Methanesulfonyl chloride → 4-Bromo-6-chloro-1H-pyrrolo[2,3-b]pyridine
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][N+:5]([O-])=[C:4]2[NH:9][CH:10]=[CH:11][C:3]=12.CS([Cl:16])(=O)=O>CN(C)C=O>[Br:1][C:2]1[CH:7]=[C:6]([Cl:16])[N:5]=[C:4]2[NH:9][CH:10]=[CH:11][C:3]=12Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 75 °C
Versuchsvorschrift
To a suspension of the 4-bromo-1H-pyrrolo[2,3-b]pyridine 7-oxide (27 mmol) in N,N-dimethylformamide (57 mL) at 50° C. was added methanesulfonyl chloride (67.5 mmol) under nitrogen. Upon completion of the addition, the reaction was stirred at 75° C. for 1 hour. The reaction was cooled to room temperature and quenched with water (60 mL). Then, it was cooled to 5° C. and 6N sodium hydroxide solution was added to raise the pH to 7. The ice bath was removed and the resulting slurry was stirred at room temperature for 3 h. The precipitate was filtered, washed with water (50 mL), and dried under high vacuum to give the title product as a white solid (89%). ESMS [M+H]+: 231.0
Aufarbeitung
- additionUpon completion of the addition
- temperatureThe reaction was cooled to room temperature
- customquenched with water (60 mL)
- temperatureThen, it was cooled to 5° C.
- addition6N sodium hydroxide solution was added
- temperatureto raise the pH to 7
- customThe ice bath was removed
- stirringthe resulting slurry was stirred at room temperature for 3 h
- filtrationThe precipitate was filtered
- washwashed with water (50 mL)
- customdried under high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-f0cbe71d787f4910b2776e6e0415baa2
- Quelldatensatz
- uspto-grants-2007_10
- Patentnummer
- US07282588B2
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