7-Trifluoromethyl-5-phenyl-2-oxo-(1H)-oxazolo[5,4-<i>b</i>]pyridine and some of its properties

Authors

  • М. В. Юре Riga Technical University, Riga LV-1658
  • Д. В. Шантаре Riga Technical University, Riga LV-1658
  • Э. Ю. Гудриниеце Riga Technical University, Riga LV-1658

Abstract

The potassium salt of 7-trifluoromethyl-5-phenyl-2-oxooxazolo[5, 4-bjpyridine (IV) was prepared from 3-aminocarbonyl-4-trifluoromethyl-6 phenyl-2(1H)-pyridone by the Hofmann reaction and was converted into 3-amino-4-trifluoromethyl-6-phenyl-2(1H)-pyridone without isolation. 1-Substituted 7-trifluoromethyl-5-phenyl-2-oxooxazolo[5,4-b]pyridines were formed by alkylation of salt IV. 6-Halogeno-7-trifluoromethyl-5-phenyl-2-oxo-(1H)-oxazolo[5,4-b]pyridines have been prepared.

How to Cite
Yure, M. V.; Shantare, D. V.; Gurdinietse, É. Y. Chem. Heterocycl. Compd. 1996, 32, 473. [Khim. Geterotsikl. Soedin. 1996, 542.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165915

Published

1996-04-25

Issue

Section

Original Papers