HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2267446Erstellt: 24. Oktober 2026
Sodium Carbonate → 1-(2-(5-(4-Chlorophenyl)-4-(thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one
https://huagongshe.com/de/reaction/2267446
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Edukt | 1-(2-(5-Bromo-4-(thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one | HCID 60204573 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-(2-(5-(4-Chlorophenyl)-4-(thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one | HCID 60204574 | — |
Reaktionsschritte
1-(2-(5-Bromo-4-(thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one (0.1 g, 0.27 mmol), 4-chlorophenylboronic acid (0.085 g, 0.54 mmol), sodium carbonate (0.27 mL of 2.0 M solution, 0.52 mmol) were added to a flask containing dioxane (1 mL). The flask was flushed with nitrogen and tetrakis(triphenylphosphine)palladium (0.062 g, 0.054 mmol) was added. The reaction was heated to 80° C. overnight. The reaction was cooled down to ambient temperature and diluted with ethyl acetate and water. The organic layer was filtered through a pad of celite and washed with saturated aqueous sodium bicarbonate, water and brine. The organic layer was then dried with sodium sulfate, concentrated and purified by column chromatography using a gradient 2 to 10% of methanol in dichloromethane to afford an off-white solid. Yield=0.04 g. MS (M+H)+ 400.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07858785B2 |
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| Quelldatensatz | uspto-grants-2010_12 |
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| ORD ID | ord-9727dfe2feca4dd89ce10a3340f68918 |
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| Quellennotiz | uspto-grants-2010_12 |
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