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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395558Generated: October 31, 2026

tert-butyl 4-(4-methoxyanilino)tetrahydro-1(2H)-pyridinecarboxylate → 1-(tert-butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

https://huagongshe.com/reaction/395558

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(4-methoxyanilino)tetrahydro-1(2H)-pyridinecarboxylateHCID 2776119—
Reactant4-Chloromethyl-2-(2-methoxyphenyl)pyridineHCID 22557973—
Product1-(tert-butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidineHCID 22557890—

Reaction Steps

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(2-methoxyphenyl)pyridine (234 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605620B1
Source datasetuspto-grants-2003_08
ORD IDord-35557f461cc0495b9046734d6021c859
Source noteuspto-grants-2003_08