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Synthesis in the 2-mercaptobenzothiazole series
Authors:E. A. Kuznetsova  S. V. Zhuravlev  T. N. Stepanova
Affiliation:(1) Institute of Pharmacology and Chemotherapy, AMS USSR, Moscow
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-(Bgr-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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