33, 337-46 (1971)]. The reaction is advantageously performed with an excess of the trialkyltin azide in refluxing toluene or dimethylformamide as inert solvent. The N-(trimethyl- stannyl) tetrazole 13 can be converted to the free tetrazole by bubbling dry gaseous hydrochloric acid in an ethereal or alcoholic solution or by treatment with aqueous sodium hydroxyde. Intermediate free tetrazole is reacted with an aralkylhalide, such as trityl chloride, which will provide a removable protecting group for the tetrazole. This reaction is best performed with trityl chloride in an inert solvent such as dichloromethane in the presence of at least one equivalent of a non-nucleophilic base such as pyridine or a trialkylamine. The bromination of 14 into the benzyl bromide 15 is performed with N-bromosuccinimide in the presence of AIBN or dibenzolyperoxide in an inert solvent such as carbon tetrachloride, the reaction medium being heated at a
temperature from 40°C to reflux of the solvent used. In some cases, it is advantageous to convert the cyanoderivative 12 into the corresponding 4-bromomethyl-2-cyano-biphenyl 16. The bromination is performed according to the procedures described above for the conversion of 14 to 15.
The 4-bromomethyl-2'-cyano-(1,1'biphenyl) derivative 16 may further be converted to the azide derivative 17 by heating at a temperature between 80°C and 120°C a mixture of 16 and of an inorganic azide salt in a high boiling solvent (preferably polar) or mixture of solvents such as dimethylformamide, toluene, xylene, N-methylpyrididone isopropanol or water. The azide 17 can be reduced to the amine 18 preferably with hydrogen in the presence of an hydrogenation catalyst such as platinum or palladium on charcoal in a solvent or mixture of solvents such as methanol, ethanol, chloroforme or acetic acid at temperatures ranging between 20°C and 50°C. C. Alkylation of the xanthine nuclei
The conversion of xanthine compounds to compound of Formula I is carried out by alkylation at the N-7 nitrogen with a derivative of type 15 as the alkylating agent (Scheme 6). The leaving group in 15 can be an halogen (with the exception of fluorine) group, a tosylate or a mesylate;
preferably a bromine atom is the leaving group. The reaction solvent can be methylene chloride, tetrahydrofurane, dioxane, water, dimethylformamide or dimethylsulfoxide and the presence of an acid binding agent such as sodium, potassium or cesium carbonate, sodium hydroxyde, triethylamine, potassium t- butoxyde, sodium hydride is required. The reaction is best performed at a temperature between 0°C and 120°C.
The alkylated xanthine derivative 17 can then be deprotected to the compounds of Formula II. A suitable method as described by Greene in "Protective Group in Organic
Synthesi s " Wiley-Interscience, 1980, can be used to remove the triphenylmethyl group. Such methods include hydrogenation in the presence of a catalyst such as palladium or platinum and hydrolysis under basic or acidic conditions. The reaction is performed in a solvent or a mixture of solvents such as acetone, water, glacial acetic acid, a lower alcohol
preferably at temperatures between 0°C and 100°C, for example at temperatures between room temperature and 50°C.
Another route to compounds of Formula II involves the alkylation with a biphenylnitrile derivative 16 of a xanthine derivative 5 or 10 (Scheme 6). The leaving group in 16 can be an halogen (with the exception of fluorine) group, a tosylate or a mesylate; preferably a bromine atom is the leaving group. The reaction solvent can be methylene
chloride, acetonitrile, tetrahydrofurane, dioxane, water. dimethylformamide or dimethylsulfoxide and the presence of an acid binding agent such as sodium, potassium or cesium carbonate, sodium hydroxyde, triethylamine, potassium
t-butoxyde, sodium hydride is required. The reaction is best performed at a temperature between 0°C and 120°C. The alkylated xanthine derivative 19 can then be transformed into a compound of Formula I by converting the . cyanide group into a tetrazole. Trialkyltinazide (K. Sisido, J. Organometal Chem., 33, 337-66, 1971) is preferably used in a high boiling temperature solvent.. The N(trimethylstanyl) intermediate is converted to the free tetrazole by the action of dilute acid. The tetrazole can also be generated by heating the cyanide derivative 19 with sodium oxide acid amonium chloride in dimethylformamide at a temperature close to reflux
temperature.
Another synthesis for compounds of Formula II utilizes the 4-amino-5-methoxycarbonyl-imidazole derivatives 24 as a pivotal intermediate. The imidazoles 24 are available from Thorpe-Ziegler cyclization of appropriate cyano
derivatives 23 as described in Scheme 5. N'- cyanoacetimidoester 21 are available from the reaction between an imidate hydrochloride 20 [P. Reynard and R. C. Moreau,
Bull. Soc. Chem. Fr., 2997, 1964] and cyanoamidine following the general procedures described by W. Lowski in Synthesis, 1971, 263 or K. R. Huffman and F. R. Schaefer in J. Org.
Chem., 28, 1816 (1963). From the reaction between the
cyanoimidate 21 and a 4-aminomethyl-2'-cyano-(1,1'-biphenyl) derivative, 18, the N' -cyanoamidine 22 is isolated. The reaction is advantageously carried out in a solvent or mixture of solvents such as methylene chloride, chloroforme, methanol, ethanol, acetonitrile or dimethylformamide in the presence of a non-nucleophilic inorganic base such as sodium carbonate or a tertiary organic base such as triethylamine. diisopropylethylamine or pyridine which may simultaneously act as the solvent, at temperatures between -25°C and 250°C, but preferably at temperatures between -10°C and the boiling point of the solvent which is used. Reaction between the
cyanoamidine 22 and α-bromo or α-chloro-ethylacetate in dimethylformamide or acetonitrile in the presence of a non- nucleophilic base such as potassium carbonate or trietlylamine at temperatures between 60-80°C (as described by K. Gewald and G. Heinhold in Monatshefte für Chemie, 107, 1413-21 (1976)) provide the N, N-dialkyl-N'-cyanoamidine 23. The derivative
23 can be converted to the 4-amino-5-alcoxycarbonyl-imidazole
24 under base catalysis. Preferably a base such as sodium or potassium alcoholate is used in a solvent or a mixture of solvents such as methanol, ethanol, t-butanol,
dimentylformamide or tetrahydrofurane at temperatures between 20°C and the boiling temperature of the solvent which is used.
The imidazole derivatives 24 are precursors to the xanthine derivatives 25. Reactions of 24 with isocyanate and thioisocyanite (R'-NCX wherein, R' and have the values in Formula I) take place very readily usually at temperatures ranging between 50°C and 150°C in solvents or mixture of solvents such as dimethylformamide, xylene, toluene preferably in the presence of a organic tertiary base such as
trietylamine or pyridine, which can also be used as solvent, and/or of a alkali salt of a lower alkyl alcohol. The xanthines 25 can be transformed into compounds of Formula II by transformations similar to those described in scheme 3.
SCHEME 1
Figure imgf000189_0001
i. NC-CH2-CO2H ii. HNO2. iii. PtO2, H2. iv. C4H9CO2H
SCHEME 2
Figure imgf000190_0001
i. NCCH2CO2H, NaOEth; HNO2. ii. PtO2, H2. iii. C4H9CO2H
SCHEME 3
Figure imgf000190_0002
i. Crotyl bromide; base. ii. Hydrogen gas 45psi; Pd on C. SCHEME 4
Figure imgf000191_0001
SCHEME 5
Figure imgf000192_0001
R0 andX2 have the previously defined values of Formula I SCHEME 6
Figure imgf000193_0001
Formula II compound wherein R0, R1 and R2 have the previously defined values. The following examples are provided to illustrate the present invention and are not intended to limit the scope thereof. Those skilled in the art will readily understand that known variations of the conditions and processes of the following preparative procedures can be used to prepare these compounds. All temperatures expressed are in degrees centigrade.
Example 1
Figure imgf000195_0001
8-(2E-butenyl)-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) [1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione;
Step A: 8-crotyl-theophylline
A mixture of 60g sodium methylate, 180g theophylline and one liter of methanol was stirred for 2 hr at 40°C. After removal of the solvent in vacuo, 750 ml water and 150g crotyl bromide were added and the mixture was stirred for 6 hours. A precipitate is filtered off, washed with methanol. The methanol filtratre was concentrated to a solid which was recrystallized from boiling water to yield 4g of the desired product (m.p.: 230-235°C).
1H NMR (CDCI3, δppm): 5.7 (m, 2H); 3.65 (s, 3H);
3.6 (d, 2H); 3.45 (s, 3H); 1.95 (bs, 1H, exchangeable); 1.72 (m, 3H). Elemental analysis (Calcd for C11H14N4O2, found):
C, 56.40, 56.23; H, 6.02, 5.98; N, 23.91, 23.69. Ste p B: 8-(2E-butenyl) -3,7-dihydro-1,3-dimethyl-7-[[2'-(N- triphenylmethyl-1H-tetrazol -5-yl) [1,1'-biphenyl]-4- yl]methyl]-1H-purine-2,6-dione An aliquot of 0.5g (2.1 mmol) of 8-crotyl- theophilline was dissolved in 35 ml of dry dimethylformamide and 2.3 ml of a 1N solution of potassium t-butoxide in tetrahydrofuran were added. After stirring at 25°C for 10 min., 1.6 g (2.8 mmol) of N-triphenylmethyl-5- [2(4'- bromomethylbiphenyl-2-yl] tetrazole were added at once. The mixture was stirred at 25°C for 16 hr. After removal of the solvents, the residue was partitioned between chloroform and water and the organic phase purified by chromatography on a silicagel column. (eluant: 10% ethyl acetate in
dichloromethane). The desired product was obtained in a yield of 65% (1g).
1H NMR (CDCI3, δ ppm): 7.95 (d, 1H, JHH = 7 Hz); 7.45 (m, 2H); 7.5-6.95 (unresolved signals, 20H); 5.45 (m, 4H); 3.62 (s, 3H); 3.4 (s, 3H); 3.3 (d, 2H); 1.65 (d, 3H).
Step C: 8-(2E -butenyl)-3,7-dihydro-1,3-dimethyl-7-[[2'-91H- tetrazol -5-yl)[1,1'-biphenl] -4-yl]methyl]-1H-Purine-2,6-dione The protected tetrazole derivative isolated in step b was stirred for 16 hr in 25 ml acetic acid containing 10% water. After removal of the solvent, the residue was disolved in ethyl acetate and the desired product precipitated with hexane. The filtered solid (m.p. = 187.5-187.6°C) weighed 450 mg. 1 H NMR (δ ppm, DMSO): 7.5-7.7 (unresolved signals; 4H); 7.11 (AB quartet, 4H0); 5.6 (s, 2H); 3.23 (s, 3H); 3.45 (s, 3H); 2.65 (t, 2H); 1.5 (m, 2H); 1.3 (m, 2H; 0.85 (t, 3H). FAB MS (M+H) : 469.
