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14-(4-acetoxy-3-methoxyphenyl)-3-acetoxy-2,10,11,12-tetramethoxy-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one | 97614-67-0

中文名称
——
中文别名
——
英文名称
14-(4-acetoxy-3-methoxyphenyl)-3-acetoxy-2,10,11,12-tetramethoxy-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one
英文别名
lamellarin B diacetate
14-(4-acetoxy-3-methoxyphenyl)-3-acetoxy-2,10,11,12-tetramethoxy-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one化学式
CAS
97614-67-0
化学式
C34H29NO11
mdl
——
分子量
627.604
InChiKey
VREUBVREFDWSPH-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

物化性质

  • 熔点:
    >250 °C(Solvent: Ethyl acetate; Hexane)
  • 密度:
    1.37±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.91
  • 重原子数:
    46.0
  • 可旋转键数:
    8.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    133.37
  • 氢给体数:
    0.0
  • 氢受体数:
    12.0

反应信息

  • 作为反应物:
    描述:
    14-(4-acetoxy-3-methoxyphenyl)-3-acetoxy-2,10,11,12-tetramethoxy-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one氢氧化钾 作用下, 以 乙醇 为溶剂, 以95%的产率得到14-(4-hydroxy-3-methoxyphenyl)-3-hydroxy-2,10,11,12-tetramethoxy-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one
    参考文献:
    名称:
    Total Synthesis of Natural and Unnatural Lamellarins with Saturated and Unsaturated D-Rings
    摘要:
    Twenty-eight natural and unnatural lamellarins with either a saturated or an unsaturated D-ring were synthesized according to our developed synthetic route. The key step involved the Michael addition/ring closure (Mi-RC) of the benzyldihydroisoquinoline and alpha-nitrocinnamate derivatives, which provided the 2-carboethoxypyrrole intermediates in moderate to good yields (up to 78% yield). Subsequent hydrogenolysis/lactonization furnished lamellarins with a saturated D-ring in excellent yields (up to 93% yield). DDQ oxidation of the saturated lamellarin acetates led directly to the corresponding unsaturated analogues in 54-95% yield. In addition, only two steps in our developed strategy require column chromatography.
    DOI:
    10.1021/jo061810h
  • 作为产物:
    描述:
    (E)-1,2,3-trimethoxy-4-(2-nitrovinyl)benzene 在 palladium on activated charcoal 4-二甲氨基吡啶 、 lithium aluminium tetrahydride 、 氢气 、 sodium hydride 、 碳酸氢钠sodium carbonate三乙胺2,3-二氯-5,6-二氰基-1,4-苯醌三氯氧磷 作用下, 以 四氢呋喃二氯甲烷乙酸乙酯N,N-二甲基甲酰胺乙腈 为溶剂, 20.0 ℃ 、517.11 kPa 条件下, 反应 51.0h, 生成 14-(4-acetoxy-3-methoxyphenyl)-3-acetoxy-2,10,11,12-tetramethoxy-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one
    参考文献:
    名称:
    Total Synthesis of Natural and Unnatural Lamellarins with Saturated and Unsaturated D-Rings
    摘要:
    Twenty-eight natural and unnatural lamellarins with either a saturated or an unsaturated D-ring were synthesized according to our developed synthetic route. The key step involved the Michael addition/ring closure (Mi-RC) of the benzyldihydroisoquinoline and alpha-nitrocinnamate derivatives, which provided the 2-carboethoxypyrrole intermediates in moderate to good yields (up to 78% yield). Subsequent hydrogenolysis/lactonization furnished lamellarins with a saturated D-ring in excellent yields (up to 93% yield). DDQ oxidation of the saturated lamellarin acetates led directly to the corresponding unsaturated analogues in 54-95% yield. In addition, only two steps in our developed strategy require column chromatography.
    DOI:
    10.1021/jo061810h
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文献信息

  • Metabolites of the marine prosobranch mollusk Lamellaria sp
    作者:Raymond J. Andersen、D. John Faulkner、Cun Heng He、Gregory D. Van Duyne、Jon Clardy
    DOI:10.1021/ja00305a027
    日期:1985.9
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