IP Library Granted Patent US 10,499,641
Granted Patent B2
US 10,499,641 · App. 15/714,109 · Granted Dec 10, 2019

Heteroarylpiperidine and -piperazine derivatives as fungicides

Inventors: Tomoki Tsuchiya (Lyons, FR); Pierre Wasnaire (Duesseldorf, DE); Sebastian Hoffmann (Neuss, DE); Pierre Cristau (Lyons, FR); Thomas Seitz (Langenfeld, DE); Joachim Kluth (Langenfeld, DE); Stefan Hillebrand (Neuss, DE); Juergen Benting (Leichlingen, DE); Daniela Portz (Vettweiss, DE); Ulrike Wachendorff-Neumann (Neuwied, DE)
Assignee: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
A01N43/80A01N43/78A01N47/22A01N47/38A01N55/00C07D417/14C07F7/0812
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,499,641
App. No.
15/714,109
Granted
Dec 10, 2019
Kind
B2
Abstract

Heteroarylpiperidine and -piperazine derivatives of the formula (I) in which the symbols A, X, Y, L 1 , L 2 , G, Q, p, R 1 , R 2 and R 10 are each as defined in the description, and salts, metal complexes and N-oxides of the compounds of the formula (I), and the use thereof for controlling phytopathogenic harmful fungi and processes for preparing compounds of the formula (I).

Claims (138)

1. A compound of formula (I)

A is pyrazol-1-yl which may contain up to two substituents, where the substituents are each independently selected from the following list:

halogen, cyano, hydroxyl, nitro, —NR 3 R 4 , C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -haloalkenyl, C 2 -C 6 -haloalkynyl, C 3 -C 6 -halocycloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylsulphonyl, C 1 -C 4 -haloalkylthio, C 1 -C 4 -haloalkylsulphonyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, hydroxy-C 1 -C 4 -alkyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -alkylcarbonyloxy or phenyl,

R 3 and R 4 are the same or different and are each independently hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cycloalkyl, benzyl or phenyl,

L 1 is NH or CH 2 ,

Y is oxygen,

X is carbon,

R 2 is hydrogen,

R 10 is oxo, alkyl, alkenyl, haloalkyl, alkoxy, halogen, cyano or hydroxyl,

p is 0,

G is

where the bond identified by “v” is bonded directly to X and where the bond identified by “w” is bonded directly to Q,

R G1 is hydrogen or halogen,

Q is

where the bond identified by “*” is bonded directly to G or L 2 , and where the bond identified by “#” is bonded directly to L 2 or G, or where the bond identified by “*” is bonded directly to L 2 , and the bond identified by “#” is at the same time bonded directly to G,

R 5 is hydrogen,

L 2 is a direct bond,

R 1 is phenyl which contains 1, 2 or 3 substituents, where the substituents are each independently selected at least once from Z 4 and optionally from the following list: fluorine, chlorine, bromine, iodine, cyano, nitro, hydroxyl, amino, —SH, —C(═O)H, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1,1-dimethylethyl, 1,2-dimethylethyl, ethenyl, ethynyl, trifluoromethyl, difluoromethyl, trichloromethyl, dichloromethyl, cyclopropyl, methoxy, ethoxy, n-propoxy, 1-methylethoxy, 1,1-dimethylethoxy, methylcarbonyl, ethylcarbonyl, trifluoromethylcarbonyl, methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, 1-methylethoxycarbonyl, 1,1-dimethylethoxycarbonyl, 1-ethenyloxy, 2-propenyloxy, 2-propynyloxy, methylcarbonyloxy, trifluoromethylcarbonyloxy, chloromethylcarbonyloxy, methylthio, ethylthio, methylsulphonyl, methylsulphonylamino, trifluoromethylsulphonylamino or -L 3 R 3 ,

L 3 is a direct bond, —CH 2 —, —C(═O)—, sulphur, oxygen, —C(═O)O—, —C(═O)NH—, —OC(═O)—or —NHC(═O)—,

