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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371122Generated: October 26, 2026

3-Chloro-4-(trifluoromethyl)aniline → N-[3-chloro-4-(trifluoromethyl)phenyl]-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carboxamide

https://huagongshe.com/reaction/2371122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-(trifluoromethyl)anilineHCID 67962—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant1-[(1-Methylpiperidin-3-yl)methyl]piperazineHCID 2736940—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChloroformHCID 6212—
ProductN-[3-chloro-4-(trifluoromethyl)phenyl]-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carboxamideHCID 115969126.7%

Reaction Steps

To a solution of di-tert-butyl dicarbonate (114.6 mg) in chloroform (2 ml) was added 4-dimethylaminopyridine (6 mg). A solution of 4-amino-2-chlorobenzotrifluoride (98.1 mg) in chloroform (2 ml) was added and the reaction mixture stirred for 20 minutes at room temperature. A solution of 1-[(1-methylpiperidin-3-yl)methyl]piperazine (98.5 mg) in chloroform (2 ml) was added and the resulting solution was stirred at reflux for 18 hours. The reaction mixture was purified by column chromatography on silica gel (20 g) using a gradient of 100% dichloromethane through to 20% methanolic ammonia in dichloromethane to give the title compound (14 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-8e0d3d9fba2e49d6a49b26fb7b1a123d
Source noteuspto-grants-2014_04