Fenspiride hydrochloride

Fenspiride hydrochloride Basic information
Pharmacological effects Indications
Product Name:Fenspiride hydrochloride
Synonyms:1-Oxa-3,8-diazaspiro[4.5]decan-2-one, 8-(2-phenylethyl)-, hydrochloride (1:1);2-OXAZOLIDINONE-5-SPIRO-4'-[N-(2-PHENYLETHYL)PIPERIDINE] HYDROCHLORIDE;FENSPIRIDE HYDROCHLORIDE;8-(2-phenylethyl)-1-oxa-3,8-diazaspiro(4.5)decan-2-onehydrochloride;8-diazaspiro(4.5)decan-2-one,8-(2-phenylethyl)-1-oxa-monohydrochloride;8-diazaspiro(4.5)decan-2-one,8-phenethyl-1-oxa-monohydrochloride;8-n-fenetil-1-oxa-2-oxo-3,8-diazaspiro-(4,5)-decanocloridrato;pneumorel
CAS:5053-08-7
MF:C15H21ClN2O2
MW:296.8
EINECS:225-752-9
Product Categories:Amines;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:5053-08-7.mol
Fenspiride hydrochloride Structure
Fenspiride hydrochloride Chemical Properties
Melting point 235-238°C (dec.)
storage temp. Refrigerator
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form powder
color white
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22
Safety Statements 36
WGK Germany 3
RTECS RO0375000
HS Code 2934.99.3000
ToxicityLD50 i.v. in mice: 106 mg/kg; orally in rats: 437 mg/kg (LeDouarec)
MSDS Information
ProviderLanguage
SigmaAldrich English
Fenspiride hydrochloride Usage And Synthesis
Pharmacological effectsAs an α adrenergic and H1 histamine receptor antagonist, Fenspiride has been shown to be antiinflammatory, anti-allergic and antioxidant. Fenspiride inhibited SO2-induced goblet cell hyperplasia in rats, with concomitant inhibition of increased hexose and fucose, indicative of mucus hypersecretion, in lavage fluid. Fenspiride also exhibits neuronal inhibitory activity. For example, in guinea pigs, it reverses capsaicin-induced and citric acid-induced bronchoconstriction and cough, and inhibits cholinergic and non-adrenergic, non-cholinergic (NANC) neural contraction of isolated bronchi.
IndicationsFenspiride hydrochloride is a bronchodilator, which was used as a drug in the treatment of certain respiratory diseases. Finsecbili hydrochloride against serotonin, dilating bronchial smooth muscle, the intensity of action is between isoproterenol and theophylline, in addition to reducing the resistance of air movement in the lungs, experiments have shown that this product has dilated bronchial smooth muscle, antitussive, antipyretic and analgesic effects. Suitable for chronic bronchitis, bronchial asthma and chronic respiratory insufficiency.  In Russia it was approved for the treatment of acute and chronic inflammatory diseases of ENT organs and the respiratory tract, as well as for maintenance treatment of asthma (like rhinopharyngitis, laryngitis, tracheobronchitis, otitis and sinusitis).
Chemical PropertiesPale Yellow Solid
OriginatorViarespan,Servier,France,1969
UsesAntiinflammatory;Bradykinin antagonist
UsesBronchodilator with anti-inflammatory properties. Inhibits mucus secretion and reduces the release of tachykinins at a prejunctional level by its anti-muscarinic action. It also may be an antagonist at α adrenergic and H1 histamine receptors.
Manufacturing ProcessA solution of 192 g of 1-phenethyl-4-hydroxy-4-aminomethyl piperidine in 800 cc of diethylcarbonate is heated for 2? hours to reflux at about 80°C in the presence of sodium methylate (prepared for immediate use from 2 g of sodium). After this time, the ethyl alcohol formed during the reaction is slowly distilled while the maximum temperature is reached. The excess ethyl carbonate is distilled under reduced pressure. A crystallized residue is then obtained, which is stirred with 400 cc of water and 400 cc of ether. The solution is filtered and 125 g (77.6%) of practically pure product melting at 232°C to 233°C, are obtained.
The starting material was prepared in a yield of 58% by reduction of the corresponding cyanohydrin. It in turn was prepared from 1-(2-phenylethyl)-4- piperidone and potassium cyanide to give the cyanohydrin which was reduced by lithium aluminum hydride.
Therapeutic FunctionBronchodilator
Fenspiride hydrochloride Preparation Products And Raw materials
Raw materials1-Phenethyl-4-piperidone-->POTASSIUM CYANIDE-->Lithium Aluminum Hydride-->Diethyl carbonate
Terbinafine Hydrochloride 1-phenethylpiperidin-4-ol 5-Methyloxazolidin-2-one 1-phenethylpiperidine emylcamate 1-AMINO-2-METHYL-PROPAN-2-OL HCL METHYL-(1-METHYL-PIPERIDIN-4-YLMETHYL)-AMINE AKOS AMR10 5-DECANONE C-(1-PROPYL-PIPERIDIN-4-YL)-METHYLAMINE 4-(Aminomethyl)-1-methyl-piperidin-4-ol Fenspiride hydrochloride C-(1-ETHYL-PIPERIDIN-4-YL)-METHYLAMINE 2-METHOXY-2-METHYL-PROPYLAMINE fenspiride 4-Methoxypiperidine (1-METHYL-4-PIPERIDINYL)METHANAMINE METHYL-PIPERIDIN-4-YLMETHYL-AMINE

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.