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Vorapaxar Sulfate

Product Name
Vorapaxar Sulfate
CAS No.
705260-08-8
Chemical Name
Vorapaxar Sulfate
Synonyms
Zontivity;Sch 530348;Vorapaxar-d5;Vorapaxar Sulfate;SCH 530348 sulfate;SCH-530348;SCH530348;vorapaxar impurity A;vorapaxar monosulfate;Vorapaxar Sulfate API;SCH 530348 (H2SO4 Salt)
CBNumber
CB92545858
Molecular Formula
C29H35FN2O8S
Formula Weight
590.66
MOL File
705260-08-8.mol
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Vorapaxar Sulfate Property

storage temp. 
4°C, away from moisture
solubility 
DMSO : 125 mg/mL (211.63 mM; Need ultrasonic)| (insoluble)
Water Solubility 
Water : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H320Causes eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

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N-Bromosuccinimide Price

TRC
Product number
V758200
Product name
VorapaxarSulfate
Packaging
100mg
Price
$580
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0014130
Product name
SCH-530348 SULPHATE
Purity
95.00%
Packaging
5MG
Price
$500.42
Updated
2021/12/16
DC Chemicals
Product number
DC8229
Product name
VorapaxarSulfate(SCH530348)
Purity
>98%
Packaging
100mg
Price
$550
Updated
2021/12/16
Crysdot
Product number
CD11069485
Product name
VorapaxarSulfate
Purity
97%
Packaging
250mg
Price
$456
Updated
2021/12/16
DC Chemicals
Product number
DC8229
Product name
VorapaxarSulfate(SCH530348)
Purity
>98%
Packaging
250mg
Price
$950
Updated
2021/12/16
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Vorapaxar Sulfate Chemical Properties,Usage,Production

Description

Merck Sharp & Dohme successfully obtained approval in the EU in 2014 for vorapaxar sulfate, marketed as Zontivity®. The drug is a first-in-class thrombin receptor (also referred to as a protease-activated or PAR-1) antagonist which, when used in conjunction with antiplatelet therapy, has been shown to reduce the chance of myocardial infarction and stroke, particularly in patients with a history of cardiac events. Antagonism of PAR-1 allows for thrombin-mediated fibrin deposition while blocking thrombinmediated platelet activation.

Uses

SCH-530348 is a novel antiplatelet agent undergoing development by Schering-Plough Corp for the treatment and prevention of atherothrombosis. acute coronary syndrome (unstable angina/non-ST segment elevation myocardial infarction) and secondary prevention of cardiovascular events in high-risk patients.

Definition

ChEBI: An organic sulfate salt obtained by combining vorapaxar with one molar equivalent of sulfuric acid. A protease-activated receptor-1 antagonist used for the reduction of thrombotic cardiovascular events in patients with a history of myocardial infarction (M ) or with peripheral arterial disease. It has been shown to reduce the rate of a combined endpoint of cardiovascular death, MI, stroke and urgent coronary revascularisation.

Synthesis

Although a variety of papers and patents describe the synthesis of vorapaxar sulfate (XXXVII), a combination of two patents describe the largest-scale synthesis reported in the literature. Retrosynthetically, the drug can be divided into olefination partners 306 and 305. Lactone 305 is further derived from synthons 300 and 299, which are readily prepared from commercially available starting materials. Dienyl acid 300 was constructed in two steps starting from commercial vinyl bromide 307, which first undergoes a Heck reaction with methacrylate (308) followed by saponification of the ester to afford the desired acid 300 in 71% over two steps.
The synthesis of alcohol 299 begins with tetrahydropyranyl (THP) protection of enantioenriched alcohol 295 to afford butyne 297 . Lithiation of this system followed by trapping with (benzyloxy)chloroformate and Dowex work-up to remove the protective functionality provided acetyl ester 298. Hydrogenation of the alkyne with Lindlar?ˉs catalyst delivered cis-allylic alcohol 299 in 93% yield. Acid 300 was then esterified with alcohol 299 by way of a 1,3-dicyclohexylcarbodiimide (DCC) coupling and, upon heating in refluxing xylenes, an intramolecular Diels¨C Alder reaction occurred. Subsequent subjection to DBU secured the tricyclic system 301 in 38% over three steps as a single enantiomer. Diastereoselective hydrogenation reduced the olefin with concomitant benzyl removal to give key fragment 302. Next, acidic revelation of the ketone followed by reductive amination with ammonium formate delivered primary amines 303a/303b as a mixture of diastereomers. These amines were then converted to the corresponding carbamates, and resolution by means of recrystallization yielded 50% of 304 as the desired diastereomer. Acid 304 was treated with oxalyl chloride and the resulting acid chloride was reduced to aldehyde 305 in 66% overall yield. Finally, deprotonation of phosphonate ester 306 followed by careful addition of 305 and acidic quench delivered vorapaxar sulfate (XXXVII) in excellent yield over the two-step protocol.
The preparation of vorapaxar phosponate ester 306 commenced from commercial sources of 5-(3-fluorophenyl)-2- methylpyridine (310). Removal of the methyl proton with LDA followed by quench with diethyl chlorophosphonate resulted in phosponate ester 306.

