HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228824Generated: October 31, 2026
Cesium carbonate → 3-(6,7-Dimethoxy-quinolin-4-yloxy)-5,6,5'-trimethyl-[2,2']bipyridine
https://huagongshe.com/reaction/228824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Reactant | 5,6,5'-Trimethyl-[2,2']bipyridin-3-ol | HCID 136385108 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(6,7-Dimethoxy-quinolin-4-yloxy)-5,6,5'-trimethyl-[2,2']bipyridine | HCID 57756451 | 29.4% |
Reaction Steps
Dimethyl sulfoxide (2.8 ml) was added to 5,6,5′-trimethyl-[2,2′]bipyridin-3-ol (60 mg), 4-chloro-6,7-dimethoxyquinoline (184 mg), cesium carbonate (274 mg), 4-(N,N-dimethylamino)-pyridine (51 mg), and cesium fluoride (64 mg) to prepare a solution which was then stirred at 140° C. overnight. The reaction solution was cooled to room temperature, water was then added to the reaction solution, 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 (33 mg, yield 29%).
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-2d83b5505904495294df572729fa61b7 |
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| Source note | uspto-grants-2009_07 |
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