Aminopyrimidinamides As Pest Control Agents

Abstract

The present application relates to novel aminopyrimidinamides, to processes for their preparation and to their use for controlling animal pests, especially arthropods, in particular insects.

1 . Compounds of the formula (I) 
       
         
           
           
               
               
           
         
         in which 
         R 1  represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, halocycloalkylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl. 
         R 2  represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl, 
         R 3  represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, alkylthioalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and hererocyclylalkyl, 
         R 4  represents a radical from the group consisting of in each case optionally substituted phenyl, naphthyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl, 
         R 5  represents a radical from the group consisting of hydrogen, halogen, cyano and in each case optionally substituted alkyl, cycloalkyl, phenyl, naphthyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl, 
         R 6  represents a radical from the group consisting of hydrogen, halogen, alkyl, haloalkyl, cyanoalkyl, alkoxyalkyl, alkylcarbonyl, haloalkylcarbonyl, cycloalkyl, halocycloalkyl, cycloalkylalkyl, alkylsulphonyl, alkenyl, alkynyl, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, alkoxycarbonylalkyl; optionally substituted phenyl, optionally substituted naphthyl, optionally substituted phenylalkyl, optionally substituted heterocyclylalkyl, optionally substituted heteroarylalkyl and optionally substituted phenylcarbonyl and 
         X represents oxygen or sulphur. 
       
     
     
         2 . Composition, characterized in that it comprises at least one compound of the formula (I) according to  claim 1  and customary extenders and/or surfactants. 
     
     
         3 . Method for controlling pests, characterized in that a compound of the formula (I) according to  claim 1  or a composition according to  claim 2  is allowed to act on the pests and/or their habitat. 
     
     
         4 . Use of compounds of the formula (I) according to  claim 1  or of compositions according to  claim 2  for controlling pests. 
     
     
         5 . Pharmaceutical compositions comprising at least one compound according to  claim 1 . 
     
     
         6 . Use of at least one compound according to  claim 1  for preparing pharmaceutical compositions for controlling parasites on animals.