EP1861369A1

EP1861369A1 - Nicotinanilides method for production thereof and agents comprising the same for prevention of fungal pests

Info

Publication number: EP1861369A1
Application number: EP06708777A
Authority: EP
Inventors: Markus Gewehr; Jochen Dietz; Thomas Grote; Carsten Blettner; Wassilios Grammenos;; Udo HÜNGER; Bernd Müller; Frank Schieweck; Anja Schwögler; Jan Klaas Lohmann; Joachim Rheinheimer; Peter Schäfer; Siegfried Strathmann; Reinhard Stierl; Jan Rether; Karl Eicken
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 2005-03-16
Filing date: 2006-03-15
Publication date: 2007-12-05
Also published as: AR053176A1; BRPI0608709A2; JP2008533097A; US20080171774A1; CN101142190A; WO2006097490A1

Abstract

The invention relates to nicotinanilides (I), where n = 0,1,2, m = 2,3, X1 = F, Cl, X2 = halogen, Y = CN, NO2, C1-C4 alkyl, C1-C4 alkyl halide, methoxy, methylthio, p = 0, 1, R1 = halogen, methyl, C1-C4 alkyl halide, methoxy, methylthio, methylsulphinyl, methylsulphonyl, R2 = H, methyl, ethyl and W = O, S, methods for production of said compounds, agents and seed comprising the same and methods for prevention of fungal pests.

Description

Nicotinic acid anilides, process for their preparation and compositions containing them for controlling harmful fungi

description

The present invention

in which the variables have the following meanings:

n is 0.1 or 2; m 2 or 3;

X ¹ F or chlorine, where in the case of n = 2, the two radicals X ^{1 may have} different meanings;

X ^{2 is} halogen, where the radicals X ^{2 may have} different meanings; Y is CN, NO _2, -C ₄ -alkyl, C _r C ₄ haloalkyl, methoxy or methylthio; p is zero or 1;

R ^{1 is} halogen, methyl, C ¹ -C 4 -haloalkyl, methoxy, methylthio, methylsulfinyl or methylsulfonyl;

R ^{2 is} hydrogen, methyl or ethyl; W oxygen or sulfur.

In addition, the invention relates to processes for the preparation of these compounds, compositions containing them and processes for their use for controlling harmful fungi.

Nicotinic acid anilides with fungicidal activity are known from the literature. Thus, for example, EP-A 545 099 describes biphenylanilides of this type which have monosubstitution on the biphenyl group.

From WO 02/059086 nicotinic anilides are known, which on the nitrogen of the

Amide group have a very specific substitution with unsaturated radicals.

From JP-A 2001/302605 2-chloro-N- (4'-chloro-6-methyl-biphenyl-2-yl) -nicotinamide is known. The object of the present invention was to find nicotinic acid anilides which show an improved fungicidal activity than the compounds of the prior art.

Accordingly, the compounds I defined above were found.

In addition, there have been found processes for preparing these compounds, compositions containing them and methods of using them to control phytopathogenic harmful fungi.

The compounds of the formula I have an over the known compounds improved activity against harmful fungi.

The compounds of the formula I can be present in various crystal modifications, which may differ in their biological activity. They are also the subject of the present invention.

In formula I, halogen is fluorine, chlorine, bromine or iodine, preferably fluorine or chlorine;

C 1 -C ₄ -alkyl is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl or 1, 1-dimethylethyl, preferably methyl or ethyl;

C 1 -C ₄ -haloalkyl represents a partially or completely halogenated C 1 -C 4 -alkyl radical, where the halogen atom (s) is / are in particular fluorine and / or chlorine, ie, for example, chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, diflu oromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2-chloro-2-fluoroethyl, 2,2,2-trifluoroethyl, 2 Chloro-1,1,2-trifluoroethyl, 2-chloro-2,2-difluoroethyl, 2-bromo-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, 1 , 1, 2,2-tetrafluoroethyl, 1,1,2,2-tetrachloroethyl, pentafluoroethyl, 2,2,3,3-tetrafluoro-m-propyl, 1,1,3,3,3,3-hexafluoro-M-propyl, 1 , 1, 1, 3,3,3-hexafluoro-2-propyl, heptafluoro-1-propyl, heptafluoro-2-propyl, 2,2,3,3,4,4,4-heptafluoro-1-butyl or nonafluoro 1-butyl, especially halomethyl, more preferably CH ₂ -CI, CH (CI) ₂ , CH ₂ -F, CH (F) ₂ , CF ₃ , CHFCl, CF ₂ Cl or CF (CI) ₂ .

The compounds I are generally obtained by reacting a carboxylic acid halide of the formula II in a manner known per se (for example, March, Advanced Organic Chemistry, 2nd Ed., 382 f., McGraw-Hill, 1977) in the presence of a Base reacted with an aniline of formula III:

The radical Hal in the formula II represents a halogen atom such as fluorine, chlorine, bromine and iodine, in particular fluorine, chlorine or bromine. This reaction is usually carried out at temperatures of (-2O) ⁰ C to 100 ⁰ C, preferably 0 ⁰ C to 50 ° C.

Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol and methylene chloride, dimethylsul - Foxid and dimethylformamide, particularly preferably toluene, methylene chloride and tetrahydrofuran.

It is also possible to use mixtures of the solvents mentioned.

Bases generally include inorganic compounds, e.g. Alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate and calcium carbonate and alkali metal hydrogencarbonates such as sodium bicarbonate and organometallic compounds, in particular alkali metal lalkyle such as methyllithium, butyl lithium and phenyllithium, alkyl magnesium halides such as methyl magnesium chloride and alkali metal and alkaline earth metal alkoxides such as sodium, sodium, potassium, potassium tert . Butanolate and dimethoxymagnesium, also organic bases, eg tertiary amines such as trimethylamine, triethylamine, di-isopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration.

Triethylamine and pyridine are particularly preferably used. The bases are generally used in equimolar amounts based on the compound II. But they can also be used in an excess of 5 mol% to 30 mol%, preferably 5 mol% to 10 mol%, or - in the case of using tertiary amines - optionally as a solvent.

