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HRID 2383931作成日:2026年10月25日

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

https://huagongshe.com/reaction/2383931

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium HydroxideHCID 14798—
反応物6-Bromo-4H-imidazo[4,5-b]pyridineHCID 911578—
反応物2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒DichloromethaneHCID 6344—
溶媒HexaneHCID 8058—
生成物6-Bromo-3-[[2-(trimethylsilyl)ethoxy]methyl]-3H-imidazo[4,5-b]pyridineHCID 1935828814.4%

反応手順

(2-Chloromethoxy-ethyl)-trimethyl-silane (508.6 mg, 3.0456 mmol), catalytic amount of benzyl triethyl-ammonium chloride and NaOH (203.04 mg, 5.076 mmol) were added to a solution of 6-bromo-3H-imidazo[4,5-b]pyridine (500 mg, 2.538 mmol) in DCM (10 mL) at 0° C. The resulting mixture was stirred room temperature for 6 hours. The reaction was monitored by TLC (80% ethylacetate in hexane). The reaction mixture was partitioned between DCM and water. The organic layer was washed with water, brine, dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (20% ethylacetate in hexane) afforded 120 mg of the product (14.4% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08263635B2
出典データセットuspto-grants-2012_09
ORD IDord-c2f7d6b69230422db0015242029973d8
出典メモuspto-grants-2012_09