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6-cyclohexyl-5-hydroxy-3-oxo-2,3-dihydro-pyridazine-4-carboxylic acid ethyl ester | 1010697-48-9

中文名称
——
中文别名
——
英文名称
6-cyclohexyl-5-hydroxy-3-oxo-2,3-dihydro-pyridazine-4-carboxylic acid ethyl ester
英文别名
ethyl 6-cyclohexyl-5-hydroxy-3-oxo-2,3-dihydro-4-pyridazinecarboxylate;ethyl 3-cyclohexyl-4-hydroxy-6-oxo-1H-pyridazine-5-carboxylate
6-cyclohexyl-5-hydroxy-3-oxo-2,3-dihydro-pyridazine-4-carboxylic acid ethyl ester化学式
CAS
1010697-48-9
化学式
C13H18N2O4
mdl
——
分子量
266.297
InChiKey
GOQQIBZDTDSGQA-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):
    2.5
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    88
  • 氢给体数:
    2
  • 氢受体数:
    5

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

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文献信息

  • Efficient synthesis of 2,6-disubstituted-5-hydroxy-3-oxo-2,3-dihydro-pyridazine-4-carboxylic acid ethyl esters
    作者:Douglas E. Murphy、Peter S. Dragovich、Benjamin K. Ayida、Thomas M. Bertolini、Lian-Sheng Li、Frank Ruebsam、Nebojsa S. Stankovic、Zhongxiang Sun、Jingjing Zhao、Yuefen Zhou
    DOI:10.1016/j.tetlet.2007.11.187
    日期:2008.1
    boxylic acid ethyl esters (6-substituted-5-hydroxy-3(2H)-pyridazinone-4-carboxylic acid ethyl esters). These compounds are shown to undergo selective alkylation at the 2-position in moderate to good yields (19–77%) to afford 2,6-disubstituted-5-hydroxy-3-oxo-2,3-dihydro-pyridazine-4-carboxylic acid ethyl esters (2,6-disubstituted-5-hydroxy-3(2H)-pyridazinone-4-carboxylic acid ethyl esters).
    描述了用于制备6-取代的5-羟基-3-氧代-2,3-二氢哒嗪-4-羧酸乙酯(6-取代的-5-羟基-3(2 H)-哒嗪酮-4-羧酸乙酯)。这些化合物显示在2位发生选择性烷基化,产率中等至良好(19-77%),可提供2,6-二取代的-5-羟基-3-羟基-3-氧代-2,3-二氢哒嗪-4-羧酸乙酯(2,6-二取代-5-羟基-3(2 H)-哒嗪酮-4-羧酸乙酯)。
  • N-Substituted Glycine Derivatives: Hydroxylase Inhibitors
    申请人:SHAW Antony N.
    公开号:US20080214549A1
    公开(公告)日:2008-09-04
    The invention described herein relates to certain pyridazinedione N-substituted glycine derivatives of formula (I) which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.
    本发明涉及某些式(I)的吡啶N-取代甘酸衍生物,它们是HIF脯酸羟化酶的拮抗剂,并且对于治疗受益于抑制该酶的疾病,如贫血等,具有用处。
  • Pyridazinone compounds
    申请人:Zhou Yuefen
    公开号:US20080275032A1
    公开(公告)日:2008-11-06
    The invention is directed to pyridazinone compounds and pharmaceutical compositions containing such compounds that are useful in treating infections by hepatitis C virus.
    这项发明涉及吡啶咪唑化合物以及包含这些化合物的药物组合物,这些化合物在治疗丙型肝炎病毒感染方面具有用处。
  • N-substituted glycine derivatives: hydroxylase inhibitors
    申请人:SmithKline Beecham, Corp.
    公开号:US07608621B2
    公开(公告)日:2009-10-27
    The invention described herein relates to certain pyridazinedione N-substituted glycine derivatives of formula (I) which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.
    本发明涉及某些式(I)的吡啶N-取代甘酸衍生物,其是HIF脯酸羟化酶的拮抗剂,对于治疗受益于抑制该酶的疾病,如贫血等,具有用途。
  • Pyridazine-dione N-substituted glycine derivatives as HIF hydroxylase inhibitors
    申请人:GlaxoSmithKline LLC
    公开号:EP2889289A1
    公开(公告)日:2015-07-01
    The invention described herein relates to certain pyridazinedione N-substituted glycine derivatives which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.
    本文所述的发明涉及某些哒嗪 N-取代甘酸衍生物,它们是 HIF 脯酰羟化酶的拮抗剂,可用于治疗因抑制该酶而获益的疾病,贫血就是其中一例。
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