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HRID 648511作成日:2026年10月26日

4-Aminobenzoic Acid → 4-[[3-Ethoxycarbonyl-7-(trifluoromethyl)-4-quinolyl]amino]benzoic acid hydrochloride

https://huagongshe.com/reaction/648511

反応式

関与物質

役割名称HCID仕込み量
反応物4-Aminobenzoic AcidHCID 978—
反応物Ethyl 4-chloro-7-(trifluoromethyl)quinoline-3-carboxylateHCID 14515676—
溶媒TetrahydrofuranHCID 8028—
生成物4-[[3-Ethoxycarbonyl-7-(trifluoromethyl)-4-quinolyl]amino]benzoic acid hydrochlorideHCID 1382503561.1%

反応手順

A mixture of ethyl 4-chloro-7-(trifluoromethyl)-3-quinoline-carboxylate (3.04 g) and 4-aminobenzoic acid (1.37 g) in tetrahydrofuran (53 ml) was stirred under reflux for 10 hours and cooled to room temperature. The precipitates were collected and washed with tetrahydrofuran to give 4-[[3-ethoxycarbonyl-7-(trifluoromethyl)-4-quinolyl]amino]benzoic acid hydrochloride (2.69 g) as yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04735952
出典データセットuspto-grants-1988_04
ORD IDord-bebe478147bd4c42b33c1475c46188a7
出典メモuspto-grants-1988_04