WO1995004046A1

WO1995004046A1 - Compounds as pde iv and tnf inhibitors

Info

Publication number: WO1995004046A1
Application number: PCT/GB1994/001631
Authority: WO
Inventors: Andrew David Morley; Malcolm Norman Palfreyman; Andrew James Ratcliffe; Brian William Sharp
Original assignee: Rhone-Poulenc Rorer Limited
Priority date: 1993-07-28
Filing date: 1994-07-28
Publication date: 1995-02-09
Also published as: GB9315595D0

Abstract

This invention is directed to an [(ether or thioether)heteroaryl or aryl] compound or an N-oxide thereof or a pharmaceutically acceptable salt thereof, which is useful for inhibiting the production or physiological effects of TNF in the treatment of a patient suffering from a disease state associated with a physiologically detrimental excess of tumor necrosis factor (TNF). Compounds within the scope of the present invention also inhibit cyclic AMP phosphodiesterase, and are useful in treating a disease state associated with pathological conditions that are modulated by inhibiting cyclic AMP phosphodiesterase, such disease states including inflammatory and autoimmune diseases, in particular type IV cyclic AMP phosphodiesterase. The present invention is therefore directed to their pharmacological use for inhibiting TNF and/or cyclic AMP phosphodiesterase, pharmacological compositions comprising the compounds and methods for their preparation.

Description

COMPOUNDS AS PDE IV AND TNF INHIBITORS

Field of the Invention

This invention is directed to [(ether or thioether)heteroaryl or aryl] compounds, their preparation, pharmaceutical compositions containing these compounds, and their pharmaceutical use in the treatment of disease states associated with proteins that mediate cellular activity.

Disease states associated with abnormally high physiological levels of cytokines such as TNF are treatable according to the invention. TNF is an important pro-inflammatory cytokine which causes hemorrhagic necrosis of tumors and possesses other important biological activities. TNF is released by activated macrophages, activated T-lymphocytes, natural killer cells, mast cells and basophils, fibroblasts, endothelial cells and brain astrocytes among other cells.

The principal in vivo actions of TNF can be broadly classified as inflammatory and catabolic. It has been implicated as a mediator of endotoxic shock, inflammation of joints and of the airways, immune deficiency states, allograft rejection, and in the cachexia associated with malignant disease and some parasitic infections. In view of the association of high serum levels of TNF with poor prognosis in sepsis, graft versus host disease and acute respiratory distress syndrome, and its role in many other immunological processes, this factor is regarded as an important mediator of general inflammation.

TNF primes or activates neutrophils, eosinophils, fibroblasts and endothelial cells to release tissue damaging mediators. TNF also activates monocytes, macrophages and T-lymphocytes to cause the production of colony stimulating factors and other pro-inflammatory cytokines such ll_ι , ll_6, ll_8 and GM-CSF, which in some case mediate the end effects of TNF. The ability of TNF to activate T-lymphocytes, monocytes, macrophages and related cells has been implicated in the progression of Human Immunodeficiency Virus (HIV) infection. In order for these cells to become infected with HIV and for HIV replication to take place the cells must be maintained in an activated state. Cytokines such as TNF have been shown to activate HIV replication in monocytes and macrophages. Features of endotoxic shock such as fever, metabolic acidosis, hypotension and intravascular coagulation are thought to be mediated through the actions of TNF on the hypothalamus and in reducing the anti-coagulant activity of vascular endothelial cells. The cachexia associated with certain disease states is mediated through indirect effects on protein catabolism. TNF also promotes bone resorption and acute phase protein synthesis.

The discussion herein related to disease states associated with TNF include those disease states related to the production of TNF itself, and disease states associated with other cytokines, such as but not limited to IL-1 , or IL-6, that are modulated by association with TNF. For example, an IL-1 associated disease state, where IL-1 production or action is exacerbated or secreted in response to TNF, would therefore be considered a disease state associated with TNF. TNF-alpha and TNF-beta are also herein referred to collectively as "TNF" unless specifically delineated otherwise, since there is a close structural homology between TNF-alpha (cachectin) and TNF-beta (lymphotoxin) and each of them has a capacity to induce similar biologic responses and bind to the same cellular receptor.

Disease states associated with pathological conditions that are modulated by inhibiting enzymes, which are associated with secondary cellular messengers, such as cyclic AMP phosphodiesterase, are also treatable according to the invention Cyclic AMP phosphodiesterase is an important enzyme which regulates cyclic AMP levels and in turn thereby regulates other important biological reactions. The ability to regulate cyclic AMP phosphodiesterase, including type IV cyclic AMP phosphodiesterase, therefore, has been implicated as being capable of treating assorted biological conditions. In particular, inhibitors of type IV cyclic AMP phosphodiesterase have been implicated as being bronchodilators and asthma-prophylactic agents and as agents for inhibiting eosinophil accumulation and of the function of eosinophils, and for treating other diseases and conditions characterized by, or having an etiology involving, morbid eosinophil accumulation. Inhibitors of cyclic AMP phosphodiesterase are also implicated in treating inflammatory diseases, proliferative skin diseases and conditions associated with cerebral metabolic inhibition.

Reported Developments

Chemical Abstracts, 108(15). April 11 , 1988, abstract no. 131583p pertains to an abstract of Japanese Patent Application Publication No. JP-A- 62 158,253 which discloses that a substituted phenyl compound of formula

is a cardiotonic, but does not disclose or suggest that the compound inhibits cyclic AMP phosphodiesterase or TNF. JP-A-62 158,253 also does not disclose or suggest that the moiety that is ortho to R^"! may be anything other than benzyloxy.

Chemical Abstracts, 99(6 , August 8, 1983, abstract no. 43556z pertains to an abstract of Japanese Patent Application Publication No. JP-A-5 869,812 which discloses that a phenyl compound of formula

is a hypoglycemic agent, but does not disclose or suggest that the compound inhibits cyclic AMP phosphodiesterase or TNF. JP-A-5 869,812 also does not disclose or suggest that the benzamido moiety may be substituted by anything other than methoxy.

Panos Grammaticakis, Bull. Soc. Chim. Fr„ 848-857 (1965) discloses a phenyl compound of the formula

Grammaticakis examines the ultraviolet and visible absorbances of compounds bearing different substituents. Grammaticakis does not disclose or suggest that the compound exhibits any pharmacological activity. JP-A-5 869,812 also does not disclose or suggest that the benzamido moiety may be substituted by anything other than methoxy.

lan W. Mathison. et al.. J. Med. Chem.. 16(4). 332-336 (1973). discloses that a phenyl compound of formula

is a hypotensive agent, but do not disclose or suggest that the compound inhibits cyclic AMP phosphodiesterase or TNF. Mathison, et al., also do not disclose or suggest that the benzamido moiety may be substituted by anything other than methoxy.

European Patent Application Publication No. EP 232199 B1 discloses that phenyl compounds of formula

wherein R2 is alpha.alpha'-disubstituted alkyl or mono- or poiycyclic cycloalkyl bonded to the phenyl moiety via a quaternary carbon, exhibit anti-inflammatory and/or anti-allergic activity. EP 232199 B1 does not disclose or suggest compounds wherein R^ is alkyl bonded to the phenyl moiety via a nonquaternary carbon, alkenyl, alkynyl, cyclothioalkyi or cyclothioalkenyl, or R³ is azaheteroaryl having a nitrogen atom thereof oxidised to the corresponding N-oxide moiety.

European Patent Application Publication No. EP 470,805 A1 discloses phenyl compounds of the formula

R^:

wherein R may be C3-7 alkyl, C3-7 cycloalkyl or

Z may be a bond; o is 1-4; a and b are independently 1-3; and c is 0-2. EP 470,805 A1 discloses that these compounds are useful intermediates for preparing PDE IV inhibitors, but does not disclose or suggest that the compounds have any pharmacological activity. EP 470,805 A1 furthermore does not disclose or suggest compounds wherein R or the methyl moiety is directly bonded to the phenyl moiety. Japanese Patent Application Publication No. JP-A-0 4360847 discloses compounds of the formula

wherein R^"! , R² and R3 may be the same or different and may be halo or lower alkoxy or lower alkyl both optionally substituted by halo; and A may be optionally substituted aryl or 5-6 membered heterocyclyl group. JP-A-0 4360847 discloses that the compounds are useful intermediates for preparing antimicrobial agents, but does not disclose or suggest that the compounds have any pharmacological activity. JP-A-0 4360847 also does not disclose or suggest that the compounds wherein the phenylacyl moiety is substituted in the 3,4-positions relative to the acyl moiety by lower alkoxy groups. Furthermore, JP-A-0 4360847 does not disclose or suggest compounds wherein R² is alkenyl, alkynyl, cyclothioalkyi or cyclothioalkenyl or R³ is azaheteroaryl having a nitrogen atom thereof oxidised to the corresponding N- oxide moiety.

WO Patent Application No. 92/12961 discloses that compounds of the formula

inhibit cyclic AMP phosphodiesterase. WO Patent Application No. 92/12961 does not disclose or suggest that these compound inhibit TNF. WO Patent Application No. 92/12961 does not disclose or suggest compounds wherein R¹ or R² is directly bonded to the phenyl moiety.

WO Patent Application No. 93/25517 discloses that compounds of the following formula inhibit PDE IV. WO Patent Application No. 93/25517 does

not disclose or suggest that these compound inhibit TNF. WO Patent Application No. 93/25517 does not disclose or suggest compounds wherein X is a direct bond and R² is alkyl, alkenyl, alkynyl, cyclothioalkyi or cyclothioalkenyl, or R³ is azaheteroaryl having a nitrogen atom thereof oxidised to the corresponding N-oxide moiety.

WO Patent Application No. 93/10228 discloses that compounds of the following formula

A-Y-B-Z

inhibit PDE IV and as such are useful in treatment of inflammatory diseases. WO Patent Application No. 93/10228 does not disclose or suggest that these compounds inhibit TNF. WO Patent Application No. 93/10228 does not disclose or suggest compounds wherein R¹ or R² is directly bonded to the phenyl moiety.

WO Patent Application No. 93/071 11 discloses that compounds of the following formula wherein X may be YR2; Y is O or S(0)_m; X₃ is halogen or

hydrogen; and A is a group of formula

inhibit PDE IV. WO Patent Application No. 93/07111 does not disclose or suggest compounds wherein the A substituent is a [(-CXNH- or -CXCH2-)aryl or heteroaryl] moiety wherein X is O or S.

WO Patent Application No. 91/16303 discloses that compounds of the following formula wherein Ri, R and R3 may be hydrogen, halogen, lower alkyl,

lower alkoxy or cycloalkoxy inhibit PDE IV. WO Patent Application No. 91/16303 does not disclose or suggest compounds wherein the lactam moiety is substituted by a [(-CXNH- or -CXCH2-)aryl or heteroaryl] moiety wherein X is O or S.

WO Patent Application No. 92/19594 discloses that compounds of the following formula wherein X may be YR₂; Y is O or S(0)_m; and X3 may be

hydrogen or halogen inhibit PDE IV. WO Patent Application No. 92/19594 does not disclose or suggest compounds wherein the lactam moiety is substituted by a [(-CXNH- or -CXCH2-)aryl or heteroaryl] moiety wherein X is 0 or S.

SUMMARY OF THE INVENTION

This invention is directed to a compound of formula I, which is useful for inhibiting the production or physiological effects of TNF in the treatment of a patient suffering from a disease state associated with a physiologically detrimental excess of tumor necrosis factor (TNF), where formula I is as follows:

wherein

R¹ is lower alkyl;

R² is alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cyclothioalkyi or cyclothioalkenyl;

R3 is aryl or heteroaryl;

Z1 and Z² are independently oxygen, sulfur or direct bond, and only one of Z¹ and Z² is a direct bond; Z3 is -CZCH2- or -CZNH-; and

Z is oxygen or sulfur,

or N-oxide thereof or a pharmaceutically acceptable salt thereof,

provided that

when Z² is a direct bond, R² is alkyl bonded to the phenyl moiety via a nonquaternary carbon, alkenyl, alkynyl, cyclothioalkyi or cyclothioalkenyl, or R³ is azaheteroaryl having a nitrogen atom thereof oxidised to the corresponding N-oxide moiety.

Compounds within the scope of the present invention also inhibit cyclic

AMP phosphodiesterase, and are useful in treating a disease state associated with pathological conditions that are modulated by inhibiting cyclic AMP phosphodiesterase, such disease states including inflammatory and autoimmune diseases, in particular type IV cyclic AMP phosphodiesterase. The present invention is therefore directed to their pharmacological use, pharmacological compositions comprising the compounds and methods for their preparation.

DETAILED DESCRIPTION OF THE INVENTION

As used above, and throughout the description of the invention, the following terms, unless otherwise indicated, shall be understood to have the following meanings:

Definitions

"Patient" includes both human and other mammals.

"Alkyl" means an aliphatic hydrocarbon group which may be straight or branched having about 1 to about 15 carbon atoms in the chain. Preferred alkyl groups have 1 to about 12 carbon atoms in the chain. Branched means that one or more lower alkyl groups such as methyl, ethyl or propyl are attached to a linear alkyl chain. "Lower alkyl" means about 1 to about 4 carbon atoms in the chain which may be straight or branched. The alkyl group is optionally substituted by one or more of halo, cycloalkyl, cycloalkenyl or cycloalkylidene groups. Exemplary alkyl groups include methyl, fluoromethyl, difluoromethyl, trifluoromethyl, cyclopropylmethyl, cyclopentylmethyl, cyclopentylfluoromethyl, cyclopentylidenemethyl, ethyl, fluoroethyl.π-propyl, /- propyl, n-butyl, f-butyl, n-pentyl, 3-pentyl, heptyl, octyl, nonyl, decyl and dodecyl; preferred are methyl, ethyl, difluoromethyl, fluoroethyl, cyclopentylmethyl and cyclopentylfluoromethyl.

"Alkenyl" means an aliphatic hydrocarbon group containing a carbon- carbon double bond and which may be straight or branched having about 2 to about 15 carbon atoms in the chain. Preferred alkenyl groups have 2 to about 12 carbon atoms in the chain; and more preferably about 2 to about 4 carbon atoms in the chain. Branched means that one or more lower alkyl groups such as methyl, ethyl or propyl are attached to a linear alkenyl chain. "Lower alkenyl" means about 2 to about 4 carbon atoms in the chain which may be straight or branched. The alkenyl group is optionally substituted by one or more halo, cycloalkyl or cycloalkenyl. Exemplary alkenyl groups include ethenyl, propenyl, π-butenyl, /-butenyl, 3-methylpropenyl, n-pentenyl, heptenyl, octenyl and decenyl.

"Alkynyl" means an aliphatic hydrocarbon group containing a carbon- carbon triple bond and which may be straight or branched having about 2 to about 15 carbon atoms in the chain. Preferred alkynyl groups have 2 to about 12 carbon atoms in the chain; and more preferably about 2 to about 4 carbon atoms in the chain. Branched means that one or more lower alkyl groups such as methyl, ethyl or propyl are attached to a linear alkynyl chain. "Lower alkynyl" means about 2 to about 4 carbon atoms in the chain which may be straight or branched. The alkynyl group is optionally substituted by one or more halo, cycloalkyl or cycloalkenyl. Exemplary alkynyl groups include ethynyl, propynyl, π-butynyl, 2-butynyI, 3-methylbutynyl, n-pentynyl, heptynyl, octynyl and decynyl.

"Cycloalkyl" means a non-aromatic mono- or multicyclic ring system of about 3 to about 10 carbon atoms. The cycloalkyl group is optionally substituted by one or more halo, methylidene (H2C=) or alkyl. Exemplary monocyclic cycloalkyl rings include cyclopentyl, fluorocyclopentyl, cyclohexyl and cycloheptyl; more preferred is cyclopentyl. Exemplary multicyclic cycloalkyl rings include 1-decalin, adamant-(1 - or 2-)yl, trinorbornyl and tricyclo[2.2.1.0²-⁶-]heptyl.

