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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | 4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine | HCID 21979972 | — |
| 반응물 | Tri(butyl)vinyltin | HCID 53438229 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(4-Vinyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine | HCID 21979942 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07160894B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-fdeb0d8ab2bd48f9bf688e687a0f3bb3 |
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| 출처 메모 | uspto-grants-2007_01 |
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