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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1285219Erstellt: 26. Oktober 2026

3-Fluorobenzoyl chloride → N-(5-Cyano-1H-imidazol-4-yl)-3-fluorobenzamide

https://huagongshe.com/reaction/1285219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Fluorobenzoyl chlorideHCID 74376—
Edukt5-amino-1H-imidazole-4-carbonitrileHCID 78777—
LösungsmittelPyridineHCID 1049—
ProduktN-(5-Cyano-1H-imidazol-4-yl)-3-fluorobenzamideHCID 13588448—

Reaktionsschritte

Under a nitrogen atmosphere a stirred solution of 4-amino-1H-imidazole-5-carbonitrile (1.1 g, 0.01 mole) and 3-fluorobenzoyl chloride (1.8 g, 0.011 mole) in 25 ml of dry pyridine was heated at reflux for one hour. The reaction mixture was cooled and the pyridine removed under reduced pressure. The residue was washed with saturated aqueous sodium bicarbonate and water. The residual solid was collected by filtration and washed sequentially with two portions of water, diethyl ether, and ethyl acetate. The solid was dried under reduced pressure; mp, 222°-240°. The solid was dissolved in ethanol and precipitated with petroleum ether, then collected by filtration and washed with diethyl ether to give after drying N-(5-cyano-1H-imidazol-4-yl)-3-fluorobenzamide (2.0 g; mp, 242°-46°).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04565875
Quelldatensatzuspto-grants-1986_01
ORD IDord-9c3ef748d9a947a0a6cda1e27811b3b8
Quellennotizuspto-grants-1986_01