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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373064생성일: 2026년 10월 26일

2,6-Di-tert-butyl-4-methylphenol → 4-(4-Vinyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/1373064

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Di-tert-butyl-4-methylphenolHCID 31404—
반응물Potassium FluorideHCID 522689—
반응물4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
반응물Tri(butyl)vinyltinHCID 53438229—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물4-(4-Vinyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979942—

반응 조건

온도110 °C

반응 단계

A suspension of Intermediate 6 (8.00 g), tri(n-butyl)vinyltin (8.63 ml), tetrakis(triphenylphosphine)palladium(0) (455 mg), and 2,6-di-tert-butyl-p-cresol (8.7 mg) in toluene (120 ml) was stirred at 110° C. for 2 hours. The reaction mixture was cooled to room temperature, then added with 10% aqueous potassium fluoride (120 ml), and stirred for 15 hours. After the precipitates were removed by filtration, the organic layer was separated, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and then the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1) to obtain the title compound (6.72 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07160894B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-fdeb0d8ab2bd48f9bf688e687a0f3bb3
출처 메모uspto-grants-2007_01