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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414218Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-Cyclopropyl-7-[3-(2-fluoroethyl)aminomethyl-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/414218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-Cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 535414—
Reactant3-(2-Fluoroethylaminomethyl)pyrrolidineHCID 14307756—
SolventAcetonitrileHCID 6342—
Product1-Cyclopropyl-7-[3-(2-fluoroethyl)aminomethyl-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1393380948.4%

Reaction Steps

A suspension of 1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (200 mg), 3-(2-fluoroethylaminomethyl)pyrrolidine (165 mg) and 1,8-diazabicyclo[5,4,0]-7-undecene (100 mg) in absolute acetonitrile (2 ml) was refluxed for an hour. After cooling, the reaction mixture was concentrated and to the residue was added acetonitrile-ether (1:1, 5 ml). The solution was allowed to stand overnight at 5° C., then the resulting precipitate was collected by filtration and recrystallized from chloroform-methanol-ether to give the title compound (140 mg), mp 134°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791118
Source datasetuspto-grants-1988_12
ORD IDord-515b307af6b4476e9316992037373974
Source noteuspto-grants-1988_12