HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888564Generated: October 26, 2026
5-Bromo-2-fluoropyridine-3-boronic Acid (contains varying amounts of Anhydride) → 5-Bromo-2-fluoro-6'-methoxy-[3,4]bipyridinyl-3'-ylamine
https://huagongshe.com/reaction/1888564
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromo-2-fluoropyridine-3-boronic Acid (contains varying amounts of Anhydride) | HCID 2783242 | — |
| Reactant | 4-Iodo-6-methoxypyridin-3-amine | HCID 11021287 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Potassium Fluoride | HCID 522689 | — |
| Product | 5-Bromo-2-fluoro-6'-methoxy-[3,4]bipyridinyl-3'-ylamine | HCID 58266519 | 71% |
Reaction Steps
A mixture of 6-methoxy-4-iodopyridin-3-amine (9.5 g, 38 mmol), 5-bromo-2-fluoropyridin-3-ylboronic acid (16.7 g, 76 mmol), and 1,1′-[bis(diphenylphosphino)ferrocene] dichloropalladium(II) (1.5 g, 2 mmol) in 1N aqueous potassium fluoride (95 mL) and acetonitrile (200 mL) was heated at 95° C. for 16 h. The cooled reaction mixture was diluted with water (100 mL) and extracted with DCM (3×100 mL). The combined organic layer was dried over sodium sulfate, filtered, and evaporated to afford a residue which was purified by flash chromotagraphy (silica, 120 g column, ISCO, 0-40% ethyl acetate in hexanes) to afford the title compound as a yellow/orange solid (8.0 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501765B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-46f763e4584a4f65bec2e8ab894e4a0d |
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| Source note | uspto-grants-2013_08 |
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