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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9413생성일: 2026년 10월 24일

Water → 7-bromo-2-ethoxymethyl-1-{2-[2-(methanesulfonyl)ethoxy]-2-methylpropyl}-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/ko/reaction/9413

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl vinyl sulfoneHCID 19354—
반응물Sodium hydrideHCID 24758—
반응물1-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-olHCID 21984028—
용매TetrahydrofuranHCID 8028—
생성물7-bromo-2-ethoxymethyl-1-{2-[2-(methanesulfonyl)ethoxy]-2-methylpropyl}-1H-imidazo[4,5-c]quinolineHCID 21984466—

반응 단계

A solution of methyl vinyl sulfone (3.0 g, 29 mmol) and 1-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol (5.4 g, 14 mmol) in anhydrous THF (57 mL) was purged with nitrogen; solid sodium hydride (available as a 60% dispersion in mineral oil, 57 mg, 1.4 mmol) was added. The reaction was stirred for 70 minutes at ambient temperature, at which time an analysis by HPLC indicated a ratio of product to starting material of 3:1. The reaction mixture was combined with material from another run, and water (100 mL) was added. The aqueous layer was separated and extracted with ethyl acetate (100 mL, 50 mL). The combined organic fractions were washed with brine (50 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluting with 95:5 dichloromethane:methanol) to provide 7-bromo-2-ethoxymethyl-1-{2-[2-(methanesulfonyl)ethoxy]-2-methylpropyl}-1H-imidazo[4,5-c]quinoline.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091214B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4e57e73174c846a0ad0b36fef32f9e8b
출처 메모uspto-grants-2006_08