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HRID 1803129作成日:2026年10月25日
2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrobenzonitrile → 5-amino-2-(3-methyl-1H-1,2,4-triazol-1-yl)benzonitrile
https://huagongshe.com/reaction/1803129
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrobenzonitrile | HCID 66858340 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-amino-2-(3-methyl-1H-1,2,4-triazol-1-yl)benzonitrile | HCID 66860053 | 70% |
反応手順
Step G (2): 10% Palladium on carbon (5.06 g) was added under an atmosphere of nitrogen to a chilled (ice-water bath) solution of 2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrobenzonitrile (10.9 g, 47.6 mmol) dissolved in methanol (100 mL). The flask was repeated evacuated and flushed with hydrogen gas (double balloon). The resulting mixture was allowed to warm to rt and left to stir for 16 h under the hydrogen atmosphere. Purged with nitrogen gas. Filtered the crude reaction mixture through a short diatomaceous earth (Celite®) plug. Rinsed reaction vessel and plug with methanol. Concentrated filtrate in vacuo. Dried residue on high vacuum overnight to afford 5-amino-2-(3-methyl-1H-1,2,4-triazol-1-yl)benzonitrile (6.59 g, 70% yield) as a brown solid. LC-MS (M+H)+ 200.0. 1H NMR (500 MHz, DMSO-d6) δ ppm 2.29-2.37 (m, 3 H) 5.99 (s, 2 H) 6.94 (dd, J=8.85, 2.44 Hz, 1 H) 7.00 (d, J=2.44 Hz, 1 H) 7.37 (d, J=8.54 Hz, 1 H) 8.69-8.81 (m, 1 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08349880B2 |
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| 出典データセット | uspto-grants-2013_01 |
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| ORD ID | ord-5ddfbb4700c54a49974f5d37cf75d967 |
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| 出典メモ | uspto-grants-2013_01 |
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