首页> 外国专利> PROCESS FOR PREPARING 3-SUBSTITUTED-2-OXINDOLE-1-CARBOXAMIDE DERIVATIVES WITH ANALGETIC AND ANTIINFLAMMATORY ACTIVITY

PROCESS FOR PREPARING 3-SUBSTITUTED-2-OXINDOLE-1-CARBOXAMIDE DERIVATIVES WITH ANALGETIC AND ANTIINFLAMMATORY ACTIVITY

机译:具有厌食和抗炎活性的3-取代的2-氧代吲哚-1-羧酰胺衍生物的制备方法

摘要

2-Oxindole-1-carboxamides of the formula: …CHEM… and their pharmaceutically acceptable base-salts, where X and Y are certain optional substituents or can be taken together to form certain ring structures; and R1 is alkyl, cycloalkyl, cycloalkenyl, optionally substituted phenyl, optionally substituted phenylalkyl, optionally substituted phenoxyalkyl, (thiophenoxy) alkyl, naphthyl, bicyclo [2.2.1]heptan-2-yl, bicyclo [2.2.1]hept-5-en-2-yl or a group of the formula -(CH2)n-Q-R0 where n is 0, 1 or 2, Q is a divalent radical which is a specified heterocycle, and R0 is H or alkyl. …??The compounds are useful as analgesic and anti-inflammatory agents. …??Also covered are certain intermediates useful in the preparation of the compounds (I), these intermediates having H in place of -COR1.
机译:下式的2-Oxindole-1-羧酰胺:……及其药学上可接受的碱盐,其中X和Y是某些可选的取代基,或可以一起形成某些环结构; R 1是烷基,环烷基,环烯基,任选取代的苯基,任选取代的苯基烷基,任选取代的苯氧基烷基,(硫代苯氧基)烷基,萘基,双环[2.2.1]庚-2-基,双环[2.2.1]庚基-5-en-2-基或式-(CH2)nQR <0>的基团,其中n为0、1或2,Q为为特定杂环的二价基团,R <0>为H或烷基。 ……该化合物可用作镇痛药和消炎药。 …还包括某些可用于制备化合物(I)的中间体,这些中间体具有H代替-COR 1。

著录项

  • 公开/公告号HU196178B

    专利类型

  • 公开/公告日1988-10-28

    原文格式PDF

  • 申请/专利权人 PFIZER INCUS;

    申请/专利号HU19850000992

  • 发明设计人 KADINSAUL B.US;

    申请日1985-03-18

  • 分类号C07D209/42;C07D401/06;C07D407/06;C07D409/06;C07D413/06;C07D417/06;C07D491/048;C07D403/06;A61K31/40;

  • 国家 HU

  • 入库时间 2022-08-22 07:00:01

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