Kdi 792 → [(Z)-5-carboxy-l-pentenyl]-4-(4-chlorophenylsulfonylamino)-1-(3-pyridylmethyl)pyrrolidine hydrochloride
Reaktionsgleichung
Cl.[C:2]([CH2:5][CH2:6][CH2:7]/[CH:8]=[CH:9]\[C@@H:10]1[CH2:14][C@@H:13]([NH:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)(=[O:18])=[O:17])[CH2:12][N:11]1[CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)([OH:4])=[O:3]>Cl>[ClH:25].[C:2]([CH2:5][CH2:6][CH2:7]/[CH:8]=[CH:9]\[CH:10]1[CH2:14][CH:13]([NH:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)(=[O:17])=[O:18])[CH2:12][N:11]1[CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)([OH:4])=[O:3]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
In 1N-hydrochloric acid (44 ml)-purified water (16 ml) was dissolved crude crystal of (2S,4R)-2-[(Z)-5-carboxy-1-pentenyl]-4-(4-chlorophenylsulfonylamino)-1-(3-pyridylmethyl)pyrrolidine hydrochloride (8.0 g, 0.016 mol) followed by addition of activated carbon (0.8 g) and the mixture was stirred at 25° C. for 1 hour. Then, clarification-filtration was carried out using a 0.25μmembrane prefilter and the filtrate was washed with 1N-hydrochloric acid (4 ml)-purified water (8 ml). While the filtrate was stirred, 1N-aqueous sodium hydroxide solution was added dropwise so as to adjust the solution to pH 2.0 (pH prior to adjustment: 0.4). The mixture was stirred at 20°-25° C. for crystallization and ripening (about 1 hour, pH decreases to 1.51). Then, 1N-aqueous sodium hydroxide solution was added thereto dropwise so as to adjust the solution to pH 2.20. The solution was cooled to 5° C. and 1N aqueous sodium hydroxide solution was added thereto dropwise so as to maintain the solution at pH 2.20. The solution was cooled to 5° C. and 1N-aqueous sodium hydroxide solution was added thereto dropwise so as to maintain the solution at pH 2.20. The solution was then allowed to stand at 0°-5° C. overnight. The next morning the crystal was collected by filtration and washed with cold purified water (8 ml). The washed crystal was dried in vacuo overnight to provide pure crystal (6.77 g) of [(Z)-5-carboxy-l-pentenyl]-4-(4-chlorophenylsulfonylamino)-1-(3-pyridylmethyl)pyrrolidine hydrochloride.