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imidazodiazepine derivatives, method for preparation and tussenpr odukten, containing medicines and therapeutic application.

机译:咪唑二氮杂卓衍生物,其制备方法和托森普度单药,含有药物和治疗用途。

摘要

Imidazodiazepine derivatives of the formula IMAGE I wherein A together with the two carbon atoms denoted as alpha and beta is selected from the group consisting of IMAGE the dotted line represents the double bond present in groups (a) and (b), D is C=O or C=S, R1 is selected from the group consisting of cyano, lower alkanoyl and a group of the formula -COOR4, R4 is selected from the group consisting of methyl, ethyl, isopropyl and 2-hydroxyethyl, R5 is selected from the group consisting of hydrogen, trifluoromethyl and halogen and R6 is selected from the group consisting of hydrogen, trifluoromethyl, halogen and lower alkyl and either R2 is hydrogen and R3 is hydrogen or lower alkyl or R2 and R3 together are trimethylene or propenylene and the carbon atom denoted as gamma has the S- or R,S-configuration, and pharmaceutically acceptable salts thereof are presented and have utility for antagonizing the central-depressant, muscle relaxant, ataxic, blood pressure-lowering and respiratory-depressant properties of 1,4-benzodiazepines which have tranquillizing activity. They can be used, for example, as antidotes in the case of intoxications in which excessive intake of 1,4-benzodiazepines which have tranquillizing participates, or for shortening an anaesthesia induced by such 1,4-benzodiazepines. They can also be used for suppressing the activities on the central nervous system of 1,4-benzodiazepines used in other fields of indication, for example of schistosomicidally-active 1,4-benzodiazepines such as (+)-5-(o-chlorophenyl)-1,3-dihydro-3-methyl-7-nitro-2H-1,4-benzodiazep in-2-one. Also presented are processes to produce the imidazodiazepine derivatives and intermediates therefor.
机译: I的咪唑二氮杂衍生物,其中A与表示为α和β的两个碳原子一起选自,虚线表示存在于(a)和(b)组中的双键, D是> C = O或> C = S,R 1选自氰基,低级链烷酰基和式-COOR 4的基团,R 4选自甲基,乙基,异丙基和2-羟乙基R 5选自氢,三氟甲基和卤素,R 6选自氢,三氟甲基,卤素和低级烷基,并且R 2为氢且R 3为氢或低级烷基或R 2和R 3一起为三亚甲基。或亚丙烯基,且表示为γ的碳原子具有S-或R,S-构型,并提供了其药学上可接受的盐,可用于拮抗中枢抑制剂,肌肉松弛剂,共济失调剂,降血压药g和具有镇静活性的1,4-苯并二氮杂respiratory的呼吸抑制特性。例如,在过量摄入具有镇静作用的1,4-苯并二氮杂pine中毒的情况下,它们可用作解毒剂,或用于缩短由1,4-苯并二氮杂s引起的麻醉。它们还可以用于抑制其他适应症领域中使用的1,4-苯并二氮杂on对中枢神经系统的活性,例如血吸虫活性的1,4-苯并二氮杂as如(+)-5-(o-氯苯基) )-1,3-二氢-3-甲基-7-硝基-2H-1,4-苯并二氮杂-2-一。还提出了生产咪唑二氮杂卓衍生物及其中间体的方法。

著录项

  • 公开/公告号NL930056I2

    专利类型

  • 公开/公告日1993-11-16

    原文格式PDF

  • 申请/专利权人 F. HOFFMANN-LA ROCHE AG;

    申请/专利号NL19930930056C

  • 发明设计人

    申请日1993-06-11

  • 分类号A61K31/55;A61K31/551;A61P33/10;A61P39/02;C07D243/14;C07D243/16;C07D243/18;C07D243/24;C07D265/26;C07D333/42;C07D487/04;C07D487/14;C07D495/04;C07D495/14;C07D495/22;C07D498/04;

  • 国家 NL

  • 入库时间 2022-08-22 04:45:17

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