Dimethylformamide → 3-Bromo-5-fluoro-2-methoxy-4-methylpyridine
Reaktionsgleichung
[Br:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[C:6]([F:9])[C:7]=1[CH3:8].CN([CH:14]=[O:15])C.C[O-].[Na+]>O>[Br:1][C:2]1[C:3]([O:15][CH3:14])=[N:4][CH:5]=[C:6]([F:9])[C:7]=1[CH3:8]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
3-bromo-2-chloro-5-fluoro-4-methylpyridine (340 mg) was added to DMF (1.8 mL). Sodium methoxide (28% solution in methanol, 5.4 mL) was added to the solution, and the mixture was stirred at 80° C. for two hours. Water was added to the reaction mixture. The precipitated solid was collected by filtration to give the title compound (240 mg).
Aufarbeitung
- filtrationThe precipitated solid was collected by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-ad0a96bf3f0247ac90b793971266620f
- Quelldatensatz
- uspto-grants-2013_10
- Patentnummer
- US08563565B2
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