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1,3-dimethyl-5-(2-(2-methylbutyl)benzylidene)pyrimidine-2,4,6(1H,3H,5H)-trione | 1268267-66-8

中文名称
——
中文别名
——
英文名称
1,3-dimethyl-5-(2-(2-methylbutyl)benzylidene)pyrimidine-2,4,6(1H,3H,5H)-trione
英文别名
1,3-Dimethyl-5-[[2-(2-methylbutyl)phenyl]methylidene]-1,3-diazinane-2,4,6-trione
1,3-dimethyl-5-(2-(2-methylbutyl)benzylidene)pyrimidine-2,4,6(1H,3H,5H)-trione化学式
CAS
1268267-66-8
化学式
C18H22N2O3
mdl
——
分子量
314.384
InChiKey
OWAOETPBACGOLY-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):
    3.5
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    57.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1,3-dimethyl-5-(2-(2-methylbutyl)benzylidene)pyrimidine-2,4,6(1H,3H,5H)-trionescandium tris(trifluoromethanesulfonate) 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 24.0h, 以97%的产率得到3-ethyl-1',3,3'-trimethyl-3,4-dihydro-1H,1'H-spiro[naphthalene-2,5'-pyrimidine]-2',4',6'(3'H)-trione
    参考文献:
    名称:
    Expeditious Construction of a Carbobicyclic Skeleton via sp3-C−H Functionalization: Hydride Shift from an Aliphatic Tertiary Position in an Internal Redox Process
    摘要:
    Described herein is the first example of an aliphatic, nonbenzylic hydride shift/cyclization sequence that contains two types of novel sp(3)-C-H functionalization: (1) construction of a tetraline skeleton via [1,5]-hydride shift/cyclization and (2) [1,6]-hydride shift/cyclization to form a five-membered ring (indane derivatives).
    DOI:
    10.1021/ja110520p
  • 作为产物:
    描述:
    邻甲基苯甲酸甲酯manganese(IV) oxide 、 lithium aluminium tetrahydride 、 正丁基锂 作用下, 以 乙醚乙醇正己烷二氯甲烷 为溶剂, 反应 22.25h, 生成 1,3-dimethyl-5-(2-(2-methylbutyl)benzylidene)pyrimidine-2,4,6(1H,3H,5H)-trione
    参考文献:
    名称:
    Expeditious Construction of a Carbobicyclic Skeleton via sp3-C−H Functionalization: Hydride Shift from an Aliphatic Tertiary Position in an Internal Redox Process
    摘要:
    Described herein is the first example of an aliphatic, nonbenzylic hydride shift/cyclization sequence that contains two types of novel sp(3)-C-H functionalization: (1) construction of a tetraline skeleton via [1,5]-hydride shift/cyclization and (2) [1,6]-hydride shift/cyclization to form a five-membered ring (indane derivatives).
    DOI:
    10.1021/ja110520p
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