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HRID 242990作成日:2026年10月27日

(5-Fluoro-2-nitrophenyl)-(6-fluoropyridin-3-yl)amine → 4-Fluoro-N2-(6-fluoropyridin-3-yl)benzene-1,2-diamine

https://huagongshe.com/reaction/242990

反応式

関与物質

役割名称HCID仕込み量
反応物(5-Fluoro-2-nitrophenyl)-(6-fluoropyridin-3-yl)amineHCID 68157161—
溶媒Ethyl AcetateHCID 8857—
生成物4-Fluoro-N2-(6-fluoropyridin-3-yl)benzene-1,2-diamineHCID 68157719104.4%

反応手順

A mixture of (5-fluoro-2-nitrophenyl)-(6-fluoropyridin-3-yl)amine (571 mg, 2.27 mmol) in EtOAc (40 mL) was degassed with a stream of nitrogen prior to addition of 10% Pd/C (57 mg) and was stirred at RT under a hydrogen atmosphere for 22 h. The mixture was filtered through a phase separator and the filtrate concentrated in vacuo to afford the title compound as a dark oil (524 mg, quantitative). LCMS (Method C): RT 2.39 min [M+H]+ 222.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653089B2
出典データセットuspto-grants-2014_02
ORD IDord-7895915473d64bf3b47ac58036aa0980
出典メモuspto-grants-2014_02