摘要:
The present invention concerns compounds of general formula (1) (I) wherein R1 is: - a hydrogen atom, or a halogen, - a straight or branched C 1 -C 6 alkyl group or a C 1 -C 3 fluoroalkyl group, - a straight or branched C 1 -C 6 alcoxy group, a carbamyl group, N-substituted or not by one or two, straight or branched C 1 -C 3 alkyl groups, or - a cyano group (CN) R2 is: - a hydrogen atom or a straight or branched C 1 -C 6 alkyl group, HaI 1 , Hal 2 and Hal 3 are: - a halogen their addition salts and the hydrates of addition salts with pharmaceutically acceptable mineral acids or organic acids, and their enantiomer forms.
摘要:
The invention relates to preparing derivatives of formula (1), wherein, in particular R1 and R2, identical or different, represent a hydrogen, fluorine or chlorine atom, a hydroxy group, an alkyl radical and an alkoxy radical, R3 is an alkyl radical, a hydroxy group or a methoxy radical, R4 is a hydrogen atom or a methyl radical and R5 and R6, identical or different, represent a hydrogen atom, an alkyl radical, an alkoxy radical, an alkylthio radical and an alkylamino radical. The inventive method consists in reducing an amid of formula (9).
摘要:
The invention relates to compounds of general formula (1) in which X and Y = a carbon with a bonded hydrogen atom (CH) or a nitrogen atom, A = a methyl, fluoromethyl, cyano, hydroxyl, methoxy group, or a chlorine or fluorine atom on condition that when A = methyl (CH3) and X and Y both = a carbon bonded to a hydrogen atom, then B = a chlorine atom, B = a chlorine or a fluorine atom, D = a hydrogen, chlorine, fluorine atom, or a cyano or trifluoromethyl group and E = a hydrogen, fluorine or chlorine atom.
摘要:
The invention concerns 3-arylthio-propyl-amino-3,4-dihydro-2H-1,5-aryloxathiepin derivatives of general formula (I), wherein: R1 and R2, identical or different, represent a hydrogen atom, a fluorine atom or a chlorine atom, a hydroxy group, an alkyl, cyclopropyl, alkoxy, cyclopropoxy radical or when they occupy adjacent positions, form with the carbon atoms bearing them a carbon-containing cycle or an oxygen-containing heterocycle with five non-aromatic rings; R3 represents an alkyl radical, a hydroxy group or a methoxy radical; R4 represents a hydrogen atom or a methyl radical; and R5 and R6, identical or different represent a hydrogen atom, an alkyl, alkoxy, alkylthio, alkylamino radical, or the groups OR4 and R5 form with the carbons which bear them a non-aromatic heterocycle with five or six rings containing at least an oxygen atom; and their pharmaceutically acceptable additions salts.
摘要:
The present invention concerns compounds of general formula (1), where in : - -a-is a single or double bond, Ar is an aromatic group, substituted or unsubstituted, R1 and R2 each independently or together are: a hydrogen atom or C 1 -C 6 alkyl group, branched or unbranched, saturated or unsaturated, substituted or unsubstituted; the groups R1 and R2 may also form a heterocycle, R3 and R3' each independently or together are a hydrogen atom or C 1 -C 6 alkyl group, X is an oxygen atom or a sulphur atom, and the addition salts of the compounds of general formula (1) with pharmaceutically acceptable mineral acids or organic acids.
摘要:
The invention relates to a new method for preparing N- [3- [ (2-methoxyphényl) sulfanyl] -2-methylpropyl] -3,4- dihydro-2H-1, 5-benzoxathiepin-3-amine.
摘要:
The invention relates to the use of a compound of formula (I) and the therapeutically-acceptable salts thereof, more particularly where u = methyl, v and w = H, x = F, y = Cl, z = F, A = H or aminomethyl and the pharmaceutically-acceptable addition salts with mineral or organic acids, for the production of a medicament for the treatment of chronic pain symptoms of neuropathological or psychogenic origin.
摘要:
The invention concerns 3-arylthio-propyl-amino-3,4-dihydro-2H-1,5-aryloxathiepin derivatives of general formula (I), wherein: R1 and R2, identical or different, represent a hydrogen atom, a fluorine atom or a chlorine atom, a hydroxy group, an alkyl, cyclopropyl, alkoxy, cyclopropoxy radical or when they occupy adjacent positions, form with the carbon atoms bearing them a carbon-containing cycle or an oxygen-containing heterocycle with five non-aromatic rings; R3 represents an alkyl radical, a hydroxy group or a methoxy radical; R4 represents a hydrogen atom or a methyl radical; and R5 and R6, identical or different represent a hydrogen atom, an alkyl, alkoxy, alkylthio, alkylamino radical, or the groups OR4 and R5 form with the carbons which bear them a non-aromatic heterocycle with five or six rings containing at least an oxygen atom; and their pharmaceutically acceptable additions salts.
摘要:
The invention concerns novel aryl-{4-fluoro-4-[(2-pyridin-2-yl-ethylamino)-methyl]-piperidin-1-yl}-methanone derivatives of formula (1) wherein X is a hydrogen, fluorine or chlorine atom, useful as medicines in particular having antidepressant, analgesic, anxiolytic and neuroprotective effects.
摘要:
The present invention relates to novel [(2-substituted-5-[3-thienyl])-benzyl]-[2-([2-isopropoxy-5-fluoro]-phenoxy)-ethyl]-amine derivatives having formula (1) and the use thereof as medicaments, especially anti-psychotic medicaments.