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Substituted N-acyl-2-substituted-4-(benzimidazolyl-or imidazopyridinyl-substituted residue)-piperidine as a tachykinin antagonist
Substituted N-acyl-2-substituted-4-(benzimidazolyl-or imidazopyridinyl-substituted residue)-piperidine as a tachykinin antagonist
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机译:取代N-酰基-2-取代的4-(苯并咪唑基或咪唑并吡啶基取代的残基)-哌啶作为速激肽拮抗剂
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摘要
The present invention relates to compounds of the following general formula (I), the N-oxides thereof, the pharmaceutically acceptable addition salts and stereochemically isomeric forms thereof, the process for their preparation, the compositions containing them and their use as medicaments:;In this formula,;n is 0, 1 or 2;;m is 1 or 2, provided that when m is 2, n is 1;;X is a covalent bond or a group of the formula-O-,-S-, or-NR3-is a radical;;= Q = O or NR3ego;;ROneArOne, Or C1-6Ar RTI ID = 0.0 OneC1-6Alkyl or di (ArOne) C1-6Alkyl;;R2Ar2, Ar2C1-6Alkyl, Het or HetC1-6Alkyl;;L is a benzimidazole or imidazopyridine derivative of the general formula (A) or (B);;ArOneIs optionally substituted phenyl;;Ar2Naphthalenyl; Or optionally substituted phenyl;;Het is an optionally substituted monocyclic or bicyclic heterocycle.
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机译:本发明涉及以下通式(I)的化合物,其N-氧化物,其药学上可接受的加成盐和立体化学异构体形式,其制备方法,包含它们的组合物及其用作药物的用途:该式中,n为0、1或2; m为1或2,条件是当m为2时,n为1; X是共价键或式-O-,-S-的基团, or-NR 3 Sup>-是基团;; = Q = O或NR 3 Sup> ego ;; R One Sup> Ar One Sup>或C 1-6 Sub> Ar 一个 Sup> C 1-6 Sub>烷基或di(Ar 1 Sup>)C 1-6 Sub>烷基;; R 2 Sup> Ar 2 Sup>,Ar 2 Sup> C 1-6 Sub>烷基,Het或HetC 1-6 Sub>烷基;; L是通式(A)或(B)的苯并咪唑或咪唑并吡啶衍生物;; Ar 一个 Sup>是任选取代的苯基;; Ar 2 Sup>萘基;或任选取代的苯基; Het为任选取代的单环或双环杂环。
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