The starting materials are generally reacted with each other in approximately equimolar amounts. It may be advantageous for the yield to use II in an excess of 1 mol% to 20 mol%, preferably 1 mol% to 10 mol%, based on III.

The starting materials of the formula II or III required for the preparation of the compounds I are known or can be synthesized analogously to known compounds (HeIv. Chim. Acta, 60, 978 (1977); Zh. Org. Khim., 26, 1527 (1990 Heterocycles 26, 1885 (1987); Izv. Akad. Nauk, SSSR Ser. Khim., 2160 (1982); THL 28, 593 (1987); THL 29, 5463 (1988)).

It has furthermore been found that compounds of the formula I are obtained by reacting, in a manner known per se, carboxylic acids of the formula IV with an aniline of the formula III in the presence of dehydrating agents and, if appropriate, an organic base.

IV III I

Suitable solvents are aliphatic hydrocarbons such as pentane, hexane,

Cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile , Ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and dimethyl sulfoxide and dimethylformamide, more preferably methylene chloride, toluene and tetrahydrofuran.

It is also possible to use mixtures of the solvents mentioned.

Suitable dehydrating agents are 1, 1'-carbonyldiimidazole, bis (2-oxo-3-oxazolidinyl) phosphoryl chloride, carbodiimides such as N, N'-dicyclohexylcarbodiimide and N- (3-dimethylaminopropyl) -N'-ethylcarbodiimide, phosphonium salts such as (benzotriazole-1 - yloxy) tris (dimethylamino) phosphonium hexafluorophosphate, bromotripyrrolidinophosphonium hexafluorophosphate, bromotris (dimethylamino) phosphonium hexafluorophosphate and Chlorotripyrrolidinophosphonium hexafluorophosphate, uronium and thiuronium salts such as O- (benzotriazol-1-yl) -N, N, N ', N'-tetramethyluronium hexafluorophosphate, O- (7-azabenzotriazol-1-yl) -N, N, N \ N'- tetramethyluronium hexafluorophosphate, S- (1-oxido-2-pyridyO-NNN'.N'-tetramethylthiuronium tetrafluoroborate, O- (2-oxo-1 (2H) pyridyl) -NNN'.N'-tetramethyluronium tetrafluoroborate and O - [(ethoxycarbonyl) cyano - methyleneamino] -N, N, N'-tetramethyluronium tetrafluoroborate, carbenium salts such as (benzotriazole-1-ynyloxy) dipyrrolidinocarbenium hexafluorophosphate, (benzotriazol-1-yloxy) dipiperidinocarbenium hexafluorophosphate, O- (3,4-dihydro-4-oxo-1 , 2,3-benzotriazine-S-y-NNN'-N'-tetramethyluronium tetrafluoroborate, chloro-N ', N'-bis (tetramethylene) formamidinium tetrafluoroborate, chlorodipyrrolidinocarbenium hexafluorophosphate, chloro-N, N, N', N ^l -bis (pentamethylene) formamidinium tetrafluoroborate, imidazolium salts such as 2-chloro-1,3-dimethylimidazolidinium tetrafluoroborate, preferably 1, 1'-carbonyldiimidazole, bis (2-oxo-3-oxazolidinyl) phosphoryl chloride, N ₁ N'-dicyclohexylcarbodiimide and N- (3-dimethylaminopropyl) -N'-ethylcarbodiimide, tracht in loading.

Suitable organic bases are tertiary amines such as trimethylamine, triethylamine, diisopropylethylamine and N-methyl-piperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylamino-pyridine and bicyclic amines. Triethylamine and pyridine are particularly preferably used. The bases are generally used in excess of from 10 mol% to 200 mol%, preferably from 50 mol% to 150 mol%, based on the compound IV.

The starting materials are generally reacted in approximately equimolar amounts with one another. It may be advantageous for the yield to use one of the compounds in an excess of 1 mol% to 20 mol%, preferably 1 mol% to 10 mol%. The dehydrating agents are generally used in excess of from 5 mol% to 100 mol%, preferably from 5 mol% to 60 mol%.

The starting materials of the formula III and IV required for the preparation of the compounds I are known or can be synthesized analogously to known compounds.

Compounds of the formula I where R ² = methyl or ethyl are obtained by reacting compounds of the formula I where R ² HH in a manner known per se in the presence of a base with an alkylating agent:

(R * = H) I (R ² = CH ₃ , C ₂ H ₅ )

Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, as well as dimethyl sulfoxide and dimethylformamide, particularly preferably diethyl ether, tert-butyl methyl ether, tetrahydrofuran and dimethylformamide.

It is also possible to use mixtures of the solvents mentioned.

Suitable alkylating agents (XCH ₃ or XC 2 H 5) are alkyl halides such as methyl iodide, ethyl iodide, methyl bromide, ethyl bromide, methyl chloride and ethyl chloride, alkyl (perfluoroalkyl sulfonates) such as methyl trifluoromethyl sulfonate and ethyl trifluoromethyl sulfonate, alkyl (alkyl sulfonates) such as methyl methyl sulfonate and ethyl methyl sulfonate, alkyl (arylsulfonate ) such as methyl p-tolylsulfonate and ethyl p-tolylsulfonate, oxonium salts such as trimethyloxonium tetrafluoroborate and triethyloxonium tetrafluoroborate.

Particularly preferred are methyl iodide, ethyl iodide, methyl bromide, ethyl bromide, methyl chloride and ethyl chloride.

Suitable bases are generally inorganic compounds, for example alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride Alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, sodium carbonate, potassium carbonate and calcium carbonate, and alkali metal hydrogen carbonates such as sodium bicarbonate or organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyllithium and phenyl-lithium, alkylmagnesium halides such as methylmagnesium chloride and alkali metal and alkaline earth metal alkoxides, such as sodium methoxide, sodium ethanolate, potassium ethanolate, potassium tert-butoxide. Particular preference is given to using sodium carbonate, potassium carbonate, sodium hydride, potassium hydride, butyllithium and potassium tert-butoxide.

