Process for preparing sulphonylurea salts

Claim 2

A process for preparing sulphonylurea salts of the formula ##STR27## in which M + represents an alkali metal ion or an alkaline earth metal ion equivalent, R 1 represents in each case optionally substituted aryl, aralkyl or heteroaryl, R 2 represents hydrogen or in each case optionally substituted alkyl, alkenyl, alkinyl or aralkyl, X represents hydrogen, halogen or alkyl, alkoxy, alkylthio or alkylamino, in each case optionally substituted by halogen or alkoxy, Y represents hydrogen, halogen or alkyl or alkoxy, in each case optionally substituted by halogen, and Z represents nitrogen, a CH group or a C-halogen group, wherein sulphonamides of the formula R.sup.1 --SO.sub.2 --NH.sub.2 (II) in which R 1 has the abovementioned meaning, are first reacted with alkali metal hydroxides or alcoholates or with alkaline earth metal hydroxides or alcoholates optionally in the presence of a diluent at temperatures between -20° C. and +150° C. (step 1) and the sulphonamide salts thus formed, of the formula R.sup.1 --SO.sub.2 --NH--M.sup.+ (IIa) in which M and R 1 have the abovementioned meaning, are then reacted with urethanes (carbamates) of the formula ##STR28## in which R 2 , X, Y and Z have the abovementioned meaning and R 3 represents alkyl, aralkyl or aryl, optionally in the presence of a diluent at temperatures between -20° C. and +150° C. (step 2) and the products of the formula (I) are isolated by conventional methods.

Claim 3

A process according to claim 1 for preparing compounds of formula (I), wherein M + represents a lithium, sodium or potassium ion, or a magnesium or calcium ion equivalent, R 1 represents in each case optionally substituted phenyl, naphthyl, benzyl, pyridyl, thienyl or pyrazolyl, where the substituents are selected from the group consisting of halogen, carboxyl, cyano, carbamoyl, nitro, amino, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylsulphinyl, C 1 -C 4 -alkylsulphonyl, di-(C 1 -C 4 -alkyl)-amino-sulphonyl, N-C 1 -C 4 -alkoxy-N-C 1 -C 4 -alkyl-amino-sulphonyl, phenyl, phenoxy, C 1 -C 4 -alkoxy-carbonyl, C 1 -C 4 -halogenoalkoxy-carbonyl, C 1 -C 2 -alkoxy-C 1 -C 2 -carbonyl, and di-(C 1 -C 4 -alkyl)-amino-alkoxy-carbonyl, R 2 represents hydrogen, C 1 -C 6 -alkyl which is optionally substituted by fluorine, cyano, C 1 -C 4 -alkoxy or C 1 -C 4 -alkylthio, C 3 -C 6 -alkenyl and C 3 -C 6 -alkinyl which are optionally substituted by fluorine or chlorine, or phenyl-C 1 -C 2 -alkyl which is optionally substituted in the phenyl moiety by fluorine, chlorine, nitro, cyano, methyl, methoxy or C 1 -C 2 -alkoxycarbonyl, X represents hydrogen, halogen or C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio or C 1 -C 4 -alkylamino, which are optionally substituted by halogen or C 1 -C 4 -alkoxy, Y represents hydrogen, halogen or C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy, which are optionally substituted by halogen, and Z represents nitrogen or a CH group.

