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7-chloro-3,3-dimethyl-9-phenyl-3,4-dihydro-2H-acridin-1-one | 851072-10-1

中文名称
——
中文别名
——
英文名称
7-chloro-3,3-dimethyl-9-phenyl-3,4-dihydro-2H-acridin-1-one
英文别名
7-chloro-3,3-dimethyl-9-phenyl-3,4-dihydroacridin-1(2H)-one;7-chloro-3,3-dimethyl-9-phenyl-2,4-dihydroacridin-1-one
7-chloro-3,3-dimethyl-9-phenyl-3,4-dihydro-2H-acridin-1-one化学式
CAS
851072-10-1
化学式
C21H18ClNO
mdl
——
分子量
335.833
InChiKey
QSSVASUDWSXNEV-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

物化性质

  • 熔点:
    209-211 °C(Solv: ethanol (64-17-5))
  • 沸点:
    511.4±50.0 °C(Predicted)
  • 密度:
    1.217±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    30
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090

SDS

SDS:3d3811032cdd36d8e1eb1615cae0781f
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反应信息

  • 作为反应物:
    描述:
    7-chloro-3,3-dimethyl-9-phenyl-3,4-dihydro-2H-acridin-1-onesodium methylate一水合肼 作用下, 以 甲醇乙醇 为溶剂, 反应 8.0h, 生成 9-chloro-4,4-dimethyl-11-phenyl-4,5-dihydro-2H-pyrazolo[3,4-a]acridine
    参考文献:
    名称:
    Efficient Protocol for Synthesis of Pyrazolo[3,4-a]acridines
    摘要:
    A new class of pyrazolo[3,4-a]acridines have been prepared. The synthon acridones were obtained in very good yield by a one-pot reaction of 2-amino-5-chloro or nitro substituted benzophenones with 1,3-cyclic diketones in the presence of freshly prepared Eaton's reagent without solvent, using Friedlander synthesis. The intermediates were reacted with ethylformate followed by hydrazine hydrate to afford pyrazolo[3,4-a]acridines. All of the compounds were purified by recrystallization only, and no chromatographic workup was required. The structures of the synthesized compounds were deduced by spectroscopic techniques, including single-crystal x-ray diffraction.
    DOI:
    10.1080/00397911.2015.1070433
  • 作为产物:
    描述:
    3,3-二甲基环己酮2-氨基-5-氯二苯甲酮苹果酸 作用下, 以 neat (no solvent) 为溶剂, 反应 1.3h, 以78%的产率得到7-chloro-3,3-dimethyl-9-phenyl-3,4-dihydro-2H-acridin-1-one
    参考文献:
    名称:
    生物有机促进的绿色弗里德兰德合成:一种通用的新苹果酸促进的无溶剂方法,用于多取代喹啉†
    摘要:
    揭示了一种新的,苹果酸促进的,生态友好的Friedländer方法用于各种多取代喹啉的发现。据我们所知,这是第一份关于苹果酸用途的报告,苹果酸被美国能源部列为12种生物基热分子之一,是有机合成中的有机促进剂,并具有许多优点,例如底物范围广,无溶剂的环境反应条件,较短的反应时间,操作简便,成本效益,高原子经济性,良好至优异的收率以及有机促进剂的可再利用性,使其成为现有方法的有价值的绿色替代品。通过成功地将其应用于一些重要的喹啉分子的靶向合成并成功扩大规模,进一步确立了该开发方法的多功能性和实用性。
    DOI:
    10.1039/c6nj03907c
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文献信息

