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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395493Generated: November 4, 2026

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

https://huagongshe.com/reaction/395493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridineHCID 12043486—
Reactant4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidineHCID 22557887—
Product4-[N-(3-Methylthiophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine TrihydrochlorideHCID 68923108—

Reaction Steps

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605620B1
Source datasetuspto-grants-2003_08
ORD IDord-6158551688ec4efc8d861895cab874fb
Source noteuspto-grants-2003_08