반응식
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:7]=[CH:8][C:9]([F:12])=[N:10][CH:11]=1.C([N-]C(C)C)(C)C.[Li+].[I:21]I.S([O-])([O-])(=O)=S.[Na+].[Na+]>C1COCC1.O>[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:7]=[C:8]([I:21])[C:9]([F:12])=[N:10][CH:11]=1참가 물질
실험 절차
Cool a solution of 5-[1,3]dioxolan-2-yl-2-fluoro-pyridine (2.0 g, 11.8 mmol) in THF (20 mL) to −75° C. Add lithium diisopropylamide (2 M in THF, 6 mL, 12 mmol) over a period of 30 min. Stir the mixture for an additional 3 hours. Add iodine (3.0 g, 11.8 mmol, dissolved in 100 mL of THF). Stir for 2 hours after the addition is complete. Add water (100 mL) to the mixture and allow the temperature to rise to room temperature over 1 hour while stirring. Treat the mixture with saturated aqueous sodium thiosulfate solution (50 mL). Extract the solution with ether. Concentrate the solution in vacuo to a brown oil. Purify by column chromatography (hexane to 20% ethyl acetate in hexane) to afford the title compound (2.1 g, 60%) as a yellow oil. MS (ES) m/z 296 [M+1]+.
후처리
- stirringStir for 2 hours
- additionafter the addition
- waitto rise to room temperature over 1 hour
- stirringwhile stirring
- extractionExtract the solution with ether
- concentrationConcentrate the solution in vacuo to a brown oil
- customPurify by column chromatography (hexane to 20% ethyl acetate in hexane)
출처 및 근거
- ORD 기록
- ord-237c637b693a4df39d152726d1b7412e
- 출처 데이터셋
- uspto-grants-2011_11
- 특허 번호
- US08063212B2
연결된 노트
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