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

HRID 334471
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HRID 334471 반응식
[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
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 693693,5-DibromopyridineHCID 123122N-Chlorodimethylamine

생성물 1

HCID 234368635-Bromo-N,N-dimethylpyridin-3-amine수율 88.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
200 °C

실험 절차

To a solution of 3,5-dibromopyridine (XLII) (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).

후처리

  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

출처 및 근거

ORD 기록
ord-c52053596b924c6ebbd5f804acf2c9b4
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08883822B2

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