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某些恶二唑啉和三唑衍生物的合成及抗菌测试

Synthesis and antimicrobial testing of certain oxadiazoline and triazole derivatives.

作者信息

Hassan E, Al-Ashmawi M I, Abd El-Fattah B

出版信息

Pharmazie. 1983 Dec;38(12):833-5.

PMID:6669612
Abstract

The synthesis of some novel oxadiazolines and triazoles is described. Cyclization of nicotinic acid hydrazones using acetic anhydride afforded 2-substituted 3-acetyl-5-(3-pyridyl)-1,3,4-oxadiazolines. Likewise, when potassium dithiocarbazate--prepared from nicotinic acid hydrazide--was reacted with hydrazine hydrate, cyclization and production of 4-amino-3-(3-pyridyl)-5-mercapto[4H]-1,2,4-triazole was achieved. Ten new azomethine derivatives were prepared through the condensation between the latter amine and different aromatic aldehydes. The novel compounds were subjected to preliminary antimicrobial testing and the data obtained are summarized.

摘要

描述了一些新型恶二唑啉和三唑的合成。使用乙酸酐使烟酸腙环化得到2-取代的3-乙酰基-5-(3-吡啶基)-1,3,4-恶二唑啉。同样,由烟酰肼制备的二硫代氨基甲酸钾与水合肼反应时,实现了4-氨基-3-(3-吡啶基)-5-巯基[4H]-1,2,4-三唑的环化和生成。通过后一种胺与不同的芳香醛缩合制备了十种新的甲亚胺衍生物。对这些新型化合物进行了初步抗菌测试,并总结了所得数据。

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