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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 335323Erstellt: 25. Oktober 2026

Pyridine → 7-bromo-N-(5-(3,4-difluorobenzylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/335323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktThionyl ChlorideHCID 24386—
Edukt3-Amino-N-(3,4-difluorobenzyl)-4-fluorobenzamideHCID 61520030—
Edukt3-[(7-Bromo-imidazo[1,2-a]pyridine-3-carbonyl)-amino]-4-fluorobenzoic acidHCID 71283443—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
Produkt7-bromo-N-(5-(3,4-difluorobenzylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 71283181—

Reaktionsschritte

A mixture comprising 7-bromoimidazo[1,2-a]pyridine-3-carboxylic acid (Intermediate 1A step 3) (1.4 g, 5.81 mmol) and thionyl chloride (8.48 ml, 116 mmol) was heated at 100° C. for 1.5 hrs. The mixture was concentrated in vacuo. 3-Amino-N-(3,4-difluorobenzyl)-4-fluorobenzamide (step 1) (1.4 g, 5.00 mmol) and pyridine (16.65 ml) was added and the resulting suspension was stirred at RT for 1 hour. EtOAc and MeOH were added and the mixture was filtered. The white solid was dried to afford the title compound;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883819B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-f935efc185b349e6904eaccceb837846
Quellennotizuspto-grants-2014_11