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2a-methyl-4-(trifluoroacetyl)-3,4,5,6-tetrahydro-2aH-2-oxa-4,10b-diazabenzo[a]cyclopenta[cd]azulen-1-one | 1238399-61-5

中文名称
——
中文别名
——
英文名称
2a-methyl-4-(trifluoroacetyl)-3,4,5,6-tetrahydro-2aH-2-oxa-4,10b-diazabenzo[a]cyclopenta[cd]azulen-1-one
英文别名
4-Methyl-6-(2,2,2-trifluoroacetyl)-3-oxa-1,6-diazatetracyclo[7.6.1.04,16.010,15]hexadeca-9(16),10,12,14-tetraen-2-one
2a-methyl-4-(trifluoroacetyl)-3,4,5,6-tetrahydro-2aH-2-oxa-4,10b-diazabenzo[a]cyclopenta[cd]azulen-1-one化学式
CAS
1238399-61-5
化学式
C16H13F3N2O3
mdl
——
分子量
338.286
InChiKey
RFIIFDUJXKQHDZ-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):
    2.8
  • 重原子数:
    24
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    51.5
  • 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

  • 作为产物:
    描述:
    benzyl 5-methylene-3-(trifluoroacetyl)-2,3,4,5-tetrahydroazepino[4,5-b]indole-6(1H)-carboxylate一溴化碘 、 sodium thiosulfate 作用下, 以 二氯甲烷 为溶剂, 以33%的产率得到benzyl 5-methyl-3-(trifluoroacetyl)-2,3-dihydroazepino[4,5-b]indole-6(1H)-carboxylate
    参考文献:
    名称:
    Formation and reactions of azepino[4,5-b]indoles: an unprecedented ozone reaction in the formation of novel benzo[c]naphthyridinones
    摘要:
    在此,我们报告了几种氮杂环[4,5-b]吲哚杂环的形成和有趣的反应性。起初,一个关键的分子内赫克反应被用来有效地生成含有一个外环双键的氮杂环[4,5-b]吲哚七分子环。用臭氧处理烯烃后,通过分子内烯烃捕获,Criegee 中间体发生了前所未有的二级反应,生成了含有桥环过氧化物的苯并[c]萘二酮。
    DOI:
    10.1039/c003742g
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文献信息

  • Formation and reactions of azepino[4,5-b]indoles: an unprecedented ozone reaction in the formation of novel benzo[c]naphthyridinones
    作者:Scott G. Stewart、Emilio L. Ghisalberti、Brian W. Skelton、Charles H. Heath
    DOI:10.1039/c003742g
    日期:——
    Herein we report the formation and interesting reactivity of several azepino[4,5-b]indole heterocycles. Initially, a key intramolecular Heck reaction is used to efficiently create the azepino[4,5-b]indole seven membered ring containing an exocyclic double bond. Treatment of the olefin with ozone results in an unprecedented secondary reaction of the Criegee intermediate, through intramolecular olefin trapping, to afford a benzo[c]naphthyridione containing a bridging cyclic peroxide.
    在此,我们报告了几种氮杂环[4,5-b]吲哚杂环的形成和有趣的反应性。起初,一个关键的分子内赫克反应被用来有效地生成含有一个外环双键的氮杂环[4,5-b]吲哚七分子环。用臭氧处理烯烃后,通过分子内烯烃捕获,Criegee 中间体发生了前所未有的二级反应,生成了含有桥环过氧化物的苯并[c]萘二酮。
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同类化合物

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