2011
DOI: 10.1016/j.tet.2011.10.045
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Two-pot synthesis of N,N-disubstituted 4H-3,1-benzothiazin-2-amines from aryl(2-isothiocyanatophenyl)methanones and secondary amines

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Cited by 6 publications
(1 citation statement)
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“…For example, exchange reactions of isocyanates, 14 the reaction of aromatic thiols with amines, 15 sodium sulfide as a sulfur source, 16 isocyanates reacting with diazonium salts, 17 but the most widely used method is substituted arylthioureas reacting with primary amines, alkyl halides or benzensulfonic acid. [18][19][20][21][22][23][24] However, these methods suffer from the disadvantages of requiring high temperatures or they give mixtures of products.…”
mentioning
confidence: 99%
“…For example, exchange reactions of isocyanates, 14 the reaction of aromatic thiols with amines, 15 sodium sulfide as a sulfur source, 16 isocyanates reacting with diazonium salts, 17 but the most widely used method is substituted arylthioureas reacting with primary amines, alkyl halides or benzensulfonic acid. [18][19][20][21][22][23][24] However, these methods suffer from the disadvantages of requiring high temperatures or they give mixtures of products.…”
mentioning
confidence: 99%