Synlett 2015; 26(01): 108-110
DOI: 10.1055/s-0034-1378922
letter
© Georg Thieme Verlag Stuttgart · New York

One-Pot Multicomponent Domino Synthesis of 4-Aminothiazole-2(3H)-thiones

Khadijeh Hajibabaei
Department of Chemistry, University of Isfahan, 81746-73441, Isfahan, Iran   Fax: +98(311)6689732   Email: h.zali@chem.ui.ac.ir
,
Hassan Zali-Boeini*
Department of Chemistry, University of Isfahan, 81746-73441, Isfahan, Iran   Fax: +98(311)6689732   Email: h.zali@chem.ui.ac.ir
› Author Affiliations
Further Information

Publication History

Received: 07 September 2014

Accepted after revision: 12 October 2014

Publication Date:
06 November 2014 (online)


Abstract

A new multicomponent domino reaction has been developed for the synthesis of 4-aminothiazole-2(3H)-thiones. Carbon disulfide was successfully used in the preparation of 4-aminothiazole-2(3H)-thione derivatives through reaction with primary amines and 2-bromo-2-arylacetonitriles in the presence of sodium carbonate and a catalytic amount of sodium iodide.

 
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  • 18 4-Aminothiazole-2(3H)-thiones 3a–n; General ProcedureNa2CO3 (1.2 mmol, 128 mg) and NaI (0.5 mmol, 75 mg) were added to a mixture of the appropriate aryl(bromo)acetonitrile (1 mmol), primary amine (1mmol), and CS2 (1.2 mmol, 73 µL) in EtOH (5 mL), and the mixture was stirred at r.t. for 10 min while the progress of the reaction was monitored by TLC (hexane–EtOAc, 5:1). When the reaction was complete, the mixture was filtered and concentrated in vacuo to give a crude product that was purified by recrystallization from a suitable solvent to afford the pure product as a yellow solid.