Hydrochloric Acid → (S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]-benzodiazepine-1-carboxylic acid
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[CH:12]=[N:13][C:14]([C:15]([O:17]CC)=[O:16])=[C:10]3[C@@H:9]3[CH2:20][CH2:21][N:8]3[C:7](=[O:22])[C:6]=2[CH:23]=1.[OH-].[Na+].Cl>C(O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[CH:12]=[N:13][C:14]([C:15]([OH:17])=[O:16])=[C:10]3[C@@H:9]3[CH2:20][CH2:21][N:8]3[C:7](=[O:22])[C:6]=2[CH:23]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
40.58 g (128.7 mmol) of ethyl (S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto-[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylate, 300 ml of ethanol and 32.5 ml (130 mmol) of 4N sodium hydroxide solution were heated to reflux on a steam bath for 1.5 hours. The alcohol was evaporated on a rotary evaporator. The aqueous phase was washed twice with methylene chloride and acidified to pH 3-4 with 32.5 ml (130 mmol) of 4N hydrochloric acid. The suspension obtained was cooled and filtered. The filter residue was washed with a small amount of ice water and dried. There were obtained 36.67 g (99%) of (S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acid of m.p. 159°-160°.
Aufarbeitung
- temperatureto reflux on a steam bath for 1.5 hours
- customThe alcohol was evaporated on a rotary evaporator
- washThe aqueous phase was washed twice with methylene chloride
- customThe suspension obtained
- temperaturewas cooled
- filtrationfiltered
- washThe filter residue was washed with a small amount of ice water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-cacbe54dc480410788994dc4e9189cab
- Quelldatensatz
- uspto-grants-1997_09
- Patentnummer
- US05665718
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