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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454570Generated: October 30, 2026

Trifluoroacetic acid → HCID 58508900, compound

https://huagongshe.com/reaction/454570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66990700HCID 66990700—
ProductHCID 58508900HCID 58508900—

Reaction Conditions

Temperature52.5 °C

Reaction Steps

A trifluoroacetic acid (4.0 mL) solution of the obtained methyl 2-(2-acetoxy-5-(pyridin-3-yl)benzamido)-4-(2-((tert-butoxycarbonyl)(ethyl)amino)phenyl)benzoate was stirred at room temperature for 2 hours and 30 minutes. The solvent was evaporated under reduced pressure, and toluene was added thereto. The solvent was evaporated under reduced pressure, and diisopropyl ether was added to the obtained residue. The solid substance was collected by filtration. Dioxane (4.0 mL) and a 1 mol/L aqueous solution of sodium hydroxide (0.40 mL) were added to the obtained solid substance, followed by stirring at 50 to 55° C. for 2 hours. The reaction mixture was cooled to room temperature and then adjusted to a pH of 7.4 with 1 mol/L hydrochloric acid. The solvent was evaporated under reduced pressure, and water was added to the obtained residue. The solid substance was collected by filtration to obtain 0.032 g of 4-(2-(ethylamino)phenyl)-2-(2-hydroxy-5-(pyridin-3-yl)benzamido)benzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-d1efa375352c4ae7ae1b6b72589f813c
Source noteuspto-grants-2013_07