反应详情

Methanesulfonyl chloride (2.32 mL, 3.44 g, 33 mmol) was added dropwise to a stirred, cooled (0° C.) solution of crude 4-aminomethyl-1-t-butoxycarbonyl-4-phenylpiperidine (7.96 g) and pyridine (3.64 mL, 3.56 g, 45 mmol) in dichloromethane (100 mL) and the mixture was stirred at room temperature for 18 h. The solvent was evaporated under reduced pressure, aqueous sodium hydrogen carbonate (saturated, 100 mL) was added and the mixture was extracted with ethyl acetate (3×100 mL). The combined organic fractions were washed with aqueous citric acid (10%, 2×100 mL), aqueous sodium hydrogen carbonate (saturated, 100 mL) and brine (100 mL), dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with ethyl acetate/hexane (30:70 increasing to 80:20) to give the title compound as a colorless solid (5.65 g, 61% from 4-cyano-4-phenylpiperidine hydrochloride), δH (250 MHz, CDCl3) 7.46-7.26 (5H, m), 3.88 (1H, br t, J 6.7 Hz), 3.72 (2H, m), 3.23 (2H, br d, J 6.7 Hz), 3.13 (2H, m), 2.71 (3H, s), 2.21 (2H, m), 1.78 (2H, m), and 1.44 (9H, s).

1. customThe solvent was evaporated under reduced pressure, aqueous sodium hydrogen carbonate (saturated, 100 mL)
2. additionwas added
3. extractionthe mixture was extracted with ethyl acetate (3×100 mL)
4. washThe combined organic fractions were washed with aqueous citric acid (10%, 2×100 mL), aqueous sodium hydrogen carbonate (saturated, 100 mL) and brine (100 mL)
5. dry with materialdried (MgSO4)
6. customthe solvent was evaporated under reduced pressure
7. customThe residue was purified by flash column chromatography on silica gel
8. washeluting with ethyl acetate/hexane (30:70 increasing to 80:20)