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2,7,7-trimethyl-5-oxo-4-(4-nitrophenyl)-1,4,5,6,7,8-hexahydroquinoline-3-carboxylic acid methyl ester

中文名称
——
中文别名
——
英文名称
2,7,7-trimethyl-5-oxo-4-(4-nitrophenyl)-1,4,5,6,7,8-hexahydroquinoline-3-carboxylic acid methyl ester
英文别名
methyl 1,4,5,6,7,8-hexahydro-2,7,7-trimethyl-4-(4-nitrophenyl)-5-oxoquinoline-3-carboxylate;methyl 2,7,7-trimethyl-4-(4-nitrophenyl)-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate;methyl 4-(4-nitrophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate;methyl 2,7,7-trimethyl-4-(4-nitrophenyl)-5-oxo-1,4,6,8-tetrahydroquinoline-3-carboxylate
2,7,7-trimethyl-5-oxo-4-(4-nitrophenyl)-1,4,5,6,7,8-hexahydroquinoline-3-carboxylic acid methyl ester化学式
CAS
——
化学式
C20H22N2O5
mdl
——
分子量
370.405
InChiKey
RNEWXZZWHLZGDL-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):
    3.1
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    101
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    对硝基苯甲醛5,5-二甲基-1,3-环己二酮乙酰乙酸甲酯 在 ammonium acetate 、 二氧化硫脲 作用下, 以 为溶剂, 反应 2.0h, 以85%的产率得到2,7,7-trimethyl-5-oxo-4-(4-nitrophenyl)-1,4,5,6,7,8-hexahydroquinoline-3-carboxylic acid methyl ester
    参考文献:
    名称:
    Combined Thiourea Dioxide–Water: An Effective Reusable Catalyst for the Synthesis of Polyhydroquinolines via Hantzsch Multicomponent Coupling
    摘要:
    研究发现,二氧化硫脲水溶液是一种高效且可重复使用的有机催化体系,可在温和的反应条件下,通过醛、二甲基酮、乙酰乙酸酯和乙酸铵的汉兹奇型偶联反应,实现多氢喹啉衍生物的一锅合成。该方法操作简单、使用的催化剂经济实惠、环境友好、产品收率高、催化剂系统可重复使用,这些都是该方法的优点。
    DOI:
    10.1246/cl.2012.920
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文献信息

  • Urea as an Ammonia Surrogate in the Hantzsch’s Synthesis of Polyhydroquinolines / 1,4-dihydropyridines under Green Reaction Conditions
    作者:G. Dhananjaya、Akula Raghunadh、P. Mahesh Kumar、S. Pulla Reddy、V. Narayana Murthy、Venkateswara Rao Anna、Manojit Pal
    DOI:10.2174/1570178617999200713144504
    日期:2021.3
    <p>Synthesis of polyhydroquinolines via Hantzsch’s multicomponent reaction (MCR) involves the use of a hygroscopic and moderately toxic ammonium salt as one of the key reactants. In our effort, we have found urea as an effective ammonia surrogate when the MCR was performed in the presence of sulphonic acid-functionalized Wang resin (Wang-OSO<sub>3</sub>H) as a polymeric and recoverable acidic catalyst under green conditions. Urea is relatively less hygroscopic/toxic than the commonly used ammonium salts used in this MCR. The methodology afforded a range of polyhydroquinolines in good yields. Depending on the nature of reaction conditions employed, the MCR afforded Biginelli product or 1,4-DHPs when the use of 1,3-diketone was omitted.</p> </sec></div> <div class="value-text ch"><p>通过汉奇多组分反应(MCR)合成聚氢喹啉,涉及使用一种吸湿性和中等毒性的铵盐作为关键反应物之一。在我们的努力中,我们发现尿素在存在磺酸基功能化王树脂(Wang-OSO<sub>3</sub>H)作为聚合物和可回收的酸性催化剂的条件下,作为有效的氨替代品。尿素比这种MCR中常用的铵盐相对更不易吸湿/有毒。该工艺提供了一系列高产率的聚氢喹啉。根据所用反应条件的性质,当省略使用1,3-二酮时,MCR会生成Biginelli产物或1,4-DHPs。