化工社化工社 化学情報印刷レポート · 研究参考用
2-Oxobutanoic Acid → 6-Bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Oxobutanoic Acid | HCID 58 | — |
| 反応物 | 3-(Trifluoromethyl)benzaldehyde | HCID 67990 | — |
| 反応物 | 4-Bromo-3-methoxyaniline | HCID 7018254 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-Bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid | HCID 67383828 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08658636B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-1f119455f58945efb2729a1ff4ef5d73 |
| 出典メモ | uspto-grants-2014_02 |