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5-(色酮基-3-次甲基)(硫代)巴比妥酸的合成 被引量:4

Synthesis of 5-(Chromon-3-ylmethylidene)(thio)barbituric Acid
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摘要 将巴比妥酸或硫代巴比妥酸、3 甲酰基色酮在乙酸 -乙酸酐溶液 (含乙酸酐 10 % )中进行缩合反应 ,制备了 5 (色酮基 3 次甲基 ) (硫代 )巴比妥酸 .并经元素分析 ,IR ,1HNMR及13 The condensation reactions between barbituric acid or thiobarbituric acid and 3-formyl chromones were carried out with heating in acetic/acetic anhydride to give 5-(chromon-3-ylmethylidene)(thio)barbituric acids. The structures of the condensed products were characterized by elemental analysis, IR, 1H NMR and 13C NMR spectroscopies.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2004年第10期1278-1280,共3页 Chinese Journal of Organic Chemistry
关键词 5-(色酮基-3-次甲基)巴比妥酸 合成 缩合反应 3-甲酰基色酮 5-(色酮基-3-次甲基)硫代巴比妥酸 formyl chromone, barbituric acid, 5-(chromon-3-ylmethylidene)(thio)barbituric acid, synthesis
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  • 1杨骏,花文廷.2,5-二取代-1,3,4-噁二唑类化合物的合成[J].化学通报,1996(9):18-26. 被引量:39
  • 2于建新,刘方明,鲁文杰,李燕萍,糟新民,刘育亭,刘丛.3-(2-二唑啉基)-色酮类化合物的合成研究[J].有机化学,2000,20(1):72-80. 被引量:11
  • 3李贵深,王春,李敬慈,张英群,李晓陆.无溶剂条件下5-亚烃基硫代巴比妥酸的合成[J].有机化学,2003,23(8):858-860. 被引量:22
  • 4陆军 李迎迎 杨玲 白银娟 田敏.有机化学,2003,23:958-958.
  • 5Nohara, A ; Umetani, T ; Sarmo, Y. Tetrahydron Lett 1973,22, 1995.
  • 6Srivastava, S K ; Pathak, R B ; Bahel, S C .J Indian Chem Soc 1991, 68, 113.
  • 7Alan, O F ; Jonathan, R F ; Peter, G H ; Hans, S .J Chem Soc, Perkin Trans 1 1979, 1691.
  • 8Yu, J.-X.; Liu, F.-M.; Lu, W.-J.; Li, Y.-P.; Zao, X.-M.;Liu, Y.-T.; Liu, C. Chin. J. Org. Chem. 2000, 20, 72 (in Chinese).(于建新,刘方明,鲁文杰,李燕萍,糟新民,刘育亭,刘丛,有机化学,2000,20,72.)
  • 9Li, G.-S.; Wang, C.; Li, J.-C.; Zhang, Y.-Q.; Li, X.-L.Chin. J. Org. Chem. 2003, 23, 858 (in Chinese).(李贵深,王春,李敬慈,张英群,李晓陆,有机化学,2003,23,858.)
  • 10Lu,J.;Li,Y.-Y.;Yang,L.;Bai,Y.-J.;Tian,M.Chin.J.Org.Chem.2003,23,958(in Chinese).(陆军,李迎迎,杨玲,白银娟,田敏,有机化学,2003,23,958.)

二级参考文献22

  • 1徐东成,杨骏,周健民,张玉霞,花文廷.2,5-二取代1,3,4-噁二唑的合成及其电子轰击质谱[J].化学通报,1996(10):61-64. 被引量:6
  • 2Toda, F. Synlett 1993, 303.
  • 3Caddick, S. Tetrahedron 1995, 51, 10403.
  • 4Deshayes, S. ; Liagre, M. ; Loupy, A. ; Luche, J. L. ; Petit, A.Tetrahedron 1999, 55, 10851.
  • 5Abdallah-Elayoubi, S. ; Texier-Boullet, F. ; Hamelin, J.Synthesis 1994, 258.
  • 6Reijo, B. ;Erkki, H. WO 9117151, 1991 [Chem. Abstr. 1992,116, 59398c].
  • 7Sabaa, M. W. ; Mohamed, N. A. ; Khalil, K. D. ; Yassin, A.A. Polym. Degrad. Stab. 2000, 70, 121.
  • 8Kazufumi, I.; Nobuaki, G.; Hajime, M.; Toshie, M..JP 03012660, 1991 [Chem. Abstr. 1991, 115, 146585i].
  • 9Dyachkou, A. I. ; Ivin, B. A. ; Smorygo, N. A. ; Sochilin, E.G. Zh. Org. Khim. 1976, 12, 1115.
  • 10Vvedenskii, V. M. ; Makukha, M. P. ; Makarina-Kibak, L. Y.Khim. Geterotsikl. Soedin. 1969, 1096.

共引文献69

同被引文献27

  • 1李贵深,王春,李敬慈,周雅璇,赵花荣,李平,耿会角.芳香醛与噻唑酮衍生物的固相缩合反应[J].应用化学,2004,21(10):1069-1071. 被引量:7
  • 2谢芳,李燕萍,刘晨江,张力.5-(取代吡唑基-4-次甲基)(硫代)巴比妥酸的合成[J].化学通报,2005,68(12):944-946. 被引量:2
  • 3葛裕华,吴亚明,薛忠俊.取代吲哚-3-甲醛类化合物的合成[J].有机化学,2006,26(4):563-567. 被引量:33
  • 4万茂生,何秋霞,赵宝祥,焦培福,王大威,苗俊英.6-氨基-2-取代吲哚-3-羧酸乙酯及其衍生物的合成与生物活性评价[J].有机化学,2006,26(9):1248-1253. 被引量:9
  • 5Agarwal A,Srivastava K,Puri S K,et al.Bioorg Med Chem Lett[J].2005,15:3133-3136.
  • 6Golob T,Liebl R,Von Angerer E.Bioorg Med Chem[J].2002(10):3941-3953.
  • 7STANKOVLCOVA H, FABIAN W M F, LACOVA M. Synthesis and theoretical study of mannich type reaction products of 3-formylchromones with triazoles and amides and nucleophilic formation of 2,3-disubstituted-4-chromanones[ J]. Molecules, 1996( 1 ) :223 - 235.
  • 8LACOVA M, PUCHALA A, SOLCANYOVA E,et al. 3- Formylchromones Ⅳ. The rearrangement of 3-formylchromone enamines as a simple, facile route to novel pyrazolo[ 3,4-b] pyridines and the synthetic utility of the latter[ J]. Molecules, 2005 (10) : 809 - 821.
  • 9PUCCETTI L, FASOLIS G, VULLO D, et al. Carbonic anhydrase inhibitors. Inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes Ⅰ , Ⅱ, Ⅸ, and Ⅻ with Schiffs bases incorporating chromone and aromatic sulfonamide moieties, and their zinc complexes [ J ]. Bioorg Med Chem Lett.2005. 15:3096-3010.
  • 10ROMA G,BRACCIO M D, CARRIERI A, et al. Coumarin, chromone, and 4 ( 3H )-pyrimidinone novel bicyclic and tricyclic derivatives as antiplatelet agents : synthesis, biological evaluation, and comparative molecular field analysis[J]. Bioorg Med Chem, 2003, 11 :123 - 138.

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