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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243540Generated: October 25, 2026

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

https://huagongshe.com/reaction/243540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBromineHCID 24408—
ReactantDithionateHCID 3082075—
ReactantN-[6-chloro-2-(4-cyanophenylamino)pyrimidin-4-yl]benzamideHCID 71465002—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductN-[5-bromo-6-chloro-2-(4-cyanophenylamino)-pyrimidin-4-yl]benzamideHCID 71465003—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653266B2
Source datasetuspto-grants-2014_02
ORD IDord-1dfb970ae5b64db5b5c2d789f77f1fe8
Source noteuspto-grants-2014_02