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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648510Generated: October 30, 2026

4-Chloro-7-(trifluoromethyl)quinoline → 4-[(4-Fluorophenyl)hydroxymethyl]-1-[4-[[7-(trifluoromethyl)-4-quinolyl]amino]benzoyl]piperidine hydrochloride

https://huagongshe.com/reaction/648510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
Reactant1-(4-Aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidineHCID 13825043—
SolventEthanolHCID 702—
Product4-[(4-Fluorophenyl)hydroxymethyl]-1-[4-[[7-(trifluoromethyl)-4-quinolyl]amino]benzoyl]piperidine hydrochlorideHCID 2014493184.7%

Reaction Steps

A mixture of 4-chloro-7-(trifluoromethyl)quinoline (0.32 g) and 1-(4-aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidine (0.45 g) in dry ethanol (10 ml) was stirred under reflux for 4 hours and concentrated to dryness in vacuo. The residue was recrystallized from a mixture of ethyl acetate and isopropanol to give 4-[(4-fluorophenyl)hydroxymethyl]-1-[4-[[7-(trifluoromethyl)-4-quinolyl]amino]benzoyl]piperidine hydrochloride (0.65 g) as pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735952
Source datasetuspto-grants-1988_04
ORD IDord-2bd6b18266c1413c914439e2c3b555d6
Source noteuspto-grants-1988_04