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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279341Generated: October 30, 2026

HCID 18426253, compound → HCID 18426266, compound

https://huagongshe.com/reaction/279341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18426253HCID 18426253—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 18426266HCID 18426266—

Reaction Steps

A solution of 1-(4-nitrobenzyl)-4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine (22.4 mg, 0.047 mmol) in EtOH (3 mL) was hydrogenated at 1 atm for 1 h in the presence of 5% palladium on charcoal (10 mg) at 25° C. The catalyst was removed by filtration and washed with EtOH (5 mL). The combined filtrate was evaporated to afford 1-(4-aminobenzyl)-4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine (compound No. 516) as a pale yellow solid (20.1 mg, 96%). The purity was determined by RPLC/MS (99%); ESI/MS m/e 449.1 (M++H, C23H27F3N4O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362177B1
Source datasetuspto-grants-2002_03
ORD IDord-ca76b13aea7b41ba8f96ba2def38a988
Source noteuspto-grants-2002_03