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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651282Generated: October 29, 2026

Dabco → Methyl 8-cyano-1-cyclopropyl-7-[(1S,6S)-2,8-diazabicyclo[4.3.0]nonan-8-yl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate

https://huagongshe.com/reaction/651282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
Reactant(1S,6S)-2,8-Diazabicyclo(4.3.0)nonaneHCID 10313138—
ReactantMethyl 8-cyano-1-cyclopropyl-7-chloro-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylateHCID 18351232—
SolventAcetonitrileHCID 6342—
ProductMethyl 8-cyano-1-cyclopropyl-7-[(1S,6S)-2,8-diazabicyclo[4.3.0]nonan-8-yl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylateHCID 15347199—

Reaction Steps

200 mg (0.625 mmol) of methyl 8-cyano-1-cyclopropyl-7-chloro-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate, 86 mg (0.683 mmol) of (1S,6S)-2,8-diazabicyclo[4.3.0]nonane and 150 mg (1.34 mmol) of 1,4-diazabicyclo[2.2.2]-octane are stirred in 6 ml of acetonitrile at room temperature for 48 hours. Thereafter, the mixture is evaporated and the residue is partitioned between 15 ml of chloroform and 20 ml of saturated sodium carbonate solution. The organic phase is separated off, the aqueous phase is extracted again with chloroform and, after drying with sodium sulfate, the combined extracts are evaporated. For purification, the residue is chromatographed over silica gel with ethyl acetate/ethanol/25% strength aqueous ammonia solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06278013B1
Source datasetuspto-grants-2001_08
ORD IDord-54db9c0c21304d0d8e3aff2fba0042cc
Source noteuspto-grants-2001_08