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E-Journal of Chemistry
Volume 9 (2012), Issue 1, Pages 55-62
http://dx.doi.org/10.1155/2012/615601

Synthesis of Peracetylated β-D-Glucopyranosyl Thioureas from Substituted 2-Aminobenzo-1ʹ, 3ʹ-thiazoles

Nguyen Dinh Thanh

Faculty of Chemistry, College of Science, Hanoi National University, 19 Le Thanh Tong, Ha Noi 10000, Vietnam

Received 6 April 2011; Accepted 7 June 2011

Copyright © 2012 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Some peracetylated glucopyranosyl thioureas containing a heterocyclic ring system, benzo-1,3-thiazole have been prepared by the condensation reaction of tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate and corresponding substituted 2-amino-(6-substituted)benzo-1,3-thiazoles. Investigated heating conditions showed that the solventless microwave-assisted method gave higher yields of these thioureas.