反应详情

Sodium hydride (0.096 g, 2.4 mmol, 60% by weight) is added to a solution of [2-oxopyrrolidin-3-(S)-yl-]-carbamic acid tert-butyl ester (0.4 g, 2 mmol) in 15 mL of THF at 0° C. The mixture is stirred for 30 minutes then a solution of 6-bromomethyl-4-chloroquinoline (0.513 g, 2 mmol) in 15 mL THF is added slowly. The resulting solution is warmed to room temperature over 4 hours. The reaction mixture is quenched with saturated ammonium chloride solution then diluted with EtOAc. The organic layer is separated, washed with brine, dried over Na2SO4, filtered and concentrated. The residue is dissolved in ethyl acetate (50 mL), and saturated with HCl gas at 0° C. The solution is stirred at 0° C. for 15 minutes, then the solution is warmed to room temperature. After four hours at room temperature, the solid that precipitates is collected, and washed with ether to give the title compound (0.445 g, 1.43 mmol) as a pale yellow solid.

1. customThe reaction mixture is quenched with saturated ammonium chloride solution
2. additionthen diluted with EtOAc
3. customThe organic layer is separated
4. washwashed with brine
5. dry with materialdried over Na2SO4
6. filtrationfiltered
7. concentrationconcentrated
8. dissolutionThe residue is dissolved in ethyl acetate (50 mL)
9. customat 0° C
10. stirringThe solution is stirred at 0° C. for 15 minutes
11. temperaturethe solution is warmed to room temperature
12. waitAfter four hours at room temperature
13. customthe solid that precipitates
14. customis collected
15. washwashed with ether