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ethyl 3-chloro-9H-imidazo<1,5-a><1,2,4>triazol<4,3-d><1,4>benzodiazepine-10-carboxylate | 163311-24-8

中文名称
——
中文别名
——
英文名称
ethyl 3-chloro-9H-imidazo<1,5-a><1,2,4>triazol<4,3-d><1,4>benzodiazepine-10-carboxylate
英文别名
ethyl 3-chloro-9H-imidazo[1,5-a][1,2,4]triazolo[4,3-d][1,4]benzodiazepine-10-carboxylate;Ethyl 15-chloro-2,4,8,10,11-pentazatetracyclo[11.4.0.02,6.08,12]heptadeca-1(13),3,5,9,11,14,16-heptaene-5-carboxylate
ethyl 3-chloro-9H-imidazo<1,5-a><1,2,4>triazol<4,3-d><1,4>benzodiazepine-10-carboxylate化学式
CAS
163311-24-8
化学式
C15H12ClN5O2
mdl
——
分子量
329.746
InChiKey
NEVSBYUBNOGFQJ-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):
    1.7
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    74.8
  • 氢给体数:
    0
  • 氢受体数:
    5

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
  • 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:
    ethyl 3-chloro-9H-imidazo<1,5-a><1,2,4>triazol<4,3-d><1,4>benzodiazepine-10-carboxylatesodium hydroxide溶剂黄146 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 反应 6.5h, 生成 3-chloro-10-(3-cyclopropyl-1,2,4-oxadiazol-5-yl)-9H-imidazo[1,5-a][1,2,4]triazolo[4,3-d][1,4]benzodiazepine
    参考文献:
    名称:
    New Tetracyclic Derivatives of Imidazo[1,5-a][1,4]benzodiazepines and of Imidazo[1,5-a]-thieno[3,2-f][1,4]-diazepines
    摘要:
    The synthesis of new tetracyclic 1,4-diazepine derivatives is described. In these compounds, an additional five-membered heterocycle is fused on the known tricyclic ring systems imidazo[1,5-a][1,4]benzodiazepine and imidazo[1,5-a]thieno[3,2-f][1,4]diazepine. Many of these new compounds display a very high affinity to the benzodiazepine receptor in mammals.
    DOI:
    10.3987/com-94-s(b)61
  • 作为产物:
    描述:
    ethyl 12-chloro-9-oxo-2,4, 8-triazatricyclo[8.4.0.02,6]tetradeca-1(14),3,5,10,12-pentaene-5-carboxylate 在 劳森试剂吡啶一水合肼 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 129.0h, 生成 ethyl 3-chloro-9H-imidazo<1,5-a><1,2,4>triazol<4,3-d><1,4>benzodiazepine-10-carboxylate
    参考文献:
    名称:
    New Tetracyclic Derivatives of Imidazo[1,5-a][1,4]benzodiazepines and of Imidazo[1,5-a]-thieno[3,2-f][1,4]-diazepines
    摘要:
    The synthesis of new tetracyclic 1,4-diazepine derivatives is described. In these compounds, an additional five-membered heterocycle is fused on the known tricyclic ring systems imidazo[1,5-a][1,4]benzodiazepine and imidazo[1,5-a]thieno[3,2-f][1,4]diazepine. Many of these new compounds display a very high affinity to the benzodiazepine receptor in mammals.
    DOI:
    10.3987/com-94-s(b)61
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文献信息

  • Discovery of the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine scaffold as a novel, potent and selective GABAA α5 inverse agonist series
    作者:Guido Achermann、Theresa M. Ballard、Francesca Blasco、Pierre-Emmanuel Broutin、Bernd Büttelmann、Holger Fischer、Martin Graf、Maria-Clemencia Hernandez、Peter Hilty、Frédéric Knoflach、Andreas Koblet、Henner Knust、Anke Kurt、James R. Martin、Raffaello Masciadri、Richard H.P. Porter、Heinz Stadler、Andrew W. Thomas、Gerhard Trube、Jürgen Wichmann
    DOI:10.1016/j.bmcl.2009.07.153
    日期:2009.10
    Through iterative design cycles we have discovered a number of novel new classes where the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine was deemed the most promising GABAA α5 inverse agonist class with potential for cognitive enhancement. This class combines a modest subtype binding selectivity with inverse agonism and has the most favourable molecular properties for further lead optimisation
    通过迭代设计周期,我们发现了许多新颖的新类,其中咪唑并[1,5- a ] [1,2,4]-三唑并[1,5- d ] [1,4]苯并二氮杂被认为是最有前途的GABA一个α5反相激动剂类的认知提高的潜力。此类具有适度的亚型结合选择性和反向激动作用,并具有最有利的分子特性,可进一步优化针对中枢神经系统(CNS)的药物。
  • Substituted imidazo [1,5-a] [1,2,4] triazolo [4,3-d] [1,4] benzodiazepine derivatives
    申请人:——
    公开号:US20020103371A1
    公开(公告)日:2002-08-01
    The present invention is a compound of formula 1 The compound and derivatives or pharmaceutically acceptable salts thereof of the invention have a good affinity and selectivity to the GABA A &agr;5 receptor and are useful for the treatment of diseases related to this receptor.
    本发明是一种化合物,化学式为1。该发明的化合物及其衍生物或药学上可接受的盐具有良好的亲和力和选择性,对GABA A &agr;5受体具有作用,并可用于治疗与该受体相关的疾病。
  • BENZODIAZEPINE DERIVATIVES AS GABA A RECEPTOR MODULATORS
    申请人:F. HOFFMANN-LA ROCHE AG
    公开号:EP1337535B1
    公开(公告)日:2004-06-09
  • US6743789B2
    申请人:——
    公开号:US6743789B2
    公开(公告)日:2004-06-01
  • New Tetracyclic Derivatives of Imidazo[1,5-a][1,4]benzodiazepines and of Imidazo[1,5-a]-thieno[3,2-f][1,4]-diazepines
    作者:Max Gerecke、Emilio Kyburz、René Boner、Walter Gassner
    DOI:10.3987/com-94-s(b)61
    日期:——
    The synthesis of new tetracyclic 1,4-diazepine derivatives is described. In these compounds, an additional five-membered heterocycle is fused on the known tricyclic ring systems imidazo[1,5-a][1,4]benzodiazepine and imidazo[1,5-a]thieno[3,2-f][1,4]diazepine. Many of these new compounds display a very high affinity to the benzodiazepine receptor in mammals.
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