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New 1-(benzoheterocyclyl-alkyl)-4-(phenyl or pyridyl)-piperidines, are tumor necrosis factor-alpha synthesis inhibitors useful for treating autoimmune or inflammatory diseases or pain
New 1-(benzoheterocyclyl-alkyl)-4-(phenyl or pyridyl)-piperidines, are tumor necrosis factor-alpha synthesis inhibitors useful for treating autoimmune or inflammatory diseases or pain
1-(Benzoheterocyclyl-alkyl)-4-(phenyl or pyridyl)-piperidine derivatives (I) are new. Piperidine derivatives of formula (I) and their salts and solvates are new. X = CH or N; R1 = H, halo or CF3; R2, R3 = H or Me; m, n = 0 or 1; W = group completing: (i) a 6-membered aromatic or saturated ring containing 1 or 2 N heteroatoms (optionally substituted by 1 or 2 of 1-4C alkyl, 1-4C alkoxy or CF3); or (ii) a 6-membered aromatic or saturated ring containing one N, O or S heteroatom (optionally substituted by 1 or 2 1-4C alkyl). An Independent claim is included for the preparation of (I).
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机译:1-(苯并杂环烷基-烷基)-4-(苯基或吡啶基)-哌啶衍生物(I)是新的。式(I)的哌啶衍生物及其盐和溶剂化物是新的。 X = CH或N; R1 = H,卤素或CF3; R2,R3 = H或Me; m,n = 0或1; W =完成的基团:(i)含有1或2个N杂原子(任选地被1-4C烷基,1-4C烷氧基或CF 3的1或2个取代)的6元芳族环或饱和环; (ii)含有一个N,O或S杂原子(可选地被1或2个1-4C烷基取代)的6元芳族环或饱和环。准备(I)包括独立权利要求。
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