HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018533Generated: October 30, 2026
Methanesulfonic Acid → Garenoxacin mesylate hydrate
https://huagongshe.com/reaction/1018533
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 68432514 | HCID 68432514 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Garenoxacin mesylate hydrate | HCID 157690 | 182.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482835B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-2aa49440462b4210bf4ef5f7edb667f9 |
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| Source note | uspto-grants-2002_11 |
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