HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228871Generated: October 30, 2026
Water → 6,7-Dimethoxy-4-(7-methoxy-quinolin-6-yloxy)-quinoline
https://huagongshe.com/reaction/228871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Reactant | 6-Hydroxy-7-methoxyquinoline | HCID 23078429 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 6,7-Dimethoxy-4-(7-methoxy-quinolin-6-yloxy)-quinoline | HCID 23078554 | 100% |
Reaction Steps
6-Hydroxy-7-methoxyquinoline (65 mg), 4-chloro-6,7-dimethoxyquinoline (100 mg), and 4-dimethylaminopyridine (148 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 155° C. overnight. The reaction solution was cooled to room temperature. Water was then added thereto, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-chloroform to give the title compound (134 mg, yield 100%).
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-6b8e2cf01bb04fc8a9e7e4d33214cc27 |
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| Source note | uspto-grants-2009_07 |
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