HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358839Generated: October 29, 2026
2-Chloroimidazoline sulfate → 2-[4-(5-Methoxythien-2-ylmethyl)phenyl]amino-imidazoline
https://huagongshe.com/reaction/1358839
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroimidazoline sulfate | HCID 12503398 | — |
| Reactant | 4-(5-Methoxythien-2-ylmethyl)-phenylamine | HCID 21876866 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[4-(5-Methoxythien-2-ylmethyl)phenyl]amino-imidazoline | HCID 21876823 | 70% |
Reaction Steps
To a solution of [4-(5-methoxythien-2-ylmethyl)-phenylamine (145 mg, 0.66 mmol) in acetonitrile (10 ml) was added 2-chloro-2-imidazoline sulfate (155 mg, 0.76 mmol) at 20-25° C. under nitrogen. The resulting suspension was heated at 80° C. for 1.5 hours. The mixture was diluted with dichloromethane and washed with 10% sodium hydroxide, water, dried (Na2SO4), and concentrated to dryness. Purification by preparative TLC, eluting with ethyl acetate/methyl alcohol/isoprolpylamine, gave 2-[4-(5-methoxythien-2-ylmethyl)phenyl]amino-imidazoline (132 mg, 70%) as a yellow oil; 1H NMR (300 MHz, CDCl3) δ 7.12 (d,J=8.4 Hz, 2H), 6.93 (d,J=8.4 Hz, 2H), 6.39 (dt, J=3.7, 1.1 Hz, 1H), 5.98 (d,J=3.7 Hz, 1H), 3.92 (bs, 2H), 3.82 (S,3H), 3.52 (S,4H), 3.15-3.35 (broad, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06596876B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-2e7280362c8f4050991db1bffd9b8ea7 |
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| Source note | uspto-grants-2003_07 |
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