HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15990Erstellt: 26. Oktober 2026
Cesium fluoride → 6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline
https://huagongshe.com/reaction/15990
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Cesium fluoride | HCID 25953 | — |
| Edukt | 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline | HCID 54775608 | — |
| Edukt | HCID 178418800 | HCID 178418800 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline | HCID 24851838 | 56% |
Reaktionsschritte
A mixture of 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (50 mg, 0.15 mmol), 4-methyl-1H-imidazole (36 mg, 0.44 mmol) and CsF (25 mg, 0.16 mmol) in acetonitrile (1.45 mL) was heated in a microwave to 160° C. for 20 minutes. The reaction was diluted with water (5 mL) and the resulting suspension was filtered. The precipitate was washed with water and then purified by column chromatography using gradient elution with methanol and dichloromethane to afford 6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (28 mg, yield 56%)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732604B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-c0952ee84e994226b7dcb2797003c9a7 |
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| Quellennotiz | uspto-grants-2010_06 |
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