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HRID 1899958作成日:2026年10月27日

N-(5-Fluoro-2-nitrophenyl)-2-methylalanine → 6-Fluoro-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-one

https://huagongshe.com/reaction/1899958

反応式

関与物質

役割名称HCID仕込み量
反応物N-(5-Fluoro-2-nitrophenyl)-2-methylalanineHCID 22912907—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物6-Fluoro-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 22912892—

反応手順

N-(5-Fluoro-2-nitrophenyl)-2-methylalanine is taken up in approximately 1 L of ethanol and divided into two lots for reduction. The reductions are done with 1.7-1.9 g of palladium on carbon (10%) under hydrogen at initial pressures of 41 and 43 psi. After 4 hr the reaction is judged complete and the catalyst is filtered off. The filtrates are combined after concentration (with heating) to about 100 ml, then further concentrated. The crude product is chromatographed on silica gel (900 ml) eluting with ethyl acetate/dichloromethane (20/80), the appropriate fractions are pooled and concentrated to give the title compound which is crystallized from methanol/dichloromethane/hexane, mp 146°-148°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05574038
出典データセットuspto-grants-1996_11
ORD IDord-2e6cd6c78ab84056a8832992efe79cc9
出典メモuspto-grants-1996_11