"Cycloalkylidene" means a non-aromatic monocyclic ring system of about 5 to about 7 carbon atoms of formula

wherein n is 1 to 3.

"Cycloalkenyl" means a non-aromatic monocyclic or multicyclic ring system containing a carbon-carbon double bond and having about 3 to about 10 carbon atoms. The cycloalkenyl group is optionally substituted by one or more halo, alkyl and methylidene (CH2=). Preferred monocyclic cycloalkenyl rings include cyclopentenyl, cyclohexenyl or cycloheptenyl; more preferred is cyclopentenyl. A preferred multicyclic cycloalkenyl ring is a norbornylenyl.

"Cyclothioalkyi" means a non-aromatic monocyclic or multicyclic ring system of about 3 to about 10 ring atoms wherein at least one of the ring atoms is sulfur and the other ring atoms are carbon. Preferred rings include about 5 to about 6 ring atoms. Also preferred are rings in which one or two of the ring atoms is/are sulfur. The cyclothioalkyi is optionally substituted by one or more halo. The thio moiety of the cyclothioalkyi ring may also be optionally oxidized to the corresponding S-oxide or S,S-dioxide. Preferred monocyclic cyclothioalkyi rings include tetrahydrothiophenyl and tetrahydrothiopyranyl; more preferred is tetrahydrothiophenyl.

"Cyclothioalkenyl" means a non-aromatic monocyclic or multicyclic ring system having about 3 to about 10 ring atoms wherein at least one of the ring atoms is sulfur and the other ring atoms are carbon and the ring system contains a carbon-carbon double bond. Preferred rings include about 5 to about 6 ring atoms. Also preferred are rings in which one or two of the ring atoms is/are sulfur. The cyclothioalkenyl is optionally substituted by one or more halo. The thio moiety of the cyclothioalkenyl may also be optionally oxidized to the corresponding S-oxide or S,S-dioxide. Preferred monocyclic cyclothioalkyi rings include dihydrothiophenyl and dihydrothiopyranyl; more preferred is dihydrothiophenyl.

"Aromatic" means aryl or heteroaryl as defined below. Preferred aromatic groups include phenyl, halo substituted phenyl and azaheteroaryl.

"Aryl" means aromatic carbocyciic radical containing about 6 to about 10 carbon atoms. Exemplary aryl include phenyl or naphthyl, or phenyl or naphthyl substituted with one or more aryl group substituents which may be the same or different, where "aryl group substituent" includes hydrogen, alkyl, aryl, aralkyl, hydroxy, hydroxyalkyl, alkoxy, aryloxy, aralkyloxy, carboxy, acyl, aroyl, halo, nitro, cyano, carboxy, alkoxycarbonyl, aryloxycarbonyl, aralkyloxycarbonyl, acylamino, aroylamino, alkylsulfonyl, arylsulfonyl, alkylsulfinyl, arylsulfinyl, alkylthio, arylthio, aralkylthio, Y Y²N-, Y¹Y²NCO- or Y¹Y²NS02-, where Y¹ and Y² are independently hydrogen, alkyl, aryl, and aralkyl. Preferred aryl group substituents include hydrogen, alkyl, hydroxy, acyl, aroyl, halo, nitro, cyano, alkoxycarbonyl, acylamino, alkylthio, Y³Y⁴N-, Y3Y NCO- and Y³Y NS02-, where Y³ and Y⁴ are independently hydrogen and alkyl.

"Heteroaryl" means about a 5- to about a 10- membered aromatic monocyclic or multicyclic hydrocarbon ring system in which one or more of the carbon atoms in the ring system is/are element(s) other than carbon, for example nitrogen, oxygen or sulfur. The heteroaryl may also be substituted by one or more aryl group substituents. "Azaheteroaryl" means a subclass of heteroaryl wherein one or more of the atoms in the ring system is/are replaced by nitrogen. Imine nitrogen (=N-) moieties of an azaheteroaryl group may also be in an oxidized state such as the corresponding N-oxide. Exemplary heteroaryl groups include pyrazinyl, furanyl, thienyl, pyridyl, pyrimidinyl, isoxazolyl, isothiazolyl, pyridazinyl, 1 ,2,4-triazinyl, quinolinyl, and isoquinolinyl. Preferred heteroaryl groups include pyrazinyl, thienyl, pyridyl, pyrimidinyl, isoxazolyl and isothiazolyl. Preferred azaheteroaryl groups include pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl or 1 ,2,4-triazinyl. "Aralkyl" means an aryl-alkyl- group in which the aryl and alkyl are as previously described. Preferred aralkyls contain a lower alkyl moiety. Exemplary aralkyl groups include benzyl, 2-phenethyl and naphthlenemethyl.

"Hydroxyalkyi" means a HO-alkyl- group in which alkyl is as previously defined. Preferred hydroxyalkyls contain lower alkyl. Exemplary hydroxyalkyi groups include hydroxymethyl and 2-hydroxyethyl.

"Acyl" means an H-CO- or alkyl-CO- group in which the alkyl group is as previously described. Preferred acyls contain a lower alkyl. Exemplary acyl groups include formyl, acetyl, propanoyl, 2-methylpropanoyl, butanoyl and palmitoyl.

"Aroyl" means an aryl-CO- group in which the aryl group is as previously described. Exemplary groups include benzoyl and 1- and 2-naphthoyl.

"Alkoxy" means an alkyl-O- group in which the alkyl group is as previously described. Exemplary alkoxy groups include methoxy, ethoxy, n-propoxy, Apropoxy, n-butoxy and heptoxy.

"Aryloxy" means an aryl-O- group in which the aryl group is as previously described. Exemplary aryloxy groups include phenoxy and naphthoxy.

"Aralkyloxy" means an aralkyl-O- group in which the aralkyl groups is as previously described. Exemplary aralkyloxy groups include benzyloxy and 1 - or 2-naphthalenemethoxy.

"Alkylthio" means an alkyl-S- group in which the alkyl group is as previously described. Exemplary alkylthio groups include methylthio, ethylthio, /-propylthio and heptylthio.

"Arylthio" means an aryl-S- group in which the aryl group is as previously described. Exemplary arylthio groups include phenylthio and naphthylthio. "Aralkylthio" means an aralkyl-S- group in which the aralkyl group is as previously described. An exemplary aralkylthio group is benzylthio.

"Y³Y⁴N-" means a substituted or unsubstituted amino group, wherein Y³ and Y⁴ are as previously described. Exemplary groups include amino (H2N-), methylamino, ethylmethylamino, dimethylamino and diethylamino.

"Alkoxycarbonyl" means an alkyl-O-CO- group. Exemplary alkoxycarbonyl groups include methoxy- and ethoxycarbonyl.

"Aryloxycarbonyl" means an aryl-O-CO- group. Exemplary aryloxycarbonyl groups include phenoxy- and naphthoxycarbonyl.

"Aralkyloxycarbonyl" means an aralkyl-O-CO- group. An exemplary aralkyloxycarbonyl group is benzyloxycarbonyl.

"Y¹Y NCO-" means a substituted or unsubstituted carbamoyl group, wherein Y^"! and Y² are as previously described. Exemplary groups are carbamoyl (H2NCO-) and dimethylcarbamoyl (Me2NCO-).

"Y^"Υ²NSθ2-" means a substituted or unsubstituted sulfamoyl group, wherein Y¹ and Y² are as previously described. Exemplary groups are sulfamoyl (H2NSO2-) and dimethylsulfamoyl (Me2NS02-).

"Acylamino" is an acyl-NH- group wherein acyl is as defined herein.

"Aroylamino" is an aroyl-NH- group wherein aroyl is as defined herein.

"Alkylsulfonyl" means an alkyI-S02- group. Preferred groups are those in which the alkyl group is lower alkyl.

"Alkylsulfinyl" means an alkyl-SO- group. Preferred groups are those in which the alkyl group is lower alkyl.

"Arylsulfonyl" means an aryl-S02- group.

"Arylsulfinyl" means an aryl-SO- group. "Halo" means fluoro, chloro, bromo, or iodo. Preferred are fluoro, chloro or bromo; more preferred are fluoro or chloro, and further preferred is fluoro.

σ I "N-oxide" means a moiety of the following structure N⁺— .

Preferred Embodiments

A compound of formula I is preferred for use in treating a disease state associated with a physiologically detrimental excess of tumor necrosis factor. Disease states associated with pathological conditions that are modulated by inhibiting tumor necrosis factor are treatable with a compound of formula I.

A compound of formula I is also preferred for use in treating a disease state associated with a physiologically detrimental excess of cyclic AMP phosphodiesterase. Disease states associated with pathological conditions that are modulated by inhibiting cyclic AMP phosphodiesterase are treatable with a compound of formula I.

According to a compound aspect of the invention, preferred compounds are described formula I,

wherein

R² is alkyl, alkenyl or cycloalkyl;

R³ is phenyl, substituted phenyl or azaheteroaryl;

Z¹ and Z² are independently oxygen or direct bond, and only one of Z^"! and Z² is a direct bond; and

Z³ is -COCH2- or -CONH-.

According to a further compound aspect of the invention, preferred compounds are described formula I, wherein

R¹ is methyl, ethyl, fluoroethyi or difluoromethyl;

R² is 2-methylpropenyl, cyclopentylfluoromethyl, cyclopentylmethyl, cyclopentyl or trinorbornyl; and

R³ is azaheteroaryl.

According to a further aspect of the invention, preferred are N-oxide compounds of formula I, that is compounds of formula I wherein R³ is azaheterocyclyl having an imine moiety thereof as an N-oxide. Also futher preferred are compounds of formula I wherein R³ is 3,5-dihalo-1-oxido-4- pyridinium.

Compounds of the invention wherein R1 is lower alkyl optionally substituted by one or more halo, preferably fluoro, are also preferred. Compounds of the invention wherein R² is substituted by one or more halo, preferably fluoro, are also preferred. It is further preferred that the halo substitution is on a position of R¹ or R² that is attached respectively to Z^"1 and Z². Where R² is cyclothioalkyi or cyclothioalkenyl substituted by halo, it is also preferred that the halo substitution is on a position adjacent to the thio moiety of the cyclothioalkyi or cyclothioalkenyl.

Among the compounds of the invention wherein R³ is substituted phenyl, the phenyl group is preferably substituted on the 2-position or on both the 2- and 6-positions; more preferably on both the 2- and 6-positions. It is also preferred that the phenyl substituent is halo; preferably chloro or fluoro.

Similarly, among compounds of the invention where R³ is substituted heteroaryl, the heteroaryl group is preferably substituted on one or both, more preferably on both, of the positions adjacent to a position of R³ that is attached to Z³.

Special embodiments of the compounds of the invention include those of formula I wherein R³ is azaheteroaryl substituted on one or both, more preferably on both, of the positions adjacent to a position of R³ that is attached to Z³, or an N-oxide thereof. Further preferred are compounds wherein R³ is a 3,5-dihalopyrid-4-yl moiety, preferably wherein halo is chloro or fluoro, or an N- oxide thereof.

Special embodiments of the compounds of the invention also include those of formula I wherein Z³ is -CZNH-, more preferably wherein Z is oxygen.

Special embodiments of the compounds of the present invention include those wherein R² is 2-methylpropenyl, cyclopentylfluoromethyl, cyclopentylmethyl, cyclopentyl, cyclopentylidenemethyl, trinorbornyl, trinorbornenyl, tricyclo[2.2.1.0²-⁶ ]heptanyl or tetrahydrothiophenyl; more preferred 2-methylpropenyl, cyclopentylfluoromethyl, cyclopentylmethyl, cyclopentyl, cyclopentylidenemethyl and trinorbornyl.

Another special embodiment of the compounds of the invention include those of formula I wherein R¹ is lower alkyl optionally substituted by halo, preferably fluoro; and R² is 2-methylpropenyl, cyclopentylfluoromethyl, cyclopentylmethyl, cyclopentyl and trinorbornyl.

According to a further aspect of the invention, preferred compounds of formula I are described wherein Z¹ is oxygen and Z² is a direct bond; Z¹ is sulfur and Z² is a direct bond; and Z¹ is a direct bond and Z² is oxygen are preferred; and more preferred are Z¹ is oxygen and Z² is a direct bond.

Preferred compounds for use according to the invention are selected from the following:

(A) N-(3,5-dichloropyrid-4-yl)-3-cyclopentylmethyl-4-methoxybenzamide;

(B) N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-ethylbenzamide;

(C) N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-methylbenzamide;

(D) N-(3,5-dichloro-1 -oxido-4-pyridinio) 3-cyclopentylmethyl-4- methoxybenzamide; (E) N-(3,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentyioxy-4- ethylbenzamide;

(F) N-(3,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentyloxy-4- methylbenzamide;

(G) N-(,5-dichloro-1 -oxido-4-pyridinio)-3-(exo)-8,9,10-trinorbornyl-2-oxy-4- ethylbenzamide;

(H) N-(,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentylidenemethyl-4- methoxybenzamide;

(I) N-(,5-dichloro-1-oxido-4-pyridinio)-3-(2-methylpropenyl)-4- methoxybenzamide;

(J) N-(,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentylidenemethyl-4- difluoromethoxybenzamide;

(K) N-(,5-dichloro-1-oxido-4-pyridinio)-3-cyclopentylfluoromethyl-4- methoxybenzamide;

(L) N-(,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentyloxy-4-(1 - fluoroethyl)benzamide;

(M) N-(3,5-dichloropyrid-4-yl)-3-(exo)-8,9,10-trinorbomyl-2-oxy-4- ethylbenzamide;

(N) N-(3,5-dichloropyrid-4-yl)-3-cyclopentylidenemethyl-4- methoxybenzamide;

(O) N-(3,5-dichloropyrid-4-yl)-3-(2-methylpropenyl)-4-methoxybenzamide;

(P) N-(3,5-dichloropyrid-4-yl)-3-cyclopentylidenemethyl-4- difluoromethoxybenzamide;

(Q) N-(3,5-dichloropyrid-4-yl)-3-cyclopentylfluoromethyl-4- methoxybenzamide; and (R) N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-(1 -fluoroethyl)benzamide.

Preferred compounds include A-R; more preferred are ?.

The letters A-R are allocated to compounds for easy reference in this specification.

Compounds of formula I may be prepared by the application or adaptation of known methods, by which is meant methods used heretofore or described in the literature.

Thus, compounds of formula I wherein R¹ , R², R³, Z¹ and

Z² are as hereinbefore defined, Z³ represents a -CZNH- linkage, and Z is oxygen, may be prepared by the reaction of compounds of formula II

wherein R1 , R², Z¹ and Z² are as hereinbefore defined, and X represents halo, such as bromo or, preferably, chloro, with a compound of the formula III

R³NH2 III

wherein R³ is as hereinbefore defined, preferably in the presence of a base such as an alkali metal hydride, such as sodium hydride, or an amine, preferably a tertiary amine, such as triethylamine or pyridine, optionally in an inert solvent, for example dichloromethane, dimethylformamide, or an ether, such as diethyl ether or tetrahydrofuran, preferably at a temperature from about 0°C to the reflux temperature or at the melting point of the reaction mixture.

Alternatively, compounds of formula I wherein R¹ , R², R³, Z¹ and Z² are as hereinbefore defined, Z³ represents a -CZNH- linkage, and Z represents oxygen, may be prepared by the reaction of compounds of formula II as hereinbefore described, with a compound of the formula IV wherein R³ is as

R CONHR³ IV

hereinbefore defined, and R⁴ represents an alkyl or cycloalkyl group containing up to 5 carbon atoms, preferably a methyl group, preferably in the presence of a base, for example an alkali metal hydride, such as sodium hydride, or an amine, preferably a tertiary amine, such as triethylamine, in an inert solvent, for example toluene, dimethylformamide, or an ether, such as tetrahydrofuran or diethyl ether, at a temperature from about 0°C to reflux, then a second base, for example an amine, such as piperidine.

