HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80105Erstellt: 24. Oktober 2026
Potassium Carbonate → 1-Naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one
https://huagongshe.com/de/reaction/80105
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| Edukt | 3-Bromo-5-(trifluoromethyl)pyridine | HCID 11127991 | — |
| Edukt | 1-Naphthalen-2-yl-imidazolidin-2-one | HCID 59636167 | — |
| Katalysator | Copper iodide | HCID 83717 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 1-Naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one | HCID 59636216 | 52% |
Reaktionsschritte
Copper iodide (12.6 mg, 0.066 mmol), trans-1,2-diamino cyclohexane (22.79 mg, 0.199 mmol) and potassium carbonate (183.5 mg, 1.32 mmol) were added to 1,4-dioxane (5 mL) and 3-bromo-5-trifluoromethyl-pyridine (150 mg, 0.66 mmol) previously degassed with argon (10 minutes). The reaction was purged with argon for a further 10 minutes, followed by the addition of 1-naphthalen-2-yl-imidazolidin-2-one (I-79b: 140 mg, 0.66 mmol) and the resulting mixture was heated to reflux at 110° C. for 15 hours. The reaction was monitored by TLC (50% ethyl acetate in hexane). The reaction mixture was filtered through celite and the bed was washed with chloroform. The organic layer was dried over Na2O4 and concentrated. Purification by column chromatography (using silica gel of mesh size of 60-120, 30% EtOAc in hexane as eluant) afforded 120 mg (52% yield) of 1-naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | USRE045173E1 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-b4701bd379cf4461a06ebbf58e991c9b |
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| Quellennotiz | uspto-grants-2014_09 |
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