Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl iodide → 5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 5-(5-Bromopyridin-3-YL)pyrrolidin-2-one | HCID 117667495 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinone | HCID 19694329 | 146.5% |
| 생성물 | 5-(5-Bromopyridin-3-YL)pyrrolidin-2-one | HCID 117667495 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09181272B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-0bcae626d45344c9a3cfcdf736f5404d |
| 출처 메모 | uspto-grants-2015_11 |