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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43147Generated: October 29, 2026

1-(4-Methoxy-benzyl)-4-(5-nitro-pyridin-2-ylmethyl)-piperazine → 6-[4-(4-Methoxy-benzyl)-piperazin-1-ylmethyl]-pyridin-3-ylamine

https://huagongshe.com/reaction/43147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Methoxy-benzyl)-4-(5-nitro-pyridin-2-ylmethyl)-piperazineHCID 66914632—
CatalystNickelHCID 935—
SolventMeOH tetrahydrofuranHCID 21899815—
Product6-[4-(4-Methoxy-benzyl)-piperazin-1-ylmethyl]-pyridin-3-ylamineHCID 5929285176%

Reaction Steps

A suspension of 1-(4-methoxy-benzyl)-4-(5-nitro-pyridin-2-ylmethyl)-piperazine (Step 111.2) (0.635 g, 1.85 mmol) and Raney Nickel (0.150 g) in MeOH/THF (1:1, v/v; 50 mL) was stirred for 24 h at rt, under a hydrogen atmosphere. The mixture was filtered through a pad of celite and the filtrate was concentrated. The residue was purified by silica gel column chromatography (DCM/MeOH/NH3aq, 98:1:1) to afford 439 mg of the title compound as a white solid. Title compound: ESI-MS: 313.3 [M+H]+; tR=1.40 min (System 1); TLC: Rf=0.18 (DCM/MeOH, 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536175B2
Source datasetuspto-grants-2013_09
ORD IDord-912f81fd168d4fe8ac7d61c053d24efe
Source noteuspto-grants-2013_09