Title of article :
Unprecedented reactivity of 3-amino-1H,3H-quinoline-2,4-diones with urea: an efficient synthesis of 2,6-dihydro-imidazo[1,5-c]quinazoline-3,5-diones
Author/Authors :
Anton??n Kl?sek، نويسنده , , Kamil Ko?istek، نويسنده , , Anton??n Ly?ka، نويسنده , , Michal Holcapek، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2003
Abstract :
Substituted 3-amino-1H,3H-quinoline-2,4-diones react with urea in acetic acid to give novel 2,6-dihydro-imidazo[1,5-c]quinazoline-3,5-diones in high yields. The same compounds were obtained, albeit with small yields, from 3-chloro-1H,3H-quinoline-2,4-diones and urea. In the proposed reaction mechanism, a molecular rearrangement of the primarily formed mono-substituted urea takes place. The prepared 2,6-dihydro-imidazo[1,5-c]quinazoline-3,5-diones were characterized by their 1H, 13C, 15N NMR and IR spectra and atmospheric pressure chemical ionisation mass spectra.
Keywords :
urea derivatives , NMR , Reaction mechanism , ?-aminoketones , MS , molecular rearrangement
Journal title :
Tetrahedron
Journal title :
Tetrahedron