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Sulfamethazine → 4-Benzylamino-N-(4,6-dimethylpyrimidin-2-yl)-benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sulfamethazine | HCID 5327 | — |
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-Benzylamino-N-(4,6-dimethylpyrimidin-2-yl)-benzenesulfonamide | HCID 10155893 | — |
反応手順
100 mg (0.36 mmol) sulfamethazine and 70.8 μl (0.60 mmol) benzyl bromide were dissolved in 4 ml methanol. Caesium carbonate (113.4 mg, 0.35 mmol) was added and solution was refluxed overnight with stirring. The reaction mixture was then evaporated to dryness, and purified on silica using gradient elution (chloroform to 2% methanol in chloroform) to obtain white crystals in a yield similar to that described in example 1 for step III. 1H NMR (CDCl3, 500 MHz): 7.93 (2H, m), 7.31 (5H, m), 6.58 (3H, m), 4.36 (2H, s), 2.34 (6H, s); MS (ESI+): m/z 369 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06767909B2 |
| 出典データセット | uspto-grants-2004_07 |
| ORD ID | ord-cbdbf0c9d743492b9dc28d251d1b0053 |
| 出典メモ | uspto-grants-2004_07 |