Methylamine → Methyl 6-(methylamino)-5-nitronicotinate
Reaktionsgleichung
Cl[C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][N:3]=1.[CH3:15][NH2:16]>>[CH3:15][NH:16][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][N:3]=1Komponenten
3
Versuchsvorschrift
1.6 g (7.4 mmol) of methyl 6-chloro-5-nitronicotinate (see Bernie et al., J. Chem. Soc. 1951, 2590) were stirred in 20 mL of 40% aqueous methylamine solution at room temperature for 30 minutes. The reaction mixture was then diluted with ice water, the yellow precipitate formed was filtered off and dried. Yield: 1.2 g (80% of theory); Rf value: 0.66 (silica gel; ethyl acetate/ethanol/glacial acetic acid=90:5:5).
Aufarbeitung
- customthe yellow precipitate formed
- filtrationwas filtered off
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-d965c41669614f89bb9338419eeebced
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06710055B2
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