1,3-Oxazines and related compounds. VI. Synthesis and some reactions of 2,6-disubstituted 4H-1,3-thiazin-4-ones.

抄録

Various of 2, 6-disubstituted 4H-1, 3-thiazin-4-ones (5) were synthesized by successive treatment of N-acylacetylcarboxamides with acid (such as 70% perchloric acid or fluorosulfonic acid) and hydrogen sulfide. Reactions of 5 were investigated ; ammonolysis with ethanolic ammonia gave the corresponding pyrimidin-4-ones; hydrolysis of 2-alkyl-1, 3-thiazine derivatives yielded ring-opened N-acyl-β-mercaptocrotonamides ; reduction with NaBH4 or LiAlH4 afforded 3, 4-dihydro-2H-1, 3-thiazin-4-one derivatives.

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