反应详情

Add triethylamine (3.19 g, 31.56 mmol) to a solution of 2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-ol (2.0 g, 10.52 mmol) in tetrahydrofuran (50 ml) at 0° C. Slowly add 1.75 mL (22.09 mMol) methanesulfonyl chloride and allow the reaction to warm to room temperature. Quench the reaction with saturated aqueous sodium bicarbonate and extract into ethyl acetate. Combine the organic layers, wash sequentially with saturated aqueous ammonium chloride, water, and saturated aqueous sodium chloride, dry over magnesium sulfate, and concentrate under reduced pressure. Add sodium hydride (0.8416 g, 21.04 mmol, 60% dispersion in mineral oil) to the resulting oil in dimethylformamide (20 ml). Quench the reaction with saturated aqueous sodium bicarbonate, concentrate to about 10 ml and extract into ethyl acetate. Combine the organic layers, wash sequentially with saturated ammonium chloride, water, and saturated aqueous sodium chloride, dry over magnesium sulfate, and concentrate under reduced pressure. Purification by flash chromatography, eluting with ethyl acetate:hexane gradient gives the title compound as an off-white solid.

1. customthe reaction
2. customQuench
3. customthe reaction with saturated aqueous sodium bicarbonate
4. extractionextract into ethyl acetate
5. washwash sequentially with saturated aqueous ammonium chloride, water, and saturated aqueous sodium chloride
6. dry with materialdry over magnesium sulfate
7. concentrationconcentrate under reduced pressure
8. customQuench
9. customthe reaction with saturated aqueous sodium bicarbonate
10. concentrationconcentrate to about 10 ml
11. extractionextract into ethyl acetate
12. washwash sequentially with saturated ammonium chloride, water, and saturated aqueous sodium chloride
13. dry with materialdry over magnesium sulfate
14. concentrationconcentrate under reduced pressure
15. customPurification by flash chromatography
16. washeluting with ethyl acetate