Ethanone, 1-(1H-pyrazolo[4,3-c]pyridin-1-yl)- → 1H-Pyrazolo[4,3-c]pyridine
Reaktionsgleichung
[N:1]1(C(=O)C)[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[N:2]1>C(O)C.[OH-].[Na+]>[NH:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[N:2]1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of 6.44 g of 1-pyrazolo[4,3-c]pyridin-1-yl-ethanone in 120 mL of ethanol, 10 mL of 5N sodium hydroxide aqueous solution was added at room temperature and stirred at this temperature for 30 minutes. After neutralization with 5N hydrochloric acid, the solvent was evaporated, the residue was washed with ethyl acetate, and the solvent of filtrate was evaporated, to afford 3.88 g of the title compound as pale yellow crystals.
Aufarbeitung
- customAfter neutralization with 5N hydrochloric acid, the solvent was evaporated
- washthe residue was washed with ethyl acetate
- customthe solvent of filtrate was evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-bc9584153d024b7d907f9748370ecf08
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07429609B2
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