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4-[(2-hydroxy-1-naphthyl)(4-methylphenyl)methyl]-5-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one | 1334395-19-5

中文名称
——
中文别名
——
英文名称
4-[(2-hydroxy-1-naphthyl)(4-methylphenyl)methyl]-5-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one
英文别名
4-[(2-hydroxy-1-naphthyl)-(p-tolyl)methyl]-5-methyl-2-phenyl-1H-pyrazol-3-one;4-[(2-hydroxynaphthalen-1-yl)-(4-methylphenyl)methyl]-5-methyl-2-phenyl-1H-pyrazol-3-one
4-[(2-hydroxy-1-naphthyl)(4-methylphenyl)methyl]-5-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one化学式
CAS
1334395-19-5
化学式
C28H24N2O2
mdl
——
分子量
420.511
InChiKey
IRXRZSTWTGABCP-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):
    6.5
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    52.6
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    苯肼 在 Ni (II) complex with 1,2-di(4-pyridyl)ethylene immobilized on nano-silica gel 作用下, 以 neat (no solvent) 为溶剂, 反应 0.06h, 生成 4-[(2-hydroxy-1-naphthyl)(4-methylphenyl)methyl]-5-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one
    参考文献:
    名称:
    Nano-SiO2@nPr@DPyE-Ni:一种用于快速生产对称二芳基硫醚和吡唑啉酮的新型纳米催化剂
    摘要:
    最初,制备了一种以纳米硅胶为基质、Ni活性中心的新型有机金属催化剂,即纳米SiO 2 @nPr@DPyE-Ni,并对其性能进行了深入的争论。然后以优异的性能应用于生产对称二芳基硫醚(14 个条目,78–98%,20–150 分钟,EtOH,70 °C)和 2-芳基-5-甲基-2,3-二氢-1 H -3-吡唑啉酮(12 个条目,91–98%,2–4 分钟,无溶剂,室温)。在两条生产路线中,纳米催化剂均可回收和重复使用七次以上,并通过回收结果、热过滤测试和ICP-OES(耦合等离子体发射光谱)方法检查和确认其异质性。 图形概要
    DOI:
    10.1007/s11164-024-05296-4
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文献信息

  • Ce/SiO2 composite as an efficient catalyst for the multicomponent one-pot synthesis of substituted pyrazolones in aqueous media and their antimicrobial activities
    作者:Adinarayana Murthy Akondi、Mannepalli Lakshmi Kantam、Rajiv Trivedi、Jagadeesh Bharatam、Sahitha Phani Babu Vemulapalli、Suresh K. Bhargava、Sudheer Kumar Buddana、Reddy Shetty Prakasham
    DOI:10.1016/j.molcata.2015.11.004
    日期:2016.1
    We describe here the preparation and characterization of a Ce/SiO2 catalyst and its application in an eco-friendly and convenient synthesis of pyrazolone derivatives via one-pot multicomponent reaction of 2-naphthol, aldehydes, phenylhydrazine and ethyl acetoacetate under aqueous media. The catalyst was prepared using sol-gel method and characterized by XRD, XPS, UV-DRS, SEM, TEM and surface area analysis
    我们在这里描述了Ce / SiO 2催化剂的制备和表征,及其在介质下通过2-萘酚,醛,苯乙酰乙酸乙酯的一锅多组分反应在吡喃酮生物的生态友好和方便的合成中的应用。该催化剂采用溶胶-凝胶法制备,并通过XRD,XPS,UV-DRS,SEM,TEM和表面积分析对其进行表征。利用2D NMR技术确定吡唑啉酮互变异构体。对新化合物的抗微生物活性进行了评估,并对大多数测试的细菌和真菌菌株表现出良好至有希望的活性。
  • Synthesis of [2,2′-Bipyridine]-1,1′-diium Tricyanomethanide as a Bifunctional Nanostructured Ionic Liquid: Application to the Synthesis of 2-Aryl-5-methyl-2,3-dihydro-1H-3-pyrazolone Derivatives
    作者:Mohammad Zolfigol、Navid Mansouri、Saeed Baghery
