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ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

中文名称
——
中文别名
——
英文名称
ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate
英文别名
2,7,7-trimethyl-5-oxo-4-(4-chlorophenyl)-1,4,5,6,7,8-hexahydroquinoline-3-carboxylic acid ethyl ester;ethyl 4-(4-chlorophenyl)-1,4,5,6,7,8-hexahydro-2,7,7-trimethyl-5-oxoquinoline-3-carboxylate;ethyl 1,4,7,8-tetrahydro-2,7,7-trimethyl-4-(4-chlorophenyl)-5(6H)-oxoquinolin-3-carboxylate;Ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydro-3-quinolinecarboxylate;ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,6,8-tetrahydroquinoline-3-carboxylate
ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate化学式
CAS
——
化学式
C21H24ClNO3
mdl
——
分子量
373.879
InChiKey
GLEFXODWLPNDKP-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):
    4.3
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate叔丁基过氧化氢 、 sodium dithionite 作用下, 以 乙酸乙酯 为溶剂, 反应 7.0h, 以73%的产率得到ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-3-carboxylate
    参考文献:
    名称:
    A new oxidation system for the oxidation of Hantzsch-1,4-dihydropyridines and polyhydroquinoline derivatives under mild conditions
    摘要:
    已开发出一种氧化系统,通过氧化1,4-二氢吡啶和多羟基喹啉衍生物,可以高产率合成吡啶衍生物。
    DOI:
    10.1039/c5ra20977c
  • 作为产物:
    描述:
    乙酰乙酸乙酯2-((4-chlorophenyl)(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)methyl)-3-hydroxy-5,5-dimethylcyclohex-2-enone 在 ammonium acetate 、 四丁基溴化铵 、 sodium carbonate 、 palladium dichloride 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以87%的产率得到ethyl 4-(4-chlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate
    参考文献:
    名称:
    钯(0)纳米颗粒:一种一锅合成聚氢喹啉的有效催化剂
    摘要:
    描述了一种温和,简洁,有效的方案,该方案通过使用Pd纳米粒子通过芳族醛,二甲酮,乙酰乙酸乙酯或氰基乙酸乙酯和乙酸铵的四组分反应合成聚氢喹啉。在一个锅中的芳基亚甲基双(3-羟基-2-环己烯-1-酮),乙酰乙酸乙酯,乙酸铵和Pd-纳米颗粒中也观察到相同的现象。本方法还允许我们从简单且容易获得的输入中合成高度官能化的标题化合物。
    DOI:
    10.1016/j.tetlet.2011.07.031
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文献信息

  • Heterogeneous Cu(<scp>ii</scp>)/<scp>l</scp>-His@Fe<sub>3</sub>O<sub>4</sub> nanocatalyst: a novel, efficient and magnetically-recoverable catalyst for organic transformations in green solvents
    作者:Masoomeh Norouzi、Arash Ghorbani-Choghamarani、Mohsen Nikoorazm
    DOI:10.1039/c6ra19776k
    日期:——
    A novel, efficient and green Cu(II)/L-His@Fe3O4 catalyst has been applied successfully in the synthesis of heterocyclic compounds. The resulting catalyst was used in the synthesis of 2,3-dihydroquinazolin-4(1H)-ones, polyhydroquinolines and 2-amino-6-(arylthio)pyridine-3,5-dicarbonitriles as biologically interesting compounds. The present research is focused on investigation of recycling, reusability
    一种新颖,高效,绿色的Cu(II)/ L- His @ Fe 3 O 4催化剂已成功用于杂环化合物的合成。所得催化剂用于合成2,3-二氢喹唑啉-4(1H)-酮,聚氢喹啉和2-氨基-6-(芳硫基)吡啶-3,5-二碳腈作为生物学上感兴趣的化合物。本研究的重点是研究相反应中催化剂的循环利用,可重复使用性和稳定性。Cu(II)/ L -His @ Fe 3 O 4该催化剂至少使用了六次,其活性与新鲜催化剂相当。通过TGA / DTG,EDS,XRD,VSM,FT-IR和SEM对催化剂的化学组成和结构进行了分析。
  • Cu-<i>S</i>-(propyl)-2-aminobenzothioate on magnetic nanoparticles: highly efficient and reusable catalyst for synthesis of polyhydroquinoline derivatives and oxidation of sulfides
    作者:Arash Ghorbani-Choghamarani、Bahman Tahmasbi、Parisa Moradi、Nasrin Havasi
    DOI:10.1002/aoc.3478
    日期:2016.8
    Cu–S‐(propyl)‐2‐aminobenzothioate supported on functionalized Fe3O4 magnetic nanoparticles is reported as a reusable and highly efficient nanocatalyst for the one‐pot synthesis of polyhydroquinoline derivatives and also for selective oxidation of sulfides to sulfoxides. The prepared nanoparticles were characterized using Fourier transform infrared spectroscopy, vibrating sample magnetometry, thermogravimetric
    官能化的Fe 3 O 4上负载的Cu- S-(丙基)-2-氨基苯甲硫醇据报道,磁性纳米颗粒是一种可重复使用的高效纳米催化剂,可用于单锅合成多氢喹啉衍生物,也可用于将硫化物选择性氧化为亚砜。使用傅里叶变换红外光谱仪,振动样品磁力分析,热重分析,透射和扫描电子显微镜,能量色散X射线光谱,X射线衍射,电感耦合等离子体原子发射光谱和原子吸收光谱对制备的纳米颗粒进行表征。使用外部磁体可以容易地回收纳米催化剂,并且可以在不显着损失其催化效率的情况下重复使用几次。版权所有©2016 John Wiley&Sons,Ltd.
