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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 712755생성일: 2026년 10월 25일

Methyl iodide → 5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinone

https://huagongshe.com/reaction/712755

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물5-(5-Bromopyridin-3-YL)pyrrolidin-2-oneHCID 117667495—
용매TetrahydrofuranHCID 8028—
생성물5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinoneHCID 19694329146.5%
생성물5-(5-Bromopyridin-3-YL)pyrrolidin-2-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181272B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-0bcae626d45344c9a3cfcdf736f5404d
출처 메모uspto-grants-2015_11