首页> 外国专利> process for the preparation of analgesic active, - 1h - azepinederivaten,method for preparation of pharmaceutical preparations, azepinederivaten - 1h - and the application obtained formed pharmaceutical preparations.

process for the preparation of analgesic active, - 1h - azepinederivaten,method for preparation of pharmaceutical preparations, azepinederivaten - 1h - and the application obtained formed pharmaceutical preparations.

机译:的镇痛活性剂的制备方法,-1h-氮杂环庚烷,药物制剂的制备方法,azepinederivaten-1h-获得的应用形成了药物制剂。

摘要

Analgesic hexahydro 1H azeoine derivs.. N3A. And their acid addn. and quat. ammonium salts are new cpds. of formula (I): (where R1 = H, (1-6C) alkyl, PhCH2, or (2-6C) alkanoyl; R2 = (1-6C)alkyl; R3 = H, (1-6C) alkyl, (2-6C) alkenyl, (2-6C) alkynyl, cyclopropylmethyl (2-6C) alkanoyl, CO2 alkyl, CHO, phenacyl, phenethyl or beta-benzoylethyl, (Ph rings may be substd); n = 3 or 4; and m = 0 or 1; with the proviso that n + m = 4; R = H or (1-6C) alkyl if m = 0 or H if m = 1). Used as analgesic and analgesic antagonists in a dose of 10-200 mg./kg.
机译:止痛六氢1H恒沸衍生物N3A。和他们的酸addn。和季。铵盐是新的cpds。式(I)的式:(其中R1 = H,(1-6C)烷基,PhCH2或(2-6C)烷酰基; R2 =(1-6C)烷基; R3 = H,(1-6C)烷基,( 2-6C)烯基,(2-6C)炔基,环丙基甲基(2-6C)烷酰基,CO2烷基,CHO,苯甲酰基,苯乙基或β-苯甲酰基乙基(Ph环可被取代); n = 3或4;以及m = 0或1;前提是n + m = 4;如果m = 0,则R = H或(1-6C)烷基;如果m = 1,则H)。用作镇痛药和镇痛药拮抗剂,剂量为10-200 mg./kg。

著录项

  • 公开/公告号NL6912483A

    专利类型

  • 公开/公告日1970-02-18

    原文格式PDF

  • 申请/专利权人

    申请/专利号NL19690012483

  • 发明设计人

    申请日1969-08-15

  • 分类号C07D41/04;A61K27/00;

  • 国家 NL

  • 入库时间 2022-08-23 11:33:47

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号