共查询到20条相似文献,搜索用时 218 毫秒
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含1,4-二氢吡啶和1,8-二氧代十氢吖啶分子片段的化合物具有扩张血管、抗菌和抗肿瘤等药理活性,因此,探讨和优化该类衍生物绿色合成方法成为药物合成领域的热点之一。基于有机小分子催化剂L-脯氨酸廉价易得、无毒无害和水溶性等特点,结合微波辐射技术快速高效等优势,以芳香醛、β-二酮 (乙酰乙酸乙酯/二甲基环己二酮)和乙酸铵为原料,乙醇为溶剂,催化剂用量20 mol/mol,微波功率300 W和80℃的条件下,通过成环缩合反应“一锅法”合成了目标化合物,收率达80%~93%。该方法具有条件温和、操作简单以及环境友好等优点。
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Asha V.Chate Umesh B.Rathod Jagdish S.Kshirsagar Pradip A.Gaikwad Kishor D.Mane Pravin S.Mahajan Mukesh D.Nikam Charansingh H.Gill 《催化学报》2016,(1):146-152
以可生物降解和可重复使用的β-环糊精为超分子催化剂,在水介质中采用简易方法合成了氮取代的1,8-二氧-十氢吖啶,所得产物的收率很高,选择性也为中等到较高.该过程为双甲酮、芳香醛和芳香胺三组分通过串联Michael加成反应一步合成得到产物.本文提供了一个高效且环境友好的合成氮取代的1,8-二氧-十氢吖啶的新方法. 相似文献
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在水相回流条件下,以芳香醛、5,5-二甲基-1,3-环己二酮(达米酮)和苯胺/对甲苯胺为原料,经过多组分一锅反应,合成了一系列N-取代吖啶二酮衍生物,收率在69%~90%之间。 该过程以水作为溶剂,无有机溶剂污染,而且操作简单,后处理方便。 相似文献
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Yagoub Mansoori Raana Sarvari Mohammad Reza Zamanloo Gholam Hassan Imanzadeh 《高分子科学》2010,28(1):21-28
<正>In the present work,new thermally stable polymers containing 1,3,4-oxadiazole units have been synthesized through Huisgen reaction of the aromatic bis-tetrazole compounds with the aromatic/aliphatic bis-acid chlorides in pyridine as solvent.The obtained polymers are insoluble or slightly soluble in polar aprotic solvents such as DMSO and DMF. Thermal analyses of the polymers using DSC and TGA techniques showed that the polymers had improved thermal stabilities.The model reaction was also investigated and the resulting bis-l,3,4-oxadiazole compounds were characterized by conventional spectroscopic methods. 相似文献
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Silver‐Catalyzed Arylation of (Hetero)arenes by Oxidative Decarboxylation of Aromatic Carboxylic Acids 下载免费PDF全文
Jian Kan Shijun Huang Jin Lin Min Zhang Prof. Weiping Su 《Angewandte Chemie (International ed. in English)》2015,54(7):2199-2203
A long‐standing challenge in Minisci reactions is achieving the arylation of heteroarenes by oxidative decarboxylation of aromatic carboxylic acids. To address this challenge, the silver‐catalyzed intermolecular Minisci reaction of aromatic carboxylic acids was developed. With an inexpensive silver salt as a catalyst, this new reaction enables a variety of aromatic carboxylic acids to undergo decarboxylative coupling with electron‐deficient arenes or heteroarenes regardless of the position of the substituents on the aromatic carboxylic acid, thus eliminating the need for ortho‐substituted aromatic carboxylic acids, which were a limitation of previously reported methods. 相似文献
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Vasant R. Choudhary Suman K. Jana Mahesh K. Chaudhari 《Journal of molecular catalysis. A, Chemical》2001,170(1-2):251-259
Performance of In- and Ga-modified ZSM-5 type zeolites (namely, In2O3/H-ZSM-5, Ga2O3/H-ZSM-5, H-GaMFI and H-GaAlMFI) and InCl3 or GaCl3 supported on high silica mesoporous MCM-41 or on Mont.-K10 in the liquid phase polycondensation of benzyl chloride to polybenzyl has been investigated. Influence of solvent (namely, dichloroethane, n-heptane and ethanol) and temperature on the rate of polycondensation of benzyl chloride over the catalyst (InCl3/Si-MCM-41) showing highest polycondensation activity has also been studied. The In- and Ga-containing solid catalysts show good or high activity in the polycondensation reaction at the reaction condition normally employed in the benzylation of aromatic compounds by benzyl chloride. However, the polycondensation is strongly influenced by the solubility of the polybenzyl polymer in the reaction medium and consequently by the solvent used as the reaction medium. 相似文献
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Andrzej Gondela 《Tetrahedron》2007,63(13):2859-2864
