反应详情

To N-(4-piperidinyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzooxepine-4-carboxamide (0.15 g) and cyclononene-1-carbaldehyde (0.085 g) dissolved in 1,2-dichloroethane (10 ml) was added under ice cooling sodium triacetoxyborohydride (0.12 g), and the resulting mixture was stirred at room temperature overnight under a nitrogen atmosphere. The reaction mixture was evaporated to remove the solvent, was neutralized with a 1 N aqueous solution of sodium hydroxide, was then concentrated and was extracted with ethyl acetate. The organic layer was washed with water and an aqueous saturated solution of sodium chloride, and was then dried with anhydrous magnesium sulfate. The resulting organic layer was evaporated under reduced pressure to remove the solvent. The residue was subjected to purification using a silica gel column (ethyl acetate) to obtain crude crystals. The crude crystals were recrystallized from ethyl acetate/hexane to obtain N-(1-(cyclononen-1-yl)methylpiperidin-4-yl)-7-(4-methylphenyl)-2,3-dihydro-1-benzooxepine-4-carboxamide (compound 59) (0.08 g) as colorless prisms.

1. additionwas added under ice
2. customThe reaction mixture was evaporated
3. customto remove the solvent
4. concentrationwas then concentrated
5. extractionwas extracted with ethyl acetate
6. washThe organic layer was washed with water
7. dry with materialan aqueous saturated solution of sodium chloride, and was then dried with anhydrous magnesium sulfate
8. customThe resulting organic layer was evaporated under reduced pressure
9. customto remove the solvent
10. customThe residue was subjected to purification
11. customto obtain crude crystals
12. customThe crude crystals were recrystallized from ethyl acetate/hexane