Synthesis of 5-Amino-2-oxo-7-aryl-2,3,4,7-tetrahydro-1,3-thiazolo[4,5-b]pyridine-6-carboxamide Derivatives under Microwave Irradiation

  • Sun Hongshun ,
  • Wang Jianqiang ,
  • Guo Cheng ,
  • Shen Linjiang
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  • a Nanjing University of Technology, Nanjing 211816;
    b Nanjing College of Chemical Technology, Nanjing 210048

Received date: 2013-04-23

  Revised date: 2013-05-28

  Online published: 2013-07-03

Supported by

Project supported by the National Natural Science Foundation of China (No. 21106069) and the Key Program of Nanjing College of Chemical Technology (No. NHKY-2013-2).

Abstract

Five new 5-amino-2-oxo-7-aryl-2,3,4,7-tetrahydro-1,3-thiazolo[4,5-b]pyridine-6-carboxamide derivatives, which are different with the products of 5-amino-2-oxo-7-aryl-2,3,4,7-tetrahydro-1,3-thiazolo[4,5-b]pyridine-6-carbonitrile derivatives in the conventional heating conditions, were synthesized by using arylmethylene malononitrile, 2,4-thiazolidinedione and ammonium acetate in one-pot via microwave irradiation techniques. And the reaction mechanism was discussed. The structures of these compounds were characterized by 1H NMR, IR, MS and elemental analysis.

Cite this article

Sun Hongshun , Wang Jianqiang , Guo Cheng , Shen Linjiang . Synthesis of 5-Amino-2-oxo-7-aryl-2,3,4,7-tetrahydro-1,3-thiazolo[4,5-b]pyridine-6-carboxamide Derivatives under Microwave Irradiation[J]. Chinese Journal of Organic Chemistry, 2013 , 33(10) : 2220 -2225 . DOI: 10.6023/cjoc201304037

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