LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Synthesis, Cytostatic and Antibacterial Evaluations of Novel 1, 2, 3-Triazolyl-tagged Pyrimidine and Furo[2, 3-d]pyrimidine Derivatives

Photo from wikipedia

C-5 alkynylated and N-1 alkylated pyrimidine derivatives were synthesized by N-alkylation reaction of 5-iodouracil in the presence of NaH, as a base, followed by Pd-catalyzed Sonogashira cross-coupling reaction of N-alkyl-5-iodouracil… Click to show full abstract

C-5 alkynylated and N-1 alkylated pyrimidine derivatives were synthesized by N-alkylation reaction of 5-iodouracil in the presence of NaH, as a base, followed by Pd-catalyzed Sonogashira cross-coupling reaction of N-alkyl-5-iodouracil derivatives (1 and 2) with corresponding terminal alkynes. Intramolecular in situ O- heteroannulation ring closure of N-1- alkyl-C-5- alkynylpyrimidine derivatives (3 and 5) generated novel 6-substituted furo[2, 3-d]pyrimidine derivatives (7 and 8). 1, 4-Disubstituted 1, 2, 3- triazole tethered 5- alkynylpyrimidines (14– 19) and 6-substituted furo[2, 3- d]pyrimidines (20–22) were successfully prepared by the copper(I)- catalyzed click reaction of 5-iodo-N- 1- propargylpyrimidine (2) using microwave irradiation, followed by Sonogashira cross- coupling reaction with corresponding terminal alkynes. In vitro antiproliferative activity of prepared compounds evaluated on human cancer cell lines cervix adenocarcinoma (HeLa), colon adenocarcinoma (CaCo- 2), chronic myeloid leukemia in blast crisis (K562), Burkitt lymphoma (Raji) revealed that pyrimidine (19) and furo[2, 3- d]pyrimidine (22) derivatives with 3, 5- difluorophenyl at pyrimidine and furo[2, 3- d]pyrimidine as well as p- (trifluoromethyl)phenyl at 1, 2, 3-triazole exhibited marked and selective inhibitory effects on the growth of K562 and Raji tumor cells. Antibacterial evaluations showed that pyrimidine derivative 14 substituted with p- tolylethynyl at C-5 of pyrimidine and benzyl at 1, 2, 3-triazole moiety was the most active of all evaluated compounds on the Gram positive bacterial strains Enterococcus faecalis. Further structure optimization of compounds 14, 19 and 22 is foreseen in order to obtain lead structural analogs with efficient and selective antitumoral and antibacterial activities.

Keywords: furo pyrimidine; pyrimidine furo; pyrimidine derivatives; pyrimidine; reaction; antibacterial evaluations

Journal Title: Croatica Chemica Acta
Year Published: 2017

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.