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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651280Generated: October 29, 2026

Potassium Bicarbonate → 8-Cyano-1-cyclopropyl-7-[(1S,6S)-2-(5methyl-2-oxo-1,3-dioxol-4-yl)methyl-2,8-diazabicyclo[4.3.0]nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/651280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BicarbonateHCID 516893—
ReactantPradofloxacinHCID 9802884—
Reactant4-(Bromomethyl)-5-methyl-1,3-dioxol-2-oneHCID 10774141—
SolventDimethylformamideHCID 6228—
Product8-Cyano-1-cyclopropyl-7-[(1S,6S)-2-(5methyl-2-oxo-1,3-dioxol-4-yl)methyl-2,8-diazabicyclo[4.3.0]nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 70108425—

Reaction Steps

100 mg (0.25 mmol) of 8-cyano-1-cyclopropyl-7-((1S,6S)-2,8-diazabicyclo[4.3.0]-nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 59 mg (0.30 mmol) of 4-bromomethyl-5-methyl-1,3-dioxol-2-one and 30 mg of potassium bicarbonate are heated at 140° C. in 2 ml of dimethylformamide for 30 minutes. The reaction solution is concentrated in vacuo, the residue is taken up in methylene chloride and the mixture is washed with water. The organic phase is dried over magnesium sulfate and concentrated in vacuo. The resulting residue is stirred with water, filtered off with suction and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06278013B1
Source datasetuspto-grants-2001_08
ORD IDord-b83e3be2654649b0a695f16018a44d6b
Source noteuspto-grants-2001_08