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HRID 1646302作成日:2026年10月25日

Benzyl Alcohol → Benzyl 3-[(2-acetylthiomethyl-3-phenylpropionyl)amino]benzoate

https://huagongshe.com/reaction/1646302

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物Benzoic acid, 3-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]-HCID 10215552—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 3-[(2-acetylthiomethyl-3-phenylpropionyl)amino]benzoateHCID 15670217—

反応手順

3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-benzoic acid prepared in Example 68-(b)-[1](0.3 g),4-dimethylaminopyridine (0.01 g) and benzyl alcohol (0.1 g) are dissolved in dichloromethane (25 ml), and thereto is added EDC·HCl (0.18 g), and the mixture is stirred at room temperature three nights. The reaction mixture is washed with saturated aqueous citric acid solution, water, saturated aqueous sodium hydrogen carbonate solution and water in this order, dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. The residue is purified by a silica gel column chromatography (eluant, chloroform) to give the title compound (0.26 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05179125
出典データセットuspto-grants-1993_01
ORD IDord-2fee52c78d91462cacc57f6c499aec62
出典メモuspto-grants-1993_01