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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 246614생성일: 2026년 10월 26일

Water → 5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1-methyl-1H-indazole

https://huagongshe.com/reaction/246614

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물HCID 178418922HCID 178418922—
반응물HCID 178455023HCID 178455023—
용매TetrahydrofuranHCID 8028—
생성물5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1-methyl-1H-indazoleHCID 7127986680.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-a51d39fae6224988a1ab16c25e5e8671
출처 메모uspto-grants-2014_02