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SafinamideIntermediate 2

SAFINAMIDE:(S)-(+)-2-[4-(3-FLUOROBENZYLOXY)BENZYLAMINO]PROPANAMIDE METHANSULFONATE

CAS: 133865-89-1

Molecular Formula: C17H19FN2O2

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SafinamideIntermediate 2 - Names and Identifiers

Name SAFINAMIDE:(S)-(+)-2-[4-(3-FLUOROBENZYLOXY)BENZYLAMINO]PROPANAMIDE METHANSULFONATE
Synonyms CS-484
FCE-26743
FCE 26743
EMD1195686
Safinamide
EMD 1195686
EMD-1195686
SafinamideIntermediate 2
Safinamide ,Safinamide base
N~2~-{4-[(3-fluorobenzyl)oxy]benzyl}-L-alaninamide
(S)-(+)-2-[4-(3-Fluorobenzyloxy)benzylamino]propanamice methansulfonate
CAS 133865-89-1
EINECS 603-772-2
InChI InChI=1/C17H19FN2O2/c1-12(17(19)21)20-10-13-5-7-16(8-6-13)22-11-14-3-2-4-15(18)9-14/h2-9,12,20H,10-11H2,1H3,(H2,19,21)/t12-/m0/s1

SafinamideIntermediate 2 - Physico-chemical Properties

Molecular FormulaC17H19FN2O2
Molar Mass302.34
Density1.189±0.06 g/cm3(Predicted)
Melting Point208-212°
Boling Point476.7±40.0 °C(Predicted)
Flash Point242.1°C
Solubility DMSO
Vapor Presure2.98E-09mmHg at 25°C
AppearanceWhite to Brown Powder
ColorWhite
Merck14,8315
pKa16.03±0.50(Predicted)
Storage Conditionunder inert gas (nitrogen or Argon) at 2–8 °C
StabilityStable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
SensitiveSensitive to heat
Refractive Index1.569
MDLMFCD00897036

SafinamideIntermediate 2 - Risk and Safety

RTECSTX1457385

SafinamideIntermediate 2 - Introduction

Safinamide (EMD 1195686; FCE 26743) is a reversible MAO-B inhibitor with IC50 of 98 nM, which is 5918 times higher than that of MAO-A.
Last Update:2022-10-16 17:13:28

SafinamideIntermediate 2 - Reference Information

Overview Safenamide (safinamide), the chemical name is (S)-2-[4-(3-fluorobenzyloxy) benzylamine] Propionamide A

Sulfonate is an anti-Parkinson's disease drug developed by Netron Pharmaceutical Company, currently in phase III clinical study

stage. Clinically, it has been shown that this drug can improve the motor and cognitive functions of patients with Parkinson's disease, prevent patients from having

current movement disorders, and has good tolerance.
Parkinson's disease new drug Safenamide (trade name: Xadago) is a new type of monoamine oxidase B(MAO-B) selective inhibitor, By blocking the voltage-dependent sodium ion channels on neurons, and then regulating the release of glutamate. This drug is recommended in combination with levodopa or other Parkinson's drugs for the treatment of advanced idiopathic Parkinson's disease.
Safenamide is a highly selective and reversible third-generation type B monoamine oxidase inhibitor (selegilan is the first generation, rasagilan is the second generation), which can increase the intracellular and extracellular dopamine in the striatum Level. Unlike the already marketed stilgilam and rasagline, Safenamide also has the effect of inhibiting the release of the neurotransmitter glutamate.
It is said that Safenamide is a "new drug", but in fact it is not so "new". In 2015, Europe has approved Safenamide for the treatment of advanced Parkinson's disease; On March 21, 2017, the US FDA approved Safenamide as an additional therapeutic drug for the treatment of Parkinson's patients who are taking levodopa/carbidopa and have "OFF" status.
as we all know, levodopa is currently the most effective and widely used drug for the treatment of Parkinson's disease, and the proportion of patients taking drugs is as high as 75%. However, with the development of the disease, the ON-Time of levodopa will gradually shorten, resulting in the so-called "wearing-off" phenomenon. At this time, we need to combine levodopa with other drugs with different mechanisms of action.
As a new selective MAO-B inhibitor, Safenamide can effectively reduce the degradation of secreted dopamine and help maintain the concentration of dopamine in the brain. In addition, Safenamide can also block voltage-dependent sodium channels on neurons, thereby inhibiting the release of glutamate. Therefore, Safenamide is a new Parkinson's disease treatment drug with both dopaminergic and non-dopaminergic mechanisms.
Preparation method 1. Solid phase synthesis: Rink amide resin is hydrolyzed to remove carboxyl groups, and (S)-2-(fluorenomethoxyamido) propionic acid undergo ammonolysis reaction, remove amino protection group, then it is condensed with 4-(triisopropylsiloxy) benzaldehyde, and is reduced by sodium triacetylborohydride, then remove the phenolic hydroxyl protecting group and then form an ether with 3-fluorobenzyl alcohol, and finally take off the product from the resin to obtain this drug. This route involves multiple protection and deprotection. The route is long and the reagents used are expensive, which is not suitable for industrial production.
2. It is prepared by the reaction of (S)-2-aminopropionamide (4) and 4-(3-fluorobenzyl) benzaldehyde (6). The total yield is about 45%. Although the route is short, the raw materials used are not easy to obtain. 3. the second method is improved: the synthesis route is as follows:



