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HRID 9413作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl vinyl sulfoneHCID 19354—
反応物Sodium hydrideHCID 24758—
反応物1-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-olHCID 21984028—
溶媒TetrahydrofuranHCID 8028—
生成物7-bromo-2-ethoxymethyl-1-{2-[2-(methanesulfonyl)ethoxy]-2-methylpropyl}-1H-imidazo[4,5-c]quinolineHCID 21984466—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091214B2
出典データセットuspto-grants-2006_08
ORD IDord-4e57e73174c846a0ad0b36fef32f9e8b
出典メモuspto-grants-2006_08