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HRID 418990作成日:2026年10月27日
3-Amino-2-bromo-5-chloropyridine → N-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-3-trifluoromethyl-benzenesulfonamide
https://huagongshe.com/reaction/418990
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 3-Amino-2-bromo-5-chloropyridine | HCID 2769640 | — |
| 反応物 | 4-Chloro-3-(trifluoromethyl)benzenesulfonyl Chloride | HCID 2780719 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | N-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-3-trifluoromethyl-benzenesulfonamide | HCID 57942594 | — |
反応手順
A mixture of 4-chloro-3-trifluoromethyl-benzenesulfonyl chloride (1.5 g, 5.3 mmol) and 2-bromo-5-chloro-pyridin-3-ylamine (500 mg, 2.4 mmol) dissolved in pyridine (20 mL) was heated at 60° C. for 16 h. The solvent was evaporated and the residue suspended in a 1:1 mixture of 2 M NaOH and methanol (20 mL) and heated at 70° C. for 30 min. The methanol was evaporated under reduced pressure and the residue diluted with 15 mL water. The solution was cooled on ice bath and the pH was adjusted to 3 by drop wise addition of concentrated HCl. The solid formed was collected by filtration and the product was purified by flash chromatography on silica gel column to afford the desired product. MS m/z: 450.8 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08093247B2 |
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| 出典データセット | uspto-grants-2012_01 |
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| ORD ID | ord-bdf7097ebde54bb28fa3f5be240f6d06 |
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| 出典メモ | uspto-grants-2012_01 |
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