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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
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)amine | HCID 62376936 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 4-Fluoro-N2-(1-methyl-1H-pyrazol-4-yl)-benzene-1,2-diamine | HCID 68157715 | 212% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08653089B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-d50d681132a24c71886a085295997328 |
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| 出典メモ | uspto-grants-2014_02 |
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