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含有薁类结构的1,4-二氢吡啶衍生物的合成 被引量:6

Synthesis of 1,4-Dihydropyridines Containing Azulenes Moiety
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摘要 在对甲基苯磺酸作用下,以1-甲酰基薁-3-甲酸甲酯、乙酰乙酸酯、醋酸铵或3-氨基巴豆酸酯为原料,进行三组分一锅法缩合,以较优的收率制备了含有薁类结构的新的1,4-二氢吡啶类衍生物,该反应收率良好、操作简单、条件温和.产物的结构经1H NMR,IR及元素分析等得以证实. New 1,4-dihydridine derivatives containing azulene moiety were synthesized by three component one-pot condensation of methyl 1-formoylazulene-3-carboxylate,acetoacetic esters and ammonium acetate or alkyl 3-amminocrotonate under p-toluenesulfonic acid as a catalyst.This method provides several advantages such as good yield and simple work-up procedure.All the products were fully characterized by ^1H NMR,IR spectra and elemental analysis.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2010年第11期1774-1777,共4页 Chinese Journal of Organic Chemistry
关键词 1-甲酰基薁-3-甲酸甲酯 1 4-二氢吡啶 合成 azulene methyl 1-formoylazulene-3-carboxylate 1 4-dihydridine synthesis
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  • 1庞冀燕,汪波,陈之朋,许遵乐.2-取代芳基苯并[b]呋喃类化合物的合成[J].有机化学,2005,25(2):176-181. 被引量:11
  • 2[1]Fujimori, K.; Fukazawa, H.; Nezu, Y.; Yamane, K.; Yasunami, M.; Takase, K. Chem. Lett. 1986, 1021.
  • 3[2](a) Matsui, K.; Nozoe, T. Chem. Ind. 1960, 1302.(b) Matsui, K. Nippon Kagaku Zasshi 1961, 82, 1517.
  • 4[3]Yamane, K.; Takeuchi, T. Bull. Chem. Soc. Jpn. 1981, 54, 2537.
  • 5[4]Fujimori, K.; Fujita, T.; Yamane, K.; Yasunami, M.; Takase, K. Chem. Lett. 1983, 1721.
  • 6Takasugi, M.; Nagao, S.; Masamura, T.; Shirata, A.; Takahashi, M. Tetrahedron Lett. 1978, 19, 797.
  • 7Mann, I. S., Widdowson, D. A. Tetrahedron 1991, 47, 7981.
  • 8Sheen, W. S.; Tsai, I. L.; Teng, C. M.; Chen, I. S. Phytochemistry 1994, 36, 213.
  • 9Jenab, M.; Thompson, L. U.; Lillian, U. Carcinogenesis 1996, 17, 1343.
  • 10Thompson, L. U.; Seidl, M. M.; Richard, S. E.; Orcheson, L. J.; Fong, H. H. S. Nutr. Cancer 1996, 26, 59.

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  • 1吴美芝,曾明,熊立武,李晓如.相转移催化氧化合成氯代苯甲酸[J].精细化工中间体,2004,24(4):42-44. 被引量:1
  • 2蔡小华,张国林.无溶剂一锅法合成1,4-二氢吡啶[J].有机化学,2005,25(8):930-933. 被引量:19
  • 3兰世林,刘卫东,兰支利.邻硝基苄基溴的合成研究[J].精细化工中间体,2006,36(2):24-25. 被引量:8
  • 4王建平,杜美菊,付永举,王建革,李宁,郑爱霞.1,4-二氢吡啶衍生物的合成方法改进[J].合成化学,2007,15(1):42-45. 被引量:7
  • 5黄池宝,任安祥.2,5-二甲基对苯二甲腈α-位溴代反应[J].精细化工,2007,24(3):231-234. 被引量:6
  • 6Gudmundsson K S, Williams J D, Drach J C, et al. Synthesis and antiviral activity of novel erythrofurano- sy] imidazo[ 1,2-a] pyridine C-nucleosides constructed via palladium coupling of iodoimidazo [ 1,2-a ] pyridines and dihydrofuran [ J ]. J Med Chem, 2003,46 : 1449 - 1455.
  • 7Kamimky J J, Doweyko A M. Synthesis, pharmacological evaluation, and structure - activity relationship and quantitative structure - activity relationship studies on novel derivatives of 2,4-diamino-6,7-dimethoxyquinazoline α1 -adrenoceptor antagonists [ J ]. J Med Chem, 1999,42:427 -437.
  • 8Tomoda H, Hirano T, Saito S, et al. Substituent effects on fluorescent properties of imidazo [ 1,2-α ] pyrldine-based compounds [ J]. J Bull Chore Soc Jap, 1999,72 : 1327 - 1334.
  • 9Szabo R, Crozet M D, Vanelle P. Microwave-assisted double Suzuki-Miyaura cross-coupling in the 6,8-di- bromoimidazo [ 1,2-α ] pyridine series [ J ]. Synthesis, 2008,1 : 127 - 135.
  • 10Koubachi J, E 1 Kazzouli S, Breteina-Raboin S, et al. Regiosclective paLladium-catalyzed arylation and het- eroarylation of imidazo[1,2-α ] pyridines [J ]. Synlett, 2006,19 : 3237 - 3242.

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