戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 248675作成日:2026年10月23日

3-Amino-4-methylbenzoic acid → 3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-4-methylbenzoic acid

https://huagongshe.com/ja/reaction/248675

反応式

関与物質

役割名称HCID仕込み量
反応物3-Amino-4-methylbenzoic acidHCID 75568—
反応物2-Acetylthiomethyl-3-phenyl-propionyl chlorideHCID 10377734—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium BicarbonateHCID 516892—
生成物3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-4-methylbenzoic acidHCID 1567016952.4%

反応手順

3-Amino-4-methylbenzoic acid (1.5 g) is dissolved in a solution of sodium hydrogen carbonate (1.68 g) in water (25 ml), and to the mixture is added dropwise a solution of 2-acetylthiomethyl-3-phenylpropionyl chloride (2.86 g) in tetrahydrofuran (8 ml) with vigorously stirring, and the mixture is stirred at room temperature for 3 hours. Tetrahydrofuran is distilled off at a low temperature under reduced pressure, and the residue is washed with diethyl ether and acidified with hydrochloric acid, and the resulting oily substance is extracted with ethyl acetate. The extract is washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and then the solvent is distilled off under reduced pressure. The oily residue is purified by a medium pressure column chromatography with CHP-20P (eluant, water-acetonitrile). The fractions containing the desired compound are collected, and acetonitrile is distilled off under reduced pressure, and the precipitated crystals are separated by filtration to give the title compound (1.93 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210266
出典データセットuspto-grants-1993_05
ORD IDord-45fd81e8e1ef4735a88d03c53e885b71
出典メモuspto-grants-1993_05