98349-24-7Relevant articles and documents
Refining method of ciprofloxacin and meglumine hydrochloride thereof
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Paragraph 0026-0028, (2021/10/27)
The invention provides a preparation process of ciprofloxacin and meglumine thereof. The intermediate product DLSX07 is stirred at Branson ° C. 20% minutes and then sonicated until the solution is cloudy, stirred at room temperature for a period 30s, stirred at room temperature 3h, cooled and slowly added to distilled water, and filtered through suction filtration and filter cake vacuum drying to obtain a pale yellow powder, and 4% the KOH mixture is subjected to ultrasonic treatment 40 - 50 °C. 1. The process is performed by stirring 5h. NCS .t. The solution is cloudy. LC-MS / MS detection powder is deltafloxacin, distilled water is added, and meglumine is mixed to obtain a deltafloxacin meglumine salt. By optimizing the preparation process, the use of the organic solvent is reduced, the reaction time is shortened, and the ice bath and the addition of the interface carrier material contribute to the improvement of the yield.
Quinolone dimers as potential antibacterial agents
Chepyala, Naveenkumar R.,Durgi, Rajashaker R.,Tatini, Lakshmi K.,Subbaraju, Gottumukkala V.,Hindupur, Rama M.,Dhanvada, Muralimohan R.
scheme or table, p. 637 - 643 (2012/06/01)
A series of novel 6-fluoro1,4-dihydro-4-oxo-3-quinoline carboxylic acid dimers (34-37), were synthesized as potential antibacterial agents from commercially available fluoro benzoic acids.
PREPARATION OF PYRIDONECARBOXYLIC ACID ANTIBACTERIALS
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Page/Page column 15, (2008/06/13)
A process for making 1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-hydroxyazetidin-1-yl)-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid, and therapeutically acceptable salts thereof, and intermediates used in the process are disclosed.