反应详情

6-Butyryl-7-chloro-3-methoxythieno[3,2-b]pyridine (1.5 g, 0.0056 mol) and 4-hydroxy-2-methylaniline (1.37 g, 0.011 mol) in anisole (30 ml) were heated under reflux in a nitrogen atmosphere for 36 hours. The solvent was evaporated under reduced pressure and the residue was partitioned between chloroform and sodium bicarbonate solution. The insoluble material was filtered off. The chloroform layer was washed with sodium bicarbonate solution (2×100 ml), dried over magnesium sulphate, filtered and evaporated to give a brown solid. The product was purified by flash chromatography using chloroform as eluant. The solid obtained was recrystallised from ethanol to give the title compound, 0.81 g, m.p. 255°-257°.

1. temperatureunder reflux in a nitrogen atmosphere for 36 hours
2. customThe solvent was evaporated under reduced pressure
3. customthe residue was partitioned between chloroform and sodium bicarbonate solution
4. filtrationThe insoluble material was filtered off
5. washThe chloroform layer was washed with sodium bicarbonate solution (2×100 ml)
6. dry with materialdried over magnesium sulphate
7. filtrationfiltered
8. customevaporated
9. customto give a brown solid
10. customThe product was purified by flash chromatography
11. customThe solid obtained
12. customwas recrystallised from ethanol