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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395557Generated: October 29, 2026

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

https://huagongshe.com/reaction/395557

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(4-methoxyanilino)tetrahydro-1(2H)-pyridinecarboxylateHCID 2776119—
Reactant4-(Chloromethyl)-2-phenylpyridineHCID 16126061—
Product1-(tert-butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]piperidineHCID 22557917—

Reaction Steps

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (612 mg) and 4-chloromethyl-2-phenylpyridine (204 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-ad0c0caae1894a62bcae8d35b294b85b
Source noteuspto-grants-2003_08