Z 3 is a phenyl radical, naphthalenyl or a 5- or 6-membered heteroaryl radical which may contain up to two substituents, where the substituents are each independently selected from the following list:

substituents on carbon: halogen, cyano, nitro, hydroxyl, amino, —SH, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 1 -C 4 -haloalkyl, C 2 -C 4 -haloalkenyl, C 2 -C 4 -haloalkynyl, C 2 -C 4 -alkoxyalkyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkoxy, C 2 -C 6 -alkenyloxy, C 2 -C 6 -alkynyloxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkylthio, C 1 -C 4 -alkylsulphonyl, C 1 -C 4 -haloalkylsulphonyl or C 1 -C 4 -alkylamino, or di(C 1 -C 4 -alkyl)amino,

substituents on nitrogen: C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -haloalkenyl, C 2 -C 6 -haloalkynyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, phenyl, benzyl, C 1 -C 4 -haloalkylsulphonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -haloalkoxycarbonyl, phenylsulphonyl, C 1 -C 4 -alkylsulphonyl, —C(=O)H, or C 1 -C 3 -alkylcarbonyl,Z 4 is cyano-C 1 -C 6 -alkyl, C 2 -C 6 -alkenylcarbonyloxy, C 2 -C 6 -alkynylthio, C 3 -C 8 -halocycloalkylcarbonyloxy, C 2 -C 6 -alkenylamino, C 2 -C 6 -alkynylamino, C 1 -C 6 -haloalkylamino, C 3 -C 8 -cycloalkyl-C 1 -C 6 -alkylamino, C 1 -C 6 -alkoxyamino, C 1 -C 6 -haloalkoxyamino, C 1 -C 6 -alkylcarbonylamino, C 1 -C 6 -haloalkylcarbonylamino, C 1 -C 6 -alkoxycarbonylamino, C 1 -C 6 -alkylcarbonyl(C 1 -C 6 -alkyl)amino, C 1 -C 6 -haloalkylcarbonyl(C 1 -C 6 -alkyl)amino, C 1 -C 6 -alkoxycarbonyl(C 1 -C 6 -alkyl)amino, —NR 3 SO 2 Z 3 , C 2 -C 6 -alkenylthio, C 1 -C 6 -haloalkoxycarbonyl, C 1 -C 6 -alkoxy-C 1 -C 4 -alkylcarbonyl, -SF 5, C 1 -C 6 -haloalkoxycarbonylamino, —NHC(═O)H, C 1 -C 6 -alkoxy(C 1 -C 4 -alkyl)aminocarbonyl, C 1 -C 6 -alkoxycarbonyl-C 1 -C 6 -alkoxy, —C(═NOR 7 )R 8 , —N=C(R 9 ) 2 , di(C 1 -C 6 -alkyl)aminocarbonylamino, di(C 1 -C 6 -alkyl)aminosulphonyl, di(C 1 -C 6 -haloalkyl)amino, C 1 -C 6 -alkylaminosulphonyl, C 1 -C 6 -alkylaminocarbonylamino, tri(C 1 -C 4 -alkyl)silyloxy, C 1 -C 6 -haloalkylsulphonyloxy, C 1 -C 6 -alkylsulphonyloxy, tri(C 1 -C 4 -alkyl)silyl-C 2 -C 4 -alkynyloxy, tri(C 1 -C 4 -alkyl)silyl-C 2 -C 4 -alkynyl or -L 4 Z 3 ,

Z 4 is cyano-C 1 -C 6 -alkyl, C 2 -C 6 -alkenylcarbonyloxy, C 2 -C 6 -alkynylthio, C 3 -C 8 -halocyclo-alkylcarbonyloxy, C 2 -C 6 -alkenylamino, C 2 -C 6 -alkynylamino, C 1 -C 6 -haloalkylamino, C 3 -C 8 -cycloalkyl-C 1 -C 6 -alkylamino, C 1 -C 6 -alkoxyamino, C 1 -C 6 -haloalkoxyamino, C 1 -C 6 -alkyl-carbonylamino, C 1 -C 6 -haloalkylcarbonylamino, C 1 -C 6 -alkoxycarbonylamino, C 1 -C 6 -alkylcarbonyl(C 1 -C 6 -alkyl)amino, C 1 -C 6 -haloalkylcarbonyl(C 1 -C 6 -alkyl)amino, C 1 -C 6 -alkoxycarbonyl(C 1 -C 6 -alkyl)amino, -NR 3 SO 2 Z 3 , C 2 -C 6 -alkenylthio, C 1 -C 6 -haloalkoxycarbonyl, C 1 -C 6 -alkoxy-C 1 -C 4 -alkylcarbonyl, -SF 5 , C 1 -C 6 -haloalkoxycarbonylamino, —NHC(═O)H, C 1 -C 6 -alkoxy(C 1 -C 4 -alkyl)aminocarbonyl, C 1 -C 6 -alkoxycarbonyl-C 1 -C 6 -alkoxy, —C(═NOR 7 )R 8 , —N═C(R 9 ) 2 , di(C 1 -C 6 -alkyl)aminocarbonylamino, di(C 1 -C 6 -alkyl)aminosulphonyl, di(C 1 -C 6 -haloalkyl)amino, C 1 -C 6 -alkylaminosulphonyl, C 1 -C 6 -alkylaminocarbonylamino, tri(C 1 -C 4 -alkyl)silyloxy, C 1 -C 6 -haloalkylsulphonyloxy, C 1 -C 6 -alkylsulphonyloxy, tri(C 1 -C 4 -alkyl)silyl-C 2 -C 4 -alkynyloxy, tri(C 1 -C 4 -alkyl)silyl-C 2 -C 4 -alkynyl or -L 4 Z 3 ,

