## Abstract For Abstract see ChemInform Abstract in Full Text.
A microwave induced cyclisation of α-phenylsulfonyl-enaminoacrylates for the preparation of 4-aryl-4H-1,4-benzothiazine 1,1-dioxide derivatives
✍ Scribed by Simón E. López; José Salazar; Oscar Rebollo; Jelem Restrepo
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 67 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
Several 4‐aryl‐4H‐1,4‐benzothiazine 1,1‐dioxide derivatives have been prepared in good yields by microwave promoted cyclisation of α‐phenylsulfonyl‐enaminoacrylate intermediates in basic media. Benzothiazines were obtained without the use of a catalyst in short reaction times.
📜 SIMILAR VOLUMES
The reaction of 3-substituted-4-hydroxyroxy-2H-1,2-be~othiazine 1,l-dioxides with aryl isocyanate under different equivalents of strong base NaH was studied. Seventeen of new derivatives were obtained whose structures were characterized by ' H NMR, IR, MS, elementary analysis and FeCls test. ## Key
A series of 1,4-benzoxathiin 4,4-dioxide derivatives have been prepared by a new synthetic route. The reactions of 2-chloro-4-nitrobenzenethiol 1 with 1 -aryl-2-chloroethanones 2 in the presence of sodium hydroxide give 1-aryl-2-(2-chloro-4-nitrophenylthio)ethanones 3 which on oxidation with \(30 \%