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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1876803생성일: 2026년 10월 26일

1,4-Dibromo-2-butanol → (4aRS,5SR,8aRS)-1-benzyl-5-(3-hydroxypyrrolidin-1-yl)perhydroquinoxaline-2,3-dione

https://huagongshe.com/reaction/1876803

반응식

참여 물질

역할이름HCID투입량
반응물1,4-Dibromo-2-butanolHCID 29570—
반응물Sodium BicarbonateHCID 516892—
반응물(4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dioneHCID 68777664—
용매AcetonitrileHCID 6342—
생성물(4aRS,5SR,8aRS)-1-benzyl-5-(3-hydroxypyrrolidin-1-yl)perhydroquinoxaline-2,3-dioneHCID 68778432—

반응 단계

(4aRS,5SR,8aRS)-5-Amino-1-benzylperhydroquinoxaline-2,3-dione (144 mg, 0.53 mmol) was dissolved in acetonitrile (16 ml), and NaHCO3 (300 mg, 3.57 mmol) and racemic 1,4-dibromobutan-2-ol (purity 85%, 1.15 g, 4.20 mmol, 0.57 ml) were added. After 24 hours, NaHCO3 was separated off and the mixture was evaporated in vacuo. The solid was taken up in CH2Cl2 and the mixture was extracted by shaking three times with HCl (1 N). The aqueous phase was then brought to pH 8 with NaOH (2 N) and extracted by shaking three times with CH2Cl2. The organic phases were dried over Na2SO4 and evaporated in vacuo. The crude product was purified by flash chromatography over silica gel 60 (40-63 μm, (Merck) Ø 2 cm, acetone/MeOH/Et2NH 9.5:0.5:0.1, l=17 cm, V=5 ml). A pale yellow solid was isolated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309725B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-7d8d99e8c42741f1b0735069a8d4fb7c
출처 메모uspto-grants-2012_11