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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69242생성일: 2026년 10월 24일

2-Iodoxybenzoic acid → (6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-[2-(2-trimethylsilanyl-ethoxymethyl)-2h-indazol-5-yl]-methanone

https://huagongshe.com/ko/reaction/69242

반응식

참여 물질

역할이름HCID투입량
반응물2-Iodoxybenzoic acidHCID 108794—
반응물(Rac)-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-[2-(2-trimethylsilanyl-ethoxymethyl)-2h-indazol-5-yl]-methanolHCID 87523362—
용매AcetoneHCID 180—
생성물(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-[2-(2-trimethylsilanyl-ethoxymethyl)-2h-indazol-5-yl]-methanoneHCID 87523378—

반응 단계

(rac)-(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-[2-(2-trimethylsilanyl-ethoxymethyl)-2H-indazol-5-yl]-methanol (Stage 195.4, 580 mg, 1.349 mmol) was dissolved in acetone (40 mL) and heated 1 h to reflux together with 2-iodoxybenzoic acid (1.133 g, 4.05 mmol). The RM was cooled down to rt and the acetone was removed under reduced pressure. The residue was mixed with 2 M NaOH solution and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and the solvent was evaporated. The residue was purified by flash chromatography (CombiFlash® Companion System®, with RediSep® silica gel column, n-hexane/EtOAc=50:50->0: 100) to afford the title compound as a light brown foam (tR 7.11 min (conditions 3), MH+=428).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822468B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-31302cce90154816ad01c97c5ad7d61b
출처 메모uspto-grants-2014_09