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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024236Generated: October 28, 2026

Trifluoroacetic acid → 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/1024236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant5-amino-2-ethyl-2H-pyrazole-3-carboxylic acid methyl esterHCID 57619416—
SolventAcetonitrileHCID 6342—
Product2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carboxylic acid methyl esterHCID 57619383—

Reaction Conditions

Temperature80 °C

Reaction Steps

To 5-amino-2-ethyl-2H-pyrazole-3-carboxylic acid methyl ester (527, 1.00 g, 5.91 mmol) in acetonitrile (27.5 mL) were added 4-fluorobenzaldehyde (528, 0.660 mL, 6.26 mmol), triethylsilane (4.77 mL, 0.0298 mol) and trifluoroacetic acid (2.38 mL, 0.0310 mol). The reaction was stirred at 80° C. for 4 hours, then concentrated, poured into aqueous potassium carbonate, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 20% to 100% ethyl acetate in hexane to give a white solid (529, 1.00 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722702B2
Source datasetuspto-grants-2014_05
ORD IDord-e14f8ecad6d14f959a37086aa260a3ac
Source noteuspto-grants-2014_05