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HRID 243190作成日:2026年10月25日

(5-fluoro-2-nitrophenyl)-(1-methyl-1H-pyrazol-4-yl)amine → 4-Fluoro-N2-(1-methyl-1H-pyrazol-4-yl)-benzene-1,2-diamine

https://huagongshe.com/reaction/243190

反応式

関与物質

役割名称HCID仕込み量
反応物(5-fluoro-2-nitrophenyl)-(1-methyl-1H-pyrazol-4-yl)amineHCID 62376936—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物4-Fluoro-N2-(1-methyl-1H-pyrazol-4-yl)-benzene-1,2-diamineHCID 68157715212%

反応条件

温度20 °C

反応手順

A mixture of (5-fluoro-2-nitrophenyl)-(1-methyl-1H-pyrazol-4-yl)amine (102 mg, 0.43 mmol) and 10% palladium on carbon (25 mg) in EtOAc (10 mL) was stirred under an atmosphere of hydrogen at atmospheric pressure and 20° C. for 6 h. A separate mixture of (5-fluoro-2-nitrophenyl)-(1-methyl-1H-pyrazol-4-yl)amine (0.19 g, 0.80 mmol) and 10% palladium on carbon (50 mg) in EtOAc (10 mL) was stirred under an atmosphere of hydrogen at atmospheric pressure and 20° C. for 5 h. The catalyst was removed by filtration and the filtrates combined and concentrated in vacuo. The resulting residue was purified by chromatography (SiO2, 0-8% (2M ammonia in methanol) in DCM) to give the title compound as a brown oil (0.188 g, 74%). LCMS (Method C): RT 1.61 min [M+H]+ 207.1

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-d50d681132a24c71886a085295997328
出典メモuspto-grants-2014_02