Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606953생성일: 2026년 10월 26일
Sodium amide → 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one
https://huagongshe.com/reaction/1606953
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium amide | HCID 24533 | — |
| 반응물 | (Chloromethyl)triphenylphosphonium chloride | HCID 197823 | — |
| 반응물 | 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde | HCID 19851584 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one | HCID 86743355 | — |
반응 단계
100 g of an equimolar mixture of chloromethyltriphenylphosphonium chloride and sodium amide were stirred for 45 minutes in 450 ml of tetrahydrofuran, whereby the temperature rose to 37°. 62.23 g (229.7 mmol) of 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde were then added portionwise thereto at room temperature and, after completion of the addition, the mixture was stirred for a further 1 hour. The reaction mixture was subsequently filtered and the filtrate was evaporated. After chromatography of the residue on silica gel while eluting with cyclohexane/ether/wasopropanol (3:3:1) there was obtained 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 205°-207°.
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-4e6d176c92604bb192e57a7ddecd8b8f |
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| 출처 메모 | uspto-grants-1989_09 |
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