首页> 外国专利> process for the production of 1 - substi - tuierter 8 - iodine - 6 - phenyl - 4h - triazolo (3,4c) thieno (2,3e) 1.4 - diazepines and their salts

process for the production of 1 - substi - tuierter 8 - iodine - 6 - phenyl - 4h - triazolo (3,4c) thieno (2,3e) 1.4 - diazepines and their salts

机译:1-取代-tuierter 8-碘-6-苯基-4h-三唑(3,4c)噻诺(2,3e)1.4-二氮杂and及其盐的生产方法

摘要

The 1-substituted 8-iodo-6-phenyl-4H-s-triazolo[3,4c]thieno[2,3e]1,4-diazepines of the formula I, as well as their physiologically tolerated acid addition salts, are prepared by cleaving a 4,1-oxazepine of the formula VII at the oxygen atom by treatment with a strong mineral acid, adding a phosphorus or sulphur halide to the hydro halide which forms, reacting the dihalide thus obtained with ammonia or substances giving rise to ammonia, and dehydrogenating the product. The substituents in the formulae I and VII have the meanings given in Patent Claim 1. Further preparation processes are given in Patent Claims 7 to 11 and 13. The compounds exhibit valuable therapeutic properties, in particular tranquillising, tension-releasing and sedative activity, as well as an intensive anticonvulsive effect, in association with extraordinarily low toxicity. In addition, they can be employed for improving feed uptake in mammals. IMAGE
机译:制备式I的1-取代的8-碘-6-苯基-4H-s-三唑并[3,4c]噻吩并[2,3e] 1,4-二氮杂s及其生理上可耐受的酸加成盐。通过用强无机酸处理在氧原子上裂解式VII的4,1-氧杂氮平,向形成的氢卤化物中添加卤化磷或卤化硫,使如此获得的二卤化物与氨或产生氨的物质反应,然后将产品脱氢。式I和VII中的取代基具有专利权利要求1中给出的含义。进一步的制备方法在专利权利要求7-11和13中给出。这些化合物显示出有价值的治疗特性,特别是镇定,释放张力和镇静活性,如以及强烈的抗惊厥作用以及极低的毒性。另外,它们可用于改善哺乳动物的饲料吸收。 <图像>

著录项

  • 公开/公告号ATA27178A

    专利类型

  • 公开/公告日1980-01-15

    原文格式PDF

  • 申请/专利权人 C.H. BOEHRINGER SOHN;

    申请/专利号AT19780000271

  • 发明设计人

    申请日1978-01-16

  • 分类号C07D495/14;

  • 国家 AT

  • 入库时间 2022-08-22 18:11:33

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