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Bilastine

CAS No.
202189-78-4
Chemical Name:
Bilastine
Synonyms
Bilastine;Bilastin;2-(4-(2-(4-(1-(2-ETHOXYETHYL)-1H-BENZO[D ]IMIDAZOL-2-YL) PIPERIDIN-1-YL)ETHY)PHEN YL)-2-METHYLPROPANOIC ACID;Bilaxten;Bilatex;Bilasten;Bilastene;Bilastine -IP/BP/;Bilastine (Form-I);Bilastine In-House
CBNumber:
CB81011081
Molecular Formula:
C28H37N3O3
Molecular Weight:
463.62
MDL Number:
MFCD09837814
MOL File:
202189-78-4.mol
Last updated:2024-11-19 20:33:22

Bilastine Properties

Melting point 202 °C
Boiling point 639.1±55.0 °C(Predicted)
Density 1.16±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
Water Solubility Insoluble in water
solubility DMSO:49.3(Max Conc. mg/mL);106.34(Max Conc. mM)
pka 4.40±0.10(Predicted)
form powder to crystal
color White to Light yellow
FDA UNII PA1123N395
ATC code R06AX29

Pharmacokinetic data

Protein binding 84-90%
Excreted unchanged in urine 28.3%
Volume of distribution 1.29(L/kg)
Biological half-life 14.5 / -

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
HS Code  2933.39.4100
NFPA 704
0
3 0

Bilastine price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical B5392 Bilastine >98.0%(HPLC)(T) 202189-78-4 250mg $104 2024-03-01 Buy
TCI Chemical B5392 Bilastine >98.0%(HPLC)(T) 202189-78-4 1g $286 2024-03-01 Buy
Cayman Chemical 28375 Bilastine 202189-78-4 25mg $44 2024-03-01 Buy
Cayman Chemical 28375 Bilastine 202189-78-4 50mg $84 2024-03-01 Buy
Cayman Chemical 28375 Bilastine 202189-78-4 100mg $155 2024-03-01 Buy
Product number Packaging Price Buy
B5392 250mg $104 Buy
B5392 1g $286 Buy
28375 25mg $44 Buy
28375 50mg $84 Buy
28375 100mg $155 Buy

Bilastine Chemical Properties,Uses,Production

Description

Bilastine, a potent and selective histamine H1 receptor antagonist, was approved in Europe in 2010 for the treatment of allergic rhinoconjunctivitis (AR) and urticaria (hives or skin rash). The original synthesis of bilastine involves alkylation of 2-piperidinyl-1H-benzimidazole with a phenethyltosylate, the para position of which is substituted with a dimethyloxazoline moiety serving as a masked carboxylic acid group. Alkylation of the benzimidazole nitrogen with 2-chloroethyl ethyl ether followed by unmasking of the oxazoline moiety with sulfuric acid provided bilastine.
In two major clinical trials, bilastine was effective at relieving allergic rhinitis as assessed by measuring the severity of nasal (obstruction, rhinorrhea, itching, sneezing) and nonnasal (ocular itching, tearing, ocular redness, itching of ears, and/or palate) symptoms.

Description

Bilastine is a histamine H1 receptor antagonist (IC50 = 180 nM). It is selective for the histamine H1 receptor in a panel of 30 receptors in vitro at 100 μM. Bilastine prevents microvascular extravasation (ED50 = 185 μg/kg, i.v.), bronchospasm (ED50 = 4.6 μg/kg, i.v.), and systemic anaphylaxis (ED50 = 0.2 μg/kg, p.o.) induced by subcutaneous histamine in guinea pigs. It prevents anaphylaxis induced by subcutaneous administration of ovalbumin or dinitrophenylated human albumin (DNP) in sensitized rats when administered at doses of 7.6 and 6.0 mg/kg, respectively. Formulations containing bilastine have been used in the treatment of urticaria and allergic rhinitis.

Originator

FAES FARMA, S.A. (Spain)

Uses

Labelled Bilastine. It is a novel, nonsedating H1-antihistamine developed for symptomatic treatment of allergic rhinitis and chronic idiopathic urticaria.

Uses

Bilastine is a novel, nonsedating H1-antihistamine developed for symptomatic treatment of allergic rhinitis and chronic idiopathic urticaria.

Definition

ChEBI: Bilastine is a member of benzimidazoles.

brand name

Bilaxten

Clinical Use

Bilastine is a selective histamine H1 antagonist approved for the treatment of allergic rhinoconjunctivitis and urticaria (hives). This drug, which has proven to be well tolerated in toxicology profiling, 46 was discovered by the Spainsh firm FAES Farma and was approved by the European Union in 2010.

Synthesis

In 2011, Collier and co-workers published a communication describing both the original synthesis of bilastine and an improved route which was amenable to gram-scale production. Collier?ˉs second generation route, shown below, relies upon a convergent approach involving the union of piperidinyl benzimidazole 49 with fully functionalized phenethyl electrophile 48.Coupling the commercially available bromophenyl acetate 44 with cyclic trioxatriborinane 45 under conventional Suzuki conditions furnished styrene 46 in good yield. Alternatively, this vinylation reaction was also performed under Stille conditions with tributyl vinyl stannane in 83% yield. Hydroboration¨Coxidation of 46 delivered phenethyl alcohol 47 which was then immediately mesylated under basic conditions in toluene to produce adduct 48. This sulfonate was then reacted with piperidine 49 (whose preparation is described in Scheme 7) followed by saponification of the resulting ester 50 to arrive at bilastene (VI) in 26% overall yield from 44.

