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HRID 1803129Erstellt: 25. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrobenzonitrileHCID 66858340—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt5-amino-2-(3-methyl-1H-1,2,4-triazol-1-yl)benzonitrileHCID 6686005370%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08349880B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-5ddfbb4700c54a49974f5d37cf75d967
Quellennotizuspto-grants-2013_01