Synthesis of new fluorinated 1,5-benzoxazepine derivatives
✍ Scribed by Maria Teresa Cocco; Cenzo Congiu; Valentina Onnis; Angela Maria Bernard; Pier Paolo Piras
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 224 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A simple approach to the fluorinated 1,5‐benzoxazepine ring system is described. By reacting commercially accessible aminophenols 1 and the trifluoroacetylvinyl ether 2, high yields of enaminones 3 were obtained. Functionalization of methyl group of compounds 3 gave rise to dieneamines 4 that were cyclized in acidic environment to benzoxazepine derivatives 5.
📜 SIMILAR VOLUMES
## Abstract A new series of 4‐(4‐methylpiperazin‐1‐yl)thieno[2,3‐__b__][1,5]benzoxazepines **1a‐k** has been synthesized from 4‐bromo‐2‐methylthiophene **6** or ethyl 2‐amino‐4,5‐dimethyl‐3‐thiophencarboxylate **10**. Preparation of the key intermediate thieno[2,3‐__b__][1,5]benzoxazepine‐4(5__H__)
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract For Abstract see ChemInform Abstract in Full Text.