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ChemicalBook CAS DataBase List Levofloxacin

Levofloxacin synthesis

9synthesis methods
109-01-3 Synthesis
1-Methylpiperazine

109-01-3
644 suppliers
$5.00/5G

100986-89-8 Synthesis
Levofloxacin carboxylic acid

100986-89-8
330 suppliers
$8.00/250mg

-

Yield:100986-85-4 97.1%

Reaction Conditions:

with potassium hydroxide in water at 55; for 24 h;Reagent/catalyst;Time;Temperature;Solvent;

Steps:

4

,3-dihydro-3-methyl-7-oxo-7H-pyrido [1,2,3-Δ] - [1,4] Benzoxazine-6-carboxylate, 4.5 g of water, 4.5 g of N-methylpiperazine and 0.22 g (81%) of potassium hydroxide were added and the reaction was incubated at 55 ° C and the alcohol , And the reaction was allowed to proceed for about 6 hours.The reaction was warmed to reflux for about 18 hours.N-methylpiperazine was replaced by N-methylpiperazine.The residue of levofloxacin crude, dissolved with chloroform and water, after acid and alkali pH adjustment, extraction, washing, concentration and other steps.(Methanol: dichloromethane = 1: 8), and the solid was combined with the cold methanol rinse to obtain the finished product of levofloxacin Yield: 97.1%.The compound was confirmed to be levofloxacin product by the same method as the product obtained in Example 1, by measuring the melting point, determining the molecular weight by high resolution mass spectrometry, and confirming the product by NMR.

References:

CN103755722,2016,B Location in patent:Paragraph 0052-0053

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