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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 405784Erstellt: 25. Oktober 2026

Sulfuric Acid → Ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/405784

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
Edukt2-Amino-5-bromopyridineHCID 70622—
EduktEthyl 2-chloro-3-hydroxyacrylate potassium saltHCID 86677443—
LösungsmittelEthanolHCID 702—
ProduktEthyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 22031055—

Reaktionsbedingungen

Temperatur78 °C

Reaktionsschritte

To a stirring suspension of 5-bromopyridin-2-amine (1.2 g, 7.05 mmol) and ethyl 2-chloro-3-hydroxyacrylate potassium salt (6.6 g, 28.19 mmol) (prepared in a similar manner as 22) in EtOH (100 mL) at room temperature was added sulfuric acid (751 μL, 14.10 mmol) dropwise. The reaction mixture was heated at 78° C. overnight. The reaction was cooled to room temperature and the solvent was concentrated. The residue was taken in water and the pH was adjusted between 6-8 with saturated sodium bicarbonate. The crude product was extracted with ethyl acetate. The organic was washed with brine and dried over anhydrous sodium sulfate. The crude product was purified by silica chromatography to yield ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s). MS m/z 270.2 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754071B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-86420139cbc04ae9b7acb9cc6abe8afd
Quellennotizuspto-grants-2014_06