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HRID 1876803作成日:2026年10月27日

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

https://huagongshe.com/reaction/1876803

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dibromo-2-butanolHCID 29570—
反応物Sodium BicarbonateHCID 516892—
反応物(4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dioneHCID 68777664—
溶媒AcetonitrileHCID 6342—
生成物(4aRS,5SR,8aRS)-1-benzyl-5-(3-hydroxypyrrolidin-1-yl)perhydroquinoxaline-2,3-dioneHCID 68778432—

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08309725B2
出典データセットuspto-grants-2012_11
ORD IDord-7d8d99e8c42741f1b0735069a8d4fb7c
出典メモuspto-grants-2012_11