1-heteroaryl-4-aryl-pyrazole microbicides

The invention relates to new 1-heteroaryl-4-arylpyrazole derivatives, a process for their preparation and their use as microbicides.
It is already known that certain heterocyclic compounds, such as, for example, N-trichloromethylthio-phthalimide and -tetrahydrophthalimide, have good fungicidal actions (compare U.S. Pat. Nos. 2,553,770, 2,553,771 and 2,553,776). Organic sulphur compounds, such as, for example, zinc ethylene-1,2-bis-(dithiocarbamate), furthermore are also compounds which have a good fungicidal action (compare, for example, R. Wegler "Chemie der Pflanzenschutz- und Schadlingsbekampfungsmittel" ("Chemistry of Plant Protection Agents and Agents for Combating Pests"), Springer Verlag, Berlin, Heidelberg, New York 1970, Volume 2, page 65 et seq.). The action of these compounds cannot always be completely satisfactory in some fields of use under certain conditions, for example when low amounts and concentrations are applied.
1,4-Diaryl-pyrazolin-5-ones, which are used as herbicides, are furthermore known. Nothing is known of a fungicidal activity (compare DE-OS (German Published Specification) No. 2,651,008).
Furthermore, 1-heteroaryl-4-aryl-pyrazolin-5-ones, such as, for example, 1-pyrimid-2-yl-4-phenyl-pyrazolin-5-one, and their microbicidal properties are known from Patent Application Ser. No. 733,450, filed May 10, 1985, now pending.
New 1-heteroaryl-4-aryl-pyrazole derivatives of the formulae (I) and (IA) ##STR3## in which R represents hydrogen or alkyl,
R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, a radical --S(O).sub.p -alkyl which is optionally substituted in the alkyl part, nitro or optionally substituted amino, or represents a fused-on carbocyclic or heterocyclic radical,
p represents the integer 0, 1 or 2,
n represents an integer from 0 to 5,
X represents .dbd.CH--, or represents a nitrogen atom,
Y represents CO or SO.sub.2 and
R.sup.2 represents hydrogen, in each case optionally substituted alkyl, cycloalkyl or aryl or a heterocyclic radical, or represents OR.sup.3, or also represents SR.sup.3, if Y is CO,
wherein
R.sup.3 represents optionally substituted alkyl or aryl, or
R.sup.2 represents a radical ##STR4## wherein R.sup.4 represents hydrogen or saturated or unsaturated optionally substituted alkyl and
R.sup.5 represents hydrogen, saturated or unsaturated, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl or an optionally substituted heterocyclic radical, or
R.sup.4 and R.sup.5, together with the nitrogen atom on which they are located, form a heterocyclic ring which optionally contains further hetero atoms and can optionally be mono- or polysubstituted by identical or different substituents.
It has furthermore been found that the new 1-heteroaryl-4-aryl pyrozole derivatives of the formulae (I) and (LA) ##STR5## in which R represents hydrogen or alkyl,
R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, a radical --S(O).sub.p -alkyl which is optionally substituted in the alkyl part, nitro or optionally substituted amino, or represents a fused-on carbocyclic or heterocyclic radical,
p represents the integer 0, 1 or 2,
n represents an integer from 0 to 5,
X represents .dbd.CH--, or represents a nitrogen atom,
Y represents CO or SO.sub.2 and
R.sup.2 represents hydrogen, in each case optionally substituted alkyl, cycloalkyl or aryl or a heterocyclic radical, or represents OR.sup.3, or also represents SR.sup.3, if Y is CO,
wherein
R.sup.3 represents optionally substituted alkyl or aryl, or
R.sup.2 represents a radical ##STR6## wherein R.sup.4 represents hydrogen or saturated or unsaturated optionally substituted alkyl and
R.sup.5 represents hydrogen, saturated or unsaturated, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl or an optionally substituted heterocyclic radical, or
R.sup.4 and R.sup.5, together with the nitrogen atom on which they are located, form a heterocyclic ring which optionally contains further hetero atoms and can optionally be mono- or polysubstituted by identical or different substituents,
are obtained by a process in which 1-heteroaryl-4-arylpyrazolin-5-ones of the formula (II) or (IIA) ##STR7## in which R, R.sup.1, X and n have the abovementioned meanings, are reacted with a reactive derivative of an acid of the formula (III)
R.sup.2 --Y--Z (III)
in which
R.sup.2 and Y have the abovementioned meanings and
Z represents halogen, an acyloxy radical, a sulphonyloxy radical or an azole radical,
if appropriate in the presence of an acid-binding agent.
Finally, it has been found that the 1-heteroaryl-4-aryl-pyrazole derivatives of the formulae (I) and (IA) can be employed for combating microbial parasites.
Surprisingly, the compounds of the formulae (I) and (IA) according to the invention exhibit a more powerful anitmicrobial activity than the active compounds already known from the prior art, such as, for example, N-trichloromethylthio-phthalimide or -tetrahydrophthalimide, zinc ethylene-1,2-bis-(dithiocarbamate) and/or N,N-dimethyl-N'-phenyl-N'-dichlorofluoro-methylthio-sulphamide. The compounds according to the invention thus represent an enrichment of the art.
Formula (I) or (IA) provides a general definition of the 1-heteroaryl-4-aryl-pyrazole derivatives according to the invention.
