ChemicalBook > CAS DataBase List > Darifenacin hydrobromide

Darifenacin hydrobromide

Product Name
Darifenacin hydrobromide
CAS No.
133099-07-7
Chemical Name
Darifenacin hydrobromide
Synonyms
Emsele;Enablex;Emselex;UK 88525-04;Darifenacin HCl;DARIFENACIN HBR;Darifenacin hydrobro;DARFENACIN HYDROBROMIDE;Darifenacin Hydrobromid;darifenacin hydrobromide
CBNumber
CB9855171
Molecular Formula
C28H31BrN2O2
Formula Weight
507.47
MOL File
133099-07-7.mol
More
Less

Darifenacin hydrobromide Property

Melting point:
228-2300C
alpha 
25D -30.3° (c = 1.0 in methylene chloride)
storage temp. 
-20°C
solubility 
DMSO: soluble20mg/mL, clear
form 
powder
color 
white to beige
optical activity
[α]/D +41 to +49°, c = 1 in methylene chloride
CAS DataBase Reference
133099-07-7(CAS DataBase Reference)
More
Less

Safety

WGK Germany 
3
HS Code 
2934990002
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML1102
Product name
Darifenacin hydrobromide
Purity
≥98% (HPLC)
Packaging
10mg
Price
$70.8
Updated
2024/03/01
Sigma-Aldrich
Product number
SML1102
Product name
Darifenacin hydrobromide
Purity
≥98% (HPLC)
Packaging
50mg
Price
$303
Updated
2024/03/01
Sigma-Aldrich
Product number
1164200
Product name
Darifenacin hydrobromide
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
150MG
Price
$958
Updated
2022/05/15
Cayman Chemical
Product number
14424
Product name
Darifenacin (hydrobromide)
Purity
≥95%
Packaging
10mg
Price
$68
Updated
2024/03/01
Cayman Chemical
Product number
14424
Product name
Darifenacin (hydrobromide)
Purity
≥95%
Packaging
25mg
Price
$161
Updated
2024/03/01
More
Less

Darifenacin hydrobromide Chemical Properties,Usage,Production

Description

Darifenacin, an orally active, once a day selective M3 receptor antagonist, was launched for the treatment of overactive bladder in patients with symptoms of urge urinary incontinence, urgency and frequency. The drug selectively inhibits M3 receptor in the detrusor muscle while sparing the M1 and M2 receptors that are believed to be involved in central nervous system and cardiovascular function respectively. The compound was originally developed by Pfizer and licensed to Novartis and Bayer.

Description

Darifenacin is an antagonist of M3 muscarinic acetylcholine receptors (mAChRs; Ki = 0.76 nM). It is selective for M3 over M1, M2, M4, and M5 mAChRs (Kis = 7.08, 44.67, 45.71, and 9.33 nM, respectively). Darifenacin selectively inhibits contractions in isolated guinea pig ileum, bladder, and trachea (pA2s = 9.44, 8.66, and 8.7, respectively), tissues that endogenously express high levels of M3 mAChRs, over isolated rabbit vas deferens and isolated guinea pig atria (pA2s = 7.9 and 7.48, respectively), which endogenously express M1 and M2 mAChRs, respectively. It inhibits micturition pressure (ED50 = 0.089 mg/kg, i.v.), as well as micturition interval and volume in rats. Formulations containing darifenacin have been used in the treatment of overactive bladder.

Chemical Properties

White Solid

Uses

calcium replenisher

Uses

acute lymphoblastic leukemia therapeutic

Uses

Darifenacin hydrobromide is used as a medication to treat urinary incontinence. It works by blocking the M3 muscarinic acetylcholine receptor.

Definition

ChEBI: The hydrobromide salt of darifenacin. A selective antagonist for the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions, it is used in the management of urinary incontinence.

brand name

Enablex (Novartis).

General Description

Darfenacin (Enablex),(s)-2-{1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]-3-pyrrolidinyl}-2,2-diphen-ylacetamide, is an antimuscarinicagent that has selectivity for the M3 muscarinicsubtype receptor. By competitively blocking of the muscarinicreceptors results in a reduction of the smoothmuscle tone, allowing for greater volume of urine to bestored in the bladder. This results in less urinary incontinence,urgency, and frequency. It is a white to almostwhite, crystalline powder, with a molecular weight of507.5. Darifenacin is metabolized by the isozymesCYP2D6 and CYP3A4 with the primary metabolic routesbeing monohydroxylation of the dihydrobenzofuran ring,opening of the dihydrobenzofuran ring, and N-dealkylationof the pyrrolidine nitrogen.

