反应详情

A flask was charged with 2-chloro-4-fluoropyridine (20 g, 152 mmol), tert-butyl carbamate (89 g, 760 mmol), tris(dibenzylideneacetone)dipalladium (1.39 g, 1.52 mmol), X-PHOS (1.48 g, 3.10 mmol), cesium carbonate (99 g, 588 mmol), and tetrahydrofuran (500 mL) under an atmosphere of dry nitrogen. This mixture was refluxed under nitrogen for 7 hours. An additional equivalent of cesium carbonate was added to drive reaction to completion. The mixture was cooled to ambient temperature and filtered through Celite, and the Celite was washed with ethyl acetate. The filtrate was partitioned between saturated sodium bicarbonate and ethyl acetate. The aqueous layer was washed with ethyl acetate twice. The combined organics were washed with brine and dried with sodium sulfate, concentrated under vacuum, and purified by column chromatography to give tert-butyl 4-fluoropyridin-2-ylcarbamate as a pale yellow solid (22.6 g).

1. temperatureThis mixture was refluxed under nitrogen for 7 hours
2. customreaction to completion
3. filtrationfiltered through Celite
4. washthe Celite was washed with ethyl acetate
5. customThe filtrate was partitioned between saturated sodium bicarbonate and ethyl acetate
6. washThe aqueous layer was washed with ethyl acetate twice
7. washThe combined organics were washed with brine
8. dry with materialdried with sodium sulfate
9. concentrationconcentrated under vacuum
10. custompurified by column chromatography