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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2417473Erstellt: 25. Oktober 2026

Sodium Hydroxide → 1-(4-Carboxybenzyl)-4-(4-chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on

https://huagongshe.com/reaction/2417473

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktSodium hydrideHCID 24758—
EduktMethyl 4-(bromomethyl)benzoateHCID 256687—
Edukt4-(4-Chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-onHCID 22632554—
LösungsmittelEthanolHCID 702—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(4-Carboxybenzyl)-4-(4-chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-onHCID 22632534—

Reaktionsschritte

300 mg (1.0 mmol) of 4-(4-chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on was dissolved in 10 ml of DMF. 48 mg (1.2 mmol) of sodium hydride was added to the obtained solution, and they were stirred at room temperature for 30 minutes. 300 mg (1.3 mmol) of methyl 4-bromomethylbenzoate was added to the obtained mixture, and they were stirred at 60° C. overnight. After the treatment with ethyl acetate as the extracting solvent, the obtained crude product was stirred together with 2 ml of THF, 2 ml of ethanol and 2 ml of 1 N aqueous sodium hydroxide solution at room temperature overnight. The obtained product was treated with ethyl acetate as the extracting solvent by an ordinary method to obtain the crude product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06825191B2
Quelldatensatzuspto-grants-2004_11
ORD IDord-205b1ef72a194d9693dacd493e87f40b
Quellennotizuspto-grants-2004_11