Method for producing substituted pyrazoles

Details Method for producing substituted pyrazoles Method for producing substituted pyrazoles

1999-12-13

2001-05-08

McKane, Joseph K. (Department: 1626)

Organic compounds -- part of the class 532-570 series

Organic compounds

Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

active

06229022

ABSTRACT:

The present invention relates to a process for preparing pyrazole derivatives.
Numerous ways of synthesizing pyrazole are described in “The Chemistry of Heterocyclic Compounds”, Volume 22, Chapters 3 and 5, for example condensation of &agr;,&bgr;-dicarbonyl compounds with hydrazines, reaction of ethynylcarbonyl compound with hydrazines and condensation of hydrazinoacetic ester with 1,2-diketones.
It is furthermore known to dehydrogenate 2-pyrazoline with chlorine, alkali metal or alkaline earth metal hypochlorites (DE-A 30 35 395), with sulfur or selenium (DE-A 30 29 160) or with aqueous hydrogen peroxide (DE-A 34 15 385) to give pyrazole. Also known are the thermal gas-phase dehydrogenation of 2-pyrazoline on palladium or platinum catalysts (DE-A 32 09 148) and the thermolysis of N-sulfonyl-2-pyrazoline to pyrazole (DE-A 30 35 394).
In addition, the dehydrogenation of 2-pyrazolines in sulfuric acid in the presence of iodine compounds has been described. In EP 0 474 037, the pyrazoline is generated in situ from an unsubstituted or substituted hydrazine and 2-butene-1,4-diol, 1-butene-3,4-diol or ethynylalkylcarbinol. In WO 95/06036, the pyrazoline is first prepared from an unsubstituted or substituted hydrazine and an &agr;,&bgr;-unsaturated carbonyl compound and is then, after mixing with sulfuric acid and the iodine catalyst, dehydrogenated. In EP 0 402 722, the pyrazoline is prepared beforehand or in situ from an unsubstituted or substituted hydrazine and a glycerol, an acrolein or vinyl alkyl ketone or a &bgr;-hydroxyethyl alkyl ketone.
However, these processes are industrially unsatisfactory, whether because they require the use of very aggressive oxidizing agents or costly catalysts, are associated with the formation of toxic by-products such as hydrogen sulfide and selenide, the compounds employed can be obtained only with difficulty, or they comprise a plurality of steps.
It is an object of the present invention to provide a process for preparing pyrazole derivatives which can be carried out industrially more simply and more economically.
We have found that this object is achieved by a process for preparing pyrazole derivatives of the formula I
where R
1
, R
2
and R
3
are, independently of one another, a hydrogen atom or an unsubstituted or substituted alkyl, cycloalkyl, aryl or aralkyl group, which comprises reacting a carbonyl compound of the formula II
where R
1
, R
2
and R
3
have the abovementioned meanings, with hydrazine, hydrazine hydrate or an acid addition salt thereof, in the presence of sulfuric acid and iodine or of a compound which liberates iodine or hydrogen iodide.
Carbonyl compounds of the formula II suitable for the novel process are those where R
1
, R
2
and R
3
are, independently of one another, selected from a hydrogen atom, a straight-chain or branched alkyl, such as C
1
-C
8
-alkyl, in particular C
1
-C
4
-alkyl, such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl and 1,1-dimethylethyl; C
3
-C
8
-cycloalkyl such as, in particular, cyclopentyl, cyclohexyl and cycloheptyl; C
6
-C
14
-aryl such as, in particular, phenyl; aralkyl such as, in particular, phenyl-C
1
-C
4
-alkyl, where the alkyl radical is as defined above, eg. benzyl and 2-phenylethyl; and corresponding organic radicals substituted by one or more halogen atoms such as F, Cl, Br or I, nitro, sulfo or sulfonyl groups, such as, in particular, chlorophenyl, nitrophenyl or tolyl.
Carbonyl compounds of the formula II preferred in the novel process are those where R
2
≠ hydrogen. R
2
is, in particular, methyl. R
3
is preferably hydrogen. It is particularly preferred for R
2
to be methyl and R
3
to be hydrogen. It is furthermore preferred for R
1
in compounds of the formula II to be hydrogen, methyl, ethyl, n-propyl, tert-butyl, phenyl, o-, m- or p-tolyl, o-, m- or p-chlorophenyl, o-, m- or p-nitrophenyl, o-, m- or p-sulfophenyl, or o-, m- or p-sulfonylphenyl.
