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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099508Generated: October 30, 2026

Potassium Carbonate → HCID 10236192, compound

https://huagongshe.com/reaction/2099508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-FluorobenzonitrileHCID 67880—
Reactant1-pyridin-2-yl-1H-pyrazol-3-yl trifluoromethanesulfonateHCID 11197128—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 10236192HCID 10236192—

Reaction Conditions

Temperature65 °C

Reaction Steps

1-Pyridin-2-yl-1H-pyrazol-3-yl trifluoromethanesulfonate (0.211 g, 0.72 mmol), 3-fluorobenzonitrile (0.111 g, 0.76 mmol) and potassium carbonate (0.209 g, 1.51 mmol) in a mixture of ethyleneglycol dimethyl ether (20 mL) and water (4 mL) was degassed by argon bubbling for 15 min., then tetrakis(triphenylphosphine)palladium(0) (20 mg, 0.017 mmol) was added the resulting solution degassed for a further 15 min. The solution was stirred at 65° C. for 12 h. The reaction mixture was quenched with water (30 mL), then extracted with EtOAc (3×30 mL) and washed with brine. The combined organic phase was dried over Na2SO4 and concentrated in vacuo. The crude residue was chromagraphed on silica gel eluting with EtOAc:hexane (2:3) to afford a white solid which was recrystallized from EtOAc-hexane to give 3-(1-pyridin-2-yl-1H-pyrazol-3-yl)benzonitrile as a white solid. 1H NMR (CD3Cl, 300 MHz) δ 8.64 (d, 1H), 8.44 (d, 1H), 8.25 (s, 1H), 8.14 (d, 1H), 8.10 (d, 1H), 7.87 (t, 1H), 7.64 (d, 1H), 7.55 (t, 1H), 7.24 (dd, 1H), 6.80 (d, 1H). MS (ESI) 247 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569592B2
Source datasetuspto-grants-2009_08
ORD IDord-f80eb8e7957b4bf6aa1cdf4ea68b9798
Source noteuspto-grants-2009_08