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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1979464생성일: 2026년 10월 26일

3-Bromocyclohexene → (3R)-(-)-2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

https://huagongshe.com/reaction/1979464

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참여 물질

역할이름HCID투입량
반응물3-BromocyclohexeneHCID 137057—
반응물Sodium BicarbonateHCID 516892—
반응물(R)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 12988641—
용매DimethylformamideHCID 6228—
생성물(3R)-(-)-2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 53946939100%

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온도50 °C

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3-Bromocyclohexene (7.06 g) and sodium bicarbonate (3.68 g) were added to a solution of (R)-(+)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (6.08 g) in anhydrous N,N-dimethylformamide (50 ml), and the mixture was stirred at 50° C. for one hour. The reaction mixture was allowed to cool, ice-water was added, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure,the residue was purified by silica gel column chromatography(ethyl acetate:n-hexane=1:3), to thereby obtain 7.84 g of the titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06239131B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-c75f7bbd45844e82a5bc132c9d783059
출처 메모uspto-grants-2001_05