Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1414906생성일: 2026년 10월 25일
alpha-Hydroxyalprazolam → 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde
https://huagongshe.com/reaction/1414906
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | alpha-Hydroxyalprazolam | HCID 162244 | — |
| 촉매 | HCID 178418406 | HCID 178418406 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde | HCID 21486011 | — |
반응 단계
A mixture of 1.3 g of 6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-methanol [cp., e.g. German `Offenlegungsschrift` No. 2,156,472, Belgian Pat. No. 775,558] , 3.4 g of manganese dioxide and 80 ml of benzene is refluxed for 2 hours. The reaction mixture is then filtered through a layer of silica gel, and the filtrate concentrated by evaporation. The residue is chromatographed through silica gel (Merck, 0.063 - 0.2 mm particle size) with various ethyl acetate/ethanol mixtures of increasing ethanol content as the eluant. The fractions eluted with ethyl acetate/ethanol (4:1) are combined and concentrated by evaporation. The residue is crystallised from ethyl acetate/petroleum ether to obtain 6-phenyl-8-chloro-4H-s-triazolo[4,3-a] [1,4]benzodiazepine-1-carboxaldehyde, M.P. 161°-163°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04002764 |
|---|
| 출처 데이터셋 | uspto-grants-1977_01 |
|---|
| ORD ID | ord-ebe97f1dc49447a3b1dc27d7a0db5031 |
|---|
| 출처 메모 | uspto-grants-1977_01 |
|---|