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Pyridine → 3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 2-Amino-5-fluoropyridine | HCID 2737701 | — |
| 反応物 | 3-Cyano-4-fluorobenzenesulfonyl chloride | HCID 2778908 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamide | HCID 59436600 | — |
反応手順
3-Cyano-4-fluorobenzenesulfonyl chloride (5 g, 20 mmol), 5-fluoropyridin-2-amine (3.37 g, 30 mmol) and pyridine (4.87 mL, 60 mmol) in dichloromethane (100 mL) were stirred at room temperature for 2 hours before concentrating in vacuo. The residue was triturated in hydrochloric acid (2 N aqueous solution, 100 mL) for 16 hours. The precipitate was filtered to afford the title compound as a pale pink solid, 6.1 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08541588B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-a8c4714f0d7c45e3a9003b24c6a5e230 |
| 出典メモ | uspto-grants-2013_09 |