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HRID 2403450作成日:2026年10月27日

Sodium hydride → 6-Bromo-3-[[2-(trimethylsilyl)ethoxy]methyl]-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/2403450

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物6-Bromo-4H-imidazo[4,5-b]pyridineHCID 911578—
反応物2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
溶媒TetrahydrofuranHCID 8028—
生成物6-Bromo-3-[[2-(trimethylsilyl)ethoxy]methyl]-3H-imidazo[4,5-b]pyridineHCID 19358288—

反応条件

温度0 °C

反応手順

To a solution of 6-bromo-3H-imidazo[4,5-b]pyridine (1.0 g) in THF (20 mL) at 0° C. was added sodium hydride (187 mg) and the reaction stirred at 0° C. for 1 h. Then, 2-(trimethylsilyl)ethoxymethyl chloride (0.94 mL) was added and the reaction stirred at room temperature for 16 h. The reaction was quenched with water (20 mL) and extracted into ethyl acetate (2×20 mL). The combined organics were washed with aqueous brine solution (2×20 mL), dried (MgSO4), reduced in vacuo and purified by column chromatography to give 6-bromo-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08802670B2
出典データセットuspto-grants-2014_08
ORD IDord-8a743374b396430f96ecd70a2fc84669
出典メモuspto-grants-2014_08