Alternatively, compounds of formula I, wherein R¹ , R², R³, Z¹ and Z² are as hereinbefore defined, Z is oxygen, and Z³ represents a -CZNH- linkage, may be prepared by the reaction of compounds of formula V wherein R¹ , R²,

Z¹ and Z² are as hereinbefore defined, with compounds of formula VI wherein

R³X VI

R³ and X are as hereinbefore defined, preferably X is chloro, and preferably the preparation takes place in the presence of a base, for example an alkali metal hydride, such as sodium hydride, an alkali metal alkoxide, such as potassium t-butoxide, an alkali metal hydroxide, such as sodium hydroxide or carbonate, or an amine, preferably a tertiary amine, such as triethylamine or pyridine, optionally in an inert solvent, for example dichloromethane, dimethylformamide, or an ether, such as diethyl ether or tetrahydrofuran, preferably at a temperature from about 0°C to reflux.

Alternatively, compounds of formula I, wherein R^"l , R² and R³ are as hereinbefore defined, Z¹ is a direct bond, Z³ represents a -CZNH- linkage, and Z and Z² are oxygen, may be prepared by the reaction of compounds of formula VII wherein R^~I , R³, Z and Z^"* are as hereinbefore defined and Z³

represents a -CZNH- linkage, and Z is oxygen, with compounds of the formula VIII wherein R² is as hereinbefore defined, preferably, X is as hereinbefore

R X VIII

defined or p-toluenesulfonate, preferably X is bromo, and preferably the preparation takes place in the presence of a base, for example an alkali metal hydride, such as sodium hydride, an alkali metal hydroxide or carbonate, such as sodium hydroxide or carbonate, or an amine, preferably a tertiary amine, such as. triethylamine or pyridine, optionally in an inert solvent, for example dichloromethane, dimethylformamide, or an ether, such as diethyl ether or tetrahydrofuran, preferably at a temperature from about 0°C to reflux, or by the reaction of the compound of formula VII above with compounds of the formula IX, wherein R² is as hereinabove defined in the presence of, for example,

R²OH IX

diisopropylazodicarboxylate and triphenylphosphine.

Alternatively, compounds of formula I, wherein R¹ , R², R³, Z¹ and Z² are as hereinbefore defined, Z³ represents a -CZCH2- linkage, and Z represents oxygen, are prepared from compounds of formula X wherein R^ , R² R³, Z1

and Z² are as hereinbefore defined, by oxidation by the application or adaptation of known methods. The oxidation is carried out, for example, by reaction with oxalyl chloride and dimethyl sulfoxide, in the presence of a base, preferably a tertiary amine, preferably triethylamine, in an inert solvent such as dichloromethane, at temperatures from about -60°C to about room temperature, preferably at a reduced temperature, or by adaptation of known methods for the preparation of ketone from a secondary alcohol, for example the application of pyridinium dichromate. Alternatively, the oxidation is carried out by reaction with chromium trioxide in the presence of 3,5-dimethylpyrazole.

According to a further feature of the present invention, compounds of formula I, wherein R¹ , R², R³, Z, Z¹ and Z² are as hereinbefore defined, Z³ represents a -CZCH2- linkage, and preferably those wherein Z represents oxygen, are prepared from compounds of formula XI wherein R¹ , R², Z,

Z^"1 and Z², are as hereinbefore defined and R⁵ and R⁶ represent lower alkyl, such as methyl, groups, by coupling with compounds of the formula XII wherein

R³CH3 XII

R³ is as hereinbefore defined, in the presence of a strong base such as lithium diisopropyiamide (usually prepared in situ from π-butyl lithium and diisopropylamine), preferably at a low temperature.

Alternatively, compounds of formula I, wherein R¹ , R², R³, Z¹ and Z² are as hereinbefore defined, Z³ represents a -CZCH2- linkage, and Z represents oxygen, are prepared from compounds of formula XIII wherein R¹ , R², Z¹ and

Z² are as hereinbefore defined, and R⁷ is alkyl, cycloalkyl or aralkyl containing up to 8 carbon atoms, by coupling with compounds of the formula XII above, wherein R³ is as hereinbefore defined, in the presence of a strong base, such as an alkali metal amide or alkyl, for example n-butyl lithium or lithium diisopropylamide (usually prepared in situ from butyl lithium and diisopropylamine), in an inert solvent, for example cyclohexane or an ether, such as tetrahydrofuran or diethyl ether, at a temperature from about -78°C to about room temperature.

According to a feature of the present invention, compounds of formula wherein R¹ , R², R³, Z¹ and Z² are as hereinbefore defined, Z³ represents a -CZCH2- linkage, and Z represents oxygen, are prepared by the reaction of compounds of formula XIV, wherein R¹ , R², Z¹ and Z² are as hereinbefore

defined, are as hereinbefore defined, with compounds of the formula XV

R³CH₂MgX XV

wherein R³ and X are as hereinbefore defined.

As another example, compounds of formula I wherein R^"! , R², R³, Z^ and Z², are as hereinbefore defined, and Z³ contains a -CS- moiety, are prepared from compounds of formula I wherein R¹ , R², R³, Z¹ and Z²are as hereinbefore defined, and Z³ contains a -CO- moiety, by reaction with phosphorus pentasulfide or 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4- diphosphetane-2,4-disulfide, preferably in a solvent such as pyridine or toluene, and preferably at a temperature from about 0°C to reflux.

As another example, compounds of formula I wherein R³ is as hereinbefore defined and contains an alkylsulfonyl, arylsulfonyl, alkylsulfinyl or arylsulfinyl group, R^"! , R², Z, Z^"! , Z² and Z³ are as hereinbefore defined, are prepared by oxidising the corresponding compounds of formula I wherein R³ is as hereinbefore defined and contains an alkylthio or arylthio group, R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, preferably wherein Z, Z^"! and Z² each represent oxygen, and R² is alkyl or cycloalkyl, preferably with a peroxyacid, such as 3-chloroperbenzoic acid, preferably in an inert solvent, such as dichloromethane, preferably at about room temperature. Alternatively, the oxidation is carried out by reaction with a peroxomonosulfate, such as potassium peroxomonosulfate, conveniently in a solvent such as methanol, buffered to about pH 5, at temperatures from about 0°C to about room temperature. This latter method is preferred for compounds containing an acid-labile group, such as those wherein the moiety R² is unsaturated, such as a cyclopent-2-enyloxy group.

As another example, compounds of formula I wherein R³ is as hereinbefore defined and contains a hydroxymethyl group, and R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, are prepared by the reduction of the corresponding compounds of formula I wherein R³ is as hereinbefore defined and contains an aryloxycarbonyl or, preferably, alkoxycarbonyl group, R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, and Z is preferably oxygen, preferably by means of reacting an alkali metal borohydride, preferably in an inert solvent, such as tetrahydrofuran, preferably at about room temperature.

As another example, compounds of formula I wherein R³ is as hereinbefore defined and contains a formyl group, and R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, are prepared by the oxidising the corresponding compounds of formula I wherein R³ is as hereinbefore defined and contains a hydroxymethyl group, R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, and Z preferably being an oxygen atom, for example with oxalyl chloride and dimethyl sulfoxide, in a solvent such as dichloromethane, and preferably at a temperature lower than about -65°C, or, preferably, by reaction with a complex of sulfur trioxide with an amine such as pyridine, preferably in the presence of an amine such as triethylamine, preferably at about room temperature.

As another example, compounds of formula I wherein R³ is as hereinbefore defined and contains an amino group, and R^"! , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, are prepared by the reducing the corresponding compounds of formula I wherein R³ is as hereinbefore defined and contains a nitro group, R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, and Z is preferably oxygen, preferably with iron in acidic conditions, such as in acetic acid, preferably at or above room temperature, more especially at the reflux temperature. Alternatively the reduction are carried out by reaction with hydrazine hydrate in the presence of ferric chloride and activated carbon, conveniently in a solvent such as methanol, at temperatures from about 25°C to about 80°C. This latter method is preferred for compounds containing an acid-labile group, such as those wherein the moiety R² is unsaturated, such as a cyclopent-2-enyloxy group.

As another example, compounds of formula I wherein R³ is as hereinbefore defined and contains an alkanoylamino or aroylamino group, and R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, are prepared from compounds of formula I wherein R³ is as hereinbefore defined and contains an amino group, R¹ , R², Z, Z^ , Z² and Z³ are as hereinbefore defined, and Z is preferably oxygen, preferably by means of reaction with the appropriate acid halide or acid anhydride in the presence of a tertiary base, such as triethylamine, optionally in an inert solvent, and preferably at a temperature from about 0°C to reflux.

Compounds of formula I wherein R³ is as hereinbefore described, including an azaheteroaryl group containing one or more nitrogen ring atoms, preferably imine (=N-), and R¹ , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, may be converted to the corresponding compounds wherein a nitrogen atom of the azaheteroaryl moiety is oxidised to an N-oxide, R¹ , R², Z, Z¹ , Z² and Z³ are hereinbefore defined, and preferably Z, Z¹ and Z² each represent oxygen, and R² is alkyl or cycloalkyl, preferably by reacting a peracid. for example peracetic acid in acetic acid or m-chloroperoxybenzoic acid in an inert solvent such as dichloromethane, at a temperature from about room temperature to reflux, preferably at elevated temperature. Preferably wherein Z, Z^ and Z² each represent oxygen, and R² is an oxidised cyclothioalkyi, such as cyclosulphinyl or sulphonyl, the reaction is carried out at a temperature from about room temperature to reflux, preferably at a reduced temperature. Alternatively, the oxidation is carried out by reaction with hydrogen peroxide in the presence of sodium tungstate at temperatures from about room temperature to about 60°C. This latter method is preferred for compounds containing an acid-labile group, such as those wherein the moiety R² contains a carbon-carbon double bond between its beta- and gamma- carbon atoms, such as a cyclopent-2-enyloxy group.

Compounds of formula ! wherein R³ represents an azaheteroaryl group containing a nitrogen ring atom as an N-oxide, and R1 , R², Z, Z¹ , Z² and Z³ are as hereinbefore defined, may be converted to the corresponding compounds wherein R³ represents an azaheteroaryl group containing one or more nitrogen ring atoms, preferably imine (=N-), and R¹ , R², Z, Z¹ , Z² and Z³ are hereinbefore defined, preferably by reacting in a deoxygenating system, for example diphosphorus tetraiodide in an inert solvent, such as dichloromethane, preferably at room temperature, or with a chlorotrialkylsilane, preferably chlorotrimethylsilane, in the presence of an alkali metal iodide, such as potassium iodide, and zinc, in an inert solvent, for example acetonitrile, at temperatures from about 0°C to about room temperature, preferably at reduced temperature.

For example, compounds of formula I wherein R1 is as hereinbefore defined and is substituted by fluorine on a carbon atom thereof alpha to the attachment of R¹ to Z¹ as sulfur, or wherein R² is as hereinbefore defined and is substituted by fluorine on a carbon atom thereof alpha to the attachment of R² to Z² as sulfur, and R³ and Z³ as hereinbefore defined, are prepared by reacting xenon difluoride with corresponding compounds of formula I wherein said alpha-carbon atoms carry hydrogen atoms instead of said fluorine atoms. The reaction is conveniently carried out in a solvent, such as dichloromethane, in the presence of a molecular sieve, and in an inert atmosphere, at a low temperature, such as at about 0°C. Alternatively, compounds of formula I wherein R¹ is a difluoromethyl group may be prepared by reacting a compound of formula I or precursor wherein Z¹ is hydroxy or thio! with HCBrF2 in the presence of a strong base in an inert solvent. Furthermore, compounds of formula I wherein R¹ or R² is halo substituted may be prepared by reacting the corresponding compound of formula I wherein R¹ or R² is hydroxy substituted with diethylaminosulphur trifluoride (DAST) in an inert solvent such as methylene chloride.

The compounds of the present invention are useful in the form of the free base or acid or in the form of a pharmaceutically acceptable salt thereof. All forms are within the scope of the invention.

Where the compound of the present invention is substituted with a basic moiety, acid addition salts are formed and are simply a more convenient form for use; and in practice, use of the salt form inherently amounts to use of the free base form. The acids which can be used to prepare the acid addition salts include preferably those which produce, when combined with the free base, pharmaceutically acceptable salts, that is, salts whose anions are non-toxic to the patient in pharmaceutical doses of the salts, so that the beneficial inhibitory effects on TNF and PDE inherent in the free base are not vitiated by side effects ascribable to the anions. Although pharmaceutically acceptable salts of said basic compounds are preferred, all acid addition salts are useful as sources of the free base form even if the particular salt, per se, is desired only as an intermediate product as, for example, when the salt is formed only for purposes of purification, and identification, or when it is used as intermediate in preparing a pharmaceutically acceptable salt by ion exchange procedures. Pharmaceutically acceptable salts within the scope of the invention are those derived from the following acids: mineral acids such as hydrochloric acid, sulfuric acid, phosphoric acid and sulfamic acid; and organic acids such as acetic acid, citric acid, lactic acid, tartaric acid, malonic acid, methanesufonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, cyclohexylsulfamic acid, quinic acid, and the like. The corresponding acid addition salts comprise the following: hydrohalides, such as hydrochloride and hydrobromide, sulfate, phosphate, nitrate, sulfamate, acetate, citrate, lactate, tartarate, malonate, oxalate, salicylate, propionate, succinate, fumarate, maleate, methylene-bis-beta-hydroxynaphthoates, gentisates, mesylates, isethionates and di-p-toluoyltartratesmethanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate, cyclohexylsulfamate and quinate, respectively. According to a further feature of the invention, acid addition salts of the compounds of this invention are prepared by reaction of the free base with the appropriate acid, by the application or adaptation of known methods. For example, the acid addition salts of the compounds of this invention are prepared either by dissolving the free base in aqueous or aqueous-alcohol solution or other suitable solvents containing the appropriate acid and isolating the salt by evaporating the solution, or by reacting the free base and acid in an organic solvent, in which case the salt separates directly or can be obtained by concentration of the solution.

The acid addition salts of the compounds of this invention can be regenerated from the salts by_. the application or adaptation of known methods. For example, parent compounds of the invention can be regenerated from their acid addition salts by treatment with an alkali, such as aqueous sodium bicarbonate solution or aqueous ammonia solution.

Where the compound of the invention is substituted with an acidic moiety, base addition salts may be formed and are simply a more convenient form for use; and in practice, use of the salt form inherently amounts to use of the free acid form. The bases which can be used to prepare the base addition salts include preferably those which produce, when combined with the free acid, pharmaceutically acceptable salts, that is, salts whose cations are non- toxic to the animal organism in pharmaceutical doses of the salts, so that the beneficial inhibitory effects on TNF and PDE inherent in the free acid are not vitiated by side effects ascribable to the cations. Pharmaceutically acceptable salts, including for example alkali and alkaline earth metal salts, within the scope of the invention are those derived from the following bases: sodium hydride, sodium hydroxide, potassium hydroxide, calcium hydroxide, aluminum hydroxide, lithium hydroxide, magnesium hydroxide, zinc hydroxide, ammonia, ethylenediamine, N-methyl-giucamine, lysine, arginine, ornithine, choline, N,N'-dibenzylethylenediamine, chloroprocaine, diethanolamine, procaine, N-benzylphenethylamine, diethylamine, piperazine, tris(hydroxymethyl)-aminomethane, tetramethylammonium hydroxide, and the like.

Metal salts of compounds of the present invention may be obtained by contacting a hydride, hydroxide, carbonate or similar reactive compound of the chosen metal in an aqueous or organic solvent with the free acid form of the compound. The aqueous solvent employed may be water or it may be a mixture of water with an organic solvent, preferably an alcohol such as methanol or ethanol, a ketone such as acetone, an aliphatic ether such as tetrahydrofuran, or an ester such as ethyl acetate. Such reactions are normally conducted at ambient temperature but they may, if desired, be conducted with heating.

