HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385486Generated: October 28, 2026
Ethyl Acrylate → 7-Methoxy-1,5-naphthyridin-2(1H)-one
https://huagongshe.com/reaction/385486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 2-Chloro-5-methoxypyridin-3-amine | HCID 20200420 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 7-Methoxy-1,5-naphthyridin-2(1H)-one | HCID 57815410 | — |
| Product | ethyl (2E)-3-(3-amino-5-methoxypyridin-2-yl)acrylate | HCID 68105232 | — |
Reaction Steps
To 1.0 g of 2-chloro-5-methoxypyridin-3-amine, 0.82 mL of ethyl acrylate, 4.2 mL of triethylamine, and 0.16 g of bis(tri-tert-butylphosphine)palladium(0) were added, and the mixture was stirred at an external temperature of 150 to 160° C. for 6 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 0.41 g of ethyl (2E)-3-(3-amino-5-methoxypyridin-2-yl)acrylate and 0.25 g of 7-methoxy-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 | US08367831B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-a086e5911642442f8b2a38298447f647 |
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| Source note | uspto-grants-2013_02 |
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