WO2015155075A1 - Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture - Google Patents
Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture Download PDFInfo
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- WO2015155075A1 WO2015155075A1 PCT/EP2015/057088 EP2015057088W WO2015155075A1 WO 2015155075 A1 WO2015155075 A1 WO 2015155075A1 EP 2015057088 W EP2015057088 W EP 2015057088W WO 2015155075 A1 WO2015155075 A1 WO 2015155075A1
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- alkyl
- methyl
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- 0 CC([C@@](C1)N=CN(*)*)=NC(OC(*)(*)CO)=C1I Chemical compound CC([C@@](C1)N=CN(*)*)=NC(OC(*)(*)CO)=C1I 0.000 description 1
- WCFDSGHAIGTEKL-UHFFFAOYSA-N CN(C)S(C)(=O)=O Chemical compound CN(C)S(C)(=O)=O WCFDSGHAIGTEKL-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P3/00—Fungicides
Definitions
- the present invention relates to novel microbiocidal, in particular fungicidal, pyridylamidine compounds. It further relates to intermediates used in the preparation of these compounds, to compositions which comprise these compounds, and to their use in agriculture or horticulture for controlling or preventing infestation of plants by
- phytopathogenic microorganisms preferably fungi.
- microbiocidal active ingredients in pesticides are microbiocidal active ingredients in pesticides.
- WO 00/46184 and WO WO 00/46184 are examples of microbiocidal active ingredients in pesticides.
- 03/093224 disclose pyridylamidines which are useful as fungicides.
- the biological properties of these known compounds are not entirely satisfactory for controlling or preventing infestation of plants by phytopathogenic microorganisms, which is why there is a need to provide other compounds which have microbicidal properties.
- the present invention relates to compounds of formula (I)
- R 1 represents hydrogen, halogen, cyano, OH, NH 2 , CrC 4 alkyl, C 3 -C 6 cycloalkyl, NH(Ci-C 4 alkyl), N(C C 4 alkyl) 2 , CO(C C 4 alkyl), C0 2 (C C 4 alkyl), C0 2 H, CONH(C C 4 alkyl), CON(C C 4 alkyl) 2 , S0 2 NH(C C 4 alkyl), S0 2 N(C C 4 alkyl) 2 , C C 4 haloalkyl, C C 4 alkoxy, C C 4 haloalkoxy, C C 4 alkyl-Ci-C 4 alkoxy or C 2 -C 4 alkynyl;
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, R 7 or -CrC 2 alkyl-R 7 , each of which may be optionally substituted by one or more groups independently selected from the group consisting halogen, C C 4 alkyl, C C 4 haloalkyl and Ci-C 4 haloalkoxy;
- R 3 and R 4 independently of each other represent hydrogen, d-C 4 alkyl or C 3 -C 6 cycloalkyl; or
- R 3 and R 4 together with the nitrogen atom to which they are attached form a 3-6- membered saturated cyclic group
- R 5 represents H, C C 4 alkyl or C C 4 haloalkyl
- R 6 represents C C 4 alkyl, C C 4 alkoxy, C C 4 haloalkyl or C C 4 haloalkoxy
- R 7 represents a three- to ten-membered monocyclic or fused bicyclic ring system which can be aromatic, partially saturated or fully saturated and can contain 1 to 4 hetero atoms selected from the group consisting of nitrogen, oxygen and sulfur, it being possible for the three- to ten-membered ring system itself to be optionally substituted by one or more groups independently selected from the group consisting halogen, CrC 4 haloalkyl, d-C 4 alkoxy and CrC 4 haloalkoxy;
- Substituents at a nitrogen atom are always different from halogen.
- a hydroxy, mercapto or amino substituent is not to be placed on an ocarbon relative to a heteroatom of a core fragment.
- Halogen either as a lone substituent or in combination with another substituent (e.g. haloalkyl) is generally fluorine, chlorine, bromine or iodine, and usually fluorine, chlorine or bromine.
