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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4,6-Dichloro-n-methylpyrimidin-2-amine | HCID 259880 | — |
| 反応物 | 4-Fluoro-benzenesulfonamide potassium salt | HCID 131721324 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide | HCID 19353544 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05932599 |
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| 出典データセット | uspto-grants-1999_08 |
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| ORD ID | ord-a78241e1c18349c4ba5dcc9fc48e642d |
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| 出典メモ | uspto-grants-1999_08 |
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