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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 559804생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/559804

반응식

참여 물질

역할이름HCID투입량
반응물FormamideHCID 713—
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-N-[4-(methylsulfonyl)benzyl]-5-(1,3-oxazol-4-yl)-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamideHCID 6672529531%

반응 단계

A mixture of 5-(bromoacetyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide (Example 50 (c), 100 mg, 0.17 mmol), formamide (135 μl, 3.4 mmol), xylene (300 μl) and conc. H2SO4 (10 μl) was heated with stirring for 2 h. The reaction was diluted with water and CH3CN and purified on preparative HPLC, affording the title compound (23 mg, 31%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063073B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-22221aa67f0245a0a1ae3bad442dde9c
출처 메모uspto-grants-2011_11