HCID 15224911, Verbindung → HCID 131718730, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:32]=[CH:31][C:5]2[O:6][C:7]3[CH:30]=[CH:29][CH:28]=[CH:27][C:8]=3[CH2:9][N:10]([C:11]([N:13]3[CH2:18][CH2:17][N:16]([C:19]([C:21]4[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=4)=[O:20])[CH2:15][CH2:14]3)=[O:12])[C:4]=2[CH:3]=1.Cl.O1CCOCC1>CO>[ClH:1].[Cl:1][C:2]1[CH:32]=[CH:31][C:5]2[O:6][C:7]3[CH:30]=[CH:29][CH:28]=[CH:27][C:8]=3[CH2:9][N:10]([C:11]([N:13]3[CH2:14][CH2:15][N:16]([C:19]([C:21]4[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=4)=[O:20])[CH2:17][CH2:18]3)=[O:12])[C:4]=2[CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The title product of Example 28 was dissolved in 10 mL of MeOH. Excess 6.9N HCl/dioxane was added to the solution. After stirring this solution for 30 minutes, all solvent was removed under reduced pressure. The residue was dissolved in water/MeOH and lyophilized to produce 0.11 g of the title product as a granular white solid.
Aufarbeitung
- customall solvent was removed under reduced pressure
- dissolutionThe residue was dissolved in water/MeOH
Quellen und Nachweise
- ORD-Eintrag
- ord-309046011f054db29182a04d8efcc9c3
- Quelldatensatz
- uspto-grants-1994_10
- Patentnummer
- US05354747
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