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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 246616생성일: 2026년 10월 26일

Potassium Hydroxide → 5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazole

https://huagongshe.com/reaction/246616

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Bromodifluoromethyl diethylphosphonateHCID 144101—
반응물Acetone cardiceHCID 18522661—
반응물3-Iodo-1-methyl-1H-indazol-5-olHCID 71279721—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazoleHCID 7127954453%

반응 단계

Diethyl bromodifluoromethylphosphonate (9 g, 10.9 mmol) was added in one portion to a cooled (dry ice-acetone bath) solution of 3-iodo-1-methyl-1H-indazol-5-ol (3 g, 37.8 mmol) and KOH (15 g, 267 mmol) in CH3CN (50 mL) and H2O (50 mL) with stirring, the reaction mixture was warmed to room temperature and stirred for 0.5 h, the mixture was diluted with EtOAc (50 mL), The organic layer was washed with H2O (50 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=3:1) to give 5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazole (1.85 g, 53%) as a white solid. LCMS: (M+H)+=325; 1H NMR (300 MHz, CDCl3), δ 7.36-7.33 (m, 1H), 7.28-7.23 (m, 1H), 7.19 (s, 1H), 6.53 (t, 1H, J=73.5 Hz), 4.09 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-0b6f2c2e918a4c72aca5771957abe10a
출처 메모uspto-grants-2014_02