or

Z 4 is —C(═O)NR 11 R 12 , —SO 2 NR 11 R 12 , -SCN, C 1 -C 3 -alkoxysulphonyl, C 3 -C 8 -cycloalkylsulphinyl or cyano(C 1 -C 3 -alkoxy)-C 1 -C 3 -alkyl,

or

Z 4 is C 1 -C 3 -alkyl which contains 1 or 2 substituents, where the substituents are each independently selected from the following list:

C 2 -C 4 -alkenyloxy, C 2 -C 4 -alkynyloxy, C 2 -C 4 -alkenylthio, C 2 -C 4 -alkynylthio, C 1 -C 3 -alkoxy-C 1 -C 3 -alkylthio, C 1 -C 3 -alkoxy-C 1 -C 3 -alkylsulphinyl, C 1 -C 3 -alkoxy-C 1 -C 3 -alkylsulphonyl, C 1 -C 3 -alkylcarbonyloxy or C 1 -C 3 -halocarbonyloxy,

or

Z 4 is substituted hydroxyl, where the substituents are each selected from the following list:

C 3 -C 8 -cycloalkylsulphonyl, C 3 -C 8 -halocycloalkylsulphonyl, C 2 -C 4 -alkenylsulphonyl or C(═O)NR 3 R 4 , or

Z 4 is C 1 -C 3 -alkoxy which contains 1 or 2 substituents, where the substituents are each independently selected from the following list:

cyano, C 1 -C 3 -alkylcarbonyloxy, C 1 -C 3 -alkoxycarbonyl, C 3 -C 8 -cycloalkoxy, C 1 -C 3 -alkylcarbonyloxy, —O(C═O)H, C 1 -C 3 -alkylthio, hydroxy-C 1 -C 3 -alkyl, C 3 -C 8 -cycloalkylsulphonyl, C 1 -C 3 -haloalkylsulphonyl, C 1 -C 3 -alkoxy-C 1 -C 3 -alkoxy, C 1 -C 3 -alkylsulphonyl,

R 7 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, benzyl or Z 3 ,

R 8 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl, C 3 -C 8 -cycloalkyl, C 1 -C 4 -alkyl-C 3 -C 8 -cycloalkyl, C 1 -C 4 -haloalkyl-C 3 -C 8 -cycloalkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -haloalkoxy-C 1 -C 4 -alkyl, benzyl or phenyl,

R 9 is the same or different and is independently C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -haloalkyl, C 3 -C 8 -cycloalkyl, benzyl or phenyl,

R 11 is C 3 -C 4 -alkenyl, C 3 -C 4 -alkynyl, cyano-C 1 -C 3 -alkyl, formyl, C 1 -C 3 -haloalkyl, benzyl, phenyl, C 1 -C 3 -alkylcarbonyl, C 3 -C 8 -cycloalkoxycarbonyl, C 1 -C 3 -alkoxycarbonyl, C 3 -C 4 -alkenyloxycarbonyl, C 3 -C 4 -alkynyloxycarbonyl, C 1 -C 3 -haloalkylcarbonyl, C 3 -C 8 -halocycloalkylcarbonyl, C 3 -C 8 -cycloalkoxycarbonyl, C 3 -C 8 -cycloalkylcarbonyl, or di(C 1 -C 3 -alkyl)aminocarbonyl,