Elemental analysis (C25 H24N8O2)
C H N
Theory: 64.01 5.16 23.91
Found: 63.92 5.19 23.46
Example 2
Figure imgf000198_0001
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione;
Step A: 8-butyl-3,7-dihydro-1,3-di menthyl-7-1H-purine-2,6- dione
An aliquot of the 8-crothyl theophilline obtained in step a) of Example 4 was hydrogenated (3 hr, 45 psi H2) in 200 ml C2H5OH and 0.8g of 10% Pd/C catalyst. After filtering out the catalyst, the crude product was identified as the desired material (m.p.: 232-235°C).
Step B: 8-butyl-3,7-dihydrom-1,3-dimethyl-7-[[2'-(N- triphenylmethyl-1H-tetrazol-5-yl) [1,1'-biphenyl]-4- yl]methyl]-1H-purine-2,6-dione.
A mixture of 0.5g (2.1 mmol) of 8-butyltheophylline (from step a), 25 ml dry dimethylformamide, and 2.4 ml in potassium t-butoxide in tetrahydrofuran were stirred for 10 min at 25°C. N-triphenylmethyl-5-[2(4'-bromomethylbiphenyl-2- yl] tetrazole (1.8g, 3.15 mmol at 70%) was added and the reaction stirred at 25°C for 16 hr. After removal of the solvents, the residue was chromatographyed on silicagel gel using 5% ethyl acetate in chloroform as the eluant. The product eluted after ~400 ml of eluate and isolated as an oil after removal of the solvent. 1 H NMR (CDCI3, δ ppm): 7.9 (d,
1H), 7.45 (m, 2H); 7.4-6.9 (unresolved signals; 20H); 5.45 (s, 2H); 3.6 (s, 3H); 3.4 (s, 3H); 2.6 (t, 2H); 1.6 9m, 2H); 1.3 (m, 2H; 1.85 (t, 3H).
The protected tetrazole derivative isolated in step b was stirred for 16 hr in 25 ml acetic acid containing 10% water. After removal of the solvent, the residue was disolved in ethyl acetate and the desired product precipitated with hexane. The filtered solid (m.p. = 187.5-187°C) weighed 450 mg.
1H NMR (δ ppm, DMSO) : 7.5-7.7 (unresolved signals; 4H); 7.11 (AB quartet, 4H; 5.6 (s, 2H); 3.23 (s, 3H); 3.45 (s, 3H); 2.65 (t, 2H); 1.5 (m, 2H); 1.3 (m, 2H; 0.85 (t, 3H).
FAB MS (M+H) : 469.
Elemental analysis (C25H26N8O2)
C H N
Theory: 63.81 5.57 23.81
Found: 63.42 5.67 23.42
Example 3
Figure imgf000200_0001
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) [1,1-biphenyl]-4-yl]methyl]-1H-purine-6-one-2-thione
This compound was prepared following the procedure of Example 2.
1H(NMR, 350 MHz, CDCI3): δ 8.05 (d, 1H); 7.6 (m,2H); 7.4
(d,1H); 7.2 (AB quartet; 1H); 5.55 (S,2H); 4.05 (t,2H); 3.3
(5,3n); 2.75 (t,2H); 1.75 (m;6H); 1.4 (m,3H); 0.95 (m, 6H). mp (0°) = 144.6-152.4.
FAB MS: 499. HRMS: calcd for C27H30N8O2 499.2570 (M+H; found: 499.2563.
Example 4
Figure imgf000201_0001
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) [1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione;
This compound was prepared in an analogous manner. 1H NMR (350 MHz, CDCI3) : δ 8.10 (d, 1H); 7.6 (m,2H); 7.4
(ol,2H); 7.2 (AB quartet; 4H); 7.55 (s,2H); 3.9 (t,2H); 3.9 (t,2H); 3.55 (t,2H); 1.7 (unresolved signals; 6H); 1.42 (m,2H); 0.95 (m, 6H). mp (°C) = 175.9 - 176.3.
FAB MS = 498.59 (M+H+).
Example 5
Figure imgf000202_0001
8-butyl-3, 7-dihydro-1, 3-diproρyl-7- [ [2 ' - (1H-tetrazol-5-yl) [1, 1 ' -biphenyl] -4-yl]methyl-1H-purine-2, 6-dione.
Step A: 1, 3-dipropyl-6-aminouracil Stoichiometric quantities (2.95g) of di-n- propylurea (5g) and of cyanoacetic acid were heated with 10ml of acetic anhydride and 10cc of acetic acid for three hours at 60°C. Acetic acid and excess anhydride were then removed under reduced pressure without raising the temperature of the reaction mixture. The residue was dissolved in about 100cc of water, made alkaline with sodium carbonate and boiled for about two hours. The products crystallized on cooling giving white solid collected by filtration. 1H NMR (δ ppm, CDCI3):
4.95 (1H, s); 3.85 (2H+2H,m); 1.7 (2H, m); 1.6 (2H, m); 1.0 (3H, t); 0.95 (3H, t). Step B: 1,3-dipropyl-5-nitroso-6-aminouracil
To an ice-cold solution of 4g of the 1,3-dipropyl- 6-aminouracil prepared as above in 40% HOAC, were added dropwise 2g of sodium nitrite in 10 mL of H2O. The reaction mixture turned purple and after a few minutes a precipitate formed, which was filtered and dried to yield 4g of
nitrosouracil. Step C: 1,3-dipropyl-5,6-diamino uracil
A solution of 4g of 1,3-dipropyl-5-nitroso-6-amino uracil in was stirred under atm H2 pressure over platinum oxide. After completion (1h) of hydrogenation, the catalyst was removed by filtration under nitrogen and the solvent evaporated in vacuo. The crystals were dried overnight in a vacuum dessicator, at 50°C. Yield: 3g.
Step D: 8-n-butyl-1,3-dipropyl xanthine,
A mixture of 3g of 1.3-dipropyl-5, 6-diaminouracil was heated at 150-160°C for 4 hrs. The reaction mixture was cooled to 25°C and aqueous solution of sodium hydrogeno carbonate was added until alkaline. A brown precipitate formed which was filtered, dried and recrystallized from hexane. This yielded lg of slightly yellow solid.
Step E : 8-buty -3,7-dihydro-1,3-dipropyl-7-([[2'-N- triphenylmethyl,-1H-tetrazol-5-yl) [1,1'-biphenyl]-4- yl]methyl]-1H-purine -2,6-dione.
A mixture of 1g of 8-n-butyl-1,3-dipropyl xanthine, 1g of 4-bromo methyl-2'-cyano-biphenyl acid and 1.5 gof potassium carbonate were stirred in 25ml acetonitrile at 60°C1 for 12 hrs. The solids were removed by filtration, and the residue concentrated under vacuum. Chromatography on SiO2 with a 3:7 mixture of ethylacetate:hexane provided 1.92g of a yellow oil.
1H NMR (CDCl3, δ ppm): 7.75 (d,1H); 7.65 (t, 1H); 7.55 (d, 2H, Jkh = 7Hz); 7.45 (m, 2H); 7.3 (d, 2H; JHH = 7Hz); 5.6 (S, 2H); 4.12 (t, 2H) 3.95 (t, 2H); 2.7 (t, 2H); 1.85 (m, 2H); 1.7 (m, 4H); 1.35 (m, 2H); 0.95 (m, 9H).
Step F: 8-buty -3.7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-
5-yl) [1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione. To the product (1.92g) isolated in step e above, were added 1.2g of trimethyltinazide in 50 ml toluene. The mixture was stirred at reflux temperature for 4 days. The toluene was removed under vacuum and 50 ml ethanol were added. Dry gazeous HCl was bubbled through the solution for 15 min and let stir for 3 hrs. After aqueous work-up, the final product was chromatographied on SiO2 with 5% ethylacetate in hexane and then 100% ethylacetate (chromatotron). The resulting oil was dissolved in 1% NaOH (80 ml) and then acidified to pH 4 with concentrated HCl under good stirring to obtain a white precepitate. The solids were collected by filtration and dried. Yield: 1.5g of a white powder (m.p. = 60 - 63°C).
Elemental analysis (C29H34N8O2.0.3 H2O):
C H N
Theory: 65.46 6.55 21.06
Found: 65.22 6.51 20.33
1 H NMR (CDCI3 δ ppm): 8.1 (d, 1H, JHH = 7Hz); 7.6 (m, 2H); 7.4 (d, 1H, JHH = 7Hz); 7.15 (m, 4H); 5.5 (s, 2H); 4.1 (t, 2H); 3.9 (t, 2H); 2.7 (t, 2H); 1.8 (m, 2H) ; 1.7 (m, 4H); 1.4 (m, 2H); 0.95 (m, 9H).
Example 6
Figure imgf000206_0001
8-(2E-butenyl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione
This compound was prepared in a manner analogous to Example 2.
1H NMR(350 MHz, CDCI3): δ 8.00 (d, 1H); 7.55 (m,2H); 7.4
(d,2H); 5.45 (s,2H); 3.9 (d,2H); 3.27 (s,3H); 2.15 (2H, 1H); 1.65 (m, 2H); 1.4 (m,2H); 0.9 (m, 9H).
mp (°C) = 165.1-166.3.
Elemental Analysis (C28H32N8O2)
C H N
Theory: 65.60 6.29 21.86
Found: 65.65 6.35 21.65 Example 7
Figure imgf000207_0001
8-butyl-3,7-dihydro-1-cyclopropylmethyl-3-methyl-7- [[2'-(1H- tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6- dione.
Step A: 1(3)-methyl-3(1)cyclgpropylmethyl-6-amino uracil.
Cyanoacetic acid (32.5g, 0.38 mol), acetic
anhydride (1 mole, 102g) and N-isopropylmethyl-N'-methyl urea (50g, 0.38mol) were mixed in 120 ml glaceal acetic acid and stirred at 60°C for 3 hrs. The reaction mixture was
concentrated, 800ml H2O and NaHCO3 added to pH=8. The resulting mixture was stirred at 80°C for 3 hrs. Upon cooling tan crystals deposited which were filtered and dried. By TLC SiO2 MeOH/CHCl3 1/10), this solid (50g; mp 86-99°C) was a mixture of the two isomers. 13 C 1H NMR indicate a ratio about 2:1 in favor of the 1-cyclopropyl-3-methyl-isomer.
1 H NMR (CDCl3, δ ppm): 5.75 (bs, 2H); 4.75 (s, 1H); 3.6 (d, 2H); 3.05 (s, 3H); 1.0 (m, 1H); 0.05-0.15 (m, 5H). 13C (CDCI3, δ ppm): 163.6; 154.9; 152.5; 77.4; 45.86; 28.091; 10.5; 4.1 (3-methyl-1-cyclopropylmethyl-6-aminouracil). 1H NMR (CDCI3 , δ ppm) : 5.75 (bs, 2H) ; 4 .75 (s, 1H) ; 3.55 (d, 2H) ; 3.15 (s, 3H) ; 1.0 (m, 1H) ; 0.05-0.15 (m, 5H) . 13C (CDCI3, δ ppm): 163.5; 155.37; 152.6; 77.4; 45.58; 29.7; 10.3; 4.4-(1-methyl-3-cyclopropylmethyl-6-aminouracil).
