Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606955생성일: 2026년 10월 27일
Water → 7-chloro-4,5-dihydro-5-methyl-3-(1-propynyl)-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one
https://huagongshe.com/reaction/1606955
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Water | HCID 962 | — |
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 7-chloro-3-ethynyl-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one | HCID 19851533 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 7-chloro-4,5-dihydro-5-methyl-3-(1-propynyl)-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one | HCID 19851568 | — |
반응 단계
2.72 g (10 mmol) of 7-chloro-3-ethynyl-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one was dissolved in 20 ml of N,N-dimethylformamide. 1.31 g (30 mmol) of sodium hydride dispersion (55% in oil) was washed with n-hexane and then introduced at room temperature into the above solution. After 10 minutes 0.95 ml (15 mmol) of methyl iodide was added thereto and the mixture was stirred at room temperature for a further 3 hours. The reaction mixture was poured into 300 ml of water and extracted four times with methylene chloride. The organic extracts were washed four times with water and dried over magnesium sulphate. After chromatography of the residue on silica gel while eluting with ethyl acetate and recrystallization from ethyl acetate, there was obtained 7-chloro-4,5-dihydro-5-methyl-3-(1-propynyl)-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 243°-244°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04863920 |
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| 출처 데이터셋 | uspto-grants-1989_09 |
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| ORD ID | ord-bb3fce22e4004d98aed4c110664b2afe |
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| 출처 메모 | uspto-grants-1989_09 |
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