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1-(2-((tert-butoxycarbonyl)amino)ethyl)-3-(phenoxymethyl)-1H-pyrazole-5-carboxylic acid ethyl ester | 1380507-28-7

中文名称
——
中文别名
——
英文名称
1-(2-((tert-butoxycarbonyl)amino)ethyl)-3-(phenoxymethyl)-1H-pyrazole-5-carboxylic acid ethyl ester
英文别名
(rac)-2-(2-tert-butoxycarbonylamino-propyl)-5-phenoxymethyl-2H-pyrazole-3-carboxylic acid ethyl ester;ethyl 1-{2-[(tert-butoxycarbonyl)amino]propyl}-3-(phenoxymethyl)-1H-pyrazole-5-carboxylate;ethyl 2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]-5-(phenoxymethyl)pyrazole-3-carboxylate
1-(2-((tert-butoxycarbonyl)amino)ethyl)-3-(phenoxymethyl)-1H-pyrazole-5-carboxylic acid ethyl ester化学式
CAS
1380507-28-7
化学式
C21H29N3O5
mdl
——
分子量
403.478
InChiKey
YOILUAMLQCOKAH-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):
    3.4
  • 重原子数:
    29
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    91.7
  • 氢给体数:
    1
  • 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:
    参考文献:
    名称:
    [EN] BICYCLIC PYRAZOLE COMPOUNDS AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS
    [FR] UTILISATION DE COMPOSÉS BICYCLIQUES DE PYRAZOLE EN TANT QUE MODULATEURS ALLOSTÉRIQUES DES RÉCEPTEURS MGLUR5
    摘要:
    在一个方面,这项发明涉及到双环吡唑化合物、其衍生物和相关化合物,这些化合物可作为代谢型谷氨酸受体亚型5(mGluR5)的正向变构调节剂;制备这些化合物的合成方法;包括这些化合物的药物组合物;以及使用这些化合物和组合物治疗与谷氨酸功能障碍相关的神经和精神疾病的方法。这个摘要旨在作为在特定领域进行搜索的扫描工具,并不意味着对本发明的限制。
    公开号:
    WO2012078817A1
  • 作为产物:
    参考文献:
    名称:
    [EN] SUBSTITUTED BICYCLIC CYCLOALKYL PYRAZOLE LACTAM ANALOGS AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS
    [FR] ANALOGUES DE LACTAME DE PYRAZOLE DE CYCLOALKYLE BICYCLIQUES SUBSTITUÉS EN TANT QUE MODULATEURS ALLOSTÉRIQUES DES RÉCEPTEURS MGLUR5
    摘要:
    在一个方面,该发明涉及替代的双环环烷基吡唑内酰胺类似物,其衍生物和相关化合物,这些化合物可用作代谢型谷氨酸受体亚型5(mGluR5)的阳性变构调节剂;制备这些化合物的合成方法;含有这些化合物的药物组合物;以及使用这些化合物和组合物治疗与谷氨酸功能障碍相关的神经和精神疾病的方法。本摘要旨在作为在特定领域进行搜索的扫描工具,并不意味着对本发明的限制。
    公开号:
    WO2013192347A1
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文献信息

  • [EN] BICYCLIC TRIAZOLE AND PYRAZOLE LACTAMS AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS<br/>[FR] UTILISATION DE LACTAMES DE TRIAZOLE ET DE PYRAZOLE BICYCLIQUES COMME MODULATEURS ALLOSTÉRIQUES DES RÉCEPTEURS MGLUR5
    申请人:UNIV VANDERBILT
    公开号:WO2012083224A1
    公开(公告)日:2012-06-21
    In one aspect, the invention relates to bicyclic triazole and pyrazole lactams, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with glutamate dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    在一个方面,该发明涉及到双环三唑和吡唑内酰胺,它们的衍生物以及相关化合物,这些化合物可用作代谢型谷酸受体亚型5(mGluR5)的正向变构调节剂;制备这些化合物的合成方法;包含这些化合物的药物组合物;以及使用这些化合物和组合物治疗与谷酸功能障碍相关的神经和精神疾病的方法。本摘要旨在作为在特定领域进行搜索的扫描工具,并不意味着对本发明的限制。
  • BICYCLIC PYRAZOLE COMPOUNDS AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS
    申请人:Conn P. Jeffrey
    公开号:US20120295913A1
    公开(公告)日:2012-11-22
    In one aspect, the invention relates to bicyclic pyrazole compounds, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with glutamate dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    本发明涉及双环吡唑化合物及其衍生物和相关化合物,它们可用作代谢型谷酸受体亚型5(mGluR5)的正向变构调节剂;合成制备这些化合物的方法;包括这些化合物的制药组合物;以及使用这些化合物和组合物治疗与谷酸功能障碍相关的神经和精神障碍的方法。本摘要旨在作为搜索特定领域的扫描工具,不限制本发明。
  • BICYCLIC TRIAZOLE AND PYRAZOLE LACTAMS AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS
    申请人:Conn P. Jeffrey
    公开号:US20120225844A1
    公开(公告)日:2012-09-06
    In one aspect, the invention relates to bicyclic triazole and pyrazole lactams, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with glutamate dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    本发明涉及双环三唑和吡唑内酰胺、其衍生物和相关化合物,可作为代谢型谷酸受体亚型5(mGluR5)的正向变构调节剂;制备这些化合物的合成方法;包含这些化合物的制药组合物;以及使用这些化合物和组合物治疗与谷酸功能障碍相关的神经和精神障碍的方法。本摘要旨在作为特定领域搜索的扫描工具,不限制本发明。
  • Bicyclic triazole and pyrazole lactams as allosteric modulators of mGluR5 receptors
    申请人:Conn P. Jeffrey
    公开号:US08592422B2
    公开(公告)日:2013-11-26
    In one aspect, the invention relates to bicyclic triazole and pyrazole lactams, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with glutamate dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    在某个方面,本发明涉及用作代谢型谷酸受体亚型5(mGluR5)正向变构调节剂的双环三唑和吡唑烯酮及其衍生物和相关化合物;制备该化合物的合成方法;包含该化合物的制药组合物;以及使用该化合物和组合物治疗与谷酸功能障碍相关的神经和精神障碍的方法。本摘要旨在作为特定领域搜索的扫描工具,不限制本发明。
  • Substituted pyrazolo[1,5-A]pyrazine compounds as allosteric modulators of mGluR5 receptors
    申请人:Conn P. Jeffrey
    公开号:US08703946B2
    公开(公告)日:2014-04-22
    In one aspect, the invention relates to substituted pyrazolo[1,5-a]pyrazine compounds, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with glutamate dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    在一个方面,本发明涉及取代的吡唑并[1,5-a]吡嗪化合物、其衍生物和相关化合物,它们是代谢型谷酸受体亚型5(mGluR5)的正向变构调节剂;制备这些化合物的合成方法;包含这些化合物的药物组合物;以及使用这些化合物和组合物治疗与谷酸功能障碍相关的神经和精神障碍的方法。本摘要旨在作为搜索特定技术领域的扫描工具,不限制本发明。
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