Chemistry is an experimental science, Application In Synthesis of 2-(1H-1,2,4-Triazol-3-yl)pyridine, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 23195-62-2, Name is 2-(1H-1,2,4-Triazol-3-yl)pyridine
A SYNTHESIS OF N-(4′-QUINAZOLON-3′-YL)-2-PYRIDINECARBOXAMIDYNES AND THEIR CONVERSION INTO 1,2,4,TRIAZOLES
Treatment of N-(2′-aminobenzoyl)-2-pyrydilamidrazone (1) with ethoxymethylenemalononitrile (EMNN) and ethyl ethoxymethylenecyanoacetate (EMCA) or ortho esters afforded the corresponding N-(2′-alkyl-4′-quinazolon-3′-yl)-2-pyridinecarboxamides (2).Furthermore, treatment of 2 with ethanolic hydrochloric acid caused the ring transformation to give corresponding 5-alkyl-3-(2′-pyridyl)-1H-1,2,4-triazoles (3).
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of 2-(1H-1,2,4-Triazol-3-yl)pyridine, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 23195-62-2, in my other articles.
Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI