反应详情

To a solution of 0.319 g (2.000 mmol) of 4,5,6,7-tetrahydrofuro[2,3-c]pyridine hydrochloride, 0.493 g (2.2 mmol) of (E)-2,3-diphenylpropenoic acid and 1.1 ml (8.0 mmol) of triethylamine in 30 ml of dichloromethane, 0.489 g (3.0 mmol) of diethyl cyanophosphonate was added dropwise under ice-cooling, followed by overnight stirring at room temperature. After the solvent was distilled off, water was added, followed by 2 extractions with ethyl acetate. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was dissolved in 10 ml of acetic acid; 0.270 ml (3.00 mmol) of 50% aqueous dimethylamine and 0.245 ml (3.00 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 120 minutes. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with 5% aqueous sodium hydrogen carbonate and extracted with ethyl acetate 2 times. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate/methanol=5/1) to yield the desired product.

1. temperaturecooling
2. distillationAfter the solvent was distilled off
3. additionwater was added
4. extractionfollowed by 2 extractions with ethyl acetate
5. washThe combined organic layer was washed with water
6. dry with materialdried over anhydrous sodium sulfate
7. distillationthe solvent was distilled off under reduced pressure
8. dissolutionThe resulting crude product was dissolved in 10 ml of acetic acid
9. stirringby stirring at 100° C. for 120 minutes
10. distillationAfter the solvent was distilled off under reduced pressure
11. extractionextracted with ethyl acetate 2 times
12. washThe combined organic layer was washed with water
13. dry with materialdried over anhydrous sodium sulfate
14. distillationthe solvent was distilled off under reduced pressure
15. customThe resulting crude product was purified by silica gel column chromatography (ethyl acetate/methanol=5/1)