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2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide

CAS No.
108605-62-5
Chemical Name:
2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide
Synonyms
Su 20;CS-862;Aubagio;Aids013145;Aids-013145;rac-A77 1626;Teriflunomide;(E/Z)-Teriflunomide;TeriflunoMide, A77 1726;Teriflunomide((E/Z) Mixture)
CBNumber:
CB6464433
Molecular Formula:
C12H9F3N2O2
Molecular Weight:
270.21
MDL Number:
MFCD00910058
MOL File:
108605-62-5.mol
Last updated:2024-11-19 23:02:33

2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide Properties

Melting point 229-232°C
Boiling point 410.8±45.0 °C(Predicted)
Density 1.424±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in DMSO (up to 30 mg/ml), or in Ethanol (up to 5 mg/ml with warming).
form Solid
pka 5.20±0.50(Predicted)
color White
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
FDA UNII 1C058IKG3B
ATC code L04AA31

Pharmacokinetic data

Protein binding >99%
Excreted unchanged in urine 22.6 (as metabolites)
Volume of distribution 11 Litres
Biological half-life 18-19 days / Unchanged

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P264-P270-P301+P310-P405-P501
Hazard Codes  Xn
Risk Statements  22
HS Code  2926900005
Toxicity mouse,LD50,intraperitoneal,100mg/kg (100mg/kg),United States Patent Document. Vol. #5494911,

2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR2878 Leflunomide Related Compound B pharmaceutical secondary standard, certified reference material 108605-62-5 50MG $634 2024-03-01 Buy
Sigma-Aldrich 1357056 Leflunomide Related Compound B United States Pharmacopeia (USP) Reference Standard 108605-62-5 20mg $1530 2024-03-01 Buy
Tocris 5069 Teriflunomide ≥99%(HPLC) 108605-62-5 50 $151 2021-12-16 Buy
TRC A771720 A771726(E/Z)Mixture 108605-62-5 50mg $80 2021-12-16 Buy
Usbiological 256904 Teriflunomide 108605-62-5 50mg $389 2021-12-16 Buy
Product number Packaging Price Buy
PHR2878 50MG $634 Buy
1357056 20mg $1530 Buy
5069 50 $151 Buy
A771720 50mg $80 Buy
256904 50mg $389 Buy

2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide Chemical Properties,Uses,Production

Description

Teriflunomide (Aubagio®), also known as A77 1726, is an immunosupressant marketed by Sanofi for the teatment of multiple sclerosis (MS). Teriflunomide is the active metabolite of leflunomide, used for treatment of patients diagnosed with rheumatoid arthritis, and therefore simultaneously can be used as a treatment for rheumatoid arthritis.Teriflunomide acts as an inhibitor of the mitochondrial enzyme dihydrorotate dehydrogenase, inhibiting pyrimidine formation, and resulting in reduced B and T cell proliferation.

Chemical Properties

White Solid

Uses

The active metabolite of Leflunomide, 2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide can be used as a potent disease-modifying antirheumatic drug used in the treatment of rheumatoid arthritis.

Definition

ChEBI: Teriflunomide is an enamide obtained by formal condensation of the carboxy group of (2Z)-2-cyano-3-hydroxybut-2-enoic acid with the anilino group of 4-(trifluoromethyl)aniline. Used for the treatment of relapsing forms of multiple sclerosis and rheumatoid arthritis. It has a role as an EC 1.3.98.1 [dihydroorotate oxidase (fumarate)] inhibitor, a tyrosine kinase inhibitor, a hepatotoxic agent, a drug metabolite and a non-steroidal anti-inflammatory drug. It is a nitrile, an enol, an aromatic amide, an enamide, a member of (trifluoromethyl)benzenes and a secondary carboxamide.

Clinical Use

Immunomodulating agent:
Treatment of relapsing remitting multiple sclerosis

Synthesis

Numerous syntheses of teriflunomide have been developed to date, most relying on the use of 4- trifluoromethyl aniline (167). The current optimized method for scale-up synthesis of teriflunomide, developed by Keshav and coworkers, begins with reaction of commercial 4-trifluoromethyl aniline 167 and ethylacetoacetate (168) in refluxing xylenes, providing acetoamidate 169 in 51% yield . The resulting acetoamidate 169 was then treated with H2O2, KBr, and concentrated HCl at room temperature, providing bromide 170 in 67% yield. Bromide 170 was reacted with NaCN in DMSO, generating teriflunomide (XXVI) in 85% yield.

Synthesis_108605-62-5

Drug interactions

Potentially hazardous interactions with other drugs
Lipid-lowering agents: effect significantly reduced by colestyramine - avoid; concentration of rosuvastatin increased - consider reducing rosuvastatin dose.
Live vaccines: risk of generalised infections - avoid.

