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-anuno-4-trifluoromethyl-6-phenyl-2(1H)-pyridone without isolation. 1-Substituted 7-trifluoromethyl-5phenyl-2-oxooxazolo[5, 4-b]pyridines were formed by alkylation of salt IV. 6-Halogeno-7-trifluoromethyl-S phenyl-2-oxo(1H)-oxazolo[5,4-b]pyridines have been prepared.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 542–545, April. 1996.
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Yure, M.V., Shantare, D.V. & Gurdinietse, É.Y. 7-Trifluoromethyl-5-phenyl-2-oxo-(1H)-oxazolo[5,4-b]pyridine and some of its properties. Chem Heterocycl Compd 32, 473–476 (1996). https://doi.org/10.1007/BF01165915
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DOI: https://doi.org/10.1007/BF01165915