Ex Parte Eliu et al - Page 4

              Appeal 2007-0549                                                                     
              Application 10/399,312                                                               

              Duennenberger (Duennenberger ‘545)  US 2,842,545  Jul. 8, 1958                       
              Duennenberger (Duennenberger ‘564)  US 2,995,564  Aug. 8, 1961                       
              Liechti US 3,407,196  Oct. 22, 1968                                                  
              Erckel  US 4,282,355  Aug. 4, 1981                                                   
              Schreiber  US 4,327,209 Apr. 27, 1982                                                
              Goda EP 0 719 774 A1  Jul. 3, 1996                                                   
              Maeder (as translated) CH 439 292 Dec. 15, 1967                                      
              2.  OBVIOUSNESS                                                                      
                    Claims 1-11 stand rejected under 35 U.S.C. § 103 as obvious over               
              Duennenberger ‘545,  Schreiber, Maeder, Liechti, Goda, and Duennenberger             
              ‘564, “each taken alone or in combination of each other, and each in view            
              of” Erckel (Answer 4-5).2                                                            
                    The Examiner cites each of the first six references as teaching                
              processes of preparing compounds of formula (1) “by reacting an amino-               
              benzene compound (e.g., 2-aminophenol) with a dicarboxylic acid (e.g.,               
              stilbene-4,4'-dicarboxylic acid or thiophene-2,5-dicarboxylic acid) in the           
              presence of an acidic catalyst (e.g., boric acid)” (Answer 5-6).                     
                    The Examiner concedes that “the prior art does not teach                       
              Appellant[s’] N-methylpyrrolidone or N,N-dimethylacetamide.  The prior art           
              teaches N,N-dimethylformamide instead in the reaction[;] see, for example,           
              Liechti et al. (column 2, lines 47-49)” (id. at 6-7).                                
                    To meet this limitation, the Examiner cites Erckel as “teach[ing] a            
              process of making bis-benzazolyl compounds by reacting an amino-benzene              
              compound (e.g., 2-aminophenol) with a carboxylic acid in the presence of an          
              acidic catalyst (e.g., boric acid)” (id. at 7).  The Examiner points out that        
                                                                                                  
              2 Examiner’s Answer mailed August 24, 2006.                                          
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