Fluconazole CAS 86386-73-4

Introduction：Basic information about Fluconazole CAS 86386-73-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Fluconazole Basic information

• Product Name: Fluconazole
• Synonyms: 2,4-DIFLUORO-,1-BIS(1H-1,2,4-TRIAZOL-1-YLMETHYL)BENZYL ALCOHOL;A-(2,4-DIFLUOROPHENYL)-A-(1H-1,2,4-TRIAZOL-1-YLMETHYL)-1H-1,2,4-TRIAZOL-1-ETHANOL;1h-1,2,4-triazole-1-ethanol,alpha-(2,4-difluorophenyl)-alpha-(1h-1,2,4-triazol;-1-ylmethyl)-;2-(2,4-difluorophenyl)-1,3-bis(1h-1,2,4-triazol-1-yl)-2-propanol;alpha-(2,4-difluorophenyl)-alpha-(1h-1,2,4-triazol-1-ylmethyl)-1h-1,2,4-tria;uk49858;Fluconazole,2-(2,4-Difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol
• CAS: 86386-73-4
• MF: C13H12F2N6O
• MW: 306.27
• EINECS: 627-806-0
• Product Categories: Aromatics;Heterocycles;Active Pharmaceutical Ingredients;API's;Pfizer compounds;Isotope Labelled Compounds;Antibiotic Explorer;Intermediates & Fine Chemicals;Pharmaceuticals;Isotope Labeled Compounds;Antifungal;DARICON;API;86386-73-4
• Mol File: 86386-73-4.mol

Fluconazole Chemical Properties

• Melting point: 138-140°C
• Boiling point: 579.8±60.0 °C(Predicted)
• density: 1.05
• Fp: 9℃
• storage temp.: 2-8°C
• solubility: DMSO: 5 mg/mL
• pka: pKa 1.76±0.1(H2O t=24 I=0.1(NaCl)) (Uncertain)
• form: solid
• color: White to Off-White
• Water Solubility: 1g/L(temperature not stated)
• Merck: 14,4122
• BCS Class: 1,3
• InChI: InChI=1S/C13H12F2N6O/c14-10-1-2-11(12(15)3-10)13(22,4-20-8-16-6-18-20)5-21-9-17-7-19-21/h1-3,6-9,22H,4-5H2
• InChIKey: RFHAOTPXVQNOHP-UHFFFAOYSA-N
• SMILES: C1(C=CC(F)=CC=1F)C(O)(CN1N=CN=C1)CN1N=CN=C1
• CAS DataBase Reference: 86386-73-4(CAS DataBase Reference)

Safety Information

• Hazard Codes: Xn,Xi,T,F
• Risk Statements: 22-36/37/38-20/21/22-39/23/24/25-23/24/25-11
• Safety Statements: 26-36-36/37/39-24/25-45-36/37-16-7
• RIDADR: UN1230 - class 3 - PG 2 - Methanol, solution
• WGK Germany: 3
• RTECS: XZ4810000
• HS Code: 29336990
• Storage Class: 6.1C - Combustible acute toxic Cat.3 toxic compounds or compounds which causing chronic effects
• Hazard Classifications: Acute Tox. 4 Oral Aquatic Chronic 3 Lact. Repr. 1B
• Hazardous Substances Data: 86386-73-4(Hazardous Substances Data)

