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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2417456Erstellt: 25. Oktober 2026

4-Nitrobenzyl chloride → 4-(4-Chlorobenzoyl)-1-(4-nitrobenzyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on

https://huagongshe.com/reaction/2417456

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitrobenzyl chlorideHCID 7482—
EduktEthyl AcetateHCID 8857—
EduktSodium hydrideHCID 24758—
Edukt4-(4-Chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-onHCID 22632554—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(4-Chlorobenzoyl)-1-(4-nitrobenzyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-onHCID 22632469—

Reaktionsschritte

110 mg (0.37 mmol) of 4-(4-chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on was dissolved in 5 ml of DMF. 17 mg (0.44 mmol) of sodium hydride was added to the obtained solution, and they were stirred at room temperature for 30 minutes. 76 mg (0.44 mmol) of 4-nitrobenzyl chloride was added to the obtained mixture and they were stirred at 60° C. overnight. The reaction mixture was treated with ethyl acetate as the extracting solvent by an ordinary method to obtain the crude product. After the purification by the silica gel column chromatography, the title compound was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06825191B2
Quelldatensatzuspto-grants-2004_11
ORD IDord-01905b1ade1a4255994994f9bea9683c
Quellennotizuspto-grants-2004_11