反应详情

A solution of acetic acid 6,7-dimethyl-2-(2-morpholin-4-yl-acetyl)-benzofuran-5-yl ester (23 mg), prepared as in Example 17, in MeOH (10 mL) was stirred while sodium bicarbonate (10 mg) was added. Then the mixture was stirred at RT overnight, followed by evaporation to dryness. The residue was purified by silica gel column, eluting with 5% MeOH in dichloromethane to give 11 mg of 1-(5-hydroxy-6,7-dimethyl-benzofuran-2-yl)-2-morpholin-4-yl-ethanone as an oil. Conversion into HCl salt gave a yellow solid. 1H NMR (CD3OD, 300 MHz) δ:: 7.60 (s, 1H), 7.20 (s, 1H), 3.78(m, 6H), 2.64(m, 4H), 2.50(s, 3H), 2.40(s, 3H) ppm. 13C NMR (CDCl3, 75 MHz)δ: 187.98, 170.20, 153.31, 152.29, 146.58, 130.44, 124.53, 122.80, 114.36, 113.15, 64.69, 53.79, 21.28, 13.47, 12.86 ppm. M/S 290 (M+H+).

1. additionwas added
2. customfollowed by evaporation to dryness
3. customThe residue was purified by silica gel column
4. washeluting with 5% MeOH in dichloromethane