HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510856Generated: October 26, 2026
Nitrogen → 1-[4-Chloro-6-(2,6-difluoropyridin-4-yl)-5-methylbiphenyl-2-yl]ethanone
https://huagongshe.com/reaction/510856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2,6-Difluoropyridine-4-boronic acid | HCID 2762747 | — |
| Reactant | 1-(6-Bromo-4-chloro-5-methylbiphenyl-2-yl)ethanone | HCID 86666787 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[4-Chloro-6-(2,6-difluoropyridin-4-yl)-5-methylbiphenyl-2-yl]ethanone | HCID 86666788 | 30% |
Reaction Steps
A biphasic solution of 1-(6-bromo-4-chloro-5-methylbiphenyl-2-yl)ethanone (0.20 g, 0.62 mmol) and (2,6-difluoropyridin-4-yl)boronic acid (0.12 g, 0.74 mmol) in 1,4-dioxane (2.0 mL) and 10% Na2CO3 in water (0.98 mL, 0.93 mmol)) was bubbled with N2 to degas. After tetrakis(triphenylphosphine)palladium(0) (29 mg, 0.025 mmol) was added the mixture was bubbled with N2 for 5 min. and heated at 100° C. overnight. The mixture was cooled to room temperature and diluted with ethyl acetate. The layers were separated and the aq. layer was extracted with more ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified on silica gel column, eluting with 0-30% of ethyl acetate in hexane, to give the desired product (60 mg, 30%). LCMS calculated for C20H15ClF2NO (M+H)+: m/z=358.1. found: 358.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096600B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-5c02a9856bba4c47b9bc7ab66ea54f41 |
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| Source note | uspto-grants-2015_08 |
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