Formation of an unusual product in the reaction of a 1,2,5-thiadiazolidine 1,1-dioxide-derived thioether with sulfuryl chloride
β Scribed by Dengfeng Dou; Erach R. Talaty; Curtis E. Moore; John C. Bullinger; David M. Eichhorn; William C. Groutas
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 284 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.136
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β¦ Synopsis
Abstract
magnified image
The treatment of a 1,2,5βthiadiazolidine 1,1βdioxideβderived phenylthiomethyl ether with sulfuryl chloride yielded an unexpected dimeric product whose structure was determined using Xβray crystallography. A plausible mechanism for the formation of this product is proposed. J. Heterocyclic Chem. (2009).
π SIMILAR VOLUMES
## 1,5-benzodiazepines / Cyclizations / Cycloadditions The reaction of o-phenylenediamine (4) with one, two or three equivalents of p-substituted 3-dimethylaminopropiophenone hydrochlorides 5a-e was studied. 4-Aryl-2,3-dihydro-1H-1,5-benzodiazepine derivatives 6a-e were obtained in good yields, alo