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1-(4-Methylpyrimidin-2-yl)-3-([1,3]thiazolo[5,4-b]pyridin-2-yl)urea | 1280215-27-1

中文名称
——
中文别名
——
英文名称
1-(4-Methylpyrimidin-2-yl)-3-([1,3]thiazolo[5,4-b]pyridin-2-yl)urea
英文别名
——
1-(4-Methylpyrimidin-2-yl)-3-([1,3]thiazolo[5,4-b]pyridin-2-yl)urea化学式
CAS
1280215-27-1
化学式
C12H10N6OS
mdl
——
分子量
286.317
InChiKey
ACQBCDCAVGURAO-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):
    1.6
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    121
  • 氢给体数:
    2
  • 氢受体数:
    6

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

反应信息

  • 作为产物:
    描述:
    噻唑并[5,4-B]2-氨基吡啶 在 sodium hydride 作用下, 以 四氢呋喃甲苯 为溶剂, 反应 20.0h, 生成 1-(4-Methylpyrimidin-2-yl)-3-([1,3]thiazolo[5,4-b]pyridin-2-yl)urea
    参考文献:
    名称:
    A New Method for Synthesizing Asymmetric Urea Containing Thiazolo[5,4-b]pyridine And Applications in Agriculture
    摘要:
    In this article, we describe the use of diphenyl carbonate (DPC) as a carbonyl source instead of isocyanate to synthesize asymmetric substituted urea derivatives. In a study aiming to discover new lead compounds with agricultural activities, thiazole[5,4-b]pyridine ureas were prepared by this method and characterized by mass spectrometry, elemental analysis, and H-1 NMR spectroscopy. The biological activities show that the title compounds have moderate activities on herbicide, fungicide, and plant growth regulation.
    DOI:
    10.1080/10426507.2010.497518
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文献信息

  • A New Method for Synthesizing Asymmetric Urea Containing Thiazolo[5,4-b]pyridine And Applications in Agriculture
    作者:Wenbin Chen、Kejian Li
    DOI:10.1080/10426507.2010.497518
    日期:2011.1.31
    In this article, we describe the use of diphenyl carbonate (DPC) as a carbonyl source instead of isocyanate to synthesize asymmetric substituted urea derivatives. In a study aiming to discover new lead compounds with agricultural activities, thiazole[5,4-b]pyridine ureas were prepared by this method and characterized by mass spectrometry, elemental analysis, and H-1 NMR spectroscopy. The biological activities show that the title compounds have moderate activities on herbicide, fungicide, and plant growth regulation.
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