Abstract
1-Substituted 4,4,6-trimethyl-1,4-dihydropyrimidine-2(3H)-thiones (2) on heating in 11M-HCl at 100–110° are converted into the corresponding 2-substituted-amino-4,6,6-trimethyl-6H-1,3-thiazines (4) and/or thioureas. But at 95–100°, Dimroth rearrangement products, e.g, the corresponding 2-substituted-amino-4,4,6-trimethyl 4H-1,3-thiazines (3) are formed.

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