Step B : 1(3)-methyl-3(1)-cyclopropylmethyl-5-nitroso-6- aminonracil
To an ice-cold solution of 10g (0.1 mole) of the mixture of isomeric amino uraciles isolated above in 40% acetic acid was added dropwise 7.6g (0.11 mole) of sodium nitrite in 10 ml water. The reaction mixture turned purple and after a few minutes a precipitate formed, which was filtered and dried to yield 19g of nitrosouracil.
Step C: 1(3)-methyl-3(1)-cyclopropylmethyl-5,6-diaminouracil To a suspension in 100 ml hot water of 10g (0.045 mole) of the mixture of isomers obtained in step a, 18g of sodium hydrosulfite were added. After a few minutes an additional 1.4g was added to complete discoloration of the solution. After standing 15 hr at 4°C, a tan precipitate was collected and air dried.
Step D: 8-butyl-3,7-dihydro -1(3)-methyl-3(1)-cyclopropyl- methyl-1H-purine-2,6-dione An aliquot (5g) of the diaminouracils from step e was stirred with 25 ml valeric acid at 160°C for 60 hr. The excess valeric acid was distilled off and diethyl ether added to the residue. A beige precipitate (2g) was collected, which identified as the 5-acylamino derivatives (J. Ruttink, Rec. Trav. Chim. 65, 751 (1946)). This solid was then stirred at 120°C in 40 ml sodium hydroxyde 30% for 1 hr. Water was added to dissolve most of the material. A small insoluble fraction was filtered off and acid was added to the filtrate (pH=3). The precipitate which formed was isolated and dried. Protron NMR still indicated the 2:1 mixture of isomers.
1H NMR (CDCl3, δ ppm): 4.05 + 3.95 (d + d, 2H); 3.65 + 3.47 (s + s; 3H); 2.87 (m, 2H); 1.8 (m, 2H), 1.4 (m, 2H).
Step E : 8-butyl -3,7-dihydro-3(1)-cyclopropylmethyl-1(3)- methyl-7-[[2'-(N-triphenylmethyl-1H-tetrazol-5-yl) [1,1'- biphenyl]-4-yplmethyl]-1H purine-2,6-dione A mixture of 555 mg (2 mmol) of the xanthine isomers mixture from step d, of 1.25g (2.1 mmol) of N- triphenylmethyl-5- [2- (4'-bromomethyl biphenyl-2-yl]tetrazole and 0.5g potassium carbonate (3.6 mmol) were stirred in 15 ml acetonitrile at 100-110°C for 3 hr. The solid were filtered off and the filtrate concentrated under vacuum. The resulting oil was chromatographied on SiO2 with 2.5% ethylacetate in chloroforme which yielded 0.7g of the mixture of the two xanthine isomers. Step F: 8-butyl-3,7-dihyriro-3 (1) -cyclopropylmethyl-1 (3) - methyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yllmethyl]-
1H purine-p2,6-dione
The material isolted in step e was dissolved in 25 ml acetic acid containing 10% water. After stirring for 16 hr, the mixture was lyophilized and the resulting mixture purified by reverse phase high performance liquid
chromatography (C18, Acetonitrile/water: 45/55). The first eluting isomer (130 mg, m.p. = 117-122°C) was identified as the 1-cyclopropylmethyl-3-methyl isomer on basis of the proton NMR spectrum. 1H NMR (CDCl3, δ ppm): 8.0 (d, 1H); 7.6 (m, 2H); 7.4 (d, 1H); 7.1 (m, 4H); 5.5 (s, 2H); 3.85 (d, 2H); 3.55 (s, 3H); 2.7 (t, 2H); 1.75 (m, 2H); 1.4 (m, 2H); 0.9 (t, 3H); 0.2 (m, 5H).
HRMS (C28H30O2N8):
Theory: 511.2570
Found: 511.2542;
Example 8
Figure imgf000211_0001
8-butyl-3,7-dihydro-1-methyl-3-cyclopropylmethyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6- dione.
The slow eluting isomer of the mixture synthesized in Example 7 was isolated in a 110 mg. yield and characterized as follows: 1H NMR (CDCI3, δ ppm): 8.05 (d, 1H); 7.6 (m, 2H);
7.4 (d, 1H); 7.15 (m, 4H); 5.5 (s, 2H); 4.05 (d, 2H); 3.3 (s, 3H); 2.7 (t, 2H); 1.75 (m, 2H); 1.4 (m, 2H); 0.9 (t, 3H); 0.25
(m, 5H).
HRMS (C28H30O2N8):
Theory: 511.2570
Found: 511.2595; Example 9
Figure imgf000212_0001
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione;
This compound was prepared in an analogous manner to Example 2.
1H NMR(350 MHz, CDCI3: δ 8.05 (d,2H); 7-7.6 (unresolved signals; 12H); 5.5 (s,2H); 3.3 (s,3H); 2.6 (t,2H); 1.6 (m,2H); 1.3 (m,2H); 0.45 (t,3H) .
mp (°C) = 125-128.
Elemental Analysis (C30H28O2.0.1H2O):
C H N
Theory: 65.44 5.49 20.35
Found: 65.22 5.23 20.03 Example 10
Figure imgf000213_0001
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1' biphenyl]-4-yl]methyl]-1H-purine-2,6-dione;
1H NMR (300 MHz, CDCI3): δ 9.89 (S,1H), 7.90 (D, 1H), 7.45 (M,2H), 7.25 (M,1H), 6.95 (s,4H), 5.34 (s,2H), 4.00 (t,2H), 2.70 (t,2H), 1.88-1.60 (m, 4H), 1.40 (m,2H), 1.00-0.85 (m, 6H) mp (°C) = 203.2, 203.3, 204.8.
Example 11
Figure imgf000214_0001
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione;
1H NMR (300 MHz, DMSO): δ 7.72-7.65 (m,2H), 7.60-7.50 (m,2H), 7.20-7.05 (dd,4H), 5.50 (s,2H), 3.88 (t,2H), 2.63 (t,2H), 1.68 (m,2H), 1.55 (m,2H), 0.87 (m, 6H) . mp (°C) = 228.3-228.5 HRMS (C26H28N8O2, M + H).
Theory: 471.2257
Found: 471.2291
Example 12
Figure imgf000215_0001
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) [1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione;
1H NMR (300 MHz, DMSO): δ 7.75-7.50 (m, 4H), 7.20-7.04 (dd, 4H), 5.59 (s,2H), 3.95 (t,2H), 3.25 (s,3H), 2.65 (t,2H), 1.73 (m,2H), 1.58 (m,2H), 0.90 (m, 6H) . mp (°C) = 122.6-122.7 mp (°C) : 122.6-122.7
Elemental Analysis (C26H28N8O2.1.25H2O):
C H N
Theory: 61.61 6.02 22.10
Found: 61.82 6.15 21.78
BIOLOGICAL EVALUATION
Assay A: Angiotensin II Binding Activity Compounds of the invention were tested for ability to bind to the smooth muscle angiotensin II receptor using a rat uterine membrane preparation. Angiotensin II (All) was purchased from Peninsula Labs. 125I-angiotensin II (specific activity of 2200 Ci/mmol) was purchased from Du Pont-New England Nuclear. Other chemicals were obtained from Sigma Chemical Co. This assay was carried out according to the method of Douglas et al [Endocrinology, 106, 120-124 (1980)].
Rat uterine membranes were prepared from fresh tissue. All procedures were carried out at 4°C. Uteri were stripped of fat and homogenized in phosphate-buffered saline at pH 7.4 containing 5 mM EDTA. The homogenate was centrifuged at 1500 x g for 20 min., and the supernatant was recentrifuged at
100,000 x g for 60 min. The pellet was resuspended in buffer consisting of 2 mM EDTA and 50 mM Tris-HCl (pH 7.5) to a final protein concentration of 4 mg/ml. Assay tubes were charged with 0.25 ml of a solution containing 5 mM MgCl2, 2 mM EDTA,
0.5% bovine serum albumin, 50 mM Tris-HCl, pH 7.5 and 125I-AII (approximately 105 cpm) in the absence or in the presence of unlabelled ligand. The reaction was initiated by the addition of membrane protein and the mixture was incubated at 25°C for 60 min. The incubation was terminated with ice-cold 50 mM Tris-HCl (pH 7.5) and the mixture was filtered to separate membrane-bound labelled peptide from the free ligand. The incubation tube and filter were washed with ice-cold buffer. Filters were assayed for radioactivity in a Micromedic gamma counter. Nonspecific binding was defined as binding in the presence of 10 μM of unlabelled All. Specific binding was calculated as total binding minus nonspecific binding. The receptor binding affinity of an All antagonist compound was indicated by the concentration (IC50) of the tested All antagonist which gives 50% displacement of the total
specifically bound 125I-AII from the high affinity All receptor. Binding data were analyzed by a nonlinear least- squares curve fitting program. Results are reported in
Table I.
Assay B: In Vitro Vascular Smooth Muscle-Response for All
The compounds of the invention were tested for antagonist activity in rabbit aortic rings. Male New Zealand white rabbits (2-2.5 kg) were sacrificed using an overdose of pentobarbital and exsanguinated via the carotid arteries. The thoracic aorta was removed, cleaned of adherent fat and connective tissue and then cut into 3-mm ring segments. The endothelium was removed from the rings by gently sliding a rolled-up piece of filter paper into the vessel lumen. The rings were then mounted in a water-jacketed tissue bath, maintained at 37°C, between moveable and fixed ends of a stainless steel wire with the moveable end attached to an FT03 Grass transducer coupled to a Model 7D Grass Polygraph for recording isometric force responses. The bath was filled with 20 ml of oxygenated (95% oxygen/5% carbon dioxide) Krebs solution of the following composition (mM) : 130 NaCl, 15
NaHCO3, 15 KCl, 1.2 NaH2PO4, 1.2 MgSO4, 2.5 CaCl2, and 11.4 glucose. The preparations were equilibrated for one hour before approximately one gram of passive tension was placed on the rings. Angiotensin II concentration-response curves were then recorded (3 X 10-10 to 1 X 10-5 M). Each concentration of All was allowed to elicit its maximal contraction, and then All was washed out repeatedly for 30 minutes before
rechallenging with a higher concentration of All. Aorta rings were exposed to the test antagonist at 10-5 M for 5 minutes before challenging with All. Adjacent segments of the same aorta ring were used for all concentration-response curves in the presence or absence of the test antagonist. The
effectiveness of the test compound was expressed in terms of pA2 values and were calculated according to H.O. Schild [Br. J. Pharmacol. Chemother., 2,189-206 (1947)]. The pA2 value is the concentration of the antagonist which increases the EC50 value for All by a factor of 2. Each test antagonist was evaluated in aorta rings from two rabbits. Results are reported in Table I.
