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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589569Generated: October 25, 2026

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

https://huagongshe.com/reaction/1589569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-Ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 9835179—
ReactantHCID 16213147HCID 16213147—
SolventAcetonitrileHCID 6342—
Product7-[2,5-Diazabicyclo(2.2.1)hept-2-yl]-1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1356580085.9%

Reaction Steps

A solution of 0.54 g (2.0 mmol) of 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 0.57 g (2.2 mmol) of 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-7ene, and 20 ml of acetonitrile was heated under reflux for one hour and stirred at room temperature for two hours. The reaction mixture was filtered and the solid was washed with ethanol to give 0.60 g of the title compound, mp 275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04571396
Source datasetuspto-grants-1986_02
ORD IDord-5552fe03e13f4ff29bde74b4d71cd05e
Source noteuspto-grants-1986_02