[C:1]([Cl:6])(=O)[C:2](Cl)=[O:3].[CH3:7][O:8][C:9]1[CH:19]=[CH:18][C:12]([CH2:13][NH:14][CH2:15][C:16]#[N:17])=[CH:11][CH:10]=1.[Cl:20]C1C=CC=CC=1>>[Cl:6][C:1]1[C:2](=[O:3])[N:14]([CH2:13][C:12]2[CH:18]=[CH:19][C:9]([O:8][CH3:7])=[CH:10][CH:11]=2)[CH:15]=[C:16]([Cl:20])[N:17]=1Oxalyl chloride (17.5 ml, 200 mmol) was added dropwise via a dropping funnel to a mixture of compound (7) (8.5 g, 48.2 mmol) in chlorobenzene (60 ml). The reaction was heated at about 90° C. for about 16 h. The solvent was removed. The resulting mixture was deposited onto silica gel and loaded onto a silica gel column and eluted with Hex/EtOAc (10:1) to afford 3,5-dichloro-1-(4-methoxybenzyl)pyrazin-2(1H)-one (4.0 g, 13.33 mmol, 27.6% yield).
読み込み中…