Preferred compounds of the formulae (I) and (IA) are those
in which
R represents hydrogen or alkyl with 1 to 4 carbon atoms,
R.sup.1 represents halogen, such as fluorine, chlorine, bromine and iodine, or hydroxyl, or represents alkyl with 1 to 4 carbon atoms, or represents halogenoalkyl with 1 or 2 carbon atoms and 1 to 5 identical or different halogen atoms, or represents alkoxy with 1 to 6 carbon atoms or halogenoalkoxy with 1 or 2 carbon atoms and 1 to 5 identical or different halogen atoms, or represents alkoxyalkoxy with 1 to 4 carbon atoms per alkyl part, or represents alkylthioalkoxy with 1 to 4 carbon atoms per alkyl part, or represents aryloxyalkoxy with 1 to 4 carbon atoms in the alkyl part and 6 to B 10 carbon atoms in the aryl part, or represents alkylthio with 1 to 6 carbon atoms, or represents halogenoalkylthio with 1 or 2 carbon atoms and 1 to 5 identical or different halogen atoms, or represents alkoxyalkylthio with 1 to 4 carbon atoms per alkyl part, or represents alkylthioalkylthio with 1 to 4 carbon atoms per alkyl part, or represents alkylsulphinyl with 1 to 6 carbon atoms, or represents halogenoalkylsulphinyl with 1 or 2 carbon atoms and 1 to 5 identical or different halogen atoms, or represents alkoxyalkylsulphinyl or alkylthioalkylsulphinyl with 1 to 4 carbon atoms per alkyl part, or represents alkylsulphonyl with 1 to 6 carbon atoms, or represents halogenoalkylsulphonyl with 1 or 2 carbon atoms and 1 to 5 identical or different halogen atoms, or represents alkoxyalkylsulphonyl or alkylthioalkylsulphonyl with 1 to 4 carbon atoms per alkyl part, or represents nitro, amino, mono- or dialkylamino with 1 to 4 carbon atoms per alkyl part, or acylamino, or represents a fused-on five-membered or six-membered carbocyclic ring which can be interrupted once or several times by identical or different atoms from the group comprising oxygen, sulphur and nitrogen atoms,
X represents .dbd.CH--, or represents a nitrogen atom,
Y represents CO or SO.sub.2 and
n represents an integer from 0 to 3, and
R.sup.2 represents hydrogen or an alkyl radical which has 1-12 carbon atoms and can be substituted by one or more halogen atoms, by a hydroxyl group, by a radical --A--R.sup.6,
in which
A represents oxygen, sulphur, SO or SO.sub.2 and
R.sup.6 represents an optionally substituted aliphatic, aromatic or heterocyclic radical,
or by the NO.sub.2 group or by a group ##STR8## in which R.sup.7 and R.sup.8 independently of one another denote hydrogen, alkyl, aryl, a heterocyclic radical or an acyl group,
or by the cyano group, a carboxylic acid ester radical or a carboxylic acid amide radical which is optionally substituted on the N atom, or by an optionally substituted aryl radical or an optionally substituted or fused heterocyclic radical, or
R.sup.2 represents cycloalkyl which has 3 to 8 ring carbon atoms and is optionally substituted by halogen, hydroxyl, alkoxy, aryloxy, alkyl or aryl or contains optionally fused-on rings, or
R.sup.2 represents aryl, which can be substituted by halogen, by a radical --A--R.sup.9,
in which
A represents oxygen, sulphur, SO or SO.sub.2 and
R.sup.9 represents an optionally substituted aliphatic, aromatic or heterocyclic radical,
or by the NO.sub.2 group, or by a dialkylamino group or acylamino group or an alkyl radical which is optionally substituted by halogen or alkoxy, or by optionally substituted aryl, or by a cyano group, a carboxyl group, a carboxylic acid ester group, a carboxylic acid amide group which is optionally substituted on the N atom or a sulphonamide group which is optionally substituted on the N atom, or by a heterocyclic radical which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms, or by a fused-on carbocyclic or heterocyclic ring which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and further substituents on the carbon and nitrogen atoms, or
R.sup.2 represents a 4- to 7-membered heterocyclic radical which, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and can contain further substituents on the carbon or nitrogen atoms in the ring, such as halogen, --A--R.sup.9, with the same meaning for A and R.sup.9 as above, an optionally substituted amino group, cyano, a carboxylic acid ester or optionally N-substituted carboxylic acid amine group, optionally substituted alkyl or aryl radicals or further heterocyclic radicals, or can contain fused-on carbocyclic or heterocyclic rings with 5 or 6 ring members, or R.sup.2 represents a radical --O--R.sup.3, or also represents S--R.sup.3 if Y represents CO,
in which
R.sup.3 denotes an alkyl group which has 1 to 12 carbon atoms and can be substituted by halogen or the radical --A--R.sup.6, with the same meaning for A and R.sup.6 as above, or by nitro, cyano or a carboxylic acid ester group, or by optionally substituted aryl; or
R.sup.3 furthermore represents an aryl group, which can optionally be substituted by halogen, nitro, cyano, the carboxylic acid ester or optionally N-substituted carboxylic acid amide group or a group --A--R.sup.9, with the same meaning for A and R.sup.9 as above, or by an alkyl group, which can optionally be substituted by one or more halogen atoms, or by a dialkylamino group or a further aryl radical, or
R.sup.2 represents a radical ##STR9## in which R.sup.4 denotes hydrogen or an optionally substituted saturated or unsaturated alkyl radical with 1-6 carbon atoms and
R.sup.5 denotes a saturated or unsaturated alkyl radical which has 1 to 12 carbon atoms and can be substituted by halogen, hydroxyl, acyloxy or the radical --A--R.sup.6, with the same meaning for A and R.sup.6 as above, or by a group ##STR10## in which R.sup.10 and R.sup.11 each independently denote a hydrogen atom, an alkyl, aryl or heterocyclic radical or an acyl group, or by the cyano group, a carboxylic acid ester radical or a carboxylic acid amide radical which is optionally substituted on the N atom, or by an optionally substituted aryl radical or an optionally substituted or fused heterocyclic radical; or furthermore
R.sup.5 represents a cycloalkyl radical which has 3 to 8 ring carbon atoms and is optionally substituted by halogen, hydroxyl, alkoxy, aryloxy, alkyl or aryl or optionally contains fused-on rings; or furthermore
R.sup.5 represents an aryl radical, which can be substituted by halogen, or by a radical --A--R.sup.9,
in which
A represents oxygen, sulphur, SO or SO.sub.2 and
R.sup.9 represents an optionally substituted aliphatic, aromatic or heterocyclic ring,
or by the NO.sub.2 group, or by a dialkylamino group or acylamino group or an alkyl radical which is optionally substituted by halogen or alkoxy, or by an optionally substituted aryl radical, or by a cyano group, a carboxylic acid ester group, a carboxylic acid amide group which is optionally substituted on the N atom or a sulphonamide group which is optionally substituted on the N atom, or by a heterocyclic radical which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms, or by a fused-on carbocyclic or heterocyclic ring which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and, on the carbon and nitrogen atoms, further substituents, or
R.sup.5 furthermore represents a 4- to 7-membered heterocyclic radical which, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and can contain further substituents on the carbon or nitrogen atoms in the ring, such as halogen, --A--R.sup.9, with the same meaning for A and R.sup.9 as above, an optionally substituted amino group, cyano, a carboxylic acid ester or optionally N-substituted carboxylic acid amide group, optionally substituted alkyl or aryl radicals or further heterocyclic radicals or fused-on carbocyclic or heterocyclic rings with 5 or 6 ring members, or furthermore
R.sup.4 and R.sup.5, together with the nitrogen atom, can form a 3- to 8-membered ring which, in addition to this N atom, can also contain further hetero atoms, such as oxygen, sulphur and nitrogen, and additional substituents and/or fused-on carbocyclic or heterocyclic rings.
Particularly preferred compounds of the formulae (I) and (IA) are those in which
R represents hydrogen or alkyl with 1 to 4 carbon atoms,
R.sup.1 represents fluorine, chlorine, bromine or hydroxyl, or represents alkyl with 1 to 4 carbon atoms, or represents halogenoalkyl with 1 or 2 carbon atoms and 1 to 3 identical or different halogen atoms, or represents alkoxy with 1 to 4 carbon atoms or halogenoalkoxy with 1 or 2 carbon atoms and 1 to 3 identical or different halogen atoms, or represents alkoxyalkoxy with 1 or 2 carbon atoms per alkyl part, or represents alkylthioalkoxy with 1 or 2 carbon atoms per alkyl part, or represents phenoxyalkoxy with 1 or 2 carbon atoms in the alkyl part, or represents alkylthio with 1 to 4 carbon atoms, or represents halogenoalkylthio with 1 or 2 carbon atoms and 1 to 3 identical or different halogen atoms, or represents alkoxyalkylthio with 1 or 2 carbon atoms per alkyl part, or represents alkylthioalkylthio with 1 or 2 carbon atoms per alkyl part, or represents alkylsulphinyl with 1 to 4 carbon atoms, or represents halogenoalkylsulphinyl with 1 or 2 carbon atoms and 1 to 3 identical or different halogen atoms, or represents alkoxyalkylsulphinyl or alkylthioalkylsulphinyl with 1 or 2 carbon atoms per alkyl part, or represents alkylsulphonyl with 1 to 4 carbon atoms, or represents halogenoalkylsulphonyl with 1 or 2 carbon atoms and 1 to 3 identical or different halogen atoms, or represents alkoxyalkylsulphonyl or alkylthioalkylsulphonyl with 1 or 2 carbon atoms per alkyl part, or represents nitro, amino, mono- or dialkylamino with 1 or 2 carbon atoms per alkyl part of acylamino, or represents a fused-on five-membered or six-membered carbocyclic ring which can be interrupted by one or more identical or different atoms from the group comprising oxygen, sulphur and nitrogen atoms,
X represents .dbd.CH--, or represents a nitrogen atom,
Y represents CO or SO.sub.2 and
n represents an integer from 0 to 3, and
R.sup.2 represents hydrogen or an alkyl radical which has 1 to 12 carbon atoms and can be substituted by one or more fluorine or chlorine atoms, by a hydroxyl group, by a radical --A--R.sup.6,
in which
A represents oxygen, sulphur, SO or SO.sub.2 and R.sup.6 represents an optionally substituted aliphatic, aromatic or heterocyclic radical,
or by the NO.sub.2 group, or by a group ##STR11## in which R.sup.7 and R.sup.8 denote a hydrogen atom, alkyl with 1 to 4 carbon atoms, phenyl, a 5- or 6-membered heterocyclic radical or an aliphatic, aromatic or heterocyclic acyl group,
or by the cyano group, a carboxylic acid ester radical or a carboxylic acid amide radical which is optionally substituted on the N atom by alkyl with 1 to 4 carbon atoms, or by an optionally substituted phenyl radical or an optionally substituted or fused 5- or 6-membered heterocyclic radical, or
R.sup.2 represents cycloalkyl which has 3 to 6 ring carbon atoms and is optionally substituted by fluorine, chlorine, hydroxyl, alkoxy, phenoxy, alkyl or phenyl or optionally contains fused-on 5- or 6-membered rings, or
R.sup.2 represents phenyl or naphthyl, which can be substituted by fluorine, chlorine or bromine, or by a radical --A--R.sup.9,
in which
A represents oxygen, sulphur, SO or SO.sub.2 and R.sup.9 represents an optionally substituted aliphatic, aromatic or heterocyclic radical,
or by the NO.sub.2 group, or by a dialkylamino group with 1 or 2 C atoms per alkyl part of acylamino group or an alkyl radical with 1 to 4 carbon atoms which is optionally substituted by halogen or alkoxy, or by an optionally substituted phenyl radical, or by a cyano group, a carboxyl group, a carboxylic acid ester group, a carboxylic acid amide group which is optionally substituted on the N atom by alkyl with 1 to 4 carbon atoms or a sulphonamide group which is optionally substituted on the N atom by alkyl with 1 to 4 carbon atoms, or by a heterocyclic radical which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms, or by a fused-on carbocyclic or heterocyclic ring which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and, on the carbon and nitrogen atoms, further substituents, or
R.sup.2 represents a 4- to 7-membered heterocyclic radical which, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and can contain further substituents on the carbon or nitrogen atoms in the ring, such as fluorine, chlorine, --A--R.sup.9, with the same meaning for A and R.sup.9 as above, an amino group which is optionally substituted by alkyl with 1 to 4 carbon atoms, cyano, a carboxylic acid ester group or a carboxylic acid amide group which is optionally N-substituted by alkyl with 1 to 4 C atoms, optionally substituted alkyl or phenyl radicals or further 5- or 6-membered heterocyclic radicals or can contain fused-on carbocyclic or heterocyclic rings with 5 or 6 ring members, or R.sup.2 represents a radical --O--R.sup.3, or also represents S--R.sup.3, if Y represents CO,
in which
R.sup.3 denotes alkyl which has 1 to 8 carbon atoms and can be substituted by fluorine, chlorine or the radical --A--R.sup.6, with the same meaning for A and R.sup.6 as above, or by nitro, cyano or a carboxylic acid ester group, or by optionally substituted phenyl, or
R.sup.3 represents phenyl, which can optionally be substituted by fluorine, chlorine, bromine, nitro, cyano, a carboxylic acid ester group or a carboxylic acid amide group which is optionally N-substituted by alkyl with 1 to 4 carbon atoms, or a group --A--R.sup.9, with the same meaning for A and R.sup.9 as above, or by an alkyl group with 1 to 4 carbon atoms, which can optionally be substituted by one or more fluorine or chlorine atoms, or by a dialkylamino group with 1 or 2 carbon atoms per alkyl part or a further phenyl radical, or
R.sup.2 represents ##STR12## in which R.sup.4 denotes hydrogen or an optionally substituted saturated or unsaturated alkyl radical with up to 4 carbon atoms and
R.sup.5 denotes a saturated or unsaturated alkyl radical which has 1 to 8 carbon atoms and can be substituted by fluorine, chlorine, hydroxyl, acetoxy or the radical --A--R.sup.6, with the same meaning for A and R.sup.6 as above,
or by a group ##STR13## in which R.sup.10 and R.sup.11 each independently denote a hydrogen atom, an alkyl, phenyl or 5- or 6-membered heterocyclic radical or an acyl group,
or by the cyano group, a carboxylic acid ester radical or a carboxylic acid amide radical which is optionally substituted on the N atom by alkyl with 1 to 4 carbon atoms, or by an optionally substituted phenyl radical or an optionally substituted or fused 5- or 6-membered heterocyclic radical, or
R.sup.5 furthermore represents cycloalkyl which has 3 to 8 ring carbon atoms and is optionally substituted by fluorine, chlorine, hydroxyl, alkoxy with 1 to 4 carbon atoms, phenoxy, alkyl with 1 to 4 carbon atoms or phenyl or contains optionally fused-on rings, or
R.sup.5 furthermore represents phenyl, which can be substituted by fluorine, chlorine or bromine, or by a radical --A--R.sup.9,
in which
A represents oxygen, sulphur, SO or SO.sub.2 and R.sup.9 represents an optionally substituted aliphatic, aromatic or heterocyclic radical,
or by the NO.sub.2 group, or by a dialkylamino group with 1 to 4 carbon atoms or an acetylamino group or an alkyl radical which has 1 to 4 C atoms and is optionally substituted by fluorine, chlorine or alkoxy with 1 to 4 C atoms, or by an optionally substituted phenyl radical, or by a cyano group, a carboxylic acid ester group, a carboxylic acid amide group which is optionally substituted on the N atom by alkyl with 1 to 4 carbon atoms or a sulphonamide group which is optionally substituted on the N atom by alkyl with 1 to 4 carbon atoms, or by a heterocyclic radical which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms, or by a fused-on carbocyclic or heterocyclic ring which has 5 or 6 ring members and, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and, on the carbon and nitrogen atoms, further substituents, or
R.sup.5 furthermore represents a 4- to 7-membered heterocyclic radical which, in addition to carbon, can contain one or more oxygen, sulphur and/or nitrogen atoms and can contain further substituents on the carbon or nitrogen atoms in the ring, such as fluorine, chlorine, --A--R.sup.9, with the same meaning for A and R.sup.9 as above, an amino group which is optionally substituted by alkyl with 1 to 4 carbon atoms, cyano, a carboxylic acid ester group or a carboxylic acid amide group which is optionally N-substituted by alkyl with 1 to 4 carbon atoms, optionally substituted alkyl or phenyl radicals or further heterocyclic radicals or fused-on carbocyclic or heterocyclic rings with 5 or 6 ring members, or
R.sup.4 and R.sup.5, together with the nitrogen atom, can also form a 3- to 8-membered ring which, in addition to this N atom, can also contain further hetero atoms, such as oxygen, sulphur and nitrogen, and additional substituents and/or fused-on carbocyclic or heterocyclic rings.
