Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.

J Org Chem

Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Building 10, Room B3C346A, 10 Center Drive, Bethesda, Maryland 20892-1003, USA.

Published: March 2009

Monohalo and dihalo 1,3-thiazole derivatives can be efficiently and selectively prepared under mild conditions from 2-amino-1,3-thiazoles. Halogenations proceed easily in the presence of copper(I) or copper(II) chlorides, bromides, or iodides directly in solution or with supported copper halides.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796164PMC
http://dx.doi.org/10.1021/jo802799cDOI Listing

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