1H-Pyrrolo(2,3-b)pyridine → (6-Bromo-pyridin-3-yl)-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone
Reaktionsgleichung
[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1.[Br:10][C:11]1[CH:19]=[CH:18][C:14]([C:15](Cl)=[O:16])=[CH:13][N:12]=1.[Cl-].[Cl-].[Cl-].[Al+3]>ClCCl>[Br:10][C:11]1[N:12]=[CH:13][C:14]([C:15]([C:3]2[C:4]3[C:5](=[N:6][CH:7]=[CH:8][CH:9]=3)[NH:1][CH:2]=2)=[O:16])=[CH:18][CH:19]=1Komponenten
Reaktionsbedingungen
- Temperatur
- -10 °C
Versuchsvorschrift
To a solution of 1H-Pyrrolo[2,3-b]pyridine (1, 1.2 g, 0.010 mol) in dichloromethane (50 mL) was added 6-bromo-nicotinoyl chloride (86, 2.6 g, 0.012 mol) at −10° C. After the solution turned clear, aluminum trichloride (10.2 g, 0.0765 mol) was added in one portion with vigorous stirring. The reaction mixture was stirred at −10° C. for 30 minutes, then was allowed to warm to room temperature and stirred at room temperature overnight. The reaction was quenched with ice water and neutralized with sodium bicarbonate. The solution was extracted with dichloromethane, washed with brine, and dried over sodium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography eluting with methanol in dichloromethane to provide the compound as a white solid (87, 0.35 g, 11%).
Aufarbeitung
- temperatureto warm to room temperature
- stirringstirred at room temperature overnight
- customThe reaction was quenched with ice water and neutralized with sodium bicarbonate
- extractionThe solution was extracted with dichloromethane
- washwashed with brine
- dry with materialdried over sodium sulfate
- customAfter removal of solvent
- customthe residue was purified by silica gel column chromatography
- washeluting with methanol in dichloromethane
Quellen und Nachweise
- ORD-Eintrag
- ord-d02c5a8176ac4410a335c0cedfd39918
- Quelldatensatz
- uspto-grants-2015_10
- Patentnummer
- US09169250B2
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