Amine salts of compounds of the present invention may be obtained by contacting an amine in an aqueous or organic solvent with the free acid form of the compound. Suitable aqueous solvents include water and mixtures of water with alcohols such as methanol or ethanol, ethers such as tetrahydrofuran, nitriles such as acetonitrile, or ketones such as acetone. Amino acid salts may be similarly prepared.

The base addition salts of the compounds of this invention can be regenerated from the salts by the application or adaptation of known methods. For example, parent compounds of the invention can be regenerated from their base addition salts by treatment with an acid, such as hydrochloric acid.

As will be self-evident to those skilled in the art, some of the compounds of this invention do not form stable salts. However, acid addition salts are most likely to be formed by compounds of this invention wherein R³ represents a nitrogen-containing heteroaryl group and/or wherein R³ contains an amino group as a substituent. Preferable acid addition salts of the compounds of the invention are those wherein R² is other than an acid labile group.

As well as being useful in themselves as active compounds, salts of compounds of the invention are useful for the purposes of purification of the compounds, for example by exploitation of the solubility differences between the salts and the parent compounds, side products and/or starting materials by techniques well known to those skilled in the art.

It will be apparent to those skilled in the art that certain compounds of formula I can exhibit isomerism, for example geometrical isomerism and optical isomerism. Optical isomers include compounds of the invention having asymmetric centers that may independently be in either the R or S configuration. Geometrical isomers include the cis and trans forms of compounds of the invention having alkenyl moieties. Individual geometrical isomers, stereoisomers and mixtures thereof are within the scope of the present invention.

Such isomers can be separated from their mixtures, by the application or adaptation of known methods, for example chromatographic techniques and recrystallization techniques, or they are separately prepared from the appropriate isomers of their intermediates, for example by the application or adaptation of methods described herein.

The starting materials and intermediates are prepared by the application or adaptation of known methods, for example methods as described in the Reference Examples or their obvious chemical equivalents.

For example, compounds of formula II above, wherein R¹, R², Z¹ and Z² are as hereinbefore defined, are prepared from compounds of formula XVI

wherein R¹ , R², Z¹ and Z² are as hereinbefore defined, by the application or adaptation of known methods for the preparation of acid halides from carboxylic acids. For example, when the moiety X in a compound of formula II represents a chloro, the reaction may be carried out by means of thionyl chloride or, preferably, oxalyl chloride in the presence of triethylamine, or as prepared by adaptation of the procedures described by K.R.Reistad et al., Acta. Chemica. Scandanavica B, 28, 667-72 (1974), incorporated herein by reference.

Compounds of formula V above, wherein R¹ , R², Z¹ and Z² are as hereinbefore defined, are prepared by reaction of the corresponding compounds of formula XVI above, wherein R^ , R², Z^ and Z² are as hereinbefore defined, with ammonia, with the aid of an acid activating group, such as oxalyl chloride, from about 0°C to about room temperature. Compounds of formula XVI above, wherein R R², Z^ and Z² are as hereinbefore defined, are prepared by hydrolysis of the corresponding compounds of formula XVII, wherein R^"! , R², Z^ and Z² are as hereinbefore

defined, R², Z¹ and Z² are as hereinbefore defined, and R⁷ is alkyl, cycloalkyl or aralkyl containing up to 8 carbon atoms, by using potassium carbonate in water and an alcohol, such as methanol or ethanol, at a temperature between 50°C and 10Q^OC.

Compounds of formula XI above, wherein R¹ , R², R⁵, R⁶, Z, Z¹ and Z² are as hereinbefore defined, are prepared from the compounds of formula XVI above, wherein R¹ , R², Z^ and Z² are as hereinbefore defined, by reaction with HNR⁴OR5, wherein R⁴ and R⁵ are as hereinbefore defined, with the aid of an acid activating group, such as oxalyl chloride, in the presence of a tertiary amine, such as triethylamine, optionally in an inert solvent, for example dichloromethane.

Compounds of formula XVIII, wherein R¹ , R², Z¹ and Z² are as

XVIII

hereinbefore defined, are prepared from reduction of compounds of formula XIII above, wherein R¹ , R², R⁷, Z¹ and Z² are as hereinbefore defined, with diiosbutylaluminium hydride in a solvent, such as diethyl ether, at low temperature, for instance -78°C to 0°C.

Compounds of formula X above, wherein R¹ , R², R³, Z¹ and Z² are as hereinbefore defined, are prepared by reaction of the compounds of formula XVIII above, wherein R1 , R², Z¹ and Z² are as hereinbefore defined, with compounds of formula XV above, wherein R³ is as hereinbefore defined. The reaction is conveniently carried out in a solvent, such as diethyl ether, at 0°C to 50°C.

Compounds of formula XIV above, wherein R¹ , R², Z¹ and Z² are as hereinbefore defined, are prepared by dehydrating compounds of formula V above, wherein R¹ , R², Z¹ and Z² are as hereinbefore defined, using chlorosulphonyl isocyanate, preferably in a solvent, such as dimethylformamide, preferably at temperatures between 0°C and room temperature.

Compounds of formulae XIX, wherein R¹ , R², R³, Z¹ and Z² are as

XKa XD b

hereinbefore defined, R⁸ is alkyl containing up to about 3 carbon atoms, and R⁹ is alkyl, alkynyl or alkenyl containing up to about 14, preferably up to 11 , carbon atoms, are prepared by reducting of compounds of formulae XX,

XXa XXb

wherein R¹ , R², R³, R⁸, R⁹, Z and Z² are as hereinbefore defined, using sodium borohydride in a solvent, such as ethanol, at between 0°C and room temperature.

Compounds of formulae (I'), wherein R¹ , R², R³, R⁸, R⁹, Z¹ and Z² are

I'a I'b

as hereinbefore defined, are prepared by the reaction of diethylaminosulphur trifluoride (DAST) with compounds of formulae XIX above, R , R², R³, R⁸, R⁹, Z^ and Z² as hereinbefore defined, in a solvent, such as dichloromethane, at low temperature e.g -78°C to -20°C.

Compounds of general formulae XX above, wherein R¹ , R², R⁸, R⁹, Z¹ and Z² as hereinbefore defined, are prepared by reaction of the corresponding compounds of formulae XXI, wherein R¹ , R², R⁸, R⁹, 7^ , Z² and X are as

XXIa XXIb

hereinbefore defined, with compounds of the formula III above, as hereinbefore defined, in the presence of a base such as an alkali metal hydride, such as sodium hydride, or an amine, preferably a tertiary amine, such as triethylamine or pyridine, optionally in an inert solvent, for example dichloromethane, dimethylformamide, or an ether, such as diethyl ether or tetrahydrofuran, preferably at a temperature from about 0°C to the reflux temperature or at the melting point of the reaction mixture-

Compounds of formulae XXI above, wherein R¹ , R², R⁸, R⁹, Z¹ , Z² and X are as hereinbefore defined, are prepared by reaction of compounds of formulae XXII, wherein R¹ , R², R⁸, R⁹, Z¹ and Z² are as hereinbefore

xxπa XXIIb

defined, by application or adaptation of known methods for the preparation of acid halides and mixed acid anhydrides.

Compounds of formulae XXII, above , wherein R¹ , R², R⁸, R⁹, Z¹ and Z² are as hereinbefore defined, are prepared from compounds of formulae XXIII, wherein R^"! , R², R⁸, R⁹, Z¹ and Z² are as hereinbefore defined, defined,

using a base, such as potassium hydroxide, preferably in a solvent, such as ethylene glycol, at temperatures between 100°C and 180°C.

Compounds of formulae XXIII above, wherein R¹ , R², R⁸, R⁹, Z¹ and Z² are as hereinbefore defined, are prepared from corresponding compounds of the formulae XXIV, wherein R¹ , R², R⁸, R⁹, Z^ and Z² are as hereinbefore

XXIVi

defined, using copper (I) cyanide and copper (II) sulphate, preferably in a solvent, such as dimethylformamide, at temperatures between 150°C and 200°C. Compounds of formulae XXIV above, wherein R¹ , R², R⁸, R⁹, ^ and Z² are as hereinbefore defined, are prepared by reacting compounds of the formulae XXVa and XXVb, wherein R¹ , R², Z¹ and Z² are as hereinbefore

defined, with compounds of formulae XXVIa and XXVIb respectively, wherein

R⁸COCl R⁹COCl

XXVIa XXVIb

R⁸ and R⁹ are as defined hereinbefore, in the presence of a Lewis acid catalyst, such as aluminium chloride, preferably in a solvent such as nitrobenzene, at temperatures between room temperature and 200°C.

Compounds of formulae XXV above, wherein R^"1 , R², Z^ and Z² are as hereinbefore defined, are prepared by alkylating compounds of formulae XXVII, wherein Z¹ and Z² are as hereinbefore defined, with compounds of

formulae VIII and XXVllI, wherein R¹ , R², and X are as hereinbefore defined,

R X R' X

VIII XXVIII with the aid of a metal hydride, such as sodium hydride, or base, such as potassium carbonate, preferably in a solvent, such as dimethylformamide, between room temperature and 100°C. Alternatively, the reaction is carried out by reacting compounds of formulae XVII above, wherein R¹ and R² are as hereinbefore defined, and , Z¹ and Z² are oxygen, with compounds of formulae IX and XXIX respectively in the presence of triphenylphosphine and

R²OH R'OH

IX XXIX

diisopropylazodicarboxylate, optionally in a solvent, such as toluene, at temperatures between 0°C and 80°C.

Compounds of formula XXXX, wherein R¹ , R², R⁷, R⁸, R⁹, Z and Z² are

XXXXa XXXXb

as hereinbefore defined, by esterifying compounds of formulae XXII above, wherein R¹ , R², R⁸, R⁹, Z^"1 and Z² are as hereinbefore defined, with compounds of formula XXXXI, wherein R⁷ is as hereinbefore defined,

R70H XXXXI

in the presence of a trace of acid, such as concentrated sulphuric acid, optionally in an inert solvent, such as toluene, at temperatures between room temperature and 100°C.

Compounds of formulae XXXXII, wherein R , R², R⁷, R⁸, R⁹, Z¹ and Z²

xxxxπa xxxxπb

are as hereinbefore defined, are prepared by reducting of compounds of formulae XXXX above, wherein R¹ , R², R⁷, R⁸, R⁹, Z¹ and Z² are as hereinbefore defined, using sodium borohydride in a solvent, such as ethanol, at between 0°C and room temperature.

Compounds of general formulae XVII', wherein R¹ , R², R⁷, R⁸, R⁹, Z^

and Z² are as hereinbefore defined, are prepared by the reaction of diethylaminosulphur trifluoride with compounds of formulae XXXXII, wherein R1 , R², R⁷, R⁸, R⁹, Z^ and Z² are as hereinbefore defined, in a solvent, such as dichloromethane, at low temperature e.g -78°C to -20°C.

Compounds of general formula (I) above, wherein R¹ , R², R³, Z¹ and Z² are as hereinbefore defined, are prepared by reduction of compounds of formulae XX above, wherein R¹ , R², R³, R⁸, R⁹, Z^ and Z² are as hereinbefore defined, using a silane, such as triethylsilane in the presence of a strong acid, such as trifluoroacetic acid, optionally in an inert solvent, such as dichloromethane, at temperatures between 0°C and room temperature.

Compounds of formula XVII above, wherein R¹ , R², R⁷, Z¹ and Z², are prepared by the reducing compounds of formulae XXXX above, wherein R¹ , R², R⁷, R⁸, R⁹, Z¹ and Z² are as hereinbefore defined, using a silane, such as triethylsilane in the presence of a strong acid, such as trifluoroacetic acid, optionally in an inert solvent, such as dichloromethane, at temperatures between 0°C and room temperature.

Compounds of formula IX above, wherein R² is alkenyl, R¹ , R⁷ and Z^"t are as hereinbefore defined, and Z² is a direct bond, are prepared from compounds of formula XXXXIII, wherein R^"* , R⁷ and Z¹ are as hereinbefore

XXXXIII

defined, with compounds of formula XXXXIV, wherein R10 represents

R 0CH₂PPh₃X XXXXIV

alkyl, alkenyl or alkynyl group containing up to about 13, preferably up to 10, carbon atoms, X is as hereinbefore defined, and Ph represents phenyl, in the presence of a base, such as butyllithium, preferably in a solvent, such as tetrahydrofuran, preferably below about 5°C.

Compounds of general formula XXXXIII, wherein R¹ , R⁷ and Z¹ are as hereinbefore defined, are prepared from compounds of the formula XXXXV,

XXXXV

wherein R⁷ and Z^"* are as hereinbefore defined, by reaction with compoundsof formula XXVllI, wherein R¹ and X are as hereinbefore defined, with the aid of a metal hydride, such as sodium hydride, or base, such as potassium carbonate, preferably in a solvent, such as dimethylformamide, between room temperature and 100°C. Compounds of general formula XXXXV, wherein R¹ and R⁷ are as hereinbefore defined, and Z¹ is a S atom, are prepared from esterification of compounds of the formula XXXXVI, wherein R¹ is as hereinbefore defined, with

XXXXVI

compounds of formula XXXXI above, wherein R⁷ is as hereinbefore defined, in the presence of a trace of acid, such as concentrated sulphuric acid, optionally in an inert solvent, such as toluene, at temperatures between room temperature and 100°C.

Compounds of formula XXXXVI, wherein R¹ is as hereinbefore defined, are prepared from compounds of the formula XXXXVII, wherein R¹ is as

XXXXVII

hereinbefore defined, using a base, such as potassium hydroxide, preferably in a solvent, such as ethylene glycol, at temperatures between 100°C and 180°C.

Compounds of formula XXXXVII above, wherein R¹ is as hereinbefore defined, are prepared from compound XXXXVIII, by reaction with compounds

XXXXVIII

of formula XXXXIX, wherein R¹ and Z¹ are as hereinbefore defined, with the aid R¹Z¹H XXXXIX

of a metal hydride, such as sodium hydride, or base, such as potassium carbonate, preferably in a solvent, such as dimethylformamide, between room temperature and 100°C.

Compounds of formula (I), wherein R1 is a group as hereinbefore defined, Z¹ is a oxygen or sulphur atom, R² is a group as hereinbefore defined, Z² is a bond , Z³ represents a CONH or COCH2 linkage, the other symbols being as hereinbefore defined, are prepared by hydrogenation of the corresponding compounds of formula (I) wherein Z² is a direct bond and R² contains a unsaturated moiety. The reaction is conveniently carried out using hydrogen in the presence of a catalyst, such as palladium on carbon, preferably in a solvent, such as ethanol, at about room temperature.

Alternatively, compounds of formulae XXII, wherein R¹, R², R⁸ and R⁹ are as hereinbefore defined, are prepared by reacting compounds of formulae XXXXX, wherein R¹ and R² are as hereinbefore defined, with compounds

XXXXXa XXXXXb

of formulae XXXXXIa and XXXXXIb respectively, wherein

R⁸MgX R⁹MgX

XXXXXIa XXXXXIb

R⁸ and R⁹ are as defined hereinbefore, in the presence of cuprous bromide in an inert solvent, such as tetrahydrofuran, at temperatures from room temperature to 80°C. Compounds of formula XVI above, wherein R¹ and R² are ethyl or methyl, Z¹ is a direct bond, Z² is oxygen, and R² is as hereinbefore defined, are prepared by alkylating compounds of formula XXXXXII, wherein R¹ is as

xxxxxii

hereinbefore defined, and Z¹ is a direct bond, with corresponding compounds of formula VIII, wherein R² and X are as hereinbefore defined, using a metal hydride, such as sodium hydride, or base, such as potassium carbonate, preferably in a solvent, such as dimethylformamide, between room temperature and 100°C.

