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8-chloro-10-(2-nitrophenyl)-5H-dibenzo[b,e][1,4]diazepin-11(10H)-one | 1628347-78-3

中文名称
——
中文别名
——
英文名称
8-chloro-10-(2-nitrophenyl)-5H-dibenzo[b,e][1,4]diazepin-11(10H)-one
英文别名
3-chloro-5-(2-nitrophenyl)-11H-benzo[b][1,4]benzodiazepin-6-one
8-chloro-10-(2-nitrophenyl)-5H-dibenzo[b,e][1,4]diazepin-11(10H)-one化学式
CAS
1628347-78-3
化学式
C19H12ClN3O3
mdl
——
分子量
365.776
InChiKey
SEGQSUPYDOCDON-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):
    4.6
  • 重原子数:
    26
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    78.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    8-chloro-10-(2-nitrophenyl)-5H-dibenzo[b,e][1,4]diazepin-11(10H)-one铁粉溶剂黄146 作用下, 反应 6.0h, 以87%的产率得到12-chloro-8,15,22-triazapentacyclo[13.7.0.02,7.09,14.016,21]docosa-1(22),2,4,6,9(14),10,12,16(21),17,19-decaene
    参考文献:
    名称:
    Dibenzodiazepinones的合成通过串联铜(I) -催化CN键的形成
    摘要:
    AbstractAn efficient, one‐pot method for the synthesis of dibenzodiazepinone derivatives involving copper‐catalyzed tandem CN bond formation is reported. The use of various halo amide and 2‐iodoaniline derivatives permitted the synthesis of an array of dibenzodiazepinone derivatives in moderate to good yields. Moreover, a dibenzodiazepinone derivative {2‐(11‐oxo‐5H‐dibenzo[b,e][1,4]diazepin‐10(11H)‐yl)benzonitrile} was utilized to synthesize the triazapentacyclic ring derivative {12‐chloro‐ 8,15,22‐triazapentacyclo[13.7.0.02,7.09,14.016,21]docosa‐1(22),2,4,6,9(14),10,12,16(21),17,19‐decaene}.magnified image
    DOI:
    10.1002/adsc.201301020
  • 作为产物:
    参考文献:
    名称:
    Dibenzodiazepinones的合成通过串联铜(I) -催化CN键的形成
    摘要:
    AbstractAn efficient, one‐pot method for the synthesis of dibenzodiazepinone derivatives involving copper‐catalyzed tandem CN bond formation is reported. The use of various halo amide and 2‐iodoaniline derivatives permitted the synthesis of an array of dibenzodiazepinone derivatives in moderate to good yields. Moreover, a dibenzodiazepinone derivative {2‐(11‐oxo‐5H‐dibenzo[b,e][1,4]diazepin‐10(11H)‐yl)benzonitrile} was utilized to synthesize the triazapentacyclic ring derivative {12‐chloro‐ 8,15,22‐triazapentacyclo[13.7.0.02,7.09,14.016,21]docosa‐1(22),2,4,6,9(14),10,12,16(21),17,19‐decaene}.magnified image
    DOI:
    10.1002/adsc.201301020
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文献信息

  • Synthesis of Dibenzodiazepinones<i>via</i>Tandem Copper(I)- Catalyzed CN Bond Formation
    作者:Sachin D. Gawande、Veerababurao Kavala、Manoj R. Zanwar、Chun-Wei Kuo、Wen-Chang Huang、Ting-Shen Kuo、Hsiu-Ni Huang、Chiu-Hui He、Ching-Fa Yao
    DOI:10.1002/adsc.201301020
    日期:2014.8.11
    AbstractAn efficient, one‐pot method for the synthesis of dibenzodiazepinone derivatives involving copper‐catalyzed tandem CN bond formation is reported. The use of various halo amide and 2‐iodoaniline derivatives permitted the synthesis of an array of dibenzodiazepinone derivatives in moderate to good yields. Moreover, a dibenzodiazepinone derivative 2‐(11‐oxo‐5H‐dibenzo[b,e][1,4]diazepin‐10(11H)‐yl)benzonitrile} was utilized to synthesize the triazapentacyclic ring derivative 12‐chloro‐ 8,15,22‐triazapentacyclo[13.7.0.02,7.09,14.016,21]docosa‐1(22),2,4,6,9(14),10,12,16(21),17,19‐decaene}.magnified image
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