Trimethyl orthoformate → 4-Bromo-2-(1,1-dimethoxyethyl)-7-methoxyfuro[2,3-c]pyridine

反応式

[C:1]([C:4]1[O:15][C:7]2=[C:8]([O:13][CH3:14])[N:9]=[CH:10][C:11]([Br:12])=[C:6]2[CH:5]=1)(=[O:3])[CH3:2].[CH3:16][O:17]C(OC)OC.O.[C:24]1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[Br:12][C:11]1[CH:10]=[N:9][C:8]([O:13][CH3:14])=[C:7]2[O:15][C:4]([C:1]([O:17][CH3:16])([O:3][CH3:24])[CH3:2])=[CH:5][C:6]=12

参加物

実験手順

A solution of 2-acetyl-4-bromo-7-methoxyfuro[2,3-c]pyridine (1.4 g), trimethylorthoformate (1.1 g) and p-toluenesulfonic acid monohydrate (1.2 g) in dry methanol (50 ml) was heated at reflux for 3 h. The mixture was cooled and the methanol removed in vacuo. The residue was taken up in ethyl acetate (100 ml), washed with saturated sodium bicarbonate solution (50 ml) and brine (50 ml), dried over magnesium sulfate, filtered and the solvent removed in vacuo. Purification by column chromatography on silica eluting with 33% ethyl acetate in hexane gave the title compound (contaminated with 15% 2-acetyl-4-bromo-7-methoxyfuro[2,3-c]pyridine) as a white solid (1.0 g).