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HRID 245200作成日:2026年10月25日

2-Oxobutanoic Acid → 6-Bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

https://huagongshe.com/reaction/245200

反応式

関与物質

役割名称HCID仕込み量
反応物2-Oxobutanoic AcidHCID 58—
反応物3-(Trifluoromethyl)benzaldehydeHCID 67990—
反応物4-Bromo-3-methoxyanilineHCID 7018254—
溶媒EthanolHCID 702—
生成物6-Bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acidHCID 6738382878%

反応手順

3-(Trifluoromethyl)benzaldehyde (21.54 g, 124 mmol) was added to a solution of 4-bromo-3-(methyloxy)aniline (25 g, 124 mmol) in ethanol (300 mL) dropwise. The mixture was stirred at reflux for 1 h, and 2-oxobutanoic acid (12.63 g, 124 mmol) was added portionwise. The reaction mixture was stirred at reflux for additional 3 h, cooled to room temperature, and stirred overnight. The mixture was filtered to collect the precipitate, and the solid was washed with ethanol and dried to give 6-bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (42.6 g, 78% yield). This material was used without further purification. MS (m/z) 442.0 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658636B2
出典データセットuspto-grants-2014_02
ORD IDord-1f119455f58945efb2729a1ff4ef5d73
出典メモuspto-grants-2014_02