CAS: 944842-54-0; (R)-2-((2-(1H-Pyrrolo[2,3-B]Pyridin-3-yl)Pyrimidin-4-yl)Amino)-2-Methyl-N-(2,2,2-Trifluoroethyl)Butanamide

该化合物是一种合成化合物,属于被称为小分子抑制剂的一类物质,主要研究其潜在的治疗用途,特别是在癌症治疗方面.VX 509作为某些信号路径的选择性抑制器,可影响细胞扩散和生存.该化合物的特征是能够调节免疫反应,使其成为免疫疗法的候选体.其化学结构包括有助于其生物活动和选择性的特定功能组.VX 509经过各种临床前科和临床评估,以评估其功效和安全性.与许多调查药物一样,其开发需要经过严格的测试,以确定最佳剂量,潜在副作用和总体治疗效益.目前围绕VX 509进行的研究反映了对有针对性的疗法的广泛兴趣,这些疗法能够提供更有效的治疗选择,其副作用比传统化学疗法要小得多.

结构式图片

上下游产品

2-((2-(1H-Pyrrolo[2,3-B]Pyridin-3-yl)Pyrimidin-4-yl)Amino)-2-Methyl-N-(2,2,2-Trifluoroethyl)Butanamide 1417421-97-6
(R)-2-(2-(1H-Pyrrolo[2,3-B]Pyridin-3-yl)Pyrimidin-4-Ylamino)-2-Methylbutanoic Acid 1417421-82-9
2-((2-(1H-Pyrrolo[2,3-B]Pyridin-3-yl)Pyrimidin-4-yl)Amino)-2-Methylbutanoic Acid 1417421-96-5
(R)-2-Methyl-2-(2-(1-Tosyl-1H-Pyrrolo[2,3-B]Pyridin-3-yl)Pyrimidin-4-Ylamino)Butanoic Acid 1417421-80-7
Methyl 2-Methyl-2-((2-(1-Tosyl-1H-Pyrrolo[2,3-B]Pyridin-3-yl)Pyrimidin-4-yl)Amino)Butanoate 1417421-95-4
(2R)-2-[(2-Chloropyrimidin-4-yl)Amino]-2-Methyl-N-(2,2,2-Trifluoroethyl)Butanamide

合成工艺路线路线简述

  • 1417421-82-9 + 753-90-2 = 944842-54-0
    反应条件:1.1 Reagents: Diisopropylethylamine Solvents: Dichloromethane; < 30 °C1.2 Reagents: Propylphosphonic Anhydride; < 20 °C; 1 H,20 °C1.3 < 20 °C; 20 °C -> 25 °C; 5 H,25 °C
    标题:Pharmaceutical Combinations Useful For Treating Rheumatoid Arthritis
    参考文献:World Intellectual Property Organization]

    1417421-82-9 + 753-90-2 = 944842-54-0
    反应条件:1.1 Reagents: Diisopropylethylamine Solvents: Dichloromethane,Water; 30 Min,< 30 °C; 30 °C -> 0 °C1.2 Reagents: Propylphosphonic Anhydride; < 20 °C; 1 H,20 °C1.3 < 20 °C; 20 °C -> 25 °C; 5 H,25 °C1.4 Reagents: Sodium Hydroxide Solvents: Isopropyl Acetate,Water; Ph 7.5 - 8,< 35 °C; 35 °C -> 10 °C; 1 H,10 °C
    标题:Processes And Intermediates For Producing Azaindoles
    参考文献:World Intellectual Property Organization]

    = 944842-54-0 [标题:Reaction Conditions
    标题:Preparation Of Isotopically Enriched Azaindoles As Janus Kinase Inhibitors
    参考文献:World Intellectual Property Organization]

    1817716-78-1 = 944842-54-0
    反应条件:1.1 Reagents: Lithium Hydroxide Solvents: Tetrahydrofuran,Water; Overnight,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified
    标题:Discovery Of Vx-509 (Decernotinib): A Potent And Selective Janus Kinase 3 Inhibitor For The Treatment Of Autoimmune Diseases
    作者:Farmer,Luc J.; Ledeboer,Mark W.; Hoock,Thomas; Arnost,Michael J.; Bethiel,Randy S.; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2015 卷标:58(18) 页码:7195-7216]

    1417421-82-9 + 753-90-2 = 944842-54-0
    反应条件:1.1 Reagents: Diisopropylethylamine,Propylphosphonic Anhydride Solvents: Dichloromethane,Water; 0 - 20 °C; 1 H,20 °C1.2 < 20 °C; 5 H,20 °C -> 25 °C1.3 Reagents: Water
    标题:Methods For Treating Inflammatory Diseases And Useful Pharmaceutical Combinations
    参考文献:World Intellectual Property Organization]

