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3,5-diacetyl-4-(4-methoxyphenyl)-1-methyl-1,4-dihydropyridine | 212623-28-4

中文名称
——
中文别名
——
英文名称
3,5-diacetyl-4-(4-methoxyphenyl)-1-methyl-1,4-dihydropyridine
英文别名
1-[5-acetyl-4-(4-methoxyphenyl)-1-methyl-4H-pyridin-3-yl]ethanone
3,5-diacetyl-4-(4-methoxyphenyl)-1-methyl-1,4-dihydropyridine化学式
CAS
212623-28-4
化学式
C17H19NO3
mdl
——
分子量
285.343
InChiKey
YJWKIERZITWKFT-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):
    1.6
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    46.6
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    3,5-diacetyl-4-(4-methoxyphenyl)-1-methyl-1,4-dihydropyridine吡啶高氯酸 作用下, 以 1,4-二氧六环 为溶剂, 反应 50.0h, 生成 Acetic acid (4S,4aR,9aR)-3,4a-diacetyl-4-(4-methoxy-phenyl)-1-methyl-1,4,4a,9a-tetrahydro-benzo[4,5]furo[2,3-b]pyridin-6-yl ester
    参考文献:
    名称:
    Novel Synthesis of Polyfunctionalized 1,4,4a,9a-Tetrahydro-1-aza-9-oxafluorenes by Unexpected Cycloaddition of 4-(4-Methoxyphenyl)-1,4-dihydropyridines and p-Benzoquinone
    摘要:
    A surprising acid-catalysed cycloaddition reaction occurs between 3,5-diacetyl-4-(4-methoxyphenyl)-1,4-dihydropyridine (4) and p-benzoquinone in dioxane/HClO4 (5%) yielding novel polyfunctionalized 1,4,4a,9a-tetrahydro-1-aza-9-oxafluorenes (9) as exclusive products. On the other hand the corresponding 4-unsubstituted 1,4-dihydropyridine (1) is oxidized by p-benzoquinone. Novel structures are characterized by standard spectroscopy and, furthermore, confirmed by acetylation. The different reactivity of the 4-substituted and 4-unsubstituted derivatives is dicussed on the basis of semiempirical MNDO calculations and redox potentials.
    DOI:
    10.3987/com-98-8189
  • 作为产物:
    描述:
    4-甲氧基苯甲醛 、 alkaline earth salt of/the/ methylsulfuric acid 在 碳酸氢铵 、 sodium hydride 作用下, 以 乙醇 为溶剂, 反应 9.0h, 生成 3,5-diacetyl-4-(4-methoxyphenyl)-1-methyl-1,4-dihydropyridine
    参考文献:
    名称:
    Novel Synthesis of Polyfunctionalized 1,4,4a,9a-Tetrahydro-1-aza-9-oxafluorenes by Unexpected Cycloaddition of 4-(4-Methoxyphenyl)-1,4-dihydropyridines and p-Benzoquinone
    摘要:
    A surprising acid-catalysed cycloaddition reaction occurs between 3,5-diacetyl-4-(4-methoxyphenyl)-1,4-dihydropyridine (4) and p-benzoquinone in dioxane/HClO4 (5%) yielding novel polyfunctionalized 1,4,4a,9a-tetrahydro-1-aza-9-oxafluorenes (9) as exclusive products. On the other hand the corresponding 4-unsubstituted 1,4-dihydropyridine (1) is oxidized by p-benzoquinone. Novel structures are characterized by standard spectroscopy and, furthermore, confirmed by acetylation. The different reactivity of the 4-substituted and 4-unsubstituted derivatives is dicussed on the basis of semiempirical MNDO calculations and redox potentials.
    DOI:
    10.3987/com-98-8189
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文献信息

  • Novel Synthesis of Polyfunctionalized 1,4,4a,9a-Tetrahydro-1-aza-9-oxafluorenes by Unexpected Cycloaddition of 4-(4-Methoxyphenyl)-1,4-dihydropyridines and p-Benzoquinone
    作者:Andreas Hilgeroth、Krystina Kuna、Uwe Kuckländer
    DOI:10.3987/com-98-8189
    日期:——
    A surprising acid-catalysed cycloaddition reaction occurs between 3,5-diacetyl-4-(4-methoxyphenyl)-1,4-dihydropyridine (4) and p-benzoquinone in dioxane/HClO4 (5%) yielding novel polyfunctionalized 1,4,4a,9a-tetrahydro-1-aza-9-oxafluorenes (9) as exclusive products. On the other hand the corresponding 4-unsubstituted 1,4-dihydropyridine (1) is oxidized by p-benzoquinone. Novel structures are characterized by standard spectroscopy and, furthermore, confirmed by acetylation. The different reactivity of the 4-substituted and 4-unsubstituted derivatives is dicussed on the basis of semiempirical MNDO calculations and redox potentials.
  • Novel functionalized 1,4,4a,9a-tetrahydro-1-aza-9-oxafluorenes by cycloaddition of 4-(4-methoxyphenyl)-1,4-dihydropyridines and<i>p</i>-benzoquinone
    作者:Andreas Hilgeroth、Krystina Kuna、Uwe Kuckländer
    DOI:10.1002/jhet.5570350310
    日期:1998.5
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