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ethyl 7-benzyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate | 775329-23-2

中文名称
——
中文别名
——
英文名称
ethyl 7-benzyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate
英文别名
——
ethyl 7-benzyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate化学式
CAS
775329-23-2
化学式
C20H17F3O3
mdl
——
分子量
362.348
InChiKey
ONHJNZNSNWMMQN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.3
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    ethyl 7-benzyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate 在 lithium hydroxide 、 盐酸 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 4.0h, 以95%的产率得到7-benzyl-2-(trifluoromethyl)-2H-chromene-3-carboxylic acid
    参考文献:
    名称:
    [EN] CHROMENE DERIVATIVES AS ANTI-INFLAMMATORY AGENTS
    [FR] DERIVES DE CHROMENE A TITRE D'AGENTS ANTI-INFLAMMATOIRES
    摘要:
    该发明涉及在治疗与环氧合酶-2介导的疾病相关的情况中具有效用的方法和化合物。特别感兴趣的化合物是由式(I)定义的苯并吡喃和它们的类似物。其中Z、X、R1、R2、R3和R4如规范中所述。
    公开号:
    WO2004087687A1
  • 作为产物:
    描述:
    ethyl 7-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylate 在 [1,1'-bis(diphenylphosphino)ferrocene]chloropalladium complex with dichloromethane potassium phosphate 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以76%的产率得到ethyl 7-benzyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate
    参考文献:
    名称:
    [EN] CHROMENE DERIVATIVES AS ANTI-INFLAMMATORY AGENTS
    [FR] DERIVES DE CHROMENE A TITRE D'AGENTS ANTI-INFLAMMATOIRES
    摘要:
    该发明涉及在治疗与环氧合酶-2介导的疾病相关的情况中具有效用的方法和化合物。特别感兴趣的化合物是由式(I)定义的苯并吡喃和它们的类似物。其中Z、X、R1、R2、R3和R4如规范中所述。
    公开号:
    WO2004087687A1
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文献信息

  • [EN] NITROSATED BENZOPYRAN COMPOUNDS AS NOVEL CYCLOOXYGENASE-2 SELECTIVE INHIBITORS<br/>[FR] COMPOSES BENZOPYRANNE NITROSES EN TANT QUE NOUVEAUX INHIBITEURS SELECTIFS DE LA CYCLOOXYGENASE-2
    申请人:PHARMACIA & UPJOHN CO LLC
    公开号:WO2006040676A1
    公开(公告)日:2006-04-20
    This invention specifically relates to novel cyclooxygenase 2 (COX-2) selective inhibitor compounds that donate, transfer or release nitric oxide, stimulate endogenous synthesis of nitric oxide, elevate endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase. Compounds of particular interest and their analogs defined by formula (I) wherein Z, X, R1, R2, R3, and R4 are as described in the specification. This invention also relates to pharmaceutical compositions and methods for treating COX-2 mediated disorders, such as inflammation and inflammation related disorders.
    这项发明特指与新型环氧合酶2(COX-2)选择性抑制剂化合物有关,这些化合物可以提供、转移或释放一氧化氮,刺激内源性一氧化氮的合成,提高内源性内皮源性舒张因子的水平,或者是一氧化氮合酶的底物。特别感兴趣的化合物及其由式(I)中定义的类似物,其中Z、X、R1、R2、R3和R4如规范中所述。这项发明还涉及用于治疗COX-2介导的疾病,如炎症和与炎症相关的疾病的药物组合物和方法。
  • [EN] CHROMENE DERIVATIVES AS ANTI-INFLAMMATORY AGENTS<br/>[FR] DERIVES DE CHROMENE A TITRE D'AGENTS ANTI-INFLAMMATOIRES
    申请人:PHARMACIA CORP
    公开号:WO2004087687A1
    公开(公告)日:2004-10-14
    The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula (I). Wherein Z, X, R1, R2, R3, and R4 are as described in the specification.
    该发明涉及在治疗与环氧合酶-2介导的疾病相关的情况中具有效用的方法和化合物。特别感兴趣的化合物是由式(I)定义的苯并吡喃和它们的类似物。其中Z、X、R1、R2、R3和R4如规范中所述。
  • [EN] SUBSTITUTED CYCLOPROPYL CHROMENE COMPOUNDS FOR USE IN THE TREATMENT AND PREVENTION OF INFLAMMATION RELATED CONDITIONS<br/>[FR] COMPOSES DE CYCLOPROPYL CHROMENE SUBSTITUES DESTINES A ETRE UTILISES DANS LE TRAITEMENT ET LA PREVENTION DE PATHOLOGIES LIEES A DES INFLAMMATIONS
    申请人:PHARMACIA & UPJOHN CO LLC
    公开号:WO2006040672A1
    公开(公告)日:2006-04-20
    The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula (1) Wherein Z, X, R1, R2, R3, and R4 are as described in the specification.
    本发明涉及在与环氧合酶-2介导的疾病相关的情况治疗中具有效用的方法和化合物。特别感兴趣的化合物是由式(1)定义的苯并吡喃和它们的类似物,其中Z、X、R1、R2、R3和R4如规范中所述。
  • Benzopyran compounds useful for treating inflammatory conditions
    申请人:Carter Jeffery
    公开号:US20050148777A1
    公开(公告)日:2005-07-07
    The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula 1 Wherein Z, X, R 1 , R 2, R 3 , and R 4 are as described in the specification.
    本发明涉及与环氧合酶-2介导的疾病相关的病症治疗方法和化合物。特别感兴趣的化合物是由公式1定义的苯并吡喃和其类似物,其中Z、X、R1、R2、R3和R4如规范中所述。
  • Benzopyran compounds for use in the treatment and prevention of inflammation related conditions
    申请人:Carter Jeffery
    公开号:US20050148627A1
    公开(公告)日:2005-07-07
    The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula 1 Wherein Z, X, R 1 , R 2 , R 3 , and R 4 are as described in the specification.
    本发明涉及用于治疗与环氧合酶-2介导的疾病相关的条件的方法和化合物。特别感兴趣的化合物是苯并吡喃和它们的类似物,其由公式1定义,其中Z、X、R1、R2、R3和R4如规范中所述。
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