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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395556Generated: October 29, 2026

1-Boc-4-AP → 1-(tert-butoxycarbonyl)-4-[N-phenyl-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

https://huagongshe.com/reaction/395556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-APHCID 1491502—
Reactant3-(3,4,5-Trimethoxyphenyl)benzyl chlorideHCID 12021157—
Product1-(tert-butoxycarbonyl)-4-[N-phenyl-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidineHCID 22557937—

Reaction Steps

1-(tert-Butoxycarbonyl)-4-phenylaminopiperidine (553 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 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-1bd0d96d19194dc8836edac65ac42fb6
Source noteuspto-grants-2003_08