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Chemical transformations of N-morpholinylacetic acid hydrazide and steric structure of its derivatives
Authors:O A Nurkenov  S D Fazylov  Zh B Satpaeva  I V Kulakov  K M Turdybekov  D M Turdybekov  S A Talipov  B T Ibragimov
Institution:1720. Institute of Organic Synthesis and Coal Chemistry of Kazakhstan, ul. Alikhanova 1, Karaganda, 100008, Kazakhstan
2720. International Research and Production Holding “Phytochemistry,”, ul. Gazalieva 4, Karaganda, 100008, Kazakhstan
3720. Multi-Profile Humanitarian-Technical University, pr. Bukhar Zhyrau 12, Karaganda, 100000, Kazakhstan
4720. Sadykov Institute of Bioorganic Chemistry, Academy of Science of Uzbekistan, Tashkent, Uzbekistan
Abstract:The reaction of N-morpholinylacetic acid hydrazide with various isothiocyanates and potassium thiocyanate resulted in the corresponding potentially biologically active thiosemicarbazide derivatives. Potassium N′-(2-morpholin-4-ylacetyl)hydrazinocarbothioate was synthesized and involved into heterocyclization in acidic environment to yield cyclic 5-(morpholinomethyl)-1,3,4-thiadiazole-2-thione. The structure of the synthesized compounds was established by IR, 1H NMR spectroscopy, mass spectrometry, and XRD analysis.
Keywords:
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