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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1800489Erstellt: 26. Oktober 2026

Potassium Carbonate → 3-(1-cyano-1-methylethyl)-N-{4-cyano-3-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

https://huagongshe.com/reaction/1800489

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-Chloro-5-nitropyridineHCID 78308—
EduktN-(4-cyano-3-hydroxyphenyl)-3-(1-cyano-1-methylethyl)benzamideHCID 68416945—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(1-cyano-1-methylethyl)-N-{4-cyano-3-[(5-nitropyridin-2-yl)oxy]phenyl}benzamideHCID 6841790824,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 2-chloro-5-nitropyridine (1.06 g, 6.68 mmol) and N-(4-cyano-3-hydroxyphenyl)-3-(1-cyano-1-methylethyl)benzamide (2.0 g, 6.55 mmol) in N,N-dimethylformamide (15 mL) was added potassium carbonate (1.35 g, 9.82 mmol), and the mixture was stirred at 80° C. for 20 hr. The reaction mixture was cooled to room temperature, the insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate (300 mL), washed with water (150 mL) and saturated brine (150 mL×2), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20→40/60), and further purified by basic silica gel column chromatography (hexane/ethyl acetate=70/30→0/100). The obtained solution was concentrated under reduced pressure to give the title compound (0.68 g, 24%) as a pale-yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08344135B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-f657c39f51f84cd8baeb78892eb4b30e
Quellennotizuspto-grants-2013_01