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2,2-Disubstd benzodioxoles - having antiinflammatory, analgesic, antitussive, CNS antiarrhythmic, and hypotensive properties

机译:2,2-二取代的苯并二恶唑-具有抗发炎,镇痛,镇咳,中枢神经系统抗心律不齐和降压特性

摘要

Title cpds. are of formula (I) (where R is H, lower alkyl, lower haloalkyl, lower hydroxyalkyl, or aryl or aralkyl opt. substd. in the aromatic ring by halogen, alkyl, OH or alkoxy, or R may be joined to an alkyl radical in the 2-posn. on the benzodioxole nucleus to form a spiran contg. 4-7C atoms; R1 is H, =1 halogen atom, a lower alkyl, lower haloalkyl, -CH2NR4R5 (where NR4R5 is opt. substd. amino) OH, alkoxy, sulphonic acid, sulphanide, N, N-dialkylsulphamido, NO2, opt. substd. amino or alkylsulphonylamino go. or R1 is a benzene nucleus condensed to the benzodioxole nucleus; R2 is H, alkyl, aryl or OH; m is 0, 1 or 2; R3 is H, lower alkyl, aryl, OH or NO2; n is 0, 1, 2 or 3; X is O or S, Y is H, aryl (opt. substd. in the aromatic ring by halogen, alkyl, OH or alkoxy), X-CH2CH2Y or NR4R5) including their optical isomers, stereoisomers and pharmaceutically acceptable salts. Some of the cpds. also have blood platelet agglutination inhibiting activity.
机译:标题cpds。式(I)的式(I)(其中R是H,低级烷基,低级卤代烷基,低级羟烷基或芳基或芳烷基在芳环中优选被卤素,烷基,OH或烷氧基取代,或R可与烷基连接)苯并二恶唑核上2位的芳基上形成螺环,含4-7C个螺环; R1为H,> = 1卤原子,低级烷基,低级卤代烷基,-CH2NR4R5(其中NR4R5为优选取代氨基) )OH,烷氧基,磺酸,硫醚,N,N-二烷基硫代氨基,NO2,取代亚氨基或烷基磺酰基氨基或.R1是缩合至苯并二恶唑核的苯核; R2是H,烷基,芳基或OH; m是0、1或2; R3是H,低级烷基,芳基,OH或NO2; n是0、1、2或3; X是O或S,Y是H,芳基(在芳环中优选) (例如卤素,烷基,OH或烷氧基),X-CH2CH2Y或NR4R5),包括它们的旋光异构体,立体异构体和可药用盐。一些cpds。还具有抑制血小板凝集的活性。

著录项

  • 公开/公告号IT1051359B

    专利类型

  • 公开/公告日1981-04-21

    原文格式PDF

  • 申请/专利权人 ISTITUTO LUSO FARMACO;

    申请/专利号IT19740024811

  • 发明设计人 MANGHISI E;MENNELLA P;SALIMBENI A;

    申请日1974-07-04

  • 分类号

  • 国家 IT

  • 入库时间 2022-08-22 15:59:20

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