Claim 4

A process according to claim 1 for preparing compounds of formula (I), wherein M + represents a sodium ion or potassium ion, R 1 represents a phenyl or benzyl which are substituted in the ortho position by fluorine, chlorine, bromine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, chloroethoxy, methoxyethoxy, ethoxyethoxy, methylthio, ethylthio, propylthio, methylsulphinyl, ethylsulphinyl, propylsulphinyl, methylsulphonyl, ethylsulphonyl, propylsulphonyl, dimethylaminosulphonyl, diethylaminosulphonyl, N-methoxy-N-methyl-aminosulphonyl, phenyl, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, chloroethoxycarbonyl, methoxyethoxycarbonyl, dimethylaminocarbonyl or diethylaminocarbonyl and are optionally substituted in a another position by halogen, or represents 3-dimethylaminocarbonyl-pyridin-2-yl or 3-ethylsulphonyl-pyridin-2-yl, 2-methoxycarbonyl-thiophen-3-yl or 1-methyl-4-methoxycarbonyl-pyrazol-5-yl, 1-methyl-4-ethoxycarbonyl-pyrazol-5-yl, 1-methyl-3-chloro-4-methoxycarbonyl-pyrazol-5-yl, 1-methyl-3-chloro-4-ethoxycarbonyl-pyrazol-5-yl or 1-pyridyl-4-methoxycarbonyl-pyrazol-5-yl, R 2 represents hydrogen or methyl, X represents hydrogen, chlorine, methyl, ethyl, trichloromethyl, trifluoromethyl, methoxymethyl, methoxy, ethoxy, difluoromethoxy, fluoromethoxy, difluoroethoxy, trifluoroethoxy, methoxyethoxy, methylthio, ethylthio, methylamino or ethylamino, Y represents hydrogen, chlorine, methyl, ethyl, trifluoromethyl, methoxy, ethoxy or difluoromethoxy, and Z represents nitrogen or a CH group.

Claim 5

A process according to claim 1, wherein the 1st process step is carried out at temperatures between 0° C. and 120° C.

Claim 6

A process according to claim 1, wherein the 2nd process step is carried out at temperatures between 0° and 100° C.

Claim 7

A process according to claim 1, wherein the 1st process step water or an alcohol is employed as the diluent.

Claim 8

A process according to claim 1, wherein the 2nd process step a ketone or a nitrile is employed as the diluent.

Claim 9

A process according to claim 1, wherein the sulphonamide of the formula (II) is introduced into an organic diluent and the alkali metal hydroxide or alcoholate or the alkaline earth metal hydroxide or alcoholate is metered in while stirring, the mixture is then stirred for some time and then concentrated under reduced pressure, and the residue which essentially contains the sulphonamide salt of the formula (IIa) is taken up in a suitable diluent and the urethane of the formula (III) is then added while stirring.

Claim 10

Process for preparing urethanes of the formula (III), ##STR29## in which R 2 represents hydrogen or in each case optionally substituted alkyl, alkenyl, alkinyl or aralkyl, X represents hydrogen, halogen or alkyl, alkoxy, alkylthio or alkylamino, in each case optionally substituted by halogen or alkoxy, Y represents hydrogen, halogen or alkyl or alkoxy, in either case optionally substituted by halogen, Z represents nitrogen, a CH grouping or a C-halogen grouping, and R 3 represents alkyl, aralkyl or aryl, characterised in that amines of the general formula (IV) ##STR30## in which R 2 , X, Y and Z have the abovementioned meaning, are reacted with chloroformic acid esters of the general formula (V) R.sup.3 --O--CO--Cl (V) in which R 3 has the abovementioned meaning, optionally in the presence of an acid acceptor, and optionally in the presence of a diluent, at temperatures between 0° C. and 150° C.

Claim 11

Process for preparing urethanes of the formula (III), ##STR29## in which R 2 represents hydrogen or in each case optionally substituted alkyl, alkenyl, alkinyl or aralkyl, X represents hydrogen, halogen or alkyl, alkoxy, alkylthio or alkylamino, in each case optionally substituted by halogen or alkoxy, Y represents hydrogen, halogen or alkyl or alkoxy, in either case optionally substituted by halogen, Z represents nitrogen, a CH grouping or a C-halogen grouping, and R 3 represents alkyl, aralkyl or aryl, characterised in that amines of the general formula (IV) ##STR30## in which R 2 , X, Y and Z have the abovementioned meaning, are reacted with chloroformic acid esters of the general formula (V) R.sup.3 --O--CO--Cl (V) in which R 3 has the abovementioned meaning, optionally in the presence of an acid acceptor, and optionally in the presence of a diluent, at temperatures between 0° C. and 150° C.

Claim 12

A process according to claim 6, wherein the alcohol is methanol or ethanol.

Claim 13

A process according to claim 7, wherein the ketone is methyl isobutyl ketone or the nitrile is acetonitrile.