- Each alkyl moiety (including the alkyl moiety of alkoxy, alkylthio, etc.) is a straight or branched chain and, depending on the number of carbon atoms it contains, is, for example, methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, / ' so-propyl, sec-butyl, / ' so-butyl, ie f-butyl, neo-pentyl, n-heptyl or 1 ,3-dimethylbutyl, and usually methyl or ethyl.
- alkenyl and alkynyl groups can be mono- or di-unsaturated and examples thereof are derived from the above mentioned alkyl groups.
- the alkenyl group is an unsaturated straight or branched chain having a carbon-carbon double bond and, depending on the number of carbon atoms it contains, is, for example ethenyl, 1 -propenyl, 2-propenyl, 1 -methyl-ethenyl, 1 -butenyl, 2-butenyl, 3-butenyl, 1 -methyl-
- the alkynyl group is an unsaturated straight or branched chain having a carbon-carbon triple bond and, depending on the number of carbon atoms it contains, is, for example ethynyl, 1 -propynyl, 2-propynyl, 1 -butynyl, 2-butynyl, 3-butynyl, 1 -methyl-2-propynyl, 1 - pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 3-methyl-1 -butynyl, 1 -methyl-2-butynyl, 1 - methyl-3-butynyl, 2-methyl-3-butynyl, 1 ,1 -dimethyl-2-propynyl, 1 -ethyl-2-propynyl, 1 -hexynyl, 2-hexynyl, 3-
- Haloalkyl moieties are alkyl moieties which are substituted by one or more of the same or different halogen atoms and are, for example, monofluoromethyl, difluoromethyl, trifluoromethyl, monochloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2,2- difluoroethyl, 2-fluoroethyl, 1 ,1 -difluoroethyl, 1 -fluoroethyl, 2-chloroethyl, pentafluoroethyl, 1 ,1 -difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl and 2,2,2-trichloroethyl, and typically trichloromethyl, difluorochloromethyl, difluoromethyl, trifluoromethyl and dichlorofluoromethyl.
- Alkoxy is, for example, methoxy, ethoxy, propoxy, / ' so-propoxy, n-butoxy, / ' so-butoxy, sec-butoxy and ie f-butoxy, and usually methoxy or ethoxy.
- Haloalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2- trifluoroethoxy, 1 ,1 ,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy, and usually difluoromethoxy, 2-chloroethoxy and trifluoromethoxy.
- Alkylthio is, for example, methylthio, ethylthio, propylthio, /so-propylthio, n-butylthio, iso- butylthio, sec-butylthio or ie f-butylthio, and usually methylthio or ethylthio.
- Alkylsulphonyl is, for example, methylsulphonyl, ethylsulphonyl, propylsulphonyl, iso- propylsulphonyl, n-butylsulphonyl, / ' so-butylsulphonyl, sec-butylsulphonyl or tert- butylsulphonyl, and usually methylsulphonyl or ethylsulphonyl.
- Alkylsulphinyl is, for example, methylsulphinyl, ethylsulphinyl, propylsulphinyl, iso- propylsulphinyl, n-butylsulphinyl, / ' so-butylsulphinyl, sec-butylsulphinyl or ie f-butylsulphinyl, and usually methylsulphinyl or ethylsulphinyl.
- Cycloalkyl may be saturated or partially unsaturated, preferably fully saturated, and is, for example, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
- Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, / ' so-propoxymethyl or / ' so-propoxyethyl.
- Aryl includes phenyl, naphthyl, anthracyl, fluorenyl and indanyl, but is usually phenyl.
- Carbocycle includes cycloalkyl groups and aryl groups.
- Heterocycloalkyl is a non-aromatic ring that may be saturated or partially unsaturated, preferably fully saturated, containing carbon atoms as ring members and at least one heteroatom selected from O, S and N as ring members.
