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HRID 253476作成日:2026年10月26日

Sodium hydride → 2-(5-fluoro-4-formyl-2-methoxy-phenoxymethyl)-1H-benzoimidazole-5-sulfonic acid dimethylamide

https://huagongshe.com/reaction/253476

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2-Fluoro-4-hydroxy-5-methoxybenzaldehydeHCID 598155—
反応物2-Chloromethyl-1h-benzoimidazole-5-sulfonic acid dimethylamide hydrochloride saltHCID 178486130—
溶媒DimethylformamideHCID 6228—
生成物2-(5-fluoro-4-formyl-2-methoxy-phenoxymethyl)-1H-benzoimidazole-5-sulfonic acid dimethylamideHCID 17849262517%

反応条件

温度60 °C

反応手順

2-Fluoro-4-hydroxy-5-methoxy-benzaldehyde (39, 0.38 g, 2.2 mmol) was dissolved in N,N-dimethylformamide (30 mL) and sodium hydride 60% dispersion in mineral oil (120 mg) was added. After 20 minutes, 2-chloromethyl-1H-benzoimidazole-5-sulfonic acid dimethylamide hydrochloride salt (217, 0.559 g, 1.80 mmol) was added to the mixture. The reaction was stirred at 60° C. overnight. The solvent was removed under reduced pressure. Ethyl acetate was added and the organic layer was washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with a gradient of ethyl acetate (20-100%) in hexane to provide the desired compound (218, 0.122 g, 17%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872018B2
出典データセットuspto-grants-2011_01
ORD IDord-6e5000b5af3948089cfc1951e1941618
出典メモuspto-grants-2011_01