HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 729526Erstellt: 25. Oktober 2026
Triethylamine → 3-chloro-1-(2-chloro-pyridin-4-yl)-1H-indazole
https://huagongshe.com/reaction/729526
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Chloro-1H-indazole | HCID 95894 | — |
| Edukt | 2-Chloropyridine-4-boronic acid, pinacol ester | HCID 5103408 | — |
| Katalysator | Cupric acetate | HCID 8895 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-chloro-1-(2-chloro-pyridin-4-yl)-1H-indazole | HCID 57832688 | — |
Reaktionsschritte
To a solution of 3-chloroindazole (1 g, 6.6 mmol) in methylene chloride (25 mL) and methanol (25 mL) were added 2-chloro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridine (3.6 g, 15 mmol) and copper(II) acetate (1.4 g, 7.5 mmol), followed by triethylamine (2 mL, 15 mmol). The resulting mixture was vigorously stirred at room temperature for 20 h. The reaction was filtered and the gray solid was discarded. The blue filtrate was concentrated in vacuo and the residue was dissolved in methylene chloride and washed with saturated sodium bicarbonate and brine and dried over MgSO4. Flash chromatography of the crude product mixture with 25:10:65 and 35:10:55 EtOAc-CH2Cl2-Hexane gave the title compound as a white solid. MS (ES+): 264.0 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07582631B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-d3de64a78146454b9dbf70b4aff034af |
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| Quellennotiz | uspto-grants-2009_09 |
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