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HRID 245244作成日:2026年10月24日

5-Bromoisatin → 6-Bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

https://huagongshe.com/ja/reaction/245244

反応式

関与物質

役割名称HCID仕込み量
反応物5-BromoisatinHCID 6889—
反応物Potassium HydroxideHCID 14797—
反応物Propiophenone, 3'-(trifluoromethyl)HCID 137064—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物6-Bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acidHCID 67383995116.4%

反応条件

温度85 °C

反応手順

Potassium hydroxide (29.8 g, 531 mmol) in water (49.2 mL) was added to an orange suspension of 5-bromoisatin (20 g, 88 mmol) in ethanol (172 mL). 1-[3-(Trifluoromethyl)phenyl]-1-propanone (19.68 g, 97 mmol) was added and the mixture was heated to 85° C. for 3 h. The solvent was removed under reduced pressure. The residue was diluted with water (400 mL) and stirred overnight. The aqueous mixture was cooled to 0° C. and adjusted to pH˜3 with concentrated HCl. The solid was collected by filtration and dried in a vacuum oven at 70° C. for 3 days to afford 6-bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (42 g, >99% yield). This material was used without further purification. MS (m/z) 411.8 (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-c3533996947e4490825591d436c4c31f
出典メモuspto-grants-2014_02