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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730634Generated: October 30, 2026

1-(1-Benzyl-4-methyl-piperidin-4-yl)-4-methyl-piperazine → 1-Methyl-4-(4-methylpiperidin-4-yl)piperazine

https://huagongshe.com/reaction/730634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Benzyl-4-methyl-piperidin-4-yl)-4-methyl-piperazineHCID 67272986—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-Methyl-4-(4-methylpiperidin-4-yl)piperazineHCID 46738261—

Reaction Steps

A suspension of 0.99 g (3.27 mmol) 1-(1-benzyl-4-methyl-piperidin-4-yl)-4-methyl-piperazine and 200 mg 10% Pd/C in 25 mL MeOH was hydrogenated at 50° C. and 50 psi hydrogen pressure for 2 h. To complete the reaction a further 200 mg catalyst were added and the reaction mixture was hydrogenated for a further 22 h at 60° C. and 50 psi hydrogen pressure. The catalyst was filtered off and the filtrate evaporated to dryness. The product was reacted further without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582625B2
Source datasetuspto-grants-2009_09
ORD IDord-e6853b6f6c264c65a4219048aaa96ddd
Source noteuspto-grants-2009_09