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2-(hydroxymethyl)-6-methyl-1,2,3,7-tetrahydroimidazo[1,2-a]pyrimidin-7-one | 315186-70-0

中文名称
——
中文别名
——
英文名称
2-(hydroxymethyl)-6-methyl-1,2,3,7-tetrahydroimidazo[1,2-a]pyrimidin-7-one
英文别名
N2,3'-anhydro-1-(2,3-dihydroxypropyl)-5-methylisocytosine;2-(hydroxymethyl)-6-methyl-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-7-one
2-(hydroxymethyl)-6-methyl-1,2,3,7-tetrahydroimidazo[1,2-a]pyrimidin-7-one化学式
CAS
315186-70-0
化学式
C8H11N3O2
mdl
——
分子量
181.194
InChiKey
ADODTNCMYYJHPU-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):
    -1.4
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    64.9
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    乙酸酐2-(hydroxymethyl)-6-methyl-1,2,3,7-tetrahydroimidazo[1,2-a]pyrimidin-7-one吡啶 作用下, 反应 16.0h, 以82.2%的产率得到(1-acetyl-6-methyl-7-oxo-1,2,3,7-tetrahydroimidazo[1,2-a]pyrimidin-2-yl)methyl acetate
    参考文献:
    名称:
    The Synthesis of Novel 6,5- and 6,6-Membered Fused Heterocyclic Compounds Derived from Thymine
    摘要:
    Novel pyrimido[1,2-a]pyrimidinones 14, 15 and 16 and imidazo[1,2-a] pyrimidinones 19 and 20, designed as conformationally constrained analogues of 1-(3-amino-2-hydroxypropyl)thymine and 1-(2-amino-3-hydroxypropyl)thymine, respective ly, were synthesized by the ring-opening/ ring-closure rearrangement of the corresponding byciclic oxygen-containing amino compounds 12 and 17.
    DOI:
    10.1080/15257770008033849
  • 作为产物:
    参考文献:
    名称:
    The Synthesis of Novel 6,5- and 6,6-Membered Fused Heterocyclic Compounds Derived from Thymine
    摘要:
    Novel pyrimido[1,2-a]pyrimidinones 14, 15 and 16 and imidazo[1,2-a] pyrimidinones 19 and 20, designed as conformationally constrained analogues of 1-(3-amino-2-hydroxypropyl)thymine and 1-(2-amino-3-hydroxypropyl)thymine, respective ly, were synthesized by the ring-opening/ ring-closure rearrangement of the corresponding byciclic oxygen-containing amino compounds 12 and 17.
    DOI:
    10.1080/15257770008033849
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