首页> 外国专利> Imidazo1,2-apyrimidines and their salts with the acids, process and intermediates for their preparation, use as medicaments and compositions containing them.

Imidazo1,2-apyrimidines and their salts with the acids, process and intermediates for their preparation, use as medicaments and compositions containing them.

机译:咪唑并[1,2-a]嘧啶及其与酸的盐,其制备方法和中间体,用作含有它们的药物和组合物。

摘要

Novel compounds selected from the group consisting of the formula IMAGE I wherein R1 is selected from the group consisting of 1,2,4-oxadiazol-5-yl and 1,3,4-thiadiazol-2-yl, both optionally substituted with alkyl of 1 to 3 carbon atoms or alkenyl of 2 to 5 carbon atoms and 1,2,4-oxadiazol-3-yl and 1,3,4-oxadiazol-2-yl, both optionally substituted with alkenyl of 2 to 5 carbon atoms, alkyl of 1 to 3 carbon atoms or alkyl of 1 to 3 carbon atoms substituted with at least one fluorine, R2 and R3 are individually selected from the group consisting of hydrogen, alkyl of 1 to 3 carbon atoms and alkenyl of 2 to 5 carbon atoms or together form alkylene of 3 to 5 carbon atoms, X is selected from the group consisting of -O- and -S-, R4 is alkyl of 1 to 3 carbon atoms and their non-toxic, pharmaceutically acceptable acid addition salts having anxiolytic sedative and hypnotic activity and a novel process and novel intermediates therefor.
机译:选自式 I的新型化合物,其中R1选自1,2,4-恶二唑-5-基和1,3,4-噻二唑-2-基,两者均任选被取代具有1至3个碳原子的烷基或2至5个碳原子的烯基和1,2,4-恶二唑-3-基和1,3,4-恶二唑-2-基,均任选被2至5个烯基取代碳原子,被至少一个氟取代的1至3个碳原子的烷基或1至3个碳原子的烷基,R 2和R 3分别选自氢,具有1至3个碳原子的烷基和具有2至3个碳原子的烯基。 5个碳原子或一起形成3至5个碳原子的亚烷基,X选自-O-和-S-,R4为1-3个碳原子的烷基及其无毒的药学上可接受的酸加成盐具有抗焦虑的镇静和催眠活性,并具有新颖的方法和新颖的中间体。

著录项

  • 公开/公告号ES8900049A1

    专利类型

  • 公开/公告日1988-11-16

    原文格式PDF

  • 申请/专利权人 ROUSSEL-UCLAF;

    申请/专利号ES19870557324

  • 发明设计人

    申请日1987-01-16

  • 分类号C07D413/14;A61K31/415;A61K31/42;A61K31/505;

  • 国家 ES

  • 入库时间 2022-08-22 06:36:31

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