  • Sulfuric acid-modified PEG-6000 (PEG-OSO3H): an efficient, bio-degradable and reusable polymeric catalyst for the solvent-free synthesis of poly-substituted quinolines under microwave irradiation
    作者:Alireza Hasaninejad、Abdolkarim Zare、Mohsen Shekouhy、Javad Ameri-Rad
    DOI:10.1039/c0gc00953a
    日期:——
    acid-modified polyethylene glycol 6000 (PEG-OSO3H) is applied as an efficient and eco-friendly polymeric catalyst for Friedländer synthesis of poly-substituted quinolines from 2-aminoaryl ketones (or anthranilonitrile) and carbonyl compounds possessing a reactive methylene group under microwave irradiation and solvent-free conditions. The reactions are completed in short times, and the products are obtained
    硫酸改性聚乙二醇6000(PEG-OSO 3 H)被用作一种高效且环保的聚合物催化剂 Friedländer合成多取代基 喹啉 由2-氨基芳基 酮类 (或者 蒽腈) 和 羰基化合物 在微波辐射下具有反应性亚甲基 溶剂无条件。反应在短时间内完成,并且以良好至优异的产率获得产物。
  • Environmentally Friendly Nafion-Mediated Friedländer Quinoline Synthesis under Microwave Irradiation: Application to One-Pot Synthesis of Substituted Quinolinyl Chalcones
    作者:Cheng-Chung Wang、Chieh-Kai Chan、Chien-Yu Lai
    DOI:10.1055/s-0039-1690088
    日期:2020.6
    An efficient and eco-friendly synthetic route for Friedländer quinoline synthesis of polysubstituted quinolines is described. This green chemical method starts from various 2-aminobenzophenones and mono- or dicarbonyl synthons and uses reusable Nafion NR50 material as a solid catalyst in ethanol under microwave irradiation. The protocol has a high generality of functional groups and provides the desired
    描述了一种用于弗里德兰德喹啉合成多取代喹啉的有效而环保的合成途径。这种绿色化学方法从各种2-氨基二苯甲酮和单或二羰基合成子开始,并在微波辐射下使用可重复使用的Nafion NR50材料作为乙醇中的固体催化剂。该方案具有很高的官能团通用性,并以良好或优异的产率提供了所需的喹啉。通过单晶X射线衍射分析确认了一些结构。
  • Sulfamic acid supported on Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>superpara magnetic nanoparticles as a recyclable heterogeneous catalyst for the synthesis of quinolines
    作者:M. A. Nasseri、B. Zakerinasab、M. M. Samieadel
    DOI:10.1039/c4ra06699e
    日期:——
    In the present study, for the first time the synthesis of sulfamic acid supported on Fe3O4@SiO2 superpara magnetic nanoparticles as a solid acid catalyst with large density of sulfamic acid groups was suggested. The structural and magnetic properties of functionalized Fe3O4@SiO2 nanoparticles are identified by TEM, IR, VSM, XRD, TGA and elemental analysis. Then, the applicability of the synthesized nanoparticles was tested as a recyclable acidic catalyst for the synthesis of quinoline derivatives, an important class of potentially bioactive compounds. The products are obtained in good to high yields (72–98%) from one-pot reaction procedure involving carbonyl compounds and 2-amino benzophenone under solvent-free conditions.
    在本项研究中,首次提出了一种新型的固体酸催化剂,即负载于Fe3O4@SiO2超顺磁性纳米粒子上的高密度磺胺酸基团合成的磺胺酸催化剂。通过透射电镜(TEM)、红外光谱(IR)、振动样品磁强计(VSM)、X射线衍射(XRD)、热重分析(TGA)和元素分析等手段,确定了功能化Fe3O4@SiO2纳米粒子的结构和磁性质。接着,对合成的纳米粒子作为可循环酸性催化剂在合成喹啉衍生物(这是一类具有潜在生物活性的重要化合物)中的应用进行了测试。在无溶剂条件下,通过羰基化合物和2-氨基二苯酮的一锅法反应,可获得良好至高产率(72–98%)的产品。
  • Friedlander Synthesis of Quinolines Promoted By Polymer-bound Sulfonic Acid
    作者:Behrooz Maleki、Esmail Rezaei Seresht、Zahra Ebrahimi
    DOI:10.1080/00304948.2015.1005986
    日期:2015.3.4
    has been shown that acid catalysis is more effective than base catalysts for the Friedlander annulation. In recent years, Bronsted and Lewis acids such as ionic liquids, sulfamic acid, hydrochloric acid, zirconium tetrakisdodecyl sulfate [Zr(DS)4], 29 silica sulfuric acid, silica supported phosphomolybdic acid [PMA.SiO2], 32 nanocrystalline aluminium oxide, dodecylphosphonic acid (DPA), poly(N-bromoethylbenzene-1
    喹啉及其衍生物在生物学上非常重要,广泛存在于天然产物中。该家族的成员显示出有趣的生理活性,并在药物化学中发现了主要应用,如抗疟疾、抗菌、抗炎、抗高血压、抗血小板和酪氨酸激酶抑制剂。它们还可用于制备具有增强的电子和光子特性的纳米和介观结构。此外,喹啉还用于生物有机、生物有机金属工艺和工业有机化学领域。因此,几十年来,探索构建喹啉骨架的有效合成方法一直受到广泛关注。在这些方法中,Friedlander 环是合成喹啉的最简单和最直接的方法之一。它涉及邻氨基芳基酮和醛与另一种具有活性α-亚甲基的羰基化合物之间的酸、碱催化或热缩合,然后进行环脱水。已经表明,对于 Friedlander 环化,酸催化比碱催化​​剂更有效。近年来,离子液体、氨基磺酸、盐酸、四十二烷基硫酸锆[Zr(DS)4]、29二氧化硅硫酸、二氧化硅负载磷钼酸[PMA.SiO2]、32纳米晶氧化铝、十二烷基膦酸 (DPA)、聚 (N-溴乙基苯-1
  • Green synthesis of trimetallic oxide nanoparticles and their use as an efficient catalyst for the green synthesis of quinoline and spirooxindoles: Antibacterial, cytotoxicity and anti-colon cancer effects
    作者:Boshra Mahmoudi、Faezeh Soleimani、Hamideh Keshtkar、Mohammad Ali Nasseri、Milad Kazemnejadi
    DOI:10.1016/j.inoche.2021.108923
    日期:2021.11
    The three-metallic oxide (Cu/Cr/Ni) nanoparticles were prepared using Echinops persicus plant extract via a simple, biocompatible, cost-effective, and non-toxic procedure, and their catalytic activity was evaluated over the synthesis of biologically active quinoline and spirooxindole derivatives. The synthesized nanoparticles were characterized by various analytical methods including UV–Vis, FTIR,
    三金属氧化物 (Cu/Cr/Ni) 纳米粒子是使用刺猬植物提取物通过简单、生物相容性、成本效益高且无毒的方法制备的,并通过合成具有生物活性的喹啉和螺环吲哚衍生物。合成的纳米粒子通过各种分析方法进行表征,包括 UV-Vis、FTIR、EDX、XRD、FE-SEM、DLS 和 TEM 分析。反应中涉及的有效参数由Design-Expert 10.0.7软件设计。Cu/Cr/Ni纳米颗粒被用作在无溶剂条件下制备喹啉和螺吲哚的有效催化剂,具有良好到优异的效率。此外,由于含有丰富的酚类物质Echinops persicus花提取物、纳米粒子对大肠杆菌、金黄色葡萄球菌和蜡状芽孢杆菌的抗菌特性通过 MIC 以及扩散方法进行了研究。此外,基于 MTT 测定,在人结肠癌 (HT29) 细胞上研究了纳米颗粒的细胞毒性和抗结肠癌活性。结果和观察清楚地表明,Cu/Cr/Ni NPs 具有显着的催化和抗菌活性,完全优于其相应的单金属纳米粒子。
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