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HRID 554338作成日:2026年10月25日

Sodium hydride → 4-Methyl-5-phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/554338

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Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
反応物4-Methyl-5-phenyl-1H-pyrrole-3-carbaldehydeHCID 71362812—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-Methyl-5-phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 8623272053%

反応手順

4-Methyl-5-phenyl-1H-pyrrole-3-carbaldehyde (185 mg) was dissolved in tetrahydrofuran (10 mL), sodium hydride (60% in oil, 60 mg) was added and the mixture was stirred at room temperature for 15 min. 15-Crown-5 (0.30 mL) was added and the mixture was further stirred at the same temperature for 15 min. 3-Pyridinesulfonyl chloride hydrochloride (231 mg) was added and the reaction mixture was stirred at room temperature for 1 hr. Water was added, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→1:1) to give the title compound as a colorless solid (yield 172 mg, 53%).

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-52613e948a3e42998139eb81acfa1e72
出典メモuspto-grants-2011_11