Biochem/physiol Actions

Darifenacin hydrobromide is an antispasmodic muscarinic antagonist, selective for blocking the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions. Darifenacin hydrobromide has 9 and 12-fold greater affinity for M3 compared to M1 and M5, respectively, and 59-fold greater affinity for M3 compared to both M2 and M4. Darifenacin is used clinically to treat urinary incontinence and overactive bladder syndrome.

Synthesis

The synthesis of darifenacin is depicted in Scheme 5. Commercially available (2S,4R)-(-)-4-hydroxy-2-pyrrolidinecarboxylic acid (17), anhydrous cyclohexanol and 2-cyclohexen-1-one were heated at 154oC to give de-carboxylated compound 18 in 69 % yield. The 3-(R)-hydroxypyrrolidine (18) was N-tosylated with p-toluenesulfonyl chloride in pyridine yielding compound 19 in 26 % yield . The N-tosylated alcohol 19 was subjected to Mitsunobu reaction in the presence of methyl ptoluenesulfonate, triphenylphosphine and diethyl azodicarboxylate (DEAD) in THF to afford N-tosyl-3(S)-(tosyloxy) pyrrolidine (20) in 70% yield, which was then condensed with 2,2-diphenylacetonitrile with NaH in refluxing toluene to give 2,2-diphenyl-2-[1-(p-toluenesulfonyloxy)pyrrolidin- 2(S)-yl]acetonitrile (21). The tosyl group of 21 was removed with 48% HBr and phenol in refluxing water to yield 2,2- diphenyl-2-[2(S)-pyrrolidinyl] acetonitrile as its corresponding hydrogen bromide salt (22), which was coupled to 2-(2, 3-dihydrobenzofuran-5-yl) acetic acid (23) by treatment with carbonyldiimidazole (CDI) in ethyl acetate to the corresponding amide 24 in a quantitative yield. The amide (24) was dissolved in toluene and reduced with sodium borohydride in THF with slow addition of boron trifluoride THF complex to keep the temperature below 10??C to give free amine in 88% yield. The free amine was converted to corresponding hydrogen bromide salt (25) with 48% HBr in methanol. Compound 25 was hydrolyzed with potassium hydroxide in refluxing 2-methyl-butan-2-ol for twenty hours to give acetamide which was crystallized from toluene as a toluene solvated form in 84% yield. Finally, the toluene solvated compound was converted to darfenacin hydrobromide (IV) with 48% HBr in 2-methyl-butan-2-ol.

References

[1]. hegde ss1,choppin a,bonhaus d,briaud s,loeb m,moy tm,loury d,eglen rm.functional role of m2 andm3muscarinic receptorsin the urinary bladder of rats in vitro and in vivo.br j pharmacol.1997 apr;120(8):1409-18.
[2]. brann mr1,ellis j,jrgensen h,hill-eubanks d,jones sv. muscarinicacetylcholinereceptorsubtypes: localization and structure/function.prog brain res.1993;98:121-7.
[3]. miller dw1,hinton m,chen f.evaluation of drug efflux transporter liabilities of darifenacin in cell culture models of the blood-brain and blood-ocular barriers. neurourol urodyn.2011 nov;30(8):1633-8. doi: 10.1002/nau.21110. epub 2011 aug 8.
[4]. haab f1,stewart l,dwyer p.darifenacin, anm3selectivereceptorantagonist, is an effective and well-tolerated once-daily treatment for overactive bladder. eur urol.2004 apr;45(4):420-9; discussion 429.

