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HRID 554324作成日:2026年10月27日

Sodium hydride → 1-[(6-Methoxypyridin-3-yl)sulfonyl]-5-phenyl-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/554324

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15-Crown-5HCID 36336—
反応物5-Phenyl-1H-pyrrole-3-carboxaldehydeHCID 11052090—
反応物6-Methoxypyridine-3-sulfonyl chlorideHCID 22344709—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-[(6-Methoxypyridin-3-yl)sulfonyl]-5-phenyl-1H-pyrrole-3-carbaldehydeHCID 8662075517.3%

反応手順

Under an argon atmosphere, 5-phenyl-1H-pyrrole-3-carbaldehyde (171 mg) was dissolved in absolute tetrahydrofuran (20 mL), and sodium hydride (60% in oil, 200 mg) was added at room temperature while stirring. After stirring at the same temperature for 15 min, 15-crown-5 (1.01 mL) was added, and the mixture was further stirred at the same temperature for 15 min. 6-Methoxypyridin-3-ylsulfonyl chloride (623 mg) was added, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→1:1) to give the title compound as an oil (yield 59 mg, 17%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08048909B2
出典データセットuspto-grants-2011_11
ORD IDord-955179d90d484b54a309cf1d101f6c00
出典メモuspto-grants-2011_11