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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 83497Erstellt: 24. Oktober 2026

8-Hydroxyquinoline → 3-(2,5-Dimethylpyrrol-1-yl)-1-(3-fluorophenyl)-1H-pyrazole

https://huagongshe.com/de/reaction/83497

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt8-HydroxyquinolineHCID 1923—
EduktCesium carbonateHCID 10796—
Edukt1-Fluoro-3-iodobenzeneHCID 70725—
EduktHCID 178425430HCID 178425430—
KatalysatorCopper oxideHCID 14829—
LösungsmittelTolueneHCID 1140—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt3-(2,5-Dimethylpyrrol-1-yl)-1-(3-fluorophenyl)-1H-pyrazoleHCID 71287753—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

To a solution of 3-(2,5-dimethylpyrrol-1-yl)-1H-pyrazole (6.8 g) in N-methyl-2-pyrrolidone (68 ml) were sequentially added cesium carbonate (27.4 g), 8-quinolinol (1.2 g), copper oxide (I) (0.6 g) and 1-fluoro-3-iodobenzene (7.4 ml), and the mixture was stirred at 110° C. for 2 hours. This reaction mixture was cooled to room temperature, and toluene (80 ml) was added thereto, and then the mixture was filtered through Celite. After adding a 1M aqueous solution of sodium hydroxide (80 ml) to the filtrate, the mixture was extracted with toluene. The resulting organic layer was sequentially washed with water and a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1) to give the titled compound (10.4 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846746B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-be681fdb8c0f4f5e8dfdcac87443dbe7
Quellennotizuspto-grants-2014_09