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(4aRS,5SR,8aRS)-1-Benzyl-5-(benzylamino)perhydroquinoxaline-2,3-dione → (4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (4aRS,5SR,8aRS)-1-Benzyl-5-(benzylamino)perhydroquinoxaline-2,3-dione | HCID 68775989 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dione | HCID 68777664 | — |
反応手順
(4aRS,5SR,8aRS)-1-Benzyl-5-(benzylamino)perhydroquinoxaline-2,3-dione (1.19 g, 3.28 mmol) was dissolved in methanol (40 ml) and NH4HCO2 (2.07 g, 32.8 mmol) was added. 120 mg of palladium-on-carbon (Merck) was furthermore added. The mixture was heated under reflux for 2 hours. The catalyst was then filtered off and the mixture was evaporated in vacuo. The residue was taken up in CH2Cl2 and the mixture was washed three times with 0.1 N NaOH. The organic phase was dried over Na2SO4 and evaporated in vacuo. A colorless solid was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08309725B2 |
| 出典データセット | uspto-grants-2012_11 |
| ORD ID | ord-d09017786fd64c849cb81b4d421530a0 |
| 出典メモ | uspto-grants-2012_11 |