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HRID 1584201作成日:2026年10月25日

4,6-Dichloro-n-methylpyrimidin-2-amine → N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide

https://huagongshe.com/reaction/1584201

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4-Fluoro-benzenesulfonamide potassium saltHCID 131721324—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamideHCID 1935354456%

反応手順

0.46 g (0.0026 mol) of (4,6-dichloro-pyrimidin-2-yl)-methylamine and 1.1 g (0.0051 mol) of 4-fluoro-benzenesulfonamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone in 150° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water and extracted. The aqueous phase was saturated with sodium chloride, evaporated briefly in a vacuum and made acid with 4N HCl, with a precipitate separating. The mixture was suctioned filtered, the extract and the solid were combined and chromatographed over silica gel with cyclohexane/ethyl acetate 2:1 as the eluent. The product was recrystallized from ethyl acetate/n-hexane. There was obtained 0.46 g (56%) of N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide as white crystals; m.p. 121-123° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05932599
出典データセットuspto-grants-1999_08
ORD IDord-a78241e1c18349c4ba5dcc9fc48e642d
出典メモuspto-grants-1999_08