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HRID 397516Erstellt: 24. Oktober 2026
1H-1,2,4-Triazole → 3-[1,2,4]Triazol-1-yl-pyridine-2-carbonitrile
https://huagongshe.com/reaction/397516
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1H-1,2,4-Triazole | HCID 9257 | — |
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | 2-Cyano-3-fluoropyridine | HCID 7060408 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-[1,2,4]Triazol-1-yl-pyridine-2-carbonitrile | HCID 21866301 | — |
Reaktionsschritte
To a solution of 2-cyano-3-fluoro-pyridine (2.99 g, 24.49 mmol) in DMF (30 ml) is added cesium carbonate (2.03 g, 29.39 mmol) and 1,2,4-triazole (2.03 g, 29.39 mmol) and the reaction mixture is stirred at 65° C. for 4 h. After cooling to room temperature, the mixture is diluted with water and extracted with EtOAc 3 times. The aqueous layer is saturated with LiCl and further extracted with EtOAc. The combined organic layer is dried on sodium sulfate, concentrated in vacuo. The crude product is purified by flash chromatography (silica gel, 2% MeOH containing 10% NH4OH in CH2Cl2 to 6%) to give 3-[1,2,4]Triazol-1-yl-pyridine-2-carbonitrile. 1H NMR (CDCl3, 400 MHz) δ8.95 (s, 1H); 8.8 (d, J=4 Hz, 1H); 8.24 (s, 1H); 8.22 (d, J=8.5 Hz, 1H); 7.75 (dd, J=4, 8.5 Hz, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06610701B2 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-f16af703873c4c6dba395327c641ea2f |
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| Quellennotiz | uspto-grants-2003_08 |
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