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A process for the preparation of Derivatives of - toina Hidan.

机译:-toina Hidan衍生物的制备方法。

摘要

Method for obtaining Derivatives of Hydantoin and its Salts, wherein R1 is c1-4 alkyl; R2 is Hydrogen or c1-4 alkyl hydroxyl hydroxyl; R3 or R5 is protected, or is hirogeno 1-6 alkyl; R4 can be several types of Radicals; and - CH2 - H2, - ch = CH - or - C = C, and N is 1 to 5.Consists in the reduction reaction of a compound in which R1, R2, R3, R4, R5, and "n" and have the same meaning with reducing Agent of the carbonyl Group, following methods convencionaes. These compounds have applications for its pharmacological activity antisecrecion gastric antiulcer, on smooth muscle and vascular activity.
机译:获得乙内酰脲及其盐的衍生物的方法,其中R1是c1-4烷基; R2是氢或c1-4烷基羟基羟基; R3或R5是被保护的,或者是hirogeno 1-6烷基; R4可以是几种自由基。 -CH 2 -H 2,-ch = CH-或-C = C,且N为1至5。包括R 1,R 2,R 3,R 4,R 5和“ n”的化合物的还原反应。按照以下方法,与羰基的还原剂具有相同的含义。这些化合物因其对平滑肌和血管活性的药理活性具有抗分泌性胃溃疡的作用。

著录项

  • 公开/公告号ES8203351A1

    专利类型

  • 公开/公告日1982-07-01

    原文格式PDF

  • 申请/专利权人 BEECHAM GROUP LIMITED;

    申请/专利号ES19810499012

  • 发明设计人

    申请日1981-01-30

  • 分类号C07D233/76;A61K31/415;

  • 国家 ES

  • 入库时间 2022-08-22 13:20:09

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