Reaktionsgleichung
[S:1]([CH:5]([N:9]1[CH:13]=[CH:12][CH:11]=[CH:10]1)[C:6](Cl)=[O:7])([OH:4])(=[O:3])=[O:2].[C:14]([O:17][CH2:18][C:19]1[CH2:26][S:25][CH:24]2[N:21]([C:22](=[O:28])[CH:23]2[NH2:27])[C:20]=1[C:29]([OH:31])=[O:30])(=[O:16])[CH3:15].C(=O)(O)[O-].[Na+]>CCOCC.O>[C:14]([O:17][CH2:18][C:19]1[CH2:26][S:25][CH:24]2[N:21]([C:22](=[O:28])[CH:23]2[NH:27][C:6](=[O:7])[CH:5]([S:1]([OH:4])(=[O:3])=[O:2])[N:9]2[CH:13]=[CH:12][CH:11]=[CH:10]2)[C:20]=1[C:29]([OH:31])=[O:30])(=[O:16])[CH3:15]Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 2-sulfo-2-(1-pyrryl)acetyl chloride (1 equivalent) in ether is added to 3-[(acetyloxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylic acid (1 equivalent) and sodium bicarbonate (about 3 equivalents) in water at about 0° C. After about 30 minutes the phases are separated, the pH adjusted to about 6.5 and the aqueous phase extracted with ethyl acetate. The ethyl acetate is dried over megnesium sulfate, filtered and evaporated to give the title compound.
Aufarbeitung
- customAfter about 30 minutes the phases are separated
- extractionthe aqueous phase extracted with ethyl acetate
- dry with materialThe ethyl acetate is dried over megnesium sulfate
- filtrationfiltered
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-dad01d312966486fa7e7e8963f0579b3
- Quelldatensatz
- uspto-grants-1979_04
- Patentnummer
- US04148998
Verknüpfte Notizen
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