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4,6,7,8-tetrahydro-7,7-dimethyl-2,4-diphenyl-5(1H)-quinolinone | 130716-55-1

中文名称
——
中文别名
——
英文名称
4,6,7,8-tetrahydro-7,7-dimethyl-2,4-diphenyl-5(1H)-quinolinone
英文别名
7,7-dimethyl-2,4-diphenyl-1,4,5,6,7,8-hexahydroquinoline-5-one;7,7-dimethyl-2,4-diphenyl-4,6,7,8-tetrahydroquinolin-5(1H)-one;7,7-dimethyl-2,4-diphenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline;7,7-dimethyl-5-oxo-2,4-diphenyl-1,4,5,6,7,8-hexahydroquinoline;7,7-dimethyl-2,4-diphenyl-5-oxo-1,4,5,6,7,8-hexahydroquinolin;7,8-dihydro-7,7-dimethyl-2,4-diphenylquinolin-5(1H,4H,6H)-one;7,7-Dimethyl-2,4-diphenyl-1,4,6,8-tetrahydroquinolin-5-one
4,6,7,8-tetrahydro-7,7-dimethyl-2,4-diphenyl-5(1H)-quinolinone化学式
CAS
130716-55-1
化学式
C23H23NO
mdl
——
分子量
329.442
InChiKey
DCKQOTCYLKBLLM-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):
    5
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:cd7bc71162f770cc0a8326549c8c45ca
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反应信息

  • 作为反应物:
    描述:
    4,6,7,8-tetrahydro-7,7-dimethyl-2,4-diphenyl-5(1H)-quinolinonesodium acetate4-氯苯甲醛 作用下, 以 溶剂黄146 为溶剂, 反应 8.0h, 以59%的产率得到7,8-dihydro-7,7-dimethyl-2,4-diphenyl-5(6H)-quinolinone
    参考文献:
    名称:
    对位取代的苯甲醛作为对苯二酚的氧化芳构化的权宜试剂
    摘要:
    四氢-5(1 H)-喹啉酮与对位取代的苯甲醛在碱存在下的Cannizzaro型反应形成相应的喹啉和芳基甲醇而不是亚芳基衍生物,因为四氢喹啉被氧化并由于从四氢喹啉到芳醛的前所未有的氢化物转移。在具有+ M效应的取代基参与底物分子的过程中,反应进行得最好。
    DOI:
    10.1002/jhet.1117
  • 作为产物:
    描述:
    3-hydroxy-5,5-dimethyl-2-(1',3'-diphenyl-1'-oxopropan-3'-yl)cyclohex-2-en-1-one 在 ammonium acetate 、 溶剂黄146 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以45%的产率得到4,6,7,8-tetrahydro-7,7-dimethyl-2,4-diphenyl-5(1H)-quinolinone
    参考文献:
    名称:
    Pati, Anita; Majumdar, Poulomi; Garnayak, Sarita, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2014, vol. 53, # 4, p. 384 - 391
    摘要:
    DOI:
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文献信息

