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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 251763Erstellt: 25. Oktober 2026

2-Aminopyridine → 2-(4-Iodophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/251763

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminopyridineHCID 10439—
Edukt2-Bromo-1-(4-iodophenyl)ethanoneHCID 256572—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
Produkt2-(4-Iodophenyl)imidazo[1,2-a]pyridineHCID 78506582%

Reaktionsschritte

Dissolving 27 g (83 mmol) of crude 2-bromo-4′-iodo acetophenone thus obtained and 8.0 g (85 mmol) of 2-aminopyridine into 200 milliliter of ethanol, adding 10 g of sodium hydrogen carbonate, the resultant suspension was refluxed under heating for 6 hours. After completion of the reaction, separation with filtration was carried out and resultant crystals were washed with water and ethanol, thereby obtaining 21 g of 2-(4-iodophenyl)-imidazo [1,2-a] pyridine (yield: 82%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07867629B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-17ed4fda02294e4a9abd48b72f4472a6
Quellennotizuspto-grants-2011_01