首页> 外国专利> PROCEDURE FOR THE PROMOTION OF NEW HETEROCYCLICAL ASSOCIATIONS.

PROCEDURE FOR THE PROMOTION OF NEW HETEROCYCLICAL ASSOCIATIONS.

机译:促进新的杂环协会的程序。

摘要

1500063 2-Indolinone and fluorenone derivatives SANDOZ Ltd 16 June 1975 [19 June 1974 (2)] 25530/75 Heading C2C Novel 2-indolinone and fluorenone derivatives of the general formula wherein Het is a radical formed by removing a hydrogen atom from the phenyl ring of 2-indolinone or fluorenone, and R is a group having one of the following Formulµ A, B, C and D in which n is 2 or 3, nSP1/SP is 1-4, X-XSP1/SP is ethylene or vinylene and in D the two C atoms adjacent to the N atom are identically unsubstituted or substituted by one or two C 1-4 alkyl groups and acid addition salts thereof are prepared by reacting Het-O-CH 2 -CH(OH)-CH 2 Y, in which Y is a leaving group, or an epoxy compound of the general Formula IIa with H-R, followed optionally by salification of the product. Pharmaceutical compositions having antiarrhythmic activity comprise, as active ingredient, a 2-indolinone or fluorenone derivative (I) or a pharmaceutically acceptable acid addition salt thereof, in association with a pharmaceutical carrier or diluent.
机译:1500063 2-吲哚啉酮和芴酮衍生物SANDOZ Ltd 1975年6月16日[1974年6月19日(2)]标题2530/75具有以下通式的新型2-吲哚啉酮和芴酮衍生物:其中Het是通过从苯基上除去氢原子而形成的基团环是2-吲哚酮或芴酮的环,R为具有以下式A,B,C和D的基团,其中n为2或3,n 1 为1-4,XX < SP> 1 是乙烯或亚乙烯基,并且在D中,与N原子相邻的两个C原子相同地未被取代或被一个或两个C 1-4烷基取代,并且其酸加成盐通过使Het-O反应而制备。 -Y 2 -CH(OH)-CH 2 Y,其中Y是离去基团,或具有HR的通式IIa的环氧化合物,随后任选地将产物盐化。具有抗心律不齐活性的药物组合物包含2-吲哚啉酮或芴酮衍生物(I)或其药学上可接受的酸加成盐以及药物载体或稀释剂作为活性成分。

著录项

  • 公开/公告号SE7506757L

    专利类型

  • 公开/公告日1975-12-22

    原文格式PDF

  • 申请/专利权人 SANDOZ AG;

    申请/专利号SE19750006757

  • 发明设计人 BERTHOLD R;TROXLER F;

    申请日1975-06-12

  • 分类号C07D403/12;

  • 国家 SE

  • 入库时间 2022-08-23 02:43:09

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