Ebastine

Ebastine Basic information
Description References
Product Name:Ebastine
Synonyms:4'-(1,1-Dimethylethyl)-γ-[4-(diphenylmethoxy)piperidin-1-yl]butyrophenone;4'-tert-Butyl-γ-[4-(diphenylmethoxy)piperidino]butyrophenone;Ebastel-OD;LAS-90;IMp. A (EP): DiphenylMethanol (Benzhydrol);Ebastine Impurity;1-butanone,1-(4-(1,1-dimethylethyl)phenyl)-4-(4-(diphenylmethoxy)-1-piperidiny;4’-tert-butyl-4-(4-(diphenylmethoxy)piperidino)butyrophenone
CAS:90729-43-4
MF:C32H39NO2
MW:469.66
EINECS:635-609-6
Product Categories:Inhibitors;Active Pharmaceutical Ingredients;Intermediates & Fine Chemicals;Pharmaceuticals;90729-43-4
Mol File:90729-43-4.mol
Ebastine Structure
Ebastine Chemical Properties
Melting point 80-82°C
Boiling point 596.3±50.0 °C(Predicted)
density 1.09±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility Slightly soluble in chloroform, methanol.
form solid
pka8.19±0.10(Predicted)
color white
Merck 14,3484
CAS DataBase Reference90729-43-4(CAS DataBase Reference)
Safety Information
WGK Germany 3
RTECS EL8140000
HS Code 2933.39.9200
MSDS Information
Ebastine Usage And Synthesis
DescriptionEbastine belongs to an effective second generation histamine H1 receptor antagonist. One important property of it is that it doesn’t penetrate the blood brain barrier. Therefore, it is capable of blocking the H1 receptor in peripheral tissue without having some specific side effects such as sedation and drowsiness. Ebastine is mainly applied for the treatment of allergic rhinitis, pruritus as well as acting as an alternative drug in Decongestant. Upon entering into the human body, it can subject to the action of hepatic cytochrome P450 3A4 to be converted to an active carboxylic acid metabolite, carebastine. The later one is the major active form in vivo. Under certain range, it can inhibit T cell proliferation and the production of Th2-type pro-inflammatory cytokines through macrophages. Ebastine generally has a high safety property without causing cognitive/psychomotor impairment and sedation, like placebo. However, it can cause side effects such as inflammation of the air-cavities around nose, sore throat, indigestion, nausea, headache, and abdominal pain.
Referenceshttps://pubchem.ncbi.nlm.nih.gov/compound/3191#section=Top
http://www.tabletwise.com/medicine/ebastine/side-effects
http://www.druginfosys.com/drug.aspx?drugcode=897&type=1

DescriptionEbastine is a new once-daily histamine Hl-receptor antagonist with no sedative effects or autonomic impairment at therapeutic doses. It is reported to be effective in the treatment of hay fever, perennial rhinitis, and uticaria. Ebastine's antihistamine activity is attributed to its carboxylic acid metabolite carebastine.
Chemical PropertiesWhite to Off-White Powder
OriginatorAlmirall (Spain)
UsesEbastine is a second-generation H1 receptor antagonist that is indicated mainly for allergic rhinitis and chronic idiopathic urticaria. It is available in 10 and 20 mg tablets and as fast-dissolving tablets, as well as in pediatric syrup. It has a recommended flexible daily dose of 10 or 20 mg, depending on disease severity.
UsesA nonsedating type histamine H1-receptor antagonist. Antihistaminic
DefinitionChEBI: Ebastine is an organic molecular entity.
Manufacturing Process(a) A mixture of 4-hydroxypiperidine (40.4 g; 0.4 moles), p-tert-butyl-ω- chlorobutyrophenone (105 g, 0.44 moles), sodium bicarbonate (67.2 g; 0.8 moles) and a crystal of potassium iodide in methyl isobutyl ketone (1 liter) was boiled under reflux for 24 hours. After cooling, the reaction mixture waswashed with water, dried (Na2SO4) and the solvent removed in vacuum. The residue was salified with the stoichiometric amount of fumaric acid in a mixture of acetone and ethanol to give 1-[3-(4-tert-butylbenzoyl)propyl]-4- hydroxypiperidine fumarate (148 g), melting point 163-165°C. This compound was converted into the free base, and 1-[3-(4-tert-butylbenzoyl)propyl]-4- hydroxypiperidine was obtained and recrystallized from a mixture of diethyl ether and petroleum ether (boiling point 50-70°C). 102 g were obtained (yield 84%), melting point 63-65°C.
(b) A mixture of 1-[3-(tert-butylbenzoyl)propyl]-4-hydroxypiperidine (60.68 g; 0.2 moles) and sodium carbonate (42.4 g; 0.4 moles) in methyl isobutyl ketone (500 ml) was heated to the boiling point and a solution of diphenylmethyl bromide (49.42 g; 0.2 moles) in methyl isobutyl ketone (75 ml) was slowly added in 1.5 hours. The resulting mixture was boiled under reflux for another 12 hours, and then another solution of diphenylmethyl bromide (24.71 g; 0.1 moles) in methyl isobutyl ketone (50 ml) was added and the mixture boiled under reflux again for 12 hours. Another solution of diphenylmethyl bromide in the same quantity was added and after refluxing for 12 additional hours the reaction mixture was cooled, washed with water, dried (Na2SO4) and the solvent removed in vacuum.
The residual oil was treated with the stoichiometric amount of fumaric acid in ethanol and 4-diphenylmethoxy-1-[3-(4-tert-butylbenzoyl)propyl]piperidine fumarate crystallized. After recrystallisation from ethanol the pure compound was obtained (88 g; yield 75%), melting point 197-198°C.

Brand nameKestine (Rhone-Poulenc Rorer);Ebastel.
Therapeutic FunctionAntihistaminic, Antiallergic, Calcium entry blocker
General DescriptionEbastine is metabolised by cytochrome P450 3A (CYP3A4) to carebastine. It is used to treat allergic rhinitis and chronic idiopathic urticaria.
Biochem/physiol ActionsEbastine is a non-sedating histamine H1 receptor antagonist, which inhibits allergen-induced bronchospasm in conscious guinea pigs. Unlike other compounds in this category, ebastine does not prolong the QT interval at up to five times the recommended therapeutic dose.
Carebastine Diphenyldimethoxysilane Methyl 2-(4-(4-chlorobutanoyl)phenyl)-2-methylpropanoate EBASTINE FUMARATE 3,4'-DIAMINODIPHENYLMETHANE EBASTINE IMPURITY D 4-Methoxyphenylacetone Ebastine-D5 Chlorodiphenylphosphine EBASTINE FUMERATE (+-) 1-BROMO-2-METHYLBUTANE 95 1-[3-(4-TERT-BUTYLBENZOYL)-PROPYL]-4-HYDROXYPIPERIDINE/INTERMEDIATE OF EBASTINE Dichlorodiphenylsilane Ebastine Ebastine Base / Fumerate 1,5-Diphenylcarbazide 1,3-Diphenyl-2-thiourea DI-TERT-BUTYL ETHER

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