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Imidazo[1,2-a]pyridine-6-carboxamide → imidazo[1,2-a]pyridine-6-carbonitrile

HRID 1654647
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인쇄 미리보기

반응식

HRID 1654647 반응식
[C:1]([C:4]1[CH:5]=[CH:6][C:7]2[N:8]([CH:10]=[CH:11][N:12]=2)[CH:9]=1)(=O)[NH2:2]>P(Cl)(Cl)(Cl)=O>[C:1]([C:4]1[CH:5]=[CH:6][C:7]2[N:8]([CH:10]=[CH:11][N:12]=2)[CH:9]=1)#[N:2]
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참가 물질

3

반응물 1

HCID 326954Imidazo[1,2-a]pyridine-6-carboxamide

생성물 1

HCID 2764471imidazo[1,2-a]pyridine-6-carbonitrile수율 86.6%

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

실험 절차

A mixture of 2.6 g of 6-carbamoylimidazo[1,2-a]pyridine and 30 ml of phosphorus oxychloride is heated under reflux for 16 hours. The excess phosphorus oxychloride is removed under reduced pressure and the residue is poured onto ice. The mixture is neutralized with sodium carbonate and extracted with ethyl acetate. The organic layer is washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is then evaporated off under reduced pressure to give 2.0 g of the above-identified compound as colorless crystals.

후처리

  1. temperatureis heated
  2. temperatureunder reflux for 16 hours
  3. customThe excess phosphorus oxychloride is removed under reduced pressure
  4. additionthe residue is poured onto ice
  5. extractionextracted with ethyl acetate
  6. washThe organic layer is washed with saturated aqueous sodium chloride solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customThe solvent is then evaporated off under reduced pressure

출처 및 근거

ORD 기록
ord-12fda8ba8ea5471a8838e4c4c414b07e
출처 데이터셋
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05409919

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