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7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridine | 1260252-92-3

中文名称
——
中文别名
——
英文名称
7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridine
英文别名
7-chloro-6,13-dihydro-5H-indolo[3,2-c]acridine
7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridine化学式
CAS
1260252-92-3
化学式
C19H13ClN2
mdl
——
分子量
304.779
InChiKey
OEKZRVLAFKHZAK-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):
    4.9
  • 重原子数:
    22
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    28.7
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridine 在 5% Pd(II)/C(eggshell) 作用下, 以 二苯醚 为溶剂, 反应 4.0h, 以31%的产率得到13H-indolo[3,2-c]acridine
    参考文献:
    名称:
    Simple and Convenient Methods for the Synthesis of Indolo[3,2-c]acridines
    摘要:
    The reaction of 2,3,4,9-tetrahydro-1H-carbazol-1-ones with anthranilic acid in POCl3 yielded 7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridines, while the same on reaction with isatin under the Pfitzinger reaction condition yielded 5,6-dihydro-13H-indolo[3,2-c]acridine-7-carboxylic acids. The latter reaction was carried out in different basic condition, because of, NaOH yielded more yield instead of KOH. Both the obtained products were treated with Pd/C in diphenyl ether to yield 13H-Indolo[3,2-c]acridines.
    DOI:
    10.1080/00397910903457365
  • 作为产物:
    描述:
    2,3,4,9-四氢-1H-咔唑-1-酮邻氨基苯甲酸三氯氧磷 、 sodium hydroxide 作用下, 以 为溶剂, 反应 48.0h, 以40%的产率得到7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridine
    参考文献:
    名称:
    Simple and Convenient Methods for the Synthesis of Indolo[3,2-c]acridines
    摘要:
    The reaction of 2,3,4,9-tetrahydro-1H-carbazol-1-ones with anthranilic acid in POCl3 yielded 7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridines, while the same on reaction with isatin under the Pfitzinger reaction condition yielded 5,6-dihydro-13H-indolo[3,2-c]acridine-7-carboxylic acids. The latter reaction was carried out in different basic condition, because of, NaOH yielded more yield instead of KOH. Both the obtained products were treated with Pd/C in diphenyl ether to yield 13H-Indolo[3,2-c]acridines.
    DOI:
    10.1080/00397910903457365
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文献信息

  • Simple and Convenient Methods for the Synthesis of Indolo[3,2-<i>c</i>]acridines
    作者:Kumaresan Prabakaran、Karnam Jayarampillai Rajendra Prasad
    DOI:10.1080/00397910903457365
    日期:2010.11.3
    The reaction of 2,3,4,9-tetrahydro-1H-carbazol-1-ones with anthranilic acid in POCl3 yielded 7-chloro-5,6-dihydro-13H-indolo[3,2-c]acridines, while the same on reaction with isatin under the Pfitzinger reaction condition yielded 5,6-dihydro-13H-indolo[3,2-c]acridine-7-carboxylic acids. The latter reaction was carried out in different basic condition, because of, NaOH yielded more yield instead of KOH. Both the obtained products were treated with Pd/C in diphenyl ether to yield 13H-Indolo[3,2-c]acridines.
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