CAS: 103-97-9; 2-Amino-N-(4-Ethoxyphenyl)Acetamide

化学文摘社编号103-97-9,主要用作止痛剂和抗过激剂的有机化合物;在水和酒精中可溶解的白白脱白结晶粉,适合各种药品配方;Phenocoll,其减少发烧和减轻疼痛的能力,其功能与其他非类止痛剂相似,其作用机制包括抑制在炎症反应中起关键作用的prostalandin合成;虽然它有效治疗轻度至中度疼痛和发烧,但由于潜在的副作用,包括过敏反应和胃肠紊乱,必须在医疗监督下使用它;此外,Phenocoll的安全性和功效导致其在特定治疗环境中的使用,尽管它可能没有在当代医学中的其他止痛剂得到广泛使用;与任何药物一样,适当的剂量和遵守准则对于确保病人安全和治疗效果至关重要.

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    上下游产品

    2-Bromo-N-(4-Ethoxyphenyl)Acetamide 34325-71-8
    2-氯-N-(4-乙氧基苯基)乙酰胺 2-Chloro-4'-Ethoxyacetanilide 04/08/2153
    Hydroxyimino-Acetic Acid P-Phenetidide 17122-74-6
    对乙氧基苯胺 4-Ethoxyaniline 156-43-4

    合成工艺路线路线简述

      📜2-氯-N-(4-乙氧基苯基)乙酰胺置于乙醇,氨体系中,化学反应生成2-氨基-N-(4-乙氧基苯基)乙酰胺
      参考文献:De59121
      标题:De59121

      专利信息


      专利号:US-2024287041-A1
      优先权日:2021-05-20
      标题 :Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms
      发明人:BALOGLU ERKAN; AUSTAD BRIAN C; ROE DAVID G; KEDUC ANDREW; GOTTSCHLING STEPHEN EDMUND; HECKER EVAN
      权利人:KARYOPHARM THERAPEUTICS INC
      摘要:The present invention relates to a method of preparing a compound represented by structural formula (VII), comprising reacting a compound represented by structural formula (II), with a compound represented by structural formula (III), in a solvent, in the presence of a Pd catalyst and one or more inorganic bases under conditions suitable to prepare a compound represented by structural formula (VII): The values and example values of the variables in structural formulas (VII), (II), and (III) are defined herein. The present invention also relates to crystalline Forms I and II of the compound represented by Structural Formula (VII), the use of the crystalline Forms in treating disease or disorders associated with CRM1 and method of preparing the crystalline Forms.

      专利号:AU-2022276509-A1
      优先权日:2021-05-20
      标题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

      专利号:US-9994558-B2
      优先权日:2013-09-20
      标题 :Multicyclic compounds and methods of using same
      发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM; MCCAULEY DILARA; LANDESMAN YOSEF; GOLAN GALI; KALID ORI; SHECHTER SHARON
      权利人:KARYOPHARM THERAPEUTICS INC
      摘要:The invention generally relates to compounds represented by Structural Formula I: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula I, or a pharmaceutically acceptable salt or composition thereof, e.g., in treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders (e.g., PAK-mediated, for example, PAK4-mediated, diseases and disorders).

      专利号:WO-2022246227-A1
      优先权日:2021-05-20
      标 题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

      专利号:US-10363247-B2
      优先权日:2015-08-18
      标 题:(S,E)-3-(6-aminopyridin-3-yl)-N-((5-(4-(3-fluoro-3-methylpyrrolidine-1-carbonyl)phenyl-7-(4-fluorophenyl)benzofuran-2-yl)methyl)acrylamide for the treatment of cancer
      发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM
      权利人:KARYOPHARM THERAPEUTICS INC
      摘要:The invention generally relates to substituted benzofuranyl compounds and, more particularly, to a compound represented by Structural Formula 1a: (I) or a pharmaceutically acceptable salt thereof. The invention also includes the synthesis and use of the compound of Structural Formula 1a, or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of diseases or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, an inflammatory diseases or an immune system disease (e.g., a T-Cell mediated autoimmune disease) in a subject in need thereof. The method comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, or a composition comprising a compound of the invention, or a pharmaceutically acceptable salt thereof.

      专利号:CA-3219525-A1
      优先权日:2021-05-20
      标 题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

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      ✅ COA系统入驻 | 共享模式

      合成参考文献


      参考文献:10.1021/jm00092a016
      摘要:Cunliffe CJ, Franklin TJ, Hales NJ, Hill GB. Novel inhibitors of prolyl 4-hydroxylase. 3. Inhibition by the substrate analogue N-oxaloglycine and its derivatives. J Med Chem. 1992 Jul 10;35(14):2652–8. doi: 10.1021/jm00092a016.
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