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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl iodideHCID 6328—
EduktHCID 178418922HCID 178418922—
EduktHCID 178455023HCID 178455023—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1-methyl-1H-indazoleHCID 7127986680,5%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658646B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-a51d39fae6224988a1ab16c25e5e8671
Quellennotizuspto-grants-2014_02