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AZABICYCLOALKANE DERIVATIVES, PREPARATION THEREOF AND USE THEREOF IN THERAPY
专利权人:
SANOFI-AVENTIS
发明人:
BEN AYAD OMAR,LECLERC ODILE,LOCHEAD ALISTAR,SAADY MOURAD,SLOWINSKI FRANCK,VACHE JULIEN
申请号:
MYPI 20093204
公开号:
MY161067A
申请日:
2008.02.04
申请国别(地区):
MY
年份:
2017
代理人:
摘要:
THE INVENTION RELATES TO COMPOUNDS OF THE GENERAL FORMULA (I) IN WHICH: R IS A HYDROGEN OR HALOGEN ATOM; OR A HYDROXYL, (C1-C6)ALKOXY, (C3-C7)CYCLOALKYL-O-OR (C3-C7)CYCLOALKYL-(C1-C3)ALKYLENE-O- GROUP; OR A HETEROCYCLOALKYL, ARYL OR HETEROARYL GROUP; WHEREIN SAID GROUP CAN OPTIONALLY BE SUBSTITUTED BY ONE OR MORE GROUPS SELECTED FROM HALOGEN ATOMS, (C1-C6)ALKYL, (C3-C7)CYCLOALKYL, (C3-C7)CYCLOALKYL-(C1-C3)ALKYLENE, (C1-C6)ALKOXY, (C3-C7)CYCLOALKYL-O-, (C3-C7)CYCLOALKYL-(C1-C3)ALKYLENE-O-, (C1-C6)FLUOROALKYL, (C1-C6)FLUOROALKOXY, NITRO, CYANO, HYDROXYL, AMINO, (C1-C6)ALKYLAMINO OR DI(C1-C6)ALKYLAMINO, HETEROCYCLOALKYL, ARYL, ARYL-(C1-C6)ALKYLENE, HETEROARYL, HETEROARYL-(C1-C6)ALKYLENE, ARYL-O-, -C(O)-(C1-C6)ALKYL GROUPS, THE HETEROCYCLOALKYL GROUP BEING OPTIONALLY SUBSTITUTED BY -C(O)O(CH3)3; N IS 1 OR 2; M IS 1 OR 2; O IS 1 OR 2; IN THE STATE OF A BASE OR AN ADDITION SALT TO AN ACID, AS WELL AS IN THE HYDRATE OR SOLVATE STATE. THE INVENTION ALSO RELATES TO A METHOD FOR PREPARING THE SAME AND TO THE APPLICATION IN THERAPY.
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