Substituted oxadiazoles for combating phytopathogenic fungi

Patent metadata

Field	Value
Publication number	US-10986839-B2
Application number	US-201716092059-A
Country	US
Kind code	B2
Filing date	Mar 31, 2017
Priority date	Apr 11, 2016
Publication date	Apr 27, 2021
Grant date	Apr 27, 2021

Abstract

The present invention relates to novel trifluoromethyloxadiazoles of the formula I, or an N-oxide and/or their agriculturally useful salts and to their use for controlling phytopathogenic fungi; to a method for combating phytopathogenic harmful fungi, which process comprises treating the fungi or the plants, the soil or seeds to be protected against fungal attack, with an effective amount of at least one compound of the formula I, or an N-oxide, or an agriculturally acceptable salt thereof; to a process for preparing compounds of the formula I; to intermediate compounds of the formula II.a for the preparation of compounds of the formula I; to agrochemical compositions comprising at least one compound of the formula I; and to agrochemical compositions further comprising seeds.

First claim

The invention claimed is:

1. A compound of formula I,

or an N-oxide or an agriculturally acceptable salt thereof;
wherein:
A is phenyl or a 6-membered aromatic heterocycle, wherein the ring member atoms of the aromatic heterocycles include besides carbon atoms 1, 2, 3 or 4 heteroatoms selected from N, O and S as ring member atoms; and wherein the group —CR 3 R 4 — is attached to the phenyl ring or to the aromatic heterocycle in para-position with regard to the trifluoromethyloxadiazole group; and wherein the phenyl ring or the aromatic heterocycle is unsubstituted or substituted with 1, or 2 identical or different groups R A ; wherein
R A is halogen, cyano, NO 2 , OH, SH, NH 2 , diC 1 -C 6 -alkylamino, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -alkylsulfonyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 8 -cycloalkyl or C 3 -C 8 -cycloalkoxy; and wherein any of the aliphatic and cyclic moieties are unsubstituted or substituted with 1, 2, 3 or 4 identical or different groups R a ; wherein
R a is halogen, cyano, NO 2 , OH, SH, NH 2 , C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio or C 3 -C 8 -cycloalkyl or C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl;

L is —(C═S)— or —S(═O) p —;
p is 0, 1 or 2;
R 1 is C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkenyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, phenyl-C 1 -C 4 alkyl, heteroaryl-C 1 -C 4 -alkyl, or phenyl, wherein any of the aliphatic or cyclic groups in R 1 are unsubstituted or substituted with 1, 2, 3 or up to the maximum possible number of identical or different groups R 1a ; wherein
R 1a is halogen, oxo, cyano, NO 2 , OH, SH, NH 2 , C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -haloalkylthio, C 3 -C 8 -cycloalkyl, NHSO 2 —(C═O)—C 1 -C 4 -alkyl, C(═O)—C 1 -C 4 -alkoxy, C 1 -C 6 -alkylsulfonyl, hydroxyC 1 -C 4 -alkyl, C(═O)—NH 2 , C(═O)—NH(C 1 -C 4 -alkyl), aminoC 1 -C 4 -alkyl, C 1 -C 4 -alkylamino-C 1 -C 4 -alkyl, diC 1 -C 4 -alkylamino-C 1 -C 4 -alkyl, aminocarbonyl-C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl;

R 2 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 3 -C 8 -cycloalkyl, or C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl; and wherein any of the aliphatic or cyclic groups in R 2 are unsubstituted or substituted with 1, 2, 3 or up to the maximum possible number of identical or different groups R 1a ;
R 3 , R 4 independently of each other are selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkenyl, C 1 -C 4 -alkynyl and C 1 -C 4 -haloalkyl;
or R 3 and R 4 together with the carbon atom to which they are bound form a 3- to 7-membered carbocycle or a saturated 3- to 6-membered heterocycle, wherein the heterocycle includes beside carbon atoms 1, 2 or 3 heteroatoms independently selected from N—R N , S, —S(═O)—, —S(═O) 2 — and O as ring member atoms; wherein
R N is H, SO 2 CH 3 , SO 2 C 6 H 4 CH 3 or SO 2 -aryl; and wherein one or two CH 2 groups of the carbocycle or heterocycle may be replaced by one or two groups independently selected from the group of —C(═O)— and —C(═S)—; and wherein the carbocycle, the heterocycle and aryl is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of identical or different groups R 3a ; wherein
R 3a is halogen, cyano, NO 2 , OH, SH, NH 2 , C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio, C 3 -C 8 -cycloalkyl, NHSO 2 —C 1 -C 4 -alkyl, (C═O)—C 1 -C 4 -alkyl, C(═O)—C 1 -C 4 -alkoxy or C 1 -C 6 -alkylsulfonyl.