Compounds of formula XIII, wherein R¹ and R² are ethyl or methyl, Z¹ is a direct bond, Z² is oxygen, and R² and R⁷ as hereinbefore defined, are prepared from corresponding compounds of formula XXXXXIII, wherein R¹ and

XXXXXIII

R⁷ are as hereinbefore defined, and Z is a direct bond, with corresponding compounds of formula VIII above, wherein R² and X are as hereinbefore defined, using a metal hydride, such as sodium hydride, preferably in a solvent, such as dimethylformamide, between room temperature and 100°C. Alternatively the reaction is carried out using compounds of formula IX above, wherein R² is as hereinbefore defined, in the presence of triphenylphosphine and diisopropyl azodicarboxylate, optionally in a solvent, such as toluene, at temperatures between 0°C and 80°C.

Compounds of formula XXXXXIII, wherein R¹ and R⁷ are as hereinbefore defined, and Z¹ is a direct bond, are prepared by esterification of the compounds of formula XXXXXII, wherein R¹ is as hereinbefore defined, and Z¹ is a direct bond, with compounds of formula XXXXI, wherein R⁷ is as hereinbefore defined, in the presence of a trace of acid, such as concentrated sulphuric acid, optionally in an inert solvent, such as toluene, at temperatures between room temperature and 100°C.

Compounds of formula XIII above, wherein R^"! , R² and R⁷ are as hereinbefore defined, Z¹ is oxygen, Z² is a direct bond, are prepared from the corresponding compounds of the formula XXXXXIV, wherein R² and

XXXXXIV

R⁷ are as hereinbefore defined, and Z² is a direct bond, by reaction with corresponding compounds of formula XXVllI, wherein R¹ and X are as hereinbefore defined, with a metal hydride, such as sodium hydride, or base, such as potassium carbonate, preferably in a solvent, such as dimethylformamide, between room temperature and 100°C.

Compounds of formula XXXXXIV, wherein R² and R⁷ are as hereinbefore defined, and Z² is a direct bond, are prepared by hydrogenation of the compounds of the formula XXXXXV, wherein R⁷ is as hereinbefore

benzylO.,

R²Z^ COOR' XXXXXV

defined, Z² is a direct bond, and R² contains an unsaturated moiety, by using hydrogen in the presence of a catalyst, such as palladium on carbon, preferably in a solvent, such as ethanol.

Compounds of formula XXXXXV above, wherein R⁷ is as hereinbefore defined, Z² is a direct bond, and R² contains an unsaturated moiety, are prepared from the reaction of compounds of formula XXXXXVI, wherein R⁷ is benzylO

HCO COOR⁷ XXXXXVI

as hereinbefore defined, with compounds of formula XXXXIV above, , wherein R10 represents

RlOCH₂PPh₃X XXXXIV

alkyl, alkenyl or alkynyl group containing up to about 13, preferably up to 10, carbon atoms, X is as hereinbefore defined, and Ph represents phenyl, in the presence of a base, such as butyliithium, preferably in the presence of a solvent, such as tetrahydrofuran, preferably below 5°C.

Compounds of formula XXXXXVI above, wherein R⁷ is as hereinbefore defined, are prepared from compounds of the formula XXXXV, wherein R⁷ and Z¹ are as hereinbefore defined, by reaction with benzyl bromide, with the aid of a metal hydride, such as sodium hydride, or base, such as potassium carbonate, preferably in a solent, such as dimethylformamide, between room temperature and 100°C.

Alternatively, compounds of formula XXIVa, wherein R² and R⁸ are as hereinbefore defined, and Z² is oxygen, are prepared from alkylation of compounds of formula XXXXXVII, wherein R⁸ is as

XXXXXVII

hereinbefore defined, with the corresponding compounds of formulae VIII above, wherein R² and X are as hereinbefore defined, with the aid of a base, such as potassium carbonate, preferably in a solvent, such as dimethylformamide, between room temperature and 100°C. Alternatively the reaction is carried out using compounds of the formula IX above, wherein R² is as hereinbefore defined, in the presence of triphenylphosphine and diisopropylazodicarboxylate, optionally in a solvent, such as toluene, at temperatures between 0°C and 80°C.

Compounds of formula XXXXXVII above, wherein R⁸ is as hereinbefore defined, are prepared from reaction of compound of formula XXXXXVIII,

H Br XXXXXVIII,

with corresponding compounds of formula XXVIa above, wherein R⁸ is as hereinbefore defined, in the presence of a Lewis acid catalyst, such as aluminiun chloride, preferably in a solvent such as nitrobenzene, at temperatures betweeen room temperature and 200°C.

The following Examples illustrate the preparation of the compounds according to the invention and the Reference Examples illustrate the preparation of the intermediates.

EXAMPLE 1 Compound A

A stirred suspension of N-(3,5-dichloropyrid-4-yl)-3- cyclopentanecarbonyl-4-methoxybenzamide (1.97 g) (prepared as described in Reference Example 2) in dry dichloromethane (ethanol-free; 9.9 mL), under nitrogen, is slowly treated with trifluoroacetic acid (2.85 g) during 5 minutes at 5-10°C. The resulting pale yellow solution is allowed to warm to 25°C during 20 minutes, then stirred at this temperature during treatment with triethylsilane (1 .28 g) during 10 minutes and for 4 hours 30 minutes thereafter. After standing for a further 3 days, the solution is diluted with dichloromethane (50 mL), washed successively with water (2 x 10 mL), saturated aqueous sodium hydrogen carbonate solution (2 x 10 mL) and water (2 x 10 mL), dried over anhydrous magnesium sulphate and the solvent removed in vacuo. The residual oil is washed with pentane (50 mL) by decantation, and subjected to flash chromatography on silica gel, using a mixture of ethyl acetate and cyclohexane (1 :3v/v), as eluent, followed by crystallisation from a mixture of tert-butyl methyl ether and diisopropyl ether (1 :1 v/v), to give N-(3,5- dichloropyrid-4-yl)-3-cyclopentylmethyl-4-methoxybenzamide (1.16 g) in the form of colourless needles, m.p. 110°C and 134°C. [Elemental analysis:- C,59.8;H,5.23;N,7.3%; Calculated:- C,60.17;H,5.31 ; N,7.39%].

EXAMPLE 2

Sodium hydride (0.36 g) is added portionwise to a stirred solution of 4-amino-3,5-dichloropyridine (0.892 g) in dry dimethylformamide (25 mL) at room temperature and the mixture is stirred under an atmosphere of nitrogen for 20 minutes. A solution of 3-cyclopentyloxy-4-ethylbenzoyl chloride (1 .04 g) (prepared as described in Reference Example 3) in dry dimethylformamide (8 mL) is added dropwise and the reaction mixture is stirred at room temperature for 2 hours and at 60°C for 90 minutes. Dimethylformamide is evaporated off under reduced pressure, water (90 mL) is added and the mixture is extracted with ethyl acetate (2 x 90 mL). The combined organic extracts are dried over magnesium sulphate, evaporated under reduced pressure and subjected to mpic, eluting with a mixture of diethyl ether and pentane (3:7v/v), to give N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4- ethylbenzamide in the form of a white solid (0.93 g),m.p. 122-123°C.

[Elemental analysis:- C,60.3;H,5.37;N,7.4%; calculated:- C,60.16;H,5.33; N,7.39%].

EXAMPLE 3

By proceeding in a similar manner to that described in Example 2, but using the appropriate quantity of 3-cyclopentyloxy-4-methy!benzoyl chloride (prepared as described in Reference Example 4), there is prepared N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-methylbenzamide in the form of a white solid, m.p. 136-138°C. [Elemental analysis:- C.58.9;

H,4.97;N,7.6;CI, 19.4%; calculated:- C,59.19;H,4.96; N,7.67;CI,19.41 %].

EXAMPLE 4

Hydrogen peroxide (3.5 mL) is added to a stirred suspension of N-(3,5- dichloropyrid-4-yl) 3-cyclopentylmethyl-4-methoxybenzamide (0.47 g, prepared as described in Example 1 ) in glacial acetic acid (10 mL). The mixture is stirred at 70-80 °C for 4 hours. After cooling, the mixture is basified by treatment with aqueous sodium hydroxide (2 M), and extracted with ethyl acetate (100 mL). The extracts are washed with brine, dried over sodium sulphate and evaporated. The resulting residue is purified by flash chromatography on silica gel, using a mixture of methanol and dichloromethane (1 :99 to 2:98 v/v) to give a white solid, which is triturated with ether/pentane to give N-(3,5-dichloro-1-oxido-4-pyridinio) 3-cyclopentylmethyl- 4-methoxybenzamide (0.11 g) in the form of a white solid, m.p. 125-129 °C. [Elemental analysis:- C57.40; H.5.24; N,6.80 %; calculated:- C,57.73; H.5.10; N,7.09 %].

EXAMPLE 5

By proceeding in a similar manner to that described in Example 2, but using the appropriate quantity of 3-(exo)-8,9,10-trinorbomyl-2-oxy-4- ethylbenzoyl chloride (prepared as described in Reference ExamplelO), there is prepared N-(3,5-dichloropyrid-4-yl)-3-(exo)-8,9,10-trinorbornyl-2-oxy-4- ethylbenzamide in the form of a white foam. [Elemental analysis:-C, 62.30; H.5.63; N.6.50 %; calculated:- C.62.23; H.5.47; N,6.90 %].

EXAMPLE 6

By proceeding in a similar manner to that described in Example 2, but using the appropriate quantity of 3-cyclopentylidenemethyl-4-methoxybenzoyl chloride (prepared as described in Reference Example 13), there is prepared N-(3,5-dichloropyrid-4-yl)-3-cyclopentylidenemethyl-4-methoxybenzamide in the form of a white solid, m.p. 155-156°C. [Elemental analysis:- C, 60.40; H,4.77; N,7.40 %; calculated:- C,60.48; H.4.80; N.7.42 %].

EXAMPLE 7

By proceeding in a similar manner to that described in Example 2, but using the appropriate quantity of 3-(2-methylpropenyl)-4-methoxybenzoyl chloride (prepared as described in Reference Example 16), there is prepared N-(3,5-dichloropyrid-4-yl)-3-(2-methylpropenyl)-4-methoxybenzamide in the form of a white solid, m.p. 154-155°C. [Elemental analysis:- C58.40; H,4.68; N.7.90 %; calculated:- C,58.13; H.4.59; N,7.97 %.] EXAMPLE 8

By proceeding in a similar manner to that described in Example 2, but using the appropriate quantity of 3-cyclopentylidenemethyl-4- difluoromethoxybenzoyl chloride (prepared as described in Reference Example 22), there is prepared N-(3,5-dichloropyrid-4-yl)-3- cyclopentylidenemethyl-4-difluoromethoxybenzamide in the form of a white solid, m.p. 122-123°C. [Elemental analysis:- C,54.60; H.4.31 ; N.6.76 %; calculated:- C.54.96; H.4.31 ; N,6.75 %].

EXAMPLE 9

N-(3,5-dichloropyrid-4-yI)-3-cyclopentylhydroxymethyl-4- methoxybenzamide (0.3 g, prepared as described in Reference Example 23) in dry dichloromethane (5 mL) is added dropwise to a solution of diethylaminosulphur trifluoride (0.12 g) in dry dichloromethane (5 mL) at -78°C. Stirring at this temperature is continued for a further 25 minutes before the reaction is quenched with water (15 mL). After allowing the mixture to warm up to room temperature the layers are separated, the aqueous layer is further extracted with dichloromethane (20 mL) and the combined organic extracts washed with saturated aqueous sodium hydrogen carbonate (25 mL), dried over magnesium sulphate and evaporated. The resulting residue is purified by flash chromatography on silica gel, using a mixture of ethyl acetate and pentane (1 :2 v/v) to give N-(3,5-dichloropyrid-4-yl)-3-cyclopentylfluoromethyl- 4-methoxybenzamide (0.1 g) in the form of a white solid, m.p. 73-75°C. [Elemental analysis:- C.57.50; H,5.06; N.6.69 %; calculated:- C.57.43; H,4.82; N.7.05 %].

EXAMPLE 10

By proceeding in a similar manner to that described in Example 9, but using the appropriate quantity of N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4- (l -hydroxyethyl)benzamide (0.3 g, prepared as described in Reference Example 29), there is prepared N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4- (l-fluoroethyl)benzamide, in the form of a white solid, m.p. 141-143°C. [Elemental analysis:- C,57.50; H,4.85; N.7.10 %; calculated:- C.57.44; H,4.82; N.7.05 %].

REFERENCE EXAMPLE 1

A stirred suspension of 3-cyano-4-methoxybenzoic acid (14.2 g) (prepared as describe in Eur. Pat. Appl. EP 279698) in dry tetrahydrofuran (142 mL) and under an atmosphere of nitrogen is treated with a solution of cyclopentyl magnesium chloride in tetrahydrofuran (126 mL; 1.4 M) during 10 minutes at 25°C. Cuprous bromide (0.4 g) is added to the orange-red solution, the mixture is heated and stirred at reflux for 6 hours, and then it is poured into a mixture of ice-water (670 mL) and aqueous hydrochloric acid (400 mL; 1 M). The crude product is extracted with ethyl acetate (1 x 400, 2 x 200 mL) and the combined extracts are washed successively with water (2 x 120 mL) and saturated aqueous sodium chloride solution

(2 x 80 mL). After drying over anhydrous magnesium sulphate the extracts are concentrated in vacuo and cooled to 25°C to give the product in the form of an off-white crystalline solid. A further quantity of this substance is obtained from the mother liquor by evaporation in vacuo and flash chromatography of the residue over silica gel, using as eluent a mixture of ethyl acetate and cyciohexane (1 :2v/v), followed by purification of the material thus obtained by sequential treatment with diisopropyl ether and ethyl acetate. The combined crops (9.8 g) of 3-cyclopentanecarbonyl-4-methoxybenzoic acid have a melting point of 184-186°C. [Elemental analysis:- C,67.2;H,6.45%; calculated:- C,67.73;H,6.50%. NMR (CDCI3):- 1.55-1.75(m;4H), 1.82- 1.90(m;4H),3.60-3.69(p;1 H),3.95-3.98(s;3H), 7.00-7.03(d;1 H),8.17- 8.21 (dd;1 H),8.26-8.28(d;1 H)].

REFERENCE EXAMPLE 2

A stirred solution/suspension of 3-cyclo-pentanecarbonyl-4- methoxybenzoic acid (11.4 g) (prepared as described in Reference Example 1) in dry tetrahydrofuran (77 mL) and under an atmosphere of nitrogen is treated with ethyl chloromethanoate (5.48 g) during 5 minutes at 17-20°C. The temperature is allowed to rise to 25°C and maintained at this temperature for 30 minutes. The resulting amber solution is then treated with dry triethylamine (5.11 g) during 10 minutes, and stirred for a further 1 hour. The suspension formed is filtered rapidly through a dry bed of diatomaceous earth and the filtrate is concentrated in vacuo to a volume of 50 mL, to give "solution A" containing 3-cyclopentane-carbonyl-4-methoxybenzoic formic anhydride.

A stirred solution of 4-amino-3,5-dichloropyridine (8.23 g) in dry tetrahydrofuran, under nitrogen, is treated with a 60% dispersion of sodium hydride in oil (4.04 g; containing 2.47 g of sodium hydride) in portions during 15 minutes at 25°C. The suspension obtained is stirred at this temperature for 1 hour. The stirred suspension is then treated with solution A during 10 minutes and then it is stirred for 30 minutes thereafter. After standing for a further 20 hours, the solution obtained is added to aqueous potassium carbonate solution (690 mL; 5%w/v) with cooling and stirring. It is then extracted with ethyl acetate (3 x 200 mL) and the combined extracts are washed successively with water (2 x 50 mL), aqueous hydrochloric acid (2 x 50 mL; 1 M), water (2 x 50 mL) and saturated aqueous sodium chloride solution (2 x 50 mL). The solution is dried using anhydrous magnesium sulphate, the solvent is evaporated in vacuo, and the residual solid is treated with tert-butyl methyl ether (200 mL), heated at reflux for 10 minutes, cooled and filtered, to give N-(3,5-dichloropyrid-4-yl)-3-cyclopentanecarbonyl-4- methoxybenzamide in the form of an off-white crystalline solid (8.5 g), m.p. 180-182°C. [Elemental analysis:- C,58.0;H,4.56;N,7.0%. calculated:- C,58.03;H,4.61 ; N.7.12%].

