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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25079생성일: 2026년 10월 26일

Ethanol → (R)-8-Methyl-5-(4-nitrophenyl)-7-(5-methyl-1,3,4-oxadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine

https://huagongshe.com/reaction/25079

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물(R)-N'-(8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-7-carbothioyl)-acetic hydrazideHCID 86593813—
촉매Mercuric acetateHCID 15337—
용매DichloromethaneHCID 6344—
생성물(R)-8-Methyl-5-(4-nitrophenyl)-7-(5-methyl-1,3,4-oxadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepineHCID 6943697551%

반응 단계

A stirred mixture of 2.2 g (5.15 mmol) of (R)—N′-(8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-7-carbothioyl)-acetic hydrazide (an intermediate of method B of Example 28), 44 ml of ethanol and 1.72 g (5.39 mmol) of mercury (II) acetate was refluxed for 2 h. The residue obtained on concentration was dissolved in dichloromethane and filtered through a neutral aluminum oxide column. After washing the column the filtrate was concentrated and the residue was purified by column chromatography using silica gel (MN Kieselgel 60) as adsorbent and a mixture of n-hexane-ethyl acetate (1:2.5) as eluent to yield 1.07 g (51%) of the title compound. Mp.: 202-204° C. after recrystallization from ethanol. [α]: −249° (c=0.22; CHCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858605B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-04778f73766b45f7825b9dbc3f96f606
출처 메모uspto-grants-2005_02