Especially preferred compounds of the formulae (I) and (IA) are those in which
R represents hydrogen, or represents alkyl with 1 to 3 carbon atoms, such as methyl, ethyl, n-propyl and iso-propyl,
R.sup.1 represents fluorine, chlorine, bromine, hydroxyl, methyl, ethyl, n-propyl, iso-propyl, tert.-butyl, trifluoromethyl, tetrachloroethyl, dichlorofluoromethyl, alkoxy with 1 to 4 carbon atoms, such as methoxy, ethoxy, n- or iso-propoxy, n-butoxy, iso-butoxy, sec.-butoxy or tert.-butoxy, trifluoromethoxy, dichlorofluoromethoxy, methoxymethoxy, ethoxymethoxy, 2-methoxyethoxy, 2-ethoxyethoxy, methylthiomethoxy, 2-methylthioethoxy, 2-ethylthioethoxy, phenoxymethoxy, 2-phenoxyethoxy, alkylthio with 1 to 4 carbon atoms, such as methylthio, ethylthio, n- or iso-propylthio, n-butylthio, sec.-butylthio, iso-butylthio, tert.-butylthio, trifluoromethylthio, dichlorofluoromethylthio, methoxymethylthio, 2-methoxyethylthio, ethoxymethylthio, 2-ethoxyethylthio, methylthiomethylthio, methylsulphinyl, ethylsulphinyl, trifluoromethylsulphinyl, methoxymethylsulphinyl, methylsulphonyl, ethylsulphonyl, trifluoromethylsulphonyl, methoxymethylsulphonyl, methylthiomethylsulphonyl, nitro, amino, cyano, dimethylamino, diethylamino, monomethylamino, monoethylamino or acetylamino, or represents a fused-on benzene ring or a 5- or 6-membered heterocyclic radical which has 1 or 2 oxygen and/or sulphur and/or nitrogen atoms and is optionally mono-, di-, tri-, tetra- or penta-substituted, such as furan, dioxolene, dioxene, thioxolene, thiophene, pyridine, pyrimidine, oxazole or thiazole,
y represents CO or SO.sub.2,
n represents the integer 0, 1, 2 or 3 and
R.sup.2 represents hydrogen, or represents saturated or unsaturated alkyl with 1 to 12 carbon atoms or halogenoalkyl with 1 to 4 carbon atoms and 1 to 3 identical or different fluorine, chlorine or bromine atoms, or represents hydroxyalkyl with 1 to 3 carbon atoms, or represents alkoxyalkyl and alkylthioalkyl with in each case 1 to 4 carbon atoms in the alkyl radicals, or represents cycloalkyl which has 3 to 7 carbon atoms and can optionally be mono-, di-, tri- or tetrasubstituted by methyl, or represents phenyl which is optionally mono-, di- or trisubstituted by identical or different substituents from the group comprising alkyl with 1 to 4 carbon atoms, fluorine, chlorine, bromine, nitro, trifluoromethyl, dichlorofluoromethyl, cyano, methoxy, ethoxy, dimethylamino, diethylamino, acetylamino, phenyl, carboxyl, or carboxylic acid amide group or a carboxylic acid ester group, or furthermore represents a 5- or 6-membered heterocyclic radical which can contain 1 to 3 identical or different oxygen, sulphur or nitrogen atoms and can contain fused-on carbocyclic or heterocyclic rings and can optionally be substituted by methyl, ethyl, fluorine, chlorine, cyano, phenyl, substituted amino or carboxyl, for example furan, tetrahydrofuran, thiophene, benzofuran, pyridine, quinoline, imidazole, benzimidazole, pyrimidine, pyridazine, pyrazine, quinazoline, quinoxaline, benzoxazole or benzothiazole, or represents OR.sup.3 or also represents SR.sup.3, if Y=CO,
wherein
R.sup.3 represents alkyl with 1 to 6 carbon atoms, halogenoalkyl with 1 to 3 carbon atoms and 1 to 5 identical or different fluorine and chlorine atoms, nitro- or cyanoalkyl with 1 to 4 carbon atoms or phenyl, which is optionally mono-, di- or trisubstituted by identical or different substituents from the group comprising methyl, ethyl, fluorine, chlorine, bromine, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -dialkylamino, nitro, cyano or a carboxylic acid ester group, or
R.sup.2 represents ##STR14## wherein R.sup.4 represents hydrogen or alkyl with 1 to 4 carbon atoms and
R.sup.5 represents hydrogen or alkyl with 1 to 6 carbon atoms, or
R.sup.4 and R.sup.5, together with the nitrogen atom on which they are located, can form a 5- to 7-membered ring which can contain further nitrogen, sulphur or oxygen atoms.
