反应详情

温度

100 °C

A vial was charged with (R)-2′-bromo-7′-(neopentyloxy)-5H-spiro[oxazole-4,9′-xanthen]-2-amine (0.050 g, 0.120 mmol), tetrakis(triphenylphosphine)palladium (0) (0.014 g, 0.012 mmol), 2-(tributylstannyl)pyridine (0.132 g, 0.359 mmol), and dioxane (0.6 mL). The reaction was stirred overnight at 100° C. The mixture was diluted with DMSO and filtered through a syringe filter, which was flushed with additional DMSO. The material was purified via Gilson HPLC (10-90% MeCN:H2O). The clean product fractions were partitioned between DCM and saturated sodium bicarbonate solution. The aqueous layer was extracted with DCM, and the combined organic layers were dried with sodium sulfate, filtered, and concentrated to afford (S)-2′-(neopentyloxy)-7′-(pyridin-2-yl)-5H-spiro[oxazole-4,9′-xanthen]-2-amine as a white solid. MS MH+ 416.4

1. filtrationfiltered through a syringe
2. filtrationfilter
3. customwhich was flushed with additional DMSO
4. customThe material was purified via Gilson HPLC (10-90% MeCN:H2O)
5. customThe clean product fractions were partitioned between DCM and saturated sodium bicarbonate solution
6. extractionThe aqueous layer was extracted with DCM
7. dry with materialthe combined organic layers were dried with sodium sulfate
8. filtrationfiltered
9. concentrationconcentrated