HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634837Generated: October 26, 2026
2-Chloroimidazoline sulfate → 2-[4-(1-Benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline
https://huagongshe.com/reaction/634837
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroimidazoline sulfate | HCID 12503398 | — |
| Reactant | 4-(1-Benzenesulfonylpiperidin-4-ylmethyl)-phenylamine | HCID 21877033 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-[4-(1-Benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline | HCID 12094396 | 89% |
Reaction Steps
A mixture of 4-(1-benzenesulfonylpiperidin-4-ylmethyl)-phenylamine (0.28 g, 0.83 mmol) and 2-chloro-2-imidazoline sulfate (0.25 g, 1.25 mmol) in 2-propanol (20 mL) was heated under reflux for 30 minutes under nitrogen atmosphere. The reaction mixture was concentrated in vacuo. The residue was basified with 10% sodium hydroxide solution and extracted with dichloromethane. The organic layer was washed with cold water and brine, dried, and solvents removed in vacuo. The residue was chromatographed on neutral aluminum oxide, eluting with 1% methanol/dichloromethane, to give 2-[4-(1-benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline (0.29 g, 89%) as a foam. Analysis for C21H26N4O2S85H20: Calc.: C, 61.89; H, 6.68; N, 13.75; Found: C, 62.00; H, 6.52; N, 13.85.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06184242B2 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-78148a89bce34817a77bab1356af4896 |
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| Source note | uspto-grants-2001_02 |
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