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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231532Erstellt: 26. Oktober 2026

p-Chlorophenacyl bromide → 8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/231532

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Chlorophenacyl bromideHCID 68303—
EduktSodium BicarbonateHCID 516892—
Edukt3-Bromo-5-chloropyridin-2-amineHCID 2763971—
LösungsmittelEthanolHCID 702—
Produkt8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 14234917—

Reaktionsschritte

17 g (82 mmol) of 2-amino-3-bromo-5-chloropyridine dissolved in 150 ml of ethanol are reacted with 29 g of 2-bromo-1-(4-chlorophenyl)-1-ethanone and 14 g of sodium hydrogen carbonate. The mixture is brought to the refluxing temperature for 6 h and cooled. The precipitate is filtered off and rinsed with CH2Cl2, and the filtrate is concentrated under reduced pressure. After recrystallization of the evaporation residue in ethyl acetate, the compound melts at 178° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04847263
Quelldatensatzuspto-grants-1989_07
ORD IDord-8a2f27f02afd4b7b85817dfa22b20cfb
Quellennotizuspto-grants-1989_07