- Examples include oxiranyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, 1 ,3-dioxolanyl, 1 ,4-dioxanyl, aziridinyl, azetidinyl, pyrrolidinyl, piperidinyl, oxazinanyl, morpholinyl, thiomorpholinyl, imidazolidinyl, pyrazolidinyl and piperazinyl, preferably morpholinyl, pyrrolidinyl, piperdinyl and piperazinyl, more preferably morpholinyl and pyrollidinyl.
- Heteroaryl is, for example, a monovalent monocyclic or bicyclic aromatic hydrocarbon radical.
- monocyclic groups include pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, furanyl, thiophenyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, and thiadiazolyl.
- bicyclic groups include quinolinyl, cinnolinyl, quinoxalinyl, benzimidazolyl, benzothiophenyl, and benzothiadiazolyl.
- Monocyclic heteroaryl groups are preferred, preferably pyridyl, pyrrolyl, imidazolyl and triazolyl, e.g. 1 ,2,4 triazolyl, pyridyl and imidazolyl being most preferred.
- heterocycle and “heterocyclic ring” are used interchangeably and are defined to include heterocycloalkyl and heteroaryl groups. Any reference herein to a heterocycle or heterocyclic ring preferably refers to the specific examples given under the definition of heteroaryl and heterocycloalkyl above, and are preferably morpholinyl, pyrrolidinyl, piperdinyl, piperazinyl pyridyl, pyrrolyl, imidazolyl and triazolyl, e.g. 1 ,2,4 triazolyl, more preferably morpholinyl, pyrollidinyl, pyridyl and imidazolyl.
- No heterocycle contains adjacent oxygen atoms, adjacent sulphur atoms, or adjacent oxygen and sulphur atoms.
- a moiety is indicated as being (optionally) substituted, e.g. alkyl, this includes those moieties where they are part of a larger group, e.g. the alkyl in the alkylthio group. The same applies, e.g. to the phenyl moiety in phenylthio etc.
- a moiety is indicated as being optionally substituted by one or more other groups, preferably there are one to five optional substituents, more preferably one to three optional substituents.
- a moiety is substituted by a cyclic group, e.g. aryl, heteroaryl, cycloalkyl, preferably there are no more than two such substituents, more preferably no more than one such substituent.
- R 1 represents hydrogen, halogen, cyano, OH, NH 2 , CrC 4 alkyl, C 3 -C 6 cycloalkyl, NH(Ci-C 4 alkyl), N(C C 4 alkyl) 2 , CO(C C 4 alkyl), C0 2 (C C 4 alkyl), C0 2 H, CONH(C C 4 alkyl), CON(Ci-C 4 alkyl) 2 , S0 2 NH(C C 4 alkyl), S0 2 N(C C 4 alkyl) 2 , C C 4 haloalkyl, C C 4 alkoxy, d-d haloalkoxy, d-d alkyl-Ci-C 4 alkoxy or C 2 -C 4 alkynyl
- R 1 represents hydrogen, halogen, cyano, OH, NH 2 , d-d alkyl, C 3 -C 6 cycloalkyl, NH(C C 4 alkyl), N(C C 4 alkyl) 2 , CO(C C 4 alkyl), C0 2 (C C 4 alkyl), C0 2 H, CONH(Ci-C 4 alkyl), CON(C C 4 alkyl) 2 , S0 2 NH(Ci-C 4 alkyl), S0 2 N(C C 4 alkyl) 2 , C C 4 haloalkyl, d-d alkoxy, d-d haloalkoxy, or C 2 -C 4 alkynyl.
- R 1 represents hydrogen, halogen, cyano, OH, NH 2 , methyl, ethyl, cyclopropyl, NH(C C 2 alkyl), N(C C 2 alkyl) 2 , CO(C C 2 alkyl), C0 2 (C C 2 alkyl), C0 2 H, CONH(Ci-C 2 alkyl), CON(C C 2 alkyl) 2 , S0 2 NH(Ci-C 2 alkyl), S0 2 N(C C 2 alkyl) 2 , C C 4 fluoroalkyl, d-d alkoxy, d-d haloalkoxy or C 2 -C 4 alkynyl.