Synthesis_202189-78-4

For the preparation of bilastine piperidine 49, commercially available piperidine 51 was first protected as the Boc-carbamate 52 prior to alkylation of the benzimidazole nitrogen atom with 1-chloro-2-ethoxyethane 53, providing compound 54. The Boc group of 54 was removed under acidic conditions to give fragment 49. This sequence produced the desired piperidine component in 86% overall yield from 51.
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Drug interactions

Potentially hazardous interactions with other drugs
Antivirals: concentration possibly increased by ritonavir.
Grapefruit juice: concentration of bilastine reduced.

Metabolism

Not significantly metabolised. Almost 95% of the administered dose was recovered in urine (28.3%) and faeces (66.5%) as unchanged bilastine

Bilastine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 270)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 20287 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29791 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32957 60
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +8618949832763 info@tnjchem.com China 2986 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29882 58
Zhejiang ZETian Fine Chemicals Co. LTD
+8618957127338 stella@zetchem.com China 2136 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 965 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28172 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58

View Lastest Price from Bilastine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Bilastine pictures 2024-11-25 Bilastine
202189-78-4
US $0.00-0.00 / kg 1kg 99%, Single impurity<0.1 1 ton Nanjing Fred Technology Co., Ltd
Bilastine pictures 2024-11-19 Bilastine
202189-78-4
US $39.00-105.00 / mg 99.61% 10g TargetMol Chemicals Inc.
Bilastine pictures 2024-03-26 Bilastine
202189-78-4
US $3.00-0.20 / KG 1KG 98% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
  • Bilastine pictures
  • Bilastine
    202189-78-4
  • US $0.00-0.00 / kg
  • 99%, Single impurity<0.1
  • Nanjing Fred Technology Co., Ltd
  • Bilastine pictures
  • Bilastine
    202189-78-4
  • US $39.00-105.00 / mg
  • 99.61%
  • TargetMol Chemicals Inc.
  • Bilastine pictures
  • Bilastine
    202189-78-4
  • US $3.00-0.20 / KG
  • 98%
  • Henan Fengda Chemical Co., Ltd
4-[2-[4-[1-(2-Ethoxyethyl)-1H-benziMidazol-2-yl]-1-piperidinyl]ethyl]-α,α-diMethylbenzeneacetic Acid Benzeneacetic acid,4-[2-[4-[1-(2-ethoxyethyl)-1H-benziMidazol-2-yl]-1-piperidinyl]ethyl]-a,a-diMethyl- BENZENEACETIC ACID, 4-(2-(4-(1-(2-ETHOXYETHYL)-1H-BENZIMIDAZOL-2-YL)-1-PIPERIDINYL)ETHYL-ALPHA, ALPHA-DIMETHYL- 2-[4-[2-[4-[1-(2-ethoxyethyl)benzoimidazol-2-yl]-1-piperidyl]ethyl]phenyl]-2-methyl-propanoic acid 4-[2-[4-[1-(2-Ethoxyethyl)-1H-benzimidazol-2-yl]-1-piperidinyl]ethyl]-alpha,alpha-dimethylbenzeneacetic acid Bilasten 2-[4-[2-[4-[1-(2-ethoxyethyl)benzimidazol-2-yl]piperidin-1-yl]ethyl]phenyl]-2-methylpropanoic acid the impurity of Bilastine 2-(4-(2-(4-(1-(2-ethoxyethyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)ethyl)phenyl)-2-methylpropanoic acid 2-[4-[2-[4-[1-(2-Ethoxyethyl)benzimidazol-2-yl]piperidin-1-yl]ethyl]phenyl]-2-methylproionic acid Bilatex Benzeneacetic acid, 4-[2-[4-[1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]-1-piperidinyl]ethyl]-α,α-dimethyl- BENZENEACETIC ACID, 4-(2-(4-(1-(2-ETHOXYETHYL)-1H-BENZIMIDAZOL-2-YL)-1-PIPERIDINYL)ETHYL-ALPHA, ALPHA-DIMETHYL- USP/EP/BP 2-[4-[2-[4-[1-(2-Ethoxyethyl)benzimidazol-2-yl]piperidin-1-y... 2-(4-(2-(4-(1-(2-ethoxyethyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)ethyl)phenyl)-3-methylpropanoic acid BilastineQ: What is Bilastine Q: What is the CAS Number of Bilastine Q: What is the storage condition of Bilastine Q: What are the applications of Bilastine Bilastine D6Q: What is Bilastine D6 Q: What is the CAS Number of Bilastine D6 Q: What is the storage condition of Bilastine D6 Q: What are the applications of Bilastine D6 Bilastine Bilastin Bilaxten 2-(4-(2-(4-(1-(2-ETHOXYETHYL)-1H-BENZO[D ]IMIDAZOL-2-YL) PIPERIDIN-1-YL)ETHY)PHEN YL)-2-METHYLPROPANOIC ACID Bilastine (Form-I) 2-[4-[2-[4-[1-(2-ethoxyethyl)benzimidazol-2-yl]piperidin-1-yl]ethyl]phenyl]-2-methylpropanoicaci Bilastine In-House Bilastene Bilastine -IP/BP/ 202189-78-4 C28H31D6N3O3 Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Isotope Labelled Compounds API