发明名称 Piperidine coumpounds for use as CCR-3 inhibitors
摘要 A compound of formula I where: Ar1 is phenyl substituted by one or more halogen atoms, Ar2 is phenyl or naphthyl which is unsubstituted or substituted by one or more substituents selected from halogen, cyano, hydroxy, nitro, C1-C8-alkyl, C1-C8-haloalkyl, C1-C8-alkoxy or C1-C8-alkoxycarbonyl, R1 is hydrogen or C1-C8-alkyl optionally substituted by hydroxy, C1-C8-alkoxy, acyloxy, N(R2)R3, halogen, carboxy, C1-C8-alkoxycarbonyl, -CON(R4)R5 or by a monovalent cyclic organic group, R2 and R3 are each independently hydrogen or C1-C8-alkyl, or R2 is hydrogen and R3 is acyl or -SO2R6, or R2 or R3 together with the nitrogen atom to which they are attached denote a 5- or 6- membered heterocyclic group, R4 and R5 are each independently hydrogen or C1-C8-alkyl, or R4 or R5 together with the nitrogen atom to which they are attached denote a 5- or 6- membered heterocyclic group, R6 is C1-C8-alkyl, C1-C8-haloalkyl, or phenyl optionally substituted by C1-C8-alkyl, and n is 1-4. This is with the proviso that when Ar1 is p-chlorophenyl and R1 is hydrogen, Ar2 is not phenyl or p-nitrophenyl. The use of the compound described above to treat conditions mediated by CCR-3 and inflammatory or allergic conditions, such as inflammatory or obstructive airway disease.
申请公布号 NZ523414(A) 申请公布日期 2004.07.30
申请号 NZ20010523414 申请日期 2001.07.10
申请人 NOVARTIS AG 发明人 HOWE, TREVOR JOHN;BHALAY, GURDIP;LE GRAND, DARREN MARK;STORZ, THOMAS
分类号 A61K31/445;A61K31/4545;A61K45/00;A61P11/06;A61P29/00;A61P37/08;A61P43/00;C07D211/32;C07D401/06;C07D405/06;C07D417/06;(IPC1-7):C07D211/32;A61K31/454 主分类号 A61K31/445
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