Assay C: In Vivo Intraduodenal Pressor Assay Response for All Αntagonists
Male Sprague-Dawley rats weighing 225-300 grams were anesthetized with Inactin (100 mg/kg, i.p.) and catheters were implanted into the trachea, femoral artery, femoral vein and duodenum. Arterial pressure was recorded from the femoral artery catheter on a Gould chart recorder (Gould, Cleveland, OH). The femoral vein catheter was used for injections of angiotensin II, mecamylamine and atropine. The tracheal catheter allows for airway patency, and the duodenal catheter was used for intraduodenal (i.d.) administration of test compounds. After surgery, the rats were allowed to
equilibrate for 30 minutes. Mecamylamine (3 mg/kg, 0.3 ml/kg) and atropine (400 ug/kg, 0.3 ml/kg) were then given i.v. to produce ganglion blockade. These compounds were administered every 90 minutes throughout the test procedure. Angiotensin II was given in bolus doses i.v. (30 ng/kg in saline with 0.5% bovine serum albumin, 0.1 ml/kg) every 10 minutes three times or until the increase in arterial pressure produced was within 3 mmHg for two consecutive All injections. The last two All injections were averaged and were taken as the control All pressor response. Ten minutes after the final control All injection, the test compound (dissolved in sodium bicarbonate) was administered i.d. at a dose of 30 mg/kg in a volume of 0.2 ml. Angiotensin II injections were then given 5, 10, 20, 30, 45, 60, 75, 90, and 120 minutes after administration of the test compound and response of arterial pressure was monitored. The response to All was calculated as percent of the control response and then the percent inhibition is calculated as 100 minus the percent control response. Duration of action of a test compound was defined as the time from peak percent inhibition to 50% of peak. One compound at one dose was tested in each rat. Each test compound was tested in two rats and the values for the two rats were averaged. Results are reported in Table I.
Figure imgf000220_0001
NT = NOT TESTED
1Assay A: Angiotensin II Binding Activity
2Assay B: In Vitro Vascular Smooth Muscle Response
3Assay C: In Vivo Intraduodenal Pressor Response
Also embraced within this invention is a class of pharmaceutical compositions comprising one or more compounds of Formula II in association with one or more non-toxic, pharmaceutically acceptable carriers and/or diluents and/or adjuvants (collectively referred to herein as "carrier" materials) and, if desired, other active ingredients. The compounds of the present invention may be administered by any suitable route, preferably in the form of a pharmaceutical composition adapted to such a route, and in a dose effective for the treatment intended. Therapeutically effective doses of the compounds of the present invention required to prevent or arrest the progress of the medical condition are readily ascertained by one of ordinary skill in the art. The compounds and composition may, for example, be administered intra- vascularly, intraperitoneally, subcutaneously, intramuscularly or topically.
For oral administration, the pharmaceutical composition may be in the form of, for example, a tablet, capsule, suspension or liquid. The pharmaceutical composition is preferably made in the form of a dosage unit containing a particular amount of the active ingredient. Examples of such dosage units are tablets or capsules. These may with advantage contain an amount of active ingredient from about 1 to 250 mg, preferably from about 25 to 150 mg. A suitable daily dose for a mammal may vary widely depending on the condition of the patient and other factors. However, a dose of from about 0.01 to 3000 mg/kg body weight, particularly from about 1 to 100 mg/kg body weight, may be appropriate.
The active ingredient may also be administered by injection as a composition wherein, for example, saline, dextrose or water may be used as a suitable carrier. A
suitable daily dose is from about 0.01 to 100 mg/kg body weight injected per day in multiple doses depending on the disease being treated. A preferred daily dose would be from about 1 to 30 mg/kg body weight. Compounds indicated for prophylactic therapy will preferably be administered in a daily dose generally in a range from about 0.1 mg to about 100 mg per kilogram of body weight per day. A more preferred dosage will be a range from about 1 mg to about 100 mg per kilogram of body weight. Most preferred is a dosage in a range from about 1 to about 50 mg per kilogram of body weight per day. A suitable dose can be administered, in multiple subdoses per day. These sub-doses may be administered in unit dosage forms. Typically, a dose or sub-dose may contain from about 1 mg to about 100 mg of active compound per unit dosage form. A more preferred dosage will contain from about 2 mg to about 50 mg of active compound per unit dosage form. Most preferred is a dosage form containing from about 3 mg to about 25 mg of active compound per unit dose.
The dosage regimen for treating a disease condition with the compounds and/or compositions of this invention is selected in accordance with a variety of factors, including the type, age, weight, sex and medical condition of the patient, the severity of the disease, the route of
administration, and the particular compound employed, and thus may vary widely.
For therapeutic purposes, the compounds of this invention are ordinarily combined with one or more adjuvants appropriate to the indicated route of administration. If administered per os, the compounds may be admixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acids, cellulose alkyl esters, talc, stearic acid, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulfuric acids, gelatin, acacia gum, sodium alginate, polyvinylpyrrolidone, and/or polyvinyl alcohol, and then tableted or encapsulated for convenient administration. Such capsules or tablets may contain a controlled-release formulation as may be provided in a dispersion of active compound in hydroxypropylmethyl cellulose. Formulations for parenteral administration may be in the form of aqueous or non-aqueous isotonic sterile injection solutions or
suspensions. These solutions and suspensions may be prepared from sterile powders or granules having one or more of the carriers or diluents mentioned for use in the formulations for oral administration. The compounds may be dissolved in water, polyethylene glycol, propylene glycol, ethanol, corn oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride, and/or various buffers. Other adjuvants and modes of administration are well and widely known in the
pharmaceutical art.
Although this invention has been described with respect to specific embodiments, the details of these
embodiments are not to be construed as limitations.

Claims

What Is Claimed Is : 1. A compound of Formula I:
Figure imgf000224_0001
wherein m is a number selected from one to four, inclusive; wherein the dotted line between seven- and eight-positions and the eight- and nine-positions represents optionally a double bond; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, haloalkyl, cycloalkyl,
cycloalkylalkyl, aralkyl, aryl, aroylalkyl, alkylalkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, alkenyl, cycloalkenyl, aralkoxycarbonyl, alkynyl, cyanoalkyl, aminoalkyl, monoalkylaminoalkyl,
dialkylaminoalkyl, mercaptoalkyl, mercaptocarbonylalkyl, mercaptothiocarbonylalkyl, alkylthiocarbonylalkyl,
alkylthiothiocarbonylalkyl, arylthiocarbonylalkyl,
arylthiothiocarbonylalkyl, aralkylthiocarbonylalkyl,
alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and radicals of the formula
Figure imgf000225_0001
wherein X is oxygen atom or sulfur atom with z being a number selected from one to four, inclusive; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R12 and R13 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein each of R2 through R11 is independently selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, formyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio,
cycloalkylalkylthio, alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio,
alkylthiothiocarbonyl, alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl,
arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, alkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cyclohetero-containing groups has one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further independently selected from amino and amido radicals of the formula K
Figure imgf000226_0001
wherein X is oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R14 and R15 taken together, R16 and R17 taken together, R18 and R19 taken together, R21 and R22 taken together and R23 and R24 taken together may each form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; and wherein each of R3 through R11 may be further
independently selected from hydroxy and acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive, and wherein A is an acidic group selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties;
wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, alkynyl, aralkyl, hydroxyalkyl, haloalkyl, halo, oxo, alkoxy, aryloxy, aralkoxy, aralkylthio, alkoxyalkyl,
cycloalkyl, cycloalkylalkyl, aryl, aroyl, cycloalkenyl, cyano, cyanoamino, nitro, alkylcarbonyloxy, alkoxycarbonyloxy, alkylcarbonyl, alkoxycarbonyl, aralkoxycarbonyl, carboxyl, mercapto, mercaptocarbonyl, alkylthio, arylthio,
alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
haloalkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl,
arylsulfinyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amino and amido radicals of the formula
Figure imgf000228_0001
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, DR32 and
Figure imgf000228_0002
wherein D is selected from oxygen atom and sulfur atom and R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl,
alkylsulfinyl, alkylsulfonyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl, and wherein each of R27, R28, R29, R30, R31, R33 and R34 is further independently selected from amino and amido radicals of the formula
Figure imgf000228_0003
wherein X is oxygen atom or sulfur atom;
wherein each of R35, R36, R37, R38, R39 and R40 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl, and wherein each of R28 and R29 taken together and each of R30 and R31 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; with the proviso that R0, R1, and R2 cannot all simultaneously be hydrido; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
2. Compound of Claim 1 of Formula II:
Figure imgf000229_0001
wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl,
hydroxyalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, mercaptoalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, alkylsulfonyl, aralkylsulfonyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amido radicals of the formula
Figure imgf000230_0001
wherein X is oxygen atom or sulfur atom with r being a number selected from one or two; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl,
aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl,
aralkylcarbonyloxyalkyl, mercaptocarbonyl,
mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio,
alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio, alkylthiothiocarbonyl,
alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl, arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio,
aralkylthiocarbonyloxy, aralkylthiocarbonylthio,
aralkylthiocarbonyl, aralkylthiocarbonylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl. aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000231_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, alkylcarbonyloxy, mercaptocarbonyl,
mercaptothiocarbonyl, alkoxycarbonyloxy, alkylthio. alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio, alkylthiothiocarbonyl, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiothiocarbonyl, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, aralkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfonyl,
aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula
Figure imgf000232_0001
wherein X is oxygen atom or sulfur atom;
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is an acidic group selected from acids containing one or more atoms selected from oxygen, sulfur, phosphorus and nitrogen atoms, and wherein said acidic group is selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, haloalkyl, oxo, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, mercaptocarbonyl, alkylthio and
alkylthiocarbonyl, and amino and amido radicals of the formula
Figure imgf000233_0001
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, and DR32 and
Figure imgf000233_0002
wherein D is selected from oxygen atom and sulfur atom, and R32 is selected from hydrido, alkyl, cycloalkyl,
cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl, alkoxycarbonyl, carboxyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
3. Compound of Claim 2 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl and cycloalkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl,
alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalklylcarbonylalkyl wherein each of said
heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein R2 may be further selected from amino and amido radicals of the formula
Figure imgf000234_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl,
cycloalkenyl, alkynyl, cyano, nitro, carboxyl,
alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylthio, arylthio, aralkylthio, mercapto, alkylsulfonyl, aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula
Figure imgf000235_0001
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000236_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R36, R37, R38 and
R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl,
cycloalkyl, cycloalkylalkyl, aryl and aralkyl; wherein each of
R35, R36, R37 and R39 may be further independently selected from amino radical of the formula
Figure imgf000236_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 and R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; wherein each of R36 and R37 may be further independently selected from hydroxy, alkoxy, alkylthio, aryloxy, arylthio, aralkylthio and aralkoxy; and the amide, ester and salt derivatives of said, acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which heterocyclic ring contains at least one hetero atom selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially
unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; and wherein any of the foregoing R1 through R26 and R35 through R41, Y and A groups having a substitutable position may be substituted by one or more groups independently
selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, oxo, haloalkyl, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro,
alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl,
mercaptocarbonyl, alkylthio and alkylthiocarbonyl, and amino and amido radicals of the formula £
Figure imgf000238_0002
wherein X is selected from oxygen atom and sulfur atom;
wherein R27 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl and DR32 and
Figure imgf000238_0001
wherein D is selected from oxygen atom and sulfur atom;
wherein R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl, alkoxycarbonyl, carboxyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
4. Compound of Claim 3 wherein m is one; wherein each of X1 and X2 is selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl,
cycloalkenyl and alkynyl with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl,
alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000239_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl,
cycloalkenyl, alkynyl, cyano, nitro, carboxyl, alkylthio, aralkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000240_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl,
cycloalkylalkyl, aryl and aralkyl; wherein each of R35 and R39 may be further independently selected from amino radical of the formula
Figure imgf000240_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 and R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms, and which heterocyclic group may be saturated or partially unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; and the amide, ester and salt derivatives of said acidic groups;
wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said
heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and A independently may be substituted at any substitutable position with one or more groups selected from alkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro,
alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
5. Compound of Claim 4 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl and alkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbony1, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy, alkoxyalkyl, alkylcarbonyl,
alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, phthalimido,
phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000243_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, phenalkyl, phenyl, benzoyl, phenoxy, phenalkyloxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through two,
inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000244_0001
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl, phenyl and benzyl; wherein each of R35 and R39 may be further
independently selected from amino radical of the formula
Figure imgf000244_0002
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
alkoxyalkyl, benzyl and phenyl; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, phenyl, phenalkyl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and A and independently may be substituted at any substitutable position with one or more groups selected from alkyl,
cycloalkyl, cycloalkylalkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro, alkylsulfonyl,
haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and
aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
6. Compound of Claim 5 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl and alkynyl; where R2 is selected from alkyl, aminoalkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy,
alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, mercaptoalkyl, mercaptocarbonyl,
alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl, phthalimido, phthalimidoalkyl, imidazoalkyl, tetrazole, tetrazolealkyl. alkylthio, cycloalkylthio, cycloalkylalkylthio, and amino and amido radicals of the formula
Figure imgf000246_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, alkoxy, phenyl, benzoyl, phenoxy, alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties consisting of CO2H, CO2CH3, SH, CH2SH, C2H4SH, PO 3H2, NHSO2CF3 , NHSO2C6F5, SO3H, CONHNH2, CONHNHSO2CF3 , CONHOCH3, CONHOC2H5 , CONHCF 3 , OH, CH2OH, C2H4OH, OPO3H2, OSO3H ,
Figure imgf000247_0001
wherein each of R42, R43 and R44 is independently selected from H, Cl, CN, NO2, CF3, C2F5, C3F7, CHF2, CH2F, CO2CH3, CO2C2H5, SO2CH3, SO2CF3, and SO2C6F5; wherein Z is selected from O, S, NR45 and CH2; wherein R45 is selected from hydrido, CH3 and CH2C6H5; and wherein said acidic moiety may be a heterocyclic acidic group attached at any two adjacent positions of R3 through R11 so as to form a fused ring system with one of the phenyl rings of the biphenyl moiety of Formula II, said biphenyl fused ring system selected from
Figure imgf000248_0001
and the esters, amides and salts of said acidic moieties;
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
7. Compound of Claim 6 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl,
n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, neopentyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclopropylmethyl, cyclopropylethyl,
cyclohexylmethyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, buten-2-yl, 3-butenyl, butyn-2-yl, butyn-3-yl, haloloweralkyl and hydroxyloweralkyl; wherein R2 is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, isopentyl, neopentyl, phenyl, cyclohexyl, cyclohexylmethyl, CH3CH=CH-CH2, SC3H7, cyclohex-3 - en-1-yl, SC4H9,
Figure imgf000249_0002
CH2S , CH3CH=CH, CH2=CH-CH2,
CH3CH2CH2CH=CH- , amino, alkoxy, aminomethyl, aminoethyl, aminopropyl, CH2OCOCH3, CH2CI, CH2OCH3, CH2OCH(CH3) 2, CH2CO2H, CH(CH3)CO2H, -CH2OCOCH2CH2 -CH2CH2CH2CO2H, -CH2CH2F, -
Figure imgf000249_0003
CH2CH2CH2F, -CH2CNO2, -CH2SH, -CH2O- CF3, CH2OH,
Figure imgf000249_0004
hydroxyalkyl, halo, 1-oxo-2-phenylethyl, 2-cyclohexylethyl, 3-cyclohexylpropyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexanoyl, 1-butenyl, buten-2-yl,
3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl and
difluoromethyl; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3, OH,
Figure imgf000249_0001
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
8. Compound of Claim 7 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl. neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl, methoxycarbonylmethyl, methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, 2-phenylethyl, 2-cyclohexylethyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3, OH,
Figure imgf000250_0001
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
9. Compound of Claim 8 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl,
n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl,
4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl. cyclohexl, cyclohexylmethyl, methoxycarbonyImethyl,
methoxycarbonylethyl,
4-hydroxybuty, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl,
n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000251_0001
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
10. Compound of Claim 9 wherein m is one; wherein X1 is an oxygen atom and X2 is a sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl,
cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl,
methoxycarbonyImethyl, methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2- phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000252_0001
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
11. Compound of Claim 10 wherein m is one; wherein X1 is an oxygen atom and X2 is an oxygen atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl,
cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl,
methoxycarbonyImethyl, methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2- phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000252_0002
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
12. Compound of Claim 6 selected from the group consisting of
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-bi2henyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-
1H-purine-2,6-dione; 8-butyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-cyclohexyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1 -biphenyl)-4-yl]methyl]-1H-purine-2, 6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2, 6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-cyclohexyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2, 6-dione;
8-cyclohexyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-cyclohexyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-thione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2, 6-thione;
8-cyclohexyl-3,7-dihydro-1-methyl-3-pheny1-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-cyclohexyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-cyclohexyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2, - dione; 8-pentyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-pentyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-pentyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-pentyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione; 8-pentyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-pentyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-pentyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(propen-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7- [[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(propen-2-yl)-3,7-dihydro-1,3-diproρyl-7-[[2'-(1H-tetrazol- 5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(propen-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine; 8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine- 2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-
7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'- (1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-(buten-2-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-
[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-
7-[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purdlne-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-(buten-2-yl)-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'- (1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-(buten-2-yl)-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(buten-2-yl)-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H- purine;
8-(cyclohex-3-en-1-yl)-3,7-dihydro-1-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol- 5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione; 8-propyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine;
8-propyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-(3-hydroxypropyl)-3-methyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-(2-carbomethoxy-ethyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-(2-hydroxyethyl)-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-methyl-3-(prop-2-en-1-yl)-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-propyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-1,3-dipropyl-7-[[2['(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione; 8-propyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- thione;
8-propyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-propyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-thione;
8-(buten-2-yl)-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine; and
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl) (1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione.
13. Compound of Claim 12 selected from the group consisting of
8-(2-butenyl)-3,7-dihydro-1-methyl-3-propyl-7-
[[2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4- yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-proρyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]- 1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-
1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-
1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3- methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)- 4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropylmethyl)-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'- (1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]- 1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]- 1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-proρyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-6- oxo-2-thioxo-1H-purine; and
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H- purine-2,6-dione.
14. Compound of Claim 13 which is 8-(2E-butenyl)- 3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
15. Compound of Claim 13 which is 8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-te razol-5-yl) [1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
16. Compound of Claim 13 which is 8-butyl-3,7- dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1- biphenyl]-4-yl]methyl]-1H-purine-6-one-2-thione.
17. Compound of Claim 13 which is 8-butyl-3,7- dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
18. Compound of Claim 13 which is 8-butyl-3,7- dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl] 4-yl]methyl-1H-purine-2,6-dione.
19. Compound of Claim 13 which is 8-(2E-butenyl)- 3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)[1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
20. Compound of Claim 13 which is 8-butyl-3,7- dihydro-1-cyclopropyl-3-methyl-7-[[2'-(1H-tetrazol-5-yl)
[1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
21. Compound of Claim 13 which is 8-butyl-3,7- dihydro-1-methyl-3-cyclopropyl-7-[[2'-(1H-tetrazol-5-yl)
[1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
22. Compound of Claim 13 which is 8-butyl-3,7- dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
23. Compound of Claim 13 which is 8-butyl-3,7- dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4- yl]methyl]-1H-purine-2,6-dione.
24. Compound of Claim 13 which is 8-propyl-3,7- dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4- yl]methyl]-1H-purine-2,6-dione.
25. Compound of Claim 13 which is 8-propyl-3,7- dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
26. A pharmaceutical composition comprising a therapeutically-effective amount of an angiotensin II
antagonist compound and a pharmaceutically-acceptable carrier or diluent, said antagonist compound selected from a family of compounds of Formula I:
Figure imgf000267_0001
wherein m is a number selected from one to four, inclusive; wherein the dotted line between seven- and eight-positions and the eight- and nine-positions represents optionally a double bond; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, haloalkyl, cycloalkyl,
cycloalkylalkyl, aralkyl, aryl, aroylalkyl, alkylalkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, alkenyl, cycloalkenyl, aralkoxycarbonyl, alkynyl, cyanoalkyl, aminoalkyl, monoalkylaminoalkyl,
dialkylaminoalkyl, mercaptoalkyl, mercaptocarbonylalkyl, mercaptothiocarbonylalkyl, alkylthiocarbonylalkyl,
alkylthiothiocarbonylalkyl, arylthiocarbonylalkyl,
arylthiothiocarbonylalkyl, aralkylthiocarbonylalkyl,
alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl. heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and radicals of the formula
Figure imgf000268_0001
wherein X is oxygen atom or sulfur atom with z being a number selected from one to four, inclusive; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R12 and R13 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein each of R2 through R11 is independently selected .from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, formyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio,
cycloalkylalkylthio, alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio,
alkylthiothiocarbonyl, alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl,
arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, alkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cyclohetero-containing groups has one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further independently selected from amino and amido radicals of the formula
p
Figure imgf000269_0001
wherein X is oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R14 and R15 taken together, R16 and R17 taken together, R18 and R19 taken together, R21 and R22 taken together and R23 and R24 taken together may each form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; and wherein each of R3 through R11 may be further
independently selected from hydroxy and acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive, and wherein A is an acidic group selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties;
wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, alkynyl, aralkyl, hydroxyalkyl, haloalkyl, halo, oxo, alkoxy, aryloxy, aralkoxy, aralkylthio, alkoxyalkyl,
cycloalkyl, cycloalkylalkyl, aryl, aroyl, cycloalkenyl, cyano, cyanoamino, nitro, alkylcarbonyloxy, alkoxycarbonyloxy, alkylcarbonyl, alkoxycarbonyl, aralkoxycarbonyl, carboxyl, mercapto, mercaptocarbonyl, alkylthio, arylthio,
alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
haloalkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl,
arylsulfinyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amino and amido radicals of the formula
Figure imgf000271_0002
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, DR32 and
Figure imgf000271_0001
wherein D is selected from oxygen atom and sulfur atom and R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl,
alkylsulfinyl, alkylsulfonyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl, and wherein each of R27' R28' R29, R30, R31, R33 and R34 is further independently selected from amino and amido radicals of the formula
Figure imgf000271_0003
wherein X is oxygen atom or sulfur atom;
wherein each of R35, R36, R37, R38, R39 and R40 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, haloalkylsulfinyl. haloalkylsulfonyl, aralkyl and aryl, and wherein each of R28 and R29 taken together and each of R30 and R31 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; with the proviso that R0, R1, and R2 cannot all simultaneously be hydrido; or a tautomer thereof or a pharmaceutically-acceptable salt thereof .
