One-Pot Synthesis of 1, 4-Dihydropyridines in PEG Under Catalyst-Free Conditions

被引:0
作者
Lv, Jing [1 ]
Jun, Liang [2 ]
Kong, Xiangfeng [1 ]
Cao, Lu [1 ]
Zhang, Ying [1 ]
Zhang, Shuwei [1 ]
机构
[1] Shandong Acad Sci, Inst Oceanog Instrumentat, Shandong Prov Key Lab Ocean Environm Monitoring T, Qingdao, Peoples R China
[2] Blue Econ Dev Ctr Qingdao West Coast Area, Qingdao, Peoples R China
来源
PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON CHEMICAL, MATERIAL AND FOOD ENGINEERING | 2015年 / 22卷
关键词
1,4-Dihydropyridines; Hatitzsch reaction; Multi component synthesis; PEG400; Catalyst free; HANTZSCH 1,4-DIHYDROPYRIDINES; POLYHYDROQUINOLINE DERIVATIVES; HETEROGENEOUS CATALYST; EFFICIENT; SOLVENT; DELIVERY; ANTAGONIST; BRAIN; ACID;
D O I
暂无
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
A simple, inexpensive, and efficient one-pot synthesis of 1,4-dihydropyridine via Hantzsch reaction was achieved in good to excellent yields under catalyst free conditions by using PEG400 as solvent. In this reaction, PEG-400 was used as the solvent, which has such advantages: absolutely nontoxic, inexpensive, thermally stable, recoverable and easy to dispose in the reaction. And the corresponding products: 1,4-Dihydropyridine derivatives are very important in organic chemistry and medicine industry, by the using of PEG, the yields of the reaction were all very high(most above 95%). Finally, as to the inexpensive of PEG-400 and the high yields of the reaction, also because of the easy-treated procedures, this kind of reaction could be easier to produce in industrial. So, Polyethylene glycol offers a convenient, inexpensive, non-ionic liquid, non-toxic and recyclable reactions.
引用
收藏
页码:351 / 354
页数:4
相关论文
共 39 条
[21]  
List B, 2001, SYNLETT, P1687
[22]  
Litvinov V.P., 1998, Russ. Chem. Bull, V47, P2053, DOI [10.1007/BF02494257, DOI 10.1007/BF02494257]
[23]   A simple and efficient one-pot synthesis of 1,4-dihydropyridines using heterogeneous catalyst under solvent-free conditions [J].
Maheswara, Muchchintala ;
Siddaiah, Vidavalur ;
Rao, Yerra Koteswara ;
Tzeng, Yew-Min ;
Sridhar, Chenchugari .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2006, 260 (1-2) :179-180
[24]   One-pot synthesis of Biginelli and Hantzsch products catalyzed by non-toxic ionic liquid (BMImSac) and structural determination of two products [J].
Ming, Li ;
Guo Wei-Si ;
Wen Li-Rong ;
Li Ya-Feng ;
Yang Hua-Zheng .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2006, 258 (1-2) :133-138
[25]  
Misra A, 2003, J PHARM PHARM SCI, V6, P252
[26]   Chemical identification of binding sites for calcium channel antagonists [J].
Nakayama, H ;
Kanaoka, Y .
HETEROCYCLES, 1996, 42 (02) :901-909
[27]  
Prokai L, 2000, MED RES REV, V20, P367, DOI 10.1002/1098-1128(200009)20:5<367::AID-MED3>3.0.CO
[28]  
2-P
[29]   A novel TMSI-mediated synthesis of Hantzsch 1,4-dihydropyridines at ambient temperature [J].
Sabitha, G ;
Reddy, GSKK ;
Reddy, CS ;
Yadav, JS .
TETRAHEDRON LETTERS, 2003, 44 (21) :4129-4131
[30]   Discovery of the first non-peptide full agonists for the human bradykinin B2 receptor incorporating 4-(2-picolyloxy)quinoline and 1-(2-picolyl)benzimidazole frameworks [J].
Sawada, Y ;
Kayakiri, H ;
Abe, Y ;
Mizutani, T ;
Inamura, N ;
Asano, M ;
Hatori, C ;
Aramori, I ;
Oku, T ;
Tanaka, H .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (11) :2853-2863