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Potassium Carbonate → 7-Bromo-1,3-dimethylimidazo[1,5-a]pyridine

HRID 879584
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HRID 879584 반응식
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH:8]([NH:10][C:11](=O)[CH3:12])[CH3:9])[CH:3]=1.P(Cl)(Cl)(Cl)=O.C(=O)([O-])[O-].[K+].[K+]>C1C=CC=CC=1>[Br:1][C:2]1[CH:7]=[CH:6][N:5]2[C:11]([CH3:12])=[N:10][C:8]([CH3:9])=[C:4]2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium Carbonate2회HCID 24813Phosphorus oxychlorideHCID 86700400N-(1-(4-bromopyridin-2-yl)ethyl)acetamide

생성물 1

HCID 838395907-Bromo-1,3-dimethylimidazo[1,5-a]pyridine

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

N-(1-(4-bromopyridin-2-yl)ethyl)acetamide (2.28 g, 9.38 mmol) was suspended in anhydrous benzene (20 mL), then phosphorus oxychloride (2.2 mL, 23.6 mmol) was added and the reaction heated to reflux for 3 hours. The crude reaction was then added portion-wise to 1M potassium carbonate solution (60 mL) and stirred until gas evolution ceased. The pH was then adjusted to pH 10 with potassium carbonate. The aqueous layer was extracted with DCM (50 mL×2), the organic were combined, dried over Na2SO4, and concentrated to afford the product, which was used without further purification. LCMS-ESI+: calc'd for C9H10BrN2: 225.1 (M+H+); Found: 225.05 (M+H+).

후처리

  1. temperaturethe reaction heated
  2. temperatureto reflux for 3 hours
  3. customThe crude reaction
  4. extractionThe aqueous layer was extracted with DCM (50 mL×2)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated
  7. customto afford the product, which
  8. customwas used without further purification

출처 및 근거

ORD 기록
ord-881d64604e604f5d9789d689afff687c
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08987250B2

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