HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510613Generated: October 26, 2026
Ethyl Acrylate → 7-Fluoro-1,5-naphthyridin-2(1H)-one
https://huagongshe.com/reaction/1510613
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 2-Bromo-5-fluoropyridin-3-amine | HCID 40427367 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 7-Fluoro-1,5-naphthyridin-2(1H)-one | HCID 46900801 | — |
| Product | ethyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate | HCID 68105283 | — |
Reaction Steps
To 0.99 g of 2-bromo-5-fluoropyridin-3-amine, 0.67 mL of ethyl acrylate, 3.5 mL of triethylamine, and 0.13 g of bis(tri-tert-butylphosphine)palladium(0) were added, and the mixture was stirred at an external temperature of 145 to 150° C. for 5 hours in a sealed tube. The reaction mixture was cooled to room temperature and the solvent was distilled off under reduced pressure. The resultant residue was purified by flash silica gel column chromatography using gradient elution with chloroform:methanol=100:0 to 90:10 to obtain 0.37 g of ethyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate and 0.15 g of 7-fluoro-1,5-naphthyridin-2(1H)-one as light brown solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211908B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-5f9e88e7673d4358b8e829909d845ee2 |
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| Source note | uspto-grants-2012_07 |
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