1174271-66-9Relevant academic research and scientific papers
Synthesis of fused 3-amino-1,2,4-triazoles via sequential addition of aryl hydrazines to isothiocyanates and I2-mediated cyclodesulfurization
Jiao, Shufeng,Wang, Zhen,Zhao, Qiongli,Yu, Wenquan,Chang, Junbiao
supporting information, p. 3069 - 3073 (2018/05/23)
A variety of fused 3-amino-1,2,4-triazole derivatives were synthesized via addition of aryl hydrazines to isothiocyanates followed by I2-mediated oxidative cyclodesulfurization. This transition-metal-free synthetic process provides facile acces
I2-Mediated Oxidative C-N and N-S Bond Formation in Water: A Metal-Free Synthesis of 4,5-Disubstituted/N-Fused 3-Amino-1,2,4-triazoles and 3-Substituted 5-Amino-1,2,4-thiadiazoles
Jatangi, Nagesh,Tumula, Nagaraju,Palakodety, Radha Krishna,Nakka, Mangarao
, p. 5715 - 5723 (2018/05/15)
An environmentally benign and convenient strategy for the synthesis of 4,5-disubstituted/N-fused 3-amino-1,2,4-triazoles and 3-substituted 5-amino-1,2,4-thiadiazoles from isothiocyanates has been developed. This metal-free method involves I2-me
Supramolecular Anion Recognition Mediates One-Pot Synthesis of 3-Amino-[1,2,4]-triazolo Pyridines from Thiosemicarbazides
Pandurangan, Komala,Aletti, Anna B.,Montroni, Devis,Kitchen, Jonathan. A.,Martínez-Calvo, Miguel,Blasco, Salvador,Gunnlaugsson, Thorfinnur,Scanlan, Eoin M.
supporting information, p. 1068 - 1071 (2017/03/14)
A facile one-pot synthesis of 3-amino-[1,2,4]-triazolo[4,3-a]pyridines from thiosemicarbazides through anion mediated synthesis is reported. Thiosemicarbazides derived from 2-hydrazino pyridine, 5-chloro 2-hydrazino pyridine, and 2-hydrazine quinoline wer
A straightforward, one-pot protocol for the synthesis of fused 3-aminotriazoles
Comas, Horacio,Bernardinelli, Gerald,Swinnen, Dominique
experimental part, p. 5553 - 5558 (2009/12/08)
(Chemical Equation Presented) A simple protocol for the synthesis of 3-amino-[1,2,4]triazolo[4,3-a]pyridines is reported. The newly developed one-pot methodology involves the reaction of hydrazinopyridine with isothiocyanates to give the corresponding thiosemicarbazides, which are further desulfurized in situ using polymer-supported Mukaiyama's reagent to promote the final cyclization and formation of the central core. Aryl isothiocyanates bearing both electron-donating and electron-withdrawing groups are well tolerated, and the expected compounds were obtained in excellent purities and yields after removal of salts with a SPE-NH2 column. This methodology proved to be robust in the extension to 3-amino-[1,2,4]triazolo[4,3-a]-pyrazines and 3-amino-[1,2,4]triazolo[4,3-c]-pyrimidines, and no significant differences were noticed in terms of purities and yields. The straightforward protocol developed, mix, filter, and evaporate, is appropriate for performing multiple reactions in parallel fashion without need of purification.