The bases are generally used in approximately equimolar amounts based on the compound I. However, they can also be used in an excess of 5 mol% to 30 mol%, preferably 5 mol% to 10 mol%.

The starting materials are generally reacted with each other in approximately equimolar amounts. However, it may also be advantageous for the yield to use the alkylating agent in an excess of 1 mol% to 20 mol%, preferably 1 mol% to 10 mol%, based on I.

Those compounds I ₁ in which W is sulfur can also be prepared by sulfurization of the corresponding compounds I ₁ in which W is oxygen (cf., for example, D. Petrova & K. Jakobcic, Croat. Chem. Acta 48, 49 (1976 ) and WO 01/42223).

With regard to the biological activity of the compounds I, the following meanings of the variables are preferred, in each case alone or in combination: n zero; X ¹ chlorine; X ² F or Cl, in particular fluorine;

Y -C ₄ -alkyl, _{Ci-C4-haloalkyl} or methoxy, in particular methyl, difluoro- methyl, trifluoromethyl or methoxy; particularly preferably methyl or trifluoromethyl; p zero; R ^{1 is} halogen, methyl, trifluoromethyl or methoxy, in particular F ₁ Cl ₁ methyl or

trifluoromethyl; particularly preferably fluorine, chlorine or trifluoromethyl, in particular chlorine or

Trifluoromethyl, most preferably chlorine; R ^{2 is} hydrogen or methyl, in particular hydrogen; W oxygen.

In the case of m = 3, the radicals X ^{2 are} preferably in the 2,4,5- or 3,4,5-position, in particular in the 3,4,5-position.

Particular preference is given to compounds I having the following substituent combinations in which the substituents have the following meanings: X ² F or chlorine;

Y -C ₄ alkyl, -C ₄ haloalkyl or methoxy, in particular methyl, Difluorme- methyl, trifluoromethyl or methoxy; R ^{1 is} halogen, methyl, trifluoromethyl or methoxy, in particular fluorine, chlorine, methyl or trifluoromethyl; R ^{2 is} hydrogen or methyl; W oxygen.

Also preferred are the following combinations of substituents with the following meanings: n zero; p zero; X ² F or chlorine;

R ^{1 is} F, Cl, methyl or trifluoromethyl, in particular fluorine or chlorine; R ^{2 is} hydrogen; W oxygen.

Also preferred are compounds I with m = 2, in particular those in which n is zero, p is zero, R ^{1 is} fluorine or chlorine, in particular chlorine, and R ^{2 is} hydrogen.

The radicals X are preferably in the 2,4- or 3,4-position, in particular in the 3,4-position.

With regard to their use as fungicides, the compounds of the general formulas I-A and I-B are particularly preferred:

(I-A) (I-B)

Table A

Table 1 :

Compounds of the general formula IA, in which R ^{1 is} Cl and R ^{2 is} hydrogen and B corresponds in each case to one row of Table A.

Table 2:

Compounds of the general formula IA, in which R ^{1 is} F and R ^{2 is} hydrogen and B corresponds in each case to one row of Table A.

Table 3:

Compounds of the general formula IA, in which R ^{1 is} methyl and R ^{2 is} hydrogen and B corresponds in each case to one row of Table A.

Table 4: Compounds of the general formula IA, in which R ^{1 is} trifluoromethyl and R ^{2 is} hydrogen and B corresponds in each case to one row of Table A.

Table 5:

Compounds of the general formula IA, in which R ^{1 is} methoxy and R ^{2 is} hydrogen and B corresponds in each case to one row of Table A. Table 6:

Compounds of the general formula IA in which R ^{1 is} Cl and R ^{2 is} methyl and B corresponds in each case to one row of Table A.

Table 7:

Compounds of the general formula IA in which R ^{1 is} F and R ^{2 is} methyl and B corresponds in each case to one row of Table A.

Table 8: Compounds of the general formula IA, in which R ^{1 is} methyl and R ^{2 is} methyl and B corresponds in each case to one row of Table A.

Table 9:

Compounds of the general formula IA, in which R ^{1 is} trifluoromethyl and R ^{2 is} methyl and B corresponds in each case to one row of Table A.

Table 10:

Compounds of the general formula IA in which R ^{1 is} methoxy and R ^{2 is} methyl and B corresponds in each case to one row of Table A.

Table n:

Compounds of general formula IA, wherein R ^{1 is} Cl and R ^{2 is} ethyl and

B corresponds in each case to one row of Table A.

Table 12:

Compounds of the general formula IA, in which R ^{1 is} F and R ^{2 is} ethyl and B corresponds in each case to one row of Table A.

Table 13: Compounds of the general formula IA, in which R ^{1 is} methyl and R ^{2 is} ethyl and B corresponds in each case to one row of Table A.

Table 14:

Compounds of the general formula IA, in which R ^{1 is} trifluoromethyl and R ^{2 is} ethyl and B corresponds in each case to one row of Table A.

Table 15:

Compounds of the general formula IA, in which R ^{1 is} methoxy and R ^{2 is} ethyl and B corresponds in each case to one row of Table A. Table 16:

Compounds of the general formula IB in which R ^{1 is} Cl and B is each one

Line of Table A corresponds.

Table 17:

Compounds of the general formula IB in which R ^{1 is} F and B corresponds in each case to one row of Table A.

Table 18: Compounds of the general formula IB in which R ^{1 is} methyl and B corresponds in each case to one row of Table A.

Table 19:

Compounds of the general formula IB in which R ^{1 is} trifluoromethyl and B corresponds in each case to one row of Table A.

Table 20:

Compounds of the general formula IB in which R ^{1 is} methoxy and B corresponds in each case to one row of Table A.

Very particular preference is given to the following nicotinic acid anilides of the formula I:

2-chloro-N- (3 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (3 ^1, 5'-dichlorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (3'-chloro-4'-fluorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (4'-chloro-3'-fluorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (3 ', 4'-difluoro-biphenyl-2-yl) -nicotinamide,

2-chloro-N- (2 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (2 ', 5'-difluoro-biphenyl-2-yl) -nicotinamide,

2-chloro-N- (4'-chloro-2'-fluorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (2 ', 4'-difluorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (4-fluoro-2 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (3 ', 4', 5'-trifluorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (2 ', 4', 5'-trifluorobiphenyl-2-yl) -nicotinamide,

2-Chloro-N- (4'-chloro-2'-fluoro-5'-methoxy-biphenyl-2-yl) -nicotinamide, 2-trifluoromethyl-N- (3 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide .

2-trifluoromethyl-N- (4-fluoro-2 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide,

2-Trifluoromethyl-N- (3 ^I, 4 ', 5'-trifluorobiphenyl-2-yl) -nicotinamide,

2-trifluoromethyl-N- (2 ', 4', 5'-trifluorobiphenyl-2-yl) -nicotinamide,

2-Trifluoromethyl-N- (4'-chloro-2'-fluoro-5'-methoxy-biphenyl-2-yl) -nicotinamide, 2-trifluoromethyl-N- (3 ', 4'-difluorobiphenyl-2-yl) -nicotinamide .

2-trifluoromethyl-N- (3 ', 5'-dichlorobiphenyl-2-yl) -nicotinamide,

2-trifluoromethyl-N- (2 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide, 2-Trifluoromethyl-N- (3'-chloro-4'-fluorobiphenyl-2-yl) nicotinamide, 2-chloro-N- (3 ', 4', 5'-trifluorobiphenyl-2-yl) -N-methylnicotinamide and 2-trifluoromethyl-N- (3 ', 4', 5'-trifluorobiphenyl-2-yl) -N-ethylnicotinamide.

The compounds I are suitable as fungicides. They are distinguished by outstanding activity against a broad spectrum of phytopathogenic fungi, in particular from the classes of the Ascomycetes, Deuteromycetes, Peronosporomyces (syn. Oomycetes) and Basidiomycetes. They are sometimes systemically effective and can be used in crop protection as foliar, soil and Beizfungizide.

They are of particular importance for the control of a large number of fungi on various crops such as wheat, rye, barley, oats, rice, corn, turf, bananas, cotton, soy, coffee, sugar cane, wine, fruit and ornamental plants and vegetables such as cucumbers. Beans, tomatoes, potatoes and pumpkins, as well as the seeds of these plants.

In particular, they are suitable for controlling the following plant diseases:

Alternaria species on vegetables, rapeseed, sugar beets and fruits and rice, e.g. A. solani or A. alternata on potatoes and tomatoes, - Aphanomyces species on sugar beet and vegetables,

Ascochyta species on cereals and vegetables,

Bipolaris and Drechslera species on corn, cereals, rice and turf, e.g. D. maydis on corn,

Blumeria graminis (powdery mildew) on cereals, - Botrytis cinerea (gray mold) on strawberries, vegetables, flowers and vines,

Bremia lactucae on salad,

Cercospora species on maize, soybeans, rice and sugar beet,

Cochliobolus species on maize, cereals, rice, e.g. Cochliobolus sativus on cereals,

Cochliobolus miyabeanus on rice, - Colletotricum species on soybeans and cotton,

Drechslera species, Pyrenophora species on corn, cereals, rice and turf, e.g. D. teres to barley or D. tritici-repentis to wheat,

Esca at grapevine, caused by Phaeoacremonium chlamydosporium, Ph.

Aleophilum and Formitipora punctata (syn. Phellinus punctatus), - Exserohilum species on maize,

Erysiphe cichoracearum and Sphaerotheca fuliginea on cucurbits,

Fusarium and Verticillium species on various plants, e.g. F. graminearum or F. culmorum on cereal or F. oxysporum on a variety of plants, e.g. Tomatoes, - Gaeumanomyces graminis on cereals,

Gibberella species on cereals and rice (e.g., Gibberella fujikuroi on rice),

Grainstaining comp / ex to rice, Helminthosporium species on corn and rice,

Michrodochium nivale on cereals,

Mycosphaerella species on cereals, bananas and peanuts, e.g. M. graminicola on wheat or M. fijiesis on bananas, - Peronospora on cabbage and onion plants, e.g. P. brassicae on cabbage or P. destructor on onion,

Phakopsara pachyrhizi and Phakopsara meibomiae on soybeans,

Phomopsis species on soybeans and sunflowers,

Phytophthora infestans on potatoes and tomatoes, Phytophthora species on various plants, e.g. P. capsici on paprika,

Plasmopara viticola on vines,

Podosphaera leucotricha on apple,

Pseudocercosporella herpotrichoides on cereals,

Pseudoperonospora on various plants, e.g. P. cubensis on cucumber or P. humili on hops,

Puccinia species on various plants, e.g. P. triticina, P. striformins, P. hordei or P. graminis on cereals or P. asparagi on asparagus,

Pyricularia oryzae, Corticium sasakii, Sarocladium oryzae, S. attenuatum, Entlyoma oryzae on rice, - Pyricularia grisea on lawn and cereals,

Pythium spp. on turf, rice, corn, cotton, oilseed rape, sunflowers, sugar beets, vegetables and other plants, e.g. P. ultimum on various plants, P. aphanidermatum on lawn,

Rhizoctonia species on cotton, rice, potatoes, turf, corn, oilseed rape, sugar beets, vegetables and on various plants, e.g. R. solani on turnips and various plants,

Rhynchosporium secalis on barley, rye and triticale,

Sclerotinia species on oilseed rape and sunflowers,

Septoria tritici and Stagonospora nodorum on wheat, - Erysiphe (syn. Uncinula) necator on grapevine,

Setospaeria species on corn and turf,

Sphacelotheca reilinia on corn,

Thievaliopsis species on soybeans and cotton,

Tilletia species on cereals, - Ustilago species on cereals, maize and sugarcane, e.g. U. maydis on corn,

Venturia species (scab) on apples and pears, e.g. V. inaequalis to apple.

