首页> 外国专利> COMBINATION OF ACTIVE INGREDIENTS FOR THE TREATMENT OF SENILE DEMENTIA OF THE ALZHEIMER TYPE

COMBINATION OF ACTIVE INGREDIENTS FOR THE TREATMENT OF SENILE DEMENTIA OF THE ALZHEIMER TYPE

机译:活性成分联合治疗老年型痴呆

摘要

in which Y is -CH- or -N- ; Rl is hydrogen, halogen, a CF3, (03-04) alkyl or (C1-C4) alkoxy group; R2 is hydrogen, halogen, hydroxyl, CF3, (C3-C4) alkyl or (C1-C4) alkoxy group; R3 and R4 each is hydrogen or (C1-C3) alkyl; X is (a) (C3-C6) alkyl; (C3-C6) alkoxy; (C3-C7) carboxyalkyl; (C1-C4) alkoxycarbonyl (C3-C6) alkyl; carboxyalkoxy,- or (C1-C4) alkoxycarbonyl (C3-C5) alkoxy; (b) a radical selected from (C3-C7) cycloalkyl, (C3- C7) cycloalkyloxy, (C3-C7) cycloalkylmethyl, (C3-C7) cycloalkylami.no and cyclohexenyl, said radical being optionally substituted by halogen, hydroxy, (C1-C4) alkoxy, carboxy, (C1-C4) alkoxycarbonyl, amino, mono or di- (C1-C4) alkylamino; or (c) a group selected from phenyl, phenoxy, phenylamino, N-(C1-C3) alkylphenylamino, phenylmethyl, phenylethyl, phenylcarbonyl, phenylthio, phenylsulfonyl, phenylsulfinyl or styryl, said phenyl group being optionally mono- or polysubstituted by halogen, CF3, (C1 c4) alkyl, (C1-C4) alkoxy, cyano, amino, mono- or di-(C1- C4) alkylamino, (C1-C4) acylamino, carboxy, (C1-C4) alkoxycarbonyl, aminocarbonyl, mono- or di-(C1-C4) alkylaminocarbonyl, amino (C1-C4) alkyl, hydroxy (€1-04) alkyl or halogeno (C1-C4) alkyl; optionally in the form of one of its pharmaceutically acceptable salts and a compound (b) active in the symptomatic treatment of DAT, optionally in the form of one of its pharmaceutically acceptable salts provided that when compound (a) is other than 1-(2-naphth-2-ylethyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine or one of its pharmaceutically acceptable salts, compound (b) is an acetylcholinesterase inhibitor.
机译:其中Y是-CH-或-N-; R1是氢,卤素,CF3,(03-04)烷基或(C1-C4)烷氧基; R2是氢,卤素,羟基,CF3,(C3-C4)烷基或(C1-C4)烷氧基; R3和R4各自为氢或(C1-C3)烷基; X为(a)(C 3 -C 6)烷基; (C3-C6)烷氧基; (C3-C7)羧烷基; (C1-C4)烷氧羰基(C3-C6)烷基;羧基烷氧基,-或(C1-C4)烷氧基羰基(C3-C5)烷氧基; (b)选自(C3-C7)环烷基,(C3-C7)环烷氧基,(C3-C7)环烷基甲基,(C3-C7)环烷基氨基和环己烯基的基团,所述基团任选地被卤素,羟基取代, C1-C4)烷氧基,羧基,(C1-C4)烷氧基羰基,氨基,单或二-(C1-C4)烷基氨基; (c)选自苯基,苯氧基,苯氨基,N-(C1-C3)烷基苯氨基,苯甲基,苯乙基,苯羰基,苯硫基,苯磺酰基,苯亚磺酰基或苯乙烯基的基团,所述苯基任选被卤素,CF3单取代或多取代,(C 1 -C 4)烷基,(C 1 -C 4)烷氧基,氰基,氨基,单或二-(C 1 -C 4)烷基氨基,(C 1 -C 4)酰基氨基,羧基,(C 1 -C 4)烷氧基羰基,氨基羰基,单-或二-(C1-C4)烷基氨基羰基,氨基(C1-C4)烷基,羟基(1-04)烷基或卤代(C1-C4)烷基;任选地以其药学上可接受的盐之一的形式和对症治疗DAT有活性的化合物(b)的形式,任选地以其药学上可接受的盐之一的形式,但前提是当化合物(a)不是1-(2)时-萘-2-基乙基)-4-(3-三氟甲基苯基)-1,2,3,6-四氢吡啶或其药学上可接受的盐之一,化合物(b)是乙酰胆碱酯酶抑制剂。

著录项

  • 公开/公告号IN1998DE03201A

    专利类型

  • 公开/公告日2007-03-09

    原文格式PDF

  • 申请/专利权人

    申请/专利号IN3201/DEL/1998

  • 申请日1998-10-30

  • 分类号A61K31/445;

  • 国家 IN

  • 入库时间 2022-08-21 20:58:27

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