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HRID 559803作成日:2026年10月26日

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/559803

反応式

関与物質

役割名称HCID仕込み量
反応物AcetamideHCID 178—
反応物Sulfuric AcidHCID 1118—
反応物O-XyleneHCID 7237—
反応物5-(bromoacetyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamideHCID 86614780—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物6-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%

反応手順

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 conc. 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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063073B2
出典データセットuspto-grants-2011_11
ORD IDord-5c21422ce5234402bdf98dc330ddeb43
出典メモuspto-grants-2011_11