反应详情

To a suspension of 0.10 g of 1-(2-(4-aminopiperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one hydrochloride in 2 mL of methanol, 0.14 g of a 28% sodium methoxide/methanol solution, 40 mg of 5-ethyl-4-methoxypyridine-2-carbaldehyde and 14 μL of acetic acid were added. Then, 30 mg of sodium cyanoborohydride was added thereto, and the mixture was stirred at room temperature for 5 hours. To the reaction mixture, chloroform and a saturated aqueous sodium hydrogen carbonate solution were added. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by basic silica gel column chromatography using gradient elution with chloroform:methanol=9:1 to 86:14 to obtain 51 mg of 1-(2-(4-(((5-ethyl-4-methoxypyridin-2-yl)methyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one as a yellow oily substance.

1. additionwere added
2. customThe organic layer was separated
3. washwashed with water
4. dry with materiala saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate
5. distillationthe solvent was distilled off under reduced pressure
6. customThe resultant residue was purified by basic silica gel column chromatography
7. washelution with chloroform