The Shocking Revelation of 61-82-5

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Pandey, YK; Mishra, A; Rai, P; Singh, J; Singh, J; Singh, RK or concate me.

Safety of 1H-1,2,4-Triazol-5-amine. In 2020.0 CURR ORG SYNTH published article about VITRO ANTIMICROBIAL ACTIVITY; MULTICOMPONENT SYNTHESIS; ONE-POT; CHEMISTRY; AGENTS; DERIVATIVES; INHIBITORS; COMPLEXES in [Pandey, Yogesh K.; Singh, Ramendra K.] Univ Allahabad, Dept Chem, Bioorgan Res Lab, Allahabad 211002, Uttar Pradesh, India; [Mishra, Anu; Rai, Pratibha; Singh, Jagdamba] Univ Allahabad, Dept Chem, Environm Benign Synth Lab, Allahabad 211002, Uttar Pradesh, India; [Singh, Jaya] LRPG Coll, Dept Chem, Sahibabad, Uttar Pradesh, India in 2020.0, Cited 51.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Aims and Objectives: An efficient and facile DBU catalysed synthesis of highly significant motif 5,7-disubstituted-1,2,4-triazolo[1,5-a]pyrimidines under solvent-free condition has been reported. Materials and Methods: To a round bottom flask, 1.0 mmol of chalcone (1), 1.5 mmol of 3-amino-1,2,4-triazole (2) and 30 mol% of DBU were added at 70 degrees C and stirred in solvent-free condition. After the completion of the reaction (monitored by TLC), water (10 ml) was added. The aqueous layer was extracted with ethyl acetate (3 x 10 ml). The combined organic layers were dried over anhydrous Na2SO4. The combined organic layers were evaporated under reduced pressure and the resulting crude product was purified by column chromatography by using ethyl acetate and hexane as eluent. Results: Reaction using chalcone and 3-amino-1,2,4-triazole as model substrates were carried out under different reaction conditions and it was observed that 30 mol% of DBU under the solvent-free condition at 70 degrees C was the optimum temperature for the proposed synthesis. Conclusion: Use of DBU (an organocatalyst) as a base, operational simplicity, high yield of products and short reaction time are some of the significant advantages associated with the proposed strategy.

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Pandey, YK; Mishra, A; Rai, P; Singh, J; Singh, J; Singh, RK or concate me.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics