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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193300Generated: October 31, 2026

Diisopropylethylamine → N,N-Dibenzyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamine

https://huagongshe.com/reaction/1193300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromopyridine HydrobromideHCID 44630127—
Reactant(Dibenzyl) [2-(4-piperidyl)ethyl]amineHCID 66798731—
Solvent1-ButanolHCID 263—
ProductN,N-Dibenzyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamineHCID 6679925753%

Reaction Steps

N,N-Dibenzyl-2-(piperidin-4-yl)ethanamine (2.4 g, 7.79 mmol, 1 eq) and 4-bromopyridine HBr (1.97 g, 10.12 mmol, 1.3 eq) were dissolved in n-butanol (30 ml) and DIPEA (3.3 ml, 19.47 mmol, 2.5 eq) and the mixture was refluxed for 48 h. After monitoring by thin-layer chromatography, the reaction solution was concentrated under reduced pressure and the residue was taken up in dichloromethane (100 ml), washed with water and sat. NaCl solution (in each case 50 ml), dried over sodium sulfate and concentrated under reduced pressure. After purification by column chromatography (silica gel, 3.5% MeOH in dichloromethane), a white solid was obtained. Yield: 53% (1.6 g, 4.15 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-46feede4f6bd453f891f58330bae694d
Source noteuspto-grants-2014_03