Synthesis, crystal structure and cytotoxic activity of novel 5‐methyl‐4‐thiopyrimidine derivatives

• Published in: Acta crystallographica. Section C, Crystal structure communications Crystal structure communications, 2018-10, Vol.74 (10), p.1138-1145
• Main Authors: Stolarczyk, Marcin, Bryndal, Iwona, Matera-Witkiewicz, Agnieszka, Lis, Tadeusz, Królewska-Golińska, Karolina, Cieślak, Marcin, Kaźmierczak-Barańska, Julia, Cieplik, Jerzy
• Format: Article
• Language: English
• Subjects: 4‐thiopyrimidine derivatives; Antineoplastic Agents - chemical synthesis; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; Aromatic compounds; Biotechnology; Cancer; Cell Survival - drug effects; Chains; Chemical bonds; Crystal structure; Crystallography, X-Ray; cytotoxic activity; Cytotoxicity; Derivatives; Endothelial cells; HeLa Cells; Human Umbilical Vein Endothelial Cells; Humans; Hydrogen Bonding; Hydrogen bonds; Infrared radiation; K562 Cells; Models, Molecular; Molecular chains; NMR; Nuclear magnetic resonance; Synthesis; Toxicity; X-ray diffraction
• ISSN: 2053-2296; 0108-2701; 2053-2296; 1600-5759
• DOI: 10.1107/S2053229618012706

This article presents the synthesis of three new 4‐thiopyrimidine derivatives obtained from ethyl 4‐methyl‐2‐phenyl‐6‐sulfanylpyrimidine‐5‐carboxylate as the starting material, namely, ethyl 4‐[(4‐chlorobenzyl)sulfanyl]‐6‐methyl‐2‐phenylpyrimidine‐5‐carboxylate, C21H19ClN2O2S, (2), {4‐[(4‐chlorobenzyl)sulfanyl]‐6‐methyl‐2‐phenylpyrimidin‐5‐yl}methanol, C19H17ClN2OS, (3), and 4‐[(4‐chlorobenzyl)sulfanyl]‐5,6‐dimethyl‐2‐phenylpyrimidine, C19H17ClN2S, (4), which vary in the substituent at the 5‐position of the pyrimidine ring. The compounds were characterized by 1H NMR, 13C NMR, IR and mass spectroscopies, and also elemental analysis. The molecular structures were further studied by single‐crystal X‐ray diffraction. Compound (2) crystallizes in the space group P with one molecule in the asymmetric unit, whereas compounds (3) and (4) crystallize in the space group P21/c with two and one molecule, respectively, in their asymmetric units. The conformation of each molecule is best defined by the dihedral angles formed between the pyrimidine ring and the planes of the two aryl substituents attached at the 2‐ and 4‐positions. The only structural difference between the three compounds is the substituent at the 5‐position of the pyrimidine ring, but they present significantly different features in the hydrogen‐bond interactions. Compound (2) displays a one‐dimensional chain formed by hydrogen bonds and the chains are further extended into a two‐dimensional network. Molecules of (3) and (4) generate one‐dimensional chains formed through intermolecular interactions. The study examines the cytotoxicity of compounds (3) and (4) against Human umbilical vein endothelial cells (HUVEC) and HeLa, K562 and CFPAC cancer cell lines. The presence of the hydroxymethyl and methyl groups in (3) and (4), respectively, offers an interesting new insight into the structures and behaviour of these derivatives. Compound (4) was found to be nontoxic against CFPAC and HUVEC; however, it shows weak activity against the HeLa and K563 cell lines. The presence of a hydroxy group in (3) significantly increases its cytotoxicity towards both, i.e. the cancer (HeLa, K562 and CFPAC) and normal (HUVEC) cell lines. The cytotoxicities of 4‐thiopyrimidine derivatives obtained from ethyl 4‐methyl‐2‐phenyl‐6‐sulfanylpyrimidine‐5‐carboxylate were examined against Human umbilical vein endothelial cells (HUVEC) and HeLa, K562 and CFPAC cancer cell lines. The presence of hydroxymethyl and methyl groups offers