戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 249663作成日:2026年10月24日

Water → 6-Amino-5-chloro-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid

https://huagongshe.com/ja/reaction/249663

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ChlorosuccinimideHCID 31398—
反応物6-Amino-2-(4-chlorophenyl)pyrimidine-4-carboxylic acidHCID 46863985—
溶媒DimethylformamideHCID 6228—
生成物6-Amino-5-chloro-2-(4-chlorophenyl)pyrimidine-4-carboxylic acidHCID 46863984—

反応条件

温度65 °C

反応手順

To a solution of 6-amino-2-(4-chlorophenyl)-4-pyrimidinecarboxylic acid (i.e. the product of Step B) (75 g, 300 mmol) in N,N-dimethylformamide (300 mL) at 50° C. was added portionwise N-chlorosuccinimide (44.1 g, 330 mmol). The temperature of the reaction mixture increased exothermically to 65° C. Then the reaction mixture was heated at 55° C. for 3 h. Additional N-chlorosuccinimide (14 g, 90 mmol) was added portionwise, and the reaction mixture was maintained at 55° C. for 30 minutes. After the reaction mixture was cooled water was added. The resulting solid was isolated by filtration, washed with water, dissolved in ethyl acetate, washed with water and dried. The solvent was removed using a rotary evaporator to afford the title product, a compound of the present invention, as a tan solid (73.68 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863220B2
出典データセットuspto-grants-2011_01
ORD IDord-8771eef4f9134e969b606860399eab85
出典メモuspto-grants-2011_01