HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44952Erstellt: 24. Oktober 2026
Pyridine → 3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrile
https://huagongshe.com/de/reaction/44952
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Pyridine | HCID 1049 | — |
| Edukt | 3-Cyanobenzoyl chloride | HCID 308483 | — |
| Edukt | HCID 178504228 | HCID 178504228 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrile | HCID 57477661 | 95,8% |
Reaktionsschritte
The crude product N-hydroxy-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridine-4-carboximidamide (0.06 gm, 0.0002 mol) was dissolved in pyridine (1.0 mL, 0.012 mol) and then 3-cyanobenzoyl chloride (0.040 g, 0.00024 mol) was added at rt. This mixture was stirred for 1 h and heated to 80° C. in an oil bath. After heating for 18 h the reaction was allowed to cool to rt and then diluted with ACN and concentrated in vacuo to give 3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrile 0.08 gm as an off white residue, LC/M S (M+H)+ 418.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541425B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-bf16f289f6114c23bb37251160b35eec |
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| Quellennotiz | uspto-grants-2013_09 |
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