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    • 61. 发明授权
    • 7-amino-decahydro-quinolines
    • 7-AMINO-DECAHYDRO-QUINOLINES
    • US3875168A
    • 1975-04-01
    • US34515473
    • 1973-03-26
    • CIBA GEIGY CORP
    • PFLEIDERER WOLFGANGZONDLER HELMUT
    • C08K5/00C07D215/38C08G59/50C08K5/3412C07D33/52
    • C08G59/506C07D215/38
    • The new 7-amino-decahydro-quinolines are manufactured by hydroxygenating 5-amino-2-( Beta -cyanoethyl)-5-cyclohexen-1-one in a manner which is in itself known. The 5-amino-2-( Beta cyanoethyl)-5-cyclohexen-1-ones used as the starting substances can be obtained by several reactions, which are disclosed by several publications. One reaction is the cyclisation of cyanoethylated aliphatic ketones in the presence of suitable catalysts. The new 7-amino-decahydro-quinolines represent valuable curing agents for epoxide resins and advantageously 0,5 to 1,3 equivalents of nitrogen-bonded active hydrogen atoms of the 7-amino-decahydro-quinolines are used per 1 equivalent of epoxide groups of the polyepoxide compound.
    • 新的7-氨基 - 十氢喹啉通过以本身已知的方式羟基化5-氨基-2-(β-氰基乙基)-5-环己烯-1-酮来制备。 用作起始物质的5-氨基-2-(β-氰基乙基)-5-环己烯-1-酮可以通过几个反应来获得,这些反应由几个出版物公开。 一个反应是在合适的催化剂存在下氰基乙基化脂族酮的环化。 新的7-氨基 - 十氢 - 喹啉代表环氧树脂的有价值的固化剂,并且每1当量的环氧基团优选使用0.5至1.3当量的7-氨基 - 十氢 - 喹啉的氮键合活性氢原子 的聚环氧化合物。
    • 62. 发明授权
    • 6H-S-TRIAZOLO{8 4,3-a{9 {8 1,4{9 BENZODIAZEPIN-6-ONES
    • 6H-S-TRIAZOLO {8 4,3-a {9 {8 1,4 {9 BENZODIAZEPIN-6-ONES
    • US3870706A
    • 1975-03-11
    • US33526873
    • 1973-02-23
    • CIBA GEIGY CORP
    • ALLGEIER HANSGAGNEUX ANDRE
    • C07D243/14C07D487/04C07D53/06C07D55/06
    • C07D487/04
    • This invention provides a new process for the production of compounds of the class of 1-substituted 6-phenyl-4H-striazolo(4,3-a)(1,4)benzodiazepines and new intermediates for this process. The compounds produced by this process have valuable pharmacological properties. In particular, they possess anticonvulsant and antiaggressive activity and inhibit somatic reflexes. According to a specific embodiment, 1(benzyloxymethyl)4,5-dihydro-8-chloro-6H-s-triazolo(4,3a)(1,4)benzodiazepin-6-one is reacted with phenylmagnesium bromide, and the resulting 1-benzyloxymethyl)-6-phenyl-8-chloro4H-s-triazolo(4,3-a)(1,4)benzodiazepine is heated with hydrobromic acid-acetic acid to yield 6-phenyl-8-chloro-4H-striazolo(4,3-a)(1,4)benzodiazepine-1-methanol.
    • 本发明提供了一种用于生产1-取代的6-苯基-4H-s-三唑并[4,3-a] [1,4]苯并二氮杂类化合物的新方法和用于该方法的新中间体。 通过该方法制备的化合物具有有价值的药理学性质。 特别是它们具有抗惊厥和抗侵袭活性并抑制体细胞反射。 根据具体实施方案,使1-(苄氧基甲基)4,5-二氢-8-氯-6H-三唑并[4,3-a] [1,4]苯并二氮杂-6-酮与苯基溴化镁反应, 并将所得的1-苄氧基甲基)-6-苯基-8-氯-4H-三唑并[4,3-a] [1,4]苯并二氮杂环庚烷与氢溴酸 - 乙酸一起加热,得到6-苯基-8 [4,3-a] [1,4]苯并二氮杂-1-甲醇。