REFERENCE EXAMPLE 3

Thionyl chloride (1.1 mL) is added to a solution of 3-cyclopentyloxy-4- ethylbenzoic acid (1.07 g) (prepared as described in Reference Example 5) in toluene (7 mL) and the mixture is heated at 80°C for 3 hours. Evaporation under reduced pressure gives 3-cyclopentyloxy-4-ethylbenzoyl chloride (1 g), in the form of a pale brown oil which is used without further purification.

REFERENCE EXAMPLE 4

By proceeding in a similar manner to that described in Reference Example 3, but using the appropriate quantity of 3-cyclopentyloxy-4- methylbenzoic acid (prepared as described in Reference Example 6), there is prepared 3-cyclopentyloxy-4-methylbenzoyl chloride, in the form of a brown oil which is used without further purification.

REFERENCE EXAMPLE 5

Sodium hydride (1.6 g of 60% dispersion in mineral oil; 40 mmol) is added portionwise to a solution of 4-ethyl-3-hydroxybenzoic acid (3.32 g) (prepared as described in D. S. Noyce and L. J. Dolby, J. Org. Chem. 26, 1732 (1961) in dry dimethyl-formamide and the mixture is stirred at room temperature for 15 minutes. Cyclopentyl bromide (2.98 g) is added and the mixture is heated at 60°C for 3 hours. Dimethylformamide is evaporated off under reduced pressure, and the dark residue is dissolved in water (100 mL), acidified by treatment with concentrated hydrochloric acid and extracted with dichloromethane (2 x 100 mL). The combined organic extracts are dried over magnesium sulphate, evaporated under reduced pressure and subjected to mplc, eluting with a mixture of ethyl acetate and pentane, to give 3-cyclopentyloxy-4-ethylbenzoic acid (1.1 g), in the form of a pale yellow solid, m.p. 101°C. [NMR (CDCI3):- 7.63(dd,1 H,J=8Hz,2Hz); 7.52(d,1H,J=2Hz), 7.22(d,1 H,J=8Hz),4.87(m,1 H);2.65(q,2H,J=8Hz),2.0-1.6(m,8H); 1.19(t,3H,J=8Hz)].

REFERENCE EXAMPLE 6

By proceeding in a similar manner to that described in Reference Example 5, but using the appropriate quantity of 3-hydroxy-4-methylbenzoic acid (prepared as described in D. S. Noyce and L. J. Dolby, J. Org. Chem. 26, 1732 (1961), there is prepared 3-cyclopentyloxy-4-methylbenzoic acid, m.p. 152-154°C. [NMR (CDCI3):- 7.6(dd,1 H,J=8Hzm,2Hz); 7.53(d,1 H,J=2Hz), 7.4(d,1 H,J=8Hz),4.85(m,1 H);2.25(s,3H),2.0-1.6(m,8H)].

REFERENCE EXAMPLE 7

To a solution of 4-ethyl-3-hydroxybenzoic acid in methanol (300 mL) is added concentrated sulphuric acid. The resulting mixture is left to stand for 2 days at room temperature, then heated to reflux for 45 minutes. After cooling, the solvent is evaporated and the residue partitioned between diethyl ether (200 mL) and water (200 mL), the layers throughly shaken, separated and the aqueous layer further extracted with diethyl ether (2 x 100 mL). The combined organic extracts are dried over magnesium sulphate and solvent evaporated. The resulting residue is purified by flash chromatography on silica gel eluting with a mixture of ethyl acetate and pentane (1 :3 v/v) to give methyl 4-ethyl-3- hydroxybenzoate (4.4 g) in the form of an off white solid, m.p. 62-63°C.

REFERENCE EXAMPLE 8

A solution of triphenylphosphine (1.45 g) in dry tetrahydrofuran (20 mL) is treated with a solution of diisopropyl azodicarboxylate (1.12 g) in dry tetrahydrofuran (4 mL). The resulting creamy precipitate is stirred at room temperature for 30 minutes, then cooled to below 5°C and treated dropwise with a solution of endo-8,9,10-trinorbomeol (0.68 g) and methyl 4-ethyl-3- hydroxybenzoate (1 g, prepared as described in Reference Example 7) in dry tetrahydrofuran (40 mL), maintaining the temperature below 5°C. The resulting mixture is then allowed to warm to room temperature and then heated at reflux for 15 hours, cooled, poured in to water (100 mL) and extracted with ethyl acetate (2 x 75 mL). The combined organic extracts are dried over magnesium sulphate, solvent evaporated, and the residue purified by flash chromatography on silica gel eluting with a mixture of ethyl acetate and pentane (1 :20 v/v) to give methyl 3-(exo)-8,9,10-trinorbomyl-2-oxy-4- ethylbenzoate (0.95 g) in the form of a colourless oil.

REFERENCE EXAMPLE 9

A stirred refluxing solution of methyl 3-(exo)-8,9,10-trinorbomyl-2-oxy-4- ethylbenzoate (0.9 g, prepared as described in Reference Example 8) in methanol (30 mL) is treated with a solution of potassium carbonate (0.58 g) in water (15 mL). The resulting suspension is heated at reflux for 24 hours, allowed to cool to room temperature and the methanol is then removed under reduced pressure. The aqueous residue is acidified to pH 1 with 1 M hydrochloric acid and extracted with dichloromethane (3 x 50 mL). The combined organic extracts are dried over magnesium sulphate and the solvent removed to give 3-(exo)-8,9,10-trinorbomyl-2-oxy-4-ethylbenzoic acid (0.8 g) in the form of a white solid, m.p. 1 10°C, which is used without further purification. REFERENCE EXAMPLE 10

By proceeding in a similar manner to that described in Reference Example 3, but using the appropriate quantity of 3-(exo)-8,9,10-trinorbomyl-2- oxy-4-ethylbenzoic acid (prepared as described in Reference Example 9), there is prepared 3-(exo)-8,9,10-trinorbomyl-2-oxy-4-ethyIbenzoyl chloride in the form of a brown oil, which is used without further purification.

REFERENCE EXAMPLE 1 1

A solution of cyclopentyltriphenylphosphonium bromide (6.68 g) in dry tetrahydrofuran (100 mL) under nitrogen is cooled to below -70°C. To this is added n-butyl lithium (2.5 M, 5.6 mL) dropwise keeping the temperature below -70°C. Once addition is complete the mixture is allowed to warm to room temperature and further stirred at this temperature for 1 hour, before recooling to below -70°C and the addition of methyl 3-formyl-4-methoxybenzoate (3.2 g) (prepared as described in WO 9217449) in dry tetrahydrofuran (60 mL) dropwise over 45 minutes, keeping the temperature below -60°C. The mixture is then stirred below -60°C for 10 minutes, before allowing to warm to room temperature and stirring for a further 30 minutes. The mixture is then quenched with water (50 mL), the layers separated and the aqueous layer further extracted with ethyl acetate (3 x 20 mL). The combined organic extracts are dried over magnesium sulphate and evaporated. The resulting residue is purified by flash chromatography on silica gel, using a mixture of ethyl acetate and pentane (2:3 v/v) to give methyl 3-cyclopentylidenemethyl-4- methoxybenzoate (1.23 g) in the form of an off white solid, m.p. 55-57°C.

REFERENCE EXAMPLE 12

By proceeding in a similar manner to that described in Reference

Example 9, but using the appropriate quantity of methyl 3-cyclopentylidene- methyl-4-methoxybenzoate (prepared as described in Reference Example 1 1 ), there is prepared 3-cyclopentylidenemethyl-4-methoxybenzoic acid in the form of a white solid, m.p. 156-158°C. REFERENCE EXAMPLE 13

By proceeding in a similar manner to that described in Reference Example 3, but using the appropriate quantity of 3-cyclopentylidenemethyl-4- methoxybenzoic acid (prepared as described in Reference Example 12), there is prepared 3-cyclopentylidenemethyl-4-methoxybenzoyl chloride in the form of a brown oil, which is used without further purification.

REFERENCE EXAMPLE 14

By proceeding in a similar manner to that described in Reference Example 1 1 , but using isopropyltriphenylphosphonium iodide as reagent instead of cyclopentyltriphenylphosphonium bromide, there is prepared methyl 3-(2-methylpropenyl)-4-methoxybenzoate in the form of a white solid, m.p. 52-53°C.

REFERENCE EXAMPLE 15

By proceeding in a similar manner to that described in Reference Example 9, but using the appropriate quantity of methyl 3-(2-methylpropenyl)- 4-methoxybenzoate (prepared as described in Reference Example14), there is prepared 3-(2-methylpropenyl)-4-methoxybenzoic acid in the form of a white solid, m.p. 170-173°C.

REFERENCE EXAMPLE 16

By proceeding in a similiar manner to that described in Reference Example 3, but using the appropriate quantity of 3-(2-methylpropenyl)-4- methoxybenzoic acid (prepared as described in Reference Example 15), there is prepared 3-(2-methylpropenyl)-4-methoxybenzoyl chloride in the form of a brown oil, which is used without further purification.

REFERENCE EXAMPLE 17

Potassium carbonate (3.03 g) is added portionwise to a solution of methyl 3-formyl-4-hydroxy benzoate (3 g) (prepared as described in Y. Suzuki and H. Takahashi, Chem. Pharm. Bull. 31, 1751 (1983) in dry dimethylformamide (30 mL), followed by the addition of benzyl bromide (3.25 g). The resulting mixture is heated to 60°C for 15 hours. On cooling the resulting precipitate is filtered off, washed with ether and the combined filtrates evaporated under reduced pressure. The resulting residue is partitioned between water (50 mL) and diethyl ether (25 mL). The layers are thoroughly stirred, separated and the aqueous phase further extracted with diethyl ether (2 x 25 mL). The combined organic extracts are dried over magnesium sulphate, evaporated, and the resulting residue is purified by flash chropmatography on silica gel, eluting with ethyl acetate and pentane (7:3 v/v) to give methyl 3-formyl-4-benzyloxybenzoate in the form of white solid, m.p. 76-78°C.

REFERENCE EXAMPLE 18

By proceeding in a similar manner to that described in Reference Example 11 , but using the appropriate quantity of methyl 3-formyl-4- benzyloxybenzoate (prepared as described in Reference Example 17), there is prepared methyl 3-cyclopentylidenemethyl-4-benzyloxy benzoate in the form of a colourless oil.

REFERENCE EXAMPLE 19

A solution of methyl 3-cyclopentylidenemethyl-4-benzyloxybenzoate (1.09 g) (prepared as described in Reference Example 18) in dry ethanol (100 mL) containing Palladium on Carbon (10%, 80 mg) is hydrogenated at room temperature and atmospheric pressure. After 3 hours the mixture is filtered through a dry bed of diatomaceous earth and the filtrate is evaporated to give methyl 3-cyclopentylmethyl-4-hydroxybenzoate (0.7 g) in the form of a colourless oil, which is used without further purification.

REFERENCE EXAMPLE 20

A solution of methyl 3-cyclopentylidenemethyl-4-hydroxybenzoate (0.7 g) (prepared as described in Reference Example 19) in dry dimethylformamide (20 mL) is treated with potassium carbonate (0.53 g) and potassium iodide (0.2 g). Chlorodifluoromethane is then bubbled through the reaction mixture at a very slow rate and the reaction mixture is then heated at 70-75°C for 4.5 hours. The mixture is then treated with water (15 mL) and extracted with ethyl acetate (4 x 15 mL). The combined ethyl acetate extracts are dried over magnesium sulphate, evaporated and the residue is purified by flash chromatography on silica gel eluting with diethyl ether and pentane (3:7 v/v) to give methyl 3-cyclopentylidenemethyl-4-difluoromethoxybenzoate (0.24 g) in the form of a colourless oil.

REFERENCE EXAMPLE 21

By proceeding in a similar manner to that described in Reference Example 9, but using the appropriate quantity of methyl 3-cyclopentylidene- methyl-4-difluoromethoxybenzoate (prepared as described in Reference Example 20), there is prepared 3-cyclopentylidenemethyl-4- difluoromethoxybenzoic acid in the form of a white solid m.p. 114-115°C.

REFERENCE EXAMPLE 22

By proceeding in a similar manner to that described in Reference Example 3, but using the appropriate quantity of 3-cyclopentylidenemethyl-4- difluoromethoxybenzoic acid (prepared as described in Reference Example 21 ), there is prepared 3-cyclopentylid enemethyl-4-difluoromethoxybenzoyl chloride in the form of a brown oil, which is used without further purification.

REFERENCE EXAMPLE 23

To a solution of N-(3,5-dichloropyrid-4-yl)-3-cyclopentanecarbonyl-4- methoxybenzamide (1.97 g, prepared as described in Reference Example 2) in a mixture of ethanol (15 mL) and tetrahydrofuran (15 mL) is added sodium borohydride (0.12 g). The resulting suspension is stirred at room temperature for 1 hour. Water is then added (150 mL) followed by ethyl acetate (50 mL). The layers are throughly stirred, separated and the aqueous layer is further extracted with ethyl acetate (50 mL). The combined organic extracts are washed with brine (2 x 10 mL), dried over magnesium sulphate and evaporated. The resulting residue is purified by flash chromatography on silica gel, using a mixture of ethyl acetate and cyclohexane (9:11 v/v) to give N-(3,5- dichloropyrid-4-yl)-3-cyclopentylhydroxymethyl-4-methoxybenzamide (1.34 g) in the form of a white solid, m.p. 90°C.

REFERENCE EXAMPLE 24

By proceeding in a similar manner to that described in Reference Example 5, but using the appropriate quantity of 4-bromo-2- hydroxyacetophenone, there is prepared 4-bromo-2-cyclopentyloxy- acetophenone in the form of an off white solid, m.p. 55-56°C.

REFERENCE EXAMPLE 25

A mixture of 4-bromo-2-cyclopentyloxyacetophenone (13.03 g, prepared as described in Reference Example 24 or as described in F. C. Chen and C. T. Chang, J. Chem. Soc, 148 (1958), copper (I) cyanide (5.15 g) and copper (II) sulphate (0.05 g) in dry dimethylformamide (39 mL) is heated to between 160-170°C for 6.5 hours. After allowing to cool, ferric chloride hexahydrate (19.7 g) and concentrated hydrochloric acid (4.9 mL) in water (160 mL) is added, and the mixture is then heated to 40°C for 20 minutes. After allowing to cool, the mixture is then filtered and the aqueous titrate extracted with diethyl ether (4 x 50 mL). The combined organic extracts are washed with water (2 x 50 mL), followed by saturated aqueous sodium hydrogen carbonate solution (50 mL), then dried over magnesium sulphate and evaporated to give 4-acetyl-3-cyclopentyloxybenzamide (8.84 g), initially as a brown oil that slowly solidifies to a dark yellow solid, m.p. 188-190°C.

REFERENCE EXAMPLE 26

To a solution of sodium hydroxide (12.92 g) in a mixture of water (32 mL) and ethanol (65 mL) at reflux is added 4-acetyl-3- cyciopentyloxybenzamide (6.46 g, prepared as described in Reference Example 25). The resulting solution is maintained under reflux for 3 hours, after which it is allowed to cool. Water is then added (90 mL) and the mixture concentrated to low bulk. Concentrated hydrochloric acid is then added (until pH 2). The resulting yellow solid is filtered off and recrystallised from a mixture of dichloromethane and peteroleum ether 80-100°C to give 4-acetyl-3- cyciopentyloxybenzoic acid (4.48 g) in the form of yellow crystals, m.p. 154-158°C.

REFERENCE EXAMPLE 27

By proceeding in a similar manner to that described in Reference Example 3, but using the appropriate quantity of 4-acetyl-3-cyclopentyloxy- benzoic acid (prepared as described in Reference Example 26), there is prepared 4-acetyl-3-cyclopentyloxybenzoyl chloride in the form of a brown oil, which is used without further purification.

