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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602085Generated: October 30, 2026

Trifluoroacetic acid → HCID 59743883, compound

https://huagongshe.com/reaction/602085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67266971HCID 67266971—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 59743883HCID 59743883—

Reaction Steps

To a solution of tert-butyl 3-(4-fluorophenyl)-4-({[6-(3-fluorophenyl)pyridin-3-yl]carbonyl}amino)piperidine-1-carboxylate (348 mg, 0.71 mmol) in CH2Cl2 (5 mL) at 0° C. was added TFA (1.2 mL). After stirring overnight at rt the the reaction was diluted with toluene (5 mL) and then the solvent removed and the residue purified by chromatography (silica, 10% MeOH/DCM) to give the desired product, 6-(3-fluorophenyl)-N-[3-(4-fluorophenyl)piperidin-4-yl]nicotinamide. (168 mg, 61% yield). 1H NMR (400 MHz, DMSO-d6) □ ppm 8.87 (1H, d, J=2.0 Hz), 8.52 (1H, s), 8.04-8.15 (2H, m), 8.00 (2H, d, J=7.9 Hz), 7.58 (1H, d, J=6.1 Hz), 7.35 (4H, dd, J=9.0, 3.5 Hz), 7.08-7.22 (2H, m), 4.60-4.72 (1H, m), 3.81 (1H, t), 3.05-3.27 (4H, m), 1.91 (1H, s). LC/MS=(M+H)=394.1 observed, 394.17 expected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902373B2
Source datasetuspto-grants-2011_03
ORD IDord-e13dcbc07f594065b1b89b5cffb852d4
Source noteuspto-grants-2011_03