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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281021Generated: October 28, 2026

Piperidine → 4-[[N-(2-amino-5-trifluoromethylbenzoyl)glycyl]aminomethyl]piperidine

https://huagongshe.com/reaction/1281021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-[{(N-(2-Amino-4,5-difluorobenzoyl)glycyl)amino}methyl]piperidineHCID 18426176—
Reactant4-[{(N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl)amino}methyl]piperidineHCID 18426225—
Reactant4-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethoxybenzoyl)glycyl}aminomethyl]piperidineHCID 18426235—
Product4-[[N-(2-amino-5-trifluoromethylbenzoyl)glycyl]aminomethyl]piperidineHCID 18426227—

Reaction Steps

4-[{(N-(2-Amino-4,5-difluorobenzoyl)glycyl)amino}methyl]piperidine, 4-[{N-(2-(tert-Butoxycarbonylamino)-5-trifluoromethoxybenzoyl)glycyl}aminomethyl]piperidine, 4-[{N-(2-(tert-butoxycarbonylamino)-4,5-difluorobenzoyl)glycyl)amino}methyl]piperidine, and 4-[{(N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl)amino}methyl]piperidine were also prepared pursuant to the above method using the corresponding reactant, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451842B1
Source datasetuspto-grants-2002_09
ORD IDord-523888255d644986a5601d4407ac1a9f
Source noteuspto-grants-2002_09