反应详情

The crude 4-(tetrahydropyranyloxy)methyl-2'-(methoxycarbonyl)amino-1,1'-biphenyl (250 mg) dissolved in 4 mL of methanol was treated with 1 mL of 10% methanolic p-toluenesulfonic acid. The reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was made basic by the addition of saturated aqueous sodium bicarbonate, then diluted with ethyl acetate. The organic layer was washed with water (2×), dried over magnesium sulfate and evaporated under vacuum. The residue was purified by preparative thin layer chromatography on silica gel, eluting with methylene chloride/methanol (100:3) to give 137 mg of the product. FAB-MS (Li+ spike): calculated for C15H15NO3 (257); found 264 (M+Li). 1H NMR (200 MHz,CDCl3): δ3.51 (s, 3H), 4.75 (s, 2H), 6.62 (br s, 11H), 7.14 (dd, 2H), 7.34 (dd, 1H), 7.4 (dd, 4H).

1. washThe organic layer was washed with water (2×)
2. dry with materialdried over magnesium sulfate
3. customevaporated under vacuum
4. customThe residue was purified by preparative thin layer chromatography on silica gel
5. washeluting with methylene chloride/methanol (100:3)