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A process for preparing compounds related to espergualina

机译:一种制备与埃斯普瓜利纳有关的化合物的方法

摘要

Preparation of espergualina Derivatives of formula (i) wherein R1 is a Lower alquileno replaced or not with a hydroxymethyl; X is H or Halogen, M and N are integers between 1 and 5, and its Salts.Are obtained by separation of the protective groups, other espergualina protected Derivative of formula (ii), where RK1 is a alquileno Lower linear chain or branched, substituted or not with a hydroxymethyl Group; R2 is a protective Group of amino; R3 is a protected amino Group and X, and M N are defined above.The Protecting groups can be separated by catalytic reduction with Palladium Black or by Treatment with Trifluoroacetic acid and cf3so3 HBR or hydrolysis with acetic acid to 0 - 50jc. These compounds are stable in aqueous solutions, inhibiting the development of micro-organisms Gam and positive and negative are antitumor agents.
机译:式(i)的espergualina衍生物的制备,其中R 1是被羟甲基取代或未被羟甲基取代的低级alquileno; X是H或卤素,M和N是1-5的整数,及其盐是通过保护基团的分离获得的,式(ii)的其他由espergualina保护的衍生物,其中RK1是alquileno低级直链或支链,被羟甲基取代或未取代; R 2是氨基的保护基; R 3是被保护的氨基,X和M N如上所定义。保护基可通过用钯黑催化还原或用三氟乙酸和cf3so3 HBR处理或用乙酸水解至0-50jc来分离。这些化合物在水溶液中稳定,可抑制微生物Gam的发育,而正负则是抗肿瘤药。

著录项

  • 公开/公告号ES8701720A1

    专利类型

  • 公开/公告日1987-03-01

    原文格式PDF

  • 申请/专利权人 MICROBIAL CHEMISTRY RESEARCH FOUNDATION;

    申请/专利号ES19850540784

  • 发明设计人

    申请日1985-02-28

  • 分类号C07C129/12;A61K31/155;

  • 国家 ES

  • 入库时间 2022-08-22 07:17:13

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