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method for preparation of new decahydroisochi - nolineverbindingen and method for preparation of pharmaceutical preparations.

机译:新的十氢异黄酮的合成方法-去甲verbindingver和药物制剂的制备方法。

摘要

1513874 1 - Ethyl - 3a - (substituted phenyl)- decahydroisoquinolines ELI LILLY & CO 3 June 1975 [7 June 1974] 23868/75 Heading C2C Novel compounds of the Formula I wherein RSP1/SP is O-(C 1-3 )alkyl, hydroxy or -OCO(C 1-3 )alkyl and pharmaceutically acceptable salts thereof may be prepared by reacting a compound VII wherein RSP11/SP is OH or -O-(C 1-3 ) alkyl with an ethyl halide and if desired converting the product I wherein RSP1/SP is OH into the corresponding compound wherein RSP1/SP is -O-(C 1-3 )alkyl or -OCO(C 1-3 )alkyl and/or forming salts thereof and/or resolving isomers thereof. The intermediates VII are described and claimed in Application No. 1693/78. The cis isomers of a precursor 1-methyl-3a-(m-methoxyphenyl - 1,2,3,3a,4,5,6,7,7a,8 - decahydro isoquinoline are described and claimed in Application No. 1694/78. Pharmaceutical compositions of the compounds I with the usual excipients are analgetic agonistic and analgetic antagonistic when administered parenterally or orally.
机译:1513874 1-乙基-3a-(取代的苯基)-十氢异喹啉ELI LILLY&CO 1975年6月3日[1974年6月7日]标题C2C其中R 1 为O-( C 1-3)烷基,羟基或-OCO(C 1-3)烷基及其药学上可接受的盐可通过使其中R SP 11为OH或-O-(C 1)的化合物VII反应来制备-3)烷基与卤代乙基,并且如果需要,将其中R 1 为OH的产物I转化为其中R 1 为-O-的相应化合物(C 1-3烷基或-OCO(C 1-3)烷基和/或其形成盐和/或其拆分异构体。在申请号1693/78中描述并要求保护中间体VII。申请号1694/78中描述了前体1-甲基-3a-(间甲氧基苯基-1,2,3,3a,4,5,6,7,7a,8-十氢异喹啉的顺式异构体当胃肠外或口服给药时,化合物I与常用赋形剂的药物组合物是镇痛激动剂和镇痛拮抗剂。

著录项

  • 公开/公告号NL7506588A

    专利类型

  • 公开/公告日1975-12-09

    原文格式PDF

  • 申请/专利号NL19750006588

  • 发明设计人

    申请日1975-06-03

  • 分类号A61K31/47;C07D217/04;

  • 国家 NL

  • 入库时间 2022-08-23 02:50:36

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