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HRID 378264作成日:2026年10月25日

4,6-Dichloro-n-methylpyrimidin-2-amine → N-[4-(6-chloro-2-methylamino-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide

https://huagongshe.com/reaction/378264

反応式

関与物質

役割名称HCID仕込み量
反応物4,6-Dichloro-n-methylpyrimidin-2-amineHCID 259880—
反応物N-(4-sulfamoyl-phenyl)-acetamide potassium saltHCID 70262342—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物N-[4-(6-chloro-2-methylamino-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamideHCID 1080813969.5%

反応手順

2.0 g (0.011 mol) of (4,6-dichlorpyrimidin-2-yl)-methylamine and 5.67 g (0.022 mol) N-(4-sulfamoyl-phenyl)-acetamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone at 140° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water, the inorganic phase was saturated with sodium chloride and the residual ethyl acetate dissolved in the aqueous phase was distilled off on a rotary evaporator. The aqueous phase was made acid with 1N HCl, the crystals which separated were filtered off under suction and washed with water. After drying there were obtained 2.72 g (68%) of N-[4-(6-chloro-2-methylamino-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide as beige crystals. m.p.: >240° C. (dec.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06030976
出典データセットuspto-grants-2000_02
ORD IDord-b283926af8594e2b95ebbd94dba9fce6
出典メモuspto-grants-2000_02