HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228790Generated: October 25, 2026
Dimethylformamide → 4-[2-(3,5-Difluoro-phenyl)-6-methyl-pyridin-3-yloxy]-6,7-dimethoxy-quinoline
https://huagongshe.com/reaction/228790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3,5-Difluorophenyl)boronic acid | HCID 2734338 | — |
| Reactant | 4-[(2-Iodo-6-methyl-3-pyridyl)oxy]-6,7-dimethoxyquinoline | HCID 10093673 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[2-(3,5-Difluoro-phenyl)-6-methyl-pyridin-3-yloxy]-6,7-dimethoxy-quinoline | HCID 57756353 | 47.6% |
Reaction Steps
N,N-Dimethylformamide (1 ml) and a 2 M aqueous potassium carbonate solution (1 ml) were added to 4-(2-iodo-6-methyl-pyridin-3-yloxy)-6,7-dimethoxy-quinoline (compound 116) (50 mg), tetrakistriphenylphosphine palladium (14 mg), and 3,5-difluorophenylboronic acid (56 mg) under an argon atmosphere, and the mixture was stirred at 70° C. for 5 hr. 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 then 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 thin layer chromatography using chloroform-methanol to give the title compound (23 mg, yield 47%).
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-17cf456e60b04877a3df7e0c1e32d90a |
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| Source note | uspto-grants-2009_07 |
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