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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;Vorapaxar sulfate salt
CBNumber:
CB92545858
Molecular Formula:
C29H35FN2O8S
Molecular Weight:
590.66
MDL Number:
MFCD16038877
MOL File:
705260-08-8.mol
Last updated:2023-09-04 16:42:00

Vorapaxar Sulfate Properties

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)
FDA UNII IN66038E6C

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
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(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC V758200 VorapaxarSulfate 705260-08-8 100mg $580 2021-12-16 Buy
American Custom Chemicals Corporation API0014130 SCH-530348 SULPHATE 95.00% 705260-08-8 5MG $500.42 2021-12-16 Buy
DC Chemicals DC8229 VorapaxarSulfate(SCH530348) >98% 705260-08-8 100mg $550 2021-12-16 Buy
Crysdot CD11069485 VorapaxarSulfate 97% 705260-08-8 250mg $456 2021-12-16 Buy
DC Chemicals DC8229 VorapaxarSulfate(SCH530348) >98% 705260-08-8 250mg $950 2021-12-16 Buy
Product number Packaging Price Buy
V758200 100mg $580 Buy
API0014130 5MG $500.42 Buy
DC8229 100mg $550 Buy
CD11069485 250mg $456 Buy
DC8229 250mg $950 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 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.

Synthesis_705260-08-8

Vorapaxar Sulfate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 183)Suppliers
Supplier Tel Email Country ProdList Advantage
Beijing Cooperate Pharmaceutical Co.,Ltd
010-60279497 sales01@cooperate-pharm.com CHINA 1811 55
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Jinan Shengqi pharmaceutical Co,Ltd
86+18663751872 christine@shengqipharm.com CHINA 491 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Beijing Ribio Biotech Co.,Ltd
010-62664360 +8613328773880 wucy@ribio.com.cn China 117 58
Beijing Yibai Biotechnology Co., Ltd
0086-182-6772-3597 sales04@yibaibiotech.com CHINA 419 58

View Lastest Price from Vorapaxar Sulfate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Vorapaxar Sulfate pictures 2023-06-26 Vorapaxar Sulfate
705260-08-8
US $200.00 / kg 1kg 99% 1000kg/Month Hebei Mingeng Biotechnology Co., Ltd
Vorapaxar sulfate pictures 2023-04-11 Vorapaxar sulfate
705260-08-8
US $100.00 / mg 10mg 99% 1000g Shijiazhuang Gantuo Biotechnology Co., Ltd
Vorapaxar sulfate pictures 2022-12-01 Vorapaxar sulfate
705260-08-8
US $200.00 / g 10g 99% 1000t/month Hebei Best Biological Technology Co., Ltd
  • Vorapaxar sulfate pictures
  • Vorapaxar sulfate
    705260-08-8
  • US $100.00 / mg
  • 99%
  • Shijiazhuang Gantuo Biotechnology Co., Ltd
  • Vorapaxar sulfate pictures
  • Vorapaxar sulfate
    705260-08-8
  • US $200.00 / g
  • 99%
  • Hebei Best Biological Technology 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) 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 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 705260-08-8 C29H33FN2O4H2SO4 C29H35FN2O8S Aromatics Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals