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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 712754Erstellt: 23. Oktober 2026

Pyridine → 1-[2-(5-Bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanone

https://huagongshe.com/de/reaction/712754

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktAcetic AnhydrideHCID 7918—
Edukt3-Bromo-5-(pyrrolidin-2-yl)pyridineHCID 4403815—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-[2-(5-Bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanoneHCID 117667240132%

Reaktionsschritte

To a solution of 3-bromo-5-(2-pyrrolidinyl)pyridine (200 mg, 0.881 mmol) and pyridine (0.2 mL, 1.96 mmol) in DCM (1 mL) in a 8-mL vial is added acetic anhydride (0.093 mL, 0.969 mmol) dropwise. The mixture is stirred at room temperature for 2.5 h. The mixture is concentrated. The resulting crude product is purified by normal phase chromatography using 0-4.5% MeOH in DCM as the gradient to afford 1-[2-(5-bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanone (313 mg, 83% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181272B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-621fe542518d4dd4a7d446037a497fb3
Quellennotizuspto-grants-2015_11