The compounds I are also suitable for controlling harmful fungi in the protection of materials (eg wood, paper, paint dispersions, fibers or fabrics) and in the protection of stored products. In wood preservation, particular attention is paid to the following harmful fungi: ascomycetes such as Ophiostoma spp., Ceratocystis spp., Aureobasidium pullulans, Sciophoma spp., Chaetomium spp., Humicola spp., Petriella spp., Trichurus spp .; Basidi- omycetes such as Coniophora spp., Coriolus spp., Gloeophyllum spp., Lentinus spp., P / et / rotus spp., Porta spp., Serpula spp. and Tyromyces spp., Deuteromycetes such as Aspergillus spp., Cladosportum spp., Penicillium spp., Trtchoderma spp., Alternaria spp., Paecilomyces spp. and Zygomycetenwe Mucorspp., in addition in the material contactor the following yeasts: Candida spp. and Saccharomyces cerevisae.

The compounds I are used by treating the fungi or the plants, seeds, materials or the soil to be protected against fungal attack with a fungicidally effective amount of the active ingredients. The application can be done both before and after the infection of the materials, plants or seeds by the fungi.

The fungicidal compositions generally contain between 0.1 and 95 wt .-%, preferably between 0.5 and 90 wt .-%, active ingredient.

The application rates in the application in crop protection, depending on the nature of the desired effect between 0.01 and 2.0 kg of active ingredient per ha.

In seed treatment, e.g. by dusting, coating or impregnating seed, in general amounts of active substance of 1 to 1000 g / 100 kg, preferably 5 to 100 g / 100 kg, of seed are required.

When used in material or storage protection, the application rate of active ingredient depends on the type of application and the desired effect. Usual application rates are, for example, 0.001 g to 2 kg, preferably 0.005 g to 1 kg of active ingredient per cubic meter of material treated in the material protection.

The compounds I can be converted into the usual formulations, e.g. Solutions, emulsions, suspensions, dusts, powders, pastes and granules. The application form depends on the respective purpose; It should in any case ensure a fine and uniform distribution of the compound I according to the invention.

The formulations are prepared in a known manner, e.g. by stretching the active compound with solvents and / or excipients, if desired with use of emulsifiers and dispersants. Suitable solvents / auxiliaries are essentially:

- Water, aromatic solvents (eg Solvesso ^® products, XyIoI), paraffins (eg petroleum fractions), alcohols (eg methanol, butanol, pentanol, benzyl alcohol), ketones (eg cyclohexanone, gamma-butyrolactone), pyrrolidones (N-methylpyrrolidone and NOP), acetates (glycol diacetate), glycols, dimethyl fatty acid amides, fatty acids and

Fatty acid ester. In principle, solvent mixtures can also be used. - Carriers such as ground natural minerals (eg kaolins, clays, talc, chalk) and ground synthetic minerals (eg fumed silica, silicates); Emulsifiers such as nonionic and anionic emulsifiers (eg polyoxyethylene fatty alcohol ethers, alkyl sulfonates and arylsulfonates) and dispersants such as lignin liquors and methylcellulose.

The surface-active substances used are alkali metal, alkaline earth metal, ammonium salts of lignin sulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkyl sulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, and condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde , Condensation products of naphthalene or naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ethers, tristerylphenyl polyglycol ethers, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene , Laurylalkoholpoly- glycol ether acetal, sorbitol esters, Ligninsulfitablaugen and methyl cellulose into consideration.

For the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions, there are mineral oil fractions of medium to high boiling point, such as kerosine or diesel oil, coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. Toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strong polar solvents, e.g. Dimethylsulfoxide, N-methylpyrrolidone or water into consideration.

Powders, dispersants and dusts may be prepared by mixing or co-grinding the active substances with a solid carrier.

Granules, e.g. Coated, impregnated and homogeneous granules can be prepared by binding the active compounds to solid carriers. Solid carriers are e.g. Mineral earths, such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulphate, magnesium oxide, ground plastics, fertilizers, e.g. Ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as cereal flour, tree bark, wood and nutshell meal, cellulose powder and other solid carriers.

Seed treatment formulations may additionally contain binders and / or gelling agents and optionally dyes. Binders can be added to increase adhesion of the active ingredients to the seed after treatment. Suitable binders are for example EO / PO block copolymer surfactants, but late also polyvinyl alcohols, Ppolyvinylpyrrolidone, polyacrylates, polymethacrylates, polybutenes, polyisobutylenes, polystyrenes, polyethyleneamines, Polyethylenamide, polyethylenimines (Lupasol ^®, Polymin ^®), polyethers, polyurethanes, polyvinyl acetates, Tylose and Copolymers of these polymers. A suitable gelling agent is, for example, carrageen (Satiagel ^®).

The formulations generally contain between 0.01 and 95% by weight, preferably between 0.1 and 90% by weight, of the active compound I. The active compounds are in a purity of 90% to 100%, preferably 95% % to 100% (according to NMR spectrum) used.

The active compound concentrations in the ready-to-use preparations can be varied within wide ranges. In general, they are between 0.0001 and 10%, preferably between 0.01 and 1%.

The active ingredients can also be used with great success in the ultra-low-volume (ULV) process, it being possible to apply formulations containing more than 95% by weight of active ingredient or even the active ingredient without additives.

For seed treatment, the formulations in question give, after dilution of from two to ten times, active compound concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-use preparations.

Examples of formulations are: 1. Products for dilution in water

A) Water Soluble Concentrates (SL)

10 parts by weight of a compound I according to the invention are dissolved with 90 parts by weight of water or a water-soluble solvent. Alternatively, wetting agents or other adjuvants are added. When diluted in water, the active ingredient dissolves. This gives a formulation with an active ingredient content of 10% by weight.

B) Dispersible Concentrates (DC)

20 parts by weight of a compound I according to the invention are dissolved in 70 parts by weight of cyclohexanone with the addition of 10 parts by weight of a dispersant, e.g. Polyvinylpyrrolidone solved. Dilution in water gives a dispersion. The active ingredient content is 20% by weight.

C) Emulsifiable Concentrates (EC)

15 parts by weight of a compound I according to the invention are dissolved in 75 parts by weight of xylene with the addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution in water results in an emulsion. The formulation has an active ingredient content of 15% by weight.

