首页> 外国专利> New process for preparing ethers Basic 2,2-dimethyl - 4 - phenyl - chromane and its Salts

New process for preparing ethers Basic 2,2-dimethyl - 4 - phenyl - chromane and its Salts

机译:制备碱性2,2-二甲基-4-苯基苯甲烷及其盐类醚的新工艺。

摘要

Compounds of the formula II are prepared IMAGE in which X is alkylene having 2 to 4 carbon atoms, Y is an oxygen or sulphur atom or a CH2 group; R1 is a hydrogen atom or lower alkyl; R2 is a hydrogen atom, lower alkyl, phenyl, tolyl or benzyl, or R2 is bonded to R1 with the formation of a 5-, 6- or 7-membered ring; R3 is aryl, aralkyl or a pyridyl, furyl, thienyl or pyrrolidyl radical, R4 is a hydrogen atom or C1-4-alkyl and R5 is a hydrogen atom or C1-4-alkyl, by reaction of an appropriate 7-OH compound with a compound Q1-X-NR1R2 or a compound Q1XQ2, in which Q1 and Q2 are groups which are easily removable by a nucleophile, and subsequent reaction with an amine HNR1R2. The compounds prepared according to the invention act on the central nervous system. Depending on the dose administered, they act as appetite suppressants or affect the mood of the person.
机译:制备式II化合物,其中X为具有2-4个碳原子的亚烷基,Y为氧或硫原子或CH 2基团; R1是氢原子或低级烷基; R2是氢原子,低级烷基,苯基,甲苯基或苄基,或R2与R1键合,形成5-,6-或7-元环;通过合适的7-OH化合物与R 3的反应,R 3是芳基,芳烷基或吡啶基,呋喃基,噻吩基或吡咯烷基,R 4是氢原子或C 1-4-烷基,R 5是氢原子或C 1-4-烷基。化合物Q1-X-NR1R2或化合物Q1XQ2,其中Q1和Q2是易于被亲核试剂除去的基团,并随后与胺HNR1R2反应。根据本发明制备的化合物作用于中枢神经系统。根据所服用的剂量,它们可作为食欲抑制剂或影响人的情绪。

著录项

  • 公开/公告号AR210500A1

    专利类型

  • 公开/公告日1977-08-15

    原文格式PDF

  • 申请/专利权人 BEECHAM GROUP LIMITED;

    申请/专利号AR19760263765

  • 发明设计人

    申请日1976-06-28

  • 分类号C07D311/04;

  • 国家 AR

  • 入库时间 2022-08-23 00:59:26

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