Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946341Generated: October 31, 2026

Triethylamine → HCID 178522345, compound

https://huagongshe.com/reaction/1946341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantHCID 178418806HCID 178418806—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 178522345HCID 17852234561.4%

Reaction Steps

To a solution of 1H-pyrazol-3-amine (160 mg, 1.93 mmol, Fluka) in acetonitrile (10 ml) was added triethylamine (0.537 ml, 3.85 mmol, Aldrich) and the stirred solution cooled in an ice-water bath. A solution of 2,6-dichlorobenzoyl chloride (0.276 ml, 1.926 mmol, Aldrich) in acetonitrile (5 ml) was added dropwise. 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 DCM (20 ml) and water (20 ml). Insoluble material precipitated. The layers were separated and the aqueous phase then extracted with ethyl acetate (approximately 50 ml). The combined organic layers were filtered through a hydrophobic frit and concentrated in vacuo to give the crude material as an off-white foam. The residue was dissolved in methanol and adsorbed onto fluorosil. The sample was 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 (0.303 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-76aa5022450c4f0e855acf8a0963068f
Source noteuspto-grants-2013_03