Ex Parte Perbost - Page 7


              Appeal No. 2004-1770                                                               Page 7                
              Application No. 09/895,050                                                                               

                     As Appellant points out, although Hirschbein teaches the advantage of using                       
              “dry” reagents during oligonucleotide synthesis, the reference uses the term “dry” to                    
              mean that the solvents used do not contain water.  Hirschbein does not suggest any                       
              advantage to removing the (non-aqueous) solvent from the activator before adding the                     
              monomer to be reacted.  Hirschbein teaches, in fact, that the activator-containing                       
              solution and the monomer-containing solution should be mixed.  See column 12, lines                      
              7-26:                                                                                                    
                     The reaction is performed by adding a solution of the phosphoramidite                             
                     monomer and a solution of an activator (or a solution containing the                              
                     phosphoramidite monomer and the activator) to the reaction vessel. . . .                          
                     The monomer and the activator either can be premixed, mixed in the valve-                         
                     block of a suitable synthesizer, mixed in a pre-activation vessel and                             
                     preequilibrated if desired, or they can be added separately to the reaction                       
                     vessel.                                                                                           


























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