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diethyl 4-(3-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate | 58029-73-5

中文名称
——
中文别名
——
英文名称
diethyl 4-(3-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
英文别名
——
diethyl 4-(3-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate化学式
CAS
58029-73-5
化学式
C20H25NO5
mdl
——
分子量
359.422
InChiKey
XLYRLDBLJJXIRH-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:
    118-120 °C
  • 沸点:
    479.4±45.0 °C(Predicted)
  • 密度:
    1.132±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    26
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    73.9
  • 氢给体数:
    1
  • 氢受体数:
    6

SDS

SDS:491340c78e6ee9a0b379966f5ca01f46
查看

反应信息

  • 作为反应物:
    描述:
    diethyl 4-(3-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 乙腈 为溶剂, 反应 0.01h, 以90%的产率得到diethyl 2,6-dimethyl-4-(m-methoxyphenyl)pyridine-3,5-dicarboxylate
    参考文献:
    名称:
    Electron Transfer-induced Aromatization of 1,4-Dihydropyridines
    摘要:
    一种广泛的3,5-二乙酰基-1,4-二氢吡啶和3,5-二酯基-1,4-二氢吡啶在室温和微波辐射下,通过2,3-二氯-5,6-二氰-p-苯醌(DDQ)被芳构化为吡啶衍生物。本反应提出了一种受电子转移诱导的机制,该机制受溶剂性质、位于1,4-二氢吡啶环的3、4和5位取代基的性质以及氧气或氩气氛围的影响。
    DOI:
    10.1515/znb-2009-1012
  • 作为产物:
    描述:
    乙酰乙酸乙酯3-甲氧基苯甲醛ammonium hydroxide 作用下, 反应 0.58h, 以70%的产率得到diethyl 4-(3-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
    参考文献:
    名称:
    二氧化硅层状的NiFe2O4上的锚固磺酸:一种可磁重复使用的纳米催化剂,用于汉茨化学合成1,4-二氢吡啶
    摘要:
    摘要研究了磺酸固定在二氧化硅层状镍铁氧体NiFe2O4 @ SiO2 @ SO3H上的方法。然后使用FT-IR,SEM,EDX,XRD和VSM分析对磺化的镍纳米催化剂进行表征。还研究了Ni-纳米复合物对1,3-二酮(乙酰乙酸乙酯或4-羟基香豆素),芳族醛和氨水在H2O中的一锅缩合反应对Hantzsch合成1,4-二氢吡啶的催化活性。 C)作为绿色溶剂。所有反应都在10-100分钟内进行,以高到极好的收率得到产物。通过检查NiFe2O4 @ SiO2 @ SO3H MNPs连续七个循环的可重复使用性,而没有明显降低催化活性,对该合成规程的绿色方面进行了更多研究。
    DOI:
    10.1016/j.poly.2019.04.035
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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<a href=https://www.molaid.com/MS_51724 target="_blank">喹啉</a>,涉及使用一种吸湿性和中等毒性的<a href=https://www.molaid.com/MS_4410 target="_blank">铵</a>盐作为关键反应物之一。在我们的努力中,我们发现<a href=https://www.molaid.com/MS_45556 target="_blank">尿素</a>在存在<a href=https://www.molaid.com/MS_64419 target="_blank">磺酸</a>基功能化王<a href=https://www.molaid.com/fenzi/4585 target="_blank">树脂</a>(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<a href=https://www.molaid.com/MS_37224 target="_blank">氨</a>替代品。<a href=https://www.molaid.com/MS_45556 target="_blank">尿素</a>比这种MCR中常用的<a href=https://www.molaid.com/MS_4410 target="_blank">铵</a>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<a href=https://www.molaid.com/MS_51724 target="_blank">喹啉</a>。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-<a href=https://www.molaid.com/MS_271138 target="_blank">DHP</a>s。</p></div> </div> </li> <li class="feature-list-item"> <div class="content-title">Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub> supported aza-crown ether complex cation ionic liquids: preparation and applications in organic reactions</div> <div class="value"> <div class="value-text"> <span>作者:</span>Dandan Li、Jinyuan Wang、Fengjuan Chen、Huanwang Jing </div> <div class="value-text"> <span>DOI:</span>10.1039/c6ra25291e </div> <div class="value-text"> <span>日期:</span>—— </div> <div class="value-text en">A series of aza-crown <span style='color:#ff0000'>ether</span> ionic liquids supported on magnetic Fe3O4@SiO2 core–shell