HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228522Generated: October 26, 2026
Phenylboronic Acid → N-[2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl]-N-phenylamine
https://huagongshe.com/reaction/228522
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinoline | HCID 23078587 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | triethylamine N,N-dimethylformamide | HCID 22056947 | — |
| Product | N-[2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl]-N-phenylamine | HCID 23156624 | 77.2% |
Reaction Steps
4-(2-Amino-4-methylphenoxy)-6,7-dimethoxyquinoline (52 mg) was dissolved in triethylamine/N,N-dimethylformamide (0.5 ml/2.5 ml), and phenylboronic acid (100 mg) and copper acetate (250 mg) were added to the solution which was then stirred at room temperature overnight. The reaction solution was filtered, 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. Next, 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 thin layer chromatography using acetone-chloroform to give the title compound (50 mg, yield 76%).
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-cb2c590698844012b3e2a9628d8f6546 |
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| Source note | uspto-grants-2009_07 |
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