82168-92-1

Upstream product

• 129585-45-1 4-Chloro-2-methyl-5-(2-nitro-phenyl)-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 111277-26-0 4-Bromo-2-methyl-5-(2-nitro-phenyl)-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 82157-87-7 5-(2-aminophenyl)-3-ethoxycarbonyl-2-methyl-1-phenyl-1H-pyrrole 
• 111277-25-9 5-(2-Amino-phenyl)-4-bromo-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 129585-46-2 5-(2-Amino-phenyl)-4-chloro-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 82157-83-3 4-Ethoxycarbonyl-5-methyl-2-(2-nitrophenyl)-1-phenylpyrrole 

Relevant academic research and scientific papers

Polycondensed Nitrogen Heterocycles. Part 23. Pyrrolocinnolines by a Japp-Klingemann Type Reaction

Pyrrolocinnoline derivatives were obtained by an unusual Japp-Klingemann reaction involving an intramolecular azadehalogenation on the pyrrole nucleus.Such an azadehalogenation represents the first example of Japp-Klingemann reaction in which the e

POLYCONDENSED NITROGEN HETEROCYCLES. PART XI. 1,3-DISUBSTITUTED 2-METHYLPYRROLOCINNOLINE AND 2-ACETYL-3-METHYLPYRROLOBENZOTRIAZINE

The diazotization of 1,3-disubstituted 2-methyl-5-(2-aminophenyl)pyrroles (2) and the intramolecular coupling reaction of the resulting diazonium salts lead to pyrrolobenzotriazine 4 when R = H.Compound 3d inhibited the germination of seeds