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Improvements in the object of Invention Patent 529608 which concerns process obtaining new derivatives of 1H-imidazol

机译:对发明专利529608的目的的改进,该发明专利涉及获得1H-咪唑的新衍生物的方法

摘要

Process for obtaining 1H-imidazole derivatives of general formula I": comprising the reaction of a compound of formula II where A is methine (-CH-) with a compound of formula III" where X is bromine or chlorine, R"' is a halogen atom selected from chlorine or fluorine in any of the 5 or 7 positions of the benzo[b]thiophene residue and joining the methylene group (-CH2-) to the benzo[b]thiophene residue in the 2 or 3 position thereof, in hexamethyl phosphorotriamide, in the presence of a mineral base, preferably sodium hydride, and at a temperature of between 0 degree C and 100 degree C for a period of time of between 1 and 24 hours, with purification by crystallization or extraction, washing, drying and chromatography, yielding addition salts by treatment with the corresponding acids. IMAGE
机译:获得通式I”的1H-咪唑衍生物的方法:包括使A为次甲基(-CH-)的式II化合物与其中X为溴或氯,R”'为A的式III''化合物反应在苯并[b]噻吩残基的5或7个位置的任何一个中选自氯或氟的卤素原子,并且在其2或3位的亚甲基(-CH 2-)与苯并[b]噻吩残基连接。六甲基磷三酰胺,在矿物碱(优选氢化钠)存在下,在0摄氏度至100摄氏度之间的温度下运行1到24小时,并通过结晶或萃取,洗涤,干燥进行纯化色谱分离,用相应的酸处理可生成加成盐。

著录项

  • 公开/公告号ES535656A0

    专利类型

  • 公开/公告日1986-02-16

    原文格式PDF

  • 申请/专利权人 FERRER INT;

    申请/专利号ES19840535656

  • 发明设计人

    申请日1984-08-06

  • 分类号C07D495/04;A61K31/415;C07D333/00;C07D233/60;

  • 国家 ES

  • 入库时间 2022-08-22 07:37:54

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