Compounds of the formula (I) or (IA) which may be mentioned in particular are those in which
R represents hydrogen, methyl or ethyl,
R.sup.1 represents methoxy, ethoxy, trifluoromethoxy, methyl, ethyl, fluorine, chlorine, bromine, trifluoromethyl, methylthio, ethylthio, trifluoromethylthio, methylenedioxy or nitro,
n represents the integer 0, 1 or 2,
X represents .dbd.CH or a nitrogen atom,
Y represents CO or SO.sub.2 and
R.sup.2 represents alkyl with 1 to 4 carbon atoms, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec.-butyl or tert.-butyl, or represents optionally substituted phenyl, methoxy, ethoxy, phenoxy, furfuryl, dimethylamino or diethylamino, piperidino or morpholino.
If, for example, 1-pyrimid-2-yl-4-phenyl-pyrazolin-5-one and acetic anhydride are used as starting substances, the course of the reaction can be represented by the following equation: ##STR15##
If, for example, 1-pyrid-2-yl-4-phenyl-pyrazolin-5-one, furan-2-carboxylic acid chloride and triethylamine are used as starting substances, the course of the reaction can be represented by the following equation. ##STR16##
If, for example, 1-pyrid-2-yl-4-phenyl-pyrazolin-5-one and phenyl isocyanate are used as starting substances, the course of the reaction can be represented by the following equation: ##STR17##
Formula (II) or (IIA) provides a general definition of the 1-pyri(mi)dyl-4-aryl-pyrazolin-5-ones to be used as starting substances in carrying out the process according to the invention. In this formula, R, R.sup.1, X and n have the meaning which has already been mentioned for these symbols in connection with the description of the substances of the formula (I) according to the invention.
The starting substances of the formula (II) or (IIA) and their preparation and use as fungicides are described in Application, Ser. No. 733,450, supra. In accordance with the statements of this patent specification, they are obtained by reaction of .alpha.-acylphenylacetic acid esters or derivatives thereof of the formula (IV) with 2-hydrazino-pyri(mi)dines (V), which themselves are known from the literature. ##STR18## wherein W represents OH, OAlk, Hal or NAlk.sub.2.
Examples which may be mentioned of starting substances of the formula (II) are: 1-pyrid-2-yl-4-phenylpyrazolin-5-one, 1-pyrid-2-yl-4-(4-fluoro-phenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(2-chloro-phenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(2-bromo-phenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(3,4-dichloro-phenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(2-methoxy-phenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(4-methoxyphenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(3-trifluoromethoxyphenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(4-trifluoromethylmercapto-phenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(4-methylphenyl)-pyrazolin-5-one, 1-pyrid-2-yl-4-(3-trifluoromethylphenyl)-pyrazolin-5-one, 1-pyrid-2-yl-3-methyl-4-phenylpyrazolin-5-one, 1-pyrid-2-yl-3-ethyl-4-phenyl-pyrazolin-5-one, 1-pyrimid-2-yl-4-(2-fluoro-phenyl)-pyrazolin-5-one, 1-pyrimid-2-yl-4-(4-chloro-phenyl)-pyrazolin-5-one, 1-pyrimid-2-yl-4-(2-fluoro-6-chloro-phenyl)-pyrazolin-5-one, 1-pyrimid-2-yl-4-(4-methoxy-phenyl)-pyrazolin- 5-one, 1-pyrimid-2-yl-4-(3,4-difluoromethylenedioxy-phenyl)-pyrazolin-5-one, 1-pyrimid-2-yl-4-(2-methoxy-phenyl)-pyrazolin-5-one, 1-pyrimid-2-yl-4-(2-chloro-5-trifluoromethyl-phenyl)-pyrazolin-5-one and 1-pyrimid-2-yl-3-methyl-4-phenyl-pyrazolin-5-one.
The acid derivatives of the formula (III) also to be used as starting substances for the preparation of the compounds according to the invention are known. They are the reactive derivatives, customary for acylation reactions, of carboxylic acids, carbonic acid esters, carbamic acids, sulphonic acids and sulphamic acids, in particular carboxylic acid halides, carboxylic acid anhydrides, mixed anhydrides of carboxylic acids and carbonic acid esters, carboxylic acid azolides, ketenes, carbonic acid ester-halides, dicarbonic acid esters, carbamic acid halides, isocyanates, sulphonic acid halides, sulphonic acid anhydrides and the like.
The reaction of the 1-pyri(mi)dyl-4-aryl-pyrazolin-5-ones of the formula (II) or (IIA) with the reactive derivatives of carboxylic acids, carbonic acid esters, carbamic acids, sulphonic acids or sulphamic acids of the formula (III) is carried out under the conditions known in principle for acylation reactions.
If carboxylic acid anhydrides, mixed anhydrides of carboxylic acids and carbonic acid esters, dicarbonic acid dialkyl esters or sulphonic acid anhydrides are used as the acylating component, this acylation can be carried out without further auxiliaries, by allowing the reaction components to act on one another, preferably in an equimolar ratio, in undiluted form or in diluents. However, it may also be advantageous to employ the acylating agent in an excess of up to a further mole or, as in the case of carboxylic acid anhydrides, to use this as the solvent in a larger excess.
The reactions are advantageously carried out in diluents, it being possible to use all the solvents which are inert towards the reaction partners. These include hydrocarbons, such as benzine or toluene, halogenohydrocarbons, such as methylene chloride, chloroform and carbon tetrachloride, ketones, such as acetone or methyl isopropyl ketone, ethers, such as diethyl ether, tetrahydrofuran or dioxane, and furthermore dimethylsulphoxide, tetrahydrothiophene dioxide and dimethylformamide.
The reaction temperatures can be varied within a substantial range. The reaction is in general carried out between -20.degree. C. and 150.degree. C., preferably between room temperature and the boiling point of the solvent used.
If carboxylic acid halides, carbonic acid esterhalides, carbamic acid halides or sulphonic acid halides are employed as the acylating component, it is advantageous to add an auxiliary base to bond the hydrogen halides liberated during the reaction. Suitable auxiliary bases are: alkali metal and alkaline earth metal hydroxides and carbonates and tertiary amines, such as, for example, triethylamine, pyridine and N,N-dimethyl-aniline.
The acylating agent and the acid-binding base are preferably employed in each case in equimolar amounts in relation to the reaction component of the formula (II) or (IIA), but it may be advantageous to employ either only the auxiliary base or the acylating component and the auxiliary base in an excess of up to a further mole.
An alternative in the reaction procedure comprises initially converting the pyrazolinone of the formula (II) or (IIA) into a metal salt in an inert solvent and then reacting this salt with the acylating agent. This can be effected, for example, with strong bases, such as sodium hydride, sodium or potassium amide or potassium tert.-butylate.
The reactions are preferably carried out in inert solvents, those already mentioned above being suitable. The reaction temperatures are -20.degree. C. to 150.degree. C., preferably 0.degree. to 100.degree. C.
If isocyanates are employed as the acylating component, the reaction is as a rule carried out with an equimolar amount of the reaction components in the abovementioned solvents. The reaction temperatures are 0.degree. to 100.degree. C. Activators, such as, for example, 1,4-diazabicyclooctane (DABCO) and tin-II octoate, can be used to accelerate the reaction.
