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5-benzyl-6-methyl-2-(propylsulfanyl)pyrimidin-4(3H)-one

中文名称
——
中文别名
——
英文名称
5-benzyl-6-methyl-2-(propylsulfanyl)pyrimidin-4(3H)-one
英文别名
5-Benzyl-6-methyl-2-(propylsulfanyl)pyrimidin-4-ol;5-benzyl-4-methyl-2-propylsulfanyl-1H-pyrimidin-6-one
5-benzyl-6-methyl-2-(propylsulfanyl)pyrimidin-4(3H)-one化学式
CAS
——
化学式
C15H18N2OS
mdl
——
分子量
274.387
InChiKey
CEBWNHYGEOOVKF-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):
    3.4
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    66.8
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • 作为反应物:
    描述:
    5-benzyl-6-methyl-2-(propylsulfanyl)pyrimidin-4(3H)-one邻苯二胺 以 melt 为溶剂, 反应 6.0h, 以26%的产率得到2,2'-(benzene-1,2-diyldiimino)bis[5-benzyl-6-methylpyrimidin-4(3H)-one]
    参考文献:
    名称:
    New general synthesis of benzo[4,5]imidazo[1,2-a]pyrimidine and benzo[4,5]imidazo[2,1-b]quinazoline derivatives
    摘要:
    The reactions of benzene-1,2-diamine with 5-substituted 2-(alkylsulfanyl)-4-methylpyrimidin-6(1H)-ones and 2-(propylsulfanyl)- and 5-iodo-2-(propylsulfanyl)-3,4-dihydroquinazolines at 175-185A degrees C under solvent-free conditions unexpectedly afforded benzo[4,5]imidazo[1,2-a]pyrimidine, benzo[4,5]imidazo[2,1-b]-quinazoline, and 2,2'-(benzene-1,2-diyldiimino)bis[pyrimidin-4(3H)-ones]. The described reaction is the first example of synthesis of these heterocyclic systems by fusion of benzimidazole to pyrimidine or quinazoline and is likely to follow ANRORC mechanism.
    DOI:
    10.1134/s1070428016070150
  • 作为产物:
    描述:
    5-苄基-2-巯基-6-甲基嘧啶-4-醇溴丙烷 在 sodium hydroxide 作用下, 以 为溶剂, 反应 15.0h, 以79%的产率得到5-benzyl-6-methyl-2-(propylsulfanyl)pyrimidin-4(3H)-one
    参考文献:
    名称:
    New general synthesis of benzo[4,5]imidazo[1,2-a]pyrimidine and benzo[4,5]imidazo[2,1-b]quinazoline derivatives
    摘要:
    The reactions of benzene-1,2-diamine with 5-substituted 2-(alkylsulfanyl)-4-methylpyrimidin-6(1H)-ones and 2-(propylsulfanyl)- and 5-iodo-2-(propylsulfanyl)-3,4-dihydroquinazolines at 175-185A degrees C under solvent-free conditions unexpectedly afforded benzo[4,5]imidazo[1,2-a]pyrimidine, benzo[4,5]imidazo[2,1-b]-quinazoline, and 2,2'-(benzene-1,2-diyldiimino)bis[pyrimidin-4(3H)-ones]. The described reaction is the first example of synthesis of these heterocyclic systems by fusion of benzimidazole to pyrimidine or quinazoline and is likely to follow ANRORC mechanism.
    DOI:
    10.1134/s1070428016070150
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文献信息

  • New general synthesis of benzo[4,5]imidazo[1,2-a]pyrimidine and benzo[4,5]imidazo[2,1-b]quinazoline derivatives
    作者:A. A. Harutyunyan
    DOI:10.1134/s1070428016070150
    日期:2016.7
    The reactions of benzene-1,2-diamine with 5-substituted 2-(alkylsulfanyl)-4-methylpyrimidin-6(1H)-ones and 2-(propylsulfanyl)- and 5-iodo-2-(propylsulfanyl)-3,4-dihydroquinazolines at 175-185A degrees C under solvent-free conditions unexpectedly afforded benzo[4,5]imidazo[1,2-a]pyrimidine, benzo[4,5]imidazo[2,1-b]-quinazoline, and 2,2'-(benzene-1,2-diyldiimino)bis[pyrimidin-4(3H)-ones]. The described reaction is the first example of synthesis of these heterocyclic systems by fusion of benzimidazole to pyrimidine or quinazoline and is likely to follow ANRORC mechanism.
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