首页> 外国专利> process for the production of 6.7 - dimethoxy - 4 - amino - 2 - (4 - (2 - furoyl) - 1 - piperazinyl) chinazolin

process for the production of 6.7 - dimethoxy - 4 - amino - 2 - (4 - (2 - furoyl) - 1 - piperazinyl) chinazolin

机译:6.7-二甲氧基-4-氨基-2-(4-(2-呋喃基)-1-哌嗪基)Chinazolin的制备方法

摘要

A novel process is provided for the preparation of 6,7-dimethoxy-4-amino-2¢4-(2-furoyl)-1-piperazinyl!quinazoline. It includes as a final step, cyclizing methyl-N-(3,4-dimethoxy-6-cyanophenyl)-¢4-(2-furoyl)-1-piperazinyl! thioformamidate by heating, together with ammonia, in a polar solvent, in the presence of an alkali metal amide. The methyl-N-(3,4-dimethoxy-6-cyanophenyl)-¢4-(2-furoyl)-1-piperazinyl!thioformamidate is preferably formed by reacting 3,4-dimethoxy-6-¢4-(2-furoyl)-1-piperazinyl-thiocarbamido!benzonitrile with methyl chloride. By this process the quinazoline ring in prazosine is produced within the molecule, rather than in a reaction between two different molecules.
机译:提供了一种制备6,7-二甲氧基-4-氨基-2¢4-(2-呋喃基)-1-哌嗪基!喹唑啉的新方法。作为最后一步,它包括将甲基-N-(3,4-二甲氧基-6-氰基苯基)-¢4-(2-呋喃基)-1-哌嗪基环化!在碱金属酰胺存在下,在极性溶剂中与氨一起加热,生成硫代甲酰胺酸盐。甲基-N-(3,4-二甲氧基-6-氰基苯基)-β4-(2-糠基)-1-哌嗪基!硫代甲酰胺酸酯优选通过使3,4-二甲氧基-6-¢4-(2-呋喃基)-1-哌嗪基-硫代氨基甲酰!通过该过程,在分子内而不是两个不同分子之间的反应中产生了哌唑嗪中的喹唑啉环。

著录项

  • 公开/公告号AT358048B

    专利类型

  • 公开/公告日1980-08-11

    原文格式PDF

  • 申请/专利权人 ORION-YHTYMAE OY;

    申请/专利号AT19770008672

  • 申请日1977-12-05

  • 分类号C07D405/14;

  • 国家 AT

  • 入库时间 2022-08-22 18:12:02

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