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5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carbonyl azide | 300554-36-3

中文名称
——
中文别名
——
英文名称
5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carbonyl azide
英文别名
——
5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carbonyl azide化学式
CAS
300554-36-3
化学式
C11H8N6O2
mdl
——
分子量
256.224
InChiKey
AKCPSKKUEWOIMR-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):
    2.42
  • 重原子数:
    19.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    113.73
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    5-甲基-6-三氟甲基吲哚啉5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carbonyl azide甲苯 为溶剂, 反应 1.0h, 以63%的产率得到5-Methyl-6-trifluoromethyl-2,3-dihydro-indole-1-carboxylic acid [5-(2-methyl-pyridin-3-yloxy)-pyrazin-2-yl]-amide
    参考文献:
    名称:
    1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines: novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/Anxiolytic agents
    摘要:
    Bisaryl ethers have been identified with excellent 5-HT2C affinity and selectivity over both 5-HT2A and 5-HT2B receptors. Compounds such as 11, 27 and 38 have potent oral activity in a centrally mediated pharmacodynamic model of 5-HT2C function and their potential as novel non-sedating anxiolytic and antidepressants is under investigation. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00364-4
  • 作为产物:
    参考文献:
    名称:
    1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines: novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/Anxiolytic agents
    摘要:
    Bisaryl ethers have been identified with excellent 5-HT2C affinity and selectivity over both 5-HT2A and 5-HT2B receptors. Compounds such as 11, 27 and 38 have potent oral activity in a centrally mediated pharmacodynamic model of 5-HT2C function and their potential as novel non-sedating anxiolytic and antidepressants is under investigation. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00364-4
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