首页> 外国专利> Isoindolonas potentiates metabotropic glutamate receptors, Pharmaceutical compositions that comprise and the use thereof in the manufacture of a Medicament for the treatment of Neurological and Psychiatric Disorders.

Isoindolonas potentiates metabotropic glutamate receptors, Pharmaceutical compositions that comprise and the use thereof in the manufacture of a Medicament for the treatment of Neurological and Psychiatric Disorders.

机译:异indolonas增强了代谢型谷氨酸受体,其包含的药物组合物及其在制备用于治疗神经和精神疾病的药物中的用途。

摘要

Pharmaceutical compositions containing the compounds, and Uses of the compounds in therapy of Neurological and Psychiatric Disorders.Claim 1: a compound according to Formula 1, wherein: R1 is - chr8r9; R2, R3 and R4, R6 and R7 are h; are selected independently from the group consisting of H, alkyl and Halogen C1 - 6; R5 is selected from the group formed by alkyl alkylaryl C0 - C1 - 6 6, - 6 and alq alquilheteroarilo C0 Uilheterociclilo C0 - 6; where, when Chemically possibleR5 can be replaced by one or more, and where any cyclical portion is optionally combined with a Ring of 5 to 7 members who may have one or more heteroatoms selected independently from the group consisting of N, o and S; a is selected from the group formed by alkyl Alkylaryl C0 - C1 - 6, 6, 6 alquilheteroarilo C0 - alquilheterociclilo C0, - 6, - 6 alkyl C0 (CO2) n (R10) 2Alkyl C0 - 6nr10 R10 (CO), alkyl C0 - 6 (SO2) n (R10) 2, CO (SO2) - alkyl 6nr10 R10 and a Ring of 5 to 7 members who may have one or more heteroatoms selected independently from the group consisting of N, o and S, where the Ring 5 to 7 members is optionally substituted by one or more r 10; R8 and R9 are selected independently between C1 - 6 h, alkyl, alkoxy alkyl C1 C1 - 6 - 6 -- (CH2) n - X - R10, fluoroalquilo Perfluoroalkyl C1 C1 - 6, 6 - or CN, R8 and R9 form or in combination a cycloalkyl group or a group heterociclilo C3 - 7 with the exception that R8 and R9 are not both h; n is 1, 2, 3, 4, 5 or 6; X is s or o, and R10 in each case is selected independently of Group F Composed of H, alkyl alkylaryl C0 - C1 - 6 6Alquilheteroarilo C0 - 6 and alquilheterociclilo C0 - 6 where any cyclical portion is optionally combined with a Ring of 5 to 7 members who may have one or more heteroatoms selected independently from the group consisting of N, o and S and any cyclical portion is optional Easily replaced with a Halo Substituent selected from hydroxyl, alkyl, alkoxy,Haloalquilo and haloalcoxi; or a Pharmaceutical acceptable Salt, solvate, hydrate, Optical isomer, or their combinations.
机译:权利要求1:根据式1的化合物,其中:R1为-chr8r9;和R2,R3和R4,R6和R7为h;选自H,烷基和卤素C 1-6; R5选自由烷基烷基芳基C0至C1-6、6-6和alq alquilheteroarilolo C0 Uilheterociclilo C0-6形成的组;其中,当化学上可能的R5可以被一个或多个取代时,并且任何环状部分任选地与5至7个成员的环结合,这些成员可以具有一个或多个独立地选自N,o和S的杂原子; a选自烷基烷基芳基C0-C1-6、6、6烷基杂杂芳基C0-烷基杂芳基C0,-6-6烷基C0(CO2)n(R10)2烷基C0-6nr10 R10(CO),烷基C0 -6(SO2)n(R10)2,CO(SO2)-烷基6nr10 R10和5至7个成员的环,这些环可具有一个或多个独立于N,o和S的杂原子,其中, 5至7个成员可选地被一个或多个r 10取代; R8和R9独立地选自C1-6小时,烷基,烷氧基烷基C1-6-6-(CH2)n-X-R10,氟代全氟烷基C1-6-6,或6-CN,R8和R9形式除了R 8和R 9都不是h以外,结合使用环烷基或C 1-7杂环基。 n是1,2,3,4,5或6; X是s或o,并且在每种情况下R 10的选择均独立于基团F,由H,烷基烷基芳基C0至C1-6 6 Alquilheteroarilo C0-6和alquilheterociclilo C0-6组成,其中任何环状部分任选地与5至5的环结合7个具有一个或多个独立地选自N,o和S以及任何环状部分的杂原子的成员是可任选的容易地被选自羟基,烷基,烷氧基,卤代喹啉和卤代烷氧基的卤代取代基取代;或药学上可接受的盐,溶剂化物,水合物,旋光异构体或其组合。

著录项

  • 公开/公告号AR060318A1

    专利类型

  • 公开/公告日2008-06-11

    原文格式PDF

  • 申请/专利权人 ASTRAZENECA AB.;

    申请/专利号AR2007P100548

  • 发明设计人 FOLMER JAMES J.;EMPFIELD JAMES R.;

    申请日2007-02-09

  • 分类号C07D209/46;C07D401/04;A61K31/4035;A61K31/4439;A61P25/28;A61P25/18;

  • 国家 AR

  • 入库时间 2022-08-21 20:08:57

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