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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 570302Erstellt: 25. Oktober 2026

3-Butenenitrile → Ethyl 6-(3-cyanoprop-1-enyl)imidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/570302

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-ButenenitrileHCID 8009—
EduktTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
EduktBis(cyclohexylmethyl)amineHCID 4594378—
EduktEthyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 22031055—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktEthyl 6-(3-cyanoprop-1-enyl)imidazo[1,2-a]pyridine-3-carboxylateHCID 78048051—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A stirring mixture of ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s) (500 mg, 1.86 mmol), allyl cyanide (224 uL, 2.79 mmol), tris(dibenzylideneacetone)dipalladium(0) (26 mg, 0.028 mmol), [(t-Bu)3PH]BF4 (16 mg, 0.056 mmol), and N,N-dicyclohexylmethylamine (433 μL, 2.04 mmol) in anhydrous 1,4-dioxane (6 mL) was heated at 95° C. overnight. The reaction was cooled to room temperature and filtered. The solvent was concentrated. The crude product was purified by silica chromatography to give ethyl 6-(3-cyanoprop-1-enyl)imidazo[1,2-a]pyridine-3-carboxylate (24v). MS m/z 256.4 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09023839B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-de6cf54cdf7049b096a94fa167ded438
Quellennotizuspto-grants-2015_05