Potassium Carbonate → 5-Bromo-N,N-dimethylpyridin-3-amine

HRID 877120

Reaktionsgleichung

Reaktionsgleichung von HRID 877120
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6](Br)[CH:7]=1.C([O-])([O-])=O.[K+].[K+].[CH3:15][N:16](Cl)[CH3:17]>CN(C=O)C>[Br:1][C:2]1[CH:7]=[C:6]([N:16]([CH3:17])[CH3:15])[CH:5]=[N:4][CH:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
200 °C

Versuchsvorschrift

To a solution of 3,5-dibromopyridine (XL) (2.37 g, 10.0 mmol) in dry DMF (20.0 mL) was added K2CO3 (4.5 g, 33 mmol) and dimethylamino hydrochloride (1.79 g, 22 mmol). The mixture was heated overnight at 200° C. in a sealed tube. The solution was cooled to room temperature and excess DMF was removed under vacuum. The residue was partitioned between EtOAc and water. The organic phase was separated. The aqueous phase was washed with EtOAc and the combined organic phases were dried over MgSO4, and concentrated to afford 5-bromo-N,N-dimethylpyridin-3-amine (XLIII) as an off-white solid (1.78 g, 8.85 mmol, 88% yield). 1H NMR (DMSO-d6, 500 MHz) δ ppm 2.94 (s, 6H), 7.25 (t, J=2 Hz, 1H), 7.91 (d, J=2 Hz, 1H), 8.07 (d, J=2 Hz, 1H); ESIMS found C7H9BrN2 m/z 201.1 (M+H).

Aufarbeitung

  1. temperatureThe solution was cooled to room temperature
  2. customexcess DMF was removed under vacuum
  3. customThe residue was partitioned between EtOAc and water
  4. customThe organic phase was separated
  5. washThe aqueous phase was washed with EtOAc
  6. dry with materialthe combined organic phases were dried over MgSO4
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-e1807483668b44d797dda5f4784374ad
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08987298B2

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