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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207998Generated: November 2, 2026

Ethanol → 1-(2,4-difluoro-phenyl)-5-(6-fluoro-4'-methanesulfonyl-biphenyl-3-yl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole

https://huagongshe.com/reaction/2207998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
Reactant5-(3-bromo-4-fluoro-phenyl)-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazoleHCID 118431754—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product1-(2,4-difluoro-phenyl)-5-(6-fluoro-4'-methanesulfonyl-biphenyl-3-yl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazoleHCID 11843218451.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

5-(3-Bromo-4-fluoro-phenyl)-1-(2,4-difluoro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (250.0 mg, 0.53 mmol) prepared in Step 5 of Preparation 7, 4-methylsulfonylphenylboronic acid (116.0 mg, 0.58 mmol), Pd(PPh3)4 (61.0 mg, cat.) and a 2N sodium carbonate solution (3.5 mL) were added to a mixed solvent of ethanol (3.5 mL) and N,N-dimethylformamide (15.0 mL). The reaction mixture was stirred at 90° C. for 3 hours and then filtered through celite pad. A saturated solution of ammonium chloride was added to the filtrate, which was then extracted with ethyl acetate three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/3) to give 150.0 mg of the titled compound as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-8c8dadd566104c0fbef8dd2e38377c58
Source noteuspto-grants-2016_06