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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Chloroimidazoline sulfate | HCID 12503398 | — |
| Edukt | 4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamine | HCID 21876857 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline | HCID 21876808 | 59,2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07141584B2 |
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| Quelldatensatz | uspto-grants-2006_11 |
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| ORD ID | ord-f4967b3a56184524b02094eb42413ce2 |
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| Quellennotiz | uspto-grants-2006_11 |
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