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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40918Erstellt: 25. 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/reaction/40918

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt3-Cyanobenzoyl chlorideHCID 308483—
EduktHCID 178504228HCID 178504228—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrileHCID 5747766195,8%

Reaktionsbedingungen

Temperatur80 °C

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/MS (M+H)+ 418.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530485B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ac254a0b10274bd3b2a0d14446a7ea0e
Quellennotizuspto-grants-2013_09