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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454742Generated: October 30, 2026

Trifluoroacetic acid → HCID 66990611, compound

https://huagongshe.com/reaction/454742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66990073HCID 66990073—
ProductHCID 66990611HCID 6699061194.9%

Reaction Steps

Trifluoroacetic acid (7.9 mL) was added to the obtained 4-(2-((tert-butoxycarbonyl)(ethyl)amino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoic acid (0.79 g), followed by stirring at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and a 30% aqueous solution of ethanol was added to the obtained residue. After adjusting the pH to 5.0 with a 4.0 mol/L aqueous solution of sodium hydroxide, the solid substance was collected by filtration to obtain 0.61 g of 4-(2-(ethylamino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoic acid as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-7244a2aa38be4b7cafc5bf1b04286b9f
Source noteuspto-grants-2013_07