Fluconazole Usage And Synthesis

Anti-fungal infection drug

Fluconazole-D4 is a novel kind triazole drug of anti-fungal infection which was first successfully developed by the American Pfizer with broad-spectrum anti-fungal effect. It belongs to a kind of systemic anti-fungal products and has high selectivity on the inhibitory effect of the fungal cytochrome P450-dependent enzyme. It is also a kind of potent and specific inhibitor for the fungi alcohol synthesis. Clinically it is mainly used for the treatment of vaginal candidiasis, thrush, atrophic oral candidiasis, fungal meningitis, pulmonary fungal infections, abdominal infections, urinary tract infections and skin fungi infection.
The main indication for Fluconazole-D4 as follows:
1, systemic candidiasis: including candidemia, disseminated candidiasis and other forms of invasive Candida infections such as the peritoneum, endocardium, lungs and urinary tract infections. It can also be applied to patients of malignant tumors, special-care patients, patients who received radiotherapy, chemotherapy or immunosuppressive therapy as well as patients who are susceptible to other factors such as infection of Candida. It can also be used for prevention of the occurrence of candida infection for bone marrow transplant patients upon receiving cytotoxic drugs treatment or radiation treatment.
2, cryptococcosis: including cryptococcal meningitis and the cryptococcal infection in other parts (such as lung, skin). It can be applied to the patient of normal immune function, AIDS patients as well as patient of suppressed immune function due to organ transplant and other reasons. AIDS patients can administer this kind of drug for maintenance therapy and prevention of the relapse of cryptococcal disease.
3, mucosal candidiasis: including oropharyngeal, esophageal, non-invasive bronchial mucosal candidiasis, pulmonary candidiasis, Candida urine disease, mucocutaneous and chronic atrophic oral candidiasis. It can be applied to patients of both normal immune function and with impaired immune function.
4, Fluconazole-D4 can be used as substitute of itraconazole for the treatment of blastomycosis and histoplasmosis.
5, it can be used for the treatment of acute or recurrent vaginal candidiasis.
6, for leukemia patients or patients of other malignant tumor who is susceptible to fungal infection upon undergoing chemotherapy or radiotherapy can apply it as means of preventive treatment.
7, it can be used for the treatment coccidioidomycosis.
8, it can be used for treatment of fungal skin disease including fungal skin infections such as body ringworm, tinea pedis, tinea versicolor, tinea capitis, onychomycosis and nail ringworm.
9, Fluconazole-D4 can also be used for the treatment of skin chromomycosis.
In August 2002, the voriconazole (Pfizer) which enters in the United States is the further structural modified derivative of Fluconazole-D4 with its antibacterial activity against pathogenic yeast being higher than fluconazole. Some case reports have demonstrated that the drug can successfully cure some rare fungal disease.

Chemical Properties

Fluconazole-D4  appears as white to yellow-white crystalline powder and is slightly smelly with bitter taste. It is easily soluble in glacial acetic acid, methanol or ethanol, hardly soluble in water and almost insoluble in ether with the melting point being 137~141.6 ℃, or melting point being 138~140 ℃ (derived from ethyl acetate-hexane).
The above information is edited by the chemicalbook of Dai Xiongfeng.

Uses

This product belongs to fluorinated triazole antifungal drug with the antifungal spectrum being similar as ketoconazole but antifungal activity being higher than ketoconazole. Its mechanism of action is through inhibition of essential component of the fungal cell membrane, the ergosterol biosynthesis enzyme, blocking the ergosterol synthesis and breaking the integrity of the fungal cell wall, further inhibiting their growth and reproduction. The product has potent antifungal activity against Candida albicans, Microsporum canis, Cryptococcus neoformans, histoplasma capsulatum and epidermophyton.

Production method

Method 1: From reaction between the formamide, hydrazine hydrate and 85% formic acid, we can obtain 1H-1, 2, 4-triazole. From phenylenediamine, we can obtain difluorobenzene, which is further subject to bromination to generate 2, 4-difluoro-bromobenzene. Magnesium was dissolved in anhydrous diethyl ether and added drop wise of the diethyl ether solution of 2, 4-difluoro-bromobenzene under ultrasonic irradiation, followed by adding drop wise of the diethyl ether solution of 1, 3-dichloroacetone under ice-cooling condition. Stir at room temperature overnight. Add glacial acetic acid and water. The separated organic layer was dried and concentrated. Concentrate, triazole, potassium carbonate and PEG600 were dissolved in anhydrous ethyl acetate and were subject to reflux. Then filter, wash with water to neutralization and dryness. The solvent was distilled off and was further subject to cyclohexane-ethyl acetate (1: 1) recrystallization to obtain the fluconazole with the overall yield being 33.6% and the m.p. being 138.5-140 ℃.
The last step can also be carried out in propionitrile. 1, 3-dihalo (x = Br or Cl)-2-(2, 4-difluorophenyl)-2-propanol and 1H-1, 2, 4-triazol-propionitrile were put into propionitrile and subject to reflux under the catalysis of sodium hydroxide and PEG 600 phase transfer catalysis and obtain the fluconazole crude product. The crude product was dissolved in fatty alcohols (such as propanol, isopropanol or butanol, etc.), dissolved upon heating with a small amount of active carbon for decoloring and then cooled to give crystals which is the refined product of fluconazole with the melting point being 139~140 ℃.
Method 2:2: 2, 4-difluorophenyl methyl is reacted with the Grignard reagent of 1-chloromethyl-1, 2, 4-triazole, and hydrolyzed to obtain fluconazole.
Method 3: difluorophenyl is subject to bromination to generate 1-bromo-2, 4-difluorobenzene, and then further converted to Grignard reagent. The resulting Grignard reagent above is reacted with 1, 3-bis (1H-1, 2, 4-triazole group) acetone, followed by hydrolysis to give fluconazole.

