首页> 外国专利> substituted aromatic arylsulfonylmethyl or arylsulfonamide compounds suitable for treating disorders responsive to dopamine d3 receptor modulation

substituted aromatic arylsulfonylmethyl or arylsulfonamide compounds suitable for treating disorders responsive to dopamine d3 receptor modulation

机译:适用于治疗对多巴胺d3受体调节敏感的疾病的取代芳基芳磺酰基甲基或芳基磺酰胺化合物

摘要

ARSULFONILMETIL OR AROMSULFONAMIDE COMPOUNDS REPLACED SUITABLE FOR TREATING DISORDERS RESPONDING TO DOPAMINE D-3 ~ RECEIVER MODULATION. The present invention relates to aromatic compounds of formula (I) wherein Ar is phenyl or a 5- or 6-membered C-linked heteroaromatic radical, wherein Ar may carry 1 radical R¬a¬ and wherein Ar may also carry 1 or 2 R sym radicals; X is N or CH; Y is O, S, -CH = N-, -CH = CH- or -N = CH-; A is CH ~ 2 ~, O or S; E is CR¬ 6¬R¬ 7¬ or NR¬ 3¬; R 1 is C 1 -C 4 alkyl, C 3 -C 4 cycloalkyl, C 3 -C 4 cycloalkylmethyl, C 3 -C 4 alkenyl, alkyl C 1 -C 4 fluorinated, C 3 -C 4 cycloalkyl fluorinated, C 3 -C 4 cycloalkylmethyl fluorinated, C 3 -C 4 fluorinated alkenyl, formyl or C 1-4 alkylcarbonyl ~ 2 ~ -C ~ 3; R¬ 1 [¬ is H, C 2 -C 4 alkyl, C 3 -C 4 cycloalkyl, C 3 -C 4 alkenyl, C 1 -C 4 alkyl fluorinated, fluorinated C 3 -C 4 cycloalkyl, or R 1 and R 2 together are (CH 2) with n being 2 or 3, or R 1 and R¬ 2 [¬ together are (CH ~ 2 ~) ~ n ~ with n being 2 or 3; R¬ 2¬ and R¬2 [¬ are independently H, CH ~ 3 ~, CH ~ 2 ~ F, CHF ~ 2 ~ or CF ~ 3 ~; R 3 is H or C 1 -C 4 alkyl; R 6, R 7, independently of each other, are selected from H, C 1 -C 2 alkyl, and C 1 -C 2 fluorinated alkyl; and their physiologically tolerated acid addition salts. The invention also relates to the use of a compound of formula I or a pharmaceutically acceptable salt thereof to prepare a pharmaceutical composition for the treatment of a medical disorder susceptible to treatment with a dopamine D3 receptor ligand.
机译:替换为适合于治疗多巴胺D-3〜受体调节的失调的阿苏糖醇或阿苏糖胺化合物。本发明涉及式(I)的芳族化合物,其中Ar是苯基或5-或6-元C-连接的杂芳族基团,其中Ar可以带有1个R aa基,并且Ar也可以带有1或2个R。 部首; X为N或CH; Y为O,S,-CH = N-,-CH = CH-或-N = CH-; A是CH〜2〜,O或S; E是CR 6 -R 7-或NR 3-; R 1为C 1 -C 4烷基,C 3 -C 4环烷基,C 3 -C 4环烷基甲基,C 3 -C 4烯基,烷基C 1 -C 4氟化,C 3 -C 4环烷基氟化,C 3- C 4为氟化的环烷基甲基,C 3 -C 4的氟化链烯基,甲酰基或C 1-4烷基羰基〜2〜-C〜3; R 1 [¬是H,C 2 -C 4烷基,C 3 -C 4环烷基,C 3 -C 4烯基,氟化的C 1 -C 4烷基,氟化的C 3 -C 4环烷基或R 1和R 2一起为(CH 2),n为2或3,或R 1和R¬2一起为(CH〜2〜)〜n〜,n为2或3; R 2和R 2 [独立地为H,CH〜3〜,CH〜2〜F,CHF〜2〜或CF〜3〜; R 3为H或C 1 -C 4烷基; R 6,R 7彼此独立地选自H,C 1 -C 2烷基和C 1 -C 2氟代烷基。及其生理上可耐受的酸加成盐。本发明还涉及式I化合物或其药学上可接受的盐在制备用于治疗易受多巴胺D3受体配体治疗的医学病症的药物组合物中的用途。

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