反应详情

4-(S)-(1-Ethoxycarbonylcyclopropyl)-3-(S)-fluoro-1-[1-(S)-phenylethyl]-2-pyrrolidinthione (6.49 g, 19.35 mmol) was dissolved in dry tetrahydrofuran (150 ml). After adding Raney nickel catalyst (15 ml), the mixture was stirred at room temperature for 30 minutes. After eliminating the catalyst by filtering through celite (washed with tetrahydrofuran), the filtrate was concentrated under reduced pressure. The residue was dissolved in diethyl ether (200 ml) and the thus obtained solution was washed with a 10% aqueous solution of ammonia (200 ml×2) and a saturated aqueous solution of sodium chloride (150 ml) and dried over anhydrous sodium sulfate. After filtering, the filtrate was concentrated under reduced pressure to obtian 5.08 g (86.0%) of the title compound as a colorless oily substance.

1. filtrationby filtering through celite (washed with tetrahydrofuran)
2. concentrationthe filtrate was concentrated under reduced pressure
3. dissolutionThe residue was dissolved in diethyl ether (200 ml)
4. washthe thus obtained solution was washed with a 10% aqueous solution of ammonia (200 ml×2)
5. dry with materiala saturated aqueous solution of sodium chloride (150 ml) and dried over anhydrous sodium sulfate
6. filtrationAfter filtering
7. concentrationthe filtrate was concentrated under reduced pressure to obtian 5.08 g (86.0%) of the title compound as a colorless oily substance