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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359027Generated: November 2, 2026

Triethylamine → HCID 67260280, compound

https://huagongshe.com/reaction/2359027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantsec-ButylhydrazineHCID 547690—
ReactantHCID 65583291HCID 65583291—
SolventDichloromethaneHCID 6344—
ProductHCID 67260280HCID 6726028021%
ProductHCID 67260571HCID 6726057116%

Reaction Steps

A mixture of 1-(5-chloro-2-thienyl)-2-(pyridin-4-yl)ethanone (0.68 mmol), secbutylhydrazin (1.37 mmol) and triethylamine (1.37 mmol) in 5 mL dichloromethane was refluxed for 2.5 h. The solvent was evaporated under reduced pressure and the residue was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate and the combined organic extracts were dried over MgSO4 filtered and concentrated. The residue was purified by chromatography on silica gel (dichloromethane:methanol 100:1 to 20:1) to afford 37 mg of 4-[1-sec-butyl-3-(5-chloro-2-thienyl)-1H-pyrazol-4-yl]pyridine (16% yield) and 48 mg of 4-[1-sec-butyl-5-(5-chloro-2-thienyl)-1H-pyrazol-4-yl]pyridine (21% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685974B2
Source datasetuspto-grants-2014_04
ORD IDord-836c52c166684ccfa282695d0e5143ee
Source noteuspto-grants-2014_04