Reaktionsgleichung
C([O:8][C:9](=[O:45])[CH2:10][C@H:11]([NH:34][C:35]([O:37][CH2:38][C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)=[O:36])[C:12]([NH:14][C:15]1[CH:20]=[C:19]([CH2:21][C:22]2[C:31]3[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=3)[C:25](=[O:32])[NH:24][N:23]=2)[CH:18]=[CH:17][C:16]=1[F:33])=[O:13])C1C=CC=CC=1.CC1C=CC(COC(NNC(C2C=NC=CN=2)=O)=O)=CC=1>C(=O)([O-])[O-].[Na+].[Na+]>[CH2:38]([O:37][C:35]([NH:34][C@H:11]([C:12]([NH:14][C:15]1[CH:20]=[C:19]([CH2:21][C:22]2[C:31]3[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=3)[C:25](=[O:32])[NH:24][N:23]=2)[CH:18]=[CH:17][C:16]=1[F:33])=[O:13])[CH2:10][C:9]([OH:45])=[O:8])=[O:36])[C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of the above crude (S)-3-benzyloxycarbonylamino-N-[2-fluoro-5-(4-oxo-3,4-dihydrophthalazin-1-ylmethyl)phenyl]succinamic acid benzyl ester (0.57 g) and saturated aqueous sodium carbonate solution (pH 9; 10 ml) was stirred at ambient temperature for 72 hours. The pH of the mixture was adjusted to pH10 by the addition of further saturated aqueous sodium carbonate solution, then the mixture was stirred at 70° C. for 4 hours until a clear solution was obtained. The cooled solution was washed with ethyl acetate (2×5 ml) and the aqueous layer was acidified by the addition of 10% hydrochloric acid. The resulting solid was collected by filtration and dried in vacuo to give (S)-3-benzyloxycarbonylamino-N-[2-fluoro-5-(4-oxo-3,4-dihydrophthalazin-1-ylmethyl)phenyl]succinamic acid (0.35 g) as an off-white solid, m.pt. 188–190° C., which was used without further purification.
Aufarbeitung
- stirringthe mixture was stirred at 70° C. for 4 hours until a clear solution
- customwas obtained
- washThe cooled solution was washed with ethyl acetate (2×5 ml)
- additionthe aqueous layer was acidified by the addition of 10% hydrochloric acid
- filtrationThe resulting solid was collected by filtration
- customdried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-65844b9017ad46ad93088862246c8dc2
- Quelldatensatz
- uspto-grants-2007_03
- Patentnummer
- US07196085B2
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