</p></div> </div> </li> <li class="feature-list-item"> <div class="content-title">Chitosan: a sustainable, reusable and biodegradable organocatalyst for green synthesis of 1,4-dihydropyridine derivatives under solvent-free condition</div> <div class="value"> <div class="value-text"> <span>作者:</span>Sara Zhaleh、Nourallah Hazeri、Mohammad Reza Faghihi、Malek Taher Maghsoodlou </div> <div class="value-text"> <span>DOI:</span>10.1007/s11164-016-2579-7 </div> <div class="value-text"> <span>日期:</span>2016.12 </div> <div class="value-text en">Abstract <span style='color:#ff0000'>Chitosan</span>, a <span style='color:#ff0000'>biodegradable</span> <span style='color:#ff0000'>green</span> <span style='color:#ff0000'>catalyst</span>, was found to be an impressive system for one-pot four-component reaction of different aldehydes, dimedone, β‐ketoesters or acetoacetanilide, and ammonium acetate leading to 1,4-dihydropyridine derivatives via Hantzsch-type condensation under solvent-free condition. This methodology produces diverse superiorities such as operational simplicity, short</div> <div class="value-text ch">摘要 壳聚糖是一种可生物降解的绿色催化剂,被发现是一种令人印象深刻的系统,可用于不同醛,二甲酮,β-酮酸酯或乙酰乙酰苯胺和乙酸铵的单锅四组分反应,通过汉茨型缩合反应生成1,4-二氢吡啶衍生物在无溶剂条件下。这种方法具有多种优势,例如操作简便,反应时间短,满意的产率和可回收的催化剂。在这项工作中,我们尝试对经典的Hantzsch转换进行一些修改,以报告一种新颖的环保方法,该方法没有以前报道的缺点。 图形概要</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Sulfuric acid heterogenized on magnetic Fe<sub>3</sub> O<sub>4</sub> nanoparticles: A new and efficient magnetically reusable catalyst for condensation reactions</div> <div class="value"> <div class="value-text"> <span>作者:</span>Lotfi Shiri、Setare Zarei、Mosstafa Kazemi、Davood Sheikh </div> <div class="value-text"> <span>DOI:</span>10.1002/aoc.3938 </div> <div class="value-text"> <span>日期:</span>2018.1 </div> <div class="value-text en">Immobilized <span style='color:#ff0000'>sulfuric</span> <span style='color:#ff0000'>acid</span> on <span style='color:#ff0000'>magnetic</span> Fe3O4 nanoparticles (Fe3O4 MNPs‐OSO3H) as a new solid <span style='color:#ff0000'>acid</span> nanocomposite was successfully synthesized and its catalytic activity in a series of condensation reactions was studied. High catalytic activity, simple separation from reaction mixture by an external magnet and good reusability are several eco‐friendly advantages of this catalytic system. It is noteworthy</div> <div class="value-text ch">成功地合成了固定在磁性Fe 3 O 4纳米颗粒上的硫酸(Fe 3 O 4 MNPs-OSO 3 H)作为一种新型固体酸纳米复合材料,并研究了其在一系列缩合反应中的催化活性。高催化活性,通过外部磁体与反应混合物的简单分离以及良好的可重复使用性是该催化系统的多项环保优势。值得注意的是,该催化体系适用于广泛范围的芳族醛,并且在温和的条件下以良好或优异的收率获得了所需的产物。从环境的角度来看,使用生态友好型溶剂也使该合成方案理想且引人入胜。