R 12 is hydrogen, C 3 -C 4 -alkenyl, C 3 -C 4 -alkynyl, cyano-C 1 -C 3 -alkyl, formyl, C 1 -C 3 -haloalkyl, benzyl, phenyl, C 1 -C 3 -alkylcarbonyl, C 3 -C 8 -cycloalkoxycarbonyl, C 1 -C 3 -alkoxycarbonyl, C 3 -C 4 -alkenyloxycarbonyl, C 3 -C 4 -alkynyloxycarbonyl, C 1 -C 3 -haloalkylcarbonyl, C 3 -C 8 -halocycloalkylcarbonyl, C 3 -C 8 -cycloalkoxycarbonyl, C 3 -C 8 -cycloalkylcarbonyl, or di(C 1 -C 3 -alkyl)aminocarbonyl,

L 4 is —C(═O)O—, —C(═O)NH—, —OC(═O)—, —NHC(═O)— or —OCH 2 C≡C—,

or a salt, metal complex and/or N-oxide of the compound of formula (I).

2. The compound of the formula (I) according to claim 1 , in which

Q is

where the bond identified by “x” is bonded directly to G and where the bond identified by “y” is bonded directly to L 2

and

R 5 is hydrogen.

3. The compound of the formula (I) according to claim 1 , in which

A is pyrazol-1-yl which may contain up to two substituents, where the substituents are each independently selected from the following list:

methyl, ethyl, chlorine, bromine, fluorine, difluoromethyl or trifluoromethyl.

4. The compound of the formula (I) according to claim 1 , in which L 1 is CH 2 .

5. The compound of the formula (I) according to claim 1 , in which

Z 3 is a phenyl radical which may contain up to two substituents, where the substituents are each independently selected from the following list:

chlorine, bromine, iodine, fluorine, cyano, nitro, hydroxyl, amino, -SH, methyl, ethyl, n-propyl, 1-methylethyl, 1,1-dimethylethyl, ethenyl, propen-2-yl, ethynyl, propyn-2-yl, trifluoromethyl, difluoromethyl, methoxymethyl, methylcarbonyl, ethylcarbonyl, trifluoromethylcarbonyl, methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, 1-methylethoxycarbonyl, 1,1-dimethylethoxycarbonyl, methoxy, ethoxy, n-propoxy, 1-methylethoxy, 1,1-dimethylethoxy, trifluoromethoxy, ethenyloxy, 2-propenyloxy, ethynyloxy, 2-propynyloxy, methylthio, ethylthio, trifluoromethylthio, methylsulphonyl, ethyl sulphonyl, propylthionyl, 1-methylethylthio, trifluoromethylsulphonyl, methylamino, ethylamino, n-propylamino, 1-methylethylamino, 1,1-dimethylethylamino or dimethylamino,

or

Z 3 is naphthalenyl.

6. A compound of the formula (I) according to claim 1 , in which

Z 4 is C 1 -C 6 -haloalkylsulphonyloxy or C 1 -C 6 -alkylsulphonyloxy.

7. A compound of the formula (I) according to claim 1 , in which

Z 4 is cyanomethyl, cyanoethyl, propenoyloxy, but-2-enoyloxy, propyn-2-ylthio, propen-2-ylamino, propyn-2-ylamino, trifluoromethylamino, difluoromethylamino, methoxyamino, ethoxyamino, propoxyamino, 1-methylethoxyamino, methoxycarbonylamino, ethoxycarbonylamino, 1-methylethoxycarbonylamino, 1,1-dimethylethoxycarbonylamino, trifluoromethylcarbonylamino, methylcarbonylamino, ethylcarbonylamino, 1-methylethylcarbonylamino, 1,1-dimethylethylcarbonylamino, phenylsulphonylamino, propen-2-ylthio, N-methoxy-N-methylaminocarbonyl, methoxycarbonylmethoxy, ethoxycarbonylmethoxy, propoxycarbonylmethoxy, 1-methylethoxycarbonylmethoxy, 1,1-dimethyl-ethylcarbonylmethoxy, —C(═NOR 7 )R 8 , dimethylaminocarbonylamino, diethyl-aminocarbonylamino, dimethylaminosulphonyl, diethylaminosulphonyl, methyl-aminosulphonyl, ethylaminosulphonyl, propylaminosulphonyl, 1-methylethyl-aminosulphony, 1,1-dimethylethylaminocarbonylamino, methylaminocarbonlamino, ethylaminocarbonylamino, propylaminocarbonylamino, 1-methlethylaminocarbonylamino, 1,1-dimethylethylaminocarbonylamino, 2-methylpropylaminocarbonylamino, 1-chlorocyclopropylcarbonyloxy, 1-fluoro-cyclopropylcarbonyloxy, trifluoromethylsulphonyloxy, trimethylsilyloxy, chloro-methylcarbonylamino, trifluoromethylcarbonylamino, methylsulphonyloxy, ethyl-sulphonyloxy, trimethylsilylethynyloxy, trimethylsilylethynyl or -L 4 Z 3 ,