Darifenacin hydrobromide Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Darifenacin hydrobromide Suppliers

Hubei Zhongshan Medical Technology Co., Ltd
Tel
027-61907345 13397111514
Fax
3443707954
Email
w13397111514@163.com
Country
China
ProdList
984
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6011
Advantage
61
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Fax
0086-571-85864795
Email
sales@capotchem.com
Country
China
ProdList
18217
Advantage
66
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9984
Advantage
60
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9552
Advantage
66
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10194
Advantage
62
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
zhangsn@titansci.com
Country
China
ProdList
14113
Advantage
59
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2127
Advantage
70
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9816
Advantage
59
More
Less

View Lastest Price from Darifenacin hydrobromide manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Darifenacin hydrobromide 133099-07-7
Price
US $0.00/g/Bag
Min. Order
100g
Purity
99%min
Supply Ability
150kg/month
Release date
2021-06-02
Henan Bao Enluo International TradeCo.,LTD
Product
Darifenacin hydrobromide 133099-07-7
Price
US $120.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000tons
Release date
2023-08-11
Baoji Guokang Healthchem co.,ltd
Product
Darifenacin hydrobromide 133099-07-7
Price
US $210.00/g
Min. Order
10g
Purity
99%
Supply Ability
100KG
Release date
2021-06-04

133099-07-7, Darifenacin hydrobromideRelated Search:


  • 2-[(3S)-1-[2-(2,3-dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-diphenyl-ethanamide hydrobromide
  • 2-[(3S)-1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-diphenyl-acetamide hydrobromide
  • Darifenacine Hydrobromide
  • Darifenacin hydrobro
  • (3S)-1-[2-(2,3-Dihydro-5-benzofuranyl)ethyl]-α-α-diphenyl-3-pyrrolidineacetaMide HydrobroMide
  • Darifenacin Hydrobromide ((3S)-1-[2-(2,3-Dihydro-5-benzofuranyl)ethyl]-a-a-diphenyl-3-pyrrolidineacetamide Hydrobromide
  • Darifenacin hydrobroMide R
  • DARFENACIN HYDROBROMIDE
  • (S)-3-(Carbamoyldiphenylmethyl)-1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]pyrrolidine hydrobromide
  • UK 88525-04
  • Darifenacin hydrobromide, >=99%
  • Darifenacin HCl
  • {1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]-3-pyrrolidnyl}-2,2-diphenylacetamide hydrobromide
  • darifenacin hydrobromide
  • DARIFENACIN HYDROBROMIDE 99.0%
  • Darifenacin hydrobromide (Under R&D)
  • (3S)-1-[2-(2,3-Dihydro-5-benzofuranyl)ethyl]-a-a-diphenyl-3-pyrrolidineacetamide Hydrobromide
  • Emsele
  • Enablex
  • DARIFENACIN HBR
  • Darifenacin Hydrobromid
  • (3S)-1-[2-(2,3-Dihydro-5-benzofuranyl)ethyl]-α-a-diphenyl-3-pyrrolidineacetamide Hydrobromide
  • Emselex
  • 2-[(3S)-1-[2-(2,3-dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-diphenylacetamide hydrobromide
  • (S)-2-[1-[2-(2,3-Dihydrobenzfuran-5-yl)ethyl]-3-pyrrolidinyl]-2,2-diphenylacetamide HBr
  • 3-Pyrrolidineacetamide, 1-[2-(2,3-dihydro-5-benzofuranyl)ethyl]-α,α-diphenyl-, hydrobromide (1:1), (3S)-
  • Darifenacin hydrobromide USP/EP/BP
  • Darifenacin Hydrobromide (10mM in DMSO)
  • Darifenacin HBr (UK88525)
  • Darifenacin D4 hydrochlorideQ: What is Darifenacin D4 hydrochloride Q: What is the CAS Number of Darifenacin D4 hydrochloride Q: What is the storage condition of Darifenacin D4 hydrochloride Q: What are the applications of Darifenacin D4 hydrochloride
  • Darifenacin HydrobromideQ: What is Darifenacin Hydrobromide Q: What is the CAS Number of Darifenacin Hydrobromide Q: What is the storage condition of Darifenacin Hydrobromide Q: What are the applications of Darifenacin Hydrobromide
  • 133099-07-7 Darifenacin hydrobromide
  • Darifenacin Hydrobromide (1164200)
  • (S)-2-(1-(2-(2,3-Dihydrobenzofuran-5-yl)ethyl)pyrrolidin-3-yl)-2,2-diphenylacetamide hydrobromide
  • 133099-07-7
  • 133099-07-1
  • 133039-07-7
  • C28H30N2O2HBr
  • C28H31BrN2O2
  • C28H30N2O2
  • C28H29BrN2O2
  • C28H30N2O2BrH
  • Amines
  • Aromatics
  • Heterocycles
  • API
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • APIs