Process for the preparation of 4-substituted 1-aryl-5-amino-pyrazoles

Claim 2

A process for the preparation of a 4-substituted 1-aryl-5-amino-pyrazole of the formula ##STR18## in which R 1 represents hydrogen or alkyl, R 2 represents alkyl or halogenoalkyl, and Ar represents polysubstituted phenyl or polysubstituted pyridyl, wherein a arylhydrazine hydrohalide of the formula Ar--NH--NH.sub.2 ×HHal in which Hal represents halogen, and Ar has the abovementioned meaning, is reacted with an acrylonitrile derivative of the formula ##STR19## in which R 1 and R 2 have the abovementioned meaning, and R 3 and R 4 , each independently represent alkyl or phenyl, or R 3 and R 4 , together with the nitrogen atom to which they are bound, represent a saturated heterocyclic ring, at temperatures between 60° C. and 90° C.

Claim 3

A process according to claim 1, wherein R 1 represents hydrogen, or straight-chain or branched alkyl having 1 to 6 carbon atoms or straight-chain or branched halogenoalkyl having 1 to 4 carbon atoms and 1 to 9 identical or different halogen atoms, and Ar represents phenyl which is disubstituted to pentasubstituted, the substituents being identical or different, or 2-pyridyl, 3-pyridyl or 4-pyridyl which is in each case disubstituted to tetrasubstituted, the substituents being identical or different and said substituents in each case being selected from the group consisting of cyano, nitro, halogen, in each case straight-chain or branched alkyl, alkoxy or alkoxycarbonyl in each case having up to 4 carbon atoms, in addition in each case straight-chain or branched halogenoalkyl or halogenoalkoxy in each case having up to 4 carbon atoms and up to 9 identical or different halogen atoms, and an --S(O) m --R 5 radical, wherein R 5 represents amino or in each case straight-chain or branched alkyl, alkylamino, dialkylamino or halogenoalkyl in each case having up to 4 carbon atoms in the individual alkyl parts and, in the case of halogenoalkyl, having up to 9 identical or different halogen atoms, and m represents a number 0, 1 or 2.

Claim 4

A process according to claim 1, wherein R 1 represents hydrogen, methyl, ethyl, n- or i-propyl, or n-, i-, s- or t-butyl, R 2 represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, trifluoromethyl, trichloromethyl, difluorochloromethyl, fluoromethyl or difluoromethyl, and Ar represents phenyl which is disubstituted to pentasubstituted, the substituents being identical or different, or 2-pyridyl or 4-pyridyl which is in each case disubstituted to tetrasubstituted, the substituents being identical or different, said substituents being selected from the group consisting of cyano, nitro, fluorine, chlorine, bromine, iodine, methyl, ethyl, n- and i-propyl, n-, i-, s- and t-butyl, methoxy, ethoxy, methoxycarbonyl, ethoxycarbonyl, trifluoromethyl, trichloromethyl, difluorochloromethyl, dichloromethyl, chloromethyl, dichloromethyl, difluoromethyl, pentafluoroethyl, tetrafluoroethyl, trifluorochloroethyl, trifluoroethyl, difluorodichloroethyl, trifluorodichloroethyl, pentachloroethyl, trifluoromethoxy, trichloromethoxy, dichlorofluoromethoxy, difluorochloromethoxy, chloromethoxy, dichloromethoxy, difluoromethoxy, pentafluoroethoxy, tetrafluoroethoxy, trifluoroethoxy, difluorodichloroethoxy, trifluorochloroethoxy, trifluorodichloroethoxy, pentachloroethoxy and an --S(O) m --R 5 radical, wherein R 5 represents amino, methylamino, ethylamino, dimethylamino, diethylamino, fluorodichloromethyl, difluoromethyl, tetrafluoroethyl, trifluorochloroethyl, trifluoromethyl, methyl or ethyl, and m represents a number 0, 1 or 2.

Claim 5

A process according to claim 1, wherein the reaction is carried out at temperatures between 70° C. and 80° C.

Claim 6

A process according to claim 1, wherein 1 to 1.5 moles of said acrylonitrile derivative is employed per mole of said arylhydrazine hydrohalide.

Claim 7

A process according to claim 1, wherein equimolar amounts of said arylhydrazine hydrohalide and said acrylonitrile derivative are employed.

Claim 8

A process according to claim 1, wherein the process is carried out in the presence of a polar organic solvent.

Claim 9

A process according to claim 1, wherein the reaction is carried out in the presence of a diluent.

Claim 10

A process according to claim 7, wherein the reaction is carried out in the presence of a mixture of a polar organic solvent and water.