Methods for onapristone synthesis dehydration and deprotection

Abstract

Methods and systems for making onapristone (ONA) using acidic hydrolysis and dehydration with sulfuric acid in an alcoholic solution are provided.

What is claimed is: 
     
         1 . A method of making onapristone comprising:
 reacting the compound of Formula I:   
       
         
           
           
               
               
           
         
         with sulfuric acid in a solvent to deprotect and dehydrate the compound of Formula I; 
         maintaining the reaction temperature below about 60° C.; 
         neutralizing the reaction with an inorganic base to form a solution; and 
         extracting the compound of Formula II 
       
       
         
           
           
               
               
           
         
         from the solution. 
       
     
     
         2 . The method of  claim 1 , wherein the sulfuric acid is diluted up to 80% with water. 
     
     
         3 . The method of  claim 2 , wherein the sulfuric acid is diluted from 30 to 60% with water. 
     
     
         4 . The method of  claim 3 , wherein the sulfuric acid is diluted with 50% water. 
     
     
         5 . The method of  claim 1 , wherein the solvent is selected from the group consisting of methanol, ethanol, acetone, n-propanol and isopropanol. 
     
     
         6 . The method of  claim 5 , wherein the solvent is methanol. 
     
     
         7 . The method of  claim 1 , wherein the temperature is maintained between about −50 to about 60° C. 
     
     
         8 . The method of  claim 7 , wherein the temperature is maintained between about −10 and 30° C. 
     
     
         9 . The method of  claim 8 , wherein the temperature is maintained from about 0 to about 15° C. 
     
     
         10 . The method of  claim 1 , wherein the inorganic base is selected from the group consisting of sodium hydrogen carbonate, sodium phosphate or ammonia. 
     
     
         11 . The method of  claim 10 , wherein the inorganic base is ammonia with a concentration between about 5 and 30%. 
     
     
         12 . The method of  claim 11 , wherein the inorganic base is 30% ammonia. 
     
     
         13 . The method of  claim 1 , wherein the reaction with the inorganic base is performed at a temperature from about 0 to about 30° C. 
     
     
         14 . The method of  claim 13 , wherein the reaction with the inorganic base is performed at a temperature from about 0 to about 15° C. 
     
     
         15 . The method of  claim 1 , wherein extraction of the compound of Formula II is performed with ethyl acetate. 
     
     
         16 . The method of  claim 1 , wherein extraction of the compound of Formula II is performed by crystallization. 
     
     
         17 . The method of  claim 1 , further comprising concentrating the solution. 
     
     
         18 . The method of  claim 17 , wherein the solution is concentrated by vacuum distillation.