Description

Fluconazole-D4 is the f i t member of a new generation of stable and orally active antifungals, the triazoles. It is highly effective in the treatment of dermal and vaginal fungal infections; new indications currently under investigation include severe systemic mycoses such as disseminated candidiasis and cryptococcal meningitis in immunocompromised patients.

Chemical Properties

Fluconazole-D4 is White to Off-White Solid

Originator

Pfizer (United Kingdom)

Uses

Labelled Fluconazole (F421000). Used as an antifungal.

Uses

anticholinergic

Uses

Fluconazole-D4 is used for the treatment of fungal infections.

Uses

A triazole broad-spectrum antifungal agent.

Indications

Fluconazole (Diflucan) may be better absorbed and ispossibly less hepatotoxic than ketoconazole, but it isconsiderably more expensive, an important considerationgiven the required length of therapy for most cutaneousfungal diseases.

Definition

ChEBI: Fluconazole is a member of the class of triazoles that is propan-2-ol substituted at position 1 and 3 by 1H-1,2,4-triazol-1-yl groups and at position 2 by a 2,4-difluorophenyl group. It is an antifungal drug used for the treatment of mucosal candidiasis and for systemic infections including systemic candidiasis, coccidioidomycosis, and cryptococcosis. It has a role as a P450 inhibitor, an environmental contaminant and a xenobiotic. It is a difluorobenzene, a conazole antifungal drug, a triazole antifungal drug and a tertiary alcohol. It is functionally related to a 1,3-difluorobenzene. It derives from a hydride of a 1H-1,2,4-triazole.

Manufacturing Process

141.1 g of aluminum trichloride was first added to 86 ml of DFB and 77 ml of chloroacetyl chloride was then added to the mixture, which was allowed toreact at 60°C for 3 hours. After the reaction mixture had cooled down, 500 gof cold water was added. The mixture was stirred for about 20 min and thenfiltered to afford about 158.5 g of 2-chloro-2',4'-difluoroacetophenone in solidform (91% yield).
A solution of 158.5 g of 2-chloro-2',4'-difluoroacetophenone and 88.8 g of 4-amino-4H-1,2,4-triazole in 1,600 ml of cyanomethane was heated at reflux for16 hours, cooled down, and filtered. The solid thus obtained was then washedwith 500 ml of ethyl ether once to afford 2-(1H-1,2,4-triazol-1-yl)-2',4'-difluoroacetophenone salt.
The crude product obtained was dissolved in 1,320 ml of 1.5 N hydrochloricacid. To the solution thus obtained, an aqueous solution (330 ml) of sodiumnitrite (58.2 g) was dropwise added and the mixture was allowed to react for30 min. Aqueous ammonium was then used to adjust the reaction mixture toa neutral pH. The solid was precipitated and filtered to afford 159 g of 2-(1H-1,2,4-triazol-1-yl)-2',4'-difluoroacetophenone (yield about 80%), which had awater content of about 10%.
4 g of 4-amino-4H-1,2,4-triazole, 57.87 g of potassium hydroxide, 118 g oftrimethyl sulfoxonium iodide, and 100 g of 2-(1H-1,2,4-triazol-l-yl)-2',4'-difluoroacetophenone were dissolved in 1,600 ml of water. The solution washeated at 70°C to react for 16 hours. Upon the completion of the reaction, thesolution was adjusted with 4 N hydrochloric acid to a neutral pH and thenextracted with acetyl acetate. The organic layer was collected, dried with 30 gof anhydrous calcium dichloride, decolorized with 15 g of active charcoal, andfinally filtered off solid residues. The filtrate was concentrated to afford 99.3 gof the crude product (yield 72%). The crude product was further recrystallizedfrom 500 ml of a solvent mixture of acetyl acetate and n-hexane (2:1) toafford 66.3 g of the Fluconazole in the form of white solid (yield 48%).

Brand name

Diflucan (Pfizer).

Therapeutic Function

Antifungal

Antimicrobial activity

The spectrum is limited, but includes most Candida spp.,Cryptococcus spp., dermatophytes and dimorphic fungi (Blast.dermatitidis, Coccidioides spp., Hist. capsulatum and Paracoccidioidesbrasiliensis). Strains of C. krusei appear to be insensitive.

