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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487257Generated: October 30, 2026

Quinoline-4-carbonyl chloride hydrochloride → 1-cyclopentyl-3-ethyl-4-cyano-5-(4-quinolinecarboxamido)-1H-pyrazole

https://huagongshe.com/reaction/487257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoline-4-carbonyl chloride hydrochlorideHCID 12373997—
Reactant1-cyclopentyl-3-ethyl-4-cyano-5-amino-1H-pyrazoleHCID 15871269—
Product1-cyclopentyl-3-ethyl-4-cyano-5-(4-quinolinecarboxamido)-1H-pyrazoleHCID 19432803214%

Reaction Conditions

Temperature250 °C

Reaction Steps

4-Quinolinecarboxylic acid chloride hydrochloride (3.8 g, 6.5 mmol) and 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carbonitrile (2.8 g, 13.7 mmol) were combined and heated in an oil bath at 250° C. for 7 minutes. The reaction mixture was cooled to room temperature and the obtained solid was collected by filtration on a glass frit and was washed with chloroform. The residue was recrystallized from ethyl acetate to afford 5.0 g (100%) of 1-cyclopentyl-3-ethyl-4-cyano-5-(4-quinolinecarboxamido)-1H-pyrazole as a white solid, m.p. 156°-161° C., after drying at 110° C. for 7 hours in high vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294612
Source datasetuspto-grants-1994_03
ORD IDord-790d31cfa60f456c92faa0e04b9ba46f
Source noteuspto-grants-1994_03