戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1035286作成日:2026年10月26日

Benzathine → Ethyl 1,4-dibenzyl-3-oxopiperazine-2-carboxylate

https://huagongshe.com/reaction/1035286

反応式

関与物質

役割名称HCID仕込み量
反応物BenzathineHCID 8793—
反応物Diethyl bromomalonateHCID 69637—
溶媒AcetonitrileHCID 6342—
溶媒Sodium HydroxideHCID 14798—
生成物Ethyl 1,4-dibenzyl-3-oxopiperazine-2-carboxylateHCID 15645950—

反応条件

温度90 °C

反応手順

To a solution of N,N′-dibenzylethylenediamine (14.12 mL, 60.2 mmol) in acetonitrile (100 mL) was added diethyl bromomalonate (5.14 mL, 30.1 mmol), and the mixture was heated with an oil bath at 90° C. (reflux) for 7 hours. The solvent was evaporated to provide a residue that was dissolved in 1 M NaOH (aqueous), and the mixture was extracted with ethyl acetate twice, dried over Na2SO4, and the solvent was evaporated. The crude mixture was purified by silica gel chromatography (Analogix IntelliFlash 280, SF40-150) eluting with 15%-30% ethyl acetate/hexanes to afford the title compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.38-7.20 (m, 10H), 4.54 (dd, J=15.0, 154.2, 2H), 4.20-4.10 (m, 2H), 4.03 (q, J=7.1, 1H), 3.96 (s, 1H), 3.61 (dd, J=13.5, 41.7, 2H), 3.27-3.14 (m, 2H), 3.05-2.95 (m, 1H), 2.60-2.52 (m, 1H), 1.23 (t, J=7.1, 3H); MS (ESI+) m/z 353.0 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08546377B2
出典データセットuspto-grants-2013_10
ORD IDord-f8dff528f719486c8df628f1de96d9a3
出典メモuspto-grants-2013_10