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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599734Generated: October 30, 2026

Ethyl 4-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-butanoate → Ethyl 4-(4-piperazin-1-yl-piperidin-1-yl)-butanoate

https://huagongshe.com/reaction/599734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-butanoateHCID 66941713—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductEthyl 4-(4-piperazin-1-yl-piperidin-1-yl)-butanoateHCID 57807571—

Reaction Steps

A suspension of 2.9 g (7.76 mmol) ethyl 4-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-butanoate and 300 mg 10% Pd/C in 60 mL MeOH was hydrogenated at RT and 50 psi hydrogen pressure for 24 h. The catalyst was filtered off, the mixture was evaporated down i.vac., the residue was taken up in a little DIPE and isopropanol and combined with 4 M HCl in 1,4-dioxane. The precipitated bis-hydrochloride salt was separated off and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897603B2
Source datasetuspto-grants-2011_03
ORD IDord-f07820ce772248f3b0faa0f76c7d5f3d
Source noteuspto-grants-2011_03