Issue 19, 1975

A new synthesis of alloxazines by the reaction of diethyl azodiformate with 6-anilinouracils

Abstract

Treatment of 6-anilinouracils with diethyl azodiformate led the corresponding alloxazines (benzo[g]pteridine-2,4-diones). This synthesis involves initial formation of Michael-type adducts [6-anilino-5-(1,2-bisethoxy-carbonylhydrazino)uracils] followed by dehydrogenative cyclization with further diethyl azodiformate.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 1907-1909

A new synthesis of alloxazines by the reaction of diethyl azodiformate with 6-anilinouracils

F. Yoneda, S. Matsumoto, Y. Sakuma and S. Fukazawa, J. Chem. Soc., Perkin Trans. 1, 1975, 1907 DOI: 10.1039/P19750001907

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