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N-(2-pyrazinyl)-2-(2-hydroxynaphthalen-1-yl)glycine | 1260490-15-0

中文名称
——
中文别名
——
英文名称
N-(2-pyrazinyl)-2-(2-hydroxynaphthalen-1-yl)glycine
英文别名
2-(2-Hydroxynaphthalen-1-yl)-2-(pyrazin-2-ylamino)acetic acid
N-(2-pyrazinyl)-2-(2-hydroxynaphthalen-1-yl)glycine化学式
CAS
1260490-15-0
化学式
C16H13N3O3
mdl
——
分子量
295.298
InChiKey
WUZNATKEGJSJGK-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):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    95.3
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    氨基吡嗪乙醛酸2-萘酚 为溶剂, 反应 4.0h, 以75%的产率得到N-(2-pyrazinyl)-2-(2-hydroxynaphthalen-1-yl)glycine
    参考文献:
    名称:
    One-Pot, Three-Component Coupling Reaction: Catalyst-Free Green Synthesis of NovelN-Heteroaryl α-Naphthylglycines
    摘要:
    A series of novel N-heteroaryl -arylglycines containing naphthol rings has been prepared by one-pot, three-component condensation reaction of glyoxalic acid, heteroaryl amines and naphthols in water at ambient temperature and under reflux conditions in moderate to high yields. The promising advantages such as removal of organic solvent, no need to catalyst, simplicity of the reaction procedure and easy product separation will be discussed in this article.
    DOI:
    10.1080/00397910903457407
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文献信息

  • One-Pot, Three-Component Coupling Reaction: Catalyst-Free Green Synthesis of Novel<i>N</i>-Heteroaryl α-Naphthylglycines
    作者:Abolfazl Olyaei、Esmat Chehrehgosha Parashkuhi、Saeed Raoufmoghaddam、Mahdieh Sadeghpour
    DOI:10.1080/00397910903457407
    日期:2010.11.16
    A series of novel N-heteroaryl -arylglycines containing naphthol rings has been prepared by one-pot, three-component condensation reaction of glyoxalic acid, heteroaryl amines and naphthols in water at ambient temperature and under reflux conditions in moderate to high yields. The promising advantages such as removal of organic solvent, no need to catalyst, simplicity of the reaction procedure and easy product separation will be discussed in this article.
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