79402-45-2Relevant academic research and scientific papers
A Novel S,N-Double Rearrangement; X-Ray Crystal Structure of 5-Carbamoyl-4-methylthio-2-phenyl-1,3-thiazin-6-one and Its 2,3-Dihydro-derivative
Yokoyama, Masataka,Nakamura, Masaki,Imamoto, Tsuneo,Yamaguchi, Kei-ichi
, p. 560 - 561 (1981)
Condensation of 2-cyano-3-mercapto-3-(methylthio)acrylamide (1) with benzoic acid in the presence of polyphosphate ester gave 5-carbamoyl-4-methylthio-2-phenyl-1,3-thiazin-6-one (5); the structures of (5) and its 2,3-dihydro-derivative (6) were determined
S,N Double Rearrangement. 2. X-ray Crystal Structures of Rearranged Products
Yokoyama, Masataka,Nakamura, Masaki,Ohteki, Hiroko,Imamoto, Tsuneo,Yamaguchi, Kei-ichi
, p. 1090 - 1094 (2007/10/02)
Condensation of 2-cyano-3-mercapto-3-(methylthio)acrylamide (1) with benzoic acid in the presence of polyphosphate ester gave 5-carbamoyl-4-(methylthio)-2-phenyl-1,3-oxazine-6-thione (6), which, on treatment with boiling ethanol, was easily converted into 5-carbamoyl-4-(methylthio)-2-phenyl-1,3-thiazin-6-one (9).Reduction of 9 with NaBH4 gave its 2,3-dihydro derivative 10.The strucures of 6,9, and 10 were determined by single-crystal X-ray diffraction.A reaction mechanism of this novel S,N double rearrangement is briefly discussed.