particles were designed, synthesized and characterized by elemental analysis, TEM, TG and FT-IR. These new aza-crown <span style='color:#ff0000'>ether</span> complex cation ionic liquids were utilized as heterogeneous acidic catalysts in Friedel–Crafts alkylation and Hantzsch <span style='color:#ff0000'>reaction</span> in good yields under convenient <span style='color:#ff0000'>reaction</span> conditions. Moreover, these</div> <div class="value-text ch">设计,合成并通过元素分析,<a href=https://www.molaid.com/MS_79832 target="_blank">TEM</a>,TG和FT-IR表征了在磁性Fe 3 O 4 @SiO 2核-壳颗粒上负载的一系列氮杂-<a href=https://www.molaid.com/fenzi/4426 target="_blank">冠醚</a><a href=https://www.molaid.com/fenzi/4437 target="_blank">离子液体</a>。这些新型的氮杂-<a href=https://www.molaid.com/fenzi/4426 target="_blank">冠醚</a>络合物阳离子<a href=https://www.molaid.com/fenzi/4437 target="_blank">离子液体</a>在便利的反应条件下,以良好的收率被用作Friedel-Crafts烷基化和Hantzsch反应中的多相酸性催化剂。而且,这些磁性颗粒负载的IL催化剂可以容易地通过外部磁体回收并重复使用五次而没有明显的活性损失。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">[Fesipmim]Cl as highly efficient and reusable catalyst for solventless synthesis of dihydropyridine derivatives through Hantzsch reaction</div> <div class="value"> <div class="value-text"> <span>作者:</span>Akansha Agrwal、Virendra Kasana </div> <div class="value-text"> <span>DOI:</span>10.1007/s12039-020-01770-9 </div> <div class="value-text"> <span>日期:</span>2020.12 </div> <div class="value-text en">catalyst were measured by vibrating sample magnetometer (VSM). The efficiency of the [Fesipmim]Cl catalyst was checked by using it for the <span style='color:#ff0000'>synthesis</span> of different derivatives of <span style='color:#ff0000'>dihydropyridine</span> through Hantzsch <span style='color:#ff0000'>reaction</span> via a three-component coupling <span style='color:#ff0000'>reaction</span> of <span style='color:#ff0000'>substituted</span> benzaldehydes, ethyl/ methyl acetoacetate and ammonium acetate. The formation and structures of all the synthesized compounds were confirmed</div> <div class="value-text ch">摘要 在本研究中,合成了磁性<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>氧体纳米粒子(<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>氧体NPs)并通过溶胶-凝胶法用<a href=https://www.molaid.com/MS_68343 target="_blank">二氧化硅</a>(ferrite @ SiO 2 NPs)进行了包覆。然后,制备<a href=https://www.molaid.com/MS_68343 target="_blank">二氧化硅</a>丙基甲基<a href=https://www.molaid.com/MS_52697 target="_blank">咪唑</a><a href=https://www.molaid.com/MS_36390 target="_blank">氯</a>化物<a href=https://www.molaid.com/fenzi/4437 target="_blank">离子液体</a>[Sipmim] Cl,并与上述制备的<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>氧体@SiO 2 NPs连接,以合成<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>氧体<a href=https://www.molaid.com/MS_68343 target="_blank">二氧化硅</a>丙基甲基<a href=https://www.molaid.com/MS_52697 target="_blank">咪唑</a><a href=https://www.molaid.com/MS_36390 target="_blank">氯</a>化物[Fesipmim] Cl催化剂。[Fesipmim] Cl催化剂的形成通过傅立叶变换红外(FT-IR)光谱分析确认。X射线衍射(XRD)分析证实了<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>氧体NPs和<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>氧体@SiO 2 NPs的结构。透射电子显微镜(<a href=https://www.molaid.com/MS_79832 target="_blank">TEM</a>)证明成功形成了<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>素体NP和<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>素体@SiO 2NP。