<p>The method for the synthesis of <i>N</i>-isopropyl-<i>N</i>′,<i>N</i>′-diorganyl-<i>N</i>-[(triethoxysilyl)-methyl]ureas was optimized. The reaction of these compounds with triethanolamine afforded the corresponding <i>N</i>-(silatranylmethyl)ureas R<sub>2</sub>NC(O)N(Pr<sup>i</sup>)CH<sub>2</sub>Si(OCH<sub>2</sub>CH<sub>2</sub>)<sub>3</sub>N (R = Me, Ph). The structures of the new compounds were confirmed by multinuclear NMR spectroscopy. The structure of the silane Ph<sub>2</sub>NC(O)N(Pr<sup>i</sup>)CH<sub>2</sub>Si(OEt)<sub>3</sub> was established by X-ray diffraction. Preliminary data on the effect of <i>N</i>-isopropyl-<i>N</i>′,<i>N</i>′-dimethyl-<i>N</i>-(silatranylmethyl)urea on the parameters of the rapeseed and wheat growth were obtained.</p>

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N-Isopropyl-N′,N′-diorganyl-N-(silylmethyl)ureas: synthesis, structure, and biological activity

  • N. F. Lazareva,
  • N. V. Filinova,
  • M. A. Alekseev,
  • M. S. Molokeev

摘要

The method for the synthesis of N-isopropyl-N′,N′-diorganyl-N-[(triethoxysilyl)-methyl]ureas was optimized. The reaction of these compounds with triethanolamine afforded the corresponding N-(silatranylmethyl)ureas R2NC(O)N(Pri)CH2Si(OCH2CH2)3N (R = Me, Ph). The structures of the new compounds were confirmed by multinuclear NMR spectroscopy. The structure of the silane Ph2NC(O)N(Pri)CH2Si(OEt)3 was established by X-ray diffraction. Preliminary data on the effect of N-isopropyl-N′,N′-dimethyl-N-(silatranylmethyl)urea on the parameters of the rapeseed and wheat growth were obtained.