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Pipemidic acid

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CAS:51940-44-4
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CAS:51940-44-4
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CAS:51940-44-4
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Company Name: Anhui Zhongda Biotechnology Co., Ltd
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CAS:51940-44-4
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Pipemidic acid manufacturers

  • Pipemidic acid
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  • $55.00 / 500mg
  • 2024-11-19
  • CAS:51940-44-4
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  • Purity: 99.9%
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  • Pipemidic acid
  • Pipemidic acid pictures
  • $55.00 / 500mg
  • 2024-11-19
  • CAS:51940-44-4
  • Min. Order:
  • Purity: 99.9%
  • Supply Ability: 10g
  • Pipemidic acid
  • Pipemidic acid pictures
  • $40.00 / 1kg
  • 2024-10-25
  • CAS:51940-44-4
  • Min. Order: 1kg
  • Purity: 0.99
  • Supply Ability: 10 tons
Pipemidic acid Basic information
Product Name:Pipemidic acid
Synonyms:8-ETHYL-5,8-DIHYDRO-5-OXO-2-[1-PIPERAZINYL]PYRIDO[2,3-D]-PYRIMIDINE-6-CARBOXYLIC ACID;LABOTEST-BB LT00772244;PIPEMIDIC ACID;1489rb;pipemid;piperamicacid;pipram;pyrido(2,3-d)pyrimidine-6-carboxylicacid,5,8-dihydro-8-ethyl-5-oxo-2-(1-piper
CAS:51940-44-4
MF:C14H17N5O3
MW:303.32
EINECS:257-530-2
Product Categories:PIPEDAC
Mol File:51940-44-4.mol
Pipemidic acid Structure
Pipemidic acid Chemical Properties
Melting point 251-255℃
Boiling point 717℃
density 1.1931 (rough estimate)
refractive index 1.7000 (estimate)
Fp >110°(230°F)
storage temp. Amber Vial, -20°C Freezer, Under inert atmosphere
solubility 1 M NaOH: soluble50mg/mL
pka4.14±0.20(Predicted)
form Powder
color White to off-white
Water Solubility Soluble in 1N sodium hydroxide or in DMSO. Insoluble in water
Sensitive Light Sensitive
CAS DataBase Reference51940-44-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 42/43
Safety Statements 22-36/37-45
WGK Germany 2
RTECS UV1153800
HS Code 29335990
ToxicityLD50 in mice (mg/kg): 4000 orally; 1000 i.p., 50 i.v. (Ficicchia)
MSDS Information
ProviderLanguage
SigmaAldrich English
Pipemidic acid Usage And Synthesis
Chemical PropertiesThe substance is a light yellow crystalline powder with an odorless, bitter taste. It has a melting point range of 251-255°C, with decomposition. It is soluble in glacial acetic acid, but only slightly soluble in methanol, acetone, and DMF. It is extremely difficult to dissolve in water, ethanol, and chloroform, and is insoluble in benzene. However, it can be dissolved in dilute alkali or acid solutions.
OriginatorPipram ,Bellon, France ,1975
UsesPipemidic acid is a quinolone antibacterial drug that is primarily used to treat gram-negative infections of the urinary tract. It is also an antibiotic and cell selection agent. Unlike nalidixic acid, pipemidic acid has a broader spectrum of antibacterial activity and is effective for treating urinary tract and ENT infections.
PreparationThe synthesis of pipemidic acid involves a series of steps. First, ethyl 2,4-dichloropyrimidine-5-carboxylate is condensed and cyclized with ethyl β-ethylaminopropionate to yield 2-chloro-5-hydroxy-7,8-dihydro-8-ethylpyridine[2,3-d]pyrimidine-6-carboxylate. This compound is then brominated and subsequently condensed with piperazine. The resulting product is hydrolyzed and neutralized to obtain pipemidic acid.
DefinitionChEBI: Pipemidic acid is a pyridopyrimidine that is 5-oxo-5,8-dihydropyrido[2,3-d]pyrimidine-6-carboxylic acid substituted at position 2 by a piperazin-1-yl group and at position 8 by an ethyl group. A synthetic broad-spectrum antibacterial, it is used for treatment of gastrointestinal, biliary, and urinary infections. It has a role as an antibacterial drug and a DNA synthesis inhibitor. It is a monocarboxylic acid, an amino acid, a N-arylpiperazine, a pyridopyrimidine and a quinolone antibiotic.
Manufacturing ProcessA mixture containing 1.33 g of 5,8-dihydro-8-ethyl-2-methylthio-5oxopyridol[2,3-d]pyrimidine-6-carboxylic acid, 1.94 g of piperazine hexahydrate and 20 ml of dimethyl sulfoxide was heated at 110°C for 1 hour with stirring. The separated solid was collected by filtration, washed with ethanol, and then dried at such a temperature that did not rise above 50°C to give 1.57 g of the trihydrate of the product as nearly colorless needles, MP 253° to 255°C.
The starting material may be produced by reacting 6-amino-2methylthiopyrimidine with ethoxymethylene malonic acid diethyl ester. The intermediate thus produced is converted by boiling in diphenyl ether to 6ethoxycarbonyl-2-methylthio-5-oxo-5,8-dihydropyrido[2,3-d]pyrimidine. That is hydrolyzed by sodium hydroxide to cleave the ethoxy group and then ethylated with diethyl sulfate to give the starting material.
Therapeutic FunctionAntibacterial (urinary)
General DescriptionChemical structure: quinolone
Pharmaceutical ApplicationsAn orally administered pyridopyrimidine derivative with a 7-piperazinyl moiety. The piperazinyl moiety at C-7 increases in-vitro activity against Ps. aeruginosa. Pipemidic acid is inactive against Gram-positive bacteria or anaerobes
It is well absorbed orally. The drug is rapidly metabolized, primarily to acetyl, formyl and oxo derivatives, which exhibit much reduced antibacterial activity. It is eliminated in the urine, 50–85% of a dose appearing over the first 24 h, less than 2% as inactive metabolites. Non-renal clearance accounts for 10–40% of a dose in the young, rising to 40–70% in elderly subjects, thereby compensating for possible renal insufficiency. No dosage adjustment is necessary in patients with mild renal insufficiency. Some of the drug is eliminated in the bile and a significant portion appears in the feces.
Nausea and vomiting are common; dizziness, weakness and grand mal seizures have been observed, principally in the elderly. A number of reactions have been sufficiently severe to require discontinuation of therapy. Clinical use is restricted to urinary tract infections.
Biochem/physiol ActionsPipemidic acid modulates (inhibits) bacterial DNA gyrase-dependent processes such as DNA polymerization, (ATP-dependent) DNA supercoiling, and chromosome fragmentation. Pipemidic acid has been shown to induce inhibition of lymphocyte DNA synthesis.
ReferencesComprehensive Heterocyclic Chemistry II Volume 7, 1996, Pages 561-624 DOI: 10.1016/B978-008096518-5.00160-X
A New Approach for Improving the Antibacterial and Tumor Cytotoxic Activities of Pipemidic Acid by Including It in Trimethyl-β-cyclodextrin doi:10.3390/ijms20020416
https://pubchem.ncbi.nlm.nih.gov/compound/Pipemidic-acid
Pipemidic Acid, a New Antibacterial Agent Active Against Pseudomonas aeruginosa: In Vitro Properties DOI: 10.1128/aac.8.2.132
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