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HRID 245152作成日:2026年10月26日

Potassium Hydroxide → 3-Methyl-6-(methylthio)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

https://huagongshe.com/reaction/245152

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Propiophenone, 3'-(trifluoromethyl)HCID 137064—
反応物5-(methylthio)-1H-indole-2,3-dioneHCID 16781205—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物3-Methyl-6-(methylthio)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acidHCID 6741835267.4%

反応手順

Potassium hydroxide (3.31 g, 59.0 mmol) in water (10 mL) was added slowly to a suspension of 5-(methylthio)-1H-indole-2,3-dione (1.9 g, 9.83 mmol) in ethanol (25 mL). 1-[3-(Trifluoromethyl)phenyl]-1-propanone (1.99 g, 9.83 mmol) was added and the mixture was heated to reflux for 1 h. The solvent was removed under reduced pressure, the residue was dissolved in water, and the aqueous mixture was washed with ether (3 times). The aqueous phase was chilled and was acidified to pH 3 with concentrated HCl. The solid material was collected by filtration, washed with water, and air dried to afford 3-methyl-6-(methylthio)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (2.5 g, 67% yield). MS (m/z) 378.0 (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-20820fad8d1647319b9ca15de2fd2c09
出典メモuspto-grants-2014_02