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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,4-Dibromo-2-butanol | HCID 29570 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | (4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dione | HCID 68777664 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (4aRS,5SR,8aRS)-1-benzyl-5-(3-hydroxypyrrolidin-1-yl)perhydroquinoxaline-2,3-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08309725B2 |
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| 出典データセット | uspto-grants-2012_11 |
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| ORD ID | ord-7d8d99e8c42741f1b0735069a8d4fb7c |
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| 出典メモ | uspto-grants-2012_11 |
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