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Phosphorus oxychloride → N-(5-bromo-2-pyridinyl)-(2-nitro)-5fluorophenylcarboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | 2-Amino-5-bromopyridine | HCID 70622 | — |
| 反応物 | 5-Fluoro-2-nitrobenzoic acid | HCID 2737420 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | N-(5-bromo-2-pyridinyl)-(2-nitro)-5fluorophenylcarboxamide | HCID 22596298 | 68.1% |
反応手順
A solution of 5-fluoro-2-nitrobenzoic acid (10.0 g, 54 mmol, 1.0 equiv), 2-amino-5-bromopyridine (12.2 g, 1.3 equiv), in 80 mL of pyridine was treated with phosphorous oxychloride (25.3 g, 3.0 equiv) for 30 min. The volatile was evaporated and the residue was redissolved into EtOAc, washed with 1N HCl, saturated aqueous NaHCO3 and saturated aqueous NaCl. The organic layer was dried over Na2SO4, filtered, and evaporated. The volatile was evaporated, and the product was triturated with diethyl ether to give N-(5-bromo-2-pyridinyl)-(2-nitro)-5-fluorophenylcarboxamide (12.5 g, 68%). MS found for C12H7BrFN3O3 (M+H)+: 340, 342.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07727982B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-b7fdc228ba5a4a11b5ad77c59bddf049 |
| 出典メモ | uspto-grants-2010_06 |