Substituted Oxadiazoles for Combating Phytopathogenic Fungi

Patent metadata

Field	Value
Publication number	US-2020045974-A1
Application number	US-201816500536-A
Country	US
Kind code	A1
Filing date	Mar 29, 2018
Priority date	Apr 7, 2017
Publication date	Feb 13, 2020
Grant date	—

Abstract

The present invention relates to novel trifluoromethyloxadiazoles of the formula I, or the N-oxides, or the agriculturally useful salts thereof; and to their use for controlling phytopathogenic fungi; and to a method for combating phytopathogenic harmful fungi, which process comprises treating the fungi, 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; and to agrochemical compositions comprising at least one compound of the formula I; and to agrochemical compositions further comprising seeds.

First claim

1 - 14 . (canceled)

15 . A compound of formula I, or an N-oxide, or an agriculturally acceptable salt thereof,

wherein:
R A is independently selected from the group consisting of halogen, cyano, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy;
n is 0, 1 or 2;
R 1 is a bicyclic carbocycle of the formula R a

wherein
C a and C b are bridgehead carbon atoms;
X is a direct single bond or a divalent group selected from the group consisting of —CH 2 —, —CH 2 —CH 2 —, —(CH 2 ) 3 —, —(CH 2 ) 4 —, —CH═CH—, —CH 2 —CH═CH—, —CH═CH—CH 2 — and —CH═CH—CH═CH—;
Y and Z independently of each other are a divalent group selected from the group consisting of —CH 2 —, —CH 2 —CH 2 —, —(CH 2 ) 3 —, —(CH 2 ) 4 —, —CH═CH—, —CH 2 —CH═CH—, —CH═CH—CH 2 — and —CH═CH—CH═CH—;
or R 1 is a tricyclic carbocycle of the formula R b

wherein
C a and C b are bridgehead carbon atoms;
X is a direct single bond or a divalent group selected from the group consisting of —CH 2 —, —CH 2 —CH 2 —, —(CH 2 ) 3 —, —(CH 2 ) 4 —, —CH═CH—, —CH 2 —CH═CH—, —CH═CH—CH 2 — and —CH═CH—CH═CH—;
Y and Z independently of each other are a divalent group selected from the group consisting of —CH 2 —, —CH 2 —CH 2 —, —(CH 2 ) 3 —, —(CH 2 ) 4 —, —CH═CH—, —CH 2 —CH═CH—, —CH═CH—CH 2 — and —CH═CH—CH═CH—; and wherein groups Y and Z are attached to the bridgehead carbon atoms C a and C b ;
T is a divalent group selected from the group consisting of —CH 2 —, —CH 2 —CH 2 —, —(CH 2 ) 3 —, —(CH 2 ) 4 —, —CH═CH—, —CH 2 —CH═CH—, —CH═CH—CH 2 — and —CH═CH—CH═CH—; and wherein the group T is attached to one carbon atom in each of the groups Y and Z;
and with the proviso that, if R 1 is a tricyclic carbocycle of the formula R b ,
wherein X is a direct single bond or a divalent group —CH 2 —, the groups T and Z independently of each other are a divalent group selected from the group consisting of —CH 2 —CH 2 —, —(CH 2 ) 3 —, —(CH 2 ) 4 —, —CH═CH—, —CH 2 —CH═CH—, —CH═CH—CH 2 — and —CH═CH—CH═CH—;
and wherein the groups R a or R b are connected to the group W through one of the ring carbon atoms;
and wherein R 1 is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of radicals selected from the group consisting of oxo, hydroxy, halogen, C 1 -C 3 -alkyl, C 1 -C 3 -haloalkyl, C 3 -C 6 -cycloalkyl, vinylidene and dichlorovinylidene;

