HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1880161Erstellt: 25. Oktober 2026
2-Cyclopenten-1-one → 3-(2-(4-(1H-Benzo[D]imidazole-2-carbonyl)phenoxy)pyridin-3-YL)cyclopent-2-enone
https://huagongshe.com/reaction/1880161
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Cyclopenten-1-one | HCID 13588 | — |
| Edukt | (1H-benzo[d]imidazol-2-yl)(4-(3-bromopyridin-2-yloxy)phenyl)methanone | HCID 59326957 | — |
| Katalysator | HCID 178418851 | HCID 178418851 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 3-(2-(4-(1H-Benzo[D]imidazole-2-carbonyl)phenoxy)pyridin-3-YL)cyclopent-2-enone | HCID 46214872 | — |
Reaktionsschritte
A suspension of (1H-benzo[d]imidazol-2-yl)(4-(3-bromopyridin-2-yloxy)phenyl)methanone (500 mg, 1.268 mmol), 2-cyclopenten-1-one (0.410 mL, 5.07 mmol), 105° C. and bis(tri-tert-butylphosphine)palladium (0) (64.8 mg, 0.127 mmol) in Dioxane (4 mL) was capped, degassed and backfilled with argon. The reaction was heated at 105° C. After 6 h, the reaction was cooled to 23° C., concentrated in vacuo and purified by silica gel chromatography (eluant: 40-100% EtOAc/hexane), affording the product as a yellow solid. MS (ESI, pos. ion) m/z: 396.1 (M+1). IC50 (uM) +++++.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08318718B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-e2e48b945aab45dc997a7491519e951e |
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| Quellennotiz | uspto-grants-2012_11 |
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