Fupentixol dihydrochloride
- Product Name
- Fupentixol dihydrochloride
- CAS No.
- 2413-38-9
- Chemical Name
- Fupentixol dihydrochloride
- Synonyms
- FLUPENTIXOL DIHYDROCHLORIDE;(E/Z)-Flupentixol Dihydrochloride;fx703;Fupentixol HCl;Flupenthixol dihydro;flupentixolhydrochloride;Fluanxol dihydrochloride;Hydrochloric Flupentixol;FUPENTIXOL DIHYDROCHLORIDE;Flupentixol dihydrochloride CRS
- CBNumber
- CB1446683
- Molecular Formula
- C23H25F3N2OS.2ClH
- Formula Weight
- 507.44
- MOL File
- 2413-38-9.mol
Fupentixol dihydrochloride Property
- Melting point:
- 237-239 °C(Solv: ethanol (64-17-5); methanol (67-56-1))
- storage temp.
- Sealed in dry,2-8°C
- solubility
- H2O: soluble
- form
- solid
- color
- white or off-white
- Water Solubility
- soluble
- CAS DataBase Reference
- 2413-38-9
N-Bromosuccinimide Price
- Product number
- Y0000064
- Product name
- Flupentixol dihydrochloride
- Purity
- European Pharmacopoeia (EP) Reference Standard
- Packaging
- y0000064
- Price
- $220
- Updated
- 2024/03/01
- Product number
- F598050
- Product name
- (E/Z)-FlupentixolDihydrochloride
- Packaging
- 500mg
- Price
- $450
- Updated
- 2021/12/16
- Product number
- API0026056
- Product name
- (E/Z)-FLUPENTIXOL DIHYDROCHLORIDE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.08
- Updated
- 2021/12/16
- Product number
- CHM0078253
- Product name
- FUPENTIXOL DIHYDROCHLORIDE
- Purity
- 95.00%
- Packaging
- 25MG
- Price
- $739.2
- Updated
- 2021/12/16
- Product number
- CHM0078253
- Product name
- FUPENTIXOL DIHYDROCHLORIDE
- Purity
- 95.00%
- Packaging
- 250MG
- Price
- $1871.1
- Updated
- 2021/12/16
Fupentixol dihydrochloride Chemical Properties,Usage,Production
Chemical Properties
Light Brown Solid
Originator
Emergil ,Labaz, France,1971
Uses
Neuroleptic agent related structurally to thiothixene. Antipsychotic; neuroleptic agent; dopamine receptor antagonist.
Definition
ChEBI: Cis-flupenthixol dihydrochloride is the dihydrochloride salt of cis-flupenthixol. It has a role as a geroprotector. It contains a cis-flupenthixol(2+).
Manufacturing Process
A mixture of 200 grams of 2-benzoyloxyethanol in 2 liters of pyridine at -5°C is treated with 275 grams of p-toluenesulfonyl chloride and the resulting mixture is stirred at 0°C for 2 hours. Water is added slowly at 0° to 5°C. Extracting with chloroform, washing the extract with dilute hydrochloric acid, water and potassium bicarbonate, and evaporating the solvent leaves benzyloxyethyl p-toluenesulfonate.
A mixture of 186 grams of the above prepared p-toluenesulfonate, 106 grams of N-ethoxycarbonylpiperazine, 44 grams of potassium carbonate and 800 ml of toluene is refluxed for 21 hours, then filtered and extracted with dilute hydrochloric acid. The extract is basified with sodium hydroxide and extracted into chloroform. Evaporation of the chloroform and distillation of the residue in vacuo gives 1-benzyloxyethyl-4-ethoxy-carbonylpiperazine, BP 153° to 156°C (0.15 mm).
Hydrolysis and decarboxylation of this ester (188 grams) is accomplished by refluxing with 155 grams of potassium hydroxide, 155 ml of water and 1,550 ml of ethanol for four days. Filtering, concentrating, adding water to the residue, acidifying with hydrochloric acid, heating to 90°C, saturating with potassium carbonate, extracting into chloroform, evaporating and distilling the chloroform gives N-benzoyloxyethylpiperazine.
