反应详情

温度

0 °C

Dihydro-2H-thiopyran-3(4H)-one (0.217 g, 1.86 mmol) was dissolved in dichloromethane (23 mL) in an oven dried flask containing 3 Å molecular sieves and stirred under argon at 0° C. TMS-OTf (0.414 g, 1.86 mmol, 0.33 mL) was added slowly to the mixture over 10 min. Ethyl 5-bromo-1H-indole-7-carboxylate (0.5 g, 1.86 mmol) was dissolved in DCM (7 mL) and added to the reaction via syringe pump over 2 hours, after which it was stirred for 3 hours between 0 and 10° C. The reaction was cooled to 0° C. and triethylsilane (0.325 g, 0.44 mL, 2.8 mmol) was added all at once and the reaction was stirred at room temperature for 18 hours. The reaction was then quenched with a saturated sodium bicarbonate solution and extracted with DCM. The combined organics were washed with water. The combined aqueous layers were back-extracted with DCM. The combined organics were washed with brine, dried with MgSO4, and concentrated. The crude compound was purified on a Combiflash silica column with 5-25% EA/Hexane to give 0.279 g (40%) of the title compound.

1. customdried flask
2. additioncontaining 3 Å molecular sieves
3. additionadded to the reaction via syringe pump over 2 hours
4. stirringafter which it was stirred for 3 hours between 0 and 10° C
5. temperatureThe reaction was cooled to 0° C.
6. stirringwas stirred at room temperature for 18 hours
7. customThe reaction was then quenched with a saturated sodium bicarbonate solution
8. extractionextracted with DCM
9. washThe combined organics were washed with water
10. extractionThe combined aqueous layers were back-extracted with DCM
11. washThe combined organics were washed with brine
12. dry with materialdried with MgSO4
13. concentrationconcentrated
14. customThe crude compound was purified on a Combiflash silica column with 5-25% EA/Hexane