AMINOAMIDINES .5. SYNTHESIS AND ACETYLATION OF N,N1,N2-TRIARYL-SUBSTITUTED BETA-AMINOAMIDINES

Authors
KORSHIN EE ZAKHAROVA LG LEVIN YA ASHRAFULLINA LK PODVALNYI EA EFREMOV YY
Citation
Ee. Korshin et al., AMINOAMIDINES .5. SYNTHESIS AND ACETYLATION OF N,N1,N2-TRIARYL-SUBSTITUTED BETA-AMINOAMIDINES, Bulletin of the Russian Academy of Sciences, Division of Chemical Sciences, 41(11), 1992, pp. 2082-2090
Citations number
13
Categorie Soggetti
Chemistry
Journal title
Bulletin of the Russian Academy of Sciences, Division of Chemical Sciences → ACNP
ISSN journal
10635211
Volume
41
Issue
11
Year of publication
1992
Part
2
Pages
2082 - 2090
Database
ISI
SICI code
1063-5211(1992)41:11<2082:A.SAAO>2.0.ZU;2-9
Abstract
Triaryl-substituted beta-aminoamidines were obtained by the reaction o f alpha,beta-unsaturated N-arylimidoyl chlorides with arylamines. Acyl ation of the products gave the products from monosubstitution at the b eta-amino group. Triaryl-substituted beta-aminomidines react with phos gene and with oxalyl chloride to form 4-aryliminoperhydropyrimidin-2-o nes and 5-aryliminoperhydro-1,4-diazepine-2,3-diones, respectively.