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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892648Generated: November 1, 2026

Potassium Carbonate → 5-iodo-2-(4-phenyl-1H-pyrazol-1-yl)pyridine

https://huagongshe.com/reaction/1892648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-PhenylpyrazoleHCID 139106—
Reactant2-Fluoro-5-iodopyridineHCID 2783179—
SolventDimethylformamideHCID 6228—
Product5-iodo-2-(4-phenyl-1H-pyrazol-1-yl)pyridineHCID 6815667394%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 2-fluoro-5-iodopyridine (368.3 mg, 1.652 mmol), 4-phenyl-1H-pyrazole (238.2 mg, 1.652 mmol), and potassium carbonate (457 mg, 3.30 mmol) in N,N-dimethylformamide (3.30 mL) was heated to 85° C. for 21 hours. The reaction was then concentrated and the crude residue diluted with water and ethyl acetate. The layers were separated and the aqueous was extracted two more times with ethyl acetate. The combined organics were dried over magnesium sulfate, filtered, and concentrated to give 5-iodo-2-(4-phenyl-1H-pyrazol-1-yl)pyridine (537.2 mg, 94%) as a white solid. 1H NMR (400 MHz, CDCl3, δ): 8.76 (s, 1H), 8.61 (d, J=1.8 Hz, 1H), 8.09 (dd, J=8.7, 2.2 Hz, 1H), 8.01 (s, 1H), 7.82 (d, J=8.6 Hz, 1H), 7.55-7.61 (m, 2H), 7.36-7.43 (m, 2H), 7.25-7.31 (m, 1H). MS (M+1): 348.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507533B2
Source datasetuspto-grants-2013_08
ORD IDord-2c6b2cb44d1e4af8bb3bd2ac240eb0a8
Source noteuspto-grants-2013_08