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2-[(4-methoxybenzyl)thio]pyrimidine

中文名称
——
中文别名
——
英文名称
2-[(4-methoxybenzyl)thio]pyrimidine
英文别名
2-[(4-Methoxyphenyl)methylsulfanyl]pyrimidine
2-[(4-methoxybenzyl)thio]pyrimidine化学式
CAS
——
化学式
C12H12N2OS
mdl
——
分子量
232.306
InChiKey
RPEGHOSCPFJLGH-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):
    2.5
  • 重原子数:
    16
  • 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:
    60.3
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-甲氧基苯硼酸2-[(4-methoxybenzyl)thio]pyrimidine四(三苯基膦)钯噻吩-2-甲酸亚铜(I) 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以73%的产率得到2-(4-甲氧基苯基)嘧啶
    参考文献:
    名称:
    An Expeditious Route toward Pyrazine-Containing Nucleoside Analogues
    摘要:
    An improved and convenient methodology for the synthesis of asymmetrically substituted pyrazines starting from 3,5-dichloropyrazin-2(1H)-ones has been elaborated. Several nucleoside analogues have been synthesized containing the pyrazine core as the organic base coupled with the sugar via a triazole linkage. The beneficial effect of microwave irradiation throughout the sequence has been demonstrated.
    DOI:
    10.1021/jo102089h
  • 作为产物:
    描述:
    2-巯基嘧啶 、 alkaline earth salt of/the/ methylsulfuric acid 在 potassium carbonate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 以33%的产率得到2-[(4-methoxybenzyl)thio]pyrimidine
    参考文献:
    名称:
    Antimycobacterial Agents. 1. Thio Analogues of Purine
    摘要:
    Thio analogues of purine, pyridine, and pyrimidine were prepared based on the initial activity screening of several analogues of these heterocycles against Mycobacterium tuberculosis (Mtb). Certain 6-thio-substituted purine analogues described herein showed moderate to good inhibitory activity. In particular, two purine analogues 9-(ethylcarboxymethyl)-6-(decylthio)9H-purine (20) and 9-(ethylcarboxymethyl)-6-(dodecylthio)-9H-purine (21) exhibited MIC values of 1.56 and 0.78 mug/mL respectively against the Mtb H(37)Rv strain. N-9-Substitution apparently enhances the antimycobacterial activity in the purine series described herein.
    DOI:
    10.1021/jm030389b
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文献信息

  • Lewis Acid Catalysed Chemoselective Amination of Alcohols Using Heterocyclic Thiones: An Avenue to Thiotetrazole Derivatives
    作者:Sudhamoyee Kataky、Pikumoni Boruah、Ashim J. Thakur
    DOI:10.1002/ejoc.202300515
    日期:2023.10.16
    Herein, the development of a Cu(OTf)2 catalysed chemoselective amination of alcohols using heterocyclic thiones is described. Notably, the method is additive, ligand or inert atmosphere free and shows good tolerance towards variety of alcohols and thiotetrazole derivatives affording good to excellent yields of the product.
    本文描述了使用杂环硫酮进行Cu(OTf) 2催化的醇的化学选择性胺化的开发。值得注意的是,该方法不含添加剂、配体或惰性气氛,并且对各种醇和硫代四唑衍生物表现出良好的耐受性,从而提供良好至优异的产物产率。
  • Antimycobacterial Agents. 1. Thio Analogues of Purine
    作者:Ashish K. Pathak、Vibha Pathak、Lainne E. Seitz、William J. Suling、Robert C. Reynolds
    DOI:10.1021/jm030389b
    日期:2004.1.1
    Thio analogues of purine, pyridine, and pyrimidine were prepared based on the initial activity screening of several analogues of these heterocycles against Mycobacterium tuberculosis (Mtb). Certain 6-thio-substituted purine analogues described herein showed moderate to good inhibitory activity. In particular, two purine analogues 9-(ethylcarboxymethyl)-6-(decylthio)9H-purine (20) and 9-(ethylcarboxymethyl)-6-(dodecylthio)-9H-purine (21) exhibited MIC values of 1.56 and 0.78 mug/mL respectively against the Mtb H(37)Rv strain. N-9-Substitution apparently enhances the antimycobacterial activity in the purine series described herein.
  • An Expeditious Route toward Pyrazine-Containing Nucleoside Analogues
    作者:Sachin G. Modha、Jalpa C. Trivedi、Vaibhav P. Mehta、Denis S. Ermolat’ev、Erik V. Van der Eycken
    DOI:10.1021/jo102089h
    日期:2011.2.4
    An improved and convenient methodology for the synthesis of asymmetrically substituted pyrazines starting from 3,5-dichloropyrazin-2(1H)-ones has been elaborated. Several nucleoside analogues have been synthesized containing the pyrazine core as the organic base coupled with the sugar via a triazole linkage. The beneficial effect of microwave irradiation throughout the sequence has been demonstrated.
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