Vorapaxar Sulfate Preparation Products And Raw materials

Raw materials

Preparation Products

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Vorapaxar Sulfate Suppliers

Shanghai Chaolan Chemical Technology Center
Tel
QQ:65489617 15618227136
Fax
21-5161 9052
Email
info@SuperLan-chem.com
Country
China
ProdList
9445
Advantage
58
Shanghai Boyle Chemical Co., Ltd.
Tel
Fax
86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2923
Advantage
55
Chemvon Biotechnology Co., Ltd
Tel
021-50790412
Fax
+86-21-50790419
Email
info@chemvon.com
Country
China
ProdList
371
Advantage
57
Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6011
Advantage
61
Chemsky (shanghai) International Co.,Ltd
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
15421
Advantage
60
Jinan Trio PharmaTech Co., Ltd.
Tel
+86 (531) 88811783
Fax
+86 (531) 55696010 QQ 1762738062
Email
sales@trio-pharmatech.com (International market)
Country
China
ProdList
1856
Advantage
62
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4647
Advantage
58
S.Z. PhyStandard Bio-Tech. Co., Ltd.
Tel
0755-83725681-603
Fax
+86 755 28094224
Country
China
ProdList
4505
Advantage
50
Beijing Yisiyan Technology Research Center
Tel
010-56645598 13366904824
Fax
01062230033
Email
bjkaida@163.com
Country
China
ProdList
1666
Advantage
59
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4428
Advantage
55
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View Lastest Price from Vorapaxar Sulfate manufacturers

Hebei Best Biological Technology Co., Ltd
Product
Vorapaxar sulfate 705260-08-8
Price
US $200.00/g
Min. Order
10g
Purity
99%
Supply Ability
1000t/month
Release date
2022-11-30
Hebei Mingeng Biotechnology Co., Ltd
Product
Vorapaxar Sulfate 705260-08-8
Price
US $200.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000kg/Month
Release date
2022-11-23
Shijiazhuang Gantuo Biotechnology Co., Ltd
Product
Vorapaxar sulfate 705260-08-8
Price
US $100.00/mg
Min. Order
10mg
Purity
99%
Supply Ability
1000g
Release date
2023-03-10

705260-08-8, Vorapaxar SulfateRelated Search:


  • Vorapaxar Sulfate
  • N-[(1R,3aR,4aR,6R,8aR,9S,9aS)-9-[(1E)-2-[5-(3-Fluorophenyl)-2-pyridinyl]ethenyl]dodecahydro-1-Methyl-3-oxonaphtho[2,3-c]furan-6-yl]carbaMic Acid Ethyl Ester Sulfate
  • Sch 530348
  • SCH 530348 (H2SO4 Salt)
  • vorapaxar impurity A
  • Carbamic acid, N-[(1R,3aR,4aR,6R,8aR,9S,9aS)-9-[(1E)-2-[5-(3-fluorophenyl)-2-pyridinyl]ethenyl]dodecahydro-1-methyl-3-oxonaphtho[2,3-c]furan-6-yl]-, ethyl ester, sulfate (1:1)
  • SCH-530348;SCH530348
  • Vorapaxar Sulfate (SCH 530348)
  • Vorapaxar-d5
  • SCH 530348 sulfate
  • vorapaxar monosulfate
  • Zontivity
  • Vorapaxar sulfateQ: What is Vorapaxar sulfate Q: What is the CAS Number of Vorapaxar sulfate Q: What is the storage condition of Vorapaxar sulfate Q: What are the applications of Vorapaxar sulfate
  • Vorapaxar Sulfate API
  • Ethyl ((1R,3aR,4aR,6R,8aR,9S,9aS)-9-((E)-2-(5-(3-fluorophenyl)pyridin-2-yl)vinyl)-1-methyl-3-oxododecahydronaphtho[2,3-c]furan-6-yl)carbamate sulfate
  • 705260-08-8
  • C29H33FN2O4H2SO4
  • C29H35FN2O8S
  • Aromatics
  • Chiral Reagents
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals