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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845743생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/845743

반응식

참여 물질

역할이름HCID투입량
반응물VesnarinoneHCID 5663—
반응물Acetyl chlorideHCID 6367—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물1-Acetyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyrilHCID 13913529—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04760064
출처 데이터셋uspto-grants-1988_07
ORD IDord-4ea69cdd5e044a10b413f71ff6440150
출처 메모uspto-grants-1988_07