摘要:
The invention relates to compounds having formula (I), wherein: X represents a group having formula (II). According to the invention, R1 and R6 represent a hydrogen atom or an alkyl group. R2 represents a radical selected from among: a (C1-C12)alkyl; a non-aromatic carbocyclic radical at (C3-C12); a (C3-C7)cycloalkylmethyl; a phenyl, a benzyl, a benzhydryl, a benzhydrylmethyl, phenethyl, a benzodioxolyl, a dihydrobenzofuranyl, a dihydrobenzodioxinyl; a methyl substituted by a benzodioxolyl, a dihydrobenzofuranyl, a dihydrobenzodioxinyl; a non-substituted 1, 2, 3, 4-tetrahydronaphtalenyl; or a heterocyclic radical, an indolyl, a substituted or non-substituted benzothiazolyl, said radicals being substituted or non-substituted. R3 represents a (C1 -C5)alkyl or a (C3-C7) cycloalkyl. R4 and R5 represent a substituted or non-substituted phenyl. The invention also relates to a method of preparing said derivatives and to the application thereof in therapeutics.
摘要:
The invention relates to 5,6-diphenylpyridine-3-carboxamide derivatives of general formula (I), where R1 = H, or (C1-C4) alkyl, R2 = a monoazo saturated heterocycle of 5 to 7 atoms, the nitrogen atom being substituted with a (C1 -C4)alkanoyl, NR10R11, a non-aromatic (C3-C10) carbocycle more than tri-substituted with (C1-C4) alkyl, a non-aromatic (C11-C12) carbocycle unsubstituted or mono- or poly-substituted with (C1-C4) alkyl, a monooxygenated saturated heterocycle with 5 to 7 atoms, more than tri-substituted with (C1-C4) alkyl, or R1 and R2, together with the nitrogen atom to which the above are bonded, form a 4-disubstituted piperidin-1-yl group, the salts, solvates and hydrates thereof. The invention further relates to a method for production and therapeutic application thereof.
摘要:
The invention concerns compounds of formula (I), wherein: R1 represents hydrogen or a C1-C4 alkyl; R2 represents a C4-C10 group, a non-aromatic carbocyclic C3-C12 radical, an indianyl, a 1,2,3,4-tetrahydronaphthalenyl -1 or 2, a heterocyclic radical, a substituted C1-C3 alkylene group, a NR10R11 group; or R1 and R2 together with the nitrogen atom whereto they are bound form a heterocyclic radical. The invention also concerns the method for preparing said compounds and their therapeutic use.
摘要:
The invention relates to compounds having formula (I), wherein: X represents a group (II); R1 represents a hydrogen atom or a (C1-C4)alkyl group; R2 represents a (C1-C12)alkyl group, a non-aromatic carbocyclic radical at (C3-C12) which may or may not be substituted, a methyl which is substituted by a non-aromatic carbocyclic radical at (C3-C12) which may or may not be substituted, a phenyl, benzyl, benzhydryl radical which may or may not be substituted, a substituted or non-substituted heterocyclic radical, a methyl substituted by a non-aromatic carbocyclic radical at (C3-C12) which may or may not be substituted; R3 represents a (C1-C5)alkyl or a (C3-C7) cycloalkyl; R4 represents a substituted or non-substituted phenyl; and R5 represents a substituted or non-substituted phenyl. The invention also relates to the preparation method thereof and the use of same in therapeutics.
摘要:
The invention relates to compounds having the formula (I), wherein A represents: a substituted or non substituted alkylene (C1-C6) group; a Formula (II) group having m = O, 1 or 2 and p = 0 or 1; R1 represents hydrogen or a (C1 -C2 )alkyl; R2 represents a substituted or non substituted (C3-C10) alkyl group, a substituted or non substituted non aromatic (C3-C12) carbocylic radical, a heterocyclic substituted or non substituted radical, an alkylene (C1-C3) substituted group, a NR10R11 group; R9 represents a functional group or a heterocyclic radical. Preparation method and use in therapy.
摘要:
The invention relates to 5,6-diphenylpyridine-3-carboxamide derivatives of general formula (I), where R1 = H, or (C1-C4) alkyl, R2 = a monoazo saturated heterocycle of 5 to 7 atoms, the nitrogen atom being substituted with a (C1 -C4)alkanoyl, NR10R11, a non-aromatic (C3-C10) carbocycle more than tri-substituted with (C1-C4) alkyl, a non-aromatic (C11-C12) carbocycle unsubstituted or mono- or poly-substituted with (C1-C4) alkyl, a monooxygenated saturated heterocycle with 5 to 7 atoms, more than tri-substituted with (C1-C4) alkyl, or R1 and R2, together with the nitrogen atom to which the above are bonded, form a 4-disubstituted piperidin-1-yl group, the salts, solvates and hydrates thereof. The invention further relates to a method for production and therapeutic application thereof.