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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Vesnarinone | HCID 5663 | — |
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Benzyl Chloride | HCID 7503 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04415572 |
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| 출처 데이터셋 | uspto-grants-1983_11 |
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| ORD ID | ord-9f8f5f37da7c44aab41dab4ec74ca058 |
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| 출처 메모 | uspto-grants-1983_11 |
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