Nawojski A, Nawrocka W, Liszkiewicz H
Pol J Pharmacol Pharm. 1985 Jan-Feb;37(1):69-72.
5-Methoxy-, ethoxy- and phenoxycarbonyl derivatives of 2-methyl-4-phenyl-1H-tetrahydro-1,5-benzodiazepine-2-carboxylic ethyl ester (1) and 4-methyl-1H-tetrahydro-1,5-benzodiazepine-2-one (2) were obtained. 5-Methoxycarbonyl- (3) and 5-phenoxycarbonyl- (5) derivatives of 1 exerted analgesic action in doses of 0.1 LD50. Compounds 3, 5 and 7 a (5-ethoxycarbonyl-) in a dose as low as 0.063 LD50, and compound 8 (5-phenoxycarbonyl-1H-tetrahydro-1,5-benzodiazepin-2-one)--in a dose of 0.004 LD50 prolonged hexobarbital sleeping time. The toxicity of all the compounds was low.
制备了2-甲基-4-苯基-1H-四氢-1,5-苯并二氮杂䓬-2-羧酸乙酯(1)和4-甲基-1H-四氢-1,5-苯并二氮杂䓬-2-酮(2)的5-甲氧基、乙氧基和苯氧基羰基衍生物。1的5-甲氧基羰基-(3)和5-苯氧基羰基-(5)衍生物在0.1 LD50剂量下具有镇痛作用。化合物3、5和7a(5-乙氧基羰基-)在低至0.063 LD50的剂量下,以及化合物8(5-苯氧基羰基-1H-四氢-1,5-苯并二氮杂䓬-2-酮)在0.004 LD50的剂量下可延长己巴比妥睡眠时间。所有化合物的毒性都很低。