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6-amino-11-(3-chlorophenyl)-11,12-dihydropyrido[3,4-c][1,9]-phenanthroline | 1401971-61-6

中文名称
——
中文别名
——
英文名称
6-amino-11-(3-chlorophenyl)-11,12-dihydropyrido[3,4-c][1,9]-phenanthroline
英文别名
5-(3-Chlorophenyl)-5,6-dihydropyrido[3,4-c][1,9]phenanthrolin-12-amine;5-(3-chlorophenyl)-5,6-dihydropyrido[3,4-c][1,9]phenanthrolin-12-amine
6-amino-11-(3-chlorophenyl)-11,12-dihydropyrido[3,4-c][1,9]-phenanthroline化学式
CAS
1401971-61-6
化学式
C21H15ClN4
mdl
——
分子量
358.83
InChiKey
USMWZMSXFUVPLM-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):
    3.7
  • 重原子数:
    26
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    64.7
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-氰基-4-甲基吡啶3-氯苯甲醛potassium tert-butylate 作用下, 反应 2.5h, 以32%的产率得到6-amino-11-(3-chlorophenyl)-11,12-dihydropyrido[3,4-c][1,9]-phenanthroline
    参考文献:
    名称:
    Synthesis and physicochemical characterization of novel 6-aminopyrido[3,4-c][1,9]phenanthrolines as aza-analogs of benzo[c]phenanthridines
    摘要:
    Based on the 6-aminobenzo[c]phenanthridines, a compound class showing noteworthy antitumor activity, an efficient one-step synthesis consisting of a base-catalyzed condensation of 2 equiv of 4-methylpyridine-3-carbonitrile and various aldehydes causing twofold ring closure is described. The obtained 6-amino-11,12-dihydropyrido[3,4-c][1,9]phenanthrolines could be aromatized with Pd/C at high temperatures to form 6-aminopyrido[3,4-c][1,9]phenanthrolines. All compounds were systematically characterized regarding both lipophilicity and solubility and a high cytotoxic potential was evaluated in preliminary in vitro studies. Compared to formerly described 6-aminobenzo[c]phenanthridines our newly developed phenanthrolines turned out to possess improved drugability, due to significantly increased water-solubility and decreased lipophilicity. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.08.047
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文献信息

  • Pyrido-phenanthroline derivatives, production and use thereof as medicaments
    申请人:Christian-Albrechts-Universitat Zu Kiel
    公开号:US11046693B2
    公开(公告)日:2021-06-29
    The invention relates to novel pyrido-phenanthroline derivatives, to the production and use thereof in the field of medicine, in particular for cancer therapy.
    本发明涉及新型吡啶-菲罗啉衍生物,以及其在医药领域,特别是癌症治疗领域的生产和使用。
  • NOVEL PYRIDO-PHENANTHROLINE DERIVATIVES, PRODUCTION AND USE THEREOF AS MEDICAMENTS
    申请人:Christian-Albrechts-Universitat Zu Kiel
    公开号:US20190292184A1
    公开(公告)日:2019-09-26
    The invention relates to novel pyrido-phenanthroline derivatives, to the production and use thereof in the field of medicine, in particular for cancer therapy.
  • Synthesis and physicochemical characterization of novel 6-aminopyrido[3,4-c][1,9]phenanthrolines as aza-analogs of benzo[c]phenanthridines
    作者:Christopher Meier、Joscha Kotthaus、Lars Stenzel、Ulrich Girreser、Dieter Heber、Bernd Clement
    DOI:10.1016/j.tet.2012.08.047
    日期:2012.11
    Based on the 6-aminobenzo[c]phenanthridines, a compound class showing noteworthy antitumor activity, an efficient one-step synthesis consisting of a base-catalyzed condensation of 2 equiv of 4-methylpyridine-3-carbonitrile and various aldehydes causing twofold ring closure is described. The obtained 6-amino-11,12-dihydropyrido[3,4-c][1,9]phenanthrolines could be aromatized with Pd/C at high temperatures to form 6-aminopyrido[3,4-c][1,9]phenanthrolines. All compounds were systematically characterized regarding both lipophilicity and solubility and a high cytotoxic potential was evaluated in preliminary in vitro studies. Compared to formerly described 6-aminobenzo[c]phenanthridines our newly developed phenanthrolines turned out to possess improved drugability, due to significantly increased water-solubility and decreased lipophilicity. (C) 2012 Elsevier Ltd. All rights reserved.
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