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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 723589Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/723589

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloroimidazoline sulfateHCID 12503398—
Edukt4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamineHCID 21876857—
LösungsmittelIsopropanolHCID 3776—
Produkt2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazolineHCID 2187680859,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07141584B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-f4967b3a56184524b02094eb42413ce2
Quellennotizuspto-grants-2006_11