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Sulfonic acid–functionalized Wang resin (Wang-OSO<sub>3</sub>H) as polymeric acidic catalyst for the ecofriendly multicomponent synthesis of polyhydroquinolines via Hantzsch condensation</div> <div class="value"> <div class="value-text"> <span>作者:</span>A. V. Dhanunjaya Rao、Rajendra Surasani、B. P. Vykunteswararao、T. Bhaskarkumar、B. Srikanth、Nivrutti R. Jogdand、Dipak Kalita、Jaydeep Kumar D. Lilakar、Vidavalur Siddaiah、Paul Douglas Sanasi、Akula Raghunadh </div> <div class="value-text"> <span>DOI:</span>10.1080/00397911.2016.1213850 </div> <div class="value-text"> <span>日期:</span>2016.9.16 </div> <div class="value-text en">efficient and green approach has been developed for the <span style='color:#ff0000'>synthesis</span> of polyhydroquinoline <span style='color:#ff0000'>derivatives</span> <span style='color:#ff0000'>via</span> <span style='color:#ff0000'>Hantzsch</span> condensation <span style='color:#ff0000'>reaction</span> directly from corresponding substituted aromatic and aliphatic aldehydes, β-keto <span style='color:#ff0000'>compounds</span>, active methylene <span style='color:#ff0000'>compounds</span>, and ammonium chloride using recyclable polymer-supported sulfonic acid catalyst under <span style='color:#ff0000'>aqueous</span> conditions. Environmental acceptability, operational simplicity</div> <div class="value-text ch">摘要 开发了一种高效、绿色的方法,通过 Hantzsch 缩合反应直接从相应的取代芳香族和脂肪族醛、β-酮化合物、活性亚甲基化合物和氯化铵合成聚氢喹啉衍生物,使用可回收聚合物负载的磺酸催化剂在水溶液下使适应。环境可接受性、操作简单性、低成本、出色的功能组兼容性和高产量是该协议的重要特征。图形概要</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Surfactant-directed one-pot preparation of novel Ti-containing mesomaterial with improved catalytic activity and reusability</div> <div class="value"> <div class="value-text"> <span>作者:</span>Dawood Elhamifar、Omolbanin Yari、Shaaker Hajati </div> <div class="value-text"> <span>DOI:</span>10.1002/aoc.4471 </div> <div class="value-text"> <span>日期:</span>2018.10 </div> <div class="value-text en">Titanium was incorporated in <span style='color:#ff0000'>ionic</span> <span style='color:#ff0000'>liquid</span> <span style='color:#ff0000'>based</span> <span style='color:#ff0000'>periodic</span> <span style='color:#ff0000'>mesoporous</span> <span style='color:#ff0000'>organosilica</span> to prepare a nanostructured catalyst (Ti@PMO‐IL) with high activity. Procedure for the <span style='color:#ff0000'>synthesis</span> of Ti@PMO‐IL was followed according the simultaneous hydrolysis and condensation of alkylimidazolium <span style='color:#ff0000'>ionic</span> <span style='color:#ff0000'>liquid</span>, tetramethoxysilane (TMOS) and tetrabutylorthotitanate (TBOT) where a surfactant template was used together with</div> <div class="value-text ch">将钛掺入基于离子液体的周期性介孔有机二氧化硅中以制备具有高活性的纳米结构催化剂(Ti @ PMO-IL)。根据烷基咪唑鎓离子液体,四甲氧基硅烷(TMOS)和四丁基甲钛酸酯(TBOT)的同时水解和缩合,遵循Ti @ PMO-IL的合成步骤,其中表面活性剂模板与简单的基于酸的催化方法一起使用。N 2研究了Ti @ PMO‐IL的吸附等温线,以测量其平均孔体积,孔径分布和比表面积。漫反射红外傅里叶变换(DRIFT)光谱用于鉴定Ti @ PMO-IL中存在的化学键。通过扫描电子显微镜(SEM)研究了这种纳米材料的形态。用透射电子显微镜(TEM)图像研究了介孔率和催化剂的结构顺序。然后研究了Ti @ PMO-IL的催化活性,发现其可有效且可重复使用以催化Hantzsch反应。