扫描电子显微镜(<a href=https://www.molaid.com/MS_301313 target="_blank">SE</a>M)结果表明,<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>氧体NPs,<a href=https://www.molaid.com/MS_4757 target="_blank">铁</a>素体@SiO 2 NPs和[Fesipmim] Cl的形态发生了变化。通过振动样品磁力计(VSM)测量[Fesipmim] Cl催化剂的磁性。[Fesipmim] Cl催化剂的效率通过使用</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Synthesis of tricarbonylchromium complexes of 4-aryl-1,4-dihydropyridines</div> <div class="value"> <div class="value-text"> <span>作者:</span>Adeleh Moshtaghi Zonouz、Mina Abkar Aras、Nasrin Abuali </div> <div class="value-text"> <span>DOI:</span>10.1007/s11243-013-9698-4 </div> <div class="value-text"> <span>日期:</span>2013.4 </div> <div class="value-text en"><span style='color:#ff0000'>Tricarbonylchromium</span> <span style='color:#ff0000'>complexes</span> of 4-aryl-1,4-dihydropyridines have been synthesized both under standard thermodynamic conditions using Cr(CO)6 and under milder <span style='color:#ff0000'>complexation</span> conditions using more labile [Cr(CO)3(NH3)3] and (η6-naphthalene)Cr(CO)3. Selective <span style='color:#ff0000'>complexation</span> of the Cr(CO)3 on the aryl ring in the presence of a 1,4-dihydropyridine ring was achieved.Graphical Abstract</div> <div class="value-text ch">4-芳基-1,4-<a href=https://www.molaid.com/fenzi/5237 target="_blank">二氢吡啶</a>的三羰基<a href=https://www.molaid.com/MS_4480 target="_blank">铬</a>配合物已在使用 Cr(CO)6 的标准热力学条件下和使用更不稳定的 [Cr(CO)3(NH3)3] 和 (η6-naphthalene )Cr(CO)3。在 1,4-<a href=https://www.molaid.com/fenzi/5237 target="_blank">二氢吡啶</a>环的存在下,实现了芳环上 Cr(CO)3 的选择性络合。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Structure-reactivity correlation for the kinetics of the reaction of substituted 4-phenyl-1,4-dihydropyridines formation</div> <div class="value"> <div class="value-text"> <span>作者:</span>Jovica Urosevic、Sasa Drmanic、Jasmina Nikolic、Ivan Juranic、Bratislav Jovanovic </div> <div class="value-text"> <span>DOI:</span>10.2298/jsc131120139u </div> <div class="value-text"> <span>日期:</span>—— </div> <div class="value-text en">Quantitative <span style='color:#ff0000'>structure-reactivity</span> correlations for the <span style='color:#ff0000'>kinetics</span> of the Hantzsch's synthesis of substituted 4-phenyl-1,4-dihydropyridines in the reaction between ethyl m- and p-substituted benzylidene acetoacetate and enamine has been studied. The reaction <span style='color:#ff0000'>kinetics</span> was followed using spectrophotometric measurements. It was found that the reaction correspond to the second-order <span style='color:#ff0000'>kinetics</span>. Quantitative</div> <div class="value-text ch">研究了间位乙基和对位取代的亚<a href=https://www.molaid.com/MS_73163 target="_blank">苄基乙酰乙酸酯</a>与烯胺的反应中汉兹许合成的取代的4-苯基-1,4-<a href=https://www.molaid.com/fenzi/5237 target="_blank">二氢吡啶</a>的动力学的定量结构-反应性相关性。使用分光光度法测量反应动力学。发现该反应对应于二级动力学。使用Hammett和扩展Hammett方程(D<a href=https://www.molaid.com/MS_15603 target="_blank">SP</a>方程),log k与相应的取代基常数(s,s +,sI和sR +)的定量结构-反应性相关性。它们与反应常数的正值(r)呈线性关系。通过线性回归分析处理获得的数据。确认迈克尔 将烯胺加至亚苄基代表在亚苄基分子上具有高正电荷的反应的缓慢步骤。进行了MO的计算,它们也与结构反应性相关性得出的结论一致。[Projekat Ministarstva nauke Republike Srbije,br。172013]</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101a07y7f428c3955N0&inchikey=XLYRLDBLJJXIRH-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_31" 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