首页> 外国专利> method for the manufacture of a pharmaceutical preparation and preparation of contraceptive operation on the basis of 2 - (halogeenfenyl) s triazolo (5.1 - (a) isochinoline derivatives and process for preparation of the usable 2 - (halogeenfenyl) s triazolo (5.1-a) isochinoline derivatives or the zuuradditiezouten thereof.

method for the manufacture of a pharmaceutical preparation and preparation of contraceptive operation on the basis of 2 - (halogeenfenyl) s triazolo (5.1 - (a) isochinoline derivatives and process for preparation of the usable 2 - (halogeenfenyl) s triazolo (5.1-a) isochinoline derivatives or the zuuradditiezouten thereof.

机译:药的制备方法和基于2-(卤代芬基)s三唑(5.1-(a)异喹啉衍生物)的避孕方法的制备方法和可用的2-(卤代芬基)s三唑(5.1-a)的制备方法)异喹啉衍生物或其zuuradditiezouten。

摘要

Triazolo-isoquinolines of formula (I) are new. (where R1 is Cl or F). (I) are prepd. by reacting 2-amino-1-(2H)-isoquinolone with an R1-substd. ethyl benzimidate, then cyclising the intermediate with base. (I) are contraceptives effective when administered after coitus or conception, and their abortion-inducing activity is not associated with other biological activities. They can be given orally or parenterally one or more times a month as necessary.
机译:式(I)的三唑-异喹啉是新的。 (其中R1是Cl或F)。 (一)准备。使2-氨基-1-(2H)-异喹诺酮与R1-取代基反应。苯磺酸二甲酯,然后用碱环化中间体。 (I)避孕药在性交或受孕后给药时有效,并且其流产诱导活性与其他生物学活性无关。可以根据需要每月一次或多次口服或胃肠外给予它们。

著录项

  • 公开/公告号NL175299C

    专利类型

  • 公开/公告日1984-10-16

    原文格式PDF

  • 申请/专利权人 GRUPPO LEPETIT S.P.A. TE MILAAN ITALIE.;

    申请/专利号NL19770004940

  • 发明设计人

    申请日1977-05-05

  • 分类号C07D471/04;A61K31/47;

  • 国家 NL

  • 入库时间 2022-08-22 09:16:22

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