A mixture of 50 grams of the above prepared piperazine, 30.1 grams of sodium carbonate and 200 ml of benzene is heated to reflux and treated with 39.5 grams of 3-bromopropanol over 1.5 hours. The resulting mixture is refluxed for 2 hours, then filtered, extracted with dilute hydrochloric acid, basified, extracted with benzene, and the extracts are concentrated and distilled to give l-benzyloxyethyl-4-(3-hydroxypropyl)-piperazine, BP 188° to 190°C (0.15 mm). The free base is converted to the dihydrochloride salt by treatment of an alcoholic solution with ethereal hydrogen chloride to separate the salt.
Thionyl chloride (67 grams) is added over 15 minutes to a mixture of 39.5 grams of the above prepared dihydrochloride salt and 400 ml of chloroform. Refluxing for 4 hours, cooling and filtering yields the dihydrochloride salt of lbenzyloxyethyl-4-(3-chloropropyl)-piperazine, MP 201° to 202°C. The salt in aqueous solution is basified. Extraction with ether and evaporation of the solvent yields the free base.
Magnesium (1.3 grams) in 8 ml of refluxing tetrahydrofuran is treated with 1 ml of ethyl bromide. A solution of 22.7 grams of l-benzyloxyethyl-4-(3chloropropyl)-piperazine in 50 ml of tetrahydrofuran is added slowly and the mixture is refluxed for 1 hour.
A solution of 13.2 grams of 2-trifluoromethyl-9-xanthenone in tetrahydrofuran is added over 1 hour to 16.0 grams of 3-(4-benzyloxyethyl-1-piperazinyl) propylmagnesium chloride, prepared as above, in tetrahydrofuran while gentlyrefluxing. Refluxing is continued for 2 hours. Concentrating, pouring the residue into ammonium chloride, ice and water, extracting with ether, evaporating the extracts and treating the residue with concentrated hydrochloric acid at 95°C for 1 hour gives a mixture of cis and trans 9-[3-(4hydroxyethyl-1-piperazinyl)propylidene]-2-trifluoromethylxanthene dihydrochloride. Fractional crystallization from ethanol-ether separates the isomers. The free bases are obtained by neutralizing an aqueous solution of the dihydrochloride, extracting into ether and evaporating the ether in vacuo.
Therapeutic Function
Tranquilizer
Biological Activity
mic: 10-100 μg/ml in most of the strainsflupenthixol, introduced in 1965 by lundbeck, marketed under brand names such asdepixol.flupenthixolis atypical antipsychoticdrugof thethioxantheneclass. in addition to single drug preparations, flupenthixol is also available asflupentixol/melitracen, which is acombination product.
in vitro
the minimum inhibitory concentration of flupenthixol was determined by the national committee for clinical laboratory standards agar dilution method. mics ranged from 10–100 μg/ml for most of the strains, whilst some strains were inhibited at even lower concentrations. the mode of action of flupenthixol was found to be bacteriostatic against staphylococcus aureus and vibrio cholerae [1].
in vivo
in the in vivo experiments, flupenthixol was able to contribute significant protection to a swiss strain of white mice challenged with 50 median lethal dose of a mouse-virulent strain at a drug concentration of 15 μg/mouse. moreover, flupenthixol reduced remarkably the number of viable bacteria in organs and blood of mice treated with flupenthixol [1].
storage
Desiccate at RT
References
[1] jeyaseeli l,gupta ad,asok kumar k,mazumdar k,dutta nk,dastidar sg. antimicrobial potentiality of the thioxanthene flupenthixol through extensive in vitro and in vivo experiments. int j antimicrob agents.2006 jan;27(1):58-62.
[2] kong ds,yeo sh. an open
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View Lastest Price from Fupentixol dihydrochloride manufacturers
- Product
- Fupentixol dihydrochloride 2413-38-9
- Price
- US $0.00-0.00/kg
- Min. Order
- 1kg
- Purity
- 99%
- Supply Ability
- 6000 kg
- Release date
- 2023-08-15
- Product
- Fupentixol dihydrochloride 2413-38-9
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 50000KG/month
- Release date
- 2023-09-20
- Product
- Fupentixol dihydrochloride 2413-38-9
- Price
- US $0.00-0.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 1Ton
- Release date
- 2022-10-17