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2-(4-methoxyphenyl)-3-(pyridin-3-ylmethyl)-1,3-thiazolidin-4-one

中文名称
——
中文别名
——
英文名称
2-(4-methoxyphenyl)-3-(pyridin-3-ylmethyl)-1,3-thiazolidin-4-one
英文别名
——
2-(4-methoxyphenyl)-3-(pyridin-3-ylmethyl)-1,3-thiazolidin-4-one化学式
CAS
——
化学式
C16H16N2O2S
mdl
——
分子量
300.381
InChiKey
VAXAJOUNWRXLNR-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):
    2.2
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    67.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-(4-methoxyphenyl)-N-(pyridin-3-ylmethyl)methanimine 、 巯基乙酸甲苯 为溶剂, 反应 0.08h, 生成 2-(4-methoxyphenyl)-3-(pyridin-3-ylmethyl)-1,3-thiazolidin-4-one
    参考文献:
    名称:
    Thiazolidin-4-ones from 3-(Aminomethyl)pyridine, Arenealdehydes and Mercaptoacetic Acid: Synthesis and Radical Scavenger Activity
    摘要:
    The efficient synthesis of fifteen novel thiazolidin-4-ones from reaction of 3-(aminomethyl) pyridine (3-picolylamine), arenealdenhydes and mercaptoacetic acid was described. The desired compounds were obtained in moderated to good yields by two methodologies: conventional heating and ultrasound irradiation. The thiazolidin-4-ones were fully identified and characterized by nuclear magnetic resonance (NMR), gas chromatography coupled to mass spectrometry (GC-MS) and high resolution mass spectrometry (HRMS) techniques. Four compounds showed radical scavenger activity in the 2,2'-azinobis-3-ethyl-benzothiazoline-6-sulfonic acid (ABTS) assay.
    DOI:
    10.5935/0103-5053.20140291
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文献信息

  • Thiazolidin-4-ones from 3-(Aminomethyl)pyridine, Arenealdehydes and Mercaptoacetic Acid: Synthesis and Radical Scavenger Activity
    作者:Adriana M. Neves、Auri R. Duval、Gabriele A. Berwaldt、Daniela P. Gouvêa、Natália P. Flores、Pâmela G. da Silva、Francieli M. Stefanello、Wilson Cunico
    DOI:10.5935/0103-5053.20140291
    日期:——
    The efficient synthesis of fifteen novel thiazolidin-4-ones from reaction of 3-(aminomethyl) pyridine (3-picolylamine), arenealdenhydes and mercaptoacetic acid was described. The desired compounds were obtained in moderated to good yields by two methodologies: conventional heating and ultrasound irradiation. The thiazolidin-4-ones were fully identified and characterized by nuclear magnetic resonance (NMR), gas chromatography coupled to mass spectrometry (GC-MS) and high resolution mass spectrometry (HRMS) techniques. Four compounds showed radical scavenger activity in the 2,2'-azinobis-3-ethyl-benzothiazoline-6-sulfonic acid (ABTS) assay.
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