Synthesis in the 2-mercaptobenzothiazole series |
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Authors: | E. A. Kuznetsova S. V. Zhuravlev T. N. Stepanova |
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Affiliation: | (1) Institute of Pharmacology and Chemotherapy, AMS USSR, Moscow |
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Abstract: | The reduction of some dihydrothiazolobenzothiazolium salts with sodium borohydride may take place in two directions: with the formation of thiazolidino[2, 3-b]benzathiazolines and with the cleavage of the C-S bond to give N-( -mercaptoethyl)benzothiazolines. The behavior of thiazolidino[2, 3-b]benzothiazoline under the conditions of acid and alkaline hydrolysis has been studied.For communication VI, see [1]. |
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