Aryloxyalkylcarbamate-type derivatives, preparation method...

C - Chemistry – Metallurgy – 07 – C

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C07C 271/16 (2006.01) A61K 31/27 (2006.01) A61K 31/33 (2006.01) C07C 269/06 (2006.01) C07C 317/28 (2006.01) C07C 323/43 (2006.01) C07D 213/65 (2006.01) C07D 215/20 (2006.01) C07D 217/02 (2006.01) C07D 239/38 (2006.01) C07D 263/58 (2006.01) C07D 277/36 (2006.01)

Patent

CA 2552565

The invention relates to a compound having general formula (I), wherein: m represents 0, 1, 2 or 3; n represents 0, 1, 2 or 3; X represents an oxygen or sulphur atom or an SO or SO¿2 ?group; R¿1? and R¿2? represent, independently of each other, a hydrogen atom or a C¿1-3?-alkyl group, or R¿1? and R¿2? together form a -(CH¿2?)¿p?- group, in which p represents an integer varying between 1 and 5, such that n + p is an integer varying between 2 and 5; R¿3? represents a hydrogen or fluorine atom or a hydroxy or methyl group; R¿4? represents a group having general formula CHR¿5?CONHR¿6? in which R¿5? represents a hydrogen atom or a C¿1-6?-alkyl group and R¿6? represents a hydrogen group or a C¿1-6?-alkyl, C¿3-7?-cycloalkyl, C¿3-7?-cycloalkyl-C¿1-6?-alkylene group; and Y represents a group that is selected, for example, from a phenyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, thiazolyl, naphthyl, quinolinyl, isoquinolinyl, phtalazinyl, quinazolinyl, quinoxalinyl, naphthyridinyl, cinnolinyl, benzofuranyl, dihydrobenzofuranyl, benzothienyl, dihydrobenzothienyl, indolyl, isoindolyl, indolinyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzothiazolyl, benzisothiazolyl, benzotriazolyl, benzoxadiazolyl, benzothiadiazolyl, said group being optionally substituted. Said compound takes the form of a base, an acid addition salt, a hydrate or a solvate. The invention also relates to the use of same in therapeutics

Composé répondant à la formule générale (I) dans laquelle m représente 0, 1, 2 ou 3 ; n représente 0, 1, 2 ou 3 ; X représente un atome d~oxygène ou de soufre ou un groupe SO ou SO2; R1 et R2 représentent, indépendamment l~un de l~autre, un atome d~hydrogène ou un groupe C1-3-alkyle, ou R1 et R2 forment ensemble un groupe -(CH2)p-, où p représente un nombre entier allant de 1 à 5 tel que n + p soit un nombre entier allant de 2 à 5 ; R3 représente un atome d~hydrogène ou de fluor ou un groupe hydroxy ou méthyle ; R4 représente un groupe de formule générale CHR5CONHR6 dans laquelle R5 représente un atome d~hydrogène ou un groupe C1-6-alkyle et R6 représente un atome d~hydrogène ou un groupe C1-6-alkyle, C3-7-cycloalkyle, C3-7-cycloalkyle-C1-6-alkylène ; Y représente un groupe choisi parmi notamment un phényle, pyridinyle, pyridazinyle, pyrimidinyle, pyrazinyle, triazinyle, thiazolyle, naphtyle, quinolinyle, isoquinolinyle, phtalazinyle, quinazolinyle, quinoxalinyle, naphthyridinyle, cinnolinyle, benzofuranyle, dihydrobenzofuranyle, benzothiényle, dihydrobenzothiényle, indolyle, isoindolyle, indolinyle, benzimidazolyle, benzoxazolyle, benzisoxazolyle, benzothiazolyle, benzisothiazolyle, benzotriazolyle, benzoxadiazolyle, benzothiadiazolyle, ce groupe étant éventuellement substitué ; à l~état de base, de sel d~addition à un acide, d~hydrate ou de solvat. Application en thérapeutique.

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