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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1888804생성일: 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/1888804

반응식

참여 물질

역할이름HCID투입량
반응물Butyl vinyl etherHCID 8108—
반응물TriethylamineHCID 8471—
반응물5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]1,2-dihydropyridine-3-carboxamideHCID 11519933—
촉매Bis(1,2-bis(diphenylphosphino)ethane)palladium(0)HCID 2724231—
용매DimethylformamideHCID 6228—
생성물5-(1-Butoxyvinyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamideHCID 6672545628.5%

반응 조건

온도100 °C

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 μmmol), 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501784B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-8a26177368884feb9d3feb4c5da1ae5b
출처 메모uspto-grants-2013_08