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101945rfcf5595c48M0&inchikey=RNEWXZZWHLZGDL-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 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title="银(1+)1-乙基-6-氟-4-氧代-7-(1-哌嗪基)-1,4-二氢-3-喹啉羧酸酯">银(1+)1-乙基-6-氟-4-氧代-7-(1-哌嗪基)-1,4-二氢-3-喹啉羧酸酯</a> </div> </div> <div class="module" id="xiangguanjiegoufenlei"> <h3 class="module-title"><i class="iconfont icon-xiangguanjiegoufenlei"></i>相关结构分类</h3> <div class="compounds-list"> <a href="https://www.molaid.com/fenzi/10" class="compound-item" title="有机杂环化合物">有机杂环化合物</a> <a href="https://www.molaid.com/fenzi/11" class="compound-item" title="苯类化合物">苯类化合物</a> <a href="https://www.molaid.com/fenzi/12" class="compound-item" title="木脂素、新木脂素和相关化合物">木脂素、新木脂素和相关化合物</a> <a href="https://www.molaid.com/fenzi/13" class="compound-item" title="苯丙烷和聚酮">苯丙烷和聚酮</a> <a href="https://www.molaid.com/fenzi/14" class="compound-item" title="脂质和类脂质分子">脂质和类脂质分子</a> <a href="https://www.molaid.com/fenzi/15" class="compound-item" title="有机酸及其衍生物">有机酸及其衍生物</a> <a href="https://www.molaid.com/fenzi/16" class="compound-item" title="有机氧化合物">有机氧化合物</a> <a href="https://www.molaid.com/fenzi/17" class="compound-item" title="生物碱及其衍生物">生物碱及其衍生物</a> <a href="https://www.molaid.com/fenzi/18" class="compound-item" title="有机硫化合物">有机硫化合物</a> <a href="https://www.molaid.com/fenzi/19" class="compound-item" title="核苷、核苷酸和类似物">核苷、核苷酸和类似物</a> <a href="https://www.molaid.com/fenzi/20" class="compound-item" title="碳氢化合物衍生物">碳氢化合物衍生物</a> <a href="https://www.molaid.com/fenzi/21" class="compound-item" title="有机氮化合物">有机氮化合物</a> <a href="https://www.molaid.com/fenzi/22" class="compound-item" title="碳氢化合物">碳氢化合物</a> <a href="https://www.molaid.com/fenzi/23" class="compound-item" title="有机卤素化合物">有机卤素化合物</a> <a href="https://www.molaid.com/fenzi/24" class="compound-item" title="有机聚合物">有机聚合物</a> <a href="https://www.molaid.com/fenzi/25" class="compound-item" title="有机金属化合物">有机金属化合物</a> <a href="https://www.molaid.com/fenzi/26" class="compound-item" title="乙炔化物 ">乙炔化物 </a> <a href="https://www.molaid.com/fenzi/27" class="compound-item" title="有机磷化合物">有机磷化合物</a> <a href="https://www.molaid.com/fenzi/28" class="compound-item" title="叠烯">叠烯</a> <a href="https://www.molaid.com/fenzi/29" class="compound-item" title="有机1,3-偶极化合物">有机1,3-偶极化合物</a> <a href="https://www.molaid.com/fenzi/30" class="compound-item" title="碳化物">碳化物</a> <a href="https://www.molaid.com/fenzi/31" class="compound-item" title="有机盐">有机盐</a> <a href="https://www.molaid.com/fenzi/32" class="compound-item" title="有机阳离子">有机阳离子</a> <a href="https://www.molaid.com/fenzi/33" class="compound-item" title="卡宾">卡宾</a> <a href="https://www.molaid.com/fenzi/34" class="compound-item" title="有机阴离子">有机阴离子</a> </div> </div> </div> <div class="right"> <div class="module"> <link rel="stylesheet" href="https://www.molaid.com/assets/css/common/hot-molecular.css?v=202504271"> <div class="component-card hot-molecular-card" style="--color: #FF4539;"> <div class="title"> <h3 class="title-name">热门分子</h3> </div> <div class="card-content"> <ul class="list"> <li class="item item-special" data-sort="TOP"> <div class="item-img"> <img src="data:image/svg+xml;base64,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