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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222866Generated: November 1, 2026

Methanesulfonic Acid → Garenoxacin mesylate

https://huagongshe.com/reaction/2222866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantGarenoxacinHCID 124093—
SolventEthanolHCID 702—
ProductGarenoxacin mesylateHCID 12409481.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

In 4 ml of ethanol is suspended 0.2 g of (R)-1-cyclopropyl-8-difluoromethoxy-7-(1-methyl-2,3-dihydro-1H-5-isoindolyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid and then the suspension is warmed to 70° C., after which 45 mg of methanesulfonic acid is added to the warmed suspension to form a uniform solution. Subsequently, the solution is stirred at the same temperature for 1 hour and then cooled to room temperature, after which the crystals deposited are collected by filtration to obtain 0.20 g of (R)-1-cyclo-propyl-8-difluoromethoxy-7-(1-methyl-2,3-dihydro-1H-5-isoindolyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371868B2
Source datasetuspto-grants-2008_05
ORD IDord-cd65c190b276499c8687eb071d3a283d
Source noteuspto-grants-2008_05