HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228521Generated: October 26, 2026
6,7-Dimethoxy-4-(4-methyl-2-nitrophenoxy)quinoline → 4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinoline
https://huagongshe.com/reaction/228521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6,7-Dimethoxy-4-(4-methyl-2-nitrophenoxy)quinoline | HCID 23078402 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | triethylamine N,N-dimethylformamide | HCID 22056947 | — |
| Product | 4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinoline | HCID 23078587 | 55% |
Reaction Steps
6,7-Dimethoxy-4-(4-methyl-2-nitrophenoxy)quinoline (480 mg) was dissolved in triethylamine/N,N-dimethylformamide (2 ml/10 ml), and palladium hydroxide (1.2 g) was added to the solution. The mixture was stirred at room temperature in a hydrogen gas atmosphere overnight. The reaction solution was filtered through Celite, and the solvent was removed therefrom by distillation under the reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine 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-chloroform to give 4-(2-amino-4-methylphenoxy)-6,7-dimethoxyquinoline (240 mg, yield 55%).
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-930b457f96284836a2aa31352c709973 |
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| Source note | uspto-grants-2009_07 |
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