| abstract |
The invention relates to the derivatives of triazolopyridine-carboxamides and triazolopyrimidine-carboxamides, of general formula (I) in whichA and X represent independently of each other, a nitrogen atom or a group CH, R1 represents an aryl group or heteroaryl, optionally substituted with one or more groups selected from halogen, (C1-C6) alkyl, halo (C1-C6) alkyl, (C1-C6) alkoxy, halo (C1-C6) alkoxy, R2 represents an aryl group, optionally substituted with one or more groups selected from a halogen atom, a methyl group, trifluoromethyl, methoxy, trifluoromethoxy.Procedure of preparation and application in therapy. |