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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250358Generated: October 31, 2026

Methanesulfonic Acid → Garenoxacin Mesylate

https://huagongshe.com/reaction/1250358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 68432514HCID 68432514—
SolventEthanolHCID 702—
ProductGarenoxacin MesylateHCID 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 numberUS06337399B1
Source datasetuspto-grants-2002_01
ORD IDord-53f26a2272544d19840de385007015a3
Source noteuspto-grants-2002_01