反应详情

Two grams of methyl 4-(3-ethoxymethylene-5,5-dicyanopent-4-en-1-yl)benzoate, 0.93 g of 2,4-diamino-6(1H)-pyrimidone, and 30 mL of acetic acid are heated at reflux with stirring for 4 hours. The reaction mixture is allowed to cool to room temperature and the solid which forms is collected by filtration, washed with water and diethyl ether and dried to yield methyl 4-[2-(2-amino-4-hydroxypyrido[2,3-d]pyrimidin-6-yl)ethyl]benzoate, m.p.>300° C; IR (KBr) vmax 3220, 2950, 1720, 1657, 1626, 1610, 1455, 1280, 1251, 1148, 1109, and 834 cm-1 ; 1H NMR (dTFA, d6DMSO) delta 8.38 (s 1H (7)-H), 7.99 (s, 1H, (5)-H), 7.55 (d, J=8.0 Hz, 2H, Ar), 6.87 (s, 1H (3)-H), 6.82 (d, J=8.0 Hz, 2H, Ar), 3.56 (s, 3H, --CH3), 2.77-281 (m, 2H, (6)-CH2 --), 2.67-2.73 (m, 2H, benzyl).

1. temperatureat reflux
2. filtrationthe solid which forms is collected by filtration
3. washwashed with water and diethyl ether
4. customdried