反应详情

温度

62.5 °C

To 3 mL of an N,N-dimethylformamide solution containing 0.12 g of 7-methoxy-4-methylquinolin-2(1H)-one, 28 mg of a 60% aqueous sodium hydride solution was added at 50° C., and the mixture was stirred at 60 to 65° C. for 30 minutes. Thereto was added 2 mL of an N,N-dimethylformamide solution containing 0.18 g of 2-(1,4-dioxaspiro[4.5]decan-8-yl)ethyl methanesulfonate at 50° C., and the mixture was stirred at 60 to 65° C. for 1 hour and 20 minutes. Thereto was added 14 mg of a 60% aqueous sodium hydride solution at the same temperature, and the mixture was stirred for 1 hour and 45 minutes. The reaction mixture was cooled to room temperature, and then water and ethyl acetate were then added thereto. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by flash silica gel column chromatography [hexane:gradient elution of ethyl acetate=40:60 to 30:70] to obtain 65 mg of a colorless oily substance, 1-(2-(1,4-dioxaspiro[4.5]decan-8-yl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-one.

1. additionwas added at 50° C.
2. stirringthe mixture was stirred at 60 to 65° C. for 1 hour and 20 minutes
3. stirringthe mixture was stirred for 1 hour and 45 minutes
4. temperatureThe reaction mixture was cooled to room temperature
5. customThe organic layer was separated
6. extractionthe aqueous layer was extracted with ethyl acetate
7. washthe resultant solution was washed with an aqueous saturated sodium chloride solution
8. dry with materialdried over anhydrous magnesium sulfate
9. customthe solvent was removed under reduced pressure
10. customThe residue thus obtained
11. customwas purified by flash silica gel column chromatography [hexane:gradient elution of ethyl acetate=40:60 to 30:70]