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HRID 914940Erstellt: 24. Oktober 2026

Methyl vinyl ketone → 2-(2-(Imidazo[1,2-a]pyridin-2-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/de/reaction/914940

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl vinyl ketoneHCID 6570—
EduktPhthalimideHCID 6809—
Edukt2-AminopyridineHCID 10439—
Edukt2-(4-Bromo-3-oxobutyl)-1H-isoindole-1,3(2H)-dioneHCID 3759744—
LösungsmittelEthanolHCID 702—
Produkt2-(2-(Imidazo[1,2-a]pyridin-2-yl)ethyl)isoindoline-1,3-dioneHCID 153126996,6%
Produkt2-(4-Bromo-3-oxobutyl)-1H-isoindole-1,3(2H)-dioneHCID 3759744—

Reaktionsschritte

2-(4-Bromo-3-oxo-butyl)-isoindole-1,3-dione is prepared by condensation of but-1-en-3-one with phthalimide followed by bromination according to known procedures (J. Med. Chem., 35:3239, 1992. A solution of 2-(4-bromo-3-oxo-butyl)-isoindole-1,3-dione (8.9 g, 30.06 mmol) and 2-aminopyridine (2.8 g, 29.75 mmol) in ethanol is heated at reflux for 4 hours. The mixture is cooled to room temperature and concentrated. The residue is purified by chromatography (silica gel, dichloromethane/ethanol 95:5); to give 4.23 g of 2-[2-(imidazo[1,2-a]pyridin-2-yl)ethyl]-isoindole-1,3-dione (49%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07265127B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-fece2ae831fe4b3c95ed9fbc3f9472fa
Quellennotizuspto-grants-2007_09