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          https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
        Synthesis  2007(7): 981-983  
DOI: 10.1055/s-2007-965978
   DOI: 10.1055/s-2007-965978
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New YorkA Microwave-Assisted Alternative Synthesis of 8-Amino-2-methyl-3,4-dihydroisoquinolin-1-one
Weitere Informationen
            
               
                  
                        
                              Received
                              29 November 2006 
                      
Publikationsdatum:
12. März 2007 (online)
            
         
      
   Publikationsverlauf
Publikationsdatum:
12. März 2007 (online)

Abstract
A shorter, alternative synthesis of 8-amino-2-methyl-3,4-dihydroisoquinolin-1-one is described in 32% overall yield, over three steps starting from commercially available 2-methyl-6-nitrobenzonitrile. The synthesis includes two ‘one-pot’ procedures in which the key process involves the microwave-assisted hydrolysis of a nitrile group followed by lactamization under elevated temperatures.
Key words
lactam - microwaves - cyclization - Bredereck’s reagent - isoquinolinone
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