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3-(2-(hydroxymethyl)-4-methoxyphenyl)-6-methoxyquinazoline-2,4(1H,3H)-dione

中文名称
——
中文别名
——
英文名称
3-(2-(hydroxymethyl)-4-methoxyphenyl)-6-methoxyquinazoline-2,4(1H,3H)-dione
英文别名
3-[2-(hydroxymethyl)-4-methoxyphenyl]-6-methoxy-1H-quinazoline-2,4-dione
3-(2-(hydroxymethyl)-4-methoxyphenyl)-6-methoxyquinazoline-2,4(1H,3H)-dione化学式
CAS
——
化学式
C17H16N2O5
mdl
——
分子量
328.324
InChiKey
JRIRAYLCMMHKLC-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):
    1.2
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    88.1
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    5-甲氧基-2-硝基苯甲酸六甲基磷酰三胺 、 lithium aluminium tetrahydride 、 硫酸 、 palladium 10% on activated carbon 、 氢气 作用下, 以 四氢呋喃甲醇乙腈 为溶剂, 反应 127.0h, 生成 3-(2-(hydroxymethyl)-4-methoxyphenyl)-6-methoxyquinazoline-2,4(1H,3H)-dione
    参考文献:
    名称:
    Concise Synthesis of Dictyoquinazol A via a Dimerisation–Cyclocondensation Sequence
    摘要:
    A two-step total synthesis of the neuroprotective alkaloid, dictyoquinazol A, has been achieved. The brevity of this synthesis was enabled by exploiting the hidden symmetry of the target molecule. Several structural analogues were also prepared using a similar strategy. These results provide a platform for future structure-activity relationship studies in the quest for a novel treatment for stroke.
    DOI:
    10.1055/s-0035-1561569
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文献信息

  • Concise Synthesis of Dictyoquinazol A via a Dimerisation–Cyclocondensation Sequence
    作者:Luke Hunter、Jonatan Wangsahardja、Gabriella Marcolin、Yuvixza Lizarme、Jonathan Morris
    DOI:10.1055/s-0035-1561569
    日期:——
    A two-step total synthesis of the neuroprotective alkaloid, dictyoquinazol A, has been achieved. The brevity of this synthesis was enabled by exploiting the hidden symmetry of the target molecule. Several structural analogues were also prepared using a similar strategy. These results provide a platform for future structure-activity relationship studies in the quest for a novel treatment for stroke.
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