PROCESS FOR THE PREPARATION OF TOLTRAZURIL AND AN INTERMEDIATE USEFUL FOR ITS PREPARATION

Abstract

Disclosed is a process for the preparation of toltrazuril of formula (I) via the intermediate N-methyl-N′-[3-methyl-4-[4-[(trifluoromethyl)thio]phenoxy]phenyl] imidodicarbonic diamide of formula (III)

##STR00001## wherein intermediate (III) is obtained via a novel intermediate without the use of potentially hazardous reagents or potentially unstable intermediates.

Claims

1. A process for the preparation of toltrazuril of formula (I) ##STR00011## which comprises: a) reacting (methylaminocarbonyl)carbamic acid phenyl ester of formula (VII) ##STR00012## with 3-methyl-4[4-(trifluoromethylthio)phenoxy]henzenamine of formula (IV) ##STR00013## to give the compound of formula (III) ##STR00014## and b) cyclizing the compound of formula (III) to give toltrazuril.

2. The process of claim 1 wherein the reaction between (IV) and (VII) is carried out at a temperature ranging from 60° C. to 80° C. in an organic solvent selected from N,N-dimethylformamide, N,N-dimethylacetamide and ethyl acetate, for a time ranging from 6 to 18 hours.

3. The process of claim 1, wherein the compound of formula (VII) is obtained reacting phenyl chloroformate with N-methylurea.

4. The process of claim 3, wherein the reaction between phenyl chloroformate and N-methylurea is carried out in a solvent selected from methylene chloride, ethyl acetate, acetone, N,N-dimethylformamide and toluene in the presence of a base selected from triethylamine and pyridine, wherein said reaction is performed at a temperature ranging from 40° C. to 60° C.

5. The compound of formula (VII) ##STR00015##

Description

DESCRIPTION OF THE INVENTION

[0011] The object of the present invention is a process for the preparation of toltrazuril which comprises: [0012] a) reaction of (methylaminocarbonyl)carbamic acid phenyl ester of formula (VII) with 3-methyl-4-[4-(trifluoromethylthio)phenoxy]benzenamine of formula (IV) to give N-methyl-N′-[3-methyl-4-[4-[(trifluoromethyl)thio]phenoxy]phenyl]-imidodicarbonic diamide of formula (III), as depicted in Scheme 6 below

##STR00008## [0013] b) cyclisation of compound (III) to give toltrazuril.

[0014] (Methylaminocarbonyl)carbamic acid phenyl ester (VII) is a novel compound that is a further object of the invention. Said compound can be obtained by reacting phenyl chloroformate of formula (VIII) with N-methylurea, as reported in Scheme 7.

##STR00009##

DETAILED DESCRIPTION OF THE INVENTION

[0015] The reaction between aniline (IV) and (methylaminocarbonyl)carbamic acid phenyl ester (VII) is carried out using equimolar amounts of the reagents or a slight molar excess (5-20%), preferably 5-10%, of (VII), at a temperature ranging from 20° C. to 90° C., preferably from 60° C. to 80° C. The reaction is carried out in an organic solvent selected from N,N-dimethylformamide, N,N-dimethylacetamide and ethyl acetate, preferably N,N-dimethylacetamide, for a time ranging from 6 to 18 hours, preferably for 12 hours.

[0016] The phenylcarbamic intermediate (VII) is obtained by reacting phenyl chloroformate (VIII) with N-methylurea in a solvent selected from methylene chloride, ethyl acetate, acetone, N,N-dimethylformamide and toluene, preferably toluene, in the presence of a base selected from triethylamine and pyridine, preferably pyridine. The reaction is conducted at a temperature ranging from 40° C. to 60° C., preferably from 50° C. to 60° C.

[0017] 3-Methyl-4-[4-(trifluoromethylthio)phenoxy]benzenamine (IV) is a known compound, which can be obtained by condensation between 4-(trifluoromethylthio)-phenol (IX) and 2-chloro-5-nitrotoluene (X) in the presence of a base, followed by reduction of the resulting nitro derivative (XI) with hydrogen and palladium-on-carbon catalysis, as disclosed, for example, in U.S. Pat. No. 4,219,552 and summarised in Scheme 8.

##STR00010##

[0018] The biuret intermediate (III) can be converted to toltrazuril by known procedures, for example by reaction with diethyl carbonate in the presence of a base, as described in U.S. Pat. No. 4,874,860.

[0019] The process according to the invention produces biuret intermediate (III) with no need to use hazardous reagents such as those described in the literature to date for its preparation, and also avoids the step involving unstable intermediates considered potentially hazardous, such as isocyanates. The invention will now be illustrated by the following examples.

EXAMPLE 1

Preparation of [(methylamino)carbonyl]carbamic acid phenyl ester

[0020] 20.5 Kg of N-methylurea (276.7 moles), 61.5 Kg of toluene and 26.3 Kg of pyridine (332.5 moles) are loaded into a reactor. The suspension is heated to 40-60° C. and, maintaining said temperature by cooling, 47.6 Kg of phenyl chloroformate (304.25 moles) is poured into it. The reaction is maintained at 50-60° C. for one hour, after which 51.3 Kg of methanol is added. The suspension is cooled to 0-10° C., after which the solid is recovered by filtration, washed with 30.8 Kg of methanol, and dried at 60-70° C. 45.1 Kg of [(methylamino)carbonyl]carbamic acid phenyl ester (232.4 moles) is obtained. HPLC purity=99%. Yield: 84%.

EXAMPLE 2

Preparation of N-methyl-N′-[3-methyl-4-[4-[(trifluoromethyl)thio]phenoxy]phenyl]imidodicarbonic diamide

[0021] 64.9 Kg of 3-methyl-4[4-[(trifluoromethylthio)]phenoxy]benzenamine (216.82 moles), 64.9 Kg of N,N-dimethylacetamide and 45.1 Kg of [(methylamino)carbonyl]carbamic acid phenyl ester (232.2 moles) are loaded into a reactor. The mass is heated at 60-80° C. for 12 hours, after which 130 Kg of toluene, 130 Kg of water and 31.8 Kg of sodium hydrate (in 30% w/w aqueous solution) are added. The lower aqueous phase is separated and eliminated, and 64.9 Kg of distilled water is added to the organic phase. The mixture is cooled to 30-45° C. (crystallisation takes place), then cooled to 0-5° C. and filtered washing first with 64.9 Kg of toluene and then with 64.9 Kg of distilled water. The resulting product is dried at 60-70° C. 74.5 Kg of N-methyl-N′-[3-methyl-4-[4-[(trifluoromethyl)thio]phenoxy]phenyl]-imidodicarbonic diamide is obtained. HPLC purity=99%. Yield 86%.