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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167106Generated: November 2, 2026

Triethylamine → N-(1-Benzylpiperidin-4-yl)[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/1167106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
Reactant4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chlorideHCID 11066000—
SolventDichloromethaneHCID 6344—
ProductN-(1-Benzylpiperidin-4-yl)[1,1'-biphenyl]-2-carboxamideHCID 15135612—

Reaction Steps

3 g (0.014 mol) of 4′-trifluoromethyl-biphenyl-2-carboxylic acid chloride, dissolved in 30 ml of dichloromethane, are added dropwise at 15 to −20° C. to a solution of 2.65 ml (0.013 mol) of 4-amino-1-benzyl-piperidine and 6 ml (0.043 mol) of triethylamine in 100 ml of dichloromethane. The mixture is stirred for 14 hours at ambient temperature. The reaction solution is extracted with a mixture of I molar sodium hydrogen carbonate solution and 1N sodium hydroxide solution. The organic phase is dried over sodium sulphate and the solvent is eliminated. The residue is recrystallised from 650 ml of ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617325B1
Source datasetuspto-grants-2003_09
ORD IDord-de8dfeeff7404ce8808f4a0d384d2ce9
Source noteuspto-grants-2003_09