반응식
[N+]([C:4]([CH3:15])=[CH:5][C:6]1[CH:7]=[CH:8][C:9]2[N:10]([CH:12]=[CH:13][N:14]=2)[CH:11]=1)([O-])=O.Cl.[OH2:17]>CCO>[N:14]1[CH:13]=[CH:12][N:10]2[CH:11]=[C:6]([CH2:5][C:4](=[O:17])[CH3:15])[CH:7]=[CH:8][C:9]=12참가 물질
실험 절차
In 25 ml of water and 25 ml of EtOH, 1.14 g of 6-(2-nitro-1-propenyl)imidazo[1,2-a]pyridine was heated to 80° C. together with 100 mg of ferrous chloride. With stirring, 2.5 ml of conc. hydrochloric acid was added at a refluxing rate and the mixture was stirred for 1 hour. Upon heating, insoluble matter was removed by filtration. After the insoluble matter was thoroughly washed with ethanol, the solvent was removed by distillation under reduced pressure. An aqueous sodium bicarbonate solution was added to the residue and the mixture was extracted with chloroform. After washing with water and drying over magnesium sulfate, chloroform was removed by distillation under reduced pressure. The residue was purified by column chromatography to obtain 500 mg of 1-(imidazo[1,2-a]pyridin-6-yl)-2-propanone.
후처리
- stirringthe mixture was stirred for 1 hour
- temperatureUpon heating
- custominsoluble matter was removed by filtration
- washAfter the insoluble matter was thoroughly washed with ethanol
- customthe solvent was removed by distillation under reduced pressure
- additionAn aqueous sodium bicarbonate solution was added to the residue
- extractionthe mixture was extracted with chloroform
- washAfter washing with water
- dry with materialdrying over magnesium sulfate, chloroform
- customwas removed by distillation under reduced pressure
- customThe residue was purified by column chromatography
출처 및 근거
- ORD 기록
- ord-36f5757ec41e4f45beb82fbff807494f
- 출처 데이터셋
- uspto-grants-1988_12
- 특허 번호
- US04791202
연결된 노트
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