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
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.