反应详情

Triphenylphosphonium bromide (6.52 g) was added to an acetonitrile solution of (S)-4-[(S)-1-(2,6-difluoropyridin-3-yl)ethyl]-2-hydroxy-6-methylmorpholin-3-one (4.3 g). The resulting reaction solution was heated under reflux for 1 hr, and triethylamine (5.28 mL) and 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde (3.42 g) were added thereto. The resulting reaction solution was heated under reflux for 1.5 hr and concentrated under reduced pressure. The residue was diluted with a 2 N hydrochloric acid aqueous solution and ethyl acetate. The water layer was separated, and the organic layer was washed with a 2 N hydrochloric acid aqueous solution. All the water layers were combined and alkalinized with a concentrated sodium hydroxide aqueous solution. The alkaline aqueous solution was extracted with ethyl acetate. The organic layer was separated, washed with saturated sodium hydrogencarbonate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: Chromatorex NH, eluting solvent; heptane:ethyl acetate=1:1 to 0:1) to give 4.06 g of the title compound. The physical property values of this compound were as follows:

1. customThe resulting reaction solution
2. temperaturewas heated
3. temperatureunder reflux for 1 hr
4. customThe resulting reaction solution
5. temperaturewas heated
6. temperatureunder reflux for 1.5 hr
7. concentrationconcentrated under reduced pressure
8. additionThe residue was diluted with a 2 N hydrochloric acid aqueous solution and ethyl acetate
9. customThe water layer was separated
10. washthe organic layer was washed with a 2 N hydrochloric acid aqueous solution
11. extractionThe alkaline aqueous solution was extracted with ethyl acetate
12. customThe organic layer was separated
13. washwashed with saturated sodium hydrogencarbonate
14. dry with materialdried over anhydrous magnesium sulfate
15. concentrationconcentrated under reduced pressure
16. customThe residue was purified by silica gel column chromatography (carrier: Chromatorex NH, eluting solvent; heptane:ethyl acetate=1:1 to 0:1)