Synthesis And Biological Activity Of New Acetylene Ethers Of Carbamates
European Journal of Molecular & Clinical Medicine,
2020, Volume 7, Issue 3, Pages 3566-3582
AbstractResearch objective: to synthesize new carbamate derivatives - ɣ-bromopropargyl ethers of carbamate derivatives for their further application as initial compounds in the synthesis of simple and asymmetric diacetylene ethers of carbamate derivatives.
Materials and methods. Infrared spectra on UR-20 and UR-10 spectrometer (“Carl Zeiss”, Germany) were applied at 3600-500 cm-1, in the form of tablets pressed with KBr. For determination of purity of the obtained compounds, a thin layer chromatography was used. As an adsorbent we used a layer of AI2O3 of the II activity degree, and an iodine vapor as a developer.
Results and Discussion. Using the method of bromination of propargyl ethers of carbamate derivatives, ɣ -bromopropargyl ethers of carbamate derivatives were obtained, used in the synthesis of simple and asymmetric diacetylene ethers of carbamate derivatives. The optimal conditions for their synthesis were established in the process of studying the effect of various factors. Besides, antifungal and herbicide activity of the synthesized compounds was studied and analyzed. Compounds with high antifungal and herbicidal activity were determined.
Conclusion. Convenient methods were developed for obtaining new ɣ-bromopropargyl ethers of carbamate derivatives during the investigation. New simple diacetylene ethers of carbamate derivatives were synthesized by the reaction of interaction on the basis of propargyl ethers and ɣ-bromopropargyl ethers of carbamate derivatives. New asymmetric diacetylene ethers of carbamate derivatives were synthesized by carrying out the reaction of interaction based on propargyl ethers and ɣ-bromopropargyl ethers of various carbamate derivatives.
- Article View: 210
- PDF Download: 386