New method for the preparation of dibenzo[b, f][1,4]thiazepines
✍ Scribed by Takayoshi Fujii; Wei Hao; Toshiaki Yoshimura
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 104 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20010
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✦ Synopsis
Abstract
The S‐amination of 9__H__‐thioxanthen‐9‐ol (2a) and 9‐substituted derivatives 2b–e (Me (b), Et (c), ^i^Pr (d), Ph (e)) with O‐mesitylenesulfonylhydroxylamine (MSH) was carried out. The expected product, 10‐amino‐9‐hydroxy‐9‐isopropyl‐9__H__‐thioxanthenium mesitylenesulfonate (3d), was obtained in 78(%) yield from the corresponding thioxanthen(9)‐ol 2d. However, in the case of 2a–c and 2e the reaction led instead to dibenzo[b,f][1,4]thiazepines 6a–c and 6e in moderate yields. © 2004 Wiley Periodicals, Inc. Heteroatom Chem 15:246–250, 2004; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20010
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