반응식
Cl.[NH2:2][C:3]1[CH:4]=[N:5][C:6]2[C:11]([C:12]=1[OH:13])=[CH:10][CH:9]=[CH:8][CH:7]=2.[C:14](OC(=O)CC)(=O)[CH2:15][CH3:16].[OH-].[Na+]>O>[CH2:15]([C:16]1[O:13][C:12]2[C:11]3[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=3[N:5]=[CH:4][C:3]=2[N:2]=1)[CH3:14]참가 물질
5
실험 절차
3-Aminoquinolin-4-ol hydrochloride (6 g) was refluxed with propanoic anhydride (8 eq.) until analysis by thin layer chromatography indicated that the reaction was complete. The reaction mixture was cooled, diluted with ice and water, made basic with 10% sodium hydroxide and then extracted with dichloromethane. The extract was washed with water and brine, dried over magnesium sulfate and then concentrated under vacuum. The residue was purified by column chromatography (silica gel eluting with methanol/ethyl acetate) to provide 4.0 g of 2-ethyloxazolo[4,5-c]quinoline.
후처리
- temperatureThe reaction mixture was cooled
- extractionextracted with dichloromethane
- washThe extract was washed with water and brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under vacuum
- customThe residue was purified by column chromatography (silica gel eluting with methanol/ethyl acetate)
출처 및 근거
- ORD 기록
- ord-45a4e05c15714b4988f1f95a245f6bd5
- 출처 데이터셋
- uspto-grants-2004_01
- 특허 번호
- US06677334B2
연결된 노트
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