Isothiazoles. Part X. New 3-substituted-2-arylpropenamidines by base catalyzed ring opening of 3-amino-4-arylisothiazole 1,1-dioxides.

Citation
Em. Beccalli et al., Isothiazoles. Part X. New 3-substituted-2-arylpropenamidines by base catalyzed ring opening of 3-amino-4-arylisothiazole 1,1-dioxides., TETRAHEDRON, 55(52), 1999, pp. 14975-14984
Citations number
12
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
55
Issue
52
Year of publication
1999
Pages
14975 - 14984
Database
ISI
SICI code
0040-4020(199912)55:52<14975:IPXN3B>2.0.ZU;2-B
Abstract
Starting from 5-unsubstituted or 5-alkyl-, aryl-, heteroarylsubstituted 3-d iethylamino-4-arylisothiazole 1,1-dioxides by base induced ring opening 3-a lkoxypropenamidines were synthesized in excellent yields in a mild and effi cient way. When 5-bromo-3-diethylamino-4-arylisothiazole 1,1-dioxide was us ed as the reagent, 3,3-dialkoxy-propenamidines, a new class of unsaturated amidines, were obtained. By using Grignard reagents 3-substituted acrylamid ines can be produced. (C) 1999 Elsevier Science Ltd. All rights reserved.