Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acrylate | HCID 8821 | — |
| Edukt | 2-Bromo-5-fluoropyridin-3-amine | HCID 40427367 | — |
| Katalysator | HCID 178418851 | HCID 178418851 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 7-Fluoro-1,5-naphthyridin-2(1H)-one | HCID 46900801 | — |
| Produkt | ethyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate | HCID 68105283 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08367831B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-d2f3bbce24b54a4fa176006bd43234d3 |
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| Quellennotiz | uspto-grants-2013_02 |
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