HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993409Generated: October 25, 2026
2-Chloroimidazoline sulfate → 2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline
https://huagongshe.com/reaction/993409
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroimidazoline sulfate | HCID 12503398 | — |
| Reactant | 4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamine | HCID 21876857 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline | HCID 21876808 | 59.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472536B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-f4f612df8b3a42efa398b3f6b28444f6 |
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| Source note | uspto-grants-2002_10 |
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