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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373331Generated: October 31, 2026

Triethylamine → HCID 12115480, compound

https://huagongshe.com/reaction/2373331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3,5-trimethyl-1H-pyrazole-4-carboxylic acidHCID 736514—
ReactantHCID 12115479HCID 12115479—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
ProductHCID 12115480HCID 1211548041%

Reaction Steps

1,3,5-Trimethylpyrazole-4-carboxylic acid (154 mg, 1 mmol) was dissolved in thionyl chloride (5 ml), and the solution was heated under reflux for 2 hours. The reaction solution was concentrated under reduced pressure, and the resulting acid chloride was added to a solution of 2-(1,3-dimethylbutyl)-4-[1-methoxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]-aniline (345 mg, 1 mmol) and triethylamine (150 mg, 1.5 mmol) in tetrahydrofuran (10 ml) under ice-cooling, after which the resulting mixture was heated under reflux for 2 hours. The reaction mixture was diluted with ethyl acetate and then washed with water. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the resulting residue was separated and purified by silica gel column chromatography. (hexane:ethyl acetate 1:2) to obtain 200 mg of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459477B2
Source datasetuspto-grants-2008_12
ORD IDord-b6c3f9bb0a3949b5ae6bd8dd67d58466
Source noteuspto-grants-2008_12