Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358846Generated: October 27, 2026

2-Chloroimidazoline sulfate → 2-[4-(1-Benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline

https://huagongshe.com/reaction/1358846

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroimidazoline sulfateHCID 12503398—
Reactant4-(1-Benzenesulfonylpiperidin-4-ylmethyl)-phenylamineHCID 21877033—
SolventIsopropanolHCID 3776—
Product2-[4-(1-Benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazolineHCID 1209439689%

Reaction Steps

A mixture of 4-(1-benzenesulfonylpiperidin-4-ylmethyl)-phenylamine (0.28 g, 0.83 mmol) and 2-chloro-2-imidazoline sulfate (0.25 g, 1.25 mmol) in 2-propanol (20 mL) was heated under reflux for 30 minutes under nitrogen atmosphere. The reaction mixture was concentrated in vacuo. The residue was basified with 10% sodium hydroxide solution and extracted with dichloromethane. The organic layer was washed with cold water and brine, dried, and solvents removed in vacuo. The residue was chromatographed on neutral aluminum oxide, eluting with 1% methanol/dichloromethane, to give 2-[4-(1-benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline (0.29 g, 89%) as a foam. Analysis for C21H26N4O2S•5H2O: Calc.: C, 61.89; H, 6.68; N, 13.75; Found: C,62.00; H, 6.52; N, 13.85.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596876B2
Source datasetuspto-grants-2003_07
ORD IDord-3554434d4f3e4212b693876daeff2d19
Source noteuspto-grants-2003_07