Issue 9, 1992

Heterocyclic transformations part 4: a facile transformation of 3-alkyl-6-methyl-1,3-oxazine-2,4(3H)-diones to 6-substituted 5-acetyluracils and 6-thioxo-1,3,5-triazine-2,4(1H,3H,5H)-diones

Abstract

3-Benzyl-6-methyl-1,3-oxazine-2,4(3H)-dione 1(R = CH2Ph) reacts under phase-transfer catalytic conditions with amides and thioamides to give 6-substituted 5-acetyluracils and with malonamide to give a bicyclic pyridopyrimidine system. Similar reactions of 1 with thioureas provide 6-thioxo-1,3,5-triazine-2,4(1H,3H,5H)-diones, but with ureas, the substituents influence the mode of the reaction and the nature of the products. The synthetic scope and utility of these reactions has been examined.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 1139-1143

Heterocyclic transformations part 4: a facile transformation of 3-alkyl-6-methyl-1,3-oxazine-2,4(3H)-diones to 6-substituted 5-acetyluracils and 6-thioxo-1,3,5-triazine-2,4(1H,3H,5H)-diones

H. Singh, P. Aggarwal and S. Kumar, J. Chem. Soc., Perkin Trans. 1, 1992, 1139 DOI: 10.1039/P19920001139

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