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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937702Generated: October 31, 2026

3-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine → 4-[N-(3,5-dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride

https://huagongshe.com/reaction/1937702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridineHCID 12043146—
Reactant4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidineHCID 22557810—
Product4-[N-(3,5-dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochlorideHCID 22558067—

Reaction Steps

4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (148 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. Yellow syrup obtained was converted to a trihydrochloroide to give the title compound as yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395753B1
Source datasetuspto-grants-2002_05
ORD IDord-5532e533947449a2a4c8080ba14949e0
Source noteuspto-grants-2002_05