derivative was obtained. The spatial structure of the product was demonstrated by 1 H NMR spectroscopy and X-ray structural analysis.Considerable importance in the years 1980-1990 was acquired by derivatives of 1,4-dihydropyridines, obtained by Hantzsch condensation, as the first representatives of highly effective vasodilators and antihypertensive agents, the calcium channel blockers (Nicardipine, Nifedipine, Felodipine, etc) [1-3]. Compounds were also discovered among the derivatives of 1,4-dihydropyridines with no less valuable pharmacological properties (antibacterial, antiviral, antidiabetic, hepatoprotecting, antiulcer, etc) [4-6], which make further searches in the 1,4-dihydropyridine series extremely urgent. Up to the present time an enormous number of symmetrical and unsymmetrical derivatives of 1,4-dihydropyridine with various functional substituents has been synthesized, and a great number of methods of obtaining them (including microwave) has been developed by further conversions and aromatization [7][8][9][10][11].Scientists of the Latvian Institute of Organic Synthesis have carried out an enormous study in executing the systematic synthesis of numerous derivatives of 1,4-dihydropyridines with the aim of searching for new cardiotonic and ionotropic preparations, and clarification of structure-activity relationships [12][13][14].However, in spite of the enormous number of synthesized derivatives of 1,4-dihydropyridines, no compounds combining in their structure a 1,4-dihydropyridine ring and certain physiologically active alkaloids have been described in the literature. It therefore seemed of interest to synthesize previously unknown 1,4-dihydropyridine derivatives from certain alkaloids, in particular, cytisine.