D) Emulsions (EW, EO)

25 parts by weight of a compound I according to the invention are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is added to water by means of an emulsifying machine (e.g., Ultraturax) in 30 parts by weight and made into a homogeneous emulsion. Dilution in water results in an emulsion. The formulation has an active ingredient content of 25% by weight.

E) suspensions (SC, OD)

20 parts by weight of a compound I according to the invention are comminuted with the addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent in a stirred ball mill to give a fine active substance suspension. Dilution in water results in a stable suspension of the active ingredient. The active ingredient content in the formulation is 20% by weight.

F) Water-dispersible and water-soluble granules (WG, SG)

50 parts by weight of a compound I according to the invention are finely ground with the addition of 50 parts by weight of dispersants and wetting agents and prepared by means of industrial equipment (for example extrusion, spray tower, fluidized bed) as water-dispersible or water-soluble granules. Dilution in water results in a stable dispersion or solution of the active ingredient. The formulation has an active ingredient content of 50% by weight.

G) Water-dispersible and Water-Soluble Powders (WP, SP) 75 parts by weight of a compound I according to the invention are ground in a rotor-stator mill with the addition of 25 parts by weight of dispersants, wetting agents and silica gel. Dilution in water results in a stable dispersion or solution of the active ingredient. The active ingredient content of the formulation is 75% by weight.

2. Products for direct application

H) dusts (DP)

5 parts by weight of a compound I according to the invention are finely ground and with 95

Parts by weight of finely divided kaolin intimately mixed. This gives a dust with an active ingredient content of 5 wt .-%.

J) Granules (GR ₁ FG ₁ GG, MG)

0.5 parts by weight of a compound I according to the invention are finely ground and with 99.5 parts by weight of carriers. Common processes are extrusion, spray drying or fluidized bed. This gives a granulate for direct application with an active ingredient content of 0.5 wt .-%.

K) ULV solutions (UL)

10 parts by weight of a compound I according to the invention are dissolved in 90 parts by weight of an organic solvent, e.g. XyIoI, solved. This gives a product for direct application with an active ingredient content of 10 wt .-%.

The active compounds may be used as such, in the form of their formulations or the forms of use prepared therefrom, e.g. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, scattering agents, granules by spraying, misting, dusting, scattering or pouring. The forms of application depend entirely on the purposes of use; In any case, they should ensure the finest possible distribution of the active compounds according to the invention.

Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (spray powders, oil dispersions) by addition of water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of wetting agents, tackifiers, dispersants or emulsifiers. But it can also be made of effective substance wetting, adhesion, dispersing or emulsifying and possibly solvent or oil concentrates, which are suitable for dilution with water.

To the active ingredients oils of various types, wetting agents, adjuvants, herbicides, fungicides, other pesticides, bactericides, optionally also just before use (tank mix), are added. These agents can usually be mixed into the compositions according to the invention in a weight ratio of 1: 100 to 100: 1, preferably 1:10 to 10: 1.

As adjuvants in this sense are in particular: organically modified polysiloxanes, eg Break Thru S 240 ^® ; Alcohol alkoxylates, eg. B. Atplus 245 ^®, Atplus MBA 1303 ^®, Plurafac LF 300 ^® and Lutensol ON 30 ^®; EO-PO block polymeεsate, z. B. Pluro- nic RPE 2035 ^® and Genapol B ^®; Alcohol ethoxylates, eg. As Lutensol XP 80 ^®; and sodium dioctylsulfosuccinate, e. B. Leophen RA ^®.

The agents according to the invention, in the form of use as fungicides, may also be present together with other active substances, e.g. with herbicides, insecticides, growth regulators such as Prohexadion-Ca, fungicides or with fertilizers. When mixing the compounds I or the agents containing them with one or more further active compounds, in particular fungicides, in many cases the spectrum of activity can be widened or resistance developments can be prevented. In many cases, synergistic effects are obtained.

The following list of fungicides with which the compounds according to the invention can be used together is intended to illustrate, but not limit, the possible combinations.

strobilurins

Azoxystrobin, dimoxystrobin, enestroburine, fluoxastrobin, kresoxim-methyl, metominostrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, orysastrobin, (2-chloro-5- [1- (3-methyl-benzyloxyimino) -ethyl] -benzyl) -carbamic acid methyl ester, (2-Chloro-5- [1- (6-methyl-pyridin-2-ylmethoxyimino) -ethyl] -benzyl) -carbamic acid methyl ester, 2- (ortho- (2,5-dimethylphenyl-oxymethylene) -phenyl) -3- methoxy-methyl acrylate;

Carboxylic acid amides - carboxylic anilides: benalaxyl, benodanil, boscalid, carboxin, mepronil, fenfuram, fenhexamide, flutolanil, furametpyr, metalaxyl, ofurace, oxadixyl, oxycarboxine, penthiopyrad, thifluzamide, tiadinil, 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid (4'-bromo-biphenyl-2-yl) -amide, 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid (4'-trifluoromethyl-biphenyl-2-yl) -amide, 4-difluoromethyl- 2-methyl-thiazole-5-carboxylic acid (4'-chloro-3'-fluorobiphenyl-2-yl) -amide, 3-difluoromethyl-1-methyl-pyrazole-4-carboxylic acid (3 ', 4' dichloro-4-fluoro-biphenyl-2-yl) -amide, 3,4-dichloro-isothiazole-5-carboxylic acid (2-cyano-phenyl) -amide;

- Carboxylic acid morpholides: Dimethomorph, Flumorph;

Benzoic acid amides: flumetover, fluopicolide (picobenzamide), zoxamide; Other carboxamides: carpropamide, diclocymet, mandipropamide, N- (2- (4- [3- (4-chloro-phenyl) -prop-2-ynyloxy] -3-methoxyphenyl) -ethyl) -2-methanesulfonylamino 3-methyl-butyramide, N- (2- (4- [3- (4-chloro-phenyl) -prop-2-ynyloxy] -3-methoxy-phenyl) -ethyl) -2-ethanesulfonyl-amino-3-methyl- butyramide;

azoles

- triazoles: bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fenbuconazole, flusilazole, fluquinconazole, flutriafol, Hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimol, triadimefon, triticonazole;

