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in zweistellung substituted 3 - aryl - 4 - oxo - 3.4 - dihydrochinazoline, their production and use

机译:韦斯特隆中的3-取代基-芳基-4-氧代-3.4-二氢杂唑啉的合成,生产和使用

摘要

Novel compounds of the general formula FORM:1038729/C2/1 and their acid addition salts, in which R is hydrogen, an alkyl or alkoxy radical containing up to 5 carbon atoms, or a halogen atom (especially chlorine), R1 is hydrogen or an alkyl radical containing up to 4 carbon atoms, R2 is an alkyl radical containing up to 4 carbon atoms, a hydroxyalkyl radical containing up to 4 carbon atoms, a cycloalkyl radical (containing 5 or 6 carbon atoms), or an amino radical, or R1 and R2 together with the adjacent nitrogen represent a saturated mononuclear heterocyclic group, especially 1-pyrrolidyl, 1-piperidyl, morpholino, or 4-alkyl- or 4-hydroxyalkyl-1-piperazinyl (the alkyl and hydroxyalkyl groups containing up to 4 carbon atoms) are prepared by condensing an amine of formula HNR1.R2 with a 2-chloro-quinazoline of the formula FORM:1038729/C2/2 The 2-chloro-quinazolines are prepared by reacting a compound of the general formula FORM:1038729/C2/3 with sulphur monochloride or sulphuryl chloride. Pharmaceutical compositions, preferably in conventional form for oral or parenteral administration, comprise a compound of the first general formula above, or an acid addition salt thereof, and a pharmaceutical carrier. They have sedative and hypnotic activity.
机译:通式的新型化合物及其酸加成盐,其中R为氢,至多5个碳原子的烷基或烷氧基或卤素原子(尤其是氯),R1为氢或含至多4个碳原子的烷基,R2为含至多4个碳原子的烷基,含至多4个碳原子的羟烷基,环烷基(含5或6个碳原子)或氨基,或R1和R2与相邻的氮原子一起代表饱和的单核杂环基,尤其是1-吡咯烷基,1-哌啶基,吗啉代或4-烷基或4-羟基烷基-1-哌嗪基(烷基和羟基烷基最多通过使式HNR1.R2的胺与式的2-氯喹唑啉缩合来制备2个氯原子。 含一氯化硫或亚硫酰氯洛里德。优选以常规形式用于口服或肠胃外给药的药物组合物包含上述第一通式的化合物或其酸加成盐和药物载体。它们具有镇静和催眠作用。

著录项

  • 公开/公告号DE000001595879A

    专利类型

  • 公开/公告日1970-03-12

    原文格式PDF

  • 申请/专利权人 BELLON LABOR SA ROGER;

    申请/专利号DE1595879A

  • 发明设计人 PESSON MARCEL;

    申请日1965-06-02

  • 分类号C07D51/48;

  • 国家 DE

  • 入库时间 2022-08-23 11:04:21

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