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                    Rearrangement of 3-(4,5-dimethoxy-2-vinylphenyl)-2-methyl-5-nitroisoquinolin-1(2H)-one to 2-(6,7-dimethoxy-1-oxoisoquinolin-2(1H)-yl)-N-methylbenzamide: a mechanistic proposal
                
                                    
                
                
                    Published:
14 November 2018
by MDPI
in The 22nd International Electronic Conference on Synthetic Organic Chemistry
session General Organic Synthesis
                
                                    
                
                
                    Abstract: 
                                    Nitro compounds are compounds of great versatility in organic synthesis due to their easy availability and transformation into a wide variety of functionalities.[1] As a part of our continued interest in nitro compounds, we few years ago reported the transformation of 3-(4,5-dimethoxy-2-vinylphenyl)-2-methyl-5-nitroisoquinolin-1(2H)-one (1) into 2-(6,7-dimethoxy-1-oxoisoquinolin-2(1H)-yl)-N-methylbenzamide (4), via 3-(4,5-dimethoxy-2-vinyl- phenyl)-2-methyl-5-nitroisoquinolin-1(2H)-one (2) and 3-(2-(2,2-dimethoxyethyl)-4,5-dimethoxy-phenyl)-2-methyl-5-nitroisoquinolin-1(2H)-one (3).[2]
A mechanistic proposal for the novel, striking rearrangement of compound 3 to compound 4 will be discussed.
                        Keywords: Nitro compounds, isoquinolines, rearrangement
                    
                
                
                
                
            