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(S)-3-chloro-N-ethyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide | 1236118-21-0

中文名称
——
中文别名
——
英文名称
(S)-3-chloro-N-ethyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide
英文别名
3-chloro-N-ethyl-4-[4-[[(6S)-7-oxo-2,8,13-triazatricyclo[7.4.0.02,6]trideca-1(9),10,12-trien-11-yl]methyl]piperazin-1-yl]benzamide
(S)-3-chloro-N-ethyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide化学式
CAS
1236118-21-0
化学式
C24H29ClN6O2
mdl
——
分子量
468.986
InChiKey
OZTSXFIBVZAPEL-NRFANRHFSA-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:
    33
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    80.8
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    (S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one 、 3-chloro-N-ethyl-4-(piperazin-1-yl)benzamide hydrochloride 在 N,N-二异丙基乙胺(cyanomethyl)trimethylphosphonium iodide 作用下, 以 丙腈 为溶剂, 反应 4.0h, 以35.3%的产率得到(S)-3-chloro-N-ethyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide
    参考文献:
    名称:
    Poly (ADP-Ribose) Polymerase (PARP) Inhibitors
    摘要:
    披露了以下公式的化合物: 其中R1、R2、R3、R4、R5、R6、R7、X和t在规范中定义。还披露了含有这些化合物的药物组合物、试剂盒和制造物品,以及用于制备这些化合物的方法和中间体,以及使用这些化合物治疗与PARP活性相关的疾病、紊乱和状况的方法。
    公开号:
    US20100190763A1
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文献信息

  • Poly (ADP-Ribose) Polymerase (PARP) INHIBITORS
    申请人:Gangloff Anthony R.
    公开号:US20110158989A1
    公开(公告)日:2011-06-30
    Disclosed are compounds of the following formula: in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , X, and t are defined in the specification. Also disclosed are pharmaceutical compositions, kits, and articles of manufacture, which contain the compounds, methods and intermediates useful for making the compounds, and methods of using the compounds to treat diseases, disorders, and conditions related to PARP activity.
    本发明涉及以下式的化合物:其中R1,R2,R3,R4,R5,R6,R7,X和t在规范中定义。本发明还涉及含有这些化合物的制药组合物、工具箱和制造物品、制备这些化合物有用的中间体和方法,以及使用这些化合物治疗与PARP活性相关的疾病、障碍和病况的方法。
  • Substituted derivatives of pyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine and pyrido[3,2-e][1,4]oxazino[4,3-a]pyrazine
    申请人:Gangloff Anthony R.
    公开号:US08450323B2
    公开(公告)日:2013-05-28
    Disclosed are compounds of the following formula: in which R1, R2, R6, R7, R12, X, and q are defined in the specification. Also disclosed are pharmaceutical compositions, kits, and articles of manufacture, which contain the compounds, methods and intermediates useful for making the compounds, and methods of using the compounds to treat diseases, disorders, and conditions related to PARP activity.
    本发明涉及以下式的化合物:其中R1、R2、R6、R7、R12、X和q在说明书中定义。本发明还涉及含有这些化合物的制药组合物、试剂盒和制造物,以及制备这些化合物的中间体和方法,以及使用这些化合物治疗与PARP活性相关的疾病、障碍和病状的方法。
  • POLY (ADP-RIBOSE) POLYMERASE (PARP) INHIBITORS
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US20130274239A1
    公开(公告)日:2013-10-17
    Disclosed are compounds of the following formula: in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , X, and t are defined in the specification. Also disclosed are pharmaceutical compositions, kits, and articles of manufacture, which contain the compounds, methods and intermediates useful for making the compounds, and methods of using the compounds to treat diseases, disorders, and conditions related to PARP activity.
    本发明涉及以下式子的化合物:其中R1、R2、R3、R4、R5、R6、R7、X和t在规范中定义。本发明还涉及含有该化合物的药物组合物、试剂盒和制造物品,制备该化合物的有用中间体和方法,以及使用该化合物治疗与PARP活性相关的疾病、疾病和情况的方法。
  • Substituted pyrido[2,3-b]pyrazines
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US08822470B2
    公开(公告)日:2014-09-02
    Disclosed are compounds of the following formula: in which R1, R2, R3, R4, R5, R6, R7, and X, are defined in the specification. Also disclosed are pharmaceutical compositions, kits, and articles of manufacture, which contain the compounds, methods and intermediates useful for making the compounds, and methods of using the compounds to treat diseases, disorders, and conditions related to PARP activity.
    本发明涉及以下式的化合物: 其中R1、R2、R3、R4、R5、R6、R7和X在说明书中定义。本发明还涉及含有该化合物的制药组合物、试剂盒和制造物,有用于制备该化合物的中间体和方法,以及使用该化合物治疗与PARP活性相关的疾病、疾病和病状的方法。
  • Substituted pyrido[3,2-e]pyrrolo[1,2-a]pyrazines as inhibitors of poly(ADP-ribose)polymerase (PARP)
    申请人:Gangloff Anthony R.
    公开号:US09187497B2
    公开(公告)日:2015-11-17
    Disclosed are compounds of the following formula: in which R1, R2, R5, R6, R7, R31, u, and X are defined in the specification. Also disclosed are pharmaceutical compositions, kits, and articles of manufacture, which contain the compounds, methods and intermediates useful for making the compounds, and methods of using the compounds to treat diseases, disorders, and conditions related to PARP activity.
    本文披露了以下化合物的结构公式:其中R1、R2、R5、R6、R7、R31、u和X的定义在说明书中。此外,还披露了含有这些化合物的药物组合物、试剂盒和制品、制备这些化合物的中间体和方法,以及使用这些化合物治疗与PARP活性相关的疾病、疾病和状况的方法。
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