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4-(2-chloro-4-fluorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester | 675200-96-1

中文名称
——
中文别名
——
英文名称
4-(2-chloro-4-fluorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester
英文别名
methyl 4-(2-chloro-4-fluorophenyl)-6-methyl-2-sulfanylidene-3,4-dihydro-1H-pyrimidine-5-carboxylate
4-(2-chloro-4-fluorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester化学式
CAS
675200-96-1
化学式
C13H12ClFN2O2S
mdl
——
分子量
314.768
InChiKey
IWKOMCDEKBZJOQ-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

物化性质

  • 沸点:
    383.9±52.0 °C(Predicted)
  • 密度:
    1.43±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    82.4
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Palladium(0)-Catalyzed, Copper(I)-Mediated Coupling of Boronic Acids with Cyclic Thioamides. Selective Carbon−Carbon Bond Formation for the Functionalization of Heterocycles<sup>†</sup>
    作者:Hana Prokopcová、C. Oliver Kappe
    DOI:10.1021/jo070408f
    日期:2007.6.1
    Employing controlled microwave irradiation at 100 °C, most cross-couplings can be completed within 2 h and proceed in high yields. An advantage of using thioamides as starting materials is the fact that the system can be tuned to an alternative carbon−sulfur cross-coupling pathway by changing to stoichiometric copper(II) under oxidative conditions. Both types of thioamide cross-couplings are orthogonal to
    描述了在化学计量的铜(I)辅因子存在下,钯催化的环硫酰胺与芳基硼酸的交叉偶联。脱硫碳-碳交叉偶联方案是在中性条件下进行的,可应用于具有嵌入的硫酰胺片段的杂环结构。成功的碳-碳交叉偶联与环大小,芳香性/非芳香性,起始硫酰胺结构中是否存在其他杂原子或其他官能团无关。通过在100°C下控制微波辐射,大多数交叉偶联可在2 h内完成,并以高收率进行。使用硫代酰胺作为起始原料的一个优点是,可以通过在氧化条件下更改为化学计量的铜(II),将系统调节至另一种碳-硫交叉偶联途径。两种类型的硫酰胺交叉偶联均与芳烃卤化物与硼酸的传统碱催化的Suzuki-Miyaura交叉偶联正交。
  • Optimized Liebeskind–Srogl coupling reaction between dihydropyrimidines and tributyltin compounds
    作者:Qi Sun、Franck Suzenet、Gérald Guillaumet
    DOI:10.1016/j.tetlet.2012.03.067
    日期:2012.5
    We developed an optimized Liebeskind-Srogl reaction in order to synthesize potentially biologically active 2-aryl-1,4-dihydropyrimidines. The pallado-catalyzed cross-coupling reaction between dihydropyrimidines and tributyltin derivatives appears particularly efficient (67-95% yields) when using CuBr.Me2S as the copper cofactor. (C) 2012 Elsevier Ltd. All rights reserved.
  • MODULATORS OF VIRUS ASSEMBLY AS ANTIVIRAL AGENTS
    申请人:INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
    公开号:US20150218182A1
    公开(公告)日:2015-08-06
    In addition to containing and protecting the viral genome, the capsid (protein shell) of hepatitis B virus (HBV) plays critical roles in the viral life cycle including regulation of intracellular trafficking and nucleic acid metabolism. Substituted pyrimidine modulators of the assembly of the HBV capsid structure and methods for their use are described.
  • ALTERNATIVE USES FOR HBV ASSEMBLY EFFECTORS
    申请人:INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
    公开号:US20150292045A1
    公开(公告)日:2015-10-15
    Described herein are methods for identifying compounds useful for the treatment of infection by hepatitis B virus (HBV).
  • US9487534B2
    申请人:——
    公开号:US9487534B2
    公开(公告)日:2016-11-08
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