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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747501Generated: October 30, 2026

Ethyl 4,4,4-trifluoroacetoacetate → HCID 178516595, compound

https://huagongshe.com/reaction/1747501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178507305HCID 178507305—
SolventAcetic AcidHCID 176—
ProductHCID 178516595HCID 17851659548%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl trifluoroacetoacetate (1.50 g, 8.15 mmol) was added to a solution of 3-{1-[5-(trifluoromethyl)pyridin-2-yl]piperidin-4-yl}-1H-pyrazol-5-amine (880 mg, 2.83 mmol) produced in Reference Example 10 in acetic acid (10 mL), and the mixture was stirred at 60° C. for 2 hours. A saturated sodium bicarbonate aqueous solution was added to the reaction solution, followed by extraction with ethyl acetate three times. The obtained organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography [NH-silica gel column, elute: ethyl acetate/methanol=100/0-96/4 (gradient)] and further purified by silica gel column chromatography [elute: hexane/ethyl acetate=60/40-0/100 (gradient)] to obtain the title compound (610 mg, yield: 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150575B2
Source datasetuspto-grants-2015_10
ORD IDord-50c842f5f2e14108a3848a44a5d76bd3
Source noteuspto-grants-2015_10