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Methyl iodide → 5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 5-(5-Bromopyridin-3-YL)pyrrolidin-2-one | HCID 117667495 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinone | HCID 19694329 | 146.5% |
| 生成物 | 5-(5-Bromopyridin-3-YL)pyrrolidin-2-one | HCID 117667495 | — |
反応手順
5-(5-Bromo-pyridin-3-yl)-pyrrolidin-2-one is prepared as described in Example 76. To a solution of 5-(5-bromo-pyridin-3-yl)-pyrrolidin-2-one (202 mg, 0.84 mmol) in THF (5.0 mL) is added 60% NaH (50 mg, 1.3 mmol). The mixture is stirred at room temperature for 5 min and methyl iodide (0.078 mL, 1.3 mmol) is then added dropwise. The mixture is stirred at room temperature for 16 h. The mixture is then concentrated and purified by normal phase chromatography to give 157 mg of 5-(5-bromo-pyridin-3-yl)-1-methyl-pyrrolidin-2-one.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09181272B2 |
| 出典データセット | uspto-grants-2015_11 |
| ORD ID | ord-0bcae626d45344c9a3cfcdf736f5404d |
| 出典メモ | uspto-grants-2015_11 |