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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1649235생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1649235

반응식

참여 물질

역할이름HCID투입량
반응물VesnarinoneHCID 5663—
반응물DimethylformamideHCID 6228—
반응물Benzyl ChlorideHCID 7503—
반응물Sodium hydrideHCID 24758—
용매WaterHCID 962—
생성물1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrateHCID 88739270—

반응 단계

6-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (500 mg) and 70 mg of 60% oily sodium hydride were mixed with 5 ml of DMF and stirred at room temperature for 1 hour. Then, to the mixture was added dropwise 3 ml of DMF solution containing 0.17 ml of benzylchloride. After stirring for 4 hours at room temperature, the reaction mixture was poured into a large amount of water and organic substances were extracted with chloroform. The chloroform layer was washed with water and dehydrated. Chloroform was distilled off and the residue was recrystallized from ethanol to give 150 mg of 1-benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate, m.p. 131.5°-132.5° C., yellow powders. Elemental Analysis for

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04415572
출처 데이터셋uspto-grants-1983_11
ORD IDord-9f8f5f37da7c44aab41dab4ec74ca058
출처 메모uspto-grants-1983_11