Acetic Acid → Ethyl 8-bromoquinoline-3-carboxylate
반응식
[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1O)=[CH:13][CH:12]=[CH:11][C:10]=2[Br:17])([O:3][CH2:4][CH3:5])=[O:2].P(Cl)(Cl)(Cl)=O.C(O)(=O)C.C(OCC)(=O)C>O1CCOCC1.[Zn]>[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][C:10]=2[Br:17])([O:3][CH2:4][CH3:5])=[O:2]참가 물질
반응 조건
- 온도
- 65 °C
실험 절차
A mixture of 2.5 g (8.4 mmol) of 3-carbethoxy-4-hydroxy-8-bromoquinoline and 10 ml of phosphorus oxychloride was heated under reflux for 1 hour. After the completion of the reaction, phosphorus oxychloride was removed and the residue was purified by NH silica gel, to give 2.6 g of a chlorinated derivative. Next, 500 mg (1.6 mmol) of the chlorinated derivative was dissolved in 20 ml of dioxane, and 1 g of powdered zinc and 3 ml of acetic acid were added thereto, followed by heating at 65° C. for 30 minutes. To the reaction mixture was added ethyl acetate, followed by filtering through Celite. The filtrate was washed with brine, dried over magnesium sulfate and concentrated. To the residue was added 1 ml of acetic acid, and the mixture was left stand for 12 hours. Then, acetic acid was removed, and the residue was subjected to silica gel column chromatography and eluted with an eluent (ethyl acetate-n-hexane=1-7), to give 180 mg of the title compound.
후처리
- temperaturewas heated
- temperatureunder reflux for 1 hour
- customwas removed
- customthe residue was purified by NH silica gel
- customto give 2.6 g of a chlorinated derivative
- filtrationby filtering through Celite
- washThe filtrate was washed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- additionTo the residue was added 1 ml of acetic acid
- customThen, acetic acid was removed
- washeluted with an eluent (ethyl acetate-n-hexane=1-7)
출처 및 근거
- ORD 기록
- ord-0629495639844b2cb4e5f8be5827e8b1
- 출처 데이터셋
- uspto-grants-2004_09
- 특허 번호
- US06787534B2
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