- R 1 represents hydrogen, halogen, cyano, OH, NH 2 , methyl, ethyl, cyclopropyl, NHMe, NMe 2 , COMe, C0 2 Me, C0 2 H, CONHMe, CONMe 2 , S0 2 NHMe, S0 2 NMe 2 , CHF 2 , CF 3 , OMe, OCHF 2 or acetylenyl.
- Ri represents hydrogen, halogen, cyano, methyl, ethyl, cyclopropyl, CHF 2 , CF 3 , OMe, or OCHF 2 .
- R 1 represents hydrogen, CI, Br, methyl, CHF 2 or cyano.
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, R 7 or -CrC 2 alkyl-R 7 , each of which may be optionally substituted by one or more groups independently selected from the group consisting halogen, d-d alkyl, d-d haloalkyl and d- haloalkoxy.
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 6 cycloalkyl, d- dcycloalkenyl, -d-dalkyl-d-dcycloalkyl, -d-C 2 alkyl-C 3 -C 6 cycloalkenyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting halogen, d-d alkyl, d- haloalkyl and d-d haloalkoxy.
- R 2 represents d-dalkyl, d-dalkenyl, d-dalkynyl, d-dcycloalkyl, d-dcycloalkenyl, -d-dalkyl-d-dcycloalkyl, -d-dalkyl-d-dcycloalkenyl which may be optionally substituted by one or more groups independently selected from the group consisting fluoro, d-C 2 alkyl, d- fluoroalkyl and d-C 2 fluoroalkoxy.
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n- pentyl, 2-methylbutyl, 2,2-dimethylpropyl, 2-methylpentyl, 3-methylpentyl, 2,3-dimethylbutyl, 2,2-dimethylbutyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl -CH 2 -cyclopropyl, -CH 2 - cyclobutyl, -CH 2 -cyclopentyl, and -CH 2 -cyclopentenyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting fluoro, methyl and difluoromethoxy.
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting fluoro and difluoromethoxy.
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl or cyclopropyl.
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl,
- R 7 or -CrC 2 alkyl-R 7 each of which may be optionally substituted by one or more groups independently selected from the group consisting halogen, CrC 4 alkyl and Ci-C 4 haloalkyl.
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 - C 6 alkynyl, C 3 -C 6 cycloalkyl, C 3 -C 5 cycloalkenyl, -Ci-C 2 alkyl-C 3 -C 6 cycloalkyl, -Ci-C 2 alkyl-C 3 - C 6 cycloalkenyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting halogen, Ci-C 2 alkyl and Ci-C 2 haloalkyl.
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 6 cycloalkyl, C 3 -C 5 cycloalkenyl, -CrC 2 alkyl-C 3 -C 6 cycloalkyl, -Ci-C 2 alkyl-C 3 - C 6 cycloalkenyl which may be optionally substituted by one or more groups independently selected from the group consisting fluoro, CrC 2 alkyl and CrC 2 fluoroalkyl.
- R 2 is n-propyl, iso-propyl, n-butyl, iso- butyl, sec-butyl, tert-butyl, n-pentyl, 2-methylbutyl, 2,2-dimethylpropyl, 2-methylpentyl, 3- methylpentyl, 2,3-dimethylbutyl, 2,2-dimethylbutyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl -CH 2 -cyclopropyl, -CH 2 -cyclobutyl, -CH 2 -cyclopentyl, and -CH 2 -cyclopentenyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting fluoro and methyl.
- R 2 is n-propyl, iso-propyl, n- butyl, iso-butyl, sec-butyl, each of which may be optionally substituted by one or more fluoro.
