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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64409Erstellt: 23. Oktober 2026

Bromoacetone → HCID 86713417, Verbindung

https://huagongshe.com/de/reaction/64409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromoacetoneHCID 11715—
EduktSodium BicarbonateHCID 516892—
EduktMethyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinateHCID 86713416—
LösungsmittelEthanolHCID 702—
ProduktHCID 86713417HCID 86713417—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a suspension of 2.15 g of methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate in 43 ml of ethanol was added 1.09 ml of bromoacetone, followed by stirring at 80° C. for 4 hours. To the reaction mixture was added 1.09 ml of bromoacetone, followed by stirring at 80° C. for 4 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and the solvent was evaporated under reduced pressure, followed by extracting with ethyl acetate and washing with saturated brine. After drying over anhydrous magnesium sulfate and then filtering, the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 1.39 g of methyl 8-[(2-fluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-6-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447090B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-2d92678427e44e14afb990b87d1e5427
Quellennotizuspto-grants-2016_09