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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946342Generated: October 25, 2026

Triethylamine → HCID 178522342, compound

https://huagongshe.com/reaction/1946342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chlorobenzoyl chlorideHCID 69110—
ReactantHCID 178418806HCID 178418806—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 178522342HCID 17852234244.7%

Reaction Steps

To a solution of 1H-pyrazol-3-amine (166 mg, 2 mmol, Aldrich) in acetonitrile (8 ml) was added triethylamine (0.558 ml, 4.0 mmol, Aldrich) and the stirred solution was cooled in an ice-water bath. To the mixture was added a solution of 2-chlorobenzoyl chloride (0.253 ml, 2.0 mmol, Aldrich) in acetonitrile (7 ml). The mixture was stirred under nitrogen and allowed to warm slowly to ambient temperature overnight. The mixture was concentrated in vacuo. The residue was partitioned between ethyl acetate (approximately 30 ml) and water (approximately 30 ml). The layers were separated and the aqueous phase was washed with further ethyl acetate (2×20 ml). The combined organic layers were filtered through a hydrophobic frit and the filtrate concentrated in vacuo to give the crude material (0.47 g). The sample was loaded in dichloromethane and purified on silica 50 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 (0.198 g); LCMS: (System 4) MH+=222, tRET=1.54 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-ec02db4d73a441b48d34783d4e550735
Source noteuspto-grants-2013_03