Method for producing 3-amidinophenylalanine derivatives

Abstract

The present invention describes a method for the synthesis of enantiomerically pure 3-amidinophenylalanine derivatives, which are used as pharmaceutically effective urokinase inhibitors, by starting from 3-cyanophenylalanine derivatives. The methods of manufacture comprising only one synthesis step lead to new intermediates, namely 3-hydroxyamidino- and 3-amidrazonophenylalanine derivatives. These intermediates or their acetyl derivatives can be reduced into the desired 3-amidino-phenylalanine derivatives under gentle conditions (H 2 or ammonium formiate formate, Pd/C (approx. 10%), ethanol/water, room temperature, normal pressure or also H 2 , Pd/C, AcOH or HCl/ethanol, 1-3 bar) in excellent yields and in an enantiomeric excess of up to 99.9%.

What is claimed is: 
     
       1. A method of synthesizing 3-amidino-phenylalanine derivatives of general formula (I) 
       
         
           
           
               
               
           
         
         or salts thereof formed with acids, which are present as either L- or D-configurated isomers and wherein R 1  is selected from the group consisting of: 
         (a) a group of formula 
       
       
         
           
           
               
               
           
         
         wherein
 (i) p=1 and r=2 and R 2  is benzyloxycarbonyl, benyzlaminocarbonyl benzylaminocarbonyl or 2-thienylhydrazinocarbonyl or 
 (ii) p=2 and r=1 and R 2  is ethoxycarbonyl, 2-propyloxycarbonyl, 2-propylcarbonyl, 2-propylaminocarbonyl, methylaminocarbonyl or methyl; and 
 
         (b) a group of formula 
       
       
         
           
           
               
               
           
         
         wherein R 3  is selected from the group consisting of methoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, dimethylaminocarbonyl, acetyl, and propionyl, 
       
       comprising the reduction of a compound of the general formula (IIa) 
       
         
           
           
               
               
           
         
       
       present as L- or D-enantiomers, as (E)- or (Z)-isomers or (E/Z)-mixtures, and wherein R 1  is selected from the group consisting of:
 (a) a group of formula 
 
       
         
           
           
               
               
           
         
         wherein
 (i) p=1 and r=2 and R 2  is benzyloxycarbonyl, benyzlaminocarbonyl benzylaminocarbonyl or 2-thienylhydrazinocarbonyl or 
 (ii) p=2 and r=1 and R 2  is ethoxycarbonyl, 2-propyloxycarbonyl, 2-propylcarbonyl, 2-propylaminocarbonyl, methylaminocarbonyl or methyl; and 
 
         (b) a group of formula 
       
       
         
           
           
               
               
           
         
         wherein R 3  is selected from the group consisting of methoxycarbonyk methoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, dimethylaminocarbonyl, acetyl, and propionyl, 
       
       in the presence of Pd/C in an alcoholic-aqueous solution with hydrogen or ammonium formiate formate. 
     
     
       2. The method of  claim 1 , wherein the compound of the general formula (IIa) is hydrogenated in the presence of Pd/C in an alcoholic, acetic acid- or hydrogen chloride-containing solution at a pressure of 1-3 bar. 
     
     
       3. The method of  claim 1 , further comprising the step of transforming the compounds of general formula (IIa) into the corresponding acetoxyamidino derivatives with acetanhydride in the presence of hydrochloric acid and reducing the derivatives with hydrogen or ammonium formiate in the presence of Pd/C in an alcoholic-aqueous solution. 
     
     
       4. The method of claim  3  1, wherein the acetoxyamidino derivatives are hydrogenated in the presence of Pd/C in an alcoholic, acetic acid- or hydrogen chloride-containing solution at a pressure of 1-3 bar. 
     
     
       5. The method of claim  3  1, wherein the transformation of the compounds of formula (IIa) into the corresponding acetoxyamidino derivatives occurs at a temperature between 20 and 60° C. 
     
     
       6. The method of  claim 1 , wherein the reduction occurs in an ethanolic-aqueous solution having a ratio of 1:1 to 20:1. 
     
     
       7. The method of  claim 1 , wherein the reduction occurs in the presence of 1 to 50% Pd/C. 
     
     
       8. The method of  claim 1 , wherein the reduction occurs at a temperature of 10 to 50° C. 
     
     
       9. The method of  claim 1 , wherein the reduction occurs with an at least 4-fold excess of ammonium formiate formate.