反应详情

To a solution of 2-amino-3-chloropyridine (6.51 g, 51 mmol) and 2-bromo-4′-fluoroacetophenone (13.0 g, 60 mmol) in ethanol (100 mL) was added sodium bicarbonate (4.91 g, 60 mmol) and the reaction mixture was heated at reflux for 6 hours. The resulting mixture was concentrated to a solid in vacuo. This residue was dissolved in ethyl acetate and the organic phase was washed with water and an aqueous sodium chloride solution. The organic phase was dried (magnesium sulfate), filtered through a silica gel pad and concentrated to give a solid. This solid was recrystallized from acetonitrile, to give 10.1 g (80%) 8-chloro-2-(4-fluorophenyl)imidazo[1,2-α]pyridine as a solid. 1H NMR (CDCl3): δ 8.06 (d, 1H), 7.96 (q, 2H), 7.86 (s, 1H), 7.25 (d, 1H), 7.13 (t, 2H), 6.73 (t, 1H); 19F NMR (CDCl3) δ −114.0; MS m/z 247 (M+1).

1. temperaturethe reaction mixture was heated
2. temperatureat reflux for 6 hours
3. concentrationThe resulting mixture was concentrated to a solid in vacuo
4. dissolutionThis residue was dissolved in ethyl acetate
5. washthe organic phase was washed with water
6. dry with materialThe organic phase was dried (magnesium sulfate)
7. filtrationfiltered through a silica gel pad
8. concentrationconcentrated
9. customto give a solid
10. customThis solid was recrystallized from acetonitrile