- imidazoles: cyazofamide, imazalil, pefurazoate, prochloraz, triflumizole; Benzimidazoles: benomyl, carbendazim, fuberidazole, thiabendazole;

- Other: ethaboxam, etridiazole, hymexazole;

Nitrogen-containing heterocyclyl compounds

Pyridines: fluazinam, pyrifenox, 3- [5- (4-chlorophenyl) -2,3-dimethylisoxazolidin-3-yl] pyridine;

Pyrimidines: bupirimate, cyprodinil, ferimzone, fenarimol, mepanipyrim, nuarimol, pyrimethanil;

- piperazine: triforin;

- Pyrroles: fludioxonil, fenpiclonil; - Morpholines: aldimorph, dodemorph, fenpropimorph, tridemorph;

Dicarboximides: iprodione, procymidone, vinclozolin;

- Other: acibenzolar-S-methyl, anilazine, captan, captafol, dazomet, diclomethine, fenoxanil, folpet, fenpropidin, famoxadone, fenamidone, octhilinone, probenazole, proquinazide, pyroquilon, quinoxyfen, tricyclazole, 5-chloro-7- (4- methyl-piperidin-1-yl) -6- (2,4,6-trifluorophenyl) - [1, 2,4] triazolo [1,5-a] pyrimidine, 2-butoxy-6-iodo-3 propylchromen-4-one, 3- (3-bromo-6-fluoro-2-methyl-indole-1-sulfonyl) - [1, 2,4] triazole-1-sulfonic acid dimethylamide;

Carbamates and Dithiocarbamates - Dithiocarbamates: Ferbam, Mancozeb, Maneb, Metiram, Metam, Propineb, Thiram, Zineb, Ziram;

Carbamates: diethofencarb, flubenthiavalicarb, iprovalicarb, propamocarb, 3- (4-chlorophenyl) -3- (2-isopropoxycarbonylamino-3-methyl-butyrylamino) -propionic acid methyl ester, N- (1 - (1 - (4- cyanophenyl) ethanesulfonyl) -but-2-yl) -carbamic acid (4-fluorophenyl) ester;

Other fungicides

- guanidines: dodin, iminoctadine, guazatine;

Antibiotics: Kasugamycin, Polyoxin, Streptomycin, Validamycin A; Organometallic compounds: fentin salts;

Sulfur-containing heterocyclyl compounds: isoprothiolane, dithianone;

Organophosphorus compounds: edifenphos, fosetyl, fosetyl-aluminum, Iprobenfos, pyrazophos, tolclofos-methyl, phosphorous acid and their salts;

Organochlorine compounds: thiophanate-methyl, chlorothalonil, dichlofluanid, toluidine, flusulfamide, phthalide, hexachlorobenzene, pencycuron, quintozene;

Nitrophenyl derivatives: binapacryl, dinocap, dinobuton; - Inorganic active substances: Bordeaux broth, copper acetate, copper hydroxide, copper oxychloride, basic copper sulphate, sulfur;

- Other: Spiroxamine, Cyflufenamid, Cymoxanil, Metrafenon.

synthesis Examples

Example 1: ΛAß ^ '- dichlorobiphenyl ^ -yl ^ -ttrifluormethyOnicotinamid To a solution of 0.20 g of 2- (trifluoromethyl) nicotinic acid and 0.21 g of triethylamine in 30 ml dichloromethane at 0 ⁰ C 0.25 g of 3', Added 4'-dichloro-2-aminobiphenyl and 0.40 g of bis (2-oxo-3-oxazolidinyl) phosphoryl chloride. The mixture was stirred at 0 ^° C. for 15 minutes and then at room temperature for 12 hours. It was then washed successively with dilute hydrochloric acid, twice with aqueous sodium bicarbonate solution and with water. The organic phase was dried and concentrated. The crude product was purified by column chromatography with cyclohexane / methyl-Fe / ϊ-butyl ether 1: 2 on silica gel. This gave 0.21 g of the desired product as beige crystals.

2-chloro-N- (4'-chloro-2'-fluoro-biphenyl-2-yl) -nicotinamide:

0.23 g of 2-chloronicotinic acid chloride were added dropwise to a solution of 0.29 g of 4'-chloro-2'-fluoro-2-aminobiphenyl and 0.15 g of pyridine in 10 ml of toluene at room temperature and the mixture was stirred at room temperature for 16 hours , 10 ml of tetrahydrofuran and 30 ml of methyl-Fe / f-butyl ether were added and the organic phase was washed successively with 2% hydrochloric acid, 2% sodium hydroxide solution and then with dilute aqueous sodium chloride solution. The organic phase was dried and concentrated in vacuo. The crude product was stirred with 5 ml of diisopropyl ether, the residual solid was separated and dried. This gave 0.34 g of the desired product as a white powder of mp. 124-126 ⁰ C.

According to the instructions given here, the compounds of general formula I indicated in Table 21 below were prepared with W = O.

Examples of the effect against harmful fungi

The fungicidal activity of the compounds of the formula I was demonstrated by the following experiments:

applications

The active compounds were prepared as a stock solution with 25 mg of active ingredient, which with a mixture of acetone and / or dimethyl sulfoxide and the emulsifier Uniperol ^® EL (wetting agent with emulsifying and dispersing action based on ethoxylated alkyl kylphenole) in the volume ratio solvent Emulsifier from 99 to 1 ad 10 ml was filled. It was then made up to 100 ml with water. This stock solution was diluted with the described solvent-emulsifier-water mixture to the desired drug concentration. Use Example 1 - Efficacy against tomato blight caused by Alternaria solani

Leaves of potted plants of the "Golden Queen" variety were sprayed to drip point with an aqueous suspension in the concentration of active compound specified below. On the following day, the leaves were infected with an aqueous spore suspension of Alternaria solani ^'m 2% biomalt solution having a density of 0.17 × 10 ⁶ spores / ml. Subsequently, the plants were placed in a water vapor-saturated chamber at temperatures between 20 and 22 ° C. After 5 days, the disease on the untreated, but infected control plants had developed so strongly that the infestation could be determined visually in%.