the specific steps are: using L-alanine (2) as raw material to prepare (S)-2-aminopropionate methyl ester hydrochloride (3), then ammonolysis to obtain 4, adding catalyst potassium iodide, replacing acetone with anhydrous ethanol as solvent, and extending the reaction time to 6 h, after extraction with toluene and recrystallization with toluene-n-hexane (1: 1), pure product 6 was prepared. The yield was increased from 78% to 91%. When preparing 1, the literature [2] condensed 4 and 6 to prepare (S)-2-[4-(3-fluorobenzyloxy) benzyimine] propionamide (7), which was then reduced with sodium cyanoborohydride, and then purified by column chromatography to obtain (S)-2-[4-(3-fluorobenzyloxy) benzylamine] propionamide (8), finally, it is salt with methanesulfonic acid to obtain 1, and the yield is 45% (calculated as 6). This method will produce the highly toxic sodium cyanide, and column chromatography purification is not suitable for large-scale production. In this study, Pd/C catalytic hydrogenation reduction was used. The product was recrystallized with toluene and then salted with methanesulfonic acid. The operation was simplified and more suitable for industrial production. The yield could be improved to 83.3%. The total yield of the improved process is 75.8%.
mechanism of action this product has a variety of mechanisms of action, which can not only inhibit monoamine oxidase B(MAO-B) with high selectivity and reversibility,

it can also inhibit dopamine reuptake, block voltage-dependent sodium channels, regulate calcium channels, and thus inhibit the release of valley

amino acid.
This product has high bioavailability of the central nervous system. Clinically, it has been shown that this drug can improve the motor and cognitive functions of patients with Parkinson's disease, prevent the patients from dyskinesia, and has good tolerance.
application can be used for the treatment of Parkinson's disease.
Adverse reactions Safenamide is a selective monoamine oxidase (MAO)B inhibitor.
The most common adverse reactions of patients taking Safenamide include uncontrolled involuntary movement, falls, nausea and insomnia.
According to the FDA, serious but uncommon risks include worsening hypertension; serotonin syndrome when used with MAO inhibitors, antidepressants or opioids; falling asleep in activities of daily living; hallucinations and psychotic behaviors; Impulse control disorders/compulsive behavior; hyperthermia and confusion after drug withdrawal; and retinopathy.
precautions FDA reminds that Safenamide should not be used in patients with severe liver dysfunction. In addition, patients taking dextromethorphan, MAO inhibitors, opioids, St. John's wort, and certain antidepressants (such as serotonin-norepinephrine reuptake inhibitors, tricyclic, tetracyclic and triazolopyridine) Or patients with cyclobenzaprine should also not take Safenamide because it may cause life-threatening serotonin syndrome.
references [1] xing ruijuan, Lu Tao, Liu leina, et al. synthesis of Safenamide [J]. china journal of pharmaceutical industry, 2012, 43(3):161-163.
[2] Pevarello P, Bonsignori A, Dostert P, et al. Synthesis and anticonvulsant activity of a new class of 2-[(arylalky)-amino] alkanamide derivatives [J]. J Med Chem, 1998, 41(4): 579-590.
Last Update:2024-04-09 15:16:47
SafinamideIntermediate 2
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CAS: 133865-89-1
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
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Email: 3623107365@qq.com
Mobile: 18916960931
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SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
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Product Name: Safinamide Visit Supplier Webpage Request for quotation
CAS: 133865-89-1
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
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MedChemExpress (MCE)
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CAS: 133865-89-1
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     tech@medchemexpress.com
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SKYRUN INDUSTRIAL CO.,LTD
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Product Name: Safinamide Visit Supplier Webpage Request for quotation
CAS: 133865-89-1
Tel: +86 0571-86722205
Email: sales@chinaskyrun.com
Mobile: +8618958170122
QQ: 2531159185 Click to send a QQ messageSend QQ message
Wechat: chinaskyrun
Shanghai Yuanye Bio-Technology Co., Ltd.
Spot supply
Product Name: Safinamide Visit Supplier Webpage Request for quotation
CAS: 133865-89-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
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SafinamideIntermediate 2
Butylperacetate
Pentane oil
FUNGUARD
RESORCINOL SOLUTION 100UG/ML IN METHANOL 5X1ML
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