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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603438Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 15859790, compound

https://huagongshe.com/reaction/1603438

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant8-Chloro-1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 9835941—
Reactanttert-Butyl 3-azabicyclo[3.2.0]heptan-1-ylcarbamateHCID 15859786—
SolventAcetonitrileHCID 6342—
ProductHCID 15859790HCID 1585979060.9%

Reaction Steps

1.22 g of 1-(t-butoxycarbonylamino)-3-azabicyclo[3.2.0]heptane, 0.96 g of 8-chloro-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid and 0.58 g of 1,8-diazabicyclo[5.4.0]-7-undecene were added to 20 ml of acetonitrile, followed by heating under reflux for 3.5 hours. After the solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (using a 100:1 mixture of chloroform and methanol as the eluent) and recrystallization (from ethyl acetate-diisopropyl ether) to obtain 0.96 g of 7-[1-(t-butoxycarbonylamino)-3-azabicyclo[3.2.0]hept-3-yl]-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (m.p. 200-202° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990106
Source datasetuspto-grants-1999_11
ORD IDord-a2656d546ec8415fb777bb28021c474b
Source noteuspto-grants-1999_11