Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222865Generated: October 31, 2026

Ethanol → Garenoxacin Mesylate

https://huagongshe.com/reaction/2222865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanesulfonic AcidHCID 6395—
ReactantGarenoxacinHCID 124093—
SolventWaterHCID 962—
ProductGarenoxacin MesylateHCID 157690—

Reaction Conditions

Temperature40 °C

Reaction Steps

In 192 ml of 50% water-containing ethanol is suspended 24 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 the suspension is warmed to 40° C., after which 5.71 g of methanesulfonic acid is added to the warmed suspension to form a uniform solution. Subsequently, the solution is stirred at the same temperature for 10 minutes and thereafter filtered, and the filtrate is concentrated, after which the crystals deposited are collected by filtration to obtain 26.64 g of (R)-1-cyclopropyl-8-difluoromethoxy-7-(1-methyl-2,3-dihydro-1H-5-isoindolyl)-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid methanesulfonate monohydrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371868B2
Source datasetuspto-grants-2008_05
ORD IDord-8ba463f6a25d4febb178db3e5d45e88d
Source noteuspto-grants-2008_05