- R 3 and R 4 independently of each other represent hydrogen, d-C 4 alkyl or C 3 -C 6 cycloalkyl; or
- R 3 and R 4 together with the nitrogen atom to which they are attached form a 3-6- membered saturated cyclic group
- R 3 and R 4 independently of each other represent hydrogen, C C 3 alkyl or C 3 -C 5 cycloalkyl; or
- R 3 and R 4 together with the nitrogen atom to which they are attached form a 4- or 5- membered saturated cyclic group.
- R 3 and R 4 independently of each other represent hydrogen, methyl, ethyl, isopropyl or cyclopropyl; or
- R 3 and R 4 together with the nitrogen atom to which they are attached form a 4- membered saturated cyclic group. ln one group of compounds, R 3 is hydrogen or methyl;
- R 4 is methyl or ethyl.
- R 3 represents hydrogen or methyl
- R 4 is ethyl
- R 5 represents H, CrC 4 alkyl or d-C 4 haloalkyl.
- R 5 represents H or d-C 4 alkyl.
- R 5 represents H or methyl
- R 5 is hydrogen
- R 6 represents C C 4 alkyl, Ci-C 4 alkoxy, C C 4 haloalkyl or Ci-C 4 haloalkoxy.
- R 6 represents C C 4 alkyl or Ci-C 4 alkoxy.
- R 6 represents methyl, ethyl, n-propyl, iso-propyl, cyclopropyl, cyclobutyl, cyclopentyl, methoxy or ethoxy.
- R 6 represents methyl, ethyl, n-propyl, iso-propyl, cyclopropyl, cyclobutyl, or cyclopentyl.
- R 6 represents methyl, ethyl, n-propyl, iso-propyl, cyclopropyl, cyclobutyl or cyclopentyl.
- R 6 represents methyl, ethyl, n-propyl, iso-propyl, or cyclopropyl.
- R 6 represents methyl, ethyl, n-propyl or iso-propyl.
- R 6 is methyl
- a racemic compound (I) is a 1 :1 mixture of the compounds of formula (la) and (lb).
- Other ratios of (la) and (lb) are possible and part of the present invention. Examples of such ratios of (la) to (lb) are 1 :99, 2:98, 5:95, 10:90, 20:80, 30:70; 40:60, 45:55; 55:45; 60;40, 70:30, 80:20, 90:10, 95:5, 98;2, and 99:1.
- the weight ratio of (lb) to (la) is weighted towards compound of formula (la), for example, the the ratio of (lb) to (la) being 1 :99, 2:98, 5:95, 10:90, 20:80, 30:70; 40:60 or 45:55.
- the compound of formula (I) consists essentially of the compound of formula (la); even more preferably, the compound of formula (I) is the compound of formula (la).
- the weight ratio of (la) to (lb) is weighted towards compound of formula (lb), for example, the the ratio of (la) to (lb) being 1 :99, 2:98, 5:95, 10:90, 20:80, 30:70; 40:60 or 45:55.
- the compound of formula (I) consists essentially of the compound of formula (lb); even more preferably, the compound of formula (I) is the compound of formula (lb).
- R 7 represents a three- to ten-membered monocyclic or fused bicyclic ring system which can be aromatic, partially saturated or fully saturated and can contain 1 to 4 hetero atoms selected from the group consisting of nitrogen, oxygen and sulfur, it being possible for the three- to ten-membered ring system itself to be optionally substituted by one or more groups independently selected from the group consisting halogen, CrC 4 haloalkyl, Ci-C 4 alkoxy and CrC 4 haloalkoxy.
- R 7 represents C 3 -C 6 cycloalkyl, C 3 -C 5 cycloalkenyl, phenyl, naphthyl, anthracyl, fluorenyl, indanyl, oxiranyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, 1 ,3- dioxolanyl, 1 ,4-dioxanyl, aziridinyl, azetidinyl, pyrrolidinyl, piperidinyl, oxazinanyl, morpholinyl, thiomorpholinyl, imidazolidinyl, pyrazolidinyl, piperazinyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl,
- R 7 represents C 3 -C 6 cycloalkyl, C 3 -C 5 cycloalkenyl, phenyl, naphthyl, anthracyl, fluorenyl, indanyl, morpholinyl, pyrrolidinyl, piperidinyl, piperazinyl, pyridyl, pyrrolyl, imidazolyl and triazolyl, each of which is optionally substituted by one or more groups independently selected from the group consisting halogen, d-C 4 haloalkyl, Ci-C 4 alkoxy and Ci-C 4 haloalkoxy.
