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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243538생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/243538

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물1-MethylpyrrolidineHCID 8454—
반응물Carbonate IonHCID 19660—
반응물2-DimethylaminopyridineHCID 21885—
반응물4-((4-Amino-6-chloropyrimidin-2-yl)amino)benzonitrileHCID 71465001—
용매WaterHCID 962—
생성물N-[6-chloro-2-(4-cyanophenylamino)pyrimidin-4-yl]benzamideHCID 71465002—

반응 조건

온도82.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653266B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-85f611c529154e2abe6e5538e9cbdacd
출처 메모uspto-grants-2014_02