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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018533Generated: October 30, 2026

Methanesulfonic Acid → Garenoxacin mesylate hydrate

https://huagongshe.com/reaction/1018533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 68432514HCID 68432514—
SolventEthanolHCID 702—
ProductGarenoxacin mesylate hydrateHCID 157690182.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

In 192 ml of 50% 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 monohydrate, and the suspension is warmed to 40° C., after which 5.71 g of methanesulfonic acid is added to form a uniform solution. Subsequently, 2.4 g of activated carbon is added and the resulting mixture is stirred at the same temperature for 10 minutes, after which the insolubles are removed by filtration. The filtrate is concentrated and 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-quinolinecarboxylic acid methanesulfonate monohydrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482835B2
Source datasetuspto-grants-2002_11
ORD IDord-2aa49440462b4210bf4ef5f7edb667f9
Source noteuspto-grants-2002_11