58064-76-9

Usage

InChI:InChI=1/C12H12N5O2S.ClH/c1-8-7-9(2)15-12(14-8)17-20(18,19)11-5-3-10(16-13)4-6-11;/h3-7H,1-2H3,(H,14,15,17);1H/q+1;/p-1

Upstream product

• 57-68-1 sulfadimesine 

Downstream Products

• 74731-81-0 2-[4-(4,6-dimethyl-pyrimidin-2-ylsulfamoyl)-phenylhydrazono]-3-oxo-butyric acid ethyl ester 
• 124259-66-1 4-[1-(2,4-Dimethoxy-3-methyl-benzoyl)-2-oxo-propylazo]-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide 
• 124279-27-2 4-[1-(2,4-Dimethoxy-6-methyl-benzoyl)-2-oxo-propylazo]-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide 
• 124435-14-9 N-(4,6-Dimethyl-pyrimidin-2-yl)-4-[1-(naphthalene-2-carbonyl)-2-oxo-propylazo]-benzenesulfonamide 
• 124259-85-4 4-[5-(2,4-Dimethoxy-6-methyl-phenyl)-3-methyl-1-(pyridine-4-carbonyl)-1H-pyrazol-4-ylazo]-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide 
• 124259-77-4 4-[5-(2,4-Dimethoxy-3-methyl-phenyl)-3-methyl-1-(pyridine-4-carbonyl)-1H-pyrazol-4-ylazo]-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide 
• 124259-75-2 4-[5-(2,4-Dimethoxy-3-methyl-phenyl)-3-methyl-1-(pyridine-4-carbonyl)-1H-pyrazol-4-ylazo]-N-pyrimidin-2-yl-benzenesulfonamide 
• 124259-81-0 4-[5-(2,4-Dimethoxy-6-methyl-phenyl)-3-methyl-1-p-tolyl-1H-pyrazol-4-ylazo]-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide 
• 124259-73-0 4-[5-(2,4-Dimethoxy-3-methyl-phenyl)-3-methyl-1-p-tolyl-1H-pyrazol-4-ylazo]-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide 

Relevant academic research and scientific papers

Synthesis, structural investigations and in vitro biological evaluation of N, N-dimethyl aniline derivatives based azo dyes as potential pharmacological agents

Three novel bioactive azo dyes were synthesized by a classical diazo-coupling method using sulfamethazine with three different N, N-dimethyl aniline derivatives as coupling components under appropriate experimental conditions. The structural features of t

Synthesis and anti-oxidant evaluation of some novel sulfa drugs

Background: Curcumins were reported to possess anti-inflammatory and antiangiogenic. Furthermore, Curcumin is a very potent free radical scavenger than vitamin E. Moreover, cyanoacetamides were reported to possess, antimicrobial antifungal, insulin releasing, antiinflammatory and antitumor. Thus the present study focuses on the synthesis of some novel structure hybrids incorporating either curcumin or cyanoacetamide with sulphonamide, aiming to reach a more potent antioxidant agent. Methods: 4-arylazoenol derivatives 12-16 and E-hydrazo derivatives 19-23 were prepared and their structure was confirmed by variable spectra analysis. The newly synthesized compounds were screened for their antioxidant activity using ABTS and Bleomycin-dependent DNA damage methods. Results: Coupling of the diazonium salts 7-11 of different sulpha drugs with curcumin 1 or with cyanoacetamide 18 afforded the corresponding 4-arylazoenol derivatives 12-16 and E-hydrazo derivatives 19-23. Among all the synthesized compounds, 12-16, 18, 20 and 22 were the most potent antioxidant compounds. Conclusion: The objective of the present study was to synthesize and evaluate the antioxidant activity of some novel sulfonamides structure hybrids incorporating either curcumin or N-[4- (aminosulfonyl) phenyl]-2-cyanoacetamide moiety with the hope of discovering new structure serving as antioxidant agent. The data showed clearly that most of compounds displayed good in vitro antioxidant activities.

Polymer complexes: XLXII-interplay of coordination π-π Stacking and hydrogen bonding in supramolecular assembly of [sulpha drug derivatives-N,S:N,O] complexes

A novel series of nickel(II) polymer complexes of 5-sulphadiazineazo-3- phenylamino-2-thio-4-thiazolidinone (HL1), 5-sulphamethazine-3- phenylamino-2-thioxo-4-thiazolidinone (HL2), 5-sulphamethoxazole-3- phenylamino-2-thioxo-4-thiazo

Synthesis of some New Pyrazolin-5-ones

Synthesis of some sufonamoylhydrazonopyrazolin-5-ones have been reported.