REFERENCE EXAMPLE 28

By proceeding in a similar manner to that described in Example 2, but using the appropriate quantity of 4-acetyI-3-cyciopentylbenzoyl chloride (prepared as described in Reference Example 27), there is prepared

N-(3,5-dichloropyrid-4-yl)-4-acetyl-3-cyclopentyloxybenzamide in the form of a pale yellow solid, m.p. 120-121.5°C.

REFERENCE EXAMPLE 29

By proceeding in a manner similar to that described in Reference Example 23, but using the appropriate quantity of N-(3,5-dichloropyrid-4-yl)-4- acetyl-3-cyclopentyloxybenzamide (prepared as described in Reference Example 28), there is prepared N-(3,5-dichloropyrid-4-yl)-4-(1-hydroxyethyl)-3- cyclopentyloxybenzamide in the form of a off white solid, m.p. 157-158.5°C.

The compounds of formula I exhibit useful pharmacological activity and accordingly are incorporated into pharmaceutical compositions and used in the treatment of patients suffering from certain medical disorders. More especially, they are cyclic AMP phosphodiesterase inhibitors, in particular type IV cyclic AMP phosphodiesterase inhibitors. The present invention provides compounds of formula I, and compositions containing compounds of formula I, which are of use in a method for the treatment of a patient suffering from, or subject to, conditions which can be ameliorated by the administration of an inhibitor of cyclic AMP phosphodiesterase. For example, compounds within the present invention are useful as bronchodilators and asthma-prophylactic agents and agents for the inhibition of eosinophil accumulation and of the function of eosinophils, such as for the treatment of inflammatory airways disease, especially reversible airway obstruction or asthma, and for the treatment of other diseases and conditions characterized by, or having an etiology involving, morbid eosinophil accumulation. As further examples of conditions which can be ameliorated by the administration of inhibitors of cyclic AMP phosphodiesterase such as compounds of formula I there may be mentioned inflammatory diseases, such as atopic dermatitis, urticaria, allergic rhinitis, psoriasis, rheumatic arthritis, ulcerative colitis, Crohn's disease, adult respiratory distress syndrome and diabetes insipidus, other proliferative skin diseases such as keratosis and various types of dermatitis, conditions associated with cerebral metabolic inhibition, such as cerebral senility, multi- infarct dementia, senile dementia (Alzheimer's disease), and memory impairment associated with Parkinson's disease, and conditions ameliorated by neuroprotectant activity, such as cardiac arrest, stroke, and intermittent claudication. A special embodiment of the therapeutic methods of the present invention is the treating of asthma.

The compounds are also inhibitors of tumor necrosis factor, especially a-TNF. Thus, the present invention provides compounds of formula I, and compositions containing compounds of formula I, which are of use in a method for treating a patient suffering from, or subject to, conditions which can be ameliorated by the administration of an inhibitor of TNF-alpha. For example compounds of the present invention are useful in joint inflammation, arthritis, rheumatoid arthritis and other arthritic conditions such as rheumatoid spondylitis and osteoarthritis. Additionally, the compounds are useful in treatment of sepsis, septic shock, gram negative sepsis, toxic shock syndrome, acute respiratory distress syndrome, asthma and other chronic pulmonary diseases, bone resorption diseases, reperfusion injury, graft vs. host reaction and allograft rejection. Furthermore, the compounds are useful in the treatment of infections such as viral infections and parasitic infections, for example malaria such as cerebral malaria, fever and myalgias due to infection, HIV, AIDS, cachexia such as cachexia secondary to AIDS or to cancer. Other disease states that may be treated with the compounds of the present invention include Crohn's disease, ulcerative colitis, pyresis, systemic lupus erythematosus, multiple sclerosis, type I diabetes mellitus, psoriasis, Beςhet's disease, anaphylactoid purpura nephritis, chronic glomerulonephritis, inflammatory bowel disease and leukemia. A special embodiment of the therapeutic methods of the present invention is the treating of joint inflammation.

According to a further feature of the invention there is provided a method for the treatment of a human or animal patient suffering from, or subject to, conditions which can be ameliorated by the administration of an inhibitor of cyclic AMP phosphodiesterase or of TNF, especially TNF-alpha, for example conditions as hereinbefore described, which comprises the administration to the patient of an effective amount of compound of formula I or a composition containing a compound of formula I. "Effective amount" is meant to describe an amount of compound of the present invention effective in inhibiting cyclic AMP phosphodiesterase and/or TNF and thus producing the desired therapeutic effect.

The present invention also includes within its scope pharmaceutical formulations which comprise at least one of the compounds of formula I in association with a pharmaceutically acceptable carrier or coating.

In practice compounds of the present invention may generally be administered parenterally, rectally or orally, but they are preferably administered by inhalation

The products according to the invention may be presented in forms permitting administration by the most suitable route and the invention also relates to pharmaceutical compositions containing at least one product according to the invention which are suitable for use in human or veterinary medicine. These compositions may be prepared according to the customary methods, using one or more pharmaceutically acceptable adjuvants or excipients. The adjuvants comprise, inter alia, diluents, sterile aqueous media and the various non-toxic organic solvents. The compositions may be presented in the form of tablets, pills, granules, powders, aqueous solutions or suspensions, injectable solutions, elixirs or syrups, and can contain one or more agents chosen from the group comprising sweeteners, flavorings, colorings, or stabilizers in order to obtain pharmaceutically acceptable preparations. The choice of vehicle and the content of active substance in the vehicle are generally determined in accordance with the solubility and chemical properties of the product, the particular mode of administration and the provisions to be observed in pharmaceutical practice. For example, excipients such as lactose, sodium citrate, calcium carbonate, dicalcium phosphate and disintegrating agents such as starch, alginic acids and certain complex silicates combined with lubricants such as magnesium stearate, sodium lauryl sulfate and talc may be used for preparing tablets. To prepare a capsule, it is advantageous to use lactose and high molecular weight polyethylene glycols. When aqueous suspensions are used they can contain emulsifying agents or agents which facilitate suspension. Diluents such as sucrose, ethanol, polyethylene glycol, propylene glycol, glycerol and chloroform or mixtures thereof may also be used.

For parenteral administration, emulsions, suspensions or solutions of the products according to the invention in vegetable oil, for example sesame oil, groundnut oil or olive oil, or aqueous-organic solutions such as water and propylene glycol, injectable organic esters such as ethyl oleate, as well as sterile aqueous solutions of the pharmaceutically acceptable salts, are used. The solutions of the salts of the products according to the invention are especially useful for administration by intramuscular or subcutaneous injection. The aqueous solutions, also comprising solutions of the salts in pure distilled water, may be used for intravenous administration with the proviso that their pH is suitably adjusted, that they are judiciously buffered and rendered isotonic with a sufficient quantity of glucose or sodium chloride and that they are sterilized by heating, irradiation or microfiltration.

Suitable compositions containing the compounds of the invention may be prepared by conventional means. For example, compounds of the invention may be dissolved or suspended in a suitable carrier for use in a nebulizer or a suspension or solution aerosol, or may be absorbed or adsorbed onto a suitable solid carrier for use in a dry powder inhaler.

Solid compositions for rectal administration include suppositories formulated in accordance with known methods and containing at least one compound of formula I. The percentage of active ingredient in the compositions of the invention may be varied, it being necessary that it should constitute a proportion such that a suitable dosage shall be obtained. Obviously, several unit dosage forms may be administered at about the same time. The dose employed will be determined by the physician, and depends upon the desired therapeutic effect, the route of administration and the duration of the treatment, and the condition of the patient. In the adult, the doses are generally from about 0.001 to about 50, preferably about 0.001 to about 5, mg/kg body weight per day by inhalation, from about 0.01 to about 100, preferably 0.1 to 70, more especially 0.5 to 10, mg/kg body weight per day by oral administration, and from about C.001 to about 10, preferably 0.01 to 1 , mg/kg body weight per day by intravenous administration. In each particular case, the doses will be determined in accordance with the factors distinctive to the subject to be treated, such as age, weight, general state of health and other characteristics which can influence the efficacy of the medicinal product.

The products according to the invention may be administered as frequently as necessary in order to obtain the desired therapeutic effect. Some patients may respond rapidly to a higher or lower dose and may find much weaker maintenance doses adequate. For other patients, it may be necessary to have long-term treatments at the rate of 1 to 4 doses per day, in accordance with the physiological requirements of each particular patient. Generally, the active product may be administered orally 1 to 4 times per day. It goes without saying that, for other patients, it will be necessary to prescribe not more than one or two doses per day.

Compounds within the scope of the present invention exhibit marked pharmacological activities according to tests described in the literature which tests results are believed to correlate to pharmacological activity in humans and other mammals. The following pharmacological test results are typical characteristics of compounds of the present invention. 1. Inhibitory effects of compounds on PDE activity.

1.1 Preparation of PDE isozymes from pig aorta.

The method is described fully by Souness and Scott (Biochem. 291.

389-395,1993). Briefly, aortas of freshly slaughtered pigs are placed in Hepes buffered krebs solution, extraneous tissue on the outside of the aorta is trimmed off and the endothelial layer on the intimal surface is removed by rubbing with a cotton swab. Smooth muscle strips are plucked from the aorta and 25 g are homogenized using a Waring Blender in homogenization buffer (20 mM Tris/HCI, pH 7.5, 2 mM MgCl2, 1 mM dithiothreitol, 5 mM EDTA and 1 mg/ml aprotinin). The homogenate is further homogenized with an Ultra- Turrax and then centrifuged (3000 g, 5 minutes). The supernatant is removed, and the pellet is sonicated in a small volume (25-50 mL) of homogenization buffer. The sonicate is centrifuged (3000 g, 5 minutes), the pellet discarded and the supernatant is pooled with that from the first centrifugation step. The pooled supernatants are centrifuged (100,000 g, 1 hour), the resulting high¬ speed supernatant is filtered (0.45 microm) and then applied to a DEAE- trisacryl (IBF) column (50 x 2.44 cm) preequilibrated in column buffer (20 mM Tris/HCI, pH 7.5, 2 mM MgCl2, 1 mM dithiothreitol, 20 microM TLCK). The column is washed with 500-700 mL of column buffer and PDE activities are eluted with 2 successive linear gradients of NaCI (0-200 mM, 400 mL and 200-300 mM, 200 mL) in column buffer. The fractions in the separated peaks of activity corresponding to the different PDE isozymes are pooled and stored at -20°C in 30% (v/v) ethylene glycol.

1 .2 Measurement of PDE activity.

PDE activity is determined by the two-step radioisotopic method of Thompson et al., Adv. Cyclic Nucl. Res.. 10, 69-92 (1979). The reaction mixture contains 20 mM Tris/HCI (pH 8.0), 10 mM MgCl2, 4 mM 2-mercaptoethanol, 0.2 mM EGTA and 0.05 mg of BSA7 mL. The concentration of substrate is 1 microM.

The IC50 values for the compounds examined are determined from concentration-response curves in which concentrations range from 0.1 nM to 40 microM. 1.3 Results.

Compounds within the scope of the invention produce up to about 50% inhibition of porcine aortic cyclic AMP-specific phosphodiesterase (PDE IV) at concentrations from about 10^-9 M up to about 10^-5 M, preferably from about 10"⁹ up to about 10"⁸ M. The compounds of the invention are from about 10, 000-fold to about 50-fold more selective for cyclic AMP phosphodiesterase IV than cyclic nucleotide phosphodiesterase types I, III or V.

2. Inhibitory effects of compounds on eosinophil superoxide generation.

2.1 Preparation of guinea-pig eosinophils.

The method is described fully in Souness et al (Biochem. Pharmacol..

42, 937-945, 1991).

2.2 Measurement of superoxide generation.

Superoxide anion generation is determined as the superoxide dismutase inhibitable reduction of p-iodonitrotetrazolium violet (INTV) (Souness et al, Biochem. Pharmacol.. 42. 937-945, 1991). Briefly, cells are incubated in 96 well microtitre plates in 0.25 mL of Hanks buffered salt solution (HBSS) containing INTV (0.5mg/mL) plus other additions for 45 minutes at 37°C. The cells are then centrifuged at 500 g for 5 minutes and the supernatant is aspirated. The pellet is solubilized by incubation overnight at room temperature in DMSO containing 0.6 M HCI and the absorbance of the reduced dye is measured at 492 nm. The results are expressed in absorbance units.

2.3 Results.

Compounds within the scope of the invention produce up to about 50% inhibition of superoxide generation from eosinophiis harvested from the peritoneal cavities of guinea-pigs at concentrations from about 10^"8 M to about 10^"5 M, preferably from about 10^~8 M up to about 10^"7 M. 3. Effects of compounds on tracheal smooth muscle contractility.

3.1 Preparation of guinea-pig tracheal strips and contractility studies.

Organ bath studies are performed essentially according to Tomkinson et al. (Br. J. Pharmacol.. 108 57-61 , 1993). Briefly, tracheas are removed from male, Dunkin-Hartley guinea-pigs (400-500 g) are placed in Krebs Ringer Bicarbonate (KRB) solution and fat and connective tissue are dissected away. Epithelium is removed by mechanical abrasion and the tracheal strips are suspended under an applied load, such that they are at their optimal length, derived from preliminary experiments, and equilibrated for 90 minutes, washing at 15 minute intervals.

Cumulative concentration-response curves to spasmogens are constructed and the concentration producing 30% of maximum contraction (EC30) is determined by computerized linear regression analysis. For relaxant studies, tissues are contracted with spasmogens (such as methacholine, histamine, leukotriene D4) (EC30) and when the response plateaus, PDE inhibitors (10 nM-100 microM) or vehicle control (DMSO) are added cumulatively. The concentration of relaxant producing 50% inhibition (IC50) of the agonist response is calculated by linear regression. Alternatively, PDE inhibitors, as above, may be added to tissues under basal tone and the concentration producing 50% relaxation (EC50) calculated as above.

3.2 Results.

Compounds within the scope of the invention produce about 50% relaxation of guinea-pig tracheal strips (under basal tone or which had been contracted by treatment with spasmogens) at concentrations from about 5x10"⁹ M to about 10^"5 M, preferably from about 5x10"⁹ M to about 10^'7 M. 4. in vivo bronchodilator actions of compounds.

4.1 Measurement of bronchodilatation.

Bronchorelaxant activity is measured in in vivo tests in the anaesthetized guinea-pig or rat according to the method described in Underwood et al., Pulm. Pharmacol.. 5, 203-212, (1992) in which the effects on bronchospasm induced by histamine (or other spasmogens such as methacholine or leukotriene D4) is determined. Nebulized aerosols generated from aqueous solutions of compounds of the invention are each administered for one minute to the anaesthetized animals. Alternatively, dry powder formulations made up from compounds of the invention and lactose are blown into the airways of the anaesthetized guinea-pigs or rats by the method described in Underwood et al., J. Pharm. Methods. 26, 203-210, 1991.

4.2 Results.

Compounds within the scope of the invention produce from about 30% up to about 90% decrease in bronchospasm when administered at effective doses of about 4 to about 1000 microg/kg, preferably about 4 to about 50 microg/kg, without any significant effect on blood pressure.

5. In vivo actions of compounds on antigen (ovalbamin)-induced eosinophilia in guinea-pigs.

5.1 Treatment of animals and measurement of eosinophil numbers.

Male Dunkin-Hartley guinea-pigs weighing 200-250 g are sensitized using 10 microg ovalbumin in 1 mL of a 100 mg/ mL suspension of aluminium hydroxide, i.p.

Sensitized guinea-pigs are anaesthetised and dry powder formulations of PDE inhibitors or lactose are administered (i.t.) into the airways. In some cases PDE inhibitors are administered orally. 23 hours later the procedure is repeated and 60 minutes later the guinea-pigs are challenged with nebulised saline or ovalbumin (1 % in saline) for 15 seconds. 24 hours after challenge the guinea-pigs are killed and the lungs are lavaged with warm saline. Total and differential cell counts are made.

