Chin. J. Org. Chem. ›› 2009, Vol. 29 ›› Issue (05): 753-757. Previous Articles     Next Articles

Original Articles

N-异壬酰基-N’-取代芳基硫脲的简便合成、晶体结构及生物活性

张有明 ; 陈小春; 陈 靖; 王爱霞; 魏太保*   

  1. (西北师范大学化学化工学院 甘肃省高分子材料重点实验室 兰州 730070)
  • 收稿日期:2008-09-16 修回日期:2008-11-23 发布日期:2009-05-20
  • 通讯作者: 魏太保

Simple Synthesis, Crystal Structure and Biological Activities of N-Isononanoyl-N’-arylthioureas

Zhang, Youming; Chen, Xiaochun ; Chen, Jing; Wang, Aixia; Wei, Taibao*

  

  1. (Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070)
  • Received:2008-09-16 Revised:2008-11-23 Published:2009-05-20
  • Contact: Wei, Taibao

A series of new N-Isononanoyl-N’-arylthiourea compounds were synthesized simply rapidly and high efficiently by serial reactions of triphosgene, isononanoic acid, potassium thiocyanate and aromatic amines, under solvent-free conditions, and confirmed by IR, 1H NMR and 13C NMR spectra. The crystal structure of compound 4g was determined by X-ray single crystal diffraction analysis. It belongs to monoclinic system with space group P2(1)/n, and a=1.4365(4) nm, b=0.7979(2) nm, c=1.5521(4) nm, β=94.814(4)°, V=1.7726(8) nm3, Dx=1.264 Mg•m-3, Z=4, F(000)=720, µ=0.200 mm-1, R=0.058, and wR=0.231. The crystal structure of compound 4g shows that the compound was assembled to a layered structure by intermolecular hydrogen bond and the force between the moleculars of each layer. The preliminary biological activity tests show that some of the title compounds have some regulating activities for the growth of rape.

Key words: isononanoic acid, crystal structu, solvent-free, thiourea, triphosgene