HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 913674Erstellt: 25. Oktober 2026
Triethylamine → 1-{[5-(2,5-Dichloro-3-pyridinyl)-1,2,4-oxadiazol-3-yl]methyl}-2-propyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile
https://huagongshe.com/reaction/913674
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,5-Dichloro-nicotinoyl chloride | HCID 2799996 | — |
| Edukt | HCID 178438386 | HCID 178438386 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-{[5-(2,5-Dichloro-3-pyridinyl)-1,2,4-oxadiazol-3-yl]methyl}-2-propyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile | HCID 57800350 | 14,2% |
Reaktionsschritte
To a solution of 2-[5-cyano-2-propyl-4-(trifluoromethyl)-1H-indol-1-yl]-N-hydroxyethanimidamide (Example 275A) (0.100 g, 0.308 mmol) in anhydrous acetonitrile (10.0 mL) under N2, was added 2,5-dichloro-3-pyridinecarbonyl chloride (0.223 g, 1.10 mmol) and triethylamine (1.0 mL, 13.6 mmol). The mixture was then heated in a microwave at 150° C. for 30 min. Upon cooling, the mixture was poured onto a biotage prepak column and the mixture was purified by flash chromatography (0-25% EtOAc-hexanes gradient) to give 0.021 g (14% yield) of pure product: MS (ES) m/z 480 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08026262B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-cb1e382331b643dd81f573eeaaf3c750 |
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| Quellennotiz | uspto-grants-2011_09 |
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