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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1589572Erstellt: 26. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-Ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[5-(phenylmethyl)-2,5-diazabicyclo(2.2.1)hept-2-yl]-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/1589572

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt1-Ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 9835179—
Edukt2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromideHCID 16637464—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[5-(phenylmethyl)-2,5-diazabicyclo(2.2.1)hept-2-yl]-3-quinolinecarboxylic acidHCID 1356582450,1%

Reaktionsschritte

A solution of 0.54 g (2.0 mmol) of 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 0.77 g (2.2 mmol) of 5-(phenylmethyl)-2,5-diazabicyclo(2.2.1)heptane dihydrobromide, (P. S. Portoghese and A. A. Mikhail, J. Org. Chem. 31, 1059 (1966)], 0.90 ml (6.0 mmol) of 1,8-diazabicyclo(5.4.0)undec-7-ene, and 20 ml of acetonitrile was heated under reflux for two hours and stirred at room temperature for two days. The mixture was filtered and the solid was washed with methanol to give 0.44 g of the title compound, mp 195°-198° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04571396
Quelldatensatzuspto-grants-1986_02
ORD IDord-01c1a2ba7b6545648357dee5608857ad
Quellennotizuspto-grants-1986_02