Particularly suitable carbonyl compounds are the following: isobutyraldehyde, methyl isopropyl ketone (2-methyl-3-butanone), ethyl isopropyl ketone (2-methyl-3-pentanone), n-propyl isopropyl ketone (2-methyl-3-hexanone), isopropyl t-butyl ketone, phenyl isopropyl ketone, tolyl isopropyl ketone, chlorophenyl isopropyl ketone, nitrophenyl isopropyl ketone, sulfonylphenyl isopropyl ketone and sulfophenyl isopropyl ketone.
Hydrazine is used as second reaction component. It is possible to employ both the free hydrazine base and its hydrates or addition salts with mineral acids, eg. the salts of hydrazine with sulfuric acid, hydrochloric acid or phosphoric acid. Since losses of yield may occur on use of salts which do not dissolve in the reaction medium, it is preferred to use the hydrate or the free base.
Sulfuric acid is used in the novel process as diluent, condensing agent and oxidizing agent. Its concentration is preferably in the range from 30 to 100% by weight, in particular in the range from 45 to 90% by weight.
It is possible, where appropriate, to employ inert organic solvents such as chlorinated hydrocarbons, eg. dichloroethane, as additional diluent.
It is possible to use as catalyst besides elemental iodine also iodine compounds such as hydrogen iodide, alkali metal and alkaline earth metal iodides such as lithium iodide, sodium iodide, potassium iodide, cesium iodide, magnesium iodide and calcium iodide, and other metal iodides. It is also possible to use other inorganic iodine compounds such as alkali metal or alkaline earth metal hypoiodites, iodites, iodates and periodates, or organic iodine compounds such as alkyl iodides, eg. methyl iodide. Iodine or the iodine compound is generally employed in this reaction in amounts of from 0.01 to 10 mol-%, in particular from 0.05 to 5 mol-%, based on hydrazine.
When hydrazine hydrate and methyl isopropyl ketone are used with hydrogen iodide as catalyst, the reaction can be represented by the following equations:
On use of isobutyraldehyde as carbonyl compound, hydrazine hydrate and hydrogen iodide as catalyst, the process reactions can be represented by the following equations:
The reaction is expediently carried out by reacting 1 mol of the hydrazine compound with from 0.5 to 2, preferably 0.8 to 1.5, mol of the carbonyl compound of the formula II in sulfuric acid in the presence of catalytic amounts of an iodine compound, it being possible to remove the water which is present in the reaction mixture and is formed additionally. This removal preferably takes place by distillation, for example under atmospheric pressure. The reaction temperatures are in the range from 50 to 250° C., preferably from 80 to 200° C. and, in particular, from 110 to 170° C. The reaction is normally carried out under atmospheric pressure. It is also possible to carry out the reaction under elevated pressure or, with appropriately raised temperature, in less concentrated sulfuric acid or under reduced pressure or, with appropriately reduced temperature, in more concentrated sulfuric acid.
The reaction can be carried out by all the reactants being placed in a vessel and brought to the reaction temperature, by feeding the reactants as mixture or separately from one another into a vessel at the reaction temperature, or by introducing part of the reactants at the reaction temperature and feeding the remaining quantity in during the reaction. It is also possible for the sulfuric acid itself or hydrazine/sulfuric acid to be initially present in the reaction vessel.
The reaction temperature is preferably reached by distilling water out. The onset of pyrazole formation is evident from the evolution of sulfur dioxide. Absorption of the sulfur dioxide with sodium hydroxide solution affords equimolar amounts of sodium bisulfite solution of high purity. The water which is distilled off contains most of the iodide employed in the form of hydrogen iodide, which can be recycled.
The reaction mixture is worked up to isolate the pyrazole by conventional processes. The dark brown reaction mixture is preferably worked up by neutralization, eg. with sodium hydroxide solution, ammon

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