HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246614Erstellt: 26. Oktober 2026
Water → 5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1-methyl-1H-indazole
https://huagongshe.com/reaction/246614
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | HCID 178418922 | HCID 178418922 | — |
| Edukt | HCID 178455023 | HCID 178455023 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1-methyl-1H-indazole | HCID 71279866 | 80,5% |
Reaktionsschritte
To a solution of 5-(tert-butyldimethylsilyloxy)-3-iodo-1H-indazole (3 g, 8.0 mmol) in THF (25 mL) was added KO-tBu (1.28 g, 11.2 mmol) at 0° C. followed by addition of MeI (1.58 g, 11.2 mmol), after the addition, the reaction mixture was warmed to room temperature and stirred for 4 hours, then H2O (25 mL) was added to the mixture and product extracted with EtOAc (100 mL). The organic layer was washed with H2O (100 mL), brine (100 mL), dried over Na2SO4 and concentrated under reduced pressure, the residue was purified by column chromatography (silica gel, 200-300 mesh, eluting with petroleum ether/EtOAc=5:1) to give 5-(tert-butyldimethylsilyloxy)-3-iodo-1-methyl-1H-indazole (2.5 g, 80.3%) as a white solid. (M+H)+=389; 1H NMR (300 MHz, CDCl3), δ 7.22-7.19 (m, 1H), 7.03-7.01 (m, 1H), 6.80 (s, 1H), 4.05 (s, 3H), 1.01 (s, 9H), 0.23 (s, 6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08658646B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-a51d39fae6224988a1ab16c25e5e8671 |
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| Quellennotiz | uspto-grants-2014_02 |
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