R 7 is hydrogen, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1,1-dimethylethyl or 2-methylpropyl,

R 8 is hydrogen, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1,1-dimethylethyl or 2-methylpropyl.

8. A compound of the formula (I) according to claim 1 , in which

R 1- is 2-{[3-(trimethylsilyl)prop-2-yn-1-yl]oxy}phenyl or

R 1- is 2-[(1E/Z)-N-hydroxyethanimidoyl]phenyl or

R 1- is 3-{(E/Z)-[(propan-2-yloxy)imino]methyl}phenyl or

R 1- is 3-[(E/Z)-(ethoxyimino)methyl]phenyl or

R 1- is 3-1E/Z)-N-(propan-2-yloxy)ethanimidoyl]phenyl or

R 1- is 3-[(E/Z)-(methoxyimino)methyl]phenyl or

R 1- is 3-[(E/Z)-(hydroxyimino)methyl]phenyl or

R 1- is 2-{(E/Z)-[(propan-2-yloxy)imino]methyl}phenyl or

R 1- is 3-[(1E/Z)-N-hydroxyethanimidoyl]phenyl or

R 1- is 3-[(1E/Z)-N-methoxyethanimidoyl]phenyl or

R 1- is 4-(acetylamino)phenyl or

R 1- is 2-[(1E/Z)-N-(propan-2-yloxy)ethanimidoyl]phenyl or

R 1- is 2- { [3 -(naphthalen-l-yl)prop-2-yn-l-yl]oxy }phenyl or

R 1- is 2-[(E/Z)-(methoxyimino)methyl]phenyl or

R 1- is 2-[(E/Z)-(ethoxyimino)methyl]phenyl or

R 1- is 2-[(1E/Z)-N-methoxyethanimidoyl]phenyl or

R 1- is 3-[(1E/Z)-N-ethoxyethanimidoyl]phenyl or

R 1- is 4-[(tert-butoxycarbonyl)amino]phenyl or

R 1- is 2-[(E/Z)-(hydroxyimino)methyl]phenyl or

R 1- is 4,5-dimethyl-2-[(methylsulphonyl)oxy]phenyl or

R 1- is 2-[(ethylsulphonyl)oxy]phenyl or

R 1- is 4-[(methylsulphonyl)oxy]phenyl or

R 1- is 2-formamidophenyl or

R 1- is 4-(2-methoxy-2-oxoethoxy)phenyl or

R 1- is 2-[(allyloxy)methyl]phenyl or

R 1- is 3-(cyanomethoxy)-2,6-difluorophenyl or

R 1- is 2-{[(2-methoxyethyl)sulphinyl]methyl}phenyl or

R 1- is 4-[(cyclopropylsulphonyl)oxy]phenyl or

R 1- is 3-chloro-2-(cyanomethoxy)phenyl or

R 1- is 2-[(4-fluorobenzoyl)oxy]phenyl or

R 1- is 3-fluoro-2-[(methylsulphonyl)oxy]phenyl or

R 1- is 2,3-dimethoxy-6-[(methylsulphonyl)oxy]phenyl or

R 1- is 2-{[(trifluoromethyl)sulphonyl]oxy}phenyl or

R 1- is 2-[(2E)-but-2-enoyloxy]phenyl or

R 1- is 2-fluoro-6-[(prop-2-yn-1-yloxy)methyl]phenyl or

R 1- is 2-[(ethylcarbamoyl)oxy]phenyl or

R 1- is 5-chloro-2-[(methylsulphonyl)oxy]phenyl or

R 1- is 2-[formyl(prop-2-yn-1-yl)amino]phenyl or

R 1- is 2-{[(1-chlorocyclopropyl)carbonyl]oxy}phenyl or

R 1- is 4-methyl-2-[(methylsulphonyl)oxy]phenyl or

R 1- is 4-chloro-2-[(methyl sulphonyl)oxy]phenyl or

R 1- is 2-fluoro-6-[(E/Z)-(methoxyimino)methyl]phenyl or

R 1- is 2-[(cyclopropylsulphonyl)oxy]-3-fluorophenyl or

R 1- is 2-(cyanomethoxy)-4-methylphenyl or

R 1- is 2-[(prop-2-yn-1-yloxy)methyl]phenyl or

R 1- is 2-[(methylsulphanyl)methoxy]phenyl or

R 1- is 2-(cyanomethoxy)-3-fluorophenyl or

R 1- is 2-methoxy-6-[(methylsulphonyl)oxy]phenyl or

R 1- is 2-(acryloyloxy)phenyl or