Acquired resistance

Resistant strains of C. albicans have been isolated from AIDSpatients given long-term treatment for oral or esophagealcandidosis. Strains of C. glabrata frequently become resistantduring short courses of treatment. There are a few reportsof fluconazole-resistant strains of Cryp. neoformans recoveredfrom AIDS patients with relapsed meningitis. Most, but notall, C. albicans and C. glabrata strains resistant to fluconazoleare cross-resistant to other azoles.

General Description

Fluconazole is used to treat adult neutropenic patients with invasive candidiasis (IC).

Pharmaceutical Applications

A synthetic bis(triazole) available for oral or parenteral administration.A prodrug formulation, fosfluconazole, is availablefor intravenous use in Japan.

Biological Activity

Triazole antifungal agent. Effective against Candida strains in vitro and in vivo .

Biochem/physiol Actions

Fluconazole is an antifungal agent. It is highly selective inhibitor of fungal cytochrome P-450 sterol C-14 α-demethyllation. Fluconazole is a potent inhibitor of CYP2C9. Fluconazole interferes with fungal ergosterol synthesis and downregulates the metallothionein gene.

Pharmacology

It has good oral absorption,is well tolerated, and is preferentially taken up in keratinized tissues, reachingconcentrations up to 50 times that in plasma. This allows for once-weeklydosing in most cases.

Pharmacokinetics

Oral absorption: >93%
C_max 50 mg oral: c. 1 mg/L after 2 h
Plasma half-life: 25–30 h
Volume of distribution: 0.6–0.8 L/kg
Plasma protein binding; <10%
Absorption
Oral absorption is rapid (1–3 h) and is not affected by food or intragastric pH. Blood concentrations increase in proportion to dosage. Maximum serum concentrations increase to about 2–3 mg/L after repeated dosing with 50 mg.
Distribution
It is widely distributed, achieving therapeutic concentrations in most tissues and body fluids. Concentrations in cerebrospinal fluid (CSF) are 50–60% of the simultaneous serum concentration in normal individuals and even higher in patients with meningitis.
Metabolism and excretion
More than 90% of an oral dose is eliminated in the urine: about 80% as unchanged drug and 10% as inactive metabolites. The drug is cleared by glomerular filtration, but there is significant tubular reabsorption. The plasma half-life is prolonged in renal failure, necessitating adjustment of the dosage.Fluconazole-D4 is removed during hemodialysis and, to a lesser extent, during peritoneal dialysis. In children the volume of distribution and plasma clearance are increased, and the half-life is considerably shorter (15–25 h).

Clinical Use

Mucosal, cutaneous and systemic candidosis
Coccidioidomycosis
Cryptococcosis
Dermatophytosis
Pityriasis versicolor

Clinical Use

Fluconazole is very effective in the treatment of infectionswith most Candida spp. Thrush in the end-stageAIDS patient, often refractory to nystatin, clotrimazole,and ketoconazole, can usually be suppressed with oralfluconazole.AIDS patients with esophageal candidiasisalso usually respond to fluconazole.
Fluconazole may be an acceptable alternative toamphotericin B in the initial treatment of mild cryptococcalmeningitis, and it has been shown to be superiorto amphotericin B in the long-term prevention of relapsingmeningitis (such patients require lifelong treatment.).Coccidioidal meningitis, previously treated withboth intravenous and intrathecal amphotericin B, appearsto respond at least as well to prolonged oral fluconazoletherapy. Aspergillosis, mucormycosis, andpseudallescheriasis do not respond to fluconazole treatment.Sporotrichosis, histoplasmosis, and blastomycosisappear to be better treated with itraconazole, althoughfluconazole does appear to have significant activityagainst these dimorphic fungi.

Side effects

Fluconazole is well tolerated. Nausea, vomiting, abdominalpain, diarrhea, and skin rash have been reported infewer than 3% of patients. Asymptomatic liver enzymeelevation has been described, and several cases of drugassociatedhepatic necrosis have been reported. Alopeciahas been reported as a common adverse event inpatients receiving prolonged high-dose therapy. Coadministrationof fluconazole with phenytoin results in increasedserum phenytoin levels.

Side effects

These are rare, but untoward reactions include nausea,abdominal discomfort, diarrhea and headache. Transientabnormalities of liver enzymes and rare serious skin reactions,including Stevens–Johnson syndrome, have beenreported.

