Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 559800생성일: 2026년 10월 26일
Butyl vinyl ether → 5-(1-Butoxyvinyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide
https://huagongshe.com/reaction/559800
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyl vinyl ether | HCID 8108 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]1,2-dihydropyridine-3-carboxamide | HCID 11519933 | — |
| 촉매 | Bis(1,2-bis(diphenylphosphino)ethane)palladium(0) | HCID 2724231 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-(1-Butoxyvinyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide | HCID 66725456 | 28.5% |
반응 단계
5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide (Example 1 (d), 101.5 mg, 0.17 mmol), bis[1,2-bis(diphenylphosphino)ethane]-palladium (0) (16.5 mg, 18.3 μmol), n-butyl vinyl ether (60 μl, 0.46 mmol), triethylamine (0.5 ml, 3.6 mmol) and DMF (6 ml) were placed in a Schlenk vessel equipped with a magnetic stirring bar. The vessel was purged with argon, sealed, and heated at 100° C. overnight. The reaction mixture was cooled and partitioned between ethyl acetate and water. The organic layer was dried over sodium sulphate, filtered and concentrated in vacuo. The residue was purified by preparative HPLC to give the title compound as a white solid (27.3 mg, 28%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08063073B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-f6f3ed1f69fb4c9a926f251a19a5551e |
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| 출처 메모 | uspto-grants-2011_11 |
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