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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514641Generated: November 3, 2026

Trifluoroacetic acid → HCID 66670206, compound

https://huagongshe.com/reaction/1514641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl 1-[2-(4-fluorophenyl)ethyl]-2-methyl-5-(1-methylpiperidin-4-yl)-1H-pyrrole-3-carboxylateHCID 66670175—
SolventDichloromethaneHCID 6344—
ProductHCID 66670206HCID 66670206—

Reaction Steps

A 230 mg portion of tert-butyl 1-[2-(4-fluorophenyl)ethyl]-2-methyl-5-(1-methylpiperidin-4-yl)-1H-pyrrole-3-carboxylate was dissolved in 2 ml of dichloromethane, and 1 ml of trifluoroacetic acid was added under ice-cooling, followed by stirring at room temperature for 1.5 hours. The reaction liquid was concentrated under a reduced pressure, and a saturated sodium bicarbonate aqueous solution was added, followed by three times extractions with chloroform. After drying the organic layer with anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (methanol:chloroform=10:90-15:85-20:80) to obtain 124 mg of 1-[2-(4-fluorophenyl)ethyl]-2-methyl-5-(1-methylpiperidin-4-yl)-1H-pyrrole-3-carboxylic acid as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222274B2
Source datasetuspto-grants-2012_07
ORD IDord-833df55f92f84f6fb33a84144abec1df
Source noteuspto-grants-2012_07