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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

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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 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063073B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-f6f3ed1f69fb4c9a926f251a19a5551e
출처 메모uspto-grants-2011_11