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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 869740생성일: 2026년 10월 24일

Sodium hydride → tert-Butyl ({4-fluoro-5-(2-fluoropyridin-3-yl)-1-[(3-methylpyridin-2-yl)sulfonyl]-1H-pyrrol-3-yl}methyl)methylcarbamate

https://huagongshe.com/ko/reaction/869740

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물15-Crown-5HCID 36336—
반응물3-Methylpyridine-2-sulfonyl chlorideHCID 12295461—
반응물tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 67176761—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl ({4-fluoro-5-(2-fluoropyridin-3-yl)-1-[(3-methylpyridin-2-yl)sulfonyl]-1H-pyrrol-3-yl}methyl)methylcarbamateHCID 6717746147.4%

반응 단계

To a suspension of sodium hydride (60% in oil, 20 mg) in tetrahydrofuran (2 mL) was added a solution of tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (161 mg), 15-crown-5 (110 mg), crude 3-methylpyridine-2-sulfonyl chloride (153 mg) in tetrahydrofuran (1.5 mL) at room temperature, and the mixture was stirred at room temperature for 72 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The separated aqueous layer was extracted again with ethyl acetate. Combined organic layers were washed with 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=9:1→11:9) to give the title compound as a colorless oil (yield 113 mg, 47%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08969387B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-f346b02d60ed4d70a17195be6fcedd35
출처 메모uspto-grants-2015_03