HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228696Generated: October 25, 2026
Water → 4-(4-Imidazol-1-yl-2-iodo-phenoxy)-6,7-dimethoxy-quinoline
https://huagongshe.com/reaction/228696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Reactant | 4-(Imidazol-1-yl)-2-iodophenol | HCID 22274493 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 4-(4-Imidazol-1-yl-2-iodo-phenoxy)-6,7-dimethoxy-quinoline | HCID 23078523 | 45.2% |
Reaction Steps
4-(Imidazol-1-yl)-2-iodophenol (123 mg), 4-chloro-6,7-dimethoxyquinoline (288 mg), and 4-dimethylaminopyridine (158 mg) were suspended in o-dichlorobenzene (3 ml), and the suspension was stirred at 140° C. for 7.5 hr. The reaction solution was cooled to room temperature, water was then added thereto, and the mixture was extracted with chloroform. The chloroform layer was washed with saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure. The residue was purified by thin layer chromatography using chloroform-methanol to give the title compound (92 mg, yield 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-08b79c1fb86e4d6f9b5bdff5798ef0eb |
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| Source note | uspto-grants-2009_07 |
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