戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2367357作成日:2026年10月27日

Dimethylformamide → N-[2-(3-Chlorophenyl)-2-oxoethyl]-4-(phenylmethyl)-2-morpholinecarboxamide

https://huagongshe.com/reaction/2367357

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物4-Benzylmorpholine-2-carboxylic acidHCID 2776353—
反応物2-Amino-1-(3-chlorophenyl)ethanoneHCID 3026272—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-[2-(3-Chlorophenyl)-2-oxoethyl]-4-(phenylmethyl)-2-morpholinecarboxamideHCID 6699093121.4%

反応条件

温度25 °C

反応手順

Oxalyl chloride (1.32 mL, 15.03 mmol) was added to the suspension of 4-(phenylmethyl)-2-morpholinecarboxylic acid (2.218 g, 10.02 mmol) and DMF (0.155 mL, 2.005 mmol) in CH2Cl2 (100 mL) at 0° C. in 10 minutes, and the resulting mixture was stirred at 25° C. for 2 hours. The mixture was concentrated, and the resulting residue was dissolved in CH2Cl2 (100 mL) and triethylamine (3.07 mL, 22.05 mmol). 2-Amino-1-(3-chlorophenyl)ethanone (1.7 g, 10.02 mmol) was added to the brown solution at 0° C., and the reaction mixture was stirred at 25° C. for 3 hours. Water (150 mL) was added to the reaction mixture, and the aqueous mixture was extracted with EtOAc (3×100 mL). The combined organic layers were dried (Na2SO4), filtered, and evaporated. The resulting residue was purified by silica gel chromatography using as eluent 50% EtOAc in petroleum ether to afford the title compound (800 mg) as a pale yellow solid. LC-MS (ES) m/z=373 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08697685B2
出典データセットuspto-grants-2014_04
ORD IDord-dc534dcd9e8b4cacba077eac4215afda
出典メモuspto-grants-2014_04