反应详情

2-Methylthio-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)pyrimidine from Reference Example 3 was reacted with 2,4-dichlorobenzyl alcohol according to the procedure described in Example 59 to afford 2-(2,4-dichlorobenzyloxy)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine (HRf): HPLC/MS: m/e=509 (M++1); Rt=5.07 min; 1H-NMR 400 MHz (CDCl3): δ 5.60 (s, 2H), 7.04 (d, J=9 Hz, 2H), 7.21 (m, 6H), 7.38-7.42 (m, 1H), 7.60 (d, J=9 Hz, 1H), 8.60 (s, 1H).