27. The composition of Claim 26 wherein said angiotensin II antagonist compound is selected from a family of compounds of Formula II:
Figure imgf000272_0001
wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl,
hydroxyalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, mercaptoalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, alkylsulfonyl, aralkylsulfonyl, arylsulfonyl.
Figure imgf000273_0001
wherein X is oxygen atom or sulfur atom with r being a numbe selected from one or two; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl,
aralkylcarbonyloxyalkyl, mercaptocarbonyl,
mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio,
alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio, alkylthiothiocarbonyl,
alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl, arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio,
aralkylthiocarbonyloxy, aralkylthiocarbonylthio,
aralkylthiocarbonyl, aralkylthiocarbonylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl,
aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000274_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, alkylcarbonyloxy, mercaptocarbonyl. mercaptothiocarbonyl, alkoxycarbonyloxy, alkylthio,
alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio, alkylthiothiocarbonyl, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiothiocarbonyl, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, aralkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfonyl,
aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula
Figure imgf000275_0001
wherein X is oxygen atom or sulfur atom;
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is an acidic group selected from acids containing one or more atoms selected from oxygen, sulfur, phosphorus and nitrogen atoms, and wherein said acidic group is selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, haloalkyl, oxo, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, mercaptocarbonyl, alkylthio and
alkylthiocarbonyl, and amino and amido radicals of the formula
Figure imgf000276_0001
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, and DR32 and
Figure imgf000276_0002
wherein D is selected from oxygen atom and sulfur atom, and R32 is selected from hydrido, alkyl, cycloalkyl,
cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl, alkoxycarbonyl, carboxyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
28. The composition of Claim 27 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl and cycloalkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl,
alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalklylcarbonylalkyl wherein each of said
heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein R2 may be further selected from amino and amido radicals of the formula
Figure imgf000278_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl,
cycloalkenyl, alkynyl, cyano, nitro, carboxyl,
alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylthio, arylthio, aralkylthio, mercapto, alkylsulfonyl, aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula
Figure imgf000278_0002
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000279_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R36, R37, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl,
cycloalkyl, cycloalkylalkyl, aryl and aralkyl; wherein each of R35, R36, R37 and R39 may be further independently selected from amino radical of the formula
Figure imgf000279_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 and R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; wherein each of R36 and R37 may be further independently selected from hydroxy, alkoxy, alkylthio, aryloxy, arylthio, aralkylthio and aralkoxy; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which heterocyclic ring contains at least one hetero atom selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially
unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; and wherein any of the foregoing R1 through R26 and R35 through R41, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, oxo, haloalkyl, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl,
mercaptocarbonyl, alkylthio and alkylthiocarbonyl, and amino and amido radicals of the formula
Figure imgf000281_0001
wherein X is selected from oxygen atom and sulfur atom;
wherein R27 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl and DR32 and
Figure imgf000281_0002
wherein D is selected from oxygen atom and sulfur atom;
wherein R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl, alkoxycarbonyl, carboxyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
29. The composition of Claim 28 wherein m is one; wherein each of X1 and X2 is selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl. alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl and alkynyl with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl,
alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000282_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl,
cycloalkenyl, alkynyl, cyano, nitro, carboxyl, alkylthio, aralkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000283_0001
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl,
cycloalkylalkyl, aryl and aralkyl; wherein each of R35 and R39 may be further independently selected from amino radical of the formula
Figure imgf000284_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 ana R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms, and which heterocyclic group may be saturated or partially unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; and the amide, ester and salt derivatives of said acidic groups;
wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said
heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and A independently may be substituted at any substitutable position with one or more groups selected from alkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro,
alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
30. The composition of Claim 29 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl,
aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl and alkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo,
haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy, alkoxyalkyl, alkylcarbonyl,
alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, phthalimido,
phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000286_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, phenalkyl, phenyl, benzoyl, phenoxy, phenalkyloxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through two, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000287_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl, phenyl and benzyl; wherein each of R35 and R39 may be further
independently selected from amino radical of the formula
Figure imgf000287_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
alkoxyalkyl, benzyl and phenyl; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said
heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, phenyl, phenalkyl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and
A and independently may be substituted at any substitutable position with one or more groups selected from alkyl,
cycloalkyl, cycloalkylalkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro, alkylsulfonyl,
haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and
aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
31. The composition of Claim 30 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is
independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl and alkynyl; where R2 is selected from alkyl, aminoalkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy,
alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, mercaptoalkyl, mercaptocarbonyl,
alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl. aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl, phthalimido, phthalimidoalkyl, imidazoalkyl, tetrazole, tetrazolealkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, and amino and amido radicals of the formula
Figure imgf000289_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, alkoxy, phenyl, benzoyl, phenoxy, alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties consisting of CO2H, CO2CH3, SH, CH2SH, C2H4SH, PO3H2, NHSO2CF3, NHSO2C6F5,
SO3H, CONHNH2, CONHNHSO2CF3, CONHOCH3, CONHOC2H5, CONHCF3, OH, CH2OH, C2H4OH, OPO3H2, OSO3H,
Figure imgf000290_0001
wherein each of R42, R43 and R44 is independently selected from H, Cl, CN, NO2, CF3, C2F5, C3F7, CHF2, CH2F, CO2CH3, CO2C2H5, SO2CH3 SO2CF3 and SO2C6F5; wherein Z is selected from O, S, NR45 and CH2; wherein R45 is selected from hydrido, CH3 and CH2C6H5; and wherein said acidic moiety may be a heterocyclic acidic group attached at any two adjacent positions of R3 through R11 so as to form a fused ring system with one of the phenyl rings of the biphenyl moiety of Formula II, said biphenyl fused ring system selected from
Figure imgf000291_0001
and the esters, amides and salts of said acidic moieties;
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
32. The composition of Claim 31 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl,
n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, neopentyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclopropylmethyl, cyclopropylethyl,
cyclohexylmethyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, buten-2-yl, 3-butenyl, butyn-2-yl, butyn-3-yl, haloloweralkyl and hydroxyloweralkyl; wherein R2 is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, isopentyl, neopentyl, phenyl. cyclohexyl, cyclohexylmethyl, CH3CH=CH-CH2, SC3H7, cyclohex-3 - en-1-yl, SC4H9, CH2S , CH3CH=CH, CH2=CH-CH2,
Figure imgf000292_0001
CH3CH2CH2CH=CH-, amino, alkoxy, aminomethyl, aminoethyl, aminopropyl, CH2OCOCH3, CH2CI, CH2OCH3, CH2OCH(CH3) 2, CH2CO2H, CH(CH3)CO2H, -CH2OCOCH2CH2 -
Figure imgf000292_0002
-CH2CH2CH2CO2H, -CH2CH2F, -
CH2CH2CH2F, -CH2ONO2, -CH2SH, -CH2O CF3, CH2OH,
Figure imgf000292_0003
hydroxyalkyl, halo, 1-oxo-2-phenylethyl, 2-cyclohexylethyl, 3-cyclohexylpropyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexanoyl, 1-butenyl, buten-2-yl,
3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl and
difluoromethyl; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3, OH,
y
Figure imgf000292_0004
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
33. The composition of Claim 32 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is
independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4- methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl,
cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl, methoxycarbonyImethyl,
methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3- hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert- butyl, n-pentyl, neopentyl, 2-phenylethyl, 2-cyclohexylethyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3,
OH,
Figure imgf000293_0001
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
34. The composition of Claim 33 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl,
n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl,
cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexl, cyclohexylmethyl, methoxycarbonyImethyl,
methoxycarbonylethyl, 4-hydroxybuty, 2-hydroxyethyl and 3- hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert- butyl, n-pentyl, neopentyl, benzyl, 2-phenylethyl, 3- phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000294_0001
> or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
35. The composition of Claim 34 wherein m is one; wherein X1 is an oxygen atom and X2 is a sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl,
methoxycarbonyImethyl, methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2- phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000295_0001
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
36. The composition of Claim 35 wherein m is one; wherein X1 is an oxygen atom and X2 is an oxygen atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl,
methoxycarbonyImethyl, methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2- phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000295_0002
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
37. The composition of Claim 36 wherein said angiotensin II antagonist compound is selected from the gorup consisting of
8-(2-butenyl)-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione; 8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl) -4-yl]methyl] -6-oxo-2-thioxo-1H-purine; and
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione.
38. The composition of Claim 37 wherein said angiotensin II antagonist compound is 8-(2E-butenyl)-3,7- dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
39. The composition of Claim 37 which is 8-butyl- 3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
40. The composition of Claim 37 which is 8-butyl-
3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1- biphenyl]-4-yl]methyl]-1H-purine-6-one-2-thione.
41. The composition of Claim 37 which is 8-butyl- 3, 7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
42. The composition of Claim 37 which is 8-butyl- 3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
43. The composition of Claim 37 which is 8-(2E- butenyl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol- 5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
44. The composition of Claim 37 which is 8-butyl- 3,7-dihydro-1-cyclopropyl-3-methyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
45. The composition of Claim 37 which is 8-butyl- 3,7-dihydro-1-methyl-3-cyclopropyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
46. The composition of Claim 37 which is 8-butyl-
3,7-dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
47. The composition of Claim 37 which is 8-butyl- 3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-
4-yl]methyl]-1H-purine-2,6-dione.
48. The composition of Claim 37 which is 8-propyl- 3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]- 4-yl]methyl]-1H-purine-2,6-dione.
