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HRID 712755作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/712755

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物5-(5-Bromopyridin-3-YL)pyrrolidin-2-oneHCID 117667495—
溶媒TetrahydrofuranHCID 8028—
生成物5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinoneHCID 19694329146.5%
生成物5-(5-Bromopyridin-3-YL)pyrrolidin-2-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181272B2
出典データセットuspto-grants-2015_11
ORD IDord-0bcae626d45344c9a3cfcdf736f5404d
出典メモuspto-grants-2015_11