Method of treating cytokine mediated diseases or conditions

A method of treating a cytokine mediated disease or condition chosen from:

• actuate and chronic pain, contact dermatitis, atherosclerosis, glomerulonephritis, reperfusion injury, bone resorption diseases, asthma, stroke, myocardial infarction, thermal injury, adult respiratory distress syndrome (ARDS), multiple organ injury secondary to trauma, dermatoses with actuate inflammatory components, acute purulent meningitis, necrotizing entrerocolities, syndromes associated with hemodialysis, septic shock, leukopherisis and granuloctye transfusion, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound of the formula (I):
• wherein
• Ar1is pyrazole optionally substituted by one or more R1, R2 or R3;
• Ar2 is:
• phenyl, naphthyl, quinoline, isoquinoline, tetrahydronaphthyl, tetrahydroquinoline, tetrahydroisoquinoline, benzimidazole, benzofuran, indanyl, indenyl or indole each being optionally substituted with one to three R2 groups;
• L is a C1-10 saturated or unsaturated branch or unbranched carbon chain;
• wherein one or more methylene groups are optionally independently replaced by O, N or S;
• and
• wherein said linking group is optionally substituted with 0-2 oxo groups and one or more C1-4 branched or unbranched alkyl which may be substituted by one or more halogen atoms;
• Q is selected from the group consisting of:
• a) pyridine, pyrimidine, pyridazine, imidazole, benzimidazole, oxazo[4,5-b]pyridine and imidazo[4,5-b]pyridine, which are optionally substituted with one to three groups selected from the group consisting of halogen, C1-6 alkyl, C1-6 alkoxy, hydroxy, mono- or di-(C1-3 alkyl)amino;
• C1-4 alkyl-S(O)m and phenylamino wherein the phenyl ring is optionally substituted with one to two groups selected from the group consisting of halogen, C1-6 alkyl and C1-6 alkoxy;
• b) morpholine, thiomorpholine, thiomorpholine sulfoxide, thiomorpholine sulfone, piperidine, piperidinone and tetrahydropyrimidone which are optionally substituted with one to three groups selected from the group consisting of C1-6 alkyl, C1-6 alkoxy, hydroxy, mono- or di-(C1-3 alkyl)amino-C13 alkyl, phenylamino-C1-3 alkyl and C1-3 alkoxy-C1-3 alkyl;
• R1 is selected from the group consisting of
• a) C3-10 branched or unbranched alkyl, which may optionally be partially or fully halogenated, and optionally substituted with one to three phenyl, naphthyl or heterocyclic groups selected from the group consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl and isothiazolyl;
• each such phenyl, naphthyl or heterocylic selected from the group hereinabove described being substituted with 0 to 5 groups selected from the halogen, C1-6 branched or unbranched alkyl which is optionally partially or fully halogenated, C3-8 cycloalkyl, C5-8 cycloalkenyl, hydroxy, cyano, C1-3 alkyloxy which is optionally partially or fully halogenated, NH2C(O) and di(C1-3) alkylaminocarbonyl;
• b) C3-7 cycloalkyl selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl and bicycloheptanyl, which may optionally be partially or fully halogenated and which may optionally be substituted with one to three C1-3alkyl groups, or an analog of such cycloalkyl group wherein one to three ring methylene groups are replaced by groups independently selected from O, S, CHOH, <C═O, <C═S and NH,
• c) C3-10 branched alkenyl which may optionally be partially or fully halogenated, and which is optionally substituted with one to three C1-5 branched or unbranched alkyl, phenyl, naphthyl or heterocyclic groups, with each such heterocyclic group being independently selected from the group consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl and isothiazolyl, and each such phenyl, naphthyl or heterocyclic group being substituted with 0 to 5 groups selected from halogen, C1-6 branched or unbranched alkyl which is optionally partially or fully halogenated, cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl and bicycloheptanyl, hydroxy, cyano, C1-3 alkyloxy which is optionally partially or fully halogenated, NH2CO(O), mono- or di(C1-3)alkylaminocarbonyl;
• d) C5-7 cycloalkenyl selected from the group consisting of cyclopentanyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl, cycloheptadienyl, bicyclohexenyl and bicycloheptenyl, wherein such cycloalkenyl group may optionally be substituted with one to three C1-3 alkyl groups;
• e) cyano;
• and,
• f) methoxycarbonyl, ethoxycarbonyl and propoxycarbonyl;
• R2 is selected from the group consisting of:
