Process for the preparation of aryloctanoyl amides

Abstract

Compounds of formula I wherein R 1 is for example 3-methoxyprop-3-yloxy, R 2 is for example methoxy, R 3 and R 4 are in each case for example isopropyl, and R 5 is H 2 NC(O)—[C(CH 3 ) 2 ]—CH 2 —, are obtainable by reaction of compounds of formula IV (IV) with a metal organic derivative of 1-(3-R 1 -4-R 2 -phen-1-yl)-2-R 3 -3-halogen propanes to form a compound of formula VI, followed by removal of the pseudoephedrine protecting group and the OH group, reaction of the resulting lactone with an amine R 5 —NH 2 and removal of protecting group Z.

What is claimed is:  
     
         1 . A process for the preparation of compounds of formula I and their physiologically acceptable salts,  
       
         
           
           
               
               
           
         
       
       wherein 
 R 1  and R 2  are, independently of one another, H, C 1 -C 6 alkyl, C 1 -C 6 halogenalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy-C 1 -C 6 alkyl, or C 1 -C 6 alkoxy-C 1 -C 6 alkyloxy, R 3  is C 1 -C 6 alkyl, R 4  is C 1 -C 6 alkyl, and R 5  is C 1 -C 6 alkyl, C 1 -C 6 hydroxyalkyl, C 1-C   6 alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 alkanoyloxy-C 1 -C 6 alkyl, C 1 -C 6 aminoalkyl, C 1 -C 6 alkylamino-C 1 -C 6 -alkyl, C 1 -C 6 -dialkylamino-C 1 -C 6 -alkyl, C 1 -C 6 -alkanoylamido-C 1 -C 6 -alkyl, HO(O)C—C 1 -C 6 -alkyl, C 1 -C 6 alkyl-O—(O)C—C 1 -C 6 alkyl, H 2 N—C(O)—C 1 -C 6 alkyl, C 1 -C 6 alkyl-HN—C(O)—C 1 -C 6 alkyl or (C 1 -C 6 alkyl) 2 N—C(O)—C 1 -C 6 -alkyl, comprising the steps  
 a) reaction of a compound of formula II,  
                     
 wherein R 4  is as defined above, with a hydroxylamine of formula ZNHOH (III), wherein Z is a removable protecting group, to form a compound of formula IV,  
                     
 b) reaction of a compound of formula IV with a metal organic derivative of a compound of formula V,  
                     
 wherein R 1 , R 2  and R 3  are as defined above and Y is Cl, Br or I, to form a compound of formula VI,  
                     
 c) removal of the hydroxyl group to form a compound of formula VII,  
                     
 d) removal of the pseudoephedrine protecting group to form compounds of formula VIII,  
                     
 or performance of step d) before step c), or of steps c) and d) together in one reaction vessel,  
 e) reaction of a compound of formula VII with an amine of formula R 5 —NH 2  to form a compound of formula IX  
                     
 f) removal of protecting group Z for the preparation of compounds of formula I.  
 
     
     
         2 . A process according to  claim 1 , comprising preparation of the 5(S)-diastereomer of formula Ia  
       
         
           
           
               
               
           
         
       
     
     
         3 . A process according to  claim 1  comprising an embodiment wherein R 1  is C 1 -C 4 alkoxy or C 1 -C 4 alkoxy-C 1 -C 4 alkyloxy, R 2  is C 1 -C 4 alkoxy, R 3  is C 1 -C 4 alkyl, R 4  is C 1 -C 4 alkyl and R 5  is H 2 NC(O)—C 1 -C 6 alkyl which if necessary is N-monosubstituted or N-di-C 1 -C 4 alkyl-substituted.  
     
     
         4 . A process according to  claim 3  comprising an embodiment wherein R 1  is methoxy-C 2 -C 4 alkyloxy, R 2  is methoxy or ethoxy, R 3  is C 2 -C 4 alkyl, R 4  is C 2 -C 4 alkyl and R 5  is H 2 NC(O)—C 1 -C 6 alkyl.  
     
     
         5 . A process according to  claim 4  comprising an embodiment wherein R 1  is 3-methoxy-prop-3-yloxy, R 2  is methoxy, R 3  and R 4  are 1-methyleth-1-yl, and R 5  is H 2 NC(O)—[C(CH 3 ) 2 ]—CH 2 —.  
     
     
         6 . A process according to  claim 1 , comprising an embodiment wherein Z in formula III is benzyl.  
     
     
         7 . A process according to  claim 1 , comprising the reaction of a compound of formula II immediately after preparation with a hydroxylamine.  
     
     
         8 . A process according to  claim 1 , comprising a reaction temperature in process step a) of −20 to 50° C.  
     
     
         9 . A process according to  claim 1 , comprising an embodiment wherein the metal organic derivatives in process step b) are those of formula X,  
       
         
           
           
               
               
           
         
       
       wherein Y 1  is an alkali metal or -MeY, wherein Y is Cl, Br or iodine and Me is Mg, Zn, Hg or Cd.  
     
     
         10 . A process according to  claim 1 , comprising a reaction temperature in process step b) of −70 to 100° C.  
     
     
         11 . A process according to  claim 1 , comprising the reaction in process step b) being carried out in the presence of a heavy metal salt, in particular cerium slats.  
     
     
         12 . A process according to  claim 1 , comprising the removal of the hydroxyl group in process step c) being carried out in an aqueous acidic medium with nascent hydrogen.  
     
     
         13 . A process according to  claim 1 , comprising the removal of the pseudoephidrine group in process step d) being carried out in an aqueous acidic medium.  
     
     
         14 . A process according to  claim 1 , comprising process steps c) and d) being carried out at the same time in one reaction vessel.  
     
     
         15 . A process according to  claim 1 , comprising the reaction in process step e) being carried out in the presence of alcohols or amines, which form activated carbonic esters or carboxamides with the carboxylic acids of formula VIII.  
     
     
         16 . A process according to  claim 1 , comprising a reaction temperature in process step e) of 40 to 150° C.  
     
     
         17 . A process according to  claim 1 , comprising the removal of the protecting group Z in process step f) being carried out catalytically by hydrogenation in the presence of homogeneous or heterogeneous precious metal catalysts or Raney-Nickel.  
     
     
         18 . A process according to  claim 1 , comprising a reaction temperature in process step f) of 0 to 200° C.  
     
     
         19 . Compounds of formula IV,  
       
         
           
           
               
               
           
         
       
       wherein R 4  and Z are as defined in  claim 1 .  
     
     
         20 . Compounds of formula XI in the form of 5(S)- or 5(R)-diastereomers or mixtures thereof,  
       
         
           
           
               
               
           
         
       
       wherein R 1 , R 2 , R 3 , R 4  and Z are as defined in  claim 1  and X 2  is H or OH.  
     
     
         21 . Compounds of formula XII in the form of 5(S)- or 5(R)-diastereomers or mixtures thereof,  
       
         
           
           
               
               
           
         
       
       wherein R 1 , R 2 , R 3 , R 4  and Z are as defined in  claim 1  and X 2  is H or OH.  
     
     
         22 . Compounds of formula XIII in the form of 5(S)- or 5(R)-diastereomers or mixtures thereof,  
       
         
           
           
               
               
           
         
       
       wherein R 1 , R 2 , R 3 , R 4 , R 5  and Z are as defined in  claim 1.