Reactions of an imidazo[4,5-c]isoxazole-6-carboxylate with dimethyl acetylenedicarboxylate; formation of the first example of a [1,4]diazepino[2,3-c]isoxazole

Citation
A. Taher et al., Reactions of an imidazo[4,5-c]isoxazole-6-carboxylate with dimethyl acetylenedicarboxylate; formation of the first example of a [1,4]diazepino[2,3-c]isoxazole, TETRAHEDR L, 41(48), 2000, pp. 9319-9321
Citations number
9
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
48
Year of publication
2000
Pages
9319 - 9321
Database
ISI
SICI code
0040-4039(20001125)41:48<9319:ROAIWD>2.0.ZU;2-M
Abstract
The synthesis of the first example of a [1,4]diazepino[2,3-c]isoxazole deri vative is reported. Reaction of an imidazo[4,5-c]isoxazole with acetylenic esters has been shown to lead to the formation of 2-pyrrol-2-yl imidazoles, Here we report an alter-native reaction pathway in which the fused imidazo le ring adds a molecule of acetylenic eater, and undergoes ring expansion t o a fused El, il]diazepine. A mechanism for the reaction is discussed. (C) 2000 Elsevier Science Ltd. All rights reserved.