SYNTHESIS AND CRYSTAL STRUCTURE OF N-ETHYL-N-CYTISINOCARBOTHIOAMIDE

2021

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DOI 10.1134/s0022476621110032
Data confidence 70 medium
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Abstract

Abstract Based on (–)-cytisine alkaloid and ethyl isothiocyanate, N-ethyl-N-cytisinocarbothioamide is synthesized and its structure is proved by 1H NMR spectroscopy and single crystal X-ray diffraction. The mesomeric effect is shown in the carbothioamide group formed. It is found that π-conjugation between nitrogen atoms and the thiocarbonyl group is weakened due to the steric hindrance between hydrogen atoms of the piperidine ring and the thioamide group.