反应详情

A solution of 2-(4-aminophenyl)-6-methoxy-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinoline (0.205 g, 0.46 mmol) and TEA (0.060 g, 0.6 mmol) in 1 mL of CH2Cl2 at 0° C. was treated with acetyl chloride (0.043 g, 0.55 mmol). The reaction mixture was warmed to room temperature and stirred for 3 hours. The reaction was quenched by the addition of saturated aqueous NaHCO3 (0.5 mL). The organic layer was separated and the aqueous layer was extracted with CH2Cl2 (3×2 mL). The combined organic layer was dried over MgSO4, then concentrated. The crude product was purified by column chromatography to provide the title compound (0.195 g, 87% yield). ES-MS, (m/z) 493 [M+H]+.

1. customThe reaction was quenched by the addition of saturated aqueous NaHCO3 (0.5 mL)
2. customThe organic layer was separated
3. extractionthe aqueous layer was extracted with CH2Cl2 (3×2 mL)
4. dry with materialThe combined organic layer was dried over MgSO4
5. concentrationconcentrated
6. customThe crude product was purified by column chromatography