反应详情

To an ice-cooled solution of 1.30 g (1.90 mmol) of (5R,6S)-3-allyl-1-((S)-1-(tert-butyldiphenylsilyloxy)butan-2-yl)-5-(3-chlorophenyl)-6-(5-chloropyridin-2-yl)-3-methylpiperidin-2-one (Example 121, Step K) in THF (55 mL) was added 11.37 mL (11.37 mmol) of a 1 M solution of TBAF in THF. The orange solution was warmed to room temperature and stirred for 3.75 h. The reaction was partitioned between 1 M HCl and EtOAc (2×), and then the combined organic layers were washed with water (2×). The organic layer was dried over Na2SO4, filtered and the filtrate was concentrated. Purification of the residue by flash chromatography on silica gel (0 to 10% MeOH/DCM, gradient elution) provided the title compound as a light yellow solid.

1. customThe reaction was partitioned between 1 M HCl and EtOAc (2×)
2. washthe combined organic layers were washed with water (2×)
3. dry with materialThe organic layer was dried over Na2SO4
4. filtrationfiltered
5. concentrationthe filtrate was concentrated
6. customPurification of the residue by flash chromatography on silica gel (0 to 10% MeOH/DCM, gradient elution)