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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300361Generated: November 2, 2026

3-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine → 4-[N-(3-Methylthiophenyl)-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/2300361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridineHCID 12043146—
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-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine TrihydrochlorideHCID 68918607—

Reaction Steps

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 3-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 numberUS06498169B1
Source datasetuspto-grants-2002_12
ORD IDord-a16fe636ac6e42e0bc1a3c48f6e9ea30
Source noteuspto-grants-2002_12