首页> 外国专利> PREPARATION OF 2-(4-(FUR-2-OYL)PIPERAZIN-1-YL)-4-AMINO-6,7-DIMETHOXYQUINAZOLINE BY DEHALOGE-NATION OF CERTAIN PRECURSORS

PREPARATION OF 2-(4-(FUR-2-OYL)PIPERAZIN-1-YL)-4-AMINO-6,7-DIMETHOXYQUINAZOLINE BY DEHALOGE-NATION OF CERTAIN PRECURSORS

机译:某些前体的脱卤反应制备2-(4-(FUR-2-OYL)哌嗪-1-基)-4-氨基-6,7-二甲氧基喹唑啉

摘要

Novel compounds of the general formula II IMAGE in which X represents a chlorine, bromine or iodine atom, and n denotes an integer from 1 to 3, are obtained by reacting a 6,7-dimethoxyquinazoline with a halogen-substituted furan. The compounds obtained can then be reacted at a temperature from 0 DEG to 150 DEG C with hydrogen in the presence of a catalytic amount of a dehalogenating catalyst and in the presence of a solvent which is inert to the reaction. The compound 2-[4-(2-furoyl)piperazin-1-yl]-4-amino-6,7-dimethoxy-quinazoline which can be prepared according to the invention is in general useful on account of its ability to lower the blood pressure in mammals having high blood pressure.
机译:通过使6,7-二甲氧基喹唑啉与卤素取代的呋喃反应,可以得到通式II的新化合物,其中X代表氯,溴或碘原子,n代表1至3的整数。然后可以在催化量的脱卤催化剂的存在下和在对反应呈惰性的溶剂的存在下,在0℃至150℃的温度下,使所获得的化合物与氢反应。可以根据本发明制备的化合物2- [4-(2-呋喃基)哌嗪-1-基] -4-氨基-6,7-二甲氧基-喹唑啉由于其降低化合物的能力而通常是有用的。具有高血压的哺乳动物的血压。

著录项

  • 公开/公告号NZ184535A

    专利类型

  • 公开/公告日1979-06-08

    原文格式PDF

  • 申请/专利权人 PFIZER INC;

    申请/专利号NZ19770184535

  • 发明设计人 HAMMEN PD;

    申请日1977-06-30

  • 分类号C07D405/12;A61Knull/null;A61K31/495;A61K31/505;C07Dnull/null;C07D239/00;C07D239/72;C07D239/84;C07D239/86;C07D239/95;C07D295/00;C07D295/12;C07D295/18;C07D307/46;C07D307/68;C07D405/06;C07D405/14;C07D407/14;

  • 国家 NZ

  • 入库时间 2022-08-22 20:38:30

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