1,2,3-THIADIAZOLYL ISOCYANATES IN THE SYNTHESIS OF BIOLOGICALLY ACTIVE COMPOUNDS. STUDY OF THE CYTOTOXIC ACTIVITY OF <i>N</i>-(4-METHYL-1,2,3-THIADIAZOLYL-5-YL)-<i>N</i>'-(4-METHYLPHENYL)UREA
DOI:
https://doi.org/10.1007/1764Keywords:
6-benzylaminopurine, cytokinin, isocyanates, 1, 2, 3-thiadiazole, thidiazuron, ureasAbstract
A simple method is proposed for the synthesis of 1,2,3-thiadiazolylureas by the reaction of 1,2,3-thiadiazolyl isocyanates with primary amines. 1,2,3-Thiadiazolyl isocyanates were obtained in situ by the Curtius rearrangement of 1,2,3-thiadiazolylcarbonyl azides. Cytokinin activity was tested for N‑(4‑methyl-1,2,3-thiadiazol-5-yl)-N'-(4-methylphenyl)urea, which is an analog of thidiazuron, differing in the presence of two methyl groups in the molecule.
How to Cite
Kalinina, T. A.; Shakhmina, Yu. S.; Glukhareva, T. V.; Morzherin, Yu. Yu.; Fan, Z.-J.; Borzenkova, R. A.; Skolobanova, E. S.; Kiseleva, I. S. Chem. Heterocycl. Compd. 2014, 50, 1039. [Khim. Geterotsikl. Soedin. 2014, 1127.]
For this article in the English edition see DOI 10.1007/s10593-014-1561-9