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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178404Generated: October 27, 2026

Benzoyl chloride → N-[4-(1-Benzoylpiperidin-4-YL)butyl]-3-pyridin-3-ylpropanamide

https://huagongshe.com/reaction/1178404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(4-piperidin-4-yl-butyl)-3-(pyridin-3-yl)-propionamideHCID 18425707—
SolventDimethylformamideHCID 6228—
ProductN-[4-(1-Benzoylpiperidin-4-YL)butyl]-3-pyridin-3-ylpropanamideHCID 9543513—

Reaction Steps

3.48 ml (30 mmol) benzoyl chloride, 8.7 g (30 mmol) N-(4-piperidin-4-yl-butyl)-3-(pyridin-3-yl)-propionamide and 16.6 g (120 mmol) potassium carbonate are stirred in 160 ml DMF at RT overnight. Subsequently, this is filtered and the filtrate is concentrated under vacuum to a large extent. The residue is taken up in 400 ml CHCl3 and washed twice, each with 100 ml water. The organic phase is dried over sodium sulfate and the solvent is removed under vacuum. The residue is chromatographically purified over silica gel with CHCl3/CH3OH (95/5) and precipitates as an amorphous solid after drawing off the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276524B2
Source datasetuspto-grants-2007_10
ORD IDord-a11497185fba4a8a922d29ae36bac0af
Source noteuspto-grants-2007_10