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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587098Generated: October 31, 2026

Potassium Carbonate → Ethyl 1-(3,4-difluorophenyl)-4[3-(ethoxycarbonyl)phenyl]-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/587098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Methoxycarbonylphenylboronic acid pinacol esterHCID 2734651—
Reactantethyl 4-bromo-1-(3,4-difluorophenyl)-1H-pyrazole-3-carboxylateHCID 89464890—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
ProductEthyl 1-(3,4-difluorophenyl)-4[3-(ethoxycarbonyl)phenyl]-1H-pyrazole-3-carboxylateHCID 89464679—

Reaction Steps

180 mg (0.54 mmol) of ethyl 4-bromo-1-(3,4-difluorophenyl)-1H-pyrazole-3-carboxylate, 156.7 mg (0.59 mmol) of methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, 158 mg (1.14 mmol) of potassium carbonate, 5.07 mg (0.011 mmol) of 2,2-dicyclohexylphosphino-2″,6″-diisopropoxybiphenyl and 1.22 mg (0.005 mmol) of palladium (II)acetate were suspended in 5 ml of ethanol and heated at the boil for 4 h. After cooling to room temperature, the solvent was removed under reduced pressure, the residue was dissolved in water and dichloromethane, the phases were separated and the organic phase was dried over magnesium sulfate. The crude product was purified by chromatography (ethyl acetate:n-heptane 1:4). This gave 84 mg (37%) of the desired product. 1H-NMR (400 MHz, CDCl3 δ, ppm) 8.15 (s, 1H); 8.05 (d, 1H); 7.96 (s, 1H); 7.74-7.69 (m, 2H); 7.53-7.47 (m, 2H); 7.28 (m, 1H); 4.48-4.34 (m, 4H); 1.43 (t, 3H); 1.29 (t, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226505B2
Source datasetuspto-grants-2016_01
ORD IDord-d81fe33f664741ed9f685641a0ae0dee
Source noteuspto-grants-2016_01