首页> 外国专利> SUBSTITUTED 4-PHENYL-4-1H-IMIDAZOL-2-YL-PIPERIDINE DERIVATIVES AND THEIR USE AS SELECTIVE NON-PEPTIDE DELTA OPIOID AGONISTS

SUBSTITUTED 4-PHENYL-4-1H-IMIDAZOL-2-YL-PIPERIDINE DERIVATIVES AND THEIR USE AS SELECTIVE NON-PEPTIDE DELTA OPIOID AGONISTS

机译:取代的4-苯基-4- [1H-咪唑-2-基]-哌啶衍生物及其作为选择性非肽δ阿片类激动剂的用途

摘要

The present invention relates to novel 4-phenyl-4-[1H-imidazol-2-yl]-piperidine derivatives according to Formula (I), the pharmaceuticallyacceptable acid or base addition salts thereof, the stereochemically isomericforms thereof, the tautomeric forms thereof and the N-oxide forms thereof. Inparticular are claimed compounds according to Formula (I) in which A=B is C=Oor SO2, X is a covalent bond, R1 is alkyloxy, alkyloxyalkyl, Ar or NR9R10,wherein R9 and R10 each independently are hydrogen or Ar; or A=B and R1together form a benzoxazolyl radical ; p is zero, R3 is benzyl optionallysubstituted with hydroxy, alkyl or alkyloxycarbonyl and R4 and R5 each arehydrogen. The invention also relates to processes for the preparation of thecompounds according to the invention and their use in medicine, in particularas selective non-peptide d-opioid agonists for use in the treatment of variouspain conditions.
机译:本发明涉及新颖的4-苯基-4- [1H-咪唑-2-基]-根据式(I)的哌啶衍生物,在药学上可接受的酸或碱加成盐,立体化学异构体形式,其互变异构形式和其N-氧化物形式。在特别是根据要求保护的根据式(I)的化合物,其中A = B为C = O或SO2,X是共价键,R1是烷氧基,烷氧基烷基,Ar或NR9R10,其中R9和R10各自独立地是氢或Ar;或A = B和R1一起形成苯并恶唑基; p为零,R 3为苄基被羟基,烷基或烷氧羰基取代的R4和R5分别为氢。本发明还涉及制备该化合物的方法。本发明的化合物及其在医学中的用途,特别是作为选择性非肽d类阿片激动剂,用于治疗各种疼痛状况。

著录项

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