Chinese Journal of Applied Chemistry ›› 2010, Vol. 27 ›› Issue (06): 646-650.DOI: 10.3724/SP.J.1095.2010.90497

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Synthesis and Auxin Activities of Acylamides with Substituted-1H-pyrazole-5-formic Acid and Substituted Thiadiazole-2-ammonia

AN Yue1*, MU Ping-Ping1, ZHANG Ying1, ZHANG Ting1, LV Jian-Zhou2, CHEN Xin2   

  1. (1.School of Chemical Engineering;2.School of Life Sciences,Liaoning Normal University,Dalian 116029)
  • Received:2009-07-24 Revised:2009-08-28 Published:2010-06-10 Online:2010-06-10
  • Contact: Anyue

Abstract:

Ethyl 3-(4-methoxy phenyl)-1H-pyrazole-5-carboxylate was synthesized by means of one-pot reaction method; and two kinds of pyrazole carboxylic acid were obtained through methylation at position 1, chlorination at position 4 and hydrolysis. Six 5-substituted-2-amino-1,3,4-thiadiazoles were obtained from substituted carboxylic acids and thiosemicarbazide using phosphorus acylchloride as the dehydrating agent. Pyrazole and 1,3,4-thiadiazole were connected together by amido bond and 12 new compounds were synthesized. The yield of the title compounds was up to 50%. All the new compounds were confirmed by means of elemental analysis, IR and 1H NMR spectroscopies. Their auxin activities are not high, and a few of them are antiblastic to wheat gemma.

Key words: pyrazole, thiadiazole, synthesis

CLC Number: