A new synthesis of 1,2,3,5-tetrahydroimidazo[2,3-b]-[1,3]benzodiazocines
✍ Scribed by Hyun In Cho; Seung Won Lee; Kee-Jung Lee
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2004
- Tongue
- English
- Weight
- 155 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A new synthesis of 6‐carbomethoxy‐1,2,3,5‐tetrahydroirnidazo[2,3‐b][1,3]benzodiazocines 13 by the intramolecular cycloaddition reaction of methyl 2‐(1‐aziridinylmethyl)‐3‐(2‐ureidophenyl)propenoates 10 under Appel's dehydration conditions is described. The latter were readily obtained from 2‐nitrobenzalde‐hyde with methyl acrylate through the Baylis‐Hillman reaction.
📜 SIMILAR VOLUMES
**The Synthesis of 2,3,4,5‐1__H__‐Tetrahydroimidazo[2,1‐__b__]quinazolin‐2,5‐diones and analogous 2,3,4,5‐1__H__‐Tetrahydroimidazo[1,2‐__a__]thieno[2,3‐__d__] (or [3,2‐__d__])‐pyrimidin‐2,5‐diones** The syntheses of various imidazo [2, 1‐__b__]quinazolinediones and their thiophene analogs are descr
## Abstract Easily accessible 2‐aroylamino‐3,3‐dichloroacrylonitriles, when treated successively with ethylenediamine, phosphorus pentasulfide, water, and methyl and benzyl halides, furnish the corresponding derivatives of 4,5,7,8‐tetrahydroimidazo[1,2‐c][1,3]thiazolo[4,5‐e][1,3,2]diazaphosphinine,