反应详情

To a suspension of 5-chloro-1H-pyrrolo[3,2-b]pyridine (20. g, 130 mmol, Adesis) in DCM (200 mL) was added benzenesulfonyl chloride (20. mL, 160 mmol, Aldrich), triethylamine (27 mL, 200 mmol) and 4-dimethylaminopyridine (0.80 g, 6.6 mmol, Aldrich). The reaction mixture was stirred overnight. Water was added and the mixture was stirred for 4 h. Layers were separated and the organic phase was washed sequentially with 1 N HCl, water, saturated solution of NaHCO3, and brine. The organic layer was dried over sodium sulfate, filtered and concentrated to give an orange solid, which was triturated with MeOH (100 mL). The solid was filtered, washed with MeOH, and dried at 40° C. under high vacuum overnight. Additional product was obtained by flash chromatography of the filtrate (eluting with a gradient from 0-60% EtOAc in hexanes). Yield: (26.8 g, 95%).

1. stirringthe mixture was stirred for 4 h
2. customLayers were separated
3. washthe organic phase was washed sequentially with 1 N HCl, water, saturated solution of NaHCO3, and brine
4. dry with materialThe organic layer was dried over sodium sulfate
5. filtrationfiltered
6. concentrationconcentrated
7. customto give an orange solid, which
8. customwas triturated with MeOH (100 mL)
9. filtrationThe solid was filtered
10. washwashed with MeOH
11. customdried at 40° C. under high vacuum overnight
12. customAdditional product was obtained by flash chromatography of the filtrate (
13. washeluting with a gradient from 0-60% EtOAc in hexanes)