Metabolism

Teriflunomide is the active metabolite of leflunomide. It is moderately metabolised and teriflunomide is the only component detected in plasma. The main biotransformation pathway is hydrolysis with oxidation being a minor pathway. Secondary pathways involve oxidation, N-acetylation and sulfate conjugation. Teriflunomide is excreted in the gastrointestinal tract mainly through the bile as unchanged drug and most likely by direct secretion.

storage

Store at +4°C

References

1) Manna et al. (1999), Immunosuppressive leflunomide metabolite (A77 1726) blocks TNF-dependent nuclear factor-kappa B activation and gene expression; J. Immunol., 162 2095 2) Davis et al. (1996), immunosuppressive metabolite of leflunomide is a potent inhibitor of human dihydroorotate dehydrogenase; Biochemistry, 35 1270 3) Seah et al. (2008), Oxidative bioactivation and toxicity of leflunomide in immortalized human hepatocytes and kinetics of the non-enzymatic conversion to its major metabolite, A77 1726; Drug Metab. Lett., 2 153

2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 170)Suppliers
Supplier Tel Email Country ProdList Advantage
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
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3009 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32957 60
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29881 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28172 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39894 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32165 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6312 58
Xi'an MC Biotech, Co., Ltd.
029-89275612 +8618991951683 mcbio_sales@163.com China 2251 58

View Lastest Price from 2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(E/Z)-Teriflunomide pictures 2024-11-19 (E/Z)-Teriflunomide
108605-62-5
US $31.00-48.00 / mg ≥95% 10g TargetMol Chemicals Inc.
A77 1726 pictures 2019-07-06 A77 1726
108605-62-5
US $1.00 / KG 1G 99% 100KG Career Henan Chemical Co
  • A77 1726 pictures
  • A77 1726
    108605-62-5
  • US $1.00 / KG
  • 99%
  • Career Henan Chemical Co

2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide Spectrum

N-(4-Trifluoromethylphenyl)-2-cyano-3-hydroxycrotonamide, 2-Cyano-3-hydroxy-N-[4-(trifluoromethyl)phenyl]-2-beuteamide, LEF-M (2Z)-2-[hydroxy-[[4-(trifluoromethyl)phenyl]amino]methylidene]-3-oxo-butanenitrile 2-Cyano-3OH-N-(4-trifluoromethylphenyl) crotonamide-d4 IMp. A (EP) as Hydrochloride: 4-(TrifluoroMethyl)aniline Hydrochloride TeriflunoMide, A77 1726 2-Cyano-3-hydroxy-N-(4-trifluoromethylphenyl)crotonamide 2-Cyano-3-hydroxy-N-[4-(trifluoromethyl)phenyl]but-2-enamide 2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide (E)-2-Cyano-3-hydroxy-N-(4-trifluoromethylphenyl)-2-butenamide 2-Butenamide, 2-cyano-3-hydroxy-N-[4-(trifluoromethyl)phenyl]- Aids013145 Aids-013145 Su 20 Teriflunomide (Z)-2-cyano-3-hydroxy-N-(4-(trifluoroMethyl)phenyl)but-2-enaMide Leflunomide Related Compound B (10 mg) (2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide) 2-Cyano-3-hydroxy-N-(4-(trifluoromethyl)phenyl)but-2-enamide,teriflunomide Leflunomide Related Compound B (20 mg) (2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide) 2-cyano-3-hydroxy-n-(4-(trifluoromethyl)phenyl)-2-butenamid n-(4-trifluoromethylphenyl)-2-cyano-2-hydroxycrotonamide N-(4-TRIFLUOROMETHYLPHENYL)-2-CYANO-3-HYDROXYCROTOAMIDE N-(4-TRIFLUOROMETHYLPHENYL)-2-CYANO-3-HYDROXYCROTONAMIDE 2-CYANO-3-OH-N-(4-TRIFLUOROMETHYLPHENYL) CROTONAMIDE 2-CYANO-3-HYDROXY-N-[4-(TRIFLUOROMETHYL)PHENYL]-2-BUTENAMIDE Teriflunomide(Random Configuration) (2Z)-2-[hydroxy-[4-(trifluoromethyl)anilino]methylidene]-3-oxobutanenitrile Leflunomide ImpuritⅡ: 2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide CS-862 2-Cyano-3-hydroxy-N-(4-trifluoromethylphenyl)cro rac-A77 1626 Leflunomide impurityⅡ[2-cyano-3-hydroxy-N-(4’-trifluoromethylphenyl)-crotone amide] Aubagio 2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide USP/EP/BP Teriflunomide((E/Z) Mixture) Leflunomide USP Related Compound B Leflunomide ImpuritⅡ: 2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide Leflunomide Related Compound B (2-Cyano-3-hydroxy-N-(4''-trifluoromethylphenyl)-crotone amide) (1357056) Leflunomide impurityⅡ [2-cyano-3-hydroxy-N-(4’ -trifluoromethylphenyl)-croton e amide (E/Z)-Teriflunomide 2-cyano-3-hydroxy-crotonic acid 4-trifluoro-methyl-anilide 2-Cyano-3-hydroxy-N-(4'-trifluoromethylphenyl)-crotone amide 108605-62-5 C12H5F3N2O2D4 Various Metabolites and Impurities Metabolites & Impurities Tyrosine Kinase Inhibitors