1-(2,4-Dinitrophenyl)-5-nitrouracil and its 3-methyl derivatives were synthesized and used as substrates in reaction with aromatic amines and amino pyridines. In the reaction of aniline with 1-(2,4-dinitrophenyl)-5-nitrouracil, only the acyclic adduct was isolated. When 1-(2,4-dinitrophenyl)-3-methyl-5-nitrouracil was treated with aniline and other aromatic amines or amino pyridines, the desired 1-aryl-5-nitrouracil derivatives were obtained in satisfactory yield. The influence of the free H-3 proton present in the uracil ring on the course of the reaction is discussed. 相似文献
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Lorenz Fehr Leonard Sewald Prof. Dr. Robert Huber Prof. Dr. Markus Kaiser 《European journal of organic chemistry》2023,26(27):e202300636
A facile multicomponent, catalyst-free oxazolidinone synthesis from primary aliphatic or aromatic amines, dibromoethane (DBE), and the usage of either cesium carbonate or cesium hydrogencarbonate as the simultaneous base and C1 source is reported. The applicability of this technically simple reaction was demonstrated by a broad scope with generally high yields, enabling concise late-stage functionalization of amino groups into N-substituted oxazolidinones. The proposed operating reaction mechanism consists of a first-step nucleophilic substitution reaction between DBE and the primary amine, followed by the formation of a carbamate or carbonate intermediate and subsequent cyclization. Additional versatility of the herein-developed protocol has been showcased in a medicinal chemistry approach by the generation of an oxazolidinone-modified dipeptidyl peptidase 8 (DPP8) inhibitor. 相似文献
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以碱性离子液体1-(2-氨基乙基)-3-甲基咪唑咪唑盐([2-aemim]im)作为催化剂,催化Knoevenagel反应和4-芳亚甲基异噁唑-5(4H)-酮衍生物的合成。实验结果表明:在无溶剂条件下,该离子液体对Knoevenagel反应具有很高的催化活性,一系列芳香醛和活泼亚甲基化合物的反应在室温条件下2 min内顺利完成,均以90%以上的高产率生成取代烯烃产物.将该碱性离子液体用于催化乙酰乙酸乙酯或苯甲酰乙酸乙酯、盐酸羟胺和芳香醛三组分一锅法缩合制备4-芳亚甲基异噁唑-5(4H)-酮衍生物,具有反应时间较短、产率较高和后处理简单的特点。离子液体经简单处理后能多次循环使用。 相似文献
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Numerical Investigation on 1,3-Butadiene/Propyne Co-pyrolysis and Insight into Synergistic Effect on Aromatic Hydrocarbon Formation 下载免费PDF全文
Tian-yu Li Jia-biao Zou Yan Zhang Chuang-chuang Cao Wei Li Wen-hao Yuan 《化学物理学报(中文版)》2017,30(3):287-294
A numerical investigation on the co-pyrolysis of 1,3-butadiene and propyne is performed to explore the synergistic effect between fuel components on aromatic hydrocarbon formation.A detailed kinetic model of 1,3-butadiene/propyne co-pyrolysis with the sub-mechanism of aromatic hydrocarbon formation is developed and validated on previous 1,3-butadiene and propyne pyrolysis experiments.The model is able to reproduce both the single component pyrolysis and the co-pyrolysis experiments,as well as the synergistic effect between 1,3-butadiene and propyne on the formation of a series of aromatic hydrocarbons.Based on the rate of production and sensitivity analyses,key reaction pathways in the fuel decomposition and aromatic hydrocarbon formation processes are revealed and insight into the synergistic effect on aromatic hydrocarbon formation is also achieved.The synergistic effect results from the interaction between 1,3-butadiene and propyne.The easily happened chain initiation in the 1,3-butadiene decomposition provides an abundant radical pool for propyne to undergo the H-atom abstraction and produce propargyl radical which plays key roles in the formation of aromatic hydrocarbons.Besides,the 1,3-butadiene/propyne co-pyrolysis includes high concentration levels of C3 and C4 precursors simultaneously,which stimulates the formation of key aromatic hydrocarbons such as toluene and naphthalene. 相似文献
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用对苯二甲醛或间苯二甲醛与5,5-二甲基-1,3-环己二酮反应,在不同条件下得到了含有双4(H)-吡喃、1,4_二氢吡啶结构单元的双一氧杂蒽衍生物、双-吖啶衍生物、以及双-AL羟基吖啶衍生物. 相似文献