Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121062Generated: November 3, 2026

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

https://huagongshe.com/reaction/2121062

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% methanovdichloromethane, 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 numberUS06693200B2
Source datasetuspto-grants-2004_02
ORD IDord-b2f329af4890436ca935711ff6dd705c
Source noteuspto-grants-2004_02