Syntheses of 7-phenyl-5h-thiazolo[5,4-e]pyrrolo[1,2-a][1,4]diazepin-10(9h)one,7-phenyl-5h-thiazolo[5,4-e][1,2,3,4]tetrazolo[5,1-c]-pyrrolo[1,2-a][1,4]diazepine and 7-phenyl-5h-thiazolo[5,4-e]-[1,3,4] triazolo [5,1-c]pyrrolo [1,2-a] [1,4] diazepines
✍ Scribed by A. Shafiee; M. Shekarchi
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2002
- Tongue
- English
- Weight
- 48 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Fused tricyclic 7‐phenyl‐5__H__‐thizolo[5,4‐e]pyrrolo[1,2‐a][1,4]diazepin‐10(9__H__)one (10) was prepared by thermolysis of 2‐phenyl‐4‐(1‐pyrrolylmethyl)thiazole‐5‐carbonyl azide (9) in acetic acid. In addition, starting from 10, 7‐phenyl‐5__H__‐thiazolo [5,4‐e][1,3,4]triazolo[5,1‐c]pyrrolo[1,2‐a][1,4]diazepines (13) and 7‐phenyl‐5__H__‐thiazolo[5,4‐e] [1,2,3,4]tetrazolo[5,1‐c]pyrrolo[ 1,2‐a] [1,4]diazepine (14) were synthesized.
📜 SIMILAR VOLUMES
A facile approach to pyrazolo [4,3-e][1,4] diazepin-5,8-diones andpyrazolo[4,3-e]pyrrolo[1,2-a][1,4]diazepin-5,10-diones is reported. Strategy involved the utility of α-amino acid as a three-atom segment in the construction of diazepine skeleton on the preformed pyrazole ring.
## Abstract The aza‐Wittig reactions of benzaldehyde‐, acetophenone‐ and benzophenone 1‐[(triphenylphosphor‐anylidene)amino]ethylidenehydrazones (**1**) with 2,3‐furandiones **6** provide a new route to 4__H__,8__H__‐1,2,4‐triazolo[1,5‐__c__][1,3]oxazepin‐4‐ones **14** or 5,6‐dihydro‐7__H__,12__H__