  • Efficient synthesis of 2,4-diaryl hexahydroquinoline-5-one derivatives in the presence of triethylamine
    作者:Zahed Karimi-Jaberi、Maryam Azadi
    DOI:10.1007/s11164-014-1773-8
    日期:2015.9
    A convenient and efficient protocol for the synthesis of 2,4-diaryl hexahydroquinoline-5-one derivatives has been accomplished by a three-component reaction of 1,3-diaryl-2-propen-1-ones, dimedone and ammonium acetate catalyzed by triethylamine under solvent-free conditions. The simple experimental procedure, use of an inexpensive catalyst, short reaction times, and excellent yields make this procedure
    一种方便有效的合成2,4-二芳基六氢喹啉-5-酮衍生物的方案是通过1,3-二芳基-2-丙烯-1-酮,二甲酮和乙酸铵的三组分反应催化的。三乙胺在无溶剂条件下使用。简单的实验程序,使用廉价的催化剂,短的反应时间和优异的收率使得该程序容易,实用和可持续。
  • Silica-supported perchloric acid (HClO4–SiO2): a mild, reusable and highly efficient heterogeneous catalyst for multicomponent synthesis of 1,4-dihydropyridines via unsymmetrical Hantzsch reaction
    作者:Syed Sheik Mansoor、Krishnamoorthy Aswin、Kuppan Logaiya、Prasanna Nitiya Sudhan、Saleem Malik
    DOI:10.1007/s11164-012-0968-0
    日期:2014.1
    Facile synthesis of some 1,4-dihydropyridine derivatives via Hantzsch reaction of 5,5-dimethyl-1,3-cyclohexanedione (dimedone), 1,3-diphenyl-2-propen-1-one derivatives and ammonium acetate under solvent-free condition in the presence of silica-supported perchloric acid (HClO4–SiO2) is described. The catalyst is easily prepared, stable, reusable and efficient under the reaction conditions.
    在无溶剂的情况下,通过5,5-二甲基-1,3-环己二酮(二甲酮),1,3-二苯基-2-丙烯-1-酮衍生物和乙酸铵的汉茨反应轻松合成某些1,4-二氢吡啶衍生物描述了在二氧化硅负载的高氯酸(HClO 4 -SiO 2)存在的条件下。该催化剂在反应条件下易于制备,稳定,可重复使用和有效。
  • A CONVENIENT SYNTHESIS OF 2,4-DIARYLPOLYHYDROQUINOLINE DERIVATIONS IN THE PRESENCE OF AMMONIUM ACETATE
    作者:Xiang-Shan Wang、Da-Qing Shi、Shu-Jiang Tu
    DOI:10.1081/scc-120014775
    日期:2002.1
    5-oxo-1,2,3,4,5,6,7,8-octahydroquinoline derivatives have been synthesized from 5,5-dimethyl-1,3-cyclohexane-dione (dimedone) and 1,3-diaryl-2-propen-1-one in DMF at 80°C in the presence of ammonium acetate with high yields (64–98%), the structure of the product was confirmed by X-ray analysis.
    摘要 从 5,5-二甲基-1,3-环己二酮(二甲酮)和 1, 合成了一系列取代的 5-氧代-1,2,3,4,5,6,7,8-八氢喹啉衍生物。 3-diaryl-2-propen-1-one 在 DMF 中于 80°C 在乙酸铵存在下以高产率 (64–98%),通过 X 射线分析证实了产物的结构。
  • Photo-oxidative aromatization and photo-rearrangement of 2, 4-diaryl-5-oxohexahydroquinolines
    作者:Fatemeh Abdollahi Rizi、Hamid R. Memarian、Hadi Amiri Rudbari、Olivier Blacque
    DOI:10.1016/j.jphotochem.2023.115414
    日期:2024.4
    radical intermediate was supported by the results of the experimental works and the DFT-computational studies. X-ray crystal structure analysis of two of 5-oxohexahydroquinoline compounds indicated that i). The C4-aryl ring occupies the pseudo-axial position of the twisted-boat conformation of the heterocyclic dihydropyridine ring and, ii). Owing to the steric ortho-repulsion, the C2-aryl ring has a non-planar
    合成了各种2,4-双芳基取代的5-氧代六氢喹啉,并研究了2-和4-取代对这些化合物的光化学行为的电子效应。这些化合物的紫外光照射导致发生两种类型的光反应:氧化 正常的光氧化和光重排反应。在这两个反应中,均观察到杂环1,4-二氢吡啶环芳构化为吡啶环。光化学结果表明自由基中间体的参与,负责芳环迁移和光重排反应的发生。实验工作和DFT计算研究的结果支持了所涉及的自由基中间体的捕获自由基稳定化的部分协同效应。两种5-氧代六氢喹啉化合物的X射线晶体结构分析表明i ) 。C 4 -芳基环占据杂环二氢吡啶环的扭船构象的假轴位置,并且, ii )。由于空间邻位排斥,C 2 -芳基环具有关于杂环的连接的C C 双键的非平面取向。这些观察结果与 DFT 计算研究和 X 射线晶体结构分析的数据非常一致。
  • Design and synthesis of 2,4-disubstituted polyhydroquinolines as prospective antihyperglycemic and lipid modulating agents
    作者:Atul Kumar、Siddharth Sharma、Vishwa Deepak Tripathi、Ram Awatar Maurya、Swayam Prakash Srivastava、Gitika Bhatia、A.K. Tamrakar、Arvind Kumar Srivastava
    DOI:10.1016/j.bmc.2009.11.061
    日期:2010.6.1
    A series of 2,4-disubstituted polyhydroquinoline were synthesized and evaluated for their in vivo antihyperglycemic as well as antidyslipidemic activities. Several synthesized compounds have exhibited promising in vivo antihyperglycemic in SLM, STZ-S, and db/db mice model along with significant lipid and TG modulating activity. All these compounds were evaluated in various in vitro models of diabetes to know the possible mechanism of their antihyperglycemic action. Interestingly, compounds 3a-r (diaryl substitution) have exhibited promising protein-tyrosine phosphatase 1B (PTP1B) inhibitory activity whereas, compounds 5a-d (acid substituted) have shown significant glycogen phosphorylase activity. (C) 2009 Published by Elsevier Ltd.
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