反应详情

温度

0 °C

To a suspension of 3-bromo-7-iodo-5H-chromeno[2,3-b]pyridin-5-one (20.00 g, 49.8 mmol) and trimethylsulfonium iodide (11.17 g, 54.7 mmol) in 250 mL DMSO under nitrogen atmosphere was added lithium tert-butoxide [1N in heptane (54.7 mL, 54.7 mmol)] drop wise over 40 minutes. After stirring for an additional 30 minutes, trimethylsilylazide (13.21 mL, 100 mmol) was added. After stirring for an additional hour, the reaction mixture was concentrated under reduced pressure. The remaining solution was diluted with water. The resulting solid was filtered off and washed with water. The solid was dissolved in 2-MeTHF, dried over MgSO4 and concentrated. The crude residue was dissolved in 200 mL THF, cooled to 0° C. and treated with LAH (1.888 g, 49.8 mmol). After stirring for 30 minutes, the cooling bath was removed, and the reaction mixture was allowed to stir for an additional 30 minutes. The reaction mixture was then cooled to 0° C. and quenched with sodium sulfate decahydrate (32.1 g, 100 mmol). The reaction mixture was vigorously stirred for one hour, filtered through a plug of celite and concentrated. Purification of the crude residue by column chromatography [0-80% (95:5 EtOAc/MeOH)/DCM] gave (5-amino-3-bromo-7-iodo-5H-chromeno[2,3-b]pyridin-5-yl)methanol (8.80 g, 20.32 mmol, 40.8% yield).

1. stirringAfter stirring for an additional hour
2. concentrationthe reaction mixture was concentrated under reduced pressure
3. additionThe remaining solution was diluted with water
4. filtrationThe resulting solid was filtered off
5. washwashed with water
6. dissolutionThe solid was dissolved in 2-MeTHF
7. dry with materialdried over MgSO4
8. concentrationconcentrated
9. dissolutionThe crude residue was dissolved in 200 mL THF
10. stirringAfter stirring for 30 minutes
11. customthe cooling bath was removed
12. stirringto stir for an additional 30 minutes
13. temperatureThe reaction mixture was then cooled to 0° C.
14. stirringThe reaction mixture was vigorously stirred for one hour
15. filtrationfiltered through a plug of celite and
16. concentrationconcentrated
17. customPurification of the crude residue by column chromatography [0-80% (95:5 EtOAc/MeOH)/DCM]