THE REACTION OF 5-ARYL(HETARYL)-2-AROYLMETHYLTHIO-1,3,4-OXADIAZOLES WITH ARYLDIAZONIUM TETRAFLUOROBORATES

Authors

  • А. Н. Красовский Chernigov Technological Institute, Chernigov 250027
  • А. П. Андрушко Chernigov Technological Institute, Chernigov 250027
  • А. М. Демченко Chernigov Technological Institute, Chernigov 250027

Keywords:

5-aryl(hetaryl)-2-aroylmethylthio-1,3,4-oxadiazoles, 5-aryl(hetaryl)-2-(1-aroyl-1-hydrazinomethylthio)-1,3,4-oxadiazole, azo coupling reaction with diazonium tetrafluoroborates

Abstract

5-Aryl(hetaryl)-2-aroylmethylthio-1,3,4-oxadiazoles behave as CH acids and readily react with aryldiazonium tetrafluoroborates at the active methylene group to give azo coupling products. The spectroscopic properties of the compounds synthesized have been studied.

How to Cite
Krasovsky, A. N.; Andrushko, A. P.; Demchenko, A. M. Chem. Heterocycl. Compd. 2001, 37, 456. [Khim. Geterotsikl. Soedin. 2001, 544.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1017612223514

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Published

2001-04-25

Issue

No. 4 (2001)

Section

Original Papers