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HRID 1876799作成日:2026年10月27日

(4aRS,5SR,8aRS)-1-Benzyl-5-(benzylamino)perhydroquinoxaline-2,3-dione → (4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dione

https://huagongshe.com/reaction/1876799

反応式

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-dioneHCID 68775989—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物(4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dioneHCID 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

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-d09017786fd64c849cb81b4d421530a0
出典メモuspto-grants-2012_11