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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774530Generated: October 27, 2026

Trifluoroacetic acid → ethyl 5-amino-1-(4-ethoxy-2,6-difluorobenzyl)-4-methyl-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/1774530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantpotassium (2Z)-3-cyano-1-ethoxy-1-oxobut-2-en-2-olateHCID 24824588—
Reactant(4-Ethoxy-2,6-difluorobenzyl)hydrazine dihydrochlorideHCID 89647959—
Solvent1,4-DioxaneHCID 31275—
Productethyl 5-amino-1-(4-ethoxy-2,6-difluorobenzyl)-4-methyl-1H-pyrazole-3-carboxylateHCID 89662197—

Reaction Steps

2.01 g potassium (2Z)-3-cyano-1-ethoxy-1-oxobut-2-en-2-olate (10.9 mmol, 1.0 eq.) were dissolved in dioxane at rt and 1.34 mL trifluoroacetic acid (17.4 mmol, 1.6 eq.) were added within 2 minutes. The slurry was stirred for 10 minutes and 3.00 g (4-ethoxy-2,6-difluorobenzyl)hydrazine dihydrochloride (10.9 mmol, 1.0 eq.) were added. The reaction mixture was stirred at 130° C. for 3 hours. The resulting solid was filtered off and washed rinsed with dioxane. The filtrate was partitioned between ethyl acetate and water. The aqueous phase was washed with ethyl acetate three times. The collected organic solutions were washed with brine, dried over a silicon filter, concentrated in vacuo and purified by flash chromatography: 1.10 g (2.42 mmol, 22%) of a 71% pure target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260412B2
Source datasetuspto-grants-2016_02
ORD IDord-f9a65ab6be8d4f58960d8a2b8b146599
Source noteuspto-grants-2016_02