돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 554324생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/554324

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물15-Crown-5HCID 36336—
반응물5-Phenyl-1H-pyrrole-3-carboxaldehydeHCID 11052090—
반응물6-Methoxypyridine-3-sulfonyl chlorideHCID 22344709—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-[(6-Methoxypyridin-3-yl)sulfonyl]-5-phenyl-1H-pyrrole-3-carbaldehydeHCID 8662075517.3%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048909B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-955179d90d484b54a309cf1d101f6c00
출처 메모uspto-grants-2011_11