4652-24-8Relevant articles and documents
Regio-controlled synthesis of 1, 4-benzothiazinones
Ghailane, Touria,Saadouni, Mohammed,Boukhris, Said,Habbadi, Nouzha,Hassikou, Amina,Kerbal, Abdelali,Garrigues, Bernard,Souizi, Abdelaziz
experimental part, p. 357 - 363 (2011/04/15)
Regio-controlled cyclization of gem-dicyanoepoxides with 2-aminothiophenol and its hydrochloride to form 1,4-benzothiazine-2-one or 3-one is described. The cyclization is highly regioselective and the reaction of the epoxides with 2-aminothiophenol under neutral reaction condition gave 1,4-benzothiazine-2-one as a sole cyclized product, whereas that with hydrochloride of 2-aminothiophenol afforded 1,4-benzothiazine-3-one predominantly. The regioselectivity resulted from the reaction condition is discussed. The Japan Institute of Heterocyclic Chemistry.
A Convenient and General Synthesis of 2-Aryl- and 2-Pyridyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazines
Jacobsen, Niels,Kolind-Andersen, Hans
, p. 911 - 914 (2007/10/02)
The reaction of bis(2-aminophenyl) disulphide 1 with methyl or ethyl aryl- or pyridylacetates and sodium hydride gives the title compounds in good yield and high purity.The reaction is general, the starting materials easily available and the workup is simple and rapid.