    DOI:10.1055/s-0035-1561420
    日期:——
    [2,2′-BPyH][C(CN) 3 ] 2 } was synthesized and fully characterized by IR, 1 H NMR, 13 C NMR, mass, X-ray diffraction patterns (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric (TG), and differential thermal (DTA) analysis. [2,2-Bipyridine]-1,1′-diium tricyanomethanide [2,2′-BPyH][C(CN) 3 ] 2 } as a bifunctional nanostructure ionic liquid beneficial
    [2,2'-BPyH][C(CN) 3 ] 2 } 合成并通过 IR、 1 H NMR、 13 C NMR、质量、X 射线衍射图 (XRD)、扫描电子显微镜 (SEM) 进行充分表征)、透射电子显微镜 (TEM)、热重 (TG) 和差热 (DTA) 分析。[2,2'-联吡啶]-1,1'-三甲烷二鎓[2,2'-BPyH][C(CN) 3 ] 2 }作为双功能纳米结构离子液体有利于催化2-芳基-5的合成-甲基-2,3-二氢-1 H -3-吡唑啉酮衍生物,通过芳香醛、乙酰乙酸乙酯、苯和β-萘酚在室温下无溶剂条件下的一锅四组分缩合反应。所提供工艺的主要优点是高效催化和催化剂的可回收性。
  • Synthesis of 4‐((2‐hydroxynaphthalen‐1‐yl)(aryl)methyl)‐5‐methyl‐2‐phenyl‐1H‐pyrazol‐3(2H)‐ones using nano‐Zn‐[2‐boromophenyl‐salicylaldimine‐methylpyranopyrazole]Cl <sub>2</sub> nanoparticles
    作者:Hamid Goudarziafshar、Ahmad Reza Moosavi‐Zare、Zahra Jalilian、Mehdi Abdolmaleki
    DOI:10.1002/jccs.201800215
    日期:2019.5
    Nano‐Zn‐[2‐boromophenyl‐salicylaldimine‐methylpyranopyrazole]Cl2 (nano‐[Zn‐2BSMP]Cl2) as a nanoparticle Schiff base complex and a catalyst was introduced for the solvent‐free synthesis of 4‐((2‐hydroxynaphthalen‐1yl)(aryl)methyl)‐5‐methyl‐2‐phenyl‐1H‐pyrazol‐3(2H)‐ones by the multicomponent condensation reaction of various aromatic aldehydes, β‐naphthol, ethyl acetoacetate, and phenyl hydrazine at
    作为纳米颗粒席夫碱配合物的纳米Zn- [2-环溴苯基-杨基亚胺基-甲基喃并吡唑] Cl 2(纳米[Zn-2BSMP] Cl 2)催化剂被引入,用于无溶剂合成4-(((2-通过各种芳香醛,β-萘酚乙酰乙酸乙酯和苯的多组分缩合反应生成羟基-1-基)(芳基)甲基)-5-甲基-2-苯基-1H-吡唑-3(2H)-在室温下。
  • A facile four-component sequential protocol in the expedient synthesis of novel 2-aryl-5-methyl-2,3-dihydro-1H-3-pyrazolones in water and their antitubercular evaluation
    作者:Pethaiah Gunasekaran、Subbu Perumal、Perumal Yogeeswari、Dharmarajan Sriram
    DOI:10.1016/j.ejmech.2011.07.029
    日期:2011.9
    A series of 2-aryl-5-methyl-2,3-dihydro-1H-3-pyrazolones has been synthesized by one-pot, four-component sequential reactions of phenylhydrazine, methyl acetoacetate, aromatic aldehydes and beta-naphthol in the presence of p-toluenesulphonic acid in water in good yields. These 2-aryl-5-methyl-2,3-dihydro-1H-3-pyrazolones were screened for in-vitro antimycobacterial activity against Mycobacterium tuberculosis H37Rv (MTB) using agar dilution method. Among the 15 compounds screened, 4-[(2,4-dichlorophenyl)(2-hydroxy-1-naphthyl)methyl]-2-(4-fluorophenyl)-5-methyl-2,3-dihydro-1H-3-pyrazolone displays the maximum potency with a minimum inhibitory concentration (MIC) of 1.6 mu M against MTB, being 2.94 and 4.75 times more active than ciprofloxacin and ethambutol respectively. (C) 2011 Elsevier Masson SAS. All rights reserved.
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