SYNTHESIS OF THIENO[3,4-B]QUINOXALIME AND DERIVATIVES

Citation
J. Pohmer et al., SYNTHESIS OF THIENO[3,4-B]QUINOXALIME AND DERIVATIVES, Journal of organic chemistry, 60(25), 1995, pp. 8283-8288
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00223263
Volume
60
Issue
25
Year of publication
1995
Pages
8283 - 8288
Database
ISI
SICI code
0022-3263(1995)60:25<8283:SOTAD>2.0.ZU;2-S
Abstract
The highly reactive o-quinonoid heterocycles thieno[3,4-b]quinoxaline (1a) and its 6,7-dimethyl derivative (1b) have been synthesized by a b ase-catalyzed Pummerer reaction and isolated in crystalline form. In c ontrast, the 1,3-dibromothieno[3,4-b]quinoxaline (8) could be characte rized in solution but not isolated in pure farm. The readily prepared 1,3-dihydrothieno[3,4-b]quinoxaline (5a) underwent a direct Knoevenage l condensation with thiophene-2-carboxaldehyde to give the stilbenoid 14a. Sulfide 5a was also converted in a two-step process to the stable 1,3-diformylthieno[3,4-b]quinoxaline 11a.