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6-piperazin-1-yl-imidazo[1,2-b]pyridazine | 946157-08-0

中文名称
——
中文别名
——
英文名称
6-piperazin-1-yl-imidazo[1,2-b]pyridazine
英文别名
6-(1-Piperazinyl)imidazo[1,2-B]pyridazine;6-piperazin-1-ylimidazo[1,2-b]pyridazine
6-piperazin-1-yl-imidazo[1,2-b]pyridazine化学式
CAS
946157-08-0
化学式
C10H13N5
mdl
MFCD27756485
分子量
203.247
InChiKey
RWXNJNDHWARRGE-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):
    0.1
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    45.5
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    6-piperazin-1-yl-imidazo[1,2-b]pyridazineN-碘代丁二酰亚胺N,N-二异丙基乙胺 作用下, 以 乙酸乙酯N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 生成 tert-butyl 4-(3-iodoimidazo[1,2-b]pyridazin-6-yl)piperazine-1-carboxylate
    参考文献:
    名称:
    [EN] IMIDAZO [1, 2 - B] PYRIDAZINE - BASED COMPOUNDS, COMPOSITIONS COMPRISING THEM, AND USES THEREOF
    [FR] COMPOSÉS À BASE D'IMIDAZO [1, 2-B] PYRIDAZINE, COMPOSITIONS LES COMPRENANT ET UTILISATIONS DE CEUX-CI
    摘要:
    基于咪唑并[1,2-b]吡啶嗪的化合物的公式(I)被披露,其中R1、R2和R3在此处被定义。还披露了包含这些化合物的组合物以及它们用于治疗、管理和/或预防由适配器相关激酶1活性介导的疾病和紊乱的方法。
    公开号:
    WO2013134219A1
  • 作为产物:
    描述:
    哌嗪6-氯咪唑并[1,2-b]哒嗪氮气乙酸乙酯magnesium sulfate 作用下, 反应 2.0h, 以to yield 5.6 g of 6-piperazin-1-yl-imidazo[1,2-b]pyridazine which的产率得到6-piperazin-1-yl-imidazo[1,2-b]pyridazine
    参考文献:
    名称:
    Imidazo[1,2-b]pyridazine-based compounds, compositions comprising them, and methods of their use
    摘要:
    公开了基于咪唑并[1,2-b]吡啶的化合物的公式:其中R1,R2和R3在此定义。还公开了包含该化合物的组合物以及使用它们治疗、管理和/或预防适配器相关激酶1活性介导的疾病和紊乱的方法。
    公开号:
    US08969565B2
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文献信息

  • Imidazo[1,2-b]pyridazine-based compounds, compositions comprising them, and methods of their use
    申请人:Bi Yingzhi
    公开号:US08969565B2
    公开(公告)日:2015-03-03
    Imidazo[1,2-b]pyridazine-based compounds of the formula: are disclosed, wherein R1, R2 and R3 are defined herein. Compositions comprising the compounds and methods of their use to treat, manage and/or prevent diseases and disorders mediated by mediated by adaptor associated kinase 1 activity are also disclosed.
    公开了基于咪唑并[1,2-b]吡啶的化合物的公式:其中R1,R2和R3在此定义。还公开了包含该化合物的组合物以及使用它们治疗、管理和/或预防适配器相关激酶1活性介导的疾病和紊乱的方法。
  • IMIDAZO[1,2-b]PYRIDAZINE-BASED COMPOUNDS, COMPOSITIONS COMPRISING THEM, AND METHODS OF THEIR USE
    申请人:BI Yingzhi
    公开号:US20130245021A1
    公开(公告)日:2013-09-19
    Imidazo[1,2-b]pyridazine-based compounds of the formula: are disclosed, wherein R 1 , R 2 and R 3 are defined herein. Compositions comprising the compounds and methods of their use to treat, manage and/or prevent diseases and disorders mediated by mediated by adaptor associated kinase 1 activity are also disclosed.
    本发明揭示了基于咪唑并[1,2-b]吡啶的化合物,其化学式如下:其中R1、R2和R3在此定义。本发明还揭示了包含这些化合物的组合物以及它们的使用方法,用于治疗、管理和/或预防由适配器相关激酶1活性介导的疾病和障碍。
  • Decahydroisoquinoline derivatives as novel non-peptidic, potent and subtype-selective somatostatin sst3 receptor antagonists
    作者:Thomas Troxler、Konstanze Hurth、Karl-Heinrich Schuh、Philippe Schoeffter、Daniel Langenegger、Albert Enz、Daniel Hoyer
    DOI:10.1016/j.bmcl.2010.01.063
    日期:2010.3
    Starting from non-peptidic sst(1)-selective somatostatin receptor antagonists, first compounds with mixed sst(1)/sst(3) affinity were identified by directed structural modifications. Systematic optimization of these initial leads afforded novel, enantiomerically pure, highly potent and sst(3)-subtype selective somatostatin antagonists based on a (4S,4aS,8aR)-decahydroisoquinoline-4-carboxylic acid core moiety. These compounds can efficiently be synthesized and show promising PK properties in rodents. (C) 2010 Elsevier Ltd. All rights reserved.
  • Discovery of novel non-peptidic β-alanine piperazine amide derivatives and their optimization to achiral, easily accessible, potent and selective somatostatin sst1 receptor antagonists
    作者:Thomas Troxler、Konstanze Hurth、Henri Mattes、Mahavir Prashad、Philippe Schoeffter、Daniel Langenegger、Albert Enz、Daniel Hoyer
    DOI:10.1016/j.bmcl.2009.01.072
    日期:2009.3
    Structural simplification of the core moieties of obeline and ergoline somatostatin sst(1) receptor antagonists, followed by systematic optimization, led to the identification of novel, highly potent and selective sst(1) receptor antagonists. These achiral, non-peptidic compounds are easily prepared and show promising PK properties in rodents. (C) 2009 Elsevier Ltd. All rights reserved.
  • IMIDAZO [1, 2 - B]PYRIDAZINE - BASED COMPOUNDS, COMPOSITIONS COMPRISING THEM, AND USES THEREOF
    申请人:Lexicon Pharmaceuticals, Inc.
    公开号:EP2822559A1
    公开(公告)日:2015-01-14
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