Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750449Generated: October 31, 2026

Water → 1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/1750449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanuric chlorideHCID 7954—
Reactant1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamideHCID 86721179—
SolventDimethylformamideHCID 6228—
Product1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carbonitrileHCID 8672128992.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamide (500 mg, 1.91 mmol) in DMF (4 mL) was added cyanuric chloride (0.267 mL, 1.91 mmol) at 0° C., and the mixture was stirred at 0° C. for 14 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 5→50% ethyl acetate/hexane) to give 1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carbonitrile (430 mg, 1.77 mmol, 92%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-a80c1ecc3f6040d0bb52459d99c939a2
Source noteuspto-grants-2015_10