首页> 外国专利> New 1-(heterocyclyl-alkyl)-4-(phenyl or pyridyl)-tetrahydropyridines, are tumor necrosis factor-alpha synthesis inhibitors useful for treating autoimmune or inflammatory diseases or pain

New 1-(heterocyclyl-alkyl)-4-(phenyl or pyridyl)-tetrahydropyridines, are tumor necrosis factor-alpha synthesis inhibitors useful for treating autoimmune or inflammatory diseases or pain

机译:新的1-(杂环基-烷基)-4-(苯基或吡啶基)-四氢吡啶类是肿瘤坏死因子-α合成抑制剂,可用于治疗自身免疫或炎性疾病或疼痛

摘要

1-(Benzoheterocyclyl-alkyl)-4-(phenyl or pyridyl)-1,2,3,6-tetrahydropyridine derivatives (I) are new. Tetrahydropyridine derivatives of formula (I) and their N-oxides, salts and solvates are new. X = CH or N; R1 = H, halo or CF3; R2, R3 = H or Me; m, n = 0 or 1; A = nitrogen-containing benzo-group of formula (a) - (i); R4 - R6 = H or 1-4C alkyl; R7, R8 = H, halo, 1-4C alkyl or 1-4C alkoxy; dotted line = optional bond; provided that if X = CH, then group A (a) is not indol-4-yl. Independent claims are included for: (1) the preparation of (I); and (2) the use of compounds (I) without the proviso (or their N-oxides, salts or solvates) in the preparation of medicaments for use as analgesics and/or treatment of diseases associatd with immunological and inflammatory disorders.
机译:1-(苯并杂环烷基-烷基)-4-(苯基或吡啶基)-1,2,3,6-四氢吡啶衍生物(I)是新的。式(I)的四氢吡啶衍生物及其N-氧化物,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; A =式(a)-(i)的含氮苯并-基团; R4-R6 = H或1-4C烷基; R7,R8 = H,卤素,1-4C烷基或1-4C烷氧基;虚线=可选键;前提是如果X = CH,则基团A(a)不是indol-4-yl。独立索赔包括:(1)(I)的制备; (2)没有附加条件的化合物(I)(或其N-氧化物,盐或溶剂化物)在制备药物中的用途,所述药物用作止痛药和/或治疗与免疫和炎性疾病有关的疾病。

著录项

  • 公开/公告号FR2823750A1

    专利类型

  • 公开/公告日2002-10-25

    原文格式PDF

  • 申请/专利权人 SANOFI-SYNTHELABO;

    申请/专利号FR20010005362

  • 申请日2001-04-20

  • 分类号C07D401/10;A61K31/4725;A61K31/4439;A61K31/4427;A61P29/00;A61P37/02;A61P25/04;

  • 国家 FR

  • 入库时间 2022-08-22 00:24:07

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