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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1888807생성일: 2026년 10월 26일

Acetamide → 6-Methyl-5-(2-methyl-1,3-oxazol-4-yl)-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide

https://huagongshe.com/reaction/1888807

반응식

참여 물질

역할이름HCID투입량
반응물AcetamideHCID 178—
반응물Sulfuric AcidHCID 1118—
반응물O-XyleneHCID 7237—
반응물5-(bromoacetyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamideHCID 86614780—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물6-Methyl-5-(2-methyl-1,3-oxazol-4-yl)-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamideHCID 6672531945%

반응 단계

A mixture of 5-(bromoacetyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide (90 mg, 0.15 mmol) and acetamide (44 mg, 0.75 mmol), xylene (300 μl) and cone. H2SO4 (10 μl) was heated with stirring for 3 h. The reaction was diluted with water and CH3CN and purified on preparative HPLC affording the title compound (37 mg, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501784B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-ef86b537969447e1b550c89bb058db9e
출처 메모uspto-grants-2013_08