Potassium Hydroxide → 4-((2-Carboxy-2-(1,3-dithiol-2-ylidene)acetyl)amino)-5-(dipropylamino)-5-oxopentanoic acid
Reaktionsgleichung
[CH2:1]([N:4]([CH2:27][CH2:28][CH3:29])[C:5](=[O:26])[CH:6]([NH:13][C:14](=[O:25])[C:15](=[C:20]1[S:24][CH:23]=[CH:22][S:21]1)[C:16]([O:18]C)=[O:17])[CH2:7][CH2:8][C:9]([O:11]C)=[O:10])[CH2:2][CH3:3].[OH-].[K+]>CO>[C:16]([C:15](=[C:20]1[S:21][CH:22]=[CH:23][S:24]1)[C:14]([NH:13][CH:6]([C:5]([N:4]([CH2:27][CH2:28][CH3:29])[CH2:1][CH2:2][CH3:3])=[O:26])[CH2:7][CH2:8][C:9]([OH:11])=[O:10])=[O:25])([OH:18])=[O:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Methyl 5-(dipropylamino)-4-((2-(1,3-dithiol-2-ylidene)-3-methoxy-3-oxopropanoyl)amino)-5-oxopentanoate (5) (111 g) was dissolved in methanol (1 l), followed by the addition of 2.5 N potassium hydroxide solution (300 ml). The resulting mixture was heated under reflux for 2 hours. The solvent was removed under reduced pressure. The resulting residue was washed several times with water, whereby 4-((2-carboxy-2-(1,3-dithiol-2-ylidene)acetyl)amino)-5-(dipropylamino)-5-oxopentanoic acid (6) was obtained as a waxy substance. Without purification, the reaction product was provided for use in the next example.
Aufarbeitung
- temperatureThe resulting mixture was heated
- temperatureunder reflux for 2 hours
- customThe solvent was removed under reduced pressure
- washThe resulting residue was washed several times with water
Quellen und Nachweise
- ORD-Eintrag
- ord-498b1fea42174e4b90db5c8457e451b2
- Quelldatensatz
- uspto-grants-1999_10
- Patentnummer
- US05962509
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