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HRID 9182Erstellt: 24. Oktober 2026

Water → 7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridine

https://huagongshe.com/de/reaction/9182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt2,4-Dichlorophenylboric acidHCID 21984477—
Edukt7-Bromo-2-ethylpyrazolo[1,5-a]pyridineHCID 21984510—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridineHCID 2198463597,9%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

After dissolving 7-bromo-2-ethylpyrazolo[1,5-a]pyridine (300 mg) in ethanol (2 mL) and toluene (4 mL), 2,4-dichlorophenylboric acid (508 mg), tetrakis(triphenylphosphine)palladium (0) complex (154 mg) and 2 M aqueous sodium carbonate (1.33 mL) were added and the mixture was heated and stirred at 80° C. for 3 hours under a nitrogen stream. Water was added to the reaction mixture, extraction was performed with ethyl acetate and the organic layer was washed with brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (380 mg) was obtained from the n-hexane:ethyl acetate (100:1) fraction as a light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091215B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-f014e611ef1f44afbd81fa386b31f468
Quellennotizuspto-grants-2006_08