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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1803129생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrobenzonitrileHCID 66858340—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물5-amino-2-(3-methyl-1H-1,2,4-triazol-1-yl)benzonitrileHCID 6686005370%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08349880B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-5ddfbb4700c54a49974f5d37cf75d967
출처 메모uspto-grants-2013_01