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Reaction of Thiosemicarbazide with Methyl Phenylpropynoate:Synthesis of 1,3-Thiazinone Derivatives

机译:硫代氨基脲与苯丙酸甲酯的反应:1,3-噻嗪酮衍生物的合成

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摘要

Condensation of thiourea with acetylenecarboxylic acid esters is well known and is used in synthesis of l,3-thiazin-4-ones [1-4].It is also known that N-ami-nothiourea (thiosemicarbazide,I)reacts with methyl propynoate in methanol to form methyl 3-thiosemicar-bazonopropanoate [5].Therefore,proceeding with studies on synthetic routes to potentially bioactive 1,3-thiazinones and condensed systems based on them,we studied the reaction of I with methyl phenyl-propynoate II.
机译:硫脲与乙炔基羧酸酯的缩合反应是众所周知的,并用于合成1,3-噻嗪-4-酮[1-4]。还已知N-氨基-硫脲(thiosemicarbazide,I)与丙炔酸甲酯反应在甲醇中生成3-硫代半胱氨酸-重氮丙酸甲酯[5]。因此,在研究可能具有生物活性的1,3-噻嗪酮的合成路线和基于它们的缩合体系后,我们研究了I与苯丙酸甲酯II的反应。

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