- R 7 represents C 3 -C 6 cycloalkyl, C 3 -C 5 cycloalkenyl, phenyl, naphthyl, morpholinyl, pyrrolidinyl, piperidinyl, piperazinyl, pyridyl, pyrrolyl, imidazolyl and triazolyl, each of which is optionally substituted by one or more groups independently selected from the group consisting halogen, d-C 4 haloalkyl, Ci-C 4 alkoxy and C C 4 haloalkoxy.
- R 7 represents C 3 -C 6 cycloalkyl, C 3 -C 5 cycloalkenyl, phenyl, morpholinyl, pyrrolidinyl, piperdinyl, piperazinyl, pyridyl, pyrrolyl, imidazolyl and triazolyl, each of which is optionally substituted by one or more groups independently selected from the group consisting halogen, CrC 4 haloalkyl, Ci-C 4 alkoxy and Ci-C 4 haloalkoxy.
- R 7 represents C 3 -C 6 cycloalkyl, C 3 -C 5 cycloalkenyl, phenyl, morpholinyl, pyrollidinyl, pyridyl and imidazolyl, each of which is optionally substituted by one or more groups independently selected from the group consisting halogen, Ci-C 4 haloalkyl, CrC 4 alkoxy and Ci-C 4 haloalkoxy.
- R 7 represents C 3 -C 6 cycloalkyl or C 3 -C 5 cycloalkenyl, each of which is optionally substituted by one or more groups independently selected from the group consisting halogen, Ci-C 4 haloalkyl, Ci-C 4 alkoxy and Ci-C 4 haloalkoxy
- R 1 represents hydrogen, halogen, cyano, OH, NH 2 , C1-C4 alkyl, C 3 -C 6 cycloalkyl, NH(C C 4 alkyl), N(C C 4 alkyl) 2 , CO(C C 4 alkyl), C0 2 (Ci-C 4 alkyl), C0 2 H, CONH(C C 4 alkyl), CON(C C 4 alkyl) 2 , S0 2 NH(C C 4 alkyl), S0 2 N(Ci-C 4 alkyl) 2 , C C 4 haloalkyl, C C 4 alkoxy, C C 4 haloalkoxy, or C 2 -C 4 alkynyl;
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 6 cycloalkyl, C 3 - C 5 cycloalkenyl, -CrC 2 alkyl-C 3 -C 6 cycloalkyl, -CrC 2 alkyl-C 3 -C 6 cycloalkenyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting halogen, C1-C4 haloalkyl and C1-C4 haloalkoxy;
- R 3 and R 4 independently of each other represent hydrogen, C1-C4 alkyl or C 3 -C 6 cycloalkyl; or
- R 3 and R 4 together with the nitrogen atom to which they are attached form a 3-6- membered saturated cyclic group
- R 5 represents H, C1-C4 alkyl or C1-C4 haloalkyl
- R 6 represents C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl or C1-C4 haloalkoxy.
- R 1 represents hydrogen, halogen, cyano, OH, NH 2 , methyl, ethyl, cyclopropyl, NH(C C 2 alkyl), N(C C 2 alkyl) 2 , CO(C C 2 alkyl), C0 2 (Ci-C 2 alkyl), C0 2 H, CONH(C C 2 alkyl), CON(C C 2 alkyl) 2 , S0 2 NH(C C 2 alkyl), S0 2 N(Ci-C 2 alkyl) 2 , C1-C4 fluoroalkyl, C1-C4 alkoxy, C C 2 haloalkoxy or C 2 -C 4 alkynyl;
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 6 cycloalkyl, C 3 -
- R 3 and R 4 independently of each other represent hydrogen, C C 3 alkyl or C 3 -C 5 cycloalkyl; or R 3 and R 4 together with the nitrogen atom to which they are attached form a 5- membered saturated cyclic group;
- R 5 represents H or CrC 4 alkyl
- R 6 represents C C 4 alkyl, CrC 4 alkoxy, Ci-C 4 haloalkyl or Ci-C 4 haloalkoxy.
