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HRID 1822849作成日:2026年10月26日

Acetic Acid → 4-[2-(Aminocarbonyl)anilino]-6,7-dimethoxy-3-quinolinecarboxamide

https://huagongshe.com/reaction/1822849

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物AnthranilamideHCID 6942—
反応物4-Chloro-6,7-dimethoxyquinoline-3-carboxamideHCID 22170204—
溶媒DimethylformamideHCID 6228—
生成物4-[2-(Aminocarbonyl)anilino]-6,7-dimethoxy-3-quinolinecarboxamideHCID 2217026641.7%

反応条件

温度100 °C

反応手順

A mixture of 4-chloro-6,7-dimethoxy-3-quinolinecarboxamide (0.046 g, 0.17 mmol), 2-aminobenzamide (0.029 g, 0.21 mmol) and acetic acid (40 μl) in DMF (0.8 ml) was heated at 100° C. for 6 h. After cooling the reaction mixture was evaporated. The residue was dissolved in a mixture of MeCN and water (1:3) containing 0.1% trifluoroacetic acid and the turbid solution was filtered through a plug of glass wool. Preparative HPLC using a gradient (containing 0.1% trifluoroacetic acid) of 10→40% MeCN in water as eluent gave, after evaporation, the title compound as the trifluoroacetic acid salt. The product was suspended in saturated aqueous NaHCO3 an absorbed on a short SPE column [ISOLUTE™ C18 (EC)] pre-conditioned subsequently with methanol and then water. The column was washed extensively with water until the pH of the eluent was neutral. The product was then eluted with methanol. After evaporation, the residue was crystallized from ethanol to give the title compound (26 mg, 41%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07037925B2
出典データセットuspto-grants-2006_05
ORD IDord-de1bf3d214084f2aa382fa73e4cc257b
出典メモuspto-grants-2006_05