  • 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">Synthesis and characterization of spinel FeAl2O4 (hercynite) magnetic nanoparticles and their application in multicomponent reactions</div> <div class="value"> <div class="value-text"> <span>作者:</span>Arash Ghorbani-Choghamarani、Masoud Mohammadi、Lotfi Shiri、Zahra Taherinia </div> <div class="value-text"> <span>DOI:</span>10.1007/s11164-019-03930-0 </div> <div class="value-text"> <span>日期:</span>2019.11 </div> <div class="value-text en">The <span style='color:#ff0000'>spinel</span> ferrite FeAl2O4 (hercynite) MNPs (magnetic <span style='color:#ff0000'>nanoparticles</span>) were applied as a reusable catalytic system for the one-pot <span style='color:#ff0000'>synthesis</span> of benzo[ a ]pyrano[2,3-c] phenazine and polyhydroquinoline derivatives via a multicomponent reaction under green reaction conditions. The structure of the prepared nanocatalyst has been characterized by XRD, FTIR, SEM, EDS, BET, and VSM techniques. The FeAl2O4</div> <div class="value-text ch">尖晶石型铁氧体FeAl 2 O 4(水铁矿)MNP(磁性纳米粒子)被用作可重复使用的催化体系,用于在以下条件下通过多组分反应一锅合成苯并[ a ]吡喃并[2,3-c]吩嗪和聚氢喹啉衍生物。绿色反应条件。制备的纳米催化剂的结构已通过XRD,FTIR,SEM,EDS,BET和VSM技术进行了表征。FeAl 2 O 4 MNP起到路易斯酸的作用,并具有许多优点,例如产物的收率高,反应时间短和后处理程序容易。此外,再循环的纳米催化剂被使用了至少四次而其活性没有明显损失。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Introduction of an efficient DABCO-based bis-dicationic ionic salt catalyst for the synthesis of arylidenemalononitrile, pyran and polyhydroquinoline derivatives</div> <div class="value"> <div class="value-text"> <span>作者:</span>Mehdi Zabihzadeh、Atefeh Omidi、Farhad Shirini、Hassan Tajik、Mohaddeseh Safarpoor Nikoo Langarudi </div> <div class="value-text"> <span>DOI:</span>10.1016/j.molstruc.2020.127730 </div> <div class="value-text"> <span>日期:</span>2020.4 </div> <div class="value-text en">Abstract —An affordable DABCO-based bis-dicationic <span style='color:#ff0000'>ionic</span> salt ([(DABCO)2C3H5OH]·2Cl) was utilized for the <span style='color:#ff0000'>synthesis</span> of arylidenemalononitrile, tetrahydrobenzo[<span style='color:#ff0000'>b</span>]<span style='color:#ff0000'>pyran</span>, pyrano[2,3-d]-pyrimidinone (thione), dihydropyrano[3,2-c]chromene, and polyhydroquinoline <span style='color:#ff0000'>derivatives</span>. The significant features of the presented method are ease of preparation and handling of the catalyst, high catalytic activity, short</div> <div class="value-text ch">摘要 —一种经济实惠的基于 DABCO 的双阳离子离子盐 ([(DABCO)2C3H5OH]·2Cl) 用于合成亚芳基丙二腈、四氢苯并[b]吡喃、吡喃并[2,3-d]-嘧啶酮(硫酮),二氢吡喃并[3,2-c]色烯和聚氢喹啉衍生物。该方法的显着特点是催化剂易于制备和处理,催化活性高,反应时间短,无需柱色谱分离,后处理程序简单。此外,催化剂可以很容易地回收并在研究的反应中重复使用几个循环。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=310166br8e9ba22e51M0&inchikey=GLEFXODWLPNDKP-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_35" class="compound-item" title="(S)-4-(叔丁基)-2-(喹啉-2-基)-4,5-二氢噁唑">(S)-4-(叔丁基)-2-(喹啉-2-基)-4,5-二氢噁唑</a> <a target="_blank" href="https://www.molaid.com/MS_48" class="compound-item" 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class="compound-item" title="阿尔马尔">阿尔马尔</a> <a target="_blank" href="https://www.molaid.com/MS_3383" class="compound-item" title="阿加曲班杂质43">阿加曲班杂质43</a> <a target="_blank" href="https://www.molaid.com/MS_3385" class="compound-item" title="阿加曲班杂质13">阿加曲班杂质13</a> <a target="_blank" href="https://www.molaid.com/MS_3405" class="compound-item" title="阿克罗宁">阿克罗宁</a> <a target="_blank" href="https://www.molaid.com/MS_4302" class="compound-item" title="铽(3+)十氧化五硼镁">铽(3+)十氧化五硼镁</a> <a target="_blank" href="https://www.molaid.com/MS_4360" class="compound-item" 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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" 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