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5-(2-hydroxy-4,4-dimethyl-6-oxocyclohexen-1-yl)-1-methyl-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-dione | 1253375-43-7

中文名称
——
中文别名
——
英文名称
5-(2-hydroxy-4,4-dimethyl-6-oxocyclohexen-1-yl)-1-methyl-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-dione
英文别名
——
5-(2-hydroxy-4,4-dimethyl-6-oxocyclohexen-1-yl)-1-methyl-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-dione化学式
CAS
1253375-43-7
化学式
C21H21N3O4
mdl
——
分子量
379.415
InChiKey
AFNLXHPACHZBOX-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):
    2.2
  • 重原子数:
    28
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    103
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    6-氨基-1-甲基尿嘧啶 、 3-Hydroxy-2-[1-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-2-oxo-2-phenylethyl]-5,5-dimethylcyclohex-2-en-1-on 在 溶剂黄146 作用下, 以 乙醇 为溶剂, 反应 9.0h, 生成 5-(2-hydroxy-4,4-dimethyl-6-oxocyclohexen-1-yl)-1-methyl-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-dione
    参考文献:
    名称:
    Generation of pyrrolo[2,3-d]pyrimidines. Unexpected products in the multicomponent reaction of 6-aminopyrimidines, dimedone, and arylglyoxal
    摘要:
    A series of 6-aryl-5-(1-cyclohexen-1-yl)pyrrolo[2,3-d]pyrimidines 9a-q were obtained by the three-component reaction between 6-aminopyrimidines 6, 7, 8, dimedone 2, and arylglyoxal 5a,b. The unexpected cyclization process was established by NMR and X-ray diffraction measurements. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.08.021
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文献信息

  • Generation of pyrrolo[2,3-d]pyrimidines. Unexpected products in the multicomponent reaction of 6-aminopyrimidines, dimedone, and arylglyoxal
    作者:Jairo Quiroga、Paola A. Acosta、Silvia Cruz、Rodrigo Abonía、Braulio Insuasty、Manuel Nogueras、Justo Cobo
    DOI:10.1016/j.tetlet.2010.08.021
    日期:2010.10
    A series of 6-aryl-5-(1-cyclohexen-1-yl)pyrrolo[2,3-d]pyrimidines 9a-q were obtained by the three-component reaction between 6-aminopyrimidines 6, 7, 8, dimedone 2, and arylglyoxal 5a,b. The unexpected cyclization process was established by NMR and X-ray diffraction measurements. (C) 2010 Elsevier Ltd. All rights reserved.
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