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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162356Generated: October 29, 2026

1-Benzyl-4-(2-methyl-4-pyridinyl)piperazine → 1-(2-Methylpyridin-4-yl)piperazine

https://huagongshe.com/reaction/1162356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(2-methyl-4-pyridinyl)piperazineHCID 23138266—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product1-(2-Methylpyridin-4-yl)piperazineHCID 16762377—

Reaction Steps

1-Benzyl-4-(2-methyl-4-pyridinyl)piperazine (10.3 g) obtained in Example 114a) and 10% palladium carbon (1.0 g) were added to methanol (200 ml), and mixed under hydrogen atmosphere at room temperature for 7 days. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified with basic silica gel column (ethyl acetate) and recrystallized from ethyl acetate-hexane to obtain the title compound as a colorless needle-like crystal (2.58 g, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820673B2
Source datasetuspto-grants-2010_10
ORD IDord-ebdfc00d2e2241ed8e23c40344042e29
Source noteuspto-grants-2010_10