Lomefloxacin

  • CAS:98079-51-7
  • MF:C17H19F2N3O3
  • Purity:99%
  • Molecular Weight:387.814
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Product Details

  • CAS: 98079-51-7
  • MF: C17H19F2N3O3
  • Appearance: off-white to yellow crystals
  • China cas 98079-51-7 factory wholesale Lomefloxacin at affordable price

    • Molecular Formula:C17H19F2N3O3
    • Molecular Weight:387.814
    • Appearance/Colour:off-white to yellow crystals 
    • Vapor Pressure:4.87E-14mmHg at 25°C 
    • Melting Point:239-240 °C 
    • Refractive Index:1.547 
    • Boiling Point:542.7 °C at 760 mmHg 
    • PKA:-0.25±0.20(Predicted) 
    • Flash Point:282 °C 
    • PSA:74.57000 
    • Density:1.342 g/cm3 
    • LogP:2.99170 

    Lomefloxacin(Cas 98079-51-7) Usage

    Manufacturing Process

    A mixture of 1.00 g of 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3- carboxylic acid, 1.10 g of 2-methylpiperazine and 10 ml of pyridine was heated for 15 minutes under reflux. The reaction mixture was evaporated and methanol was added to the residue. The precipitate was filtered and recrystallized from ethanol to give 0.36 g of the 1-ethyl-6,8-difluoro-1,4- dihydro-7-(3-methyl-1-piperazinyl)-4-oxoquinoline-3-carboxylic acid as colorless needles, melting point 239.0-240.5°C.By the usual manner the hydrochloride was prepared and recrystallized from water as colorless needles, melting point 290-300°C (decomp.).

    Therapeutic Function

    Antibacterial

    Pharmaceutical Applications

    A difluoropiperazinyl quinolone formulated as the hydrochloride salt for oral administration. The in-vitro activity is very similar to that of norfloxacin . It is active against Enterobacteriaceae and fastidious Gram-negative bacilli, including L. pneumophila. Activity against Campylobacter spp., Ps. aeruginosa, Acinetobacter and Chlamydia spp. is poor. It has reduced activity against staphylococci and poor activity against streptococci, L. monocytogenes, anaerobes and Mycobacterium spp.A 400 mg oral dose achieves a concentration of 3–5 mg/L after 1–1.5 h. In escalating oral doses of 100, 400 and 800 mg to volunteers, the AUC was essentially proportional to the dosage, the mean plasma concentrations following 100, 400 and 800 mg doses being approximately 1.1, 4.7 and 7.5 mg/L, respectively.Several metabolites have been described, accounting for <5% of the oral dose. Elimination occurs principally via the kidneys and 50–70% of a dose appears in the urine over 24 h. In patients with impaired renal function given 400 mg orally, the apparent elimination half-life ranged from 8 to 44 h, depending on the degree of renal failure. Non-renal clearance was also impaired, but there was no significant change in other pharmacokinetic parameters. The daily dosage (400 mg) should be reduced to 280 mg when the creatinine clearance falls below 30 mL/min. Hemodialysis has no effect on the plasma concentration. The effect of lomefloxacin on the plasma concentration of theophylline is clinically insignificant and no dosage adjustment is required.The main adverse event is phototoxicity; other adverse events (mainly diarrhea, abdominal pain, skin reactions, dizziness, headache and insomnia) occur in about 10% of patients.It is chiefly used in urinary tract infection, but is no longer widely available.

    Definition

    ChEBI: A fluoroquinolone antibiotic, used (generally as the hydrochloride salt) to treat bacterial infections including bronchitis and urinary tract infections. It is also used to prevent urinary tract infections prior to surgery.

    Brand name

    Uniquin

    InChI:InChI=1/C17H21F2N3O3/c1-3-21-8-11(17(24)25)16(23)10-6-12(18)15(13(19)14(10)21)22-5-4-20-9(2)7-22/h6,9,11,20H,3-5,7-8H2,1-2H3,(H,24,25)

    98079-51-7 Relevant articles

    The crystal structure of DL-lomenfloxacin hydrate

    Shu, Zhan,Li, Hai Yan,Ma, Lin Lin,Chen, Wei Liang,Jin, Zhi Min

    , p. 384 - 388 (2009)

    The DL-lomenfloxacin hydrate is an inner...

    Preparation method of lomefloxacin hydrochloride

    -

    Paragraph 0025-0029, (2019/12/25)

    The invention discloses a preparation me...

    NOVEL METHOD OF SYNTHESIS OF FLUOROQUINOLONES

    -

    Page/Page column 6, (2009/04/24)

    The invention relates to a method of pre...

    Regioselective nucleophilic substitution of halogen derivatives of 1-substituted 4-oxo-1,4-dihydroquinoline-3-carboxylic acids

    Hermecz, Istvan,Vasvari-Debreczy, Lelle,Podanyi, Benjamin,Kereszturi, Geza,Balogh, Maria,Horvath, Agnes,Varkonyi, Peter

    , p. 1111 - 1116 (2007/10/03)

    The rate of the nucleophilic displacemen...

    98079-51-7 Process route

    (RS)-2-methylpiperazine
    109-07-9

    (RS)-2-methylpiperazine

    ethyl 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate
    100501-62-0

    ethyl 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate

    lomefloxacin
    98079-51-7

    lomefloxacin

    Conditions
    Conditions Yield
    (RS)-2-methylpiperazine; ethyl 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate; With potassium carbonate; In water; at 90 - 95 ℃; for 10h;
    With hydrogenchloride; water; at 20 ℃; for 3h; pH=7.5;
    96%
    ethyl 1-ethyl-6,8-difluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxoquinoline-3-carboxylate
    98079-83-5

    ethyl 1-ethyl-6,8-difluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxoquinoline-3-carboxylate

    lomefloxacin
    98079-51-7

    lomefloxacin

    Conditions
    Conditions Yield
    With hydrogenchloride; In ethanol;

    98079-51-7 Upstream products

    • 75338-42-0
      75338-42-0

      1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

    • 109-07-9
      109-07-9

      (RS)-2-methylpiperazine

    • 98079-83-5
      98079-83-5

      ethyl 1-ethyl-6,8-difluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxoquinoline-3-carboxylate

    • 100501-62-0
      100501-62-0

      ethyl 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate

    98079-51-7 Downstream products

    • 98079-47-1
      98079-47-1

      8-desfluoro-lomefloxacin

    • 195259-11-1
      195259-11-1

      8-Fluoro-9-(3-methyl-piperazin-1-yl)-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid

    • 111234-01-6
      111234-01-6

      8-chloro-1-ethyl-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxoquinoline-3-carboxylic acid

    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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