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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289527Generated: November 1, 2026

4-(4-Benzylpiperazin-1-yl)-6-chloropyrimidine → 4-(Piperazin-1-yl)pyrimidine

https://huagongshe.com/reaction/2289527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Benzylpiperazin-1-yl)-6-chloropyrimidineHCID 18698052—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(Piperazin-1-yl)pyrimidineHCID 1832113776%

Reaction Steps

1-(Benzyl)-4-(4-chloropyrimidin-6-yl)piperazine (58.0 g) was dissolved, with some heating, in methanol (700 ml), treated with 10% Pd on activated carbon (11.6 g) and agitated and hydrogenated at atmospheric pressure for 8 h. The catalyst was removed by filtering through celite. The filtrate thus obtained was then evaporated under reduced pressure to a yellow-brown viscous gum which was chromatographed through 60 υm silica gel, eluting with 5% methanol, 1% ammonium hydroxide and 94% dichloromethane to obtain 4-(4-pyrimidinyl)piperazine, as a white solid, 25 g (76% yield based on prehydrogenation substrate);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093718
Source datasetuspto-grants-2000_07
ORD IDord-8a55d6c0af4e4710bfb64becf0de1071
Source noteuspto-grants-2000_07