Hydrochloric Acid → (3-Fluoro-4-methylpyridin-2-yl)methanamine dihydrochloride
Reaktionsgleichung
[C:1]([C:3]1[C:8]([F:9])=[C:7]([CH3:10])[CH:6]=[CH:5][N:4]=1)#[N:2].[ClH:11]>C(O)C.[Pd]>[ClH:11].[ClH:11].[NH2:2][CH2:1][C:3]1[C:8]([F:9])=[C:7]([CH3:10])[CH:6]=[CH:5][N:4]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A stirred solution of 332 mg (2.44 mmol) of 2-cyano-3-fluoro4-methylpyridine 5-3 in 15 mL of ethanol and 0.61 mL (7.32 mmol) of conc. HCl was hydrogenated over 175 mg of 10% palladium on carbon at 55 psi for 16 h. The catalyst was removed by filtration and the solvents removed at reduced pressure to give 5-4 as a yellow solid: 1H NMR (CD3OD) δ 8.41 (d, 1H, 5.1 Hz), 7.54 (dd, 1H, 5.5, 5.5 Hz), 4.40 (s, 2H), 2.44 (s, 3H).
Aufarbeitung
- customThe catalyst was removed by filtration
- customthe solvents removed at reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-e83b94b3a16e4ab9ac6c7151a24609da
- Quelldatensatz
- uspto-grants-2002_09
- Patentnummer
- US06455532B1
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