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HRID 243540作成日:2026年10月26日

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

https://huagongshe.com/reaction/243540

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物BromineHCID 24408—
反応物DithionateHCID 3082075—
反応物N-[6-chloro-2-(4-cyanophenylamino)pyrimidin-4-yl]benzamideHCID 71465002—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物N-[5-bromo-6-chloro-2-(4-cyanophenylamino)-pyrimidin-4-yl]benzamideHCID 71465003—

反応手順

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.

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-1dfb970ae5b64db5b5c2d789f77f1fe8
出典メモuspto-grants-2014_02