Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406474Generated: October 29, 2026

Triethylamine → 3,5-difluoro-N-{2-oxo-2-[3-(4-phenyl-piperidin-1-yl)-pyrrolidin-1-yl]-ethyl}-benzamide

https://huagongshe.com/reaction/406474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Difluorobenzoyl chlorideHCID 145600—
Reactant2-Amino-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanoneHCID 59764695—
SolventDichloromethaneHCID 6344—
Product3,5-difluoro-N-{2-oxo-2-[3-(4-phenyl-piperidin-1-yl)-pyrrolidin-1-yl]-ethyl}-benzamideHCID 5976494655%

Reaction Steps

To a solution of 2-amino-1-[3-(4-phenyl-piperidin-1-yl)-pyrrolidin-1-yl]-ethanone (preparation #9) (0.026 g, 0.09 mmol) and triethylamine (0.025 mL, 0.18 mmol) in DCM (0.7 mL) was added a solution of 3,5-difluoro-benzoyl chloride (0.016 g, 0.09 mmol) in dichloromethane (0.2 mL). The reaction mixture was stirred at ambient temperature for about 3 h then concentrated in vacuo. The residue was purified by flash chromatography on silica gel using 10% MeOH/EtOAc as the mobile phase to give 3,5-difluoro-N-{2-oxo-2-[3-(4-phenyl-piperidin-1-yl)-pyrrolidin-1-yl]-ethyl}-benzamide (0.021 g, 55%). RP-HPLC (Table 1, Method b) Rt 1.51 min; m/z: (M+H)+ 428.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754107B2
Source datasetuspto-grants-2014_06
ORD IDord-6313b5d7dcbc4671a49de9437e68ae74
Source noteuspto-grants-2014_06