77202-06-3

Upstream product

• 67-51-6 3,5-dimethyl-1H-pyrazole 

Downstream Products

• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 77202-09-6 4,6-dimethyl-1,2,3-triazine 
• 122481-14-5 4-Chloro-3,5-dimethyl-pyrazol-1-ylamine 
• 109520-02-7 5-chloro-4,6-dimethyl-1,2,3-triazine 
• 122481-15-6 4-Iodo-3,5-dimethyl-pyrazol-1-ylamine 
• 99214-51-4 Bis-(3,5-dimethyl-pyrazol-1-yl)-diazene 
• 99214-50-3 Bis-(3,5-dimethyl-pyrazol-1-yl)-diazene 
• 137968-25-3 1-(Benzylamino)-3,5-dimethylpyrazole 
• 137968-18-4 1-(Benzylideneamino)-3,5-dimethylpyrazole 

Relevant academic research and scientific papers

Synthesis of new N-(4-pyridyl)-1-aminopyrazoles and their muscarinic and adrenergic properties

The synthesis of new N-(4-pyridyl)-1-aminopyrazoles is described. Their binding properties were tested for muscarinic and other neurotransmitter receptors, together with their acetylcholinesterase inhibitory activity. The series derived from 3,5-dimethyl-1H-pyrazole showed moderate activities in both muscarinic and adrenergic receptor binding tests.

1,2,3-Triazines,III. - Synthesis of N-Aminopyrazoles and their Oxidation to 1,2,3-Triazines. Molecular Structure of 1,2,3-Triazine

Oxidation of the N-aminopyrazoles 4a-i affords the 1,2,3-triazines 5a-i.Spectra and reactions - such as oxidation, reduction, and cycloaddition reactions - of some 1,2,3-triazines 5 are described.The X-ray analysis of 5a is presented.

Oxidation of 1-Aminopyrazoles and Synthesis of 1,2,3-Triazines

Unsubstituted and various substituted monocyclic 1,2,3-triazines were synthesized from 1-aminopyrazoles by oxidation with lead tetraacetate, lead dioxide-CF3CO2H, and/or nickel peroxide-AcOH.