W is #1-(C═O)—NR 2 -#2, #1-NR 2 —(C═O)-#2, #1-(C═S)—NR 2 -#2, #1-NR 2 —(C═S)-#2, #1-S(═O) p —NR 2 -#2 or #1-NR 2 —S(═O) p -#2; wherein #1 denotes the position, which is attached to the group —CR 3 R 4 — or, if m is 0, to the phenyl group, and #2 denotes the position, which is attached to R 1 ;
p is 0, 1 or 2;
R 2 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -alkoxy, C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkenyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl, phenyl-C 1 -C 4 -alkyl, phenyl, C(═O)—(C 1 -C 6 -alkyl) or C(═O)—(C 1 -C 6 -alkoxy); and wherein any of the aliphatic or cyclic groups are unsubstituted or substituted with 1, 2, 3 or up to the maximum possible number of identical or different radicals selected from the group consisting of halogen, hydroxy, cyano, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy and C 3 -C 8 -cycloalkyl;
m is 0 or 1;
R 3 , R 4 independently of each other are selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -alkenyl, C 1 -C 4 -alkynyl, C 1 -C 4 -haloalkyl and C 1 -C 4 -alkoxy;
or R 3 and R 4 together with the carbon atom to which they are bound form a monocyclic 3- to 5-membered saturated heterocycle or saturated carbocycle; and wherein the saturated heterocycle includes beside one or more carbon atoms no heteroatoms or 1 or 2 heteroatoms independently selected from the group consisting of N, O and S as ring member atoms; and wherein the heterocycle or the carbocycle is unsubstituted or substituted 1, 2, 3, 4 or up to the maximum possible number of identical or different radicals selected from the group consisting of halogen, cyano and C 1 -C 2 -alkyl;
with the exception of compounds of the formula I, wherein
m is 0;
W is #1-NR 2 —(C═O)-#2, #1-NR 2 —(C═S)-#2 or #1-NR 2 —S(═O) p -#2, wherein the variables p and R 2 are defined as above for compounds of the formula I; and
R 1 is a bicyclic carbocycle of the formula R a .

16 . The compound of claim 15 having formula 1.3,

wherein n is 0 or 1, and wherein the meaning of the variables R A , R 1 , W and R 2 are as defined for compounds of the formula I in claim 15 .

17 . The compound of claim 15 , wherein n is 0.

18 . The compound of claim 15 , wherein W is #1-(C═O)—NR 2 -#2, #1-(C═S)—NR 2 -#2 or #1-S(═O) p —NR 2 -#2.

19 . The compound of claim 15 , wherein R 3 and R 4 independently of each other are selected from the group consisting of hydrogen, halogen, C 1 -C 6 -alkyl and C 1 -C 6 -haloalkyl; or R 3 and R 4 together with the carbon atom to which they are bound form a cyclopropyl ring.

20 . The compound of claim 15 , wherein R 1 is a bicyclic carbocycle selected from the group consisting of radicals R 1 .10, R 1 .15, R 1 .22, R 1 .23, R 1 .24, R 1 .25, R 1 .26, R 1 .27 and R 1 .31 as defined herein; and wherein each radical may be connected to the group W through one of the ring carbon atoms by substitution of one hydrogen atom; and wherein R 1 is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of radicals selected from the group consisting of oxo, hydroxy, halogen and C 1 -C 3 -alkyl.

21 . The compound of claim 15 , wherein R 1 is a bicyclic carbocycle selected from the group consisting of radicals R 1 .32, R 1 .33, R 1 .34 and R 1 .35 as defined herein; and wherein R 1 is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of radicals selected from the group consisting of oxo, hydroxy, halogen and C 1 -C 3 -alkyl.

22 . The compound of claim 15 , wherein R 1 is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of radicals selected from the group consisting of hydrogen, fluorine, chlorine, methyl and ethyl.

23 . The compound of claim 15 , wherein R 2 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkenyl, ethynyl, propargyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl or phenyl; and wherein any of the aliphatic or cyclic groups are unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of identical or different radicals selected from the group consisting of halogen and C 1 -C 6 -alkyl.

24 . 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 claim 15 .

25 . The agrochemical composition of claim 24 , wherein the auxiliary is selected from the group consisting of ionic and non-ionic surfactants.

26 . The agrochemical composition claim 24 , 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.

27 . A method for combating p

Assignees

• Basf Se

Inventors

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

Classifications

• C07D271/06 Primary

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

• A01N43/82 Primary

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