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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32011생성일: 2026년 10월 24일

Sodium Thiosulfate Pentahydrate → 1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanone

https://huagongshe.com/ko/reaction/32011

반응식

참여 물질

역할이름HCID투입량
반응물Sodium Thiosulfate PentahydrateHCID 61475—
반응물TriacetoxyperiodinaneHCID 159087—
반응물Sodium BicarbonateHCID 516892—
반응물1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanolHCID 21114171—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanoneHCID 2111417271%

반응 단계

A solution of 1-[6-(4-bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanol 10i (44 mg, 0.096 mmol) and the Dess-Martin periodinane (49 mg, 0.12 mmol) in CH2Cl2 (1.5 mL) is stirred for 1.5 hours at room temperature. The reaction mixture is diluted with ether (3 mL). Saturated aqueous NaHCO3 (1 mL) containing sodium thiosulfate pentahydrate (74 mg) is added. The resulting mixture is stirred for 10 minutes and diluted with EtOAc. The organic layer is washed with saturated aqueous NaHCO3 and brine, dried over MgSO4, filtered, and concentrated in vacuo to give a crude material which is purified by flash chromatography (1.5% MeOH in CH2Cl2) to afford the desired product (31 mg, 71%): MS APCI (+) m/z 456, 458 (M+, Br pattern) detected.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425637B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-e9c32509e51d4cc49e566892f3e4e21e
출처 메모uspto-grants-2008_09