2. The compound of claim 1 , wherein A is phenyl.

3. The compound of claim 1 , wherein A is unsubstituted or substituted with 1 or 2 identical or different groups R A ; and wherein R A is fluorine, chlorine or C 1 -C 6 -alkyl.

4. The compound of claim 1 , wherein R 2 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl; and R 1 is C 3 -C 8 -cycloalkyl; and wherein the cycloalkyl group in R 1 is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of identical or different radicals selected from halogen or C 1 -C 6 -alkyl.

5. The compound of claim 1 , wherein:
R 2 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl;
R 1 is C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkenyl, C 2 -C 6 -alkenyl, or C 2 -C 6 -alkynyl; and
any of the aliphatic or cyclic groups in R 1 or R 2 are independently unsubstituted or substituted with 1, 2, 3 or up to the maximum possible number of identical or different groups R 1a .

6. The compound of claim 1 , wherein R 3 and R 4 independently of each other are hydrogen, fluorine, methyl or trifluoromethyl; or R 3 and R 4 together with the carbon atom to which they are bound form an unsubstituted 3-membered carbocyclic ring.

7. An agrochemical composition, which comprises an auxiliary and at least one compound of the formula I, or an N-oxide, or an agriculturally acceptable salt thereof, as defined in any one of claim 1 .

8. An agrochemical composition according to claim 7 comprising at least one further pesticidally active substance selected from the group consisting of herbicides, safeners, fungicides, insecticides, and plant growth regulators.

9. An agrochemical composition according to claim 7 , further comprising seed, wherein the amount of the compound of the formula I, or an N-oxide, or an agriculturally acceptable salt thereof, is from 0.1 g to 10 kg per 100 kg of seed.

10. A process for preparing compounds of the formula I as defined in claim 1 , which comprises the process step of reacting an amine compound of the formula II

wherein the variables A, R 2 , R 3 and R 4 are as defined for compounds of the formula I in claim 1 , under basic conditions with a compound of the formula III
LG-L-R 1   III,

wherein L and R 1 are as defined for compounds of the formula I in claim 1 ; and wherein LG is a leaving group selected from the group consisting of chlorine, bromine, fluorine, azide and the group —O-L-R 1 , wherein the variables R 1 and L are as defined for compounds of the formula I in claim 1 .

11. A method for combating phytopathogenic harmful fungi, which process comprises treating the fungi or the plants, the soil or seeds to be protected against fungal attack, with an effective amount of at least one compound of formula I, or an N-oxide, or an agriculturally acceptable salt thereof, as defined in claim 1 .

12. The method of claim 11 , wherein A is phenyl.

13. The method of claim 12 , wherein A is unsubstituted or substituted with 1 or 2 identical of different groups R A ; and wherein R A is fluorine, chlorine or C 1 -C 6 -alkyl.

14. The method of claim 11 , wherein R 2 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl; and R 1 is C 3 -C 8 -cycloalkyl; and wherein the cycloalkyl group in R 1 is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of identical or different radicals selected from halogen or C 1 -C 6 -alkyl.

Assignees

• Basf Se

Inventors

• Terteryan-Seiser Violeta
• Grammenos Wassilios
• Wiebe Christine
• Kretschmer Manuel
• Craig Ian Robert
• Escribano Cuesta Ana
• Fehr Marcus
• Mentzel Tobias
• Quintero Palomar Maria Angelica
• Grote Thomas
• Cambeis Erica
• Mueller Bernd
• Lohmann Jan Klaas
• Winter Christian Harald

Classifications

• C07D417/10

  linked by a carbon chain containing aromatic rings · CPC title

• C07D413/04

  directly linked by a ring-member-to-ring-member bond · CPC title

• A01N43/82 Primary

  five-membered rings with three ring hetero atoms · CPC title

• C07D271/06

  1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles · CPC title