SYNTHESIS OF NEW THIAZOLES FROM α-HALOHETARYL KЕTONES

Authors

  • T. Loloiu Faculty of Pharmacy, Org. Chem. Dept., University of Medicine and Pharmacy "Carol Davila", 6 Traian Vuia street, Bucharest
  • I. Saramet Faculty of Pharmacy, Org. Chem. Dept., University of Medicine and Pharmacy "Carol Davila", 6 Traian Vuia street, Bucharest
  • G. Loloiu Faculty of Chemistry, Org. Chem. Dept., University of Bucharest, 90-92 Panduri Road, 76233
  • C. Drăghici "C. D. Nenitescu" – Institute of Organic Chemistry Romanian Academy, Spl. Independentei 202B, Bucharest
  • О. Maior Faculty of Chemistry, Org. Chem. Dept., University of Bucharest, 90-92 Panduri Road, 76233

Keywords:

2,4-disubstituted thiazoles, α-bromoketones, p-(arylsulphonyl)thiobenzamides

Abstract

Reactions of α-bromoacetylphenoxathiin, α-bromoacetylphenoxathiin 10,10-dioxide, or α-bromoacetyl-thianthrene with certain p-(arylsulfonyl)thiobenzamides lead to the formation of the corresponding 2,4‑disubstituted thiazoles. The new compounds were characterized through elemental analysis and spectral data (IR, 1H NMR, and 13C NMR).

How to Cite
Loloiu, T.; Saramet, I.; Loloiu, G.; Draghici, C.; Maior, V. Chem. Heterocycl. Compd. 2001, 37, 353. [Khim. Geterotsikl. Soedin. 2001, 383.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1017567302267

 

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Published

2001-03-25

Issue

No. 3 (2001)

Section

Original Papers