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6-methyl-N-phenyl-4-(2-thienyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbothioamide | 1574646-67-5

中文名称
——
中文别名
——
英文名称
6-methyl-N-phenyl-4-(2-thienyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbothioamide
英文别名
6-methyl-N-phenyl-2-sulfanylidene-4-thiophen-2-yl-3,4-dihydro-1H-pyrimidine-5-carbothioamide
6-methyl-N-phenyl-4-(2-thienyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbothioamide化学式
CAS
1574646-67-5
化学式
C16H15N3S3
mdl
——
分子量
345.513
InChiKey
QFABYNWGAAKJCC-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):
    2.9
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    129
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-噻吩甲醛硫脲丁硫代酰胺,3-羰基-N-苯基-硼酸溶剂黄146 作用下, 以68%的产率得到6-methyl-N-phenyl-4-(2-thienyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbothioamide
    参考文献:
    名称:
    2-Acylthioacetamides in the Biginelli Reaction
    摘要:
    We have demonstrated for the first time a Biginelli reaction of 2-acylthioacetamides with aromatic aldehydes and ureas or thioureas, leading to N-Ar-1-4-Ar-2-6-R-1-1-R-2-2-oxo(thioxo)-1,2,3,4-tetrahydro-pyrimidine-5-carbothioamides. The regioselectivity of this process matched the concept of hard/soft Lewis acids and bases. It was established that nitrous acid or other oxidants converted the synthesized compounds into N-Ar-1-4-Ar-2-6-R-1-1-R-2-2-oxo(thioxo)-1,2,3,4-tetrahydropyrimidine-5-carboxamides, and not the expected 4-Ar-2-6-R-1-1-R-2-5-(1,3-benzothiazol-2-yl)-1,2,3,4-tetrahydropyrimidin-2-ones(thiones).
    DOI:
    10.1007/s10593-014-1429-z
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文献信息

  • 2-Acylthioacetamides in the Biginelli Reaction
    作者:M. N. Kurmach、A. B. Ryabitskiy、V. N. Britsun
    DOI:10.1007/s10593-014-1429-z
    日期:2014.3
    We have demonstrated for the first time a Biginelli reaction of 2-acylthioacetamides with aromatic aldehydes and ureas or thioureas, leading to N-Ar-1-4-Ar-2-6-R-1-1-R-2-2-oxo(thioxo)-1,2,3,4-tetrahydro-pyrimidine-5-carbothioamides. The regioselectivity of this process matched the concept of hard/soft Lewis acids and bases. It was established that nitrous acid or other oxidants converted the synthesized compounds into N-Ar-1-4-Ar-2-6-R-1-1-R-2-2-oxo(thioxo)-1,2,3,4-tetrahydropyrimidine-5-carboxamides, and not the expected 4-Ar-2-6-R-1-1-R-2-5-(1,3-benzothiazol-2-yl)-1,2,3,4-tetrahydropyrimidin-2-ones(thiones).
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