反应详情

To a solution of 4.8 g (17.4 mmol) l-biphenyl-3-yl-5-hydroxy-2-methylpyridin-4(1H)-one in 150 ml of DMF was added 4.1 g (26.1 mmol) PMBCl, and 12.0 g (87.0 mmol) K2CO3. The reaction was stirred at rt for 2 h, after which time water was added and a precipitate formed. The solid was collected by filtration and purified by flash chromatography (100 g silica gel, 0-20% MeOH;EtOAc) to afford 1-biphenyl-3-yl-5-[(4-methoxybenzyl)oxy]-2-methylpyridin-4(1H)-one.  H NM δ (ppm)(DMSO-d6): 7.84 (1H, d, J=7.86 Hz), 7.77 (2H, d, J=7.71 Hz), 7.73 (1H, s), 7.64 (1H, t, J=7.84 Hz), 7.53-7.47 (3H, m), 7.46-7.39 (2H, m), 7.38-7.30 (3H, m), 6.93 (2H, d, J=8.32 Hz), 6.23 (1H, s), 4.89 (2H, s), 3.77-3.70 (3H, m), 2.03 (3H, s). LCMS (M+H)+=398.3.

1. customa precipitate formed
2. filtrationThe solid was collected by filtration
3. custompurified by flash chromatography (100 g silica gel, 0-20% MeOH;EtOAc)