Stannous chloride dihydrate → 5-Bromo-2-(piperidin-1-yl)pyridin-3-amine
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([N+:14]([O-])=O)[C:5]([N:8]2[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)=[N:6][CH:7]=1.O.O.[Sn](Cl)Cl>CCOC(C)=O>[Br:1][C:2]1[CH:3]=[C:4]([NH2:14])[C:5]([N:8]2[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)=[N:6][CH:7]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 90 °C
Versuchsvorschrift
To a stirred mixture of 5-bromo-3-nitro-2-(piperidin-1-yl)pyridine (5.88 g, 20.5 mmol) in EtOAc (50 mL) was added tin(II) chloride dihydrate (23.5 g, 104 mmol) in portions. Upon complete addition of the reducing agent, the mixture was carefully heated to 90° C. After 1 h, the reaction was cooled in an ice bath, then washed with 1M NaOH, water, and brine. After drying over anhydrous sodium sulfate and filtration, the organic solvent was removed under reduced pressure. The residue was purified with silica gel chromatography (0-15% EtOAc in hexanes) to provide a white solid as 5-bromo-2-(piperidin-1-yl)pyridin-3-amine. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.57 (1H, d, J=2.2 Hz), 7.09 (1H, d, J=2.3 Hz), 5.04 (2H, s), 2.98 (4H, m), 1.73 (4H, m), 1.58 (2H, m).
Aufarbeitung
- additionUpon complete addition of the reducing agent
- temperaturethe reaction was cooled in an ice bath
- washwashed with 1M NaOH, water, and brine
- dry with materialAfter drying over anhydrous sodium sulfate and filtration
- customthe organic solvent was removed under reduced pressure
- customThe residue was purified with silica gel chromatography (0-15% EtOAc in hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-cb217b42873c4e26b36a07b85ef7d915
- Quelldatensatz
- uspto-grants-2015_01
- Patentnummer
- US08940724B2
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