HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1799577Erstellt: 25. Oktober 2026
Triethylamine → (E)-Ethyl 3-(5-amino-2-iodopyrimidin-4-yl)acrylate
https://huagongshe.com/reaction/1799577
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl Acrylate | HCID 8821 | — |
| Edukt | 2,4-Diiodopyrimidin-5-amine | HCID 58216643 | — |
| Katalysator | Tetrabutylammonium Chloride | HCID 70681 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | (E)-Ethyl 3-(5-amino-2-iodopyrimidin-4-yl)acrylate | HCID 58216629 | — |
Reaktionsschritte
A 3-necked roundbottom flask was purged and maintained under an atmosphere of nitrogen. 2,4-Diiodopyrimidin-5-amine (135 g, 389.4 mmol) in dioxane (1400 ml) was added followed by palladium(II) acetate (4.8 g, 19.63 mmol), triethylamine (157 g, 1.55 mol), ethyl acrylate (390 g, 3.90 mol), and tetrabutylammonium chloride (108 g, 389.9 mmol). The resulting solution was allowed to react, with stirring, for 16 hours while the temperature was maintained at 90° C. Upon completion, the mixture was concentrated under reduced pressure. The resulting residue was purified via silica gel chromatography eluting with 1:4 to 1:1 ethyl acetate/petroleum ether to afford the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08344144B2 |
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| Quelldatensatz | uspto-grants-2013_01 |
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| ORD ID | ord-51a338a645dc43a3a71091f1c69ca483 |
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| Quellennotiz | uspto-grants-2013_01 |
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