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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Quinoline-4-carbonyl chloride hydrochloride | HCID 12373997 | — |
| Reactant | 1-cyclopentyl-3-ethyl-4-cyano-5-amino-1H-pyrazole | HCID 15871269 | — |
| Product | 1-cyclopentyl-3-ethyl-4-cyano-5-(4-quinolinecarboxamido)-1H-pyrazole | HCID 19432803 | 214% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05294612 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-790d31cfa60f456c92faa0e04b9ba46f |
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| Source note | uspto-grants-1994_03 |
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