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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502651Generated: November 2, 2026

Water → 1-(6-(1H-pyrazol-1-yl)pyridin-3-yl)ethanone

https://huagongshe.com/reaction/1502651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyrazoleHCID 1048—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Acetyl-2-bromopyridineHCID 15668195—
SolventDimethylformamideHCID 6228—
Product1-(6-(1H-pyrazol-1-yl)pyridin-3-yl)ethanoneHCID 5916197081.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

407.9 mg (corresponding to 5.99 mmol) of pyrazole was dissolved in 10 mL of dimethylformamide. Then, 400.0 mg (corresponding to 1.99 mmol) of 5-acetyl-2-bromopyridine and 827.9 mg (corresponding to 5.99 mmol) of potassium carbonate were added thereto. The resulting solution was heated at 100° C. for 5 hours. After the completion of the reaction, the reaction solution was cooled down to room temperature, supplemented with water, and extracted twice with dichloromethane. The combined dichloromethane layer was washed with water and a saturated saline solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (elution solvent: dichloromethane/ethyl acetate=50/1), to obtain 304.0 mg (corresponding to 1.62 mmol) of 5-acetyl-2-(pyrazole-1-yl)pyridine (FIG. 5, step 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211350B2
Source datasetuspto-grants-2015_12
ORD IDord-cff99f09e2a346b794d243da66f76852
Source noteuspto-grants-2015_12