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Convenient and simple synthesis of 2-aminothiazoles by the reaction of α-halo ketone carbonyls with ammonium thiocyanate in the presence of N-methylimidazole

Authors :
Meshram, H.M.
Thakur, Pramod B.
Madhu Babu, B.
Bangade, Vikas M.
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Sep2012, Vol. 53 Issue 39, p5265-5269. 5p.
Publication Year :
2012

Abstract

Abstract: Substituted 2-aminothiazole derivatives were obtained as a result of N-methylimidazole catalyzed cyclization of α-halo ketone carbonyls with ammonium thiocyanate in water–alcoholic media. The generality of the method has been demonstrated by screening a series of aromatic/heteroaromatic/aliphatic α-halo ketones, α-halo β-diketones, and α-halo β-ketoesters. The developed method is simple, mild, and general route for the preparation of diversely functionalized 2-aminothiazoles in good to moderate yields from readily available starting materials. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404039
Volume :
53
Issue :
39
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
79558009
Full Text :
https://doi.org/10.1016/j.tetlet.2012.07.080