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Vorapaxar Sulfate

CAS No.
705260-08-8
Chemical Name:
Vorapaxar Sulfate
Synonyms
Vorapaxar-d5;Zontivity;Sch 530348;Vorapaxar Sulfate;SCH 530348 sulfate;SCH-530348;SCH530348;vorapaxar impurity A;vorapaxar monosulfate;Vorapaxar Sulfate API;Vorapaxar sulfate salt
CBNumber:
CB92545858
Molecular Formula:
C29H35FN2O8S
Molecular Weight:
590.66
MDL Number:
MFCD16038877
MOL File:
705260-08-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41

Vorapaxar Sulfate Properties

storage temp. 4°C, away from moisture
solubility DMSO : 125 mg/mL (211.63 mM; Need ultrasonic)| (insoluble)
form Solid
color White to off-white
Water Solubility Water : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C)
FDA UNII IN66038E6C

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H320-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338

Vorapaxar Sulfate price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0002462 Vorapaxar sulfate 99.81% 705260-08-8 5mg $97 2026-06-04 Buy
ChemScene CS-0002462 Vorapaxar sulfate 99.81% 705260-08-8 10mg $162 2026-06-04 Buy
ChemScene CS-0002462 Vorapaxar sulfate 99.81% 705260-08-8 25mg $303 2026-06-04 Buy
ChemScene CS-0002462 Vorapaxar sulfate 99.81% 705260-08-8 50mg $487 2026-06-04 Buy
ChemScene CS-0002462 Vorapaxar sulfate 99.81% 705260-08-8 100mg $780 2026-06-04 Buy
Product number Packaging Price Buy
CS-0002462 5mg $97 Buy
CS-0002462 10mg $162 Buy
CS-0002462 25mg $303 Buy
CS-0002462 50mg $487 Buy
CS-0002462 100mg $780 Buy

Vorapaxar Sulfate Chemical Properties,Uses,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 Lindlarˉs 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.

Synthesis_705260-08-8

Vorapaxar Sulfate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 190)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2915 55
Chemvon Biotechnology Co., Ltd 021-50790412 info@chemvon.com China 371 57
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 5996 61
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15350 60
Jinan Trio PharmaTech Co., Ltd. 0531-88811783 sales@trio-pharmatech.com China 1856 62
Dalian Meilun Biotech Co., Ltd. 0411-62910999 13889544652 sales@meilune.com China 4765 58
S.Z. PhyStandard Bio-Tech. Co., Ltd. 0755-83725681-603 China 4484 50
Beijing Yisiyan Technology Research Center 010-56645598 13366904824; bjkaida@163.com China 1596 59
Guangzhou Isun Pharmaceutical Co., Ltd 020-39119399 18927568969 isunpharm@qq.com China 4773 55
TargetMol Chemicals Inc. 021-021-33632979 15002134094 marketing@targetmol.com China 7993 58

View Lastest Price from Vorapaxar Sulfate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Vorapaxar Sulfate  pictures 2026-09-14 Vorapaxar Sulfate
705260-08-8
1g More Than 99% 100kg/Month BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
Vorapaxar sulfate pictures 2026-07-27 Vorapaxar sulfate
705260-08-8
$32.00-72.00 99.99% 10g TargetMol Chemicals Inc.
Vorapaxar Sulfate pictures 2023-06-26 Vorapaxar Sulfate
705260-08-8
$200.00 1kg 99% 1000kg/Month Hebei Mingeng Biotechnology Co., Ltd
  • Vorapaxar Sulfate  pictures
  • Vorapaxar Sulfate
    705260-08-8
  • $0.00
  • More Than 99%
  • BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.

Vorapaxar Sulfate Spectrum

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) 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 Vorapaxar sulfate salt 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 Vorapaxar sulfate, 10 mM in DMSO Vorapaxar-d5 705260-08-8 C29H33FN2O4H2SO4 C29H35FN2O8S Aromatics Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals