Issue 0, 1982

Novel synthesis of di-imines by the transformation of 1-aryl-4,6-disubstituted pyrimidin-2(1H)-ones

Abstract

The di-imines (4), which are versatile starting materials for the synthesis of heterocycles, are obtained in fair yields when the 1-aryl-4,6-disubstituted pyrimidin-2(1H)-ones (3) are treated with alkoxide, both photochemically and thermally. The di-imines (4) thus obtained, when treated with carbon disulphide, give the 1,3-thiazine-2-thiones (8) and/or the 1-arylpyrimidine-2(1H)-thiones (9).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 2149-2152

Novel synthesis of di-imines by the transformation of 1-aryl-4,6-disubstituted pyrimidin-2(1H)-ones

T. Nishio and Y. Omote, J. Chem. Soc., Perkin Trans. 1, 1982, 2149 DOI: 10.1039/P19820002149

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