CAS: 40507-23-1; 4-(4-Fluorophenyl)-7-Methyl-1-Propan-2-Ylquinazolin-2-One

该化合物是一种化学化合物,被归类为非类固醇抗炎药物(NSAID),主要用于其止痛和抗炎特性,其特点是能够抑制环氧酶酶,这对合成蛋白质具有关键作用,从而减轻疼痛和炎症.该化合物一般在有机溶剂中表现出中等溶解性,在水中不易溶性,从而影响其生物利用率和药用动力.氟丙酮经常用于治疗各种情况,包括关节炎和其他炎症.其化学结构包括一个五氯硝基苯环,有助于其药用活动.与许多非氨基苯一样,潜在副作用可能包括胃肠问题,心血管风险和肾损伤,因此需要在临床使用中仔细考虑.

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MSDS等安全信息

    上下游产品

    1-Isopropyl-7-Methyl-Quinazolin-2,4(1H,3H)-Dione

    合成工艺路线路线简述

      📜1-Isopropyl-4-(4-Fluorophenyl)-7-Methyl-4A,5,6,8A-Tetrahydro-2(1H)-Quinazolinone 以 甲醇,二氯甲烷,萘烷 作为反应溶剂,化学反应生成 氟丙喹宗
      参考文献:Tetrahydro-2(1H)-Quinazolinones And Cyclohexene Nitriles
      标题:Tetrahydro-2(1H)-Quinazolinones And Cyclohexene Nitriles
      摘要:一种生产4-苯基-2(1H)-喹唑啉酮和-4A,5,6,8A-四氢-2(1H)-喹唑啉酮的过程,包括通过格氏试剂反应将所需的苯基基团引入相应的喹唑啉-2,4(1H,3H)-二酮中,然后对所得产物进行水解.

      海关参考信息

      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:US-4778805-A
      优先权日:1987-06-18
      标题:4,7-benzofurandione derivatives useful as inhibitors of leukotriene synthesis
      发明人:ADAMS JULIAN; GUINDON YVAN; BELANGER PATRICE C; BELLEY MICHEL L; ROKACH JOSHUA
      权利人:MERCK FROSST CANADA
      摘要:4,7-Benzofurandione derivatives of Formula I, pharmaceutical compositions, and methods of treatment are disclosed. These compounds are useful as inhibitors of mammalian leukotriene biosynthesis. As such, these compounds are useful therapeutic agents for treating allergic conditions, asthma, cardiovascular disorders, inflammation, psoriasis and allergic conjunctivitis. The compounds are also useful as analgesics and as cytoprotective agents. Also disclosed are novel intermediates useful for the preparation of the 4,7-benzofurandiones of this invention. ##STR1##

      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.

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      ✅ COA系统入驻 | 共享模式

      主要参考文献


      1: Orwig BA, Dugger HA, Bhuta SI, Talbot KC, Schwarz HJ. The biotransformation of fluproquazone in man and several animal species. Arzneimittelforschung. 1981;31(5a):904-11. German. English, German.

      合成参考文献


      摘要:Arzneimittel-Forschung. Drug Research., 34(879), 1984 []
      摘要:Arzneimittel-Forschung. Drug Research., 31(882), 1981 []
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