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HRID 487268Erstellt: 24. Oktober 2026

Sodium → 1-cyclopentyl-3-ethyl-6-imidazo[1,2-a]pyridin-6-yl-2H-pyrazolo[3,4-d]pyrimidin-4-one

https://huagongshe.com/de/reaction/487268

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodiumHCID 5360545—
EduktEthyl imidazo[1,2-a]pyridine-6-carboxylateHCID 11830209—
Edukt5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
LösungsmittelEthanolHCID 702—
Produkt1-cyclopentyl-3-ethyl-6-imidazo[1,2-a]pyridin-6-yl-2H-pyrazolo[3,4-d]pyrimidin-4-oneHCID 17843783462%

Reaktionsschritte

Sodium metal (0.21 g, 9.2 mmol) was dissolved in ethanol (25 ml) and 6-carboethoxyimidazo[1,2-a]pyridine (1.75 g, 9.2 mmol) and 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (1.02 g, 4.6 mmol) were added. The reaction mixture was heated to reflux for 24 hours, cooled to room temperature and stirred for 60 hours. The solvent was removed in vacuo, the residue was dissolved in water (100 ml) and the solution was neutralized by the addition of concentrated HCl. A precipitate was obtained which was collected by filtration through a glass frit. The solid was recrystallized from ethanol and washed with ether to afford 0.98 g (62%) of 1-cyclopentyl-3-ethyl-6-(6-imidazo[1,2-a]pyridinyl)-pyrazolo[3,4-d]pyrimidin-4-one as white crystals, m.p. >300° C. when dried for 18 hours at 120° C. in high vacuum.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05294612
Quelldatensatzuspto-grants-1994_03
ORD IDord-19b4b463815840d1850298edd2de8c12
Quellennotizuspto-grants-1994_03