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5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carboxylic acid methyl ester | 300554-35-2

中文名称
——
中文别名
——
英文名称
5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carboxylic acid methyl ester
英文别名
Methyl 5-(2-methylpyridin-3-yl)oxypyrazine-2-carboxylate;methyl 5-(2-methylpyridin-3-yl)oxypyrazine-2-carboxylate
5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carboxylic acid methyl ester化学式
CAS
300554-35-2
化学式
C12H11N3O3
mdl
——
分子量
245.238
InChiKey
OVSHJRURMRSHMS-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):
    1.2
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    74.2
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carboxylic acid methyl ester盐酸一水合肼 、 sodium nitrite 作用下, 以 甲醇 为溶剂, 反应 4.5h, 生成 5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carbonyl azide
    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:
    描述:
    3-羟基-2-甲基吡啶5-氯吡嗪-2-羧酸甲酯 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 以94%的产率得到5-(2-Methyl-pyridin-3-yloxy)-pyrazine-2-carboxylic acid methyl ester
    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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文献信息

  • 1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines: novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/Anxiolytic agents
    作者:Steven M. Bromidge、Steven Dabbs、Susannah Davies、D.Malcolm Duckworth、Ian T. Forbes、Graham E. Jones、Jerome Jones、Frank D. King、Damian V. Saunders、Thomas P. Blackburn、Vicky Holland、Guy A. Kennett、Sean Lightowler、Derek N. Middlemiss、Graham J. Riley、Brenda Trail、Martyn D. Wood
    DOI:10.1016/s0960-894x(00)00364-4
    日期:2000.8
    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.
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