Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 443793생성일: 2026년 10월 25일
Pyridine → 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one
https://huagongshe.com/reaction/443793
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Temazepam | HCID 5391 | — |
| 반응물 | 2-Propylvaleryl chloride | HCID 76240 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one | HCID 23465564 | — |
반응 단계
A solution of 15 g of 1-methyl-7-chloro-3-hydroxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one (Temazepam) and 5 g of absolute pyridine is cooled in 40 ml of freshly distilled dimethyl formamide to -5° and is mixed drop by drop with 10.5 g of dipropyl acetic acid chloride with the exclusion of atmospheric moisture. The mixture is stirred for an additional 4 hours at -5° and is allowed to stand over night at 0°, and then the mixture is poured on ice. The separated oil crystallizes while rubbed on with ethanol. By recrystallization from petroleum ether or isopropanol using activated charcoal, one will obtain the 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one as a colorless powder with a melting point of 134°-136°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04261987 |
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| 출처 데이터셋 | uspto-grants-1981_04 |
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| ORD ID | ord-b58383cd293c40228718e3d99a150283 |
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| 출처 메모 | uspto-grants-1981_04 |
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