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[F:1][C:2]1[C:7]([CH:8]=[O:9])=[C:6](I)[CH:5]=[CH:4][N:3]=1.[CH2:11]([O:13][C:14]([Sn](CCCC)(CCCC)CCCC)=[CH2:15])[CH3:12].[F-].[K+]>O1CCOCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:14]([O:13][C:11]([C:6]1[CH:5]=[CH:4][N:3]=[C:2]([F:1])[C:7]=1[CH:8]=[O:9])=[CH2:12])[CH3:15]참가 물질
실험 절차
There are mixed in succession 8 g (31.9 mmol) of 2-fluoro-4-iodo-3-pyridinecarbaldehyde (described in J.O.C, 1993, 58, pp. 7832), 12.7 g (35.96 mmol) of 1-ethoxyvinyltributyltin and 740 mg of tetrakis(triphenylphosphine)palladium (2% molar) in 280 ml of dioxane. The reaction mixture is heated at reflux until the starting material has disappeared completely. After returning to room temperature a solution of potassium fluoride is added to the reaction mixture. Vigorous stirring is maintained for 10 minutes in order to cause precipitation of the tributyltin fluoride, which is filtered off. The filtrate is plunged into a sodium chloride solution. The aqueous phase is extracted 3 times with dichloromethane and then the organic phases are combined, dried over magnesium sulphate, concentrated and purified by chromatography over a silica column, using a dichloromethane/cyclohexane mixture (95/5) as eluant to yield the expected product.
후처리
- temperatureThe reaction mixture is heated
- temperatureat reflux until the starting material
- customAfter returning to room temperature
- additionis added to the reaction mixture
- temperatureis maintained for 10 minutes in order
- customprecipitation of the tributyltin fluoride, which
- filtrationis filtered off
- extractionThe aqueous phase is extracted 3 times with dichloromethane
- dry with materialdried over magnesium sulphate
- concentrationconcentrated
- custompurified by chromatography over a silica column
출처 및 근거
- ORD 기록
- ord-b1911e1b043043799444f39d04e81d1e
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06699876B2
연결된 노트
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