The reaction products are isolated in the customary manner by distilling off the solvent and, thoroughly washing the amine hydrochloride which may be formed in the reaction, or by precipitation with water in the case where the reaction is carried out in a water-miscible solvent.
The active compounds according to the invention exhibit a powerful microbicidal action and can be employed in practice for combating undesired microorganisms. The active compounds are suitable for use as plant protection agents, in particular as fungicides or can be used in the preservation of materials for the preservation of industrial materials.
Fungicidal agents in plant protection are employed for combating Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes.
Bactericidal agents are used in plant protection for combating Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
Some causative organisms of fungal and bacterial diseases which come under the generic names listed above may be mentioned as examples, but not by way of limitation: Xanthomonas species, such as, for example, Xanthomonas campestris pv.oryzal; Pseudomonas species, such as, for example, Pseudomonas oyringae pv. lachrymans; Erwinia species, such as, for example, Erwinia amylovora; Pythium species, such as, for example, Pythium ultimum; Phytophthora species, such as, for example, Phytophthora infestans; Pseudoperonospora species, such as, for example, Pseudoperonospora humuli or Pseudoperonospora cubense; Plasmopara species, such as, for example, Plasmopara viticola; Peronospora species, such as, for example, Peronospora pisi or P. brassicae; Erysiphe species, such as, for example, Erysiphe graminis; Sphaerotheca species, such as, for example, Sphaerotheca fuliginea; Podosphaera species, such as, for example, Podosphaera leucotricha; Venturia species, such as, for example, Venturia inaequalis; Pyrenophora species, such as, for example, Pyrenophora teres or P. graminea (conidia form: Drechslera, syn: Helminthosporium); Cochliobolus species, such as, for example, Cochliobolus sativus (conidia form: Drechslera, syn: Helminthosporium); Uromyces species, such as, for example, Uromyces appendiculatus; Puccinia species, such as, for example, Puccinia recondita; Tilletia species, such as, for example, Tilletia caries; Ustilago species, such as, for example, Ustilago nuda or Ustilago avenae; Pellicularia species, such as, for example, Pellicularia sasakii; Pyricularia species, such as, for example, Pyricularia oryzae; Fusarium species, such as, for example, Fusarium culmorum; Botrytis species, such as, for example, Botrytis cinerea; Septoria species, such as, for example, Septoria nodorum; Leptosphaeria species, such as, for example, Leptosphaeria nodorum; Cercospora species, such as, for example, Cercospora canescens; Alternaria species, such as, for example, Alternaria brassicae; and Pseudocercosporella species, such as, for example, Pseudocercosporella herpotrichoides.
The good toleration, by plants, of the active compounds, at the concentrations required for combating plant diseases, permits treatment of above-ground parts of plants, of vegetative propagation stock and seeds; and of the soil.
The active compounds can be converted to the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine capsules in polymeric substances and in coating compositions for seed, and ULV formulations.
These formulations are produced in known manner, for example by mixing the active compounds with extenders, that is, liquid solvents, liquefied gases under pressure, and/or solid carriers, optionally with the use of surface-active agents, that is, emulsifying agents and/or dispersing agents, and/or foam-forming agents. In the case of the use of water as an extender, organic solvents can, for example, also be used as auxiliary solvents. As liquid solvents, there are suitable in the main: aromatics, such as xylene, toluene or alkyl naphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example mineral oil fractions, alcohols, such as butanol or glycol as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethylformamide and dimethylsulphoxide, as well as water. By liquefied gaseous extenders or carriers are meant liquids which are gaseous at normal temperature and under normal pressure, for example aerosol propellants, such as halogenated hydrocarbons as well as butane, propane, nitrogen and carbon dioxide. As solid carriers there are suitable: for example ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as highly dispersed silicic acid, alumina and silicates. As solid carriers for granules there are suitable: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, as well as synthetic granules of inorganic and organic meals, and granules of organic material such as sawdust, coconut shells, corn cobs and tobacco stalks. As emulsifying and/or foam-forming agents there are suitable: for example non-ionic and anionic emulsifiers, such as polyoxyethylene-fatty acid esters, polyoxyethylene-fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulphonates, alkyl sulphates, aryl sulphonates as well as albumin hydrolysis products. As dispersing agents there are suitable: for example lignin-sulphite waste liquors and methylcellulose.
Adhesives such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules and latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, as well as natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids, can be used in the formulations. Other additives can be mineral and vegetable oils.
It is possible to use colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyestuffs, such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
The formulations in general contain between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%.
The active compounds according to the invention can be present in the formulations as a mixture with other known active compounds, such as fungicides, insecticides, acaricides and herbicides, and as mixtures with fertilizers and growth regulators.
The active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, emulsifiable concentrates, emulsions, foams, suspensions, wettable powders, pastes, soluble powders, dusts and granules. They are used in the customary manner, for example by watering, spraying, atomizing, scattering, dusting, foaming, brushing on and the like. It is furthermore possible to apply the active compounds by the ultra-low volume method or to inject the active compound formulation or the active compound itself into the soil. The seed of the plants can also be treated.
In the treatment of parts of plants, the active compound concentrations in the use forms can be varied within a substantial range. They are, in general, between 1 and 0.0001% by weight, preferably between 0.5 and 0.001%.
In the treatment of seed, amounts of active compound of 0.001 to 50 g per kilogram of seed, preferably 0.01 to 10 g, are generally required.
For the treatment of soil, active compound concentrations of 0.00001 to 0.1% by weight, preferably 0.0001 to 0.02% by weight, are required at the place of action.
The compounds of the formula (I) according to the invention show good actions against causative organisms of cereal diseases, against causative organisms of rice diseases (Pyricularia oryzae) and against causative organisms of vegetable and fruit diseases (Botrytis cinerea). When used accordingly, the compounds likewise also have a bactericidal action, and they also show an action in the plate test.
According to the invention, industrial materials are non-living materials which have been prepared for use in industry. Industrial materials which are to be preserved by active compounds according to the invention from microbial change or destruction can be, for example, adhesives, sizes, paper and card, textiles, leather, wood, paints and articles made of plastic, cooling lubricants and other materials which can be attacked or decomposed by microorganisms. Components of production plants, for example cooling water circulation, which can be impaired by multiplication of microorganisms may also be mentioned in the context of materials to be preserved. Adhesives, sizes, paper and card, leather, wood, paints, cooling lubricants and cooling circulations may be mentioned as preferred industrial materials in the context of the present invention.
Examples which may be mentioned of microorganisms which can cause degradation of or a change in the industrial materials are bacteria, fungi, yeasts, algae and slime organisms. The active compounds according to the invention act preferentially against fungi, in particular moulds, fungi which discolor wood and destroy wood (Basidiomycetes) and against slime organisms and algae.
