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10-(4-chlorophenyl)-9-(4-methylphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridin-1,8-dione | 141076-61-1

中文名称
——
中文别名
——
英文名称
10-(4-chlorophenyl)-9-(4-methylphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridin-1,8-dione
英文别名
10-(4-chlorophenyl)-3,3,6,6-tetramethyl-9-(p-tolyl)-3,4,6,7,9,10-hexahydroacridine-1,8(2H,5H)-dione;10-(4-chlorophenyl)-3,3,6,6-tetramethyl-9-(4-methylphenyl)-4,5,7,9-tetrahydro-2H-acridine-1,8-dione
10-(4-chlorophenyl)-9-(4-methylphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridin-1,8-dione化学式
CAS
141076-61-1
化学式
C30H32ClNO2
mdl
——
分子量
474.043
InChiKey
YFSMPARABLBVKN-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):
    6.7
  • 重原子数:
    34
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    10取代的3,3,6,6-四甲基-9-芳基-3,4,6,7,9,10-六氢ac啶-1,8(2H,5H)-二酮衍生物的合成,结构和生物活性
    摘要:
    一系列10取代的-3,3,6,6-四甲基-9-芳基-3,4,6,7,9,10-六氢吖-1,8-(2 ħ,5 ħ) -二酮衍生物2分别为通过化合物1与胺反应合成。在室温下,在少量L-脯氨酸作为催化剂存在下,由5,5-二甲基环己烷-1,3-二酮和醛有效制备化合物1。所有化合物均通过IR,MS和1 H NMR表征。通过X射线单晶衍射收集1b和2d的晶体数据,化合物2b和2d对HepG2细胞表现出更好的抑制活性。
    DOI:
    10.1002/jhet.2925
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文献信息

  • Ionic liquid immobilized on Fe3O4 nanoparticles: a magnetically recyclable heterogeneous catalyst for one-pot three-component synthesis of 1,8-dioxodecahydroacridines
    作者:Heshmatollah Alinezhad、Mahmood Tajbakhsh、Neda Ghobadi
    DOI:10.1007/s11164-015-2003-8
    日期:2015.12
    A magnetically recoverable nanocatalyst based on 1-methylimidazolium hydrogen sulfate ionic liquid has been synthesized by reaction of 1-methylimidazole with 3-(trimethoxysilyl)propyl chloride group, leading to formation of 1-methyl-3-(triethoxysilyl)propyl imidazolium chloride ([pmim]Cl). The ionic liquid was anchored onto silica-coated magnetic Fe3O4 particles, and Cl− anion exchange by treatment with H2SO4 afforded the corresponding immobilized ionic liquid MNP-[pmim]HSO4. The synthesized catalyst was characterized by various techniques such as Fourier-transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), transmission electron microscopy (TEM), (differential) thermogravimetry (TG/DTG), CHN analysis, and vibrating-sample magnetometry (VSM), revealing the superparamagnetic nature of the particles. From electron microscopy (SEM and TEM) studies it can be inferred that the particles were mostly spherical in shape with average size of 20 nm. The loading amount of ionic liquid supported on the magnetic particles was indicated to be 0.98 mmol/g by the results of elemental and thermogravimetric analyses (CHN and TG). The catalytic activity of the supported ionic liquid was examined in synthesis of 1,8-dioxodecahydroacridines by condensation reaction of cyclic diketones with aromatic aldehydes and ammonium acetate or primary amines under solvent-free conditions. The catalyst could be easily recovered by applying an external magnetic field and reused for at least nine runs without deterioration in catalytic activity.
    一种基于1-甲基咪唑硫酸氢盐离子液体的磁性可回收纳米催化剂已通过1-甲基咪唑与3-(三甲氧基硅基)丙基氯反应合成,导致形成1-甲基-3-(三乙氧基硅基)丙基咪唑氯([pmim]Cl)。将该离子液体固定在涂有二氧化硅的磁性Fe3O4粒子上,并通过用H2SO4处理置换Cl−阴离子,得到了相应的固定化离子液体MNP-[pmim]HSO4。该合成的催化剂通过傅里叶变换红外(FT-IR)光谱、X射线衍射(XRD)分析、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、(差示)热重分析(TG/DTG)、CHN元素分析和振动样品磁力计(VSM)等多种技术进行表征,显示了粒子的超顺磁性质。从电子显微镜(SEM和TEM)研究可以推断,粒子大多呈球形,平均尺寸为20 nm。根据元素和热重分析(CHN和TG)的结果,固定在磁性粒子上的离子液体的负载量为0.98 mmol/g。在无溶剂条件下,通过环状二酮与芳香醛和乙酸铵或伯胺的缩合反应,研究了该固定化离子液体的催化活性,用于合成1,8-二氧十氢吖啶。该催化剂可通过施加外部磁场轻松回收,并可重复使用至少九次而不会降低催化活性。
  • One-Pot, Facile, Highly Efficient, and Green Synthesis of Acridinedione Derivatives Using Vitamin B<sub>1</sub>
