戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 243538作成日:2026年10月26日

Benzoyl chloride → N-[6-chloro-2-(4-cyanophenylamino)pyrimidin-4-yl]benzamide

https://huagongshe.com/reaction/243538

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物1-MethylpyrrolidineHCID 8454—
反応物Carbonate IonHCID 19660—
反応物2-DimethylaminopyridineHCID 21885—
反応物4-((4-Amino-6-chloropyrimidin-2-yl)amino)benzonitrileHCID 71465001—
溶媒WaterHCID 962—
生成物N-[6-chloro-2-(4-cyanophenylamino)pyrimidin-4-yl]benzamideHCID 71465002—

反応条件

温度82.5 °C

反応手順

1400 ml of N-methylpyrrolidine and 140 g of 4-(4-Amino-6-chloropyrimidin-2-ylamino)benzonitrile was charged into a reaction vessel. To this were added 85.49 g of dimethylamino pyridine and 87.21 g of diazabicyclo undecene and stirred for 30 mins. To the reaction mixture was added 27.36 g of benzoyl chloride and stirred at RT for 30 mins. and heated to 80-85° C. and maintained the same for 4 hrs. After completion of the reaction, the reaction mass was cooled to RT and 1400 ml of water was added, followed by 1400 ml of 50% carbonate solution. The reaction mass was extracted with 1400 ml of dichloromethane and the dichloromethane layer was washed with 700 ml of water. The organic layers were separated and dried over anhydrous sodium sulfate and filtered; distilled off dichloromethane and the solid was isolated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653266B2
出典データセットuspto-grants-2014_02
ORD IDord-85f611c529154e2abe6e5538e9cbdacd
出典メモuspto-grants-2014_02