193486-05-4Relevant articles and documents
A facile synthesis of new [1,2,4]triazolo[3,4-d][1,3,5]dithiazines involving acid-labile methanesulphinyl leaving group
Yadav, L. D. S.,Vaish, Anjum,Sharma, Sangeeta
, p. 442 - 444 (2007/10/03)
Nucleophilic addition of the amine function of 5-aryl-3-methanesulphinylmethylthio-1,2,4-triazoles 2a, b to carbon disulphide and aryl/cyclohexyl isothiocyanates furnishes adducts 4a-h which undergo a facile intramolecular cyclization via a nucleophilic displacement to yield the corresponding [1,2,4]triazolo[3,4-d][1,3,5]dithiazines 5a-h with the loss of the acid-labile methanesulphinyl leaving group as methanesulphenic acid.