32787-80-7Relevant articles and documents
Syntheses, in vitro α-amylase and α-glucosidase dual inhibitory activities of 4-amino-1,2,4-triazole derivatives their molecular docking and kinetic studies
Aboaba, Sherifat A.,Chigurupati, Sridevi,Hameed, Shehryar,Kannan Maharajan, Mari,Kanwal,Mohammed Khan, Khalid.,Perveen, Shahnaz,Shamim, Shahbaz,Taha, Muhammad,Ur Rehman, Ashfaq,Wadood, Abdul,Yeye, Emmanuel Oloruntoba
, (2020/04/23)
Thirty-three 4-amino-1,2,4-triazole derivatives 1–33 were synthesized by reacting 4-amino-1,2,4-triazole with a variety of benzaldehydes. The synthetic molecules were characterized via 1H NMR and EI-MS spectroscopic techniques and evaluated for
REACTION OF SCHIFF BASES OBTAINED FROM 4-AMINOANTIPYRINE AND 4-AMINO-1,2,4-TRIAZOLE WITH KETONES
Letunov, V. I.
, p. 145 - 149 (2007/10/02)
With acetophenone and p-nitroacetophenone in alcohol and benzene media in the presence of acid N-arylidene-4-aminoantipyrines form α,β-unsaturated ketones, and with antipyrine the form aryldiantipyrylmethanes.With the same ketones N-arylidene-4-amino-1,2,4-triazoles form the products from addition at the azomethine bond.In both cases reaction with benzylideneacetone was not detected.