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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248372Erstellt: 25. Oktober 2026

Sodium hydride → 2-[N-butyryl-N-[4-(4-chloro-2-cyano-1-pyrrolyl)benzyl]amino]-4-methyl-3-nitropyridine

https://huagongshe.com/reaction/248372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt1-(4-Bromomethylphenyl)-4-chloropyrrole-2-carbonitrileHCID 18961926—
Edukt2-Butyrylamino-4-methyl-3-nitropyridineHCID 21464239—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt2-[N-butyryl-N-[4-(4-chloro-2-cyano-1-pyrrolyl)benzyl]amino]-4-methyl-3-nitropyridineHCID 19759566—

Reaktionsschritte

To a suspension of sodium hydride (114 mg, 60% oil dispersion) in dimethyl sulfoxide (5 ml) was added dropwise a solution of 2-butyrylamino-4-methyl-3-nitropyridine (605 mg) in dimethyl sulfoxide (10 ml) at ambient temperature under nitrogen atmosphere. The mixture was stirred at the same temperature for one hour and a solution of 1-(4-bromomethylphenyl)-4-chloropyrrole-2-carbonitrile (800 ml) in dimethyl sulfoxide (10 ml) was added therein. The reaction mixture was stirred at ambient temperature for 2 hours and quenched with ice water. The separated oil was extracted twice with ethyl acetate. The combined extracts were washed with water, dried, and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluted by n-hexane/ethylacetate (2/1-1/1) to yield 2-[N-butyryl-N-[4-(4-chloro-2-cyano-1-pyrrolyl)benzyl]amino]-4-methyl-3-nitropyridine (723 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05210092
Quelldatensatzuspto-grants-1993_05
ORD IDord-3bca4c37b7a34ab79886e7008dd9a727
Quellennotizuspto-grants-1993_05