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7-噁-1-aza-螺[4.4]壬烷 | 128389-81-1

中文名称
7-噁-1-aza-螺[4.4]壬烷
中文别名
——
英文名称
7-oxa-1-azaspiro[4.4]nonane
英文别名
——
7-噁-1-aza-螺[4.4]壬烷化学式
CAS
128389-81-1
化学式
C7H13NO
mdl
MFCD14581262
分子量
127.186
InChiKey
MYBGAQSNYATOKI-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

物化性质

  • 沸点:
    207.8±13.0 °C(Predicted)
  • 密度:
    1.04±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.2
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2934999090

反应信息

  • 作为反应物:
    描述:
    7-噁-1-aza-螺[4.4]壬烷铁粉potassium carbonate氯化铵 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 反应 25.0h, 生成 5-chloro-2-{7-oxa-1-azaspiro[4.4]nonan-1-yl}aniline
    参考文献:
    名称:
    [EN] TRPML MODULATORS
    [FR] MODULATEURS DE TRPML
    摘要:
    本发明提供了化合物、药学上可接受的组合物以及使用这些化合物的方法。
    公开号:
    WO2021127337A1
点击查看最新优质反应信息

文献信息

  • 6-(4-Hydroxy-phenyl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
    申请人:SANOFI
    公开号:US20130150340A1
    公开(公告)日:2013-06-13
    The present invention relates to 1H-pyrazolo[3,4-b]pyridine compounds of the formula I, in which R 1 , R 2 , R 3 and R 4 are defined as indicated below. The compounds of the formula I are kinase inhibitors, and are useful for the treatment of diseases associated with diabetes and diabetic complications, such as, diabetic nephropathy, diabetic neuropathy and diabetic retinopathy, for example. The invention furthermore relates to the use of compounds of the formula I, in particular as active ingredients in pharmaceuticals, and pharmaceutical compositions comprising them.
    本发明涉及式I的1H-吡唑并[3,4-b]吡啶化合物,其中R1、R2、R3和R4如下所示。式I的化合物是激酶抑制剂,对于治疗与糖尿病及糖尿病并发症相关的疾病,如糖尿病肾病、糖尿病神经病变和糖尿病视网膜病变等,具有用处。此外,本发明还涉及将式I的化合物用作药物中的活性成分,以及包含它们的药物组合物。
  • [EN] 6-(4-HYDROXY-PHENYL)-1H-PYRAZOLO[3,4-B]PYRIDINE-4-CARBOXYLIC ACID AMIDE DERIVATIVES AS KINASE INHIBITORS<br/>[FR] DÉRIVÉS D'AMIDE DE L'ACIDE 6-(4-HYDROXY-PHÉNYL)-1H-PYRAZOLO[3,4-B]PYRIDINE-4-CARBOXYLIQUE EN TANT QU'INHIBITEURS DE KINASES
    申请人:SANOFI SA
    公开号:WO2013060636A1
    公开(公告)日:2013-05-02
    The present invention relates to 1 H-pyrazolo[3,4-b]pyridine compounds of the formula (I) in which R1, R2, R3 and R4 are defined as indicated below. The compounds of the formula I are protein kinase C (PKC) inhibitors, and are useful for the treatment of diseases associated with diabetes and diabetic complications, such as, diabetic nephropathy, diabetic neuropathy and diabetic retinopathy, for example. The invention furthermore relates to the use of compounds of the formula, in particular as active ingredients in pharmaceuticals, and pharmaceutical compositions comprising them.
    本发明涉及式(I)的1H-吡唑并[3,4-b]吡啶化合物,其中R1、R2、R3和R4的定义如下所示。式I的化合物是蛋白激酶C(PKC)抑制剂,对于治疗与糖尿病及糖尿病并发症相关的疾病,如糖尿病肾病、糖尿病神经病变和糖尿病视网膜病变等,具有益处。此外,本发明还涉及利用该式化合物,特别是作为药物中的活性成分以及包含它们的药物组合物。
  • 6-(4-HYDROXY-PHENYL)-3-STYRYL-1H-PYRAZOLO[3,4-b]PYRIDINE-4-CARBOXYLIC ACID AMIDE DERIVATIVES AS KINASE INHIBITORS
