首页> 外国专利> A process for the preparation of bis-indole-alkaloids and acid addition salts thereof and new bis-indole-alkaloids, pharmaceutical compositions containing them and their use as antitumour agents.

A process for the preparation of bis-indole-alkaloids and acid addition salts thereof and new bis-indole-alkaloids, pharmaceutical compositions containing them and their use as antitumour agents.

机译:一种双吲哚生物碱及其酸加成盐和新的双吲哚生物碱的制备方法,含有它们的药物组合物及其作为抗肿瘤剂的用途。

摘要

A process for the preparation of diindolealkaloids, especially new compounds corresponding to vinblastine or leurosine, in which the N-methyl group is replaced by an N-CH2-OC2H5 group having antitumor properties. The starting compounds are subjected to oxidation by chromic acid or an alkali metal dichromate at temperatures from -90 DEG C. to -30 DEG C. but preferably below about -45 DEG C. when the new compounds are to be produced, ethanol being present in this case.
机译:一种制备二吲哚生物碱,特别是相应于长春碱或亮氨酸的新化合物的方法,其中N-甲基被具有抗肿瘤特性的N-CH2-OC2H5基团取代。当要生产新化合物时,在-90℃至-30℃但优选低于约-45℃的温度下,用铬酸或碱金属重铬酸盐对起始化合物进行氧化。在这种情况下。

著录项

  • 公开/公告号ES8105008A1

    专利类型

  • 公开/公告日1981-05-16

    原文格式PDF

  • 申请/专利权人 RICHTER GEDEON VEGYESZETI GYAR RT.;

    申请/专利号ES19800490758

  • 发明设计人

    申请日1980-04-22

  • 分类号C07D519/04;A61K31/48;

  • 国家 ES

  • 入库时间 2022-08-22 15:48:26

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