• a C1-4 branched or unbranched alkyl which may optionally be partially or fully halogenated, acetyl, aroyl, C1-4 branched or unbranched alkoxy, which may optionally be partially or fully halogenated, halogen, methoxycarbonyl and phenylsulfonyl;
• R5 is selected from the group consisting of:
• a) a phenyl, naphthyl or heterocyclic group selected from the group consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, tetrahydrofuryl, isoxazlyl, isothiazolyl, quinolinyl, isoquinolinyl, indolyl, benzimidazoly, benzofuranyl, benzoxazolyl, benzisoxazolyl, benzpyrazolyl, benzothiofuranyl, cinnolinyl, pterindinyl, pththalazinyl, naphthypyridinyl, quinoxalinyl, quinazolinyl, purinyl and indazolyl, wherein such phenyl, naphthyl or heterocyclic group is optionally substituted with one to five groups selected from the group consisting of a C1-6 branched or unbranched alkyl, phenyl, naphthyl, heterocycle selected from the group hereinabove described, C1-4 branched or unbranched alkyl which is optionally partially or fully halogenated, cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl, bicycloheptanyl, phenyl C1-5alkyl, naphthyl C1-5 alkyl, halo, hydroxy, cyano, C1-5 alkyloxy which may optionally be partially or fully halogenated, phenyloxy, naphthyloxy, heteraryloxy wherein the heterocyclic moiety is selected from the group hereinabove described, nitro, amino, mono- or Di-(C1-3)alkylamino, phenylamino, naphthylamino, heterocyclclamino wherein the heterocyclyl moiety is selected from the group hereinabove described, NH2C(O), a mono- or di-(C1-3)alkyl aminocarbonyl, C1-5 alkyl-C(O)-C1-4alkyl, amino-C1-5 alkyl, mono- or di-(C1-3)alkylamino-C1-5 alkyl, amino-S(O)2, di-(C1-3)alkylamino-S(O)2, R4-C1-5alkyl, R5-C1-5alkoxy, R6-C())-C1-5 alkyl and R7-C1-5 alkyl(R8)N;
• b) a fused aryl selected from the group consisting of benzocyclobutanyl, indanyl, indenyl, dihydronaphthyl, tetrahydronaphthyl, benzocycloheptanyl and benzocycloheptenyl, or a fused heterocyclyl selected from the group consisting of cyclopentenopyridine, cyclohexanopyridine, cyclopentanopytimidine, cyclohexanopyrimidine, cyclopentanopyrazine, cyclohexanopyrazine, cyclopentanopyridazine, cyclohexanopyridazine, cyclopentanoquinoline, cyclohexanoquinoline, cyclopentanoisoquinoline, cycloheanoisoquinoline, cyclopentanoindole, cyclohexanoindole, cyclopentanobenzimidazole, cyclohexanobenzimidazole, cyclopentanobenzoxazole, cyclohexanobenzoxazole, cyclopentanoimidazole, cyclohexanolmidazole, cyclopentanothiophene and cyclohexanothiophene;
• wherein the fused aryl or fused heterocyclyl ring is substituted win 0 to 3 groups independently selected from phenyl, naphthyl and heterocycl selected from the group consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl, and isothiazolyl, C1-6 branched or unbranched alkyl which is optionally partially or fully halogenated, halo, cyano, C1-2 alkyloxy which is optionally partially or fully halogenated, phenyloxy, naphthyloxy, heterocyclyloxy wherein the heterocyclyl moiety is selected from the group hereinabove described, nitro, amino, mono- or di-(C1-3)alkylamino, phenylamino, naphthylamino;
• heterocyclylamino wherein the heterocyclyl moiety is selected from the group hereinabove described, NH2C(O), a mono- or di-(C1-3)alkyl aminocarbonyl, C1-4 alkyl-OC(O), C1-5 alkyl-C(O)-C1-4 branched or unbranched alkyl, an amino-C1-5 alkyl, mono- or di-(C1-3)alkylamino-C1-5 alkyl, R9-C1-5 alkyl, R10-C1-5alkoxy, R11—C(O)—C1-5 alkyl and R12-C1-5 alkyl(R13)N;
• c) cycloalkyl selected from the group consisting of cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl and bicycloheptanyl, which the cycloalkyl may optionally be partially or fully halogenated and which may optionally be substituted with one to three C1-3 alkyl groups;
• d) C5-7cycloalkenyl, selected from the group consisting of cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl, cycloheptadienyl, bicyclohexenyl and bicycloheptenyl, wherein such cycloalkenyl group may optionally be substituted with one to three C1-5 alkyl groups;
• and
• e) acetyl, aroyl, alkoxycarbonylalkyl or phenylsulfonyl;
• f) C1-6 branched or unbranched alkyl which may optionally be partially or fully halogenated;
• wherein
• or R1 and R2 taken together may optionally form a fused phenyl or pyridinyl ring;
• each R8, R13 is independently selected from the group consisting of hydrogen and C1-4 branched or unbranched alkyl which may optionally be partially or fully halogenated;
• each R4, R5, R6, R7, R9, R10, R11 and R12 is independently selected from the group consisting of:
• morpholine, piperidine, piperazine, imidazole and tetrazole;
• m=0, 1, 2;
• X=O or S and physiologically acceptable acids or salts thereof.