Issue 6, 1992

Oxazol-5(4H)-ones. Part 7. New synthesis of oxazolo[5,4-b]pyridines

Abstract

Oxazolo[5,4-b]pyridines 4 are synthesized by heating the iminophosphoranes 1 and alkylideneoxazol-5(4H)-ones 2. At room temperature the reaction of 4-ethoxymethyleneoxazol-5(4H)-one 2f with iminophosphorane 1a yields the enamino lactone 6, which is, in turn, transformed by heating in acetic acid into the 2(1H)-pyridone 7.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 701-705

Oxazol-5(4H)-ones. Part 7. New synthesis of oxazolo[5,4-b]pyridines

M. L. Gelmi, D. Pocar, M. Viziano, R. Destro and F. Merati, J. Chem. Soc., Perkin Trans. 1, 1992, 701 DOI: 10.1039/P19920000701

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