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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 634834Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/634834

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 vacua. 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 vacua. 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
PatentnummerUS06184242B2
Quelldatensatzuspto-grants-2001_02
ORD IDord-defd4999d63849a5a49cf176ccee5808
Quellennotizuspto-grants-2001_02