5.2 Results.

Compounds within the scope of the invention, administered one hour before challenge, inhibit by at least 50% ovalbumin-induced eosinophilia in guinea-pigs which is measured 24 hours after challenge, at oral doses of about 1 to about 50 mg/kg, preferably about 1 to 10 mg/kg and inhaled doses of about 4 to 1000 microg/kg, preferably.4 to 50 microg/kg.

6 In Vitro Inhibitory Effects on TNF-alpha Release by Human Monocytes.

The effects of compounds on TNF-alpha production by human peripheral blood monocytes (PBMs) are examined as follows:

6.1. Preparation of blood leukocytes.

Blood is drawn from normal donors, mixed with dextran, and the erythrocytes allowed to sediment for 35 minutes at 37°C. Leukocytes are fractionated by centrifugation through a discontinuous (18, 20 and 22%) metrizamide gradient. The mononuclear cell fraction comprising 30-40% PBMs is suspended in HBSS and stored at 4°C until use.

6.2. Measurement of TNF-alpha.

Cells from the PBM-rich metrizamide fraction are spun down (200 g for 10 minutes at 20°C), resuspended at 10⁶ PBMs/ mL of medium; RPMI 1640 containing 1%v/v FCS, 50 U/ mL penicillin and 50 mg/ mL streptomycin (Gibco, U.K.), then plated out in 96 well plates at 2 x1θ5 cells/ well. The medium

(200 microL) is changed to remove any non-adherent cells and the remaining, adherent PBMs left in the incubator overnight (18 hours). One hour prior to challenge, the medium is changed to that containing compound for test or drug vehicle. Control treatments and compounds for test are assayed in quadruplicate wells. Compounds are tested within the concentration range of 3 x 10-^{1 0} M to 3 x l O'⁶ M. Medium (50 μL) with or without 10ng/ml LPS (E. Coli, 055 B5 from Sigma, U.K.) is then added. The incubation is then continued for a further 4 hours. Cell supematants are removed for storage at -20°C.

TNF-alpha levels in cell supematants are quantified using a standard sandwich ELISA technique. ELISA plates (Costar, U.K.) are coated ovemight at 4°C with 3 mg/ mL polyclonal goat anti-human TNF-alpha antibody (British Biotechnology, U.K.) in pH 9.9 bicarbonate buffer. Rabbit polyclonal anti- human TNF-alpha antiserum (Janssen Biochimicha, Belgium) at 1/500 dilution is used as the second antibody and polyclonal goat anti-rabbit IgG horseradish peroxidase (Calbiochem, U.S.A.) at 1/8000 dilution is used as the detection antibody. Color development is measured by absorbance at 450 nm using a Titertek plate reader.

TNF-alpha levels are calculated by interpolation from a standard curve using recombinant human TNF-alpha (British Biotechnology U.K.)(0.125-8 ng/ mL). Data (log-cone. vs. log-resp) are fitted by linear regression (p > 0.99) using a Multicalc (Wallac Pharmacia, U.K.) software program. Basal TNF-alpha levels are less than 100 pg/ mL whilst LPS stimulation of the PBMs increases TNF-alpha levels to 3-10 ng/ mL.

6.3 Results.

Compounds within the scope of the invention produce 50% inhibition of LPS-induced TNF-alpha release from human PBMs at concentrations within the range of about 10^-9 M to about 10^-6 M., preferably about 10^-9 M to about 10^"8 M.

7. Inhibitory effects of compounds on antigen-induced bronchoconstriction in the conscious guinea-pig.

7.1. Sensitisation of guinea-pigs and measurement of antigen - induced bronchoconstriction.

Male, Dunkin-Hartley guinea-pigs (550-700 g) are sensitized as above. Specific airways resistance (SRaw) is measured in conscious animals by whole body plethysmography using a variation of the method of Pennock et al., (J. Appl. Phvsio 46 ,399, 1979). Test compounds or vehicle (lactose carrier) are instilled into the airways as dry powders through a metal gavage needle. 30 minutes later, the animals are injected with mepyramine (30 mg/kg i.p.) to prevent anaphylactic collapse and placed into the plethysmography chambers where SRaw is determined at 1 minute intervals. Resting SRaw is then determined. Animals are challenged with an aerosol of ovalbumin and SRaw is determined every 5 minutes for 15 minutes.

7.2. Results.

Compounds within the scope of the invention inhibit antigen-induced bronchoconstriction by up to 80% at doses of between about 1 to about 1000 μg/kg (i.t.), preferably about 1 to about 20 μg/kg (i.t.).

8. Inhibitory effects of compounds on serum TNF-alpha levels in LPS - challenged mice.

8.1. Treatment of animals and measurement of murine TNF-alpha.

Female Balb/c mice (age 6-8 weeks, weight 20-22 g from Charles River, U.K.) in groups of five or more animals are dosed p.o. with compounds suspended in 1.5% (w/v) carboxymethyl cellulose then challenged after a minimum period of 30 min with 30 mg of LPS i.p. After 90 min the animals are killed by CO2 asphyxiation and bled by cardiac puncture. Blood is allowed to clot at 4°C, centrifuged (12,000 g for 5 minutes) and serum taken for TNF-alpha analysis.

TNF-alpha levels are measured using a commercially available murine TNF-alpha ELISA kit, purchased from Genzyme (Cat. no. 1509.00 ), as recommended by the manufacturer. Values for TNF-alpha are calculated from a recombinant murine TNF-alpha standard curve.

8.2 Results.

Compounds within the scope of the invention inhibit LPS-induced serum TNF-alpha at doses between about 10 and about 10,000 mg/kg, preferably about 10 to about 250 μg/kg. The value of the compounds of the invention is enhanced by their very low mammalian toxicity levels.

The following Composition Examples illustrate pharmaceutical compositions according to the present invention.

Composition Example 1

5-Cyclopentylmethyl-N-(3,5-dichloropyrid-4-yl)-6-methoxybenzamide (1 g) (mean particle size 3.5 microns) and lactose (99 g) (mean particle size 72 microns) are blended together for 30 minutes in a mechanical shaker/mixer. The resulting blend is filled, to a fill weight of 25 mg, into No.3 hard gelatine capsules, to give a product suitable for use, for example, with a dry powder inhaler.

Composition Example 2

No. 2 size gelatin capsules each containing:-

5-cyclopentylmethyl-N-(3,5-dichloro-pyrid-4-yl)-

6-methoxybenzamide 20 mg lactose 100 mg starch 60 mg dextrin 40 mg magnesium stearate 1 mg

are prepared in accordance with the usual procedure.

Compositions similar to those above are prepared from other compounds of formula I.

The present invention may be embodied in other specific forms without departing from the spirit or essential attributes thereof.

Claims

WHAT IS CLAIMED:

1. A compound of formula I

wherein

R^"1 is lower alkyl;

R³ is aryl or heteroaryl;

7^ and Z² are independently oxygen, sulfur or direct bond, and only one of Z^"! and Z² is a direct bond;

Z³ is -CZCH2- or -CZNH-; and

Z is oxygen or sulfur,

or N-oxide thereof or a pharmaceutically acceptable salt thereof,

provided that

The compound according to claim 1 wherein

R² is alkyl, alkenyl or cycloalkyl; R³ is phenyl, substituted phenyl or azaheteroaryl;

Z^"1 and Z² are independently oxygen or direct bond, and only one of Z¹ and Z² is a direct bond; and

Z³ is -COCH2- or -CONH-.

3. The compound according to claim 2 wherein

R¹ is methyl, ethyl, fluoroethyl or difluoromethyl;

R³ is azaheteroaryl.

4. The compound according to claim 1 wherein R³ is azaheterocyclyl having an imine moiety thereof as an N-oxide.

5. The compound according to claim 1 wherein R³ is phenyl substituted on the 2-position or on both the 2- and 6-positions.

6. The compound according to claim 1 wherein R³ is heteroaryl substituted on one or both of the positions adjacent to the position of R³ that is attached to

Z³.

7. The compound according to claim 1 wherein R³ is azaheteroaryl substituted on one or both, more preferably on both, of the positions adjacent to a position of R³ that is attached to Z³.

8. The compound according to claim 7 wherein R³ is a 3,5-dihalo- pyrid-4-yl.

9. The compound according to claim 8 wherein 3, 5-dihalo-1-oxido-4- pyridinium. 10. The compound according to claim 1 wherein Z² is -CZNH-.

11. The compound according to claim 10 wherein Z is oxygen.

12. The compound according to claim 1 wherein Z¹ is oxygen and Z² is a direct bond; Z¹ is sulfur and Z² is a direct bond; or Z¹ is a direct bond and Z² is oxygen are preferred.

13. The compound according to claim 12 wherein Z^"* is oxygen and Z² is a direct bond.

14. The compound according to claim 1 wherein R¹ is lower alkyl optionally substituted by one or more halo.

15. The compound according to claim 14 wherein the substitutition is on a position of R¹ that is attached to ^ .

16. The compound according to claim 1 wherein R² is lower alkyl, cycloalkyl or cyclothioalkyi optionally substituted by one or more halo.

17. The compound according to claim 1 wherein the substitutition is on a position of R² that is attached to Z².

18. The compound according to claim 17 wherein R² is cyclothioalkyi substituted on a position of R² that is attached to Z² or on a position adjacent to the thio moiety of the cyclothioalkyi.

19. The compound according to claim 1 wherein R² is 2-methylpropenyl, cyclopentylfluoromethyl, cyclopentylmethyl, cyclopentyl, cyclopentylidenemethyl or trinorbornyl.

20. The compound according to claim 1 wherein R² is cyclothioalkyi oxidized to the corresponding S-oxide or S,S-dioxide.

21. The compound according to claim 1 wherein R¹ is lower alkyl optionally substituted by halo; and R² is 2-methylpropenyl, cyclopentylfluoromethyl, cyclopentylmethyl, cyclopentyl, cyclopentylidenemethyl or trinorbornyl. 22. The compound according to claim 1 which is:

N-(3,5-dichloropyrid-4-yl)-3-cyclopentylmethyl-4-methoxybenzamide;

N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-ethylbenzamide;

N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-methylbenzamide;

N-(3,5-dichloro-1-oxido-4-pyridinio) 3-cyclopentylmethyl-4- methoxybenzamide;

N-(3,5-dichloro-1-oxido-4-pyridinio)-3-cyclopentyloxy-4-ethylbenzamide;

N-(3,5-dichloro-1-oxido-4-pyridinio)-3-cyclopentyloxy-4-methylbenzamide;

N-(,5-dichloro-1-oxido-4-pyridinio)-3-(exo)-8,9,10-trinorbomyl-2-oxy-4- ethylbenzamide;

N-(,5-dichloro-1-oxido-4-pyridinio)-3-cyclopentylidenemethyl-4- methoxybenzamide;

N-(,5-dichloro-1-oxido-4-pyridinio)-3-(2-methylpropenyl)-4- methoxybenzamide;

N-(,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentylidenemethyl-4- difluoromethoxybenzamide;

N-(,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentylfluoromethyl-4- methoxybenzamide;

N-(,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentyloxy-4-(1- fluoroethyl)benzamide;

N-(3,5-dichloropyrid-4-yl)-3-(exo)-8,9,10-trinorbomyl-2-oxy-4-ethylbenzamide;

N-(3,5-dichloropyrid-4-yl)-3-cyclopentylidenemethyl-4-methoxybenzamide; N-(3,5-dichloropyrid-4-yl)-3-(2-methylpropenyl)-4-methoxybenzamide;

N-(3,5-dichloropyrid-4-yl)-3-cyclopentylidenemethyl-4- difluoromethoxybenzamide;

N-(3,5-dichloropyrid-4-yl)-3-cyclopentylfluoromethyl-4-methoxybenzamide; or

N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-(1-fluoroethyl)benzamide.

23. The compound according to claim 1 which is:

N-(3,5-dichioropyrid-4-yl)-3-cyclopentylmethyl-4-methoxybenzamide

24. The compound according to claim 1 which is:

N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-ethylbenzamide;

25. The compound according to claim 1 which is:

N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-methylbenzamide;

26. The compound according to claim 1 which is:

N-(3,5-dichloro-1-oxido-4-pyridinio) 3-cyclopentylmethyl-4- methoxybenzamide;

27. The compound according to claim 1 which is:

N-(3,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentyloxy-4-ethylbenzamide;

28. The compound according to claim 1 which is:

N-(3,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentyloxy-4-methylbenzamide;

29. The compound according to claim 1 which is: N-(,5-dichloro-1-oxido-4-pyridinio)-3-(exo)-8,9,10-trinorbomyl-2-oxy-4- ethylbenzamide;

30. The compound according to claim 1 which is:

31. The compound according to claim 1 which is:

N-(,5-dichloro-1-oxido-4-pyridinio)-3-(2-methylpropenyl)-4- methoxybenzamide;

32. The compound according to claim 1 which is:

N-(,5-dichloro-1-oxido-4-pyridinio)-3-cyclopentylidenemethyl-4- difluoromethoxybenzamide;

33. The compound according to claim 1 which is:

34. The compound according to claim 1 which is:

N-(,5-dichloro-1 -oxido-4-pyridinio)-3-cyclopentyloxy-4-(1 - fiuoroethyl)benzamide;

35. The compound according to claim 1 which is:

N-(3,5-dichloropyrid-4-yl)-3-(exo)-8,9,10-trinorbomyl-2-oxy-4-ethylbenzamide;

36. The compound according to claim 1 which is:

N-(3,5-dichloropyrid-4-yl)-3-cyclopentylidenemethyl-4-methoxybenzamide;

37. The compound according to claim 1 which is: N-(3,5-dichloropyrid-4-yl)-3-(2-methylpropenyl)-4-methoxybenzamide;

38. The compound according to claim 1 which is:

39. The compound according to claim 1 which is:

N-(3,5-dichloropyrid-4-yl)-3-cyclopentylfluoromethyl-4-methoxybenzamide; or

40. The compound according to claim 1 which is:

N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-(1-fluoroethyl)benzamide.

41. A pharmaceutical composition comprising a pharmaceutically acceptable amount of the compound of claim 1 and a pharmaceutically acceptable carrier.

42. A method for treating a disease state capable of being modulated by inhibiting TNF comprising administering to a patient suffering from said disease state an effective amount of the compound of claim 1.

43. The method of claim 42 wherein said disease state is an inflammatory disease or autoimmune disease.

44. The method of claim 42 wherein said disease state is selected from the group consisting of joint inflammation, arthritis, rheumatoid arthritis, rheumatoid spondylitis and osteoarthritis, sepsis, septic shock, gram negative sepsis, toxic shock syndrome, acute respiratory distress syndrome, asthma, bone resorption diseases, reperfusion injury, graft vs host reaction, allograft rejection malaria, myalgias , HIV, AIDS, cachexia, Crohn's disease, ulcerative colitis, pyresis, systemic lupus erythematosus, multiple sclerosis, type I diabetes mellitus, psoriasis, Bechet's disease, anaphylactoid purpura nephritis, chronic glomerulonephritis, inflammatory bowel disease and leukemia. 45. The method of claim 44 wherein the disease state is joint inflammation.

46. A method for treating a disease state capable of being modulated by inhibiting production of cyclic AMP phosphodiesterase comprising administering to a patient suffering from said disease state an effective amount of the compound of claim 1.

47. The method of claim 46 wherein said disease state is a pathological condition associated with a function of cyclic AMP phophodiesterase, eosinophil accumulation or a function of the eosinophil.

48. The method of claim 47 wherein said pathological condition is asthma, atopic dermatitis, urticaria, allergic rhinitis, psoriasis, rheumatic arthritis, ulcerative colitis, Crohn's disease, adult respiratory distress syndrome, diabetes insipidus, keratosis, dermatitis, cerebral senility, multi-infarct dementia, senile dementia, memory impairment associated with Parkinson's disease, cardiac arrest, stroke and intermittent claudication.

49. The method of claim 48 wherein the pathological condition is asthma.

50. A process for preparing the compound of claim 1 substantially as hereinbefore described.