In this test, the plants treated with 250 mg / l of the compounds 21.1, 21.2, 21.3, 21.4, 21.5 and 2i.7 from Table 21 showed a maximum of 20% infestation, while the untreated plants were 64% infected.

Application Example 2 - Efficacy against barley spot disease caused by Pyrenophora teres at 1 day of protective application

Leaves of pot-grown barley seedlings of the "Hanna" variety were sprayed to drip point with aqueous suspension in the concentration of active compound specified below. 24 hours after the spray coating had dried on, the test plants were incubated with an aqueous spore suspension of Pyrenophora [syn. Drechslera] teres, the causative agent of net blotch inoculation. Subsequently, the test plants were placed in the greenhouse at temperatures between 20 and 24 ° C and 95 to 100% relative humidity. After 6 days, the extent of disease development was determined visually as% of total leaf area.

In this test, the plants treated with 250 mg / l of the compounds 21.1, 21.2, 21.3, 21.4, 21.5 and 21.7 from Table 21 showed a maximum of 15% infestation, while the untreated plants were 80% infected.

Claims

claims:

1. nicotinic acid anilides of the formula I.

in which the variables have the following meanings:

n is 0.1 or 2; m 2 or 3;

X ^{2 is} halogen, where the radicals X ^{2 may have} different meanings;

Y is CN, _NO2, Ci-C ₄ alkyl, -C ₄ haloalkyl, methoxy or methylthio; p is zero or 1;

R ^{1 is} halogen, methyl, C ¹ -C ⁴ -haloalkyl, methoxy, methylthio, methylsulfinyl or methylsulfonyl;

R ^{2 is} hydrogen, methyl or ethyl;

W oxygen or sulfur.

2. nicotinic acid anilides of the formula I according to claim 1, in which the variables have the following meanings:

X ² F or chlorine;

Y _Ci-C4 alkyl, _{Ci-C4-haloalkyl} or methoxy; R ^{1 is} halogen, methyl, trifluoromethyl or methoxy; R ^{2 is} hydrogen or methyl; W oxygen.

3. nicotinic acid anilides of the formula I according to claim 1, in which the variables have the following meanings:

X ² F or chlorine; Y is methyl, difluoromethyl, trifluoromethyl or methoxy;

R ^{1 is} F, Cl, methyl or trifluoromethyl;

R ^{2 is} hydrogen or methyl;

W oxygen. 4. nicotinic acid anilides of the formula I according to any one of claims 1 to 3, in which the variables have the following meanings: n is zero;

P Well;

X ² F or chlorine;

R ^{1 is} F ₁ Cl, methyl or trifluoromethyl;

R ^{2 is} hydrogen;

W oxygen.

Nicotinic acid anilides of the formula I according to one of claims 1 to 3, in which the

Variables have the following meanings: n zero;

P zero;

X ² F or chlorine;

R ^{1 is} F or chlorine;

R ^{2 is} hydrogen;

W oxygen.

6. nicotinic acid anilides of the formula I according to claim 1, selected from the group consisting of:

2-chloro-N- (3 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (3', 5 ^l -dichlorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (3'-chloro-4'-fluorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (4'-chloro-3'-fluorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (3 ', 4'-difluoro-biphenyl-2-yl) -nicotinamide,

2-chloro-N- (2 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (2', 5'-difluorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (4'-chloro-2'-fluoro-biphenyl-2-yl) nicotinamide, 2-chloro-N- (2 ', 4 ^I -difluorobiphenyl-2-yl) nicotinamide, 2-chloro-N- (4-fluoro -2 ', 4 ^l -dichlorobiphenyl-2-yl) -nicotinamide,

2-chloro-N- (3 ', 4', 5'-trifluorobiphenyl-2-yl) nicotinamide, 2-chloro-N- (2 ', 4', 5 ¹ -trifluorbiphenyl-2-yl) nicotinamide _l 2-Chloro-N- (4'-chloro-2'-fluoro-5'-methoxy-biphenyl-2-yl) -nicotinamide, 2-trifluoromethyl-N- (3 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide , 2-trifluoromethyl-N- (4-fluoro-2 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide,

2-trifluoromethyl-N- (3 ^I, ^I 4, 5'-trifluorobiphenyl-2-yl) nicotinamide, 2-trifluoromethyl-N- (2 ', 4', 5'-trifluorobiphenyl-2-yl) -nicotinamide, 2-Trifluoromethyl-N- (4 ^I -chloro-2'-fluoro-5'-methoxy-biphenyl-2-yl) -nicotinamide; 2-trifluoromethyl-N- (3 ', 4 ^I -difluoro-biphenyl-2-yl) -nicotinamide , 2-trifluoromethyl-N- (3 ', 5'-dichlorobiphenyl-2-yl) -nicotinamide,

2-trifluoromethyl-N- (2 ', 4'-dichlorobiphenyl-2-yl) -nicotinamide, 2-trifluoromethyl-N- (3'-chloro-4'-fluorobiphenyl-2-yl) -nicotinamide, 2-chloro-N- (3 ^I , 4 ^L , 5'-trifluorobiphenyl-2-yl) -N-methylnicotinamide and 2-trifluoromethyl-N- (3 ¹ _I 4 ', 5'-trifluorobiphenyl-2-yl) - N-ethylnicotinamide.

7. A composition for controlling phytopathogenic harmful fungi, comprising a fungicidal amount of a compound of formula I according to any one of claims 1 to 6 and at least one inert additive.

8. Composition according to claim 7, containing in addition a further active ingredient.

9. A method for controlling phytopathogenic harmful fungi, characterized in that the harmful fungi, their habitat and / or to be protected against fungal attack materials, plants, the soil or seeds with a fungicidally effective amount of a compound of formula I according to any one of claims 1 treated until 6.

10. Use of the compounds I according to any one of claims 1 to 6 for controlling phytopathogenic harmful fungi.

11. Seed containing a compound of formula I according to any one of claims 1 to 6 in an amount of 1 to 1000 g / 100 kg.