反应详情

To a solution of 1.1 g (2.76 mmol) of 2-(((1S,2R)-2-(3-chlorophenyl)-1-(4-chlorophenyl)but-3-enylamino)methyl)phenol (Example 115, Step B) and triethylamine (0.85 mL, 6.08 mmol) in a mixture of THF (5.0 mL) and DCM (5.0 mL) was added acetic anhydride (0.55 mL, 5.80 mmol) at 0° C. The temperature of the reaction was slowly allowed to rise to room temperature and the mixture was stirred at ambient temperature overnight. When LCMS indicated completion of the reaction, 100 ml of ethyl acetate was added and the combined organics were washed consecutively with water (30 ml), citric acid (30 ml, 1M), NaHCO3 solution (30 ml) and sat. NaCl solution (30 ml), dried over MgSO4, filtered and the filtrate was concentrated to give the title compound. The crude product was used without further purification.

1. customto rise to room temperature
2. additionwas added
3. washthe combined organics were washed consecutively with water (30 ml), citric acid (30 ml, 1M), NaHCO3 solution (30 ml) and sat. NaCl solution (30 ml)
4. dry with materialdried over MgSO4
5. filtrationfiltered
6. concentrationthe filtrate was concentrated