首页> 外国专利> method rauhoittavina lääkeaineina feasible for 6 - phenyl - 4h - s - t riatsolo - (1,5a) (1,4) - benzodiazepines produce.

method rauhoittavina lääkeaineina feasible for 6 - phenyl - 4h - s - t riatsolo - (1,5a) (1,4) - benzodiazepines produce.

机译:方法作为可行的镇静剂,可用于6-苯基-4h-s-t riazolo-(1,5a)(1,4)-苯并二氮杂produce。

摘要

1336744 Substituted 2-amino-5-phenyl-3H- 1,4-benzodiazepine derivatives TAKEDA YAKUHIN KOGYO KK 16 Nov 1970 [15 Nov 1969] 32303/73 Divided out of 1336743 Heading C2C Novel compounds of the Formulµ IV and V wherein R is alkyl, aryl or amlkyl in which the aromatic ring of the aryl or aralkyl group is unsubstituted or substituted by one or more C 1-3 alkyl, C 2-4 alkenyl, C 1-3 alkoxy, C 2-7 acylamino, halo or nitro; RSP1/SP is hydrogen, C 1-6 alkyl, R 1 is C 1-3 alkyl; the rings A and/or B are unsubstituted or substituted by one or more halogen, nitro, trifluoromethyl, alkyl or alkoxy and the nitrogen at the 4-position is optionally linked to an oxygen atom may be prepared by reacting an amine II: with an ortho ester R-C(OR 1 ) 3 to form a compound IV and optionally reacting this product with ammonia to form a compound V and after each step, for products carrying an N-oxide optionally deoxygenating IV or V. Pharmaceutical compositions of IV and V show muscle relaxant, anti-convulsant, tranquillizing and sleep-inducing activity when administered orally or parenterally with the usual excipients.
机译:1336744取代的2-氨基-5-苯基-3H-1,4-苯并二氮杂衍生物TAKEDA YAKUHIN KOGYO KK 1970年11月16日[1969年11月15日] 32303/73从1336743标题C2C中分离出式IV和V的新型化合物,其中R为烷基,芳基或芳基,其中芳基或芳烷基的芳环未被取代或被一个或多个C 1-3烷基,C 2-4烯基,C 1-3烷氧基,C 2-7酰基氨基,卤素或硝基R 1 是氢,C 1-6烷基,R 1是C 1-3烷基;环A和/或B未被取代或被一个或多个卤素,硝基,三氟甲基,烷基或烷氧基取代,并且4-位的氮任选与氧原子相连,可通过使胺II与原酸酯RC(OR 1)3形成化合物IV,然后使该产物与氨反应形成化合物V,并且在每个步骤之后,对于带有N-氧化物的产物,可以对IV或V进行脱氧。IV和V的药物组合物显示与普通的赋形剂口服或胃肠外给药时,具有肌肉松弛,抗惊厥,镇静和诱导睡眠的作用。

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