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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395544Generated: October 26, 2026

Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate → 1-(tert-butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

https://huagongshe.com/reaction/395544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylateHCID 1491503—
Reactant4-Chloromethyl-2-(3,4,5-trimethoxyphenyl) pyridineHCID 12019237—
Product1-(tert-butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidineHCID 22557808—

Reaction Steps

1-(tert-Butoxycarbonyl)-4-[(4-chlorophenyl)amino]piperidine (621 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605620B1
Source datasetuspto-grants-2003_08
ORD IDord-aea10e9e54fa41ae8a24162568ffc196
Source noteuspto-grants-2003_08