Microorganisms of the following genera may be mentioned as examples: Alternaria, such as Alternaria tenuis, Aspergillus, such as Aspergillus niger, Chaetomium, such as Chaetomium globosum, Coniophora, such as Coniophora puteana, Lentinus, such as Lentinus tigrinus, Penicillium, such Penicillium glaucum, Polyporus, such as Polyporus versicolor, Aureobasidium, such as Auerobasidium pullulans, Sclerophoma, such as Sclerophoma pityophila, Trichoderma, such as Trichoderma viride, Escherichia, such as Escherichia coli, Pseudomonas, such as Pseudomonas aeruginosa and Staphylococcus, such as Staphylococcus aureus.
An active compound according to the invention can be converted into the customary formulations according to the field of use, such as solutions, emulsions, suspensions, powders, pastes and granules.
These can be prepared in a manner which is known per se, for example by mixing the active compounds with an extender consisting of liquid solvent and/or solid excipients, if appropriate using surface-active agents, such as emulsifiers and/or dispersing agents, and, in the case of the use of water as an extender, organic solvents, such as alcohols, can, if appropriate, be used as auxiliaries.
Liquid solvents for the active compounds can be, for example, water, alcohols, such as lower aliphatic alcohols, preferably ethanol or isopropanol, or benzyl alcohol, ketones, such as acetone or methyl ethyl ketone, liquid hydrocarbons, such as benzine fractions, or halogenated hydrocarbons, such as 1,2-dichloroethane.
Microbicidal agents in general contain the active compounds in an amount of 1 to 95%, preferably 10 to 75%.
The use concentrations of the active compounds according to the invention depend on the nature and occurrence of the microorganisms to be combated and on the composition of the material to be preserved. The optimum amount to be used can be determined by test series. The use concentrations are in general in the range from 0.001 to 5% by weight, preferably 0.05 to 1.0% by weight, based on the material to be preserved.
The active compounds according to the invention can also be present as a mixture with other known active compounds. The following active compounds may be mentioned as examples: benzyl alcohol mono(poly)hemiformal and other compounds which split off formaldehyde, benzimidazolyl methylcarbamates, tetramethylthiuram disulphide, zinc salts of dialkyldithiocarbamates, 2,4,5,6-tetrachloroisophthalonitrile, thiazolylbenzimidazole, mercaptobenzothiazole, 2-thiocyanatomethylthiobenzothiazole, organo-tin compounds, methylenebisthiocyanate and phenol derivatives, such as 2-phenylphenol, (2,2'-dihydroxy-5,5'-dichloro)diphenylmethane and 3-methyl-4-chloro-phenol.

PREPARATION EXAMPLES
Example 1 ##STR19##
23.7 g (0.1 mole) of 1-pyrid-2-yl-4-phenyl-pyrazolin-5-one are boiled under reflux in 150 ml of acetic anhydride for 6 hours. Excess acetic anhydride and the acetic acid formed are distilled off in vacuo. The residue which remains is dissolved in 100 ml of ethyl acetate and the solution is cooled in ice for several hours. The crystals which have separated out are filtered off with suction and dried.
20.4 g (73% of theory) of a mixture of 1-pyrid-2-yl-2-acetyl-4-phenyl-pyrazolin-5-one and 1-pyrid-2-yl-4-phenyl-5-acetoxypyrazole in a ratio of 60:40 (according to the .sup.1 H-proton resonance spectrum) of melting point: 158.degree.-162.degree. C. are obtained.
The following compounds are obtained in an analogous manner:
Example 2
1-Pyrimid-2-yl-2-acetyl-4-phenyl-pyrazol-5-one
Melting point: 171.degree.-173.degree. C. (from ethyl acetate).
Example 3
1-Pyrimid-2-yl-2-acetyl-3-methyl-4-phenyl-pyrazol-5-one
Melting point: 138.degree.-140.degree. C. (from toluene).
According to the .sup.1 H-proton resonance spectrum, the compounds according to Examples 2 and 3 are single compounds and, according to the .sup.13 C nuclear magnetic resonance spectrum, contain the acetyl radical in the 2-position.
Example 4 ##STR20##
26.7 g (0.1 mole) of 1-pyrid-2-yl-4-(4-methoxy-phenyl)-pyrazolin-5-one are dissolved in 200 ml of dioxane. 10.1 g (0.1 mole) of triethylamine and 0.2 g of 4-dimethylaminopyridine are added and 7.9 g (0.1 mole) of acetyl chloride are then added dropwise at room temperature. The mixture is subsequently stirred at room temperature for a further hour and at 90.degree. C. for 3 hours, cooled and stirred into 1 l of water. The crystals which have separated out are filtered off with suction, dried in air and recrystallized from cleaner's naphtha. 20.7 g (67% of theory) of 1-pyrid-2-yl-2-acetyl-4-(4-methoxy-phenyl)-pyrazolin-5-one of melting point 98.degree.-100.degree. C., which is contaminated only by a little 5-acetoxy derivative, are obtained.
The following compounds are obtained in an analogous manner:
__________________________________________________________________________ ##STR21## MeltingExample X R.sup.1 n R.sup.2 R point (.degree.C.) Recrystallized from__________________________________________________________________________ 5a N -- 0 C(CH.sub.3).sub.3 H 140-141 Toluene 6a CH -- 0 ##STR22## H 114-116 Cleaner's naphtha 7a CH 4-OCH.sub.3 1 ##STR23## H 156-157 Toluene 8a CH -- 0 ##STR24## CH.sub.3 115-117 Cleaner's naphtha 9a N -- 0 ##STR25## H 221-223 Butanol 9b N -- 0 ##STR26## H 128-130 Carbon tetrachloride10a CH -- 0 OCH.sub.3 CH.sub.3 150-152 Cleaner's naphtha11a N -- 0 OCH.sub.3 H 174 Toluene12a N -- 0 ##STR27## H 162-164 Toluene/ligroin13a N 2-CH.sub.3 1 ##STR28## H 128.5 Ethanol14a CH 2-CH.sub.3 1 ##STR29## H 88-89 Diisopropyl ether15a CH 2-CH.sub.3 1 ##STR30## H 102-104 Diisopropyl ether16a CH 2-Cl, 6-F 2 ##STR31## H 121-122 Toluene17a N 2-Cl, 6-F 2 ##STR32## H 116-118 Diisopropyl ether18a CH -- 0 ##STR33## H 77-79 Cleaner's naphtha19a CH -- 0 ##STR34## H 212-214 Toluene20a CH 3-Cl 1 ##STR35## H 88-90 Cleaner's naphtha21a CH 4-CH.sub.3 1 ##STR36## H 114-116 Cleaner's naphtha22a CH 4-CF.sub.3 1 ##STR37## H 132-134 Cleaner's naphtha23a CH 4-Cl 1 ##STR38## H 134-136 Cleaner's naphtha23b CH 2-Cl, 6-F 2 ##STR39## H 107-109 Diisopropyl ether23c N -- 0 ##STR40## H 159-160 Carbontetrachloride23d N 3-CH.sub.3 1 ##STR41## H 126-128 Cleaner's naphtha23e CH 4-Cl 1 ##STR42## H 115-117 Carbontetrachloride23f N 4-OCH.sub.3 1 ##STR43## H 124-125 Carbontetrachloride__________________________________________________________________________
Example 24 ##STR44##
23.7 g (0.1 mole) of 1-pyrid-2-yl-4-phenyl-pyrazolin-5-one are dissolved in 200 ml of dioxane. After addition of 10.1 g (0.1 mole) of triethylamine, 11.5 g (0.1 mole) of methanesulphonyl chloride are added dropwise at room temperature, while cooling gently. The mixture is subsequently stirred at room temperature for a further 2 hours and at 70.degree. C. for 5 hours, cooled and stirred into 1 l of water. The crystals are filtered off with suction, dried in air and recrystallized from ethanol. 22.5 g (71% of theory) of 1-pyrid-2-yl-2-methylsulphonyl-4-phenyl-pyrazolin-5-one of melting point 112.degree.-114.degree. C. are obtained.
