Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897954Generated: November 3, 2026

Trifluoroacetic acid → HCID 66890546, compound

https://huagongshe.com/reaction/1897954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66890859HCID 66890859—
SolventChloroformHCID 6212—
ProductHCID 66890546HCID 66890546—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 195 mg of tert-butyl 2-((4-((6-((1-tert-butyl-1H-pyrazol-5-yl)amino)pyridin-2-yl)methyl)-1-(2-fluoro-3-(trifluoromethyl)benzoyl)piperidin-4-yl)carbonyl)hydrazinecarboxylate in 4 ml of chloroform was added 2 ml of trifluoroacetic acid at 0° C. The reaction mixture was stirred at 0° C. for 2 hours and at room temperature for 2 hours, followed by concentrating in vacuo. The resulting residue was basified with saturated aqueous sodium bicarbonate solution, and extracted with ethyl acetate. The ethyl acetate solution was dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated in vacuo. The resulting residue was purified by a silica gel column chromatography (eluent: chloroform to chloroform/methanol=10/1) to give the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519136B2
Source datasetuspto-grants-2013_08
ORD IDord-a329cdca615e40228024b145e9ff2929
Source noteuspto-grants-2013_08