反应详情

3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(methyl)amino]cyclopropyl]-1-[1-(S)-phenylethyl]pyrrolidin-2-one (7.53 g, 21.0 mmol) was dissolved in anhydrous tetrahydrofuran (70 ml) and a 1.0M borane-tetrahydrofuran complex/tetrahydrofuran solution (63.0 ml, 63.0 mmol) was added dropwise gradually thereto while stirring and cooling with ice. After completion of dripping, it was stirred at room temperature for 20 hours. After slowly adding an aqueous solution (72 ml) of potassium carbonate (7.22 g) while cooling with ice, it was heated under reflux for 1.5 hours. After letting the reaction solution cool to room temperature, water (150 ml) was added, extraction with ethyl acetate (200 ml×2) was performed, and then the combined organic layer was washed with saturated saline solution (200 ml) and then dried over anhydrous sodium sulfate. After filtering, the filtrate was concentrated under a reduced pressure, the concentrate was applied to a silica gel chromatography, and 7.19 g (99%) of the title compound was obtained in the form of a colorless syrup from a chloroform:methanol=50:1 eluate.

1. temperaturecooling with ice
2. stirringit was stirred at room temperature for 20 hours
3. temperaturewhile cooling with ice, it
4. temperaturewas heated
5. temperatureunder reflux for 1.5 hours
6. extractionextraction with ethyl acetate (200 ml×2)
7. washthe combined organic layer was washed with saturated saline solution (200 ml)
8. dry with materialdried over anhydrous sodium sulfate
9. filtrationAfter filtering
10. concentrationthe filtrate was concentrated under a reduced pressure