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Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
Published on: April 27, 2017
One-pot synthesis of 4,5-biphenyl-2-pyrimidinylguanidine derivatives
Zun-Ting Zhang1, Fei-Fei Xu, Mi-Xiang Gao
1Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, and School of Chemistry and Materials Science, Shaanxi Normal University, Xi'an 710062, PR China. zhangzt@snnu.edu.cn
Abstract:
A simple and straightforward methodology toward the synthesis of novel 4,5-biphenyl-2-pyrimidinylguanidine compounds has been developed by one-pot reaction of biguaninde or dimethyldiguanide with isoflavones. A series of 20 new compounds was reported. All of them were characterized by FT-IR, NMR, and elemental analysis. A typical compound was determined by X-ray diffraction. A variety of substrates can participate in the process with good yields and high purities, making this methodology suitable for library synthesis in drug discovery.

