反应详情

温度

150 °C

To a stirred solution consisting of 1,3-dihydro-1-propylamino-2H-indol-2-one (5.06 g), phenol (13.2 g) and p-toluenesulfonic acid hydrate (0.25 g), heated at 150° C., was added 4-chloro-3-fluoropyridine hydrochloride (5.37 g). Heating was continued at 150° C. for 10.75 hours at which time additional 4-chloro-3-fluoropyridine (2.05 g) was added and heating continued an additional 6.5 hours. Upon cooling to room temperature, the reaction mixture was dissolved in dichloromethane and dilute aqueous sodium bicarbonate. The layers were separated and the organic layer extracted with dilute aqueous sodium bicarbonate (2×). The combined aqueous layers were back-extracted with dichloromethane and ether. The combined organic layers were washed with brine, dried (K2CO3), filtered, and concentrated. Purification via flash column chromatography (silica gel, 2% triethylamine/ether) and another column (silica gel, EtOAc) afforded the desired product as a solid.

1. temperatureHeating
2. additionwas added
3. temperatureheating
4. temperatureUpon cooling to room temperature
5. customThe layers were separated
6. extractionthe organic layer extracted with dilute aqueous sodium bicarbonate (2×)
7. extractionThe combined aqueous layers were back-extracted with dichloromethane and ether
8. washThe combined organic layers were washed with brine
9. dry with materialdried (K2CO3)
10. filtrationfiltered
11. concentrationconcentrated
12. customPurification via flash column chromatography (silica gel, 2% triethylamine/ether)