    = 944842-54-0 [标题:Reaction Conditions
    标题:Preparation Of The Prodrug Compound And Their Medical Applications
    参考文献:World Intellectual Property Organization]

    = 944842-54-0 [标题:Reaction Conditions
    标题:Azaindoles Useful As Inhibitors Of Janus Kinases And Their Preparation And Use In The Treatment Of Diseases
    参考文献:World Intellectual Property Organization
(R)-2-Methyl-2-(2-(1-Tosyl-1H-Pyrrolo[2,3-B]Pyridin-3-yl)Pyrimidin-4-Ylamino)Butanoic Acid置于水,N,N-二异丙基乙胺,Potassium Hydroxide体系中,用 二氯甲烷,水 作为反应溶剂,化学反应 11.5H,反应生成 Decernotinib(vx-509)抑制剂
参考文献: Processes And Intermediates For Producing Azaindoles[fr] Procédés Et Intermédiaires Pour Produire Des Azaindoles
标题: Processes And Intermediates For Producing Azaindoles[fr] Procédés Et Intermédiaires Pour Produire Des Azaindoles

海关参考信息

专利信息


专利号:US-2025206743-A1
优先权日:2022-03-25
标 题:Tyk2 inhibitor synthesis and intermediates thereof
发明人:MASSE CRAIG E; PHADKE AVINASH S; LAWSON JON P; LEVY STUART; YANG XIAOWEI; WU GUISHENG; FAN SHUFENG
权利人:TAKEDA PHARMACEUTICALS CO
摘要:Described herein are methods of synthesis of a tyrosine-protein kinase 2 (TYK2) inhibitor and to intermediate compounds of the synthesis and methods of making the intermediates. Also provided are pharmaceutically acceptable compositions including compounds prepared by the synthetic method and methods of treating disorders using the same.

专利号:US-10906888-B2
优先权日:2016-07-14
标 题:Pyrimidine carboxamides as inhibitors of Vanin-1 enzyme
发明人:CASIMIRO-GARCIA AGUSTIN; STROHBACH JOSEPH WALTER; HEPWORTH DAVID; LOVERING FRANK ELDRIDGE; CHOI CHULHO; ALLAIS CHRISTOPHE PHILIPPE; WRIGHT STEPHEN WAYNE
权利人:PFIZER
摘要:Compounds, pharmaceutically acceptable salts thereof, are disclosed wherein the compounds have the structure of (I) as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

专利号:US-10308615-B2
优先权日:2015-05-29
标 题:Heterocyclic compounds as inhibitors of Vanin-1 enzyme
发明人:CASIMIRO-GARCIA AGUSTIN; CONDON JEFFREY SCOTT; FLICK ANDREW CHRISTOPHER; GOPALSAMY ARIAMALA; KIRINCICH STEVEN J; MATHIAS JOHN PAUL; STROBACH JOSEPH WALTER; XIANG JASON SHAOYUN; XING LI HUANG; WANG XIAOLUN
权利人:PFIZER
摘要:Compounds, pharmaceutically acceptable salts thereof, are disclosed wherein the compounds have the structure of n nas defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

专利号:CN-118922420-A
优先权日:2022-03-25
标题 :Synthesis of TYK2 inhibitors and their intermediates

专利号:US-2018230127-A1
优先权日:2015-08-13
标题 :Bicyclic-Fused Heteroaryl Or Aryl Compounds
发明人:ANDERSON DAVID RANDOLPH; CURRAN KEVIN JOSEPH; GAVRIN LORI KRIM; GOLDBERG JOEL ADAM; LEE ARTHUR; LOWE MICHAEL DENNIS; PATNY AKSHAY; PIERCE BETSY SUSAN; SAIAH EDDINE; TRZUPEK JOHN DAVID
权利人:PFIZER
摘要:Compounds, tautomers and pharmaceutically acceptable salts of the compounds of Formula (Ia) are disclosed which are inhibitors of Interleukin-1 receptor associated kinase (IRAK4). Methods of treatment, methods of synthesis, and intermediates are also disclosed as defined in the specification.

专利号:US-2023119606-A1
优先权日:2020-02-18
标 题:Immune cell modulators
发明人:SHERDEN NATHANIEL; YU SHEN; STONER ISAAC
权利人:OCTAGON THERAPEUTICS INC
摘要:Disclosed are immune cell-selective small molecule compounds that modulate certain immune cell-specific receptors and enzymes, and methods of their synthesis and use to treat proliferative disorders.
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✅ COA系统入驻 | 共享模式

主要参考文献


1: Kyttaris VC. Kinase inhibitors: a new class of antirheumatic drugs. Drug Des Devel Ther. 2012;6:245-50. doi: 10.2147/DDDT.S25426. Epub 2012 Sep 21. Review.

合成参考文献


摘要:S55 | ZINC15PHARMA | Pharmaceuticals from ZINC15 | DOI:10.5281/zenodo.3247749
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