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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 429044Erstellt: 24. Oktober 2026

Cyanide → HCID 86757583, Verbindung

https://huagongshe.com/de/reaction/429044

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanideHCID 5975—
EduktSodium CyanideHCID 8929—
Eduktethyl 4-chloro-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 10491120—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 86757583HCID 8675758340%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 4-chloro-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester (10.0 g, 39.5 mmol) in DMF (50 mL) and ethanol (10 mL) was added either sodium cyanide (3.9 g, 80.0 mmol) or tetrabutylarimonium cyanide (11.8 g, 1.1 eq) or tetrabutylammonium chloride (14.7 g, 1.0 eq) and sodium cyanide (2.4 g, 1.2 eq) together. This solution or suspension was warmed up to 60° C. until reaction was completed as judged by TLC. The reaction mixture was then diluted with water (200 mL) and stirred gently at rt for 10 min. A large amount of precipitate formed. The solid was filtered and rinsed thoroughly with water to afford the title compound as an off-white solid after drying: 40-80% yield. This material was >95% pure as judged by HPLC and was used directly without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06316438B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-f29d4bde23a8479e8594b6e02fd39747
Quellennotizuspto-grants-2001_11