反应详情

A suspension of 6-fluoro-2-(2-methoxyphenyl)-3H-quinazolin-4-one (14.0 g, 52 mmol), N,N-dimethylaniline (6.6 mL, 52 mmol), and phosphorus oxychloride (4.8 mL, 52 mmol) in benzene (100 mL) was heated at reflux until a clear, dark solution was obtained (1 hour). The reaction mixture was cooled to room temperature, and the volume was reduced under reduced pressure. The black, oily residue was poured into 300 g of ice. Dichloromethane (600 mL) was added with vigorous stirring, and the temperature was kept below 5° C. at all times. The pH was monitored, and aqueous 1 N sodium hydroxide was added until the pH was 10-11. The mixture was stirred for one hour at a temperature below 5° C., and the pH was kept between 10-11 by addition of 1 N aqueous sodium hydroxide. The layers were separated, and the organic layer was washed with ice-cold 1 N aqueous sodium hydroxide (2×200 mL). Heptanes (300 mL) were added to the organic layer. This mixture was filtered through a short plug of silica gel and eluted with dichloromethane/heptanes (2:1). All fractions containing product were combined and evaporated to dryness. The residue was triturated with heptanes to yield 4-chloro-6-fluoro-2-(2-methoxyphenyl)-quinazoline (11.5 g, 76%) as a white solid.

1. temperaturewas heated
2. temperatureat reflux until a clear, dark solution
3. customwas obtained (1 hour)
4. customwas kept below 5° C. at all times
5. customThe layers were separated
6. washthe organic layer was washed with ice-cold 1 N aqueous sodium hydroxide (2×200 mL)
7. additionHeptanes (300 mL) were added to the organic layer
8. filtrationThis mixture was filtered through a short plug of silica gel
9. washeluted with dichloromethane/heptanes (2:1)
10. additionAll fractions containing product
11. customevaporated to dryness
12. customThe residue was triturated with heptanes