| 摘要 |
The invention relates to triazolopyridine carboxamide derivatives of general formula (I) in which X represents a hydrogen atom, a halogen atom, a (C-C)alkyl, (C-C)alkoxy, halo(C-C)alkyl, S(O)R', hydroxyl or cyano group, A is absent or else represents a bond, an oxygen atom, a sulphur atom, an NR, C(O)NR' or SONR' group, a (C-C)alkylene group, or a (C)alkenyl group, Rand Rrepresent, independently of one another, one or more groups chosen from a hydrogen atom, a (C-C)alkyl group, a (C-C)alkoxy group, a (C-C)cycloalkyl group, a (C-C)cycloalkyl-(C-C)alkyl group, a (C-C)cycloalkyl(C-C)alkoxy group, a halogen atom, a cyano group, a C(O)R', C(O)OR', C(O)NRRor NOgroup, an NRRor NRC(O)-Rgroup, the (C-C)alkyl and (C-C)alkoxy groups being optionally substituted by one or more atoms or groups chosen independently from one another from halogen atoms, and hydroxyl, amino or NRRgroups. Preparation method and therapeutic use thereof.
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