HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82230Generated: October 27, 2026
Picolinic acid → Ethyl 1,5-naphthyridin-3-ylacetate
https://huagongshe.com/reaction/82230
Participants
| Role | Name | HCID | Charge |
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| Reactant | Picolinic acid | HCID 1018 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,2-Diethylpropanedioate | HCID 6951563 | — |
| Reactant | 3-Bromo-1,5-naphthyridine | HCID 12878818 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 1,5-naphthyridin-3-ylacetate | HCID 70817520 | 402.5% |
Reaction Steps
A mixture of 3-bromo-1,5-naphthyridine (540 mg, 2.58 mmol), diethylmalonate (0.8 mL, 5.17 mmol) and cesium carbonate (2.53 g, 7.75 mmol) in 1,4-dioxane (6 mL) was degassed with argon for 15 min then picolinic acid (64 mg, 0.517 mmol) and CuI (50 mg, 0.258 mmol) was added. The mixture was heated in a sealed tube at 110° C. for 24 hours then cooled to room temperature, diluted with ethyl acetate (10 mL), washed with water (10 mL) and brine (10 mL). The organic phase was dried over sodium sulphate then evaporated in vacuo and purified by column chromatography on silica gel (hexane:EtOAc 70:30) to afford 450 mg of ethyl 1,5-naphthyridin-3-ylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846698B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-dbf074aa3cb349a3be97092eb8999ff6 |
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| Source note | uspto-grants-2014_09 |
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