The following compounds are obtained in an analogous manner:
__________________________________________________________________________ ##STR45## Melting point RecrystallizedExample X R.sup.1 n R.sup.2 R (.degree.C.) from__________________________________________________________________________25 CH -- 0 ##STR46## 132-134 Toluene26 CH 4-OCH.sub.3 1 ##STR47## 133-135 To,uene27 CH -- 0 N(CH.sub.3).sub.2 135-137 Toluene28 N -- 0 N(CH.sub.3).sub.2 166-168 Toluene29 CH 2-Cl 1 ##STR48## H 135 Ethanol30 CH 2-Cl, 6-F 2 ##STR49## H 128-130 Diisopropyl ether31 N 2-Cl, 6-F 2 ##STR50## H 198-200 Butanol32 CH 2-CH.sub.3 1 ##STR51## H 119-121 Cleaner's naphtha33 CH 3-Cl 1 ##STR52## H 124-126 Cleaner's naphtha34 CH 4-CH.sub.3 1 ##STR53## H 132-134 Toluene35 CH 4-CF.sub.3 1 ##STR54## H 159-161 Toluene36 CH 4-Cl 1 ##STR55## H 138-140 Butanol__________________________________________________________________________
USE EXAMPLES
The compound shown below is employed as the comparison substance in the use examples which follow: ##STR56## Zinc ethylene-1,2-bis-(dithiocarbamate)
Example A
Pyricularia test (rice)/protective
Solvent: 12.5 parts by weight of acetone
Emulsifier: 0.3 parts by weight of alkylaryl polyglycol ether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water and the stated amount of emulsifier, to the desired concentration.
To test for protective activity, young rice plants are sprayed with the preparation of active compound until dripping wet. After the spray coating has dried on, the plants are inoculated with an aqueous spore suspension of Pyricularia oryzae. The plants are then placed in a greenhouse at 100% relative atmospheric humidity and 25.degree. C.
Evaluation of the disease infestation is carried out 4 days after the inoculation.
In this test, a clearly superior activity compared with the prior art is shown, for example, by the compounds according to the following preparation examples: 1, 2, 9a and 24.
Example B
The minimum inhibitory concentrations (MIC) of active compounds according to the invention are determined to demonstrate the activity against fungi:
Active compounds according to the invention are added in concentrations of 0.1 mg/l to 5,000 mg/l to an agar prepared from beer wort and peptone. After the agar has solidified, it is contaminated with pure cultures of the test organisms listed in the table. After storage at 28.degree. C. and 60 to 70% relative atmospheric humidity for 2 weeks, the MIC is determined. The MIC is the lowest concentration of active compound at which the species of microbe used shows no growth at all. Good actions on the listed test organisms are shown, for example, by the compounds according to Preparation Examples 2, 6a, 12a, 9b, 24 and 25:
Alternaria tenuis
Aspergillus niger
Aureobasidium pullulans
Chaetomium globosum
Cladosporium cladosporioides
Lentinus tigrinus
Penicillium glaucum
Polyporus versicolor
Sclerophoma pityophila
Example C
Action against bacteria
Active compounds according to the invention are added in concentrations of 1 to 5,000 ppm to an agar containing broth as the nutrient medium. The nutrient medium is then infected with in each case the test organisms listed in Table C and the infected medium is kept at 28.degree. C. and 60 to 70% relative atmospheric humidity for 2 weeks. The MIC is the lowest concentration of active compound at which the species of microbe used shows no growth at all. The compounds according to Preparation Examples 2, 6a, 12a, 9b, 13 and 14 show good actions.
TABLE C______________________________________MIC values in mg/l on action of the active compounds shownbelow on bacteria. MIC in mg/l of the active compounds Example No.Test organisms 2 6a 12a 9b 24 25______________________________________Escherichia coli 750 350 200 200 50 1,000Staphylococcus 1,000 100 500 500 50 20aureus______________________________________
Example D
Action against slime organisms
Substances according to the invention are used in concentrations of in each case 0.1 to 100 mg/l in Allen's nutrient solution (Arch. Mikrobiol. 17, 34 to 53 (1952)), which contains, in 4 l of sterile water, 0.2 g of ammonium chloride, 4.0 g of sodium nitrate, 1.0 g of dipotassium hydrogen phosphate, 0.2 g of calcium chloride, 2.05 g of magnesium sulphate, 0.02 g of iron chloride and 1% of caprolactam, dissolved in a little acetone. Shortly beforehand, the nutrient solution is infected with slime organisms (about 10.sup.6 germs/ml) which have been isolated from spinning water circulations used in polyamide production. Nutrient solutions which contain the minimum inhibitory concentration (MIC) or larger concentrations of active compound are still completely clear after culture at room temperature for 3 weeks, i.e. the pronounced multiplication of the microbes and slime formation noticeable after 3 to 4 days in nutrient solutions containing no active compound is absent. A good action is shown by the compound according to Preparation Example 13.
TABLE D______________________________________MIC value in mg/l on action of the substance shown below onslime organismsActive compound MIC in mg/l______________________________________Example No. 24 2-<5______________________________________
It is understood that the specification and examples are illustrative but not limitative of the present invention and that other embodiments within the spirit and scope of the invention will suggest themselves to those skilled in the art.

Number	Date	Country
0167888	Jun 1985	EPX
0165448	Dec 1985	EPX
0167893	Jan 1986	EPX
2643262	Sep 1976	DEX
3316891	Jul 1983	DEX
7044290	Dec 1970	FRX

1-heteroaryl-4-aryl-pyrazole microbicides

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Chem. Abstracts vol. 64 No. 7 Mar. 28, 1966.
Chem. Abstracts vol. 70 No. 3 Jan. 20, 1969.