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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236838Generated: October 31, 2026

Trifluoroacetic acid → HCID 68696215, compound

https://huagongshe.com/reaction/2236838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantHCID 68695860HCID 68695860—
SolventEthanolHCID 702—
ProductHCID 68696215HCID 68696215—

Reaction Steps

To a suspension of 1-(6-fluoro-5-nitropyridin-2-yl)-4-methylpiperazine.trifluoroacetic acid salt (0.38 g, 1.1 mmol) in ethanol (30 mL) is added triethylamine dropwise with agitation until all of the solid had dissolved. The mixture is then degassed with dry ice and treated with an aqueous slurry of Raney nickel (approx 1.5 mL). After shaking under 50 psi of hydrogen, the reaction mixture is filtered through a pad of diatomaceous earth and concentrated under reduced pressure to give 2-fluoro-6-(4-methyl-piperazin-1-yl)-pyridin-3-ylamine (contaminated with triethylammonium trifluoroacetate) as a red wine colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-801fdd4893134ff19bf7ca6db3ca6132
Source noteuspto-grants-2010_05