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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68552Generated: October 25, 2026

1-Benzyl-4-(pyridin-3-yl)piperazine → 1-(Pyridin-3-yl)piperazine

https://huagongshe.com/reaction/68552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(pyridin-3-yl)piperazineHCID 21815409—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-(Pyridin-3-yl)piperazineHCID 43723462%

Reaction Steps

31.3 g 1-Benzyl-4-pyridin-3-yl-piperazin was hydrogenated at 5 bar on 4 g 10% palladium on charcoal in 300 mL methanol at 50° C. for 25 h. The reaction was filtered. The filtrate was evaporated and purified by chromatography on silica gel (dichlormethane/methanol/ammonia (9/1/0.1)). 12.5 g of the desired compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822464B2
Source datasetuspto-grants-2014_09
ORD IDord-fe990aa700d7442d94c6508d1f0b7864
Source noteuspto-grants-2014_09