R 1- is 3-chloro-2-[(methylsulphonyl)oxy]phenyl or

R 1- is 2-[(trimethylsilyl)ethynyl]phenyl or

R 1- is 3-[(cyclopropylsulphonyl)oxy]phenyl or

R 1- is 2-[(cyclopropylsulphonyl)oxy]-5-fluorophenyl or

R 1- is 4-(cyanomethoxy)phenyl or

R 1- is 2-(dimethylcarbamothioyl)phenyl or

R 1- is 5-chloro-2-(cyanomethoxy)phenyl or

R 1- is 2-(cyanomethoxy)-6-fluorophenyl or

R 1- is 2-[(cyclopropylsulphonyl)oxy]phenyl or

R 1- is 2-{[(2-methoxyethyl)sulphonyl]methyl}phenyl or

R 1- is 2-chloro-6-[(methyl sulphonyl)oxy]phenyl or

R 1- is 4-chloro-2-(cyanomethoxy)phenyl or

R 1- is 3- { [3-(1-naphthyl)prop-2-yn-l-yl]oxy }phenyl or

R 1- is 4-[(ethylsulphonyl)oxy]phenyl or

R 1- is 3-[(ethylsulphonyl)oxy]phenyl or

R 1- is 2-{[(2-methoxyethyl)sulphanyl]methyl}phenyl or

R 1- is 2,6-difluoro-3-[(methylsulphonyl)oxy]phenyl or

R 1- is 5-methyl-2-[(methylsulphonyl)oxy]phenyl or

R 1- is 2-(cyanomethoxy)phenyl or

R 1- is 2-(cyanomethoxy)-5-methylphenyl or

R 1- is 2-{[(4-methylphenyl)sulphonyl]oxy}phenyl or

R 1- is 2-[(cyanomethyl)(formyl)amino]phenyl or

R 1- is 3-(cyanomethoxy)phenyl or

R 1- is 2-chloro-6-(cyanomethoxy)phenyl.

9. A method for controlling phytopathogenic harmful fungi, comprising applying one or more compounds of the formula (I) according to claim 1 to the phytopathogenic harmful fungi and/or their habitat.

10. A composition for controlling phytopathogenic harmful fungi, comprising at least one compound of the formula (I) according to claim 1 , in addition to one or more extenders and/or surfactants.

11. A process for producing compositions for controlling phytopathogenic harmful fungi, comprising mixing one or more compounds of the formula (I) according to claim 1 with extenders and/or surfactants.

12. The method according to claim 9 , comprising treatment of transgenic plants.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2018
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 047420/0466 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 2, 2018
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 047403/0243 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2017
From: TSUCHIYA, TOMOKI; WASNAIRE, PIERRE; HOFFMANN, SEBASTIAN; CRISTAU, PIERRE; SEITZ, THOMAS; KLUTH, JOACHIM; HILLEBRAND, STEFAN; BENTING, JUERGEN; PORTZ, DANIEL; WACHENDORFF-NEUMANN, ULRIKE
To: BAYER CROPSCIENCE AG
Reel/Frame 043990/0830 →
Priority Claims (2)
EP 10174012 · Aug 25, 2010 · regional
EP 11154453 · Feb 15, 2011 · regional
Continuity (6)
Continuation 14821898 · Aug 10, 2015
Division 14225978 · Mar 26, 2014
Continuation 13216033 · Aug 23, 2011
Provisional Application 61442967 · Feb 15, 2011
Provisional Application 61377229 · Aug 26, 2010
Related Publication 20180007903A1 · Jan 11, 2018
Cited By (1)
US 12,503,465