Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][NH:5][C:4](=[O:8])[CH:3]=1.Br[CH2:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12]>>[Br:1][C:2]1[CH:7]=[CH:6][N:5]([CH2:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[C:4](=[O:8])[CH:3]=1Komponenten
3
Versuchsvorschrift
4.9 g (28.4 mmol) of 4-bromopyridin-2(1H)-one and 1.2 eq. of tert-butyl 2-bromoacetate were reacted according to General Method 4B at 120° C. After aqueous work-up, the crude product was reacted further without further purification. Yield: 8.6 g (purity 91%, 95% of theory)
Aufarbeitung
- customaccording to General Method 4B at 120° C
Quellen und Nachweise
- ORD-Eintrag
- ord-0ebd5d658add447c96942101750407a7
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09434690B2
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