Arylalklcarbamate derivatives, preparation method thereof and use of same in therapeutics

A compound of the formula (I):

• in which
• n represents an integer between 1 and 6;
• A is a group X;
• X represents a C1-2-alkylene group optionally substituted with one or more C1-12-alkyl, C3-7-cycloalkyl or C3-7-cycloalkyl-C1-6-alkylene groups;
• R1 represents a hydrogen atom, a halogen atom, or a hydroxyl, cyano, nitro, C1-3-alkyl, C1-3-alkoxy, C1-3-thioalkyl, C1-3-fluoroalkyl, C1-3-fluoroalkoxy or C1-3-fluorothioalkyl group;
• R2 represents a hydrogen atom, a halogen atom, or a cyano, nitro, hydroxyl, C1-3-alkyl, C1-3-alkoxy, C1-3-thioalkyl, C1-3-fluoroalkyl, C1-3-fluoroalkoxy or C1-3-fluorothioalkyl group;
• or a group chosen from a phenyl, naphthalenyl, biphenyl, phenylethylenyl, naphthylethylenyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazinyl, indanyl, indenyl, quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, phthalazinyl, cinnolinyl, thienyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, thiadiazolyl, oxadiazolyl, triazolyl, benzothienyl, benzofuryl, dibenzofuryl, benzimidazolyl, benzotriazolyl, indolyl, isoindolyl, indazolyl, benzoxazolyl, benzisoxazolyl, benzothiazolyl, benzisothiazolyl, dihydroindolyl, pyrrolopyridinyl, furopyridinyl, thienopyridinyl, imidazopyridinyl, oxazolopyridinyl, thiazolopyridinyl, pyrazolopyridinyl, isoxazolopyridinyl, isothiazolopyridinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, phenyloxy, phenylthio, phenylsulfonyl, benzoyl, phenylmethoxy, phenylethoxy, phenylpropoxy, naphthalenyloxy, naphthalenylmethoxy, naphthalenylethoxy, naphthalenylpropoxy, quinolinoxy and isoquinolinoxy, and optionally substituted with one or more substituents chosen from a halogen atom, and the following groups:
• hydroxyl, cyano, nitro, C1-4-alkyl, C1-4-alkoxy, C1-4-thioalkyl, C1-3-fluoroalkyl, C1-3-fluoroalkoxy, C1-3-fluorothioalkyl, phenyloxy, benzyloxy, piperidyl, pyrrolidinyl, morpholinyl, NH2, NHR6, NR6R7, NHCOR6, COR6, CO2R6, SO2R6, —O—(C1-3-alkylene)-O—, 4-piperazinyl optionally substituted with a C1-3-alkyl or with a benzyl;
• R3 represents either a 2,2,2-trifluoroethyl group, or a phenyl group optionally substituted with one or more halogen atoms or cyano, nitro, C1-3-alkyl, C1-3-alkoxy, trifluoromethyl or trifluoromethoxy groups, and
• R6 and R7 represent, independently of one another, a C1-3-alkyl group or a phenyl;
• with the proviso that:
• when R3 represents a 2,2,2-trifluoroethyl group and the group -[A]n- represents a —CH2— group, then R1 is other than a hydrogen atom or a methoxy group;
• and
• when R3 represents an optionally substituted phenyl group and the group -[A]n- represents a —CH2—, —CH2CH2—, —CH(CH3)— or —CH(CH3)—CH2— group, then R1 is other than a hydrogen or chlorine atom or a methyl or methoxy group and R2 is other than a hydrogen atom;
• and
• wherein said compound is in the form of a base, or an addition salt with an acid, or a hydrate or a solvate.