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methyl 10H-azepino<1,2-a>indole-8-carboxylate | 76293-08-8

中文名称
——
中文别名
——
英文名称
methyl 10H-azepino<1,2-a>indole-8-carboxylate
英文别名
methyl 10H-azepino[1,2-a]indole-8-carboxylate
methyl 10H-azepino<1,2-a>indole-8-carboxylate化学式
CAS
76293-08-8
化学式
C15H13NO2
mdl
——
分子量
239.274
InChiKey
IDVRKLPZFWXRMP-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):
    2.9
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    31.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    methyl 2-azidodiphenylmethane-4'-carboxylate 以34%的产率得到
    参考文献:
    名称:
    HAYES P. C.; JONES G., J. CHEM. SOC. CHEM. COMMUN., 1980, NO 17, 844
    摘要:
    DOI:
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文献信息

  • Intramolecular nitrene insertions into aromatic and heteroaromatic systmes. Part 7. Insertions into electron-deficient rings
    作者:Robert N. Carde、Peter C. Hayes、Gurnos Jones、Cynthia J. Cliff
    DOI:10.1039/p19810001132
    日期:——
    thermolysis at 200 °C gave azepino-indoles (48) and (51), the first examples of ring expansion by an arylnitrene of benzene rings with electron-with drawing substituents. Also reported are syntheses of 3- and 4-(2-azidobenzyl)pyridines (38) and (39), and of 2-(2-azidobenzyl)thiazole (40); decomposition of these azides gave mainly polymers.
    描述了许多制备邻氨基三苯基甲烷的途径,其中一个苯环或两个苯环带有潜在的酯基。最有用的合成子显示为1,3-二恶烷-2-基取代基,并使用该2-氨基二苯基甲烷4'-羧酸甲酯(18)和2-氨基三苯基甲烷-4',4''-二羧酸二甲酯(28 )已经准备好了。在200°C下热分解时,来自这些化合物(19)和(29)的叠氮化物产生了氮杂环庚烷-吲哚(48)和(51),这是苯环的芳基亚硝基苯带有带吸电子取代基的芳环扩大的第一个例子。还报道了3-和4-(2-叠氮基苄基)吡啶(38)和(39),以及2-(2-叠氮基苄基)噻唑(40)的合成。这些叠氮化物的分解主要得到聚合物。
  • CARDE R. N.; HAYES P. C.; JONES G.; CLIFF C. J., J. CHEM. SOC. PERKIN TRANS., PART 1, 1981, NO 4, 1132-1142
    作者:CARDE R. N.、 HAYES P. C.、 JONES G.、 CLIFF C. J.
    DOI:——
    日期:——
  • Hayes, Peter C.; Jones, Gurnos, Journal of the Chemical Society Chemical Communications, 1980, # 17, p. 844
    作者:Hayes, Peter C.、Jones, Gurnos
    DOI:——
    日期:——
  • HAYES P. C.; JONES G., J. CHEM. SOC. CHEM. COMMUN., 1980, NO 17, 844
    作者:HAYES P. C.、 JONES G.
    DOI:——
    日期:——
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