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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946340Generated: October 29, 2026

Triethylamine → HCID 178522343, compound

https://huagongshe.com/reaction/1946340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluorobenzoyl chlorideHCID 9808—
ReactantHCID 178418806HCID 178418806—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 178522343HCID 17852234355.6%

Reaction Steps

To a solution of 1H-pyrazol-3-amine (249 mg, 3 mmol, Aldrich) in acetonitrile (10 ml) was added triethylamine (0.836 ml, 6.0 mmol, Aldrich) and the stirred solution cooled in an ice-water bath. A solution of 2-fluorobenzoyl chloride (0.358 ml, 3.0 mmol, Alfa Aesar) in acetonitrile (10 ml) was added dropwise. The mixture was stirred under nitrogen and allowed to warm slowly to ambient temperature overnight. The solvent was concentrated in vacuo. The residue was partitioned between ethyl acetate (˜50 ml) and water approximately 50 ml). The phases were separated and the aqueous phase washed with further ethyl acetate (2×approximately 30 ml). The combined organic layers were filtered through a hydrophobic frit and the filtrate concentrated in vacuo to give the crude material (0.64 g). The sample was loaded in dichloromethane and purified on silica 70 g using 0-100% ethyl acetate-cyclohexane. The appropriate fractions were combined and concentrated in vacuo to give the title compound as a colourless solid (342 mg); LCMS: (System 4) MH+=206, tRET=1.50 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-280e9bb139544fefa7ed37b27a0a5169
Source noteuspto-grants-2013_03