Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2002-12-12
2004-01-20
Morris, Patricia L. (Department: 1625)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
06680388
ABSTRACT:
The invention relates to a novel process for preparing 5-amino-N-phenyl-1,2,4-triazole-3-sulfonamides, which are familiar as intermediates for active ingredients in agriculture, in particular for substituted, herbicidally active 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides.
It is known that triazolopyrimidinesulfonamides may be prepared by reacting triazole pyrimidine sulfonyl chlorides with alkylamines or aniline (GB-A 951 652, EP-A 0 142 152, DE-A 36 40 155, U.S. Pat. No. 4,740,233). However, in these processes, the amine first has to be partially activated by metallation using n-butyllithium or alkali metal hydrides. The preparation of triazolopyrimidinesulfonamides having a substitution pattern desirable for herbicidal effectiveness by a multistage reaction from other triazolopyrimidinesulfonamides comprising oxidative cleavage of the pyrimidine ring and subsequent ring reclosure (U.S. Pat. No. 4,734,123; J. Heterocyclic Chem., 30, 169 (1993)) or from other triazolopyrimidinesulfonamides in a multistep reaction by intermediate conversion to trialkylsilyl derivatives (U.S. Pat. No. 4,910,306) has also been described. The use of organometallic compounds and also losses in introducing and cleaving protecting groups and in the transformations are disadvantageous in these synthetic routes to the herbicidally active triazolopyrimidinesulfonamides.
The preparation of the triazolopyrimidinesulfonamides by another route with high yield and efficiency is accordingly desirable.
To this end, it has been suggested that triazolopyrimidinesulfonamides could be prepared from 5-amino-1,2,4-triazole-3-sulfonamides which have previously been obtained by reacting an appropriate chlorosulfonyltriazole with a substituted aniline derivative (EP-A 0 375 061). However, it was found that the preparation of the compound 5-amino-N-(2,6-dichloro-3-methylphenyl)-1,2,4-triazole-3-sulfonamide from the reaction of 2,6-dichloro-3-methylaniline with 5-amino-3-chlorosulfonyl-1,2,4-triazole in the presence of an organic solvent only leads to a yield of 67% after an extremely long reaction time of 5 days. Likewise, the same reaction step when acetic acid is used as solvent also only gives a 67% yield after 5.5 hours of reaction time.
Further known processes for preparing 5-amino-N-phenyl-1,2,4-triazole-3-triazolesulfonamides are likewise not completely satisfactory with regard to the achievable yields (EP-A 0 246 749).
According to the invention, it has been found that the substituted 5-amino-1,2,4-triazole-3-sulfonamides required for preparing triazolopyrimidinesulfonamides surprisingly succeeds by reacting the appropriate slow-reacting, dihalogenated aniline derivatives with the appropriate chlorosulfonyltriazole derivatives in very good yields with negligible formation of by-products when the reaction is carried out as an aniline melt even without addition of an auxiliary base and in the absence of a solvent at a short reaction time of from 30 minutes to 6 hours. In the process according to the invention, both the reaction product and the unconverted aniline may be particularly efficiently isolated in high purity.
It has accordingly been found that substituted 5-amino-N-phenyl-1,2,4-triazole-3-sulfonamides of the general formula (I)
where
X is halogen (in particular fluorine, chlorine or bromine), cyano or nitro,
R is hydrogen or optionally halogen-substituted C
1
-C
4
-alkyl, and
n is 1 or 2,
are obtained in very good yields and in high purity
on reacting 5-amino-3-chlorosulfonyl-1,2,4-triazole of the formula (II)
with a substituted aniline of the general formula (III)
where
X, n and R are as defined above,
in the absence of a solvent.
In formula (I), X is preferably fluorine, chlorine or bromine.
The process according to the invention is particularly advantageous for preparing 5-amino-N-(2,6-dichloro-3-methylphenyl)-1,2,4-triazole-3-sulfonamide of the formula (Ia)
In this case, the product is obtained by reacting 5-amino-3-chlorosulfonyl-1,2,4-triazole of the formula (II)
with 2,6-dichloro-3-methylaniline of the formula (IIIa)
in the absence of a solvent according to the invention.
In the process according to the invention, it is also generally unnecessary to add an auxiliary base (for example, potassium carbonate).
The direct reaction in the melt and not using the solvent described in the exemplary examples of EP-A 0 375 061 surprisingly provides a novel process which allows the preparation of 5-amino-N-phenyl-1,2,4-triazole-3-sulfonamides in very good yields and in high purity after a short reaction time.
Carrying out the reaction of the process according to the invention in the absence of a solvent provides the further advantage of avoiding the otherwise necessary, complicated recovery of the organic solvent after carrying out the reaction. Since no auxiliary base is required either, no waste products are formed. A substantial advance of the process according to the invention is the short reaction time. Even after 30 minutes to 6 hours, virtually quantitative yields are achieved.
Finally, the process according to the invention is notable in that only gaseous HCl is by-produced, which is easy to bind. The excess aniline can be simply removed by extraction and can accordingly be efficiently recovered.
A preferred embodiment of the process according to the invention is accordingly the variant which involves extracting the excess aniline in a further reaction step after the reaction of the starting materials using a water-immiscible organic solvent and then isolating it. This achieves quantitative recovery of excess aniline in high purity in a simple manner.
In a further preferred embodiment, the reaction product of the reaction is isolated by precipitating out of an aqueous solution using a salt-forming acid, preferably HCl, and subsequent filtration.
The process according to the invention accordingly provides an enrichment of the prior art, since it allows very advantageous preparation of 5-amino-N-phenyl-1,2,4-triazole-3-sulfonamides. This eases access to the herbicidal 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides based on these intermediates.
The 5-amino-3-chlorosulfonyl-1,2,4-triazole of the formula (II) to be used as the starting compound in the process according to the invention and also the substituted anilines of the formula (III) and the 2,6-dichloro-3-methylaniline of the formula (IIIa) are already known and may be prepared by known processes (cf., for example, EP-A 0 375 061).
The reaction according to the invention of the substituted anilines with 5-amino-3-chlorosulfonyl-1,2,4-triazole is generally carried out at temperatures of from 90° C. to 150° C., preferably from 115° C. to 145° C.
The reaction according to the invention of the substituted anilines with 5-amino-3-chlorosulfonyl-1,2,4-triazole is generally carried out for reaction times of from 30 minutes to 6 hours, preferably from 30 to 120 minutes.
To carry out the process according to the invention, preference is given to using the aniline in excess for preparing the compounds of the formula (I). In general, from 1.2 to 10 moles, preferably from 1.5 to 5 moles, of the aniline of the formula (III) are used per mole of 5-amino-3-chlorosulfonyl-1,2,4-triazole of the formula (II).
The above-described, preferred embodiment of the process according to the invention involves admixing the reaction mixture after the end of the reaction with an aqueous basic solution (preferably aqueous sodium hydroxide) and shaking it with a virtually water-immiscible organic solvent, for example, dichloromethane or toluene, washing the organic phase with water, drying it, and isolating the unconverted aniline of the formula (III) used as the starting material after evaporating off this solvent.
The compounds of the formula (I) can be worked up and isolated in a customary manner. Preference is given to admixing the reaction mixture after the end of the reaction with an aqueous basic solution (preferably aqueous sodium hydroxide) and shaking it with a virtually water-immiscible organic solvent, such as dichloromethane, to obtain a
Beier Christian
Lantzsch Reinhard
Bayer Cropscience AG
Henderson Richard E. L.
Morris Patricia L.
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