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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 251778Erstellt: 26. Oktober 2026

4-Bromophenacyl bromide → 2-(4-Bromo-phenyl)-6-phenyl-imidazo [1,2-a] pyridine

https://huagongshe.com/reaction/251778

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromophenacyl bromideHCID 7454—
EduktSodium BicarbonateHCID 516892—
Edukt2-Amino-3,5-diphenylpyridineHCID 11572327—
LösungsmittelEthanolHCID 702—
Produkt2-(4-Bromo-phenyl)-6-phenyl-imidazo [1,2-a] pyridineHCID 2308856082%

Reaktionsschritte

Dissolving crude 3,5-diphenyl-2-amino-pyridine obtained and 5.5 g (20 mmol) of 2,4′-dibromo acetophenone into 80 milliliter of ethanol, adding 3.0 g of sodium hydrogen carbonate, the resultant suspension was refluxed under heating for 7 hours. After completion of the reaction, separation with filtration was carried out and resultant crystals were washed with water and methanol, thereby obtaining 6.9 g of 2-(4-bromo-phenyl)-6-phenyl-imidazo [1,2-a] pyridine (yield: 82%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07867629B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-5e6630f5c8bf47f0891df99080789d75
Quellennotizuspto-grants-2011_01