Cycloaddition reactions of 2-acetylamino-, 2-alkylamino-, 8-ethylamino-, and 8-acetylamino-1-azaazulenes with dimethyl acetylenedicarboxylate
        Bulletin of the Chemical Society of Japan Volume 65 Issue 7
        Page 1784-1793
        
published_at 1992
            Title
        
        Cycloaddition reactions of 2-acetylamino-, 2-alkylamino-, 8-ethylamino-, and 8-acetylamino-1-azaazulenes with dimethyl acetylenedicarboxylate
        
        
    
                
                    Creators
                
                    Fukazawa Yoshimasa
                
                
            
            
                
                    Creators
                
                    Hirai Yoshimasa
                
                
            
            
                
                    Creators
                
                    Sakurai Tosio
                
                
            
            
                
                    Creators
                
                    Urushido Kunio
                
                
            
            
                
                    Creators
                
                    Kakehi Akikazu
                
                
            
    The reactions of 2- and 8-(substituted amino)-1-azaazulenes with dimethyl acetylenedicarboxylate (DMAD) were investigated. Treatment of ethyl 2-acetylamino-1-azaazulene-3-carboxylate with DMAD in refluxing acetonitrile gave 9-ethyl 1,2,3-trimethyl 3a-azacyclopent[a]azulene-1,2,3,9-tetracarboxylate, 5-ethyl 1,2,2a,3-tetramethyl 4-acetyl-2a,3-dihydro-4H-4, 10b-diazapentaleno[1,6-aj]azulene-1,2,2a,3,5-pentacarboxylate (3a), and dimethyl (10-ethoxycarbonyl-4-methoxycarbonyl-2,4a-dihydro-2-oxo-2H-1,4a-diazabenz[a]azulen-3-yl)maleate. Compound 3a thermally rearranged to 9-ethyl 2,3,10,11-tetramethyl 1-acetyl-2,3,4,4a-tetrahydro-1H-1,4-diaza-3,4a-ethenofluorene-2,3,9,10,11-pentacarboxylate. The reaction of ethyl 2-alkylamino-1-azaazulene-3-carboxylate with DMAD gave the corresponding 4-alkyl-2a,3-dihydro-4H-4,10b-diazapentaleno[1,6-aj]azulene derivatives, and the etheno-bridged 1-azaheptalene derivative. The reaction of 8-ethylamino-3-phenyl-1-azaazulene with DMAD gave trimethyl 1-phenyl-2a-azabenz[cd]azulene-3,4,5-tricarboxylate, tetramethyl 6-ethyl-1-phenyl-4a,5-dihydro-6H-2a,6-diazapentaleno[1,6-cd]azulene-3,4,4a,5-tetracarboxylate, tetramethyl 3-phenyl-9b-azaindeno[1,6,7-bcd]azulene-1,2,8,9-tetracarboxylate, and dimethyl [8-phenyl-1,2,3-tris(methoxycarbonyl)-8H-3a-azacyclopent[1,2-a]inden-8-yl]maleate. However, the reaction of 8-acetylamino-3-phenyl-1-azaazulene with DMAD gave dimethyl-1-phenyl-2a,5-diazabenz[cd]azulene-3,4-dicarboxylate, trimethyl 3-phenyl-8,9b-diazaindeno[1,6,7-bcd]azulene-1,2,9-tricarboxylate, dimethyl 3-phenyl-8,9b-diazaindeno[1,6,7-bcd]azulene-1,2-dicarboxylate, tetramethyl 6-acetyl-1-phenyl-4a,5-dihydro-6H-2a,6-diazapentaleno[1,6,7-cd]azulene-3,4,4a,5-tetracarboxylate. The structures of the obtained compounds were determined by inspections of their physical and spectral data, and by single-crystal X-ray analyses of some of these compounds. The reaction mechanisms of these reactions are discussed.
        
        
            Languages
        
            eng
    
    
        
            Resource Type
        
        journal article
    
    
        
            Publishers
        
            日本化学会
    
    
        
            Date Issued
        
        1992
    
    
        
            File Version
        
        Not Applicable (or Unknown)
    
    
        
            Access Rights
        
        metadata only access
    
    
            Relations
        
            
                
                
                [ISSN]0009-2673
            
            
                
                
                [NCID]AA00580132
            
            
            
                [isVersionOf]
                
                [URI]http://www.jstage.jst.go.jp/browse/bcsj/-char/en
            
    
        
            Schools
        
            大学院医学系研究科(理学)
    
                
