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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

反応式

関与物質

役割名称HCID仕込み量
反応物2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrobenzonitrileHCID 66858340—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物5-amino-2-(3-methyl-1H-1,2,4-triazol-1-yl)benzonitrileHCID 6686005370%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08349880B2
出典データセットuspto-grants-2013_01
ORD IDord-5ddfbb4700c54a49974f5d37cf75d967
出典メモuspto-grants-2013_01