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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 712755Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt5-(5-Bromopyridin-3-YL)pyrrolidin-2-oneHCID 117667495—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(5-Bromo-3-pyridinyl)-1-methyl-2-pyrrolidinoneHCID 19694329146,5%
Produkt5-(5-Bromopyridin-3-YL)pyrrolidin-2-oneHCID 117667495—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181272B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-0bcae626d45344c9a3cfcdf736f5404d
Quellennotizuspto-grants-2015_11