Notes

A New Synthesis of 2-Amino-4,5-substituted Pyrimidine Derivatives

  • Deng Lanqing ,
  • Xu Zhonghai ,
  • Shang Yunfeng ,
  • Dai Wenjing ,
  • Hu Huimin ,
  • Deng Suiping ,
  • Ouyang Jianming
Expand
  • a Key Laboratory of Yueyang Chinese Herbal Utilization, Yueyang Vocational Technical College, Yueyang 414000;
    b Institute of Biomineralization and Lithiasis Research, Jinan University, Guangzhou 510632

Received date: 2011-09-22

  Revised date: 2011-12-20

  Online published: 2012-02-14

Supported by

Project supported by the National Natural Science Foundation of China (No. 30672103) and the Fundation of Hunan Educational Committee (No. 10C0336).

Abstract

In this paper, a novel synthetic method for 2-amino-4,5-substituted pyrimidine derivatives was reported, which began from cheap and simple four aromatic aldehydes and three aliphatic aldehydes. 12 compounds of 2-amino-4,5-substituted pyrimidine derivatives were synthesized by four steps with yields of 40%~70%. The structures of terminational compounds were determined by 1H NMR, 13C NMR and LC-MS techniques.

Cite this article

Deng Lanqing , Xu Zhonghai , Shang Yunfeng , Dai Wenjing , Hu Huimin , Deng Suiping , Ouyang Jianming . A New Synthesis of 2-Amino-4,5-substituted Pyrimidine Derivatives[J]. Chinese Journal of Organic Chemistry, 2012 , 32(06) : 1141 -1145 . DOI: 10.6023/cjoc1109222

References

[1] Wu, Q.; Song, A.-B.; Jin, L.-H.; Hu, D.-Y. Chin. J. Org. Chem.2009, 29(3), 365 (in Chinese).(吴琴, 宋宝安, 金林红, 胡德禹, 有机化学, 2009, 29(3), 365.)  
[2] Wang, Z.; Xu, Y.; Dong, W.; Liang, P.; Yang, X.-L. Chin. J. Org.Chem. 2011, 31(4), 567 (in Chinese).(王振, 徐焱, 董玮, 梁沛, 杨新玲, 有机化学, 2011, 31(4), 567.)  
[3] Li, Y.-X.; Lin, L.; Chen, Q. Chin. J. Org. Chem. 2011, 31(3), 306(in Chinese).(李元祥, 林龙, 陈琼, 有机化学, 2011, 31(3), 306.)  
[4] Bridges, A.-J. Chem. Rev. 2001, 101, 2541.  
[5] Pranab, K.; Mahata U.-K.; Syam, K.-V.; Sriram, H.-I.; Junjappa, H.Tetrahedron 2003, 59, 2631.  
[6] Deshmukh, M.-B.; Salunkhe, S.-M.; Patil, D.-R.; Anbhule, P.-V.Eur. J. Med. Chem. 2009, 44, 2651.
[7] Takahashi, S.; Togo, H. Heterocycles 2010, 1(82), 593.
[8] Aggarwal, V.-K.; Vicente, J.-D.; Pelotier, B.; Holmes, I.-P.;Bonnert, R.-V. Tetrahedron Lett. 2000, 41, 10327.  
[9] Fulton, J.-R.; Aggarwal, V.-K.; Vicente, J.-D. Eur. J. Org. Chem.2005, 1479.  
[10] Angle, S.-R.; Neitzel, M.-L. J. Org. Chem. 2000, 65, 6458.  
[11] Angle, S.-R.; Neitzel, M.-L. J. Org. Chem. 1999, 64, 8754.  
[12] Kil, K.-E; Ding, Y.-S; Lin, K.-S. Nucl. Med. Biol. 2007, 34, 153.  
[13] Plate, R.; Plaum, M.-J.-M.; Deboer, T. Bioorg. Med. Chem. 1996, 4,227.  
[14] Chen, Q.-F.; Zhang, H.-D.; Gong, S.-C. Chin. J. Appl. Chem. 2011,4, 382 (in Chinese).  
Outlines

/