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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1782353생성일: 2026년 10월 24일

3-Methyl-2-(tributylstannyl)pyridine → tert-butyl methyl{[5-(3-methylpyridin-2-yl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]methyl}carbamate

https://huagongshe.com/ko/reaction/1782353

반응식

참여 물질

역할이름HCID투입량
반응물3-Methyl-2-(tributylstannyl)pyridineHCID 16427098—
반응물tert-Butyl {[5-bromo-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 57522258—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물tert-butyl methyl{[5-(3-methylpyridin-2-yl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]methyl}carbamateHCID 6697466722.3%

반응 단계

A solution of 3-methyl-2-(tributylstannyl)pyridine (1.0 g), tert-butyl {[5-bromo-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate (563 mg) and tetrakis(triphenylphosphine)palladium (454 mg) in toluene was stirred under a nitrogen atmosphere at 120° C. for 30 hr. The mixture was cooled to room temperature and the solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: hexane-ethyl acetate=4:1) to give the title compound as a colorless oil (yield 129 mg, 22%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07498337B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-7e097de107c94f40815c9390fe085e9f
출처 메모uspto-grants-2009_03