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HRID 1869153作成日:2026年10月27日

Lithium hydroxide, monohydrate → 1-(2-(Trifluoromethyl)quinolin-4-yl)-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1869153

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indoleHCID 68970592—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-(Trifluoromethyl)quinolin-4-yl)-1H-indole-3-carboxylic acidHCID 68972955—

反応手順

0.204 g (4.9 mmol) of lithium hydroxide monohydrate and 8 cm3 of water are added to 0.6 g (1.62 mmol) of 3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole dissolved in 8 cm3 of tetrahydrofuran. After stirring at reflux for 15 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give a residue which is taken up in 20 cm3 of water (pH=10). The resulting aqueous solution is washed with 30 cm3 of ethyl acetate, adjusted to pH 6 with N hydrochloric acid and extracted with 50 cm3 of ethyl acetate. The organic phase is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The solid obtained is triturated in 20 cm3 of isopropyl ether and filtered off, resulting in 0.3 g of 3-carboxy-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole in the form of a yellow powder. Mass spectrum (EI): m/e 356 (M+•), m/e 311.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07638521B2
出典データセットuspto-grants-2009_12
ORD IDord-d37b4a9f20ea4fc38641b5986370be79
出典メモuspto-grants-2009_12