HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047588Generated: November 2, 2026
Water → Ethyl 5-bromo-5'-methyl-2,3'-bipyridine-4-carboxylate
https://huagongshe.com/reaction/2047588
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Methylpyridine-3-boronic acid | HCID 2762708 | — |
| Reactant | Ethyl 2,5-dibromoisonicotinate | HCID 46311329 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 5-bromo-5'-methyl-2,3'-bipyridine-4-carboxylate | HCID 58394285 | — |
Reaction Steps
To a solution ethyl 2,5-dibromoisonicotinate (1-2, 1.5 g, 4.86 mmol) in degassed dimethylformamide (24 mL) at 25° C. was added (5-methylpyridin-3-yl)boronic acid (0.665 g, 4.86 mmol), PdCl2dppf (0.355 g, 0.486 mmol), cesium carbonate (4.75 g, 14.6 mmol) and water (0.262 mL, 14.57 mmol). The reaction flask was purged with nitrogen, sealed and stirred at 50° C. overnight. The crude reaction mixture was partitioned between water and EtOAc, separating layers and washing the organic layer with saturated sodium bicarbonate solution and brine. The solvent was removed by rotary evaporation and the crude product was purified by normal phase column chromatography (0 to 50% EtOAc in hexanes) to afford the product (1-3) as a white solid. ESI+MS[M]+C14H13BrN2O2=321.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592457B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-5ebfb4a674c04f07ae2a65ce5bfc633e |
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| Source note | uspto-grants-2013_11 |
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