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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243540생성일: 2026년 10월 25일

Dichloromethane → N-[5-bromo-6-chloro-2-(4-cyanophenylamino)-pyrimidin-4-yl]benzamide

https://huagongshe.com/reaction/243540

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물BromineHCID 24408—
반응물DithionateHCID 3082075—
반응물N-[6-chloro-2-(4-cyanophenylamino)pyrimidin-4-yl]benzamideHCID 71465002—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물N-[5-bromo-6-chloro-2-(4-cyanophenylamino)-pyrimidin-4-yl]benzamideHCID 71465003—

반응 단계

1500 ml of dichloromethane and 150 g of N-[6-chloro-2-(4-cyanophenylamino)pyrimidin-4-yl]benzamide were added to a reaction vessel and to this was added 750 ml of acetic acid and 44.2 mL of liquid bromine solution at 27±3° C. and stirred for 11 hrs. After completion of the reaction, to the reaction mixture was added 375 ml of water under stirring and maintained for 45 mins. To the reaction mixture was further added metabisulphate solution (60 g in 375 ml of water) and stirred further for 30 mins. The solid was filtered and washed with 300 ml of water and suck dried. The wet cake and 1500 ml of water were charged into a clean RB and adjusted pH 9.0±0.5 with 50% potassium carbonate solution. The reaction mass was stirred and filtered; the solid was washed with 150 ml of water followed by 150 ml of dichloromethane. The obtained solid was dried under vacuum at 73±2° C. to yield the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653266B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-1dfb970ae5b64db5b5c2d789f77f1fe8
출처 메모uspto-grants-2014_02