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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952097Generated: November 2, 2026

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

https://huagongshe.com/reaction/1952097

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 numberUS08404700B2
Source datasetuspto-grants-2013_03
ORD IDord-300bcd566294422a87f2a8c20fcbd094
Source noteuspto-grants-2013_03