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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 845743Erstellt: 27. Oktober 2026

Vesnarinone → 1-Acetyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/845743

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVesnarinoneHCID 5663—
EduktAcetyl chlorideHCID 6367—
EduktSodium hydrideHCID 24758—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Acetyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyrilHCID 13913529—

Reaktionsschritte

Sodium hydride (60% in oil, 263 mg) was suspended in dimethylformamide (DMF) (30 ml). To the suspension was added 6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (2 g) and the mixture was stirred at 70° to 80° C. for 30 minutes. After cooling, to the mixture was added slowly acetyl chloride (0.43 m/g) with stirring and under ice-cooling, and the mixture was stirred at the same temperature for 5 minutes. After completion of reaction, the reaction mixture was poured into ice-water and extracted with chloroform. The chloroform layer was washed successively with water and saturated saline solution and dried over magnesium sulfate. The chloroform extract was evaporated under reduced pressure. The resultant residue was purified by silica-gel column chromatography (eluent:dichloromethane:methanol=100:1) and recrystallized from a mixture of dichloromethane and diethyl ether to give 1-acetyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (700 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04760064
Quelldatensatzuspto-grants-1988_07
ORD IDord-4ea69cdd5e044a10b413f71ff6440150
Quellennotizuspto-grants-1988_07