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remifentanil optionally in the form of a pharmaceutically acceptable acid addition salt, including the remifentanil hydrochloride

机译:瑞芬太尼(可选)呈药学上可接受的酸加成盐形式,包括盐酸瑞芬太尼

摘要

N-Phenyl-N-(4-piperdinyl)amide derivatives are disclosed having the general formula (I). CHEM wherein: X is a member selected from the group consisting of: alkoxy-carbonyl-lower alkyl, lower alkyl-carbonyloxy-lower alkyl, alkenyloxy-carbonyl-lower alkyl, and (C1-2)alkoxy-(C1-2)alkoxy-carbonyl-lower alkyl. Ar is a member selected from the group consisting of phenyl, mono-, di- and tri-substituted phenyl, wherein each subtitutuent is independently selected from the group consisting of halo, lower alkyl, lower alkoxy and trifluoromethyl; R is a member selected from the group consisting of lower alkyl, and lower alkoxy-lower alkyl; R1 is a member selected from the group consisting of hydrogen, lower alkoxy-carbonyl, and methoxymethyl; and R2 is a member selected from the group consisting of hydrogen and methyl; and the diastereomeric and enantiomeric isomers thereof, and the acid addition salts of said compounds and isomers. The compounds exhibit analgesic activity having relatively short durations of analgesic action. The invention embraces the compounds (I), pharmaceutical compositions of (I) and methods of providing analgesia with (I). Also included are certain novel intermediates for making (I).
机译:公开了具有通式(I)的N-苯基-N-(4-哌啶基)酰胺衍生物。 其中:X是选自由以下组成的组的成员:烷氧基-羰基-低级烷基,低级烷基-羰基氧基-低级烷基,烯基氧基-羰基-低级烷基和(C1-2)烷氧基-(C1-2 )烷氧基-羰基-低级烷基。 Ar是选自苯基,单,二和三取代的苯基的成员,其中每个取代基独立地选自卤素,低级烷基,低级烷氧基和三氟甲基; R是选自低级烷基和低级烷氧基-低级烷基的成员; R 1为选自氢,低级烷氧基-羰基和甲氧基甲基的成员。 R 2为选自氢和甲基的成员。及其非对映异构体和对映异构体,以及所述化合物和异构体的酸加成盐。该化合物显示出具有相对较短的止痛作用持续时间的止痛活性。本发明包括化合物(I),(I)的药物组合物和为(I)提供镇痛作用的方法。还包括某些用于制备(I)的新型中间体。

著录项

  • 公开/公告号LU90011I2

    专利类型

  • 公开/公告日1997-03-11

    原文格式PDF

  • 申请/专利权人 GLAXO WELLCOME INC.;

    申请/专利号LU19970090011C

  • 发明设计人

    申请日1997-01-24

  • 分类号A61K;A61K31/445;A61K31/4465;A61P25/04;C07B57;C07D;C07D211/14;C07D211/58;

  • 国家 LU

  • 入库时间 2022-08-22 03:26:39

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