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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1045435Erstellt: 25. Oktober 2026

tert-Butyl acrylate → Ethyl 6-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)imidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1045435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl acrylateHCID 15458—
EduktTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
EduktBis(cyclohexylmethyl)amineHCID 4594378—
EduktEthyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 22031055—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktEthyl 6-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)imidazo[1,2-a]pyridine-3-carboxylateHCID 78048034—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A stirring mixture of ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s) (500 mg, 1.86 mmol), tert-butyl acrylate (408 uL, 2.79 mmol), tris(dibenzylideneacetone)diplalladium(0) (51 mg, 0.056 mmol), [(t-Bu)3PH]BF4 (27 mg, 0.093 mmol) and N,N-dicyclohexylmethylamine (738 uL, 3.48 mmol) in anhydrous 1,4-dioxane (5 mL) was heated at 95° C. overnight. The reaction was cooled to room temperature and filtered. The solvent was concentrated and the crude product was purified by silica chromatography to yield ethyl 6-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)imidazo[1,2-a]pyridine-3-carboxylate (70). MS m/z 317.14 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08569283B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-3d041e9dd9234cc884cca02f76a12913
Quellennotizuspto-grants-2013_10