49. The composition of Claim 37 which is 8-propyl- 3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
50. A therapeutic method for treating a circulatory disorder, said method comprising administering to a subject susceptible to or afflicted with such disorder a therapeutically-effective amount of a compound of Formula I:
Figure imgf000298_0001
wherein m is a number selected from one to four, inclusive; wherein the dotted line between seven- and eight-positions and the eight- and nine-positions represents optionally a double bond; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, haloalkyl, cycloalkyl,
cycloalkylalkyl, aralkyl, aryl, aroylalkyl, alkylalkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, alkenyl, cycloalkenyl, aralkoxycarbonyl, alkynyl, cyanoalkyl, aminoalkyl, monoalkylaminoalkyl,
dialkylaminoalkyl, mercaptoalkyl, mercaptocarbonylalkyl, mercaptothiocarbonylalkyl, alkylthiocarbonylalkyl,
alkylthiothiocarbonylalkyl, arylthiocarbonylalkyl,
arylthiothiocarbonylalkyl, aralkylthiocarbonylalkyl,
alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and radicals of the formula
Figure imgf000299_0001
wherein X is oxygen atom or sulfur atom with z being a number selected from one to four, inclusive; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R12 and R13 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein each of R2 through R11 is independently selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, formyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio,
cycloalkylalkylthio, alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio,
alkylthiothiocarbonyl, alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl,
arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonyIthio, alkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cyclohetero-containing groups has one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further independently selected from amino and amido radicals of the formula
Figure imgf000301_0001
wherein X is oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R14 and R15 taken together, R16 and R17 taken together, R18 and R19 taken together, R21 and R22 taken together and R23 and R24 taken together may each form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical and which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; and wherein each of R3 through R11 may be further
independently selected from hydroxy and acidic moieties of the formula -YnA wherein n is a number selected from zero through three, inclusive, and wherein A is an acidic group selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties;
wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, alkynyl, aralkyl, hydroxyalkyl, haloalkyl, halo, oxo, alkoxy, aryloxy, aralkoxy, aralkylthio, alkoxyalkyl,
cycloalkyl, cycloalkylalkyl, aryl, aroyl, cycloalkenyl, cyano, cyanoamino, nitro, alkylcarbonyloxy, alkoxycarbonyloxy, alkylcarbonyl, alkoxycarbonyl, aralkoxycarbonyl, carboxyl, mercapto, mercaptocarbonyl, alkylthio, arylthio,
alkylthiocarbonyl, alkylsulfinyl, alkylsulfonyl,
haloalkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl,
arylsulfinyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amino and amido radicals of the formula
Figure imgf000302_0001
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, DR32 and
Figure imgf000302_0002
wherein D is selected from oxygen atom and sulfur atom and R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl,
alkylsulfinyl, alkylsulfonyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl, and wherein each of R27, R28, R29, R30, R31, R33 and R34 is further independently selected from amino and amido radicals of the formula
Figure imgf000303_0001
wherein X is oxygen atom or sulfur atom;
wherein each of R35, R36, R37, R38, R39 and R40 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl, and wherein each of R28 and R29 taken together and each of R30 and R31 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino or amido radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
51. The method of Claim 50 wherein said compound is of Formula II:
Figure imgf000304_0001
wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl,
hydroxyalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, mercaptoalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, alkylsulfonyl, aralkylsulfonyl, arylsulfonyl, heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms, and amido radicals of the formula
Figure imgf000304_0002
wherein X is oxygen atom or sulfur atom with r being a number selected from one or two; wherein each of R12 and R13 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from hydrido, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl,
aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl,
aralkylcarbonyloxyalkyl, mercaptocarbonyl,
mercaptothiocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio,
alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio, alkylthiothiocarbonyl,
alkylthiothiocarbonylthio, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiocarbonylthio, arylthiothiocarbonyl, arylthiothiocarbonylthio, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio,
aralkylthiocarbonyloxy, aralkylthiocarbonylthio,
aralkylthiocarbonyl, aralkylthiocarbonylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl,
aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000306_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, alkylcarbonyloxy, mercaptocarbonyl,
mercaptothiocarbonyl, alkoxycarbonyloxy, alkylthio,
alkylthiocarbonyl, alkylcarbonylthio, alkylthiocarbonyloxy, alkylthiocarbonylthio, alkylthiothiocarbonyl, arylthio, arylthiocarbonyl, arylcarbonylthio, arylthiocarbonyloxy, arylthiothiocarbonyl, aralkylthio, aralkylthiocarbonyl, aralkylcarbonylthio, aralkylthiocarbonyloxy,
aralkylthiocarbonylthio, aralkylthiocarbonyl,
aralkylthiocarbonylthio, mercapto, alkylsulfonyl,
aralkylsulfonyl and arylsulfonyl, and amino and amido radicals of the formula
Figure imgf000307_0001
wherein X is oxygen atom or sulfur atom;
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is an acidic group selected from acids containing one or more atoms selected from oxygen, sulfur, phosphorus and nitrogen atoms, and wherein said acidic group is selected to contain at least one acidic hydrogen atom, and the amide, ester and salt derivatives of said acidic moieties; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl, aralkyl and heteroaryl having one or more ring atoms selected from oxygen, sulfur and nitrogen atoms; and wherein any of the foregoing R1 through R26, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, haloalkyl, oxo, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, mercaptocarbonyl, alkylthio and
alkylthiocarbonyl, and amino and amido radicals of the formula
Figure imgf000308_0001
wherein X is oxygen atom or sulfur atom; wherein each of R27 through R31 is independently selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, and DR32 and
Figure imgf000308_0002
wherein D is selected from oxygen atom and sulfur atom, and R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl, alkoxycarbonyl, carboxyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
52. The method of Claim 51 wherein m is one; wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl, alkynyl and cycloalkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl,
alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, aralkylthiocarbonylthio, mercapto, alkylsulfinyl,
alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and cycloheteroalklylcarbonylalkyl wherein each of said
heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein R2 may be further selected from amino and amido radicals of the formula
Figure imgf000309_0001
wherein X is selected from oxygen atom or sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl,
cycloalkenyl, alkynyl, cyano, nitro, carboxyl,
alkylcarbonyloxy, mercaptocarbonyl, alkoxycarbonyloxy, alkylthio, arylthio, aralkylthio, mercapto, alkylsulfonyl, aralkylsulfonyl and arylsulfonyl, and aminό and amido radicals of the formula
Figure imgf000310_0001
wherein each of R14, R15, R16, R17, R18 and R19 is
independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000310_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R36, R37, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl,
cycloalkyl, cycloalkylalkyl, aryl and aralkyl; wherein each of R35, R36, R37 and R39 may be further independently selected from amino radical of the formula
Figure imgf000311_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 and R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms and which heterocyclic group may be saturated or partially unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; wherein each of R36 and R37 may be further independently selected from hydroxy, alkoxy, alkylthio, aryloxy, arylthio, aralkylthio and aralkoxy; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of
heterocyclic rings of four to about nine ring members, which heterocyclic ring contains at least one hetero atom selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially
unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; and wherein any of the foregoing R1 through R26 and R35 through R41, Y and A groups having a substitutable position may be substituted by one or more groups independently selected from hydroxy, alkyl, alkenyl, aralkyl, hydroxyalkyl, halo, oxo, haloalkyl, alkoxy, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, carboxyl, cyano, nitro, alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl,
mercaptocarbonyl, alkylthio and alkylthiocarbonyl, and amino and amido radicals of the formula
Figure imgf000312_0001
wherein X is selected from oxygen atom and sulfur atom;
wherein R27 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl and DR32 and
Figure imgf000312_0002
wherein D is selected from oxygen atom and sulfur atom;
wherein R32 is selected from hydrido, alkyl, cycloalkyl, cycloalkylalkyl, aralkyl and aryl; wherein each of R27, R28, R29, R30, R31, R33 and R34 is independently selected from hydrido, alkyl, cycloalkyl, cyano, hydroxyalkyl, haloalkyl, cycloalkylalkyl, alkoxyalkyl, alkanoyl, alkoxycarbonyl, carboxyl, haloalkylsulfinyl, haloalkylsulfonyl, aralkyl and aryl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
53. The method of Claim 52 wherein m is one;
wherein each of X1 and X2 is selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, alkenyl, cycloalkenyl and alkynyl with the proviso that R0 and R1 cannot simultaneously be hydrido; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, aroyl, aryloxy, aryloxyalkyl, aralkoxy, alkoxyalkyl,
alkylcarbonyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, arylthio, aralkylthio, mercapto, alkylsulfinyl, alkylsulfonyl, aralkylsulfinyl, aralkylsulfonyl, arylsulfinyl, arylsulfonyl, phthalimido, phthalimidoalkyl, heteroaryl, heteroarylalkyl. cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000314_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, monoalkylamino, dialkylamino, hydroxyalkyl, cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, aralkyl, aryl, aroyl, aryloxy, aralkoxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl,
cycloalkenyl, alkynyl, cyano, nitro, carboxyl, alkylthio, aralkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula -YnA wherein n is a number selected from zero through three, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000315_0002
Figure imgf000315_0003
-OH, -SH, -NR35 , -C-WH, -S-WH, and
Figure imgf000315_0004
Figure imgf000315_0005
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl,
cycloalkylalkyl, aryl and aralkyl; wherein each of R35 and R39 may be further independently selected from amino radical of the formula
Figure imgf000315_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
cycloalkylalkyl, alkoxyalkyl, aralkyl and aryl, and wherein R40 and R41 taken together may form a heterocyclic group having five to seven ring members including the nitrogen atom of said amino radical, which heterocyclic group may further contain one or more hetero atoms as ring members selected from oxygen, nitrogen and sulfur atoms, and which heterocyclic group may be saturated or partially unsaturated; wherein R40 and R41 taken together may form an aromatic heterocyclic group having five ring members including the nitrogen atom of said amino radical and which aromatic heterocyclic group may further contain one or more hetero atoms as ring atoms selected from oxygen, nitrogen and sulfur atoms; and the amide, ester and salt derivatives of said acidic groups;
wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said
heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and A independently may be substituted at any substitutable position with one or more groups selected from alkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro,
alkylsulfonyl, haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
54. The method of Claim 53 wherein m is one;
wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl and alkynyl; wherein R2 is selected from alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy, alkoxyalkyl, alkylcarbonyl,
alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl, alkylcarbonyloxy,
alkylcarbonyloxyalkyl, alkoxycarbonylalkyl,
aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl,
mercaptocarbonyl, mercaptoalkyl, alkoxycarbonyloxy, alkylthio, cycloalkylthio, cycloalkylalkylthio, phthalimido,
phthalimidoalkyl, heteroaryl, heteroarylalkyl,
cycloheteroalkyl, cycloheteroalkylalkyl and
cycloheteroalkylcarbonylalkyl wherein each of said heteroaryl- and cycloheteroalkyl-containing groups has one or more hetero ring atoms selected from oxygen, sulfur and nitrogen atoms, and wherein each of R2 through R11 may be further
independently selected from amino and amido radicals of the formula
Figure imgf000317_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, alkoxy, phenalkyl, phenyl, benzoyl, phenoxy, phenalkyloxy, alkoxyalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties of the formula
-YnA wherein n is a number selected from zero through two, inclusive; wherein A is selected from carboxylic acid and bioisosteres of carboxylic acid selected from
Figure imgf000318_0002
wherein each W is independently selected from oxygen atom, sulfur atom and NR39; wherein each of R35, R38 and R39 is independently selected from hydrido, alkyl, haloalkyl, haloalkylsulfonyl, haloalkylcarbonyl, cycloalkyl, phenyl and benzyl; wherein each of R35 and R39 may be further
independently selected from amino radical of the formula
Figure imgf000318_0001
wherein each of R40 and R41 is independently selected from hydrido, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl,
alkoxyalkyl, benzyl and phenyl; and the amide, ester and salt derivatives of said acidic groups; wherein said bioisostere of carboxylic acid may be further selected from heterocyclic acidic groups consisting of heterocyclic rings of four to about nine ring members, which ring contains at least one hetero atom, selected from oxygen, sulfur and nitrogen atoms, which heterocyclic ring may be saturated, fully unsaturated or partially unsaturated, and which heterocyclic ring may be attached at a single position selected from R3 through R11 or may be attached at any two adjacent positions selected from R3 through R11 so as to form a fused-ring system with one of the phenyl rings of Formula II; and the amide, ester and salt derivatives of said
heterocyclic acidic groups; wherein Y is a spacer group independently selected from one or more of alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, phenyl, phenalkyl and aralkyl; wherein each of R1 through R26, R35 and R38 through R41, Y and
A and independently may be substituted at any substitutable position with one or more groups selected from alkyl,
cycloalkyl, cycloalkylalkyl, hydroxy, halo, oxo, haloalkyl, alkoxycarbonyl, cyano, nitro, alkylsulfonyl,
haloalkylsulfonyl, aryl, aralkyl, alkoxy, aryloxy and
aralkoxy; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
55. The method of Claim 54 wherein m is one;
wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is
independently selected from hydrido, alkyl, hydroxyalkyl, mercaptoalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, aralkyl, aryl, alkoxyalkyl, alkoxycarbonylalkyl,
alkylcarbonyloxyalkyl, alkenyl and alkynyl; where R2 is selected from alkyl, aminoalkyl, hydroxyalkyl, halo, haloalkyl, cycloalkyl, cycloalkylalkyl,
cycloalkylhaloalkyl, cycloalkylcarbonyl, alkoxy, aralkyl, aralkylhaloalkyl, aryl, benzoyl, phenoxy, phenoxyalkyl, phenalkyloxy, phenylthio, phenalkylthio, aralkoxy,
alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl, cyano, nitro, carboxyl, carboxyalkyl,
alkylcarbonyloxy, mercaptoalkyl, mercaptocarbonyl,
alkoxycarbonyloxy, alkylcarbonyloxyalkyl, alkoxycarbonylalkyl, aralkoxycarbonylalkyl, aralkylcarbonyloxyalkyl, phthalimido, phthalimidoalkyl, imidazoalkyl, tetrazole, tetrazolealkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, and amino and amido radicals of the formula
Figure imgf000320_0001
wherein X is selected from oxygen atom and sulfur atom; wherein each r is a number independently selected from zero to six, inclusive; wherein each of R14 through R26 is independently selected from hydrido, alkyl, cycloalkyl, cyano, amino, hydroxyalkyl, alkoxyalkyl, phenalkyl and phenyl; wherein each of R3 through R11 is independently selected from hydrido, hydroxy, alkyl, hydroxyalkyl, halo, haloalkyl, alkoxy, phenyl, benzoyl, phenoxy, alkoxyalkyl, acetyl, alkoxycarbonyl, alkenyl, cyano, nitro, carboxyl, alkylthio and mercapto; and wherein each of R3 through R11 may be further
independently selected from acidic moieties consisting of CO2H, CO2CH3, SH, CH2SH, C2H4SH, PO 3H2, NHSO2CF3 , NHSO2C6F5, SO3H, CONHNH2, CONHNHSO2CF3 , CONHOCH 3 , CONHOC2H5 , CONHCF 3 , OH, CH2OH, C2H4OH, OPO 3H2, OSO 3H ,
Figure imgf000322_0001
wherein each of R42, R43 and R44 is independently selected from H, Cl, CN, NO2, CF3, C2F5, C3F7, CHF2, CH2F, CO2CH3, CO2C2H5, SO2CH3 SO2CF3 and SO2C6F5; wherein Z is selected from O, S, NR45 and CH2; wherein R45 is selected from hydrido, CH3 and CH2C6H5; and wherein said acidic moiety may be a heterocyclic acidic group attached at any two adjacent positions of R3 through R11 so as to form a fused ring system with one of the phenyl rings of the biphenyl moiety of Formula II, said biphenyl fused ring system selected from
Figure imgf000323_0001
and the esters, amides and salts of said acidic moieties;
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
56. The method of Claim 55 wherein m is one;
wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl,
n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, neopentyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclopropylmethyl, cyclopropylethyl,
cyclohexylmethyl, alkoxycarbonylalkyl, alkylcarbonyloxyalkyl, buten-2-yl, 3-butenyl, butyn-2-yl, butyn-3-yl, haloloweralkyl and hydroxyloweralkyl; wherein R2 is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, isopentyl, neopentyl, phenyl, cyclohexyl, cyclohexylmethyl, CH3CH=CH-CH2, SC3H7, cyclohex-3 - en-1-yl, SC4H9,
Figure imgf000324_0002
CH2S , CH3CH=CH, CH2=CH-CH2,
CH3CH2CH2CH=CH-, amino, alkoxy, aminomethyl, aminoethyl, aminopropyl, CH2OCOCH3, CH2CI, CH2OCH3, CH2OCH (CH3) 2, CH2CO2H, CH(CH3)CO2H, -CH2OCOCH2CH2 -CH2CH2CH2CO2H, -CH2CH2F, -
Figure imgf000324_0003
CH2CH2CH2F, -CH2ONO2, -CH2SH, -CH2O , CF3, CH2OH,
Figure imgf000324_0004
hydroxyalkyl, halo, 1-oxo-2-phenylethyl, 2-cyclohexylethyl, 3-cyclohexylpropyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexanoyl, 1-butenyl, buten-2-yl,
3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl and
difluoromethyl; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3, OH,
Figure imgf000324_0001
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
57. The method of Claim 56 wherein m is one;
wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein R0 and R1 is
independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4- methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl,
cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl, methoxycarbonyImethyl,
methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3- hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tertbutyl, n-pentyl, neopentyl, 2-phenylethyl, 2-cyclohexylethyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3 through R11 is hydrido with the proviso that at least one of R5, R6, R8 and R9 is an acidic group selected from CO2H, SH, PO3H2, SO3H, CONHNH2, CONHNHSO2CF3 ,
OH,
Figure imgf000325_0001
wherein each of R42 and R43 is independently selected from chloro, cyano, nitro, trifluoromethyl, methoxycarbonyl and trifluoromethylsulfonyl; or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
58. The method of Claim 57 wherein m is one;
wherein each of X1 and X2 is independently selected from oxygen atom and sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl,
n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl. cyclohexl, cyclohexylmethyl, methoxycarbonylmethyl,
methoxycarbonylethyl,
4-hydroxybuty, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl,
n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2-phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000326_0001
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
59. The method of Claim 58 wherein m is one;
wherein X1 is an oxygen atom and X2 is a sulfur atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl,
methoxycarbonylmethyl, methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2- phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000327_0001
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
60. The method of Claim 59 wherein m is one;
wherein X1 is an oxygen atom and X2 is an oxygen atom; wherein each of R0 and R1 is independently selected from hydrido, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 4-methylbutyl, n-pentyl, neopentyl, cyclopropylmethyl, cyclopropylethyl, propenyl, phenyl, benzyl, phenethyl, cyclohexyl, cyclohexylmethyl,
methoxycarbonylmethyl, methoxycarbonylethyl, 4-hydroxybutyl, 2-hydroxyethyl and 3-hydroxypropyl; wherein R2 is selected from ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, 4-methylbutyl, tert-butyl, n-pentyl, neopentyl, benzyl, 2- phenylethyl, 3-phenylpropyl, cyclohexylmethyl, cyclohexyl, propoxy, butoxy, 1-butenyl, buten-2-yl, 3-butenyl, butyn-1-yl, butyn-2-yl, butyn-3-yl, propylthio and butylthio; wherein each of R3, R4, R6, R7, R8, R10 and R11 is hydrido; wherein one of R5 and R9 is hydrido and the other of R5 and R9 is an acidic group selected from CO2H and
Figure imgf000327_0002
or a tautomer thereof or a pharmaceutically-acceptable salt thereof.
61. The method of Claim 60 wherein said compound is selected from the group consisting of
8-(2-butenyl)-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H- tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6- dione;
8-butyl-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-(cyclopropyl-methyl)-3-methyl-7-[[2'- (1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2, 6-dione;
8-butyl-3,7-dihydro-1-methyl-3-(cyclopropyl-methyl)-7-[[2'-
(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl]methyl]-1H-purine-
2,6-dione;
8-butyl-3,7-dihy ro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-3-propyl-7-[[2'-(1H-tetrazol-5- yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-propyl-3,7-dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-
5-yl)(1,1'-biphenyl)-4-yl]methyl]-1H-purine-2,6-dione;
8-butyl-3,7-dihydro-1-propyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dionn; 8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-6-oxo-2-thioxo-1H-purine; and
8-butyl-3,7-dihydro-1-methyl-7-[[2'-(1H-tetrazol-5-yl)(1,1'- biphenyl)-4-yl]methyl]-1H-purine-2,6-dione.
62. The method of Claim 61 which is 8-(2E- butenyl)-3,7-dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
63. The method of Claim 61 which is 8-butyl-3,7- dihydro-1,3-dimethyl-7-[[2'-(1H-tetrazol-5-yl) [1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
64. The method of Claim 61 which is 8-butyl-3,7- dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1- biphenyl]-4-yl]methyl]-1H-purine-6-one-2-thione.
65. The method of Claim 61 which is 8-butyl-3,7- dihydro-1-propyl-3-methyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
66. The method of Claim 61 which is 8-butyl-3,-7- dihydro-1,3-dipropyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]- 4-yl]methyl-1H-purine-2,6-dione.
67. The method of Claim 61 which is 8- (2E- butenyl)-3,7-dihydro-1-methyl-3-isobutyl-7-[[2'-(1H-tetrazol- 5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
68. The method of Claim 61 which is 8-butyl-3,7- dihydro-1-cyclopropyl-3-methyl-7-[[2'-(1H-tetrazol-5-yl)
[1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
69. The method of Claim 61 which is 8-butyl-3,7- dihydro-1-methyl-3-cyclopropyl-7-[[2'-(1H-tetrazol-5-yl)
[1,1'-biphenyl]-4-yl]methyl-1H-purine-2,6-dione.
70. The method of Claim 61 which is 8-butyl-3,7- dihydro-1-methyl-3-phenyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
71. The method of Claim 61 which is 8-butyl-3,7- dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4- yl]methyl]-1H-purine-2,6-dione.
72. The method of Claim 61 which is 8-propyl-3,7' dihydro-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4- yl]methyl]-1H-purine-2,6-dione.
73. The method of Claim 61 which is 8-propyl-3,7' dihydro-1-methyl-3-propyl-7-[[2'-(1H-tetrazol-5-yl)[1,1'- biphenyl]-4-yl]methyl]-1H-purine-2,6-dione.
74. The method of Claim 50 wherein said circulatory disorder is a cardiovascular disorder.
75. The method of Claim 50 wherein said cardiovascular disorder is hypertension.
76. The method of Claim 50 wherein said cardiovascular disorder is congestive heart failure.
PCT/US1991/007426 1990-10-25 1991-10-16 Biphenylalkyl xanthine compounds for treatment of cardiovascular disorders WO1992007852A1 (en)

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