Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846642Generated: November 1, 2026

1-(2-(Piperidin-4-yl)ethyl)piperidine → HCID 67321965, compound

https://huagongshe.com/reaction/1846642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-(Piperidin-4-yl)ethyl)piperidineHCID 296292—
Reactant4-chloro-n-cyclopropyl-3-nitrobenzamideHCID 881839—
SolventAcetonitrileHCID 6342—
ProductHCID 67321965HCID 6732196579.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 0.612 g (2.51 mmol) of 4-chloro-N-cyclopropyl-3-nitro-benzamide and 0.50 g (2.5 mmol) of 1-(2-piperidin-4-yl-ethyl)-piperidine in acetonitrile (0.5 mL) are heated at 110° C. for 30 minutes in a microwave reactor. The mixture is cooled to room temperature and concentrated under reduced pressure. The residue is purified by flash silica gel chromatography to provide 0.80 g (79%) of N-cyclopropyl-3-nitro-4-[4-(2-piperidin-1-yl-ethyl)-piperidin-1-yl]-benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952004B2
Source datasetuspto-grants-2015_02
ORD IDord-c3e7674e77474d05bf5a90491ba5f0af
Source noteuspto-grants-2015_02