An efficient two-step synthesis of novel 2-amino-substituted pyrazolo[1,5-a][1,3,5] triazines

2018-09-262018-09-262012https://repositorio.minciencias.gov.co/handle/20.500.14143/21975A series of novel 2-amino-substituted pyrazolo[1,5-a][1,3,5]triazines were selectively synthesized by a two-step reaction between 5-amino-3-hetaryl-1H-pyrazoles and hetaroyl isothiocyanates with subsequent amination and cyclization promoted by the couple HgCl2/TEA and DMF as solvent. This approach provided the title compounds in good to excellent yields and under mild reaction conditions. The structures of the new compounds were unambiguously established by spectroscopic and analytical techniques.pdf4 páginasenginfo:eu-repo/semantics/embargoedAccessAn efficient two-step synthesis of novel 2-amino-substituted pyrazolo[1,5-a][1,3,5] triazinesArtículo científico10.1016/j.tetlet.2013.01.073Síntesis (química orgánica)Radicales (química)Amino H-pyrazolesPyrazolo[1,5-a][1,3,5]triazinesPyrazolylthioureasGuanylationNucleophilic aminationMercury(II) chlorideReacciones químicasTecnología químicaCompuestos orgánicosQuímica orgánicaResiduos orgánicos