    申请人:LOEHN Matthias
    公开号:US20130065894A1
    公开(公告)日:2013-03-14
    The present invention relates to pyrazolo[3,4-b]pyridine compounds of the formula I, in which R 1 , R 2 , R 3 , R 4 and R 5 are defined as indicated below. The compounds of the formula I are kinase inhibitors, and are useful for the treatment of diseases associated with diabetes and diabetic complications, such as, diabetic nephropathy, diabetic neuropathy and diabetic retinopathy, for example. The invention furthermore relates to the use of compounds of the formula I, in particular as active ingredients in pharmaceuticals, and pharmaceutical compositions comprising them.
    本发明涉及式I的吡唑啉[3,4-b]吡啶化合物,其中R1、R2、R3、R4和R5如下所示。式I的化合物是激酶抑制剂,可用于治疗与糖尿病及糖尿病并发症相关的疾病,如糖尿病肾病、糖尿病神经病变和糖尿病视网膜病变等。此外,该发明还涉及式I的化合物的用途,特别是作为药物中的活性成分,以及包含它们的药物组合物。
  • [EN] 6-(4-HYDROXY-PHENYL)-3-STYRYL-1H-PYRAZOLO[3,4-B]PYRIDINE-4-CARBOXYLIC ACID AMIDE DERIVATIVES AS KINASE INHIBITORS<br/>[FR] DÉRIVÉS AMIDES D'ACIDE 6-(4-HYDROXYPHÉNYL)-3-STYRYL-1H-PYRAZOLO[3,4-B]PYRIDINE-4-CARBOXYLIQUE EN TANT QU'INHIBITEURS DE KINASE
    申请人:SANOFI SA
    公开号:WO2013037390A1
    公开(公告)日:2013-03-21
    The present invention relates to pyrazolo[3,4-b]pyridine compounds of the formula I, in which R1, R2, R3, R4 and R5 are defined as indicated below. The compounds of the formula I are kinase inhibitors, and are useful for the treatment of diseases associated with diabetes and diabetic complications, such as, diabetic nephropathy, diabetic neuropathy and diabetic retinopathy, for example. The invention furthermore relates to the use of compounds of the formula I, in particular as active ingredients in pharmaceuticals, and pharmaceutical compositions comprising them.
    本发明涉及具有以下式I的吡唑并[3,4-b]吡啶化合物,其中R1、R2、R3、R4和R5如下所示。式I的化合物是激酶抑制剂,可用于治疗与糖尿病及糖尿病并发症相关的疾病,例如糖尿病肾病、糖尿病神经病变和糖尿病视网膜病变等。此外,该发明还涉及将式I的化合物用作药物中的活性成分,以及包含它们的药物组合物。
  • 6-(4-Hydroxy-phenyl)-3-alkyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
    申请人:SANOFI
    公开号:US20130085128A1
    公开(公告)日:2013-04-04
    The present invention relates to pyrazolo[3,4-b]pyridine compounds of the formula I, in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are defined as indicated below. The compounds of the formula I are kinase inhibitors, and are useful for the treatment of diseases associated with diabetes and diabetic complications, such as, diabetic nephropathy, diabetic neuropathy and diabetic retinopathy, for example. The invention furthermore relates to the use of compounds of the formula I, in particular as active ingredients in pharmaceuticals, and pharmaceutical compositions comprising them.
    本发明涉及式I的吡唑并[3,4-b]吡啶化合物,其中R1、R2、R3、R4、R5、R6和R7如下所示。式I的化合物是激酶抑制剂,适用于治疗与糖尿病及糖尿病并发症相关的疾病,如糖尿病肾病、糖尿病神经病变和糖尿病视网膜病变等。此外,本发明还涉及式I的化合物的用途,特别是作为药物中的活性成分以及包含它们的药物组合物。
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