A new tautomeric zwitterion form of 2-acylamino-4H-1,3,4-oxadiazino[5,6-b]quinoxalines in solution

Citation
Y. Kurasawa et al., A new tautomeric zwitterion form of 2-acylamino-4H-1,3,4-oxadiazino[5,6-b]quinoxalines in solution, J HETERO CH, 35(6), 1998, pp. 1333-1338
Citations number
6
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF HETEROCYCLIC CHEMISTRY
ISSN journal
0022152X → ACNP
Volume
35
Issue
6
Year of publication
1998
Pages
1333 - 1338
Database
ISI
SICI code
0022-152X(199811/12)35:6<1333:ANTZFO>2.0.ZU;2-T
Abstract
The reaction of 2-acylamino-8-chloro-4-methyl-4H-1,3,4-oxadiazino[5,6-b]qui noxalines 2a-d with methyl iodide/base gave the 8-chloro-4,10-dimethyl-4H-1 ,3,4-oxadiazino[5,6-b]quinoxaline-10-ium-2-acylamidates 4a-d, respectively. Comparison of the nmr spectral data between compounds 2a-d and 4a-d in deu teriodimethyl sulfoxide or in deuteriotrifluoroacetic acid established that compounds 2a-d existed as the zwitterionic tautomers 2'a-d in solution.