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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723589Generated: October 26, 2026

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

https://huagongshe.com/reaction/723589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroimidazoline sulfateHCID 12503398—
Reactant4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamineHCID 21876857—
SolventIsopropanolHCID 3776—
Product2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazolineHCID 2187680859.2%

Reaction Steps

A mixture of 4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamine (0.64 g, 2.31 mmol) and 2-chloro-2-imidazoline sulfate (0.70 g, 3.47 mmol) in 2-propanol (20 mL) was heated under reflux for 30 minutes. The reaction mixture was concentrated in vacuo. The residue was diluted with water, basified with 10% sodium hydroxide solution and extracted into dichloromethane. The organic layer was washed with water and brine, dried (Na2SO4), and concentrated in vacuo. The crude product was chromatographed on neutral aluminum oxide, eluting with 5% methanol/dichloromethane, and crystallized from ethyl acetate containing some ethanol, to give 2-[4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline (0.47 g, 59%) as a white solid, m.p. 191–192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141584B2
Source datasetuspto-grants-2006_11
ORD IDord-f4967b3a56184524b02094eb42413ce2
Source noteuspto-grants-2006_11