Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747502Generated: November 1, 2026

Ethyl 4,4,4-trifluoroacetoacetate → HCID 178516597, compound

https://huagongshe.com/reaction/1747502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178507306HCID 178507306—
SolventAcetic AcidHCID 176—
ProductHCID 178516597HCID 17851659739.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl trifluoroacetoacetate (1.28 g, 6.97 mmol) was added to a solution of 3-[1-(5-chloropyridin-2-yl)piperidin-4-yl]-1H-pyrazol-5-amine (0.484 g, 1.74 mmol) produced in Reference Example 20 in acetic acid (8 mL), and the mixture was stirred at 60° C. for 1.5 hours. A saturated sodium bicarbonate aqueous solution was added to the reaction solution, followed by extraction with ethyl acetate twice. 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=100/0-95/5 (gradient)] and further purified by silica gel column chromatography [elute: hexane/ethyl acetate=20/80-0/100 (gradient)] to obtain the title compound (0.283 g, yield: 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150575B2
Source datasetuspto-grants-2015_10
ORD IDord-f64b1a3ea22744bf9187e2ccc7b97b6c
Source noteuspto-grants-2015_10