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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10531생성일: 2026년 10월 25일

Tetramethyltin → 4-(4-Methyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/10531

반응식

참여 물질

역할이름HCID투입량
반응물TetramethyltinHCID 11661—
반응물2,6-Di-tert-butyl-4-methylphenolHCID 31404—
반응물4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물4-(4-Methyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979807—

반응 조건

온도150 °C

반응 단계

A solution of Intermediate 71 (313 mg) in toluene (6 ml) was added with tetrakis(triphenylphosphine)palladium(0) (17.9 mg, Aldrich), tetramethyltin (165 μl, Kanto Chemicals) and 2,6-di-tert-butyl-4-methylphenol (several pellets, Tokyo Kasei Kogyo) and stirred in a sealed tube at 150° C. for 48 hours. The reaction mixture was cooled to room temperature, filtered through Celite and concentrated under reduced pressure. The residue was added with saturated brine (30 ml) and extracted three times with ethyl acetate (30 ml for each time). The organic layers were combined and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain the title compound (61.7 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094789B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-2e9115487cd940a38efae8fd5e24df8a
출처 메모uspto-grants-2006_08