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Facile and convenient synthesis of 2,4-disubstituted and 2,3,4-trisubstituted 1,3-thiazoles.
- Source :
-
Journal of Sulfur Chemistry . Apr2016, Vol. 37 Issue 2, p162-175. 14p. - Publication Year :
- 2016
-
Abstract
- An efficient route for the synthesis of (E)-2-(2-(2-nitrobenzylidene)-hydrazinyl)-4-phenylthiazol-3-ium bromide, (E)-2-(2(substituted benzylidene)hydrazinyl)-4-phenylthiazoles and (E)-4-(4-bromophenyl)-2-(cycloalkylidenehydrazono)-3-phenyl-2,3-dihydrothiazoles by reaction of 1-aryl-2-bromoethanones with 2-(1-substituted methylidene)hydrazinecarbothioamides and cycloalkylidene-N-phenyl-hydrazinecarbothioamides. The structure of the products has been confirmed by using IR, NMR, mass spectrometry and single-crystal X-ray analyses. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 17415993
- Volume :
- 37
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- Journal of Sulfur Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 113945438
- Full Text :
- https://doi.org/10.1080/17415993.2015.1114621