    作者:Ahmet Işık、Burak Aday、Ramazan Ulus、Muharrem Kaya
    DOI:10.1080/00397911.2015.1109127
    日期:2015.12.17
    Abstract An efficient methodology for the synthesis of acridinedione derivatives 4a–o has been achieved by one-pot, multicomponent condensation of dimedone 1, various amines 2a–d, and substitute aromatic aldehydes 3a–k, in the presence of the easily available, inexpensive, and nontoxic catalyst vitamin B1 (VB1) as a versatile biodegradable. Synthesis of acridine-type compounds was performed in good
    摘要 一种合成吖啶二酮衍生物 4a-o 的有效方法是通过二甲酮 1、各种胺 2a-d 和取代芳香醛 3a-k 的一锅多组分缩合,在容易获得、廉价的和无毒催化剂维生素 B1 (VB1) 作为一种多功能的生物可降解材料。在作为绿色溶剂的水中以良好的收率合成了吖啶类化合物。其高产效率;清洁、环保、简单的后处理程序;除了溶剂环保外,该方法的主要优点是易于纯化。合成的化合物使用光谱分析(FTIR、1H NMR、13C NMR 和高分辨率质谱)技术进行表征。图形概要
  • Synthesis of New Nonclassical Acridines, Quinolines, and Quinazolines Derived from Dimedone for Biological Evaluation
    作者:Osama I. El- Sabbagh、Mohamed A. Shabaan、Hanan H. Kadry、Ehab Saad Al-Din
    DOI:10.1002/ardp.200900296
    日期:——
    New nonclassical acridines, quinolines, and quinazolines were prepared starting from cyclic β‐diketones, namely dimedone, through application of Hantzsch addition, Michael addition, and Mannich reactions, respectively. The antimicrobial activity revealed that decahydroacridin‐1,8‐dione 2e bearing a 3‐nitrophenyl group and hexahydroquinoline 4e having a 2,4‐dichlorophenyl moiety were the most active
    以环状β-二酮即二甲酮为原料,分别通过Hantzsch加成、Michael加成和Mannich反应制备了新的非经典吖啶、喹啉和喹唑啉。抗菌活性表明,基于使用圆盘扩散,带有 3-硝基苯基的十氢吖啶 - 1,8-二酮 2e 和带有 2,4-二氯苯基部分的六氢喹啉 4e 是对革兰氏阳性菌和革兰氏阴性菌最有效的化合物方法。使用 MTT 细胞活力测定法对十氢吖啶 - 1,8 - 二酮 2a - e 对肝癌细胞 (HepG2) 的细胞毒活性研究表明,带有 4 - 甲基苯基部分 2d 的十氢吖​​啶 - 1,8 - 二酮表现出更高的细胞毒活性 (IC50 = 4.42 µg/mL) 比其他衍生物。
  • Pt NPs@GO as a highly efficient and reusable catalyst for one-pot synthesis of acridinedione derivatives
    作者:Handan Pamuk、Burak Aday、Fatih Şen、Muharrem Kaya
    DOI:10.1039/c5ra06441d
    日期:——
    and highly efficient catalyst for the synthesis of acridinedione derivatives from dimedone, aromatic aldehydes and various amines with great catalytic performance. All the acridinedione compounds were synthesized in DMF in a single process through two successive reactions (aldol condensation and Michael addition) in the presence of highly efficient Pt NPs@GO. The synthesized catalyst was characterized
    用铂纳米粒子修饰的氧化石墨烯(Pt NPs @ GO)首次用作高度稳定,可重复使用,可分离,可瓶装,长寿命且高效的催化剂,用于由二甲酮,芳族醛和二甲基吡啶合成a啶二酮衍生物。具有良好催化性能的各种胺。在高效Pt NPs @ GO存在的情况下,通过两个连续的反应(醛醇缩合和迈克尔加成反应),在一个单一的过程中通过DMF合成了所有的cr啶二酮化合物。通过透射电子显微镜(TEM),高分辨率电子显微镜(HRTEM),X射线衍射(XRD),原子力显微镜(AFM)和X射线光电子能谱(XPS)对合成的催化剂进行了表征。使用Pt NPs @ GO获得的所有产品均通过FT-IR表征,1 H-NMR, 13 C-NMR和HRMS技术。
  • Ferric (III) complex supported on superparamagnetic Fe3O4@SiO2 as a reusable Lewis acid catalyst: a new highly efficient protocol for the synthesis of acridinedione and spiroquinazolin-4(3H)-one derivatives
    作者:Hadi Mohammadi、Hamid Reza Shaterian
    DOI:10.1007/s11164-019-03942-w
    日期:2020.1
    very easy reaction conditions, simple work-up, excellent yields, high purity of the desired product, short reaction time and one-pot reaction to synthesize Fe3O4@SiO2-HBP-FeCl3. The recycling studies revealed that catalyst could be easily recovered using an external magnet and reused five times without significant loss of its catalytic activity.
    制备纳米Fe 3 O 4 @SiO 2 -3,4-二羟基苯甲醛/巴比妥酸/邻苯二甲酰-FeCl 3(纳米Fe 3 O 4 @SiO 2 -HBP-FeCl 3),并通过常规分析和光谱技术鉴定。将制备的纳米Fe 3 O 4 @SiO 2 -HBP-FeCl 3应用于a啶二酮和螺喹唑啉-4(3 H)-绿色条件下的一种衍生物。此外,这项研究还提供了许多优势,例如非常容易的反应条件,简单的后处理,优异的收率,所需产物的高纯度,较短的反应时间和一锅法反应以合成Fe 3 O 4 @SiO 2 -HBP- FeCl 3。回收研究表明,使用外磁体可以轻松回收催化剂,并重复使用五次,而不会明显降低其催化活性。
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