彭司勋, 杨桢祥, 濮家溎, 盛时, 李明华. 5,6-取代-3-吲(口朶)乙胺衍生物的合成J. 药学学报, 1966, 13(1): 24-29.
引用本文: 彭司勋, 杨桢祥, 濮家溎, 盛时, 李明华. 5,6-取代-3-吲(口朶)乙胺衍生物的合成J. 药学学报, 1966, 13(1): 24-29.
PENG SZU-HSUN YANG CHEN-HSIANG PU JIA-GUEI SHENG SHIH LEE MING-HWA, . Synthesis of Derivatives of 5,6-Disubstituted 3(β-Aminoethyl) lndoleJ. Acta Pharmaceutica Sinica, 1966, 13(1): 24-29.
Citation: PENG SZU-HSUN YANG CHEN-HSIANG PU JIA-GUEI SHENG SHIH LEE MING-HWA, . Synthesis of Derivatives of 5,6-Disubstituted 3(β-Aminoethyl) lndoleJ. Acta Pharmaceutica Sinica, 1966, 13(1): 24-29.

5,6-取代-3-吲(口朶)乙胺衍生物的合成

Synthesis of Derivatives of 5,6-Disubstituted 3(β-Aminoethyl) lndole

  • 摘要: 5,6-二甲氧基及5,6-次甲二氧基吲(口朶)用草酰氯法引入乙胺侧链,合成了两类5,6-取代-3-吲(口朶)乙胺衍生物共19个。药理系统筛选结果,表明两类化合物多具有不同程度的安定、抗惊、及镇痛作用。其中以化合物(Ⅱ)7的作用较显著,详细的药理研究结果,将另文报导。

     

    Abstract: Nineteen derivatives of 3-indolylethyl amine were synthesized by treating substituted indoles with oxalyl chloride to form 3-indolyl glyoxylyl chloride, which on treatment with the requisite amines and subsequent reduction of the corresponding amides obtained with lithium aluminium hydride gave the required products. Pharmacological tests showed that the compound (Ⅱ)7 possesses tranquilizing, anticonvulsant, and analgesic properties. Detailed pharmacological results will be reported elsewhere.

     

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