Veterinary Drugs and Treatments

Fluconazole may have use in veterinary medicine in the treatmentof systemic mycoses, including cryptococcal meningitis, blastomycosis,and histoplasmosis. It may also be useful for superficialcandidiasis or dermatophytosis. Because of the drug’s unique pharmacokineticqualities, it is probably more useful in treating CNSinfections or fungal urinary tract infections than other azole derivatives.Fluconazole does not have appreciable effects (unlike ketoconazole)on hormone synthesis and may have fewer side effectsthan ketoconazole in small animals.

Drug interactions

Potentially hazardous interactions with other drugs
Aminophylline: concentration of aminophylline possibly increased.
Analgesics: increases concentration of celecoxib - halve celecoxib dose; concentration of flurbiprofen, ibuprofen and methadone increased; increases concentration of parecoxib - reduce parecoxib dose; inhibits metabolism of alfentanil; concentration of fentanyl possibly increased.
Anti-arrhythmics: avoid concomitant use with amiodarone due to risk of QT prolongation.
Antibacterials: avoid with erythromycin; increases rifabutin levels - reduce dose; metabolism accelerated by rifampicin; concentration of bedaquiline possibly increased - avoid if fluconazole for >14 days.
Anticoagulants: potentiates effect of coumarins.
Antidepressants: avoid concomitant use with reboxetine; concentration of amitriptyline and nortriptyline increased.
Antidiabetics: possibly enhances hypoglycaemic effect of nateglinide; increases concentration of sulphonylureas. Antiepileptics: increases fosphenytoin and phenytoin levels; possibly increased carbamazepine concentration. Antimalarials: avoid concomitant administration with artemether/lumefantrine and piperaquine with artenimol.
Antipsychotics: increased risk of ventricular arrhythmias with pimozide - avoid concomitant use; possibly increases lurasidone concentration; possibly increased quetiapine levels - reduce dose of quetiapine.
Antivirals: increases nevirapine, ritonavir, tipranavir and zidovudine levels, and possibly saquinavir: concentration of simeprevir possibly increased - avoid.
Anxiolytics and hypnotics: increases diazepam and midazolam levels.
Avanafil: concentration of avanafil possibly increased.
Bosentan: increased bosentan levels - avoid concomitant use.
Ciclosporin: increases blood/serum ciclosporin levels.
Clopidogrel: possibly reduced antiplatelet effect.
Cytotoxics: possibly increased side effects of cyclophosphamide; concentration of bosutinib and possibly olaparib increased - avoid or reduce dose of bosutinib; possibly increases ibrutinib concentration - reduce ibrutinib dose; reduce dose of ruxolitinib.
Dapoxetine: reduce dose of dapoxetine.
Diuretics: increased eplerenone levels - avoid concomitant use; concentration of fluconazole increased by hydrochlorothiazide.
Ergot alkaloids: increased risk of ergotism - avoid concomitant use.
Guanfacine: possibly increased guanfacine dose - halve dose of guanfacine.
Ivabradine: increased ivabradine levels - reduce initial dose.
Ivacaftor: increased concentration of ivacaftor.
Lipid-lowering drugs: possibly increased risk of myopathy with atorvastatin or simvastatin; concentration of fluvastatin increased possibly increased risk of myopathy; avoid with lomitapide.
Retinoids: possibly increased risk of tretinoin toxicity.
Sirolimus: may increase sirolimus concentration.
Tacrolimus: increases blood/serum tacrolimus levels.
Theophylline: possibly increases theophylline levels.

Metabolism

Fluconazole is metabolised only to a minor extent. Of a radioactive dose, only 11% is excreted as metabolites in the urine. The major route of excretion is renal, with approximately 80% of the administered dose appearing in the urine as unchanged medicinal product. Fluconazole clearance is proportional to creatinine clearance. There is no evidence of circulating metabolites.

storage

Store at +4°C

Fluconazole Preparation Products And Raw materials

• Raw materials: Ethanol-->Diethyl ether-->Toluene-->Potassium carbonate-->Isopropyl alcohol-->tert-Butanol-->Cyclohexane-->Methanesulfonic acid-->m-Phenylenediamine-->1,2,4-Triazole-->1,3-Difluorobenzene-->1,3-Dichloroacetone-->1-Bromo-2,4-difluorobenzene-->METHYL 2,4-DIFLUOROBENZOATE-->2,4 DIFLUOROBENZENE-->Aluminum chloride-->Chloroacetyl chloride-->Trimethylsulfoxonium iodide-->Potassium hydroxide