Ammonia → 4-amino-1-benzyl-3-nitro-1H-pyridin-2-one
Reaktionsgleichung
[NH3:1].[CH2:2]([N:9]1[CH:14]=[CH:13][C:12](OCC2C=CC=CC=2)=[C:11]([N+:23]([O-:25])=[O:24])[C:10]1=[O:26])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>ClCCl>[NH2:1][C:12]1[CH:13]=[CH:14][N:9]([CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)[C:10](=[O:26])[C:11]=1[N+:23]([O-:25])=[O:24]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
20 ml of a saturated ethanolic ammonia solution were added to a solution of 5.5 g (16.3 mmol) of 1-benzyl-4-benzyloxy-3-nitro-pyridin-2-one in 50 ml dichloromethane and stirred for 3 days at ambient temperature in the sealed flask. The solution was evaporated to dryness, the residue was triturated with diethyl ether, suction filtered and dried.
Aufarbeitung
- customThe solution was evaporated to dryness
- customthe residue was triturated with diethyl ether, suction
- filtrationfiltered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-acf982725c804f048c9961e2e0d4844a
- Quelldatensatz
- uspto-grants-2006_09
- Patentnummer
- US07109192B2
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