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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989853Generated: November 1, 2026

Triethylamine → N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/1989853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(4-Benzylpiperazin-1-yl)anilineHCID 737259—
Reactant4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chlorideHCID 11066000—
SolventDichloromethaneHCID 6344—
ProductN-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamideHCID 2249940190.6%

Reaction Steps

A mixture of 4-[4-(phenylmethyl)-1-piperazinyl]-benzenamine (0.3 mol) and triethylamine (0.36 mol) in DCM (1500 ml) was stirred at room temperature for 15 minutes. 4′-(Trifluoromethyl)-[1,1′-biphenyl]-2-carbonyl chloride (0.36 mol) was added dropwise over 30 minutes. The mixture was stirred at room temperature for 3 hours and then washed twice with water, then washed with a saturated NaCl solution. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was stirred in DIPE (800 ml). The precipitate was filtered off, washed twice with DIPE and dried in vacuo at 50° C., yielding 140.2 g of N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 1, mp. 180° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642378B2
Source datasetuspto-grants-2010_01
ORD IDord-83b8f7893b7c47aeb7d2924ceb12d5cb
Source noteuspto-grants-2010_01