Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  API >  Synthetic Anti-infective Drugs >  Quinolones >  Grepafloxacin hydrochloride

Grepafloxacin hydrochloride

Basic information Safety Supplier Related

Grepafloxacin hydrochloride Basic information

Product Name:
Grepafloxacin hydrochloride
Synonyms:
  • GREPAFLOXACIN HCL
  • 1-Cyclopropyl-6-fluoro-1,4-dihydro-5-methyl-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid hydrochloride (1:1)
  • D02178
  • Gpfx
  • Grepafloxacin hydrochloride (jan/usan)
  • Raxar
  • Raxar (tn)
  • Grepafloxacin hydrochloride
CAS:
161967-81-3
MF:
C19H22FN3O3
MW:
395.86
Mol File:
161967-81-3.mol
More
Less

Grepafloxacin hydrochloride Chemical Properties

storage temp. 
Store at -20°C
solubility 
H2O : ≥ 13.33 mg/mL (33.67 mM)
form 
Solid
color 
Yellow to orange
More
Less

Grepafloxacin hydrochloride Usage And Synthesis

Originator

Raxar,Glaxo Wellcome,UK

Uses

Antibacterial.

Uses

Grepafloxacin Hydrochloride is a useful compound for treatment of ophthalmic and otic infections.

Manufacturing Process

To 3-(3-methyl-1-piperazinyl)-4-fluoro-5-methyl-6-nitro-N-cyclopropylaniline is added diethyl ethoxymethylenemalonate and the mixture is heated at 150°C for 25 hours. After cooling, the reaction product is purified by silica-gel column-chromatography (dichloromethane:methanol = 100:1) to give diethyl[N-cyclopropyl-N-[3-(3-methyl-1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl] aminomethylene]malonate. The product is dissolved in acetic anhydride and thereto conc. sulfuric acid is added dropwise at 50-60°C, followed by stirring for 30 min. The mixture is poured into ice-water, neutralized, extracted with dichloromethane and the extract is dried. The solvent is distilled off under reduced pressure. Purification by silica-gel column-chromatography (dichloromethane:methanol = 10:1) to give ethyl 7- (3-methyl-1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4- oxoquinoline-3-carboxylate. To these compound is 10% aqueous solution of sodium hydroxide and ethanol, and the mixture is refluxed for 1 hour. After cooling, the reaction mixture is diluted with water and washed with dichloromethane. The aqueous layer is made acidic with acetic acid and then made weakly alkaline with an aqueous sodium hydrogen carbonate. The product is extracted with dichloromethane and the extract is dried. The solvent is distilled off under reduced pressure and to the residue is added ethanol. The precipitated crystals are filtered and recrystallized from DMFA to give 7-(3-methyl-1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro- 4-oxoquinoline-3-carboxylic acid (12 mg), as white powder, m.p. 206-208°C.
7-(3-methyl-1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4- oxoquinoline-3-carboxylicacid may be transformed to hydrochloride.

brand name

Raxar (Otsuka).

Therapeutic Function

Antibacterial

Grepafloxacin hydrochlorideSupplier

Pharmacodia (Beijing) Co.,Ltd
Tel
+86-400-851-9921
Email
sales@pharmacodia.com
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
CONIER CHEM AND PHARMA LIMITED
Tel
+8618523575427
Email
sales@conier.com
career henan chemical co
Tel
+86-0371-86658258 +8613203830695
Email
factory@coreychem.com
Shanghai?Medlife?Pharm-Tech?Co.,?Ltd
Tel
021-59167510 18117107507
Email
vip@med-life.cn