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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782736Generated: October 29, 2026

4-(4-Benzylpiperazin-1-yl)-2-chloropyrimidine → 4-(Piperazin-1-yl)pyrimidine

https://huagongshe.com/reaction/1782736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Benzylpiperazin-1-yl)-2-chloropyrimidineHCID 18321300—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(Piperazin-1-yl)pyrimidineHCID 18321137—

Reaction Steps

A solution of 7.4 g (0.0256 mol) of 1-(2-chloro-4-pyrimidinyl)-4-(phenylmethyl)piperazine in 100 ml of ethanol was hydrogenated in the presence of 2 g of 10% palladium/charcoal for 4 hours at 40° C. under 5 bar of hydrogen pressure. The crude product obtained after conventional working up was purified by column chromatography over silica gel (30-60 μm) using FM1/cyclohexane 9/1 (v/v) as eluant. Colourless crystals, Rf=0.3 (FM1/cyclohexane 9/1 (v/v)); Macherey-Nagel POLYGRAM® SIL G/UV254, ready-made films for TLC). Yield: 1.7 g (40.7% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498325B2
Source datasetuspto-grants-2009_03
ORD IDord-d5eced98e88047eaa4bbdc008c01c5b9
Source noteuspto-grants-2009_03