戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1016628作成日:2026年10月25日

Sodium Bicarbonate → N-[(S)-2-(3,4-Dichlorophenyl)-4-hydroxybutyl]-N-methyl-3-cyano-1-naphthamide

https://huagongshe.com/reaction/1016628

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物(gammaS)-gamma-(Aminomethyl)-3,4-dichlorobenzenepropanolHCID 20794251—
反応物3-Cyano-1-naphthoyl chlorideHCID 22636686—
溶媒DichloromethaneHCID 6344—
生成物N-[(S)-2-(3,4-Dichlorophenyl)-4-hydroxybutyl]-N-methyl-3-cyano-1-naphthamideHCID 5367934278%

反応条件

温度0 °C

反応手順

(S)-2-(3,4-Dichlorophenyl)-4-hydroxybutylamine (20.8 g, 83.8 mmol) was dissolved in DCM (700 mL). To the stirred solution was added 10% aqueous sodium bicarbonate (300 mL), and the mixture cooled to 0° C. A solution of 3-cyano-1-naphthoyl chloride (17.4 g, 80.6 mmol) in DCM (300 mL) was added dropwise over 30 minutes. The mixture was then allowed to warm to ambient temperature and stir for 20 h. The layers were separated, and the aqueous phase washed with DCM (300 mL). The combined organic layers were dried (Na2SO4), filtered, and evaporated in vacuo to give a white foam. Purification by chromatography (silica gel; 0-25% acetonitrile in DCM) provided the desired product as a white foam (27.0 g, 78%). 1H-NMR (DMSO-d6) δ1.46-1.60 (m, 1H, CH); 1.77-1.91 (m, 3H, CH); 4.3-4.41 (t, 1H, CH); 4.5-4.57 (t, 2H, CH); 6.43 (broad, 1H, OH); 6.8-7.26 (m, 2H, aromatic); 7.44-7.54 (m, 3H, aromatic); 7.57-7.80 (m, 7H, aromatic); 8.04-8.33 (m, 2H, aromatic); 8.61 (s, 1H, aromatic).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06476077B1
出典データセットuspto-grants-2002_11
ORD IDord-daa73d049a6e4a49a4eb412ae57fa2ed
出典メモuspto-grants-2002_11