HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228640Generated: October 29, 2026
Bromosalicylchloranilide → HCID 57756539, compound
https://huagongshe.com/reaction/228640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromosalicylchloranilide | HCID 77254 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 57756539 | HCID 57756539 | 25.7% |
Reaction Steps
4-Chloro-6,7-dimethoxyquinoline (100 mg), 5-bromo-4′-chlorosalicylanilide (653 mg), and 4-dimethylaminopyridine (244 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 120° C. overnight. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give the title compound (59 mg, yield 23%).
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-490f7a0df62946948cde51cb5fbc5628 |
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| Source note | uspto-grants-2009_07 |
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