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3-benzoyl-1,2-dimethoxybonylindolizine-5-carbaldehyde | 135489-61-1

中文名称
——
中文别名
——
英文名称
3-benzoyl-1,2-dimethoxybonylindolizine-5-carbaldehyde
英文别名
Dimethyl 3-benzoyl-5-formylindolizine-1,2-dicarboxylate
3-benzoyl-1,2-dimethoxybonylindolizine-5-carbaldehyde化学式
CAS
135489-61-1
化学式
C20H15NO6
mdl
——
分子量
365.342
InChiKey
WSEMBJUNEGJODS-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

  • 密度:
    1.30±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    27
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    91.2
  • 氢给体数:
    0
  • 氢受体数:
    6

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-benzoyl-1,2-dimethoxybonylindolizine-5-carbaldehyde 在 sodium cyanoborohydride 、 间氯过氧苯甲酸三氟乙酸酐 作用下, 以 甲醇二氯甲烷甲苯 为溶剂, 反应 1.0h, 生成
    参考文献:
    名称:
    A New Entry to [2.3.4]Cyclazines
    摘要:
    Treatment of 2,3-dihydro-2-methyl-3-phenyl-1H-pyrazino[3,4,5-cd]indolizine 2-oxides (5) with trifluoroacetic anhydride gave new heterocyclic six-membered betaines (6) which underwent 1,3-dipolar cycloaddition reaction with dimethyl acetylenedicarboxylate and maleimides in hot toluene to yield the corresponding cycloadducts (7) and (8). Treatment of the maleimide adducts (8) with p-toluenesulfonic acid in boiling acetic acid gave the [2.3.4]cyclazines (9).
    DOI:
    10.3987/com-91-5665
  • 作为产物:
    参考文献:
    名称:
    A New Entry to [2.3.4]Cyclazines
    摘要:
    Treatment of 2,3-dihydro-2-methyl-3-phenyl-1H-pyrazino[3,4,5-cd]indolizine 2-oxides (5) with trifluoroacetic anhydride gave new heterocyclic six-membered betaines (6) which underwent 1,3-dipolar cycloaddition reaction with dimethyl acetylenedicarboxylate and maleimides in hot toluene to yield the corresponding cycloadducts (7) and (8). Treatment of the maleimide adducts (8) with p-toluenesulfonic acid in boiling acetic acid gave the [2.3.4]cyclazines (9).
    DOI:
    10.3987/com-91-5665
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文献信息

  • A Convenient Synthesis of 3-Benzoylindolizine-5-carbaldehydes
    作者:J. Zhou、Y. Hu、H. Hu
    DOI:10.1080/00397919808004447
    日期:1998.9
    3-Benzoylindolizine-5-carbaldehydes (4a-f), which could be used as derivatization reagents for amino compounds in HPCE were synthesized based on the 1,3-dipolar cycloaddition of 1-phenacyl-2-(1,3-dioxolan-2-yl)pyridinium ylide with alkenes in the presence of TPCD.
  • A New Entry to [2.3.4]Cyclazines
    作者:Yasuyoshi Miki、Hiroko Hachiken、Masami Yoshikawa、Shoji Takemura
    DOI:10.3987/com-91-5665
    日期:——
    Treatment of 2,3-dihydro-2-methyl-3-phenyl-1H-pyrazino[3,4,5-cd]indolizine 2-oxides (5) with trifluoroacetic anhydride gave new heterocyclic six-membered betaines (6) which underwent 1,3-dipolar cycloaddition reaction with dimethyl acetylenedicarboxylate and maleimides in hot toluene to yield the corresponding cycloadducts (7) and (8). Treatment of the maleimide adducts (8) with p-toluenesulfonic acid in boiling acetic acid gave the [2.3.4]cyclazines (9).
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