- R 1 represents hydrogen, halogen, cyano
- R 2 represents C 3 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 6 cycloalkyl, C 3 - C 5 cycloalkenyl, -CrC 2 alkyl-C 3 -C 6 cycloalkyl, -CrC 2 alkyl-C 3 -C 6 cycloalkenyl which may be optionally substituted by one or more groups independently selected from the group consisting fluoro, Ci-C 2 alkyl, Ci-C 2 fluoroalkyl and Ci-C 2 fluoroalkoxy;
- R 3 and R 4 independently of each other represent hydrogen, methyl, ethyl, isopropyl or cyclopropyl; or
- R 3 and R 4 together with the nitrogen atom to which they are attached form a 5- membered saturated cyclic group
- R 5 represents H or methyl
- R 6 represents C C 4 alkyl or Ci-C 4 alkoxy.
- Ri represents hydrogen, halogen, cyano, methyl, ethyl, cyclopropyl, CHF 2 , CF 3 , OMe, or OCHF 2 ;
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, 2-methylbutyl,
- R 3 is hydrogen or methyl
- R 4 is methyl or ethyl
- R 5 represents H or methyl
- R 6 represents methyl, ethyl, n-propyl, iso-propyl, cyclopropyl, cyclobutyl, cyclopentyl, methoxy or ethoxy.
- R 1 represents hydrogen, CI, Br, methyl, CHF 2 or cyano
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting fluoro and difluoromethoxy;
- R 3 represents hydrogen or methyl;
- R 4 is ethyl
- R 5 is hydrogen or methyl
- R 6 represents methyl, ethyl, n-propyl, iso-propyl, cyclopropyl, cyclobutyl, cyclopentyl, methoxy or ethoxy.
- R 1 represents hydrogen, CI, Br, methyl, CHF 2 or cyano
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting fluoro and difluoromethoxy;
- R 3 represents hydrogen or methyl
- R 4 is ethyl
- R 5 is hydrogen or methyl
- R 6 represents methyl, ethyl, n-propyl, iso-propyl, cyclopropyl, cyclobutyl or cyclopentyl.
- R 1 represents hydrogen, CI, Br, methyl
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting fluoro and difluoromethoxy;
- R 3 represents hydrogen or methyl
- R 4 is ethyl
- R 5 is hydrogen or methyl
- R 6 represents methyl, ethyl, n-propyl or iso-propyl.
- R 1 represents hydrogen, CI, Br, methyl, CHF 2 or cyano
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, each of which may be optionally substituted by one or more groups independently selected from the group consisting fluoro and difluoromethoxy;
- R 3 represents hydrogen or methyl
- R 4 is ethyl
- R 5 is hydrogen or methyl
- R 6 is methyl
- R 1 represents hydrogen, CI, Br, methyl, CHF 2 or cyano
- R 2 is n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl or cyclopropyl;
- R 3 represents hydrogen or methyl;
- R 4 is ethyl
- R 5 is hydrogen
- R 6 is methyl
- the invention is further illustrated by making available the following individual compounds of formula (I) listed below in Tables 1 to 22.
- Table 1 Each of Tables 1 to 22, which follow Table A below, make available 47 compounds of the formula (I) in which R 2 , R 3 , R 4 , R 5 and R 6 are the substituents defined in Table A and R 1 is the substituent defined in the relevant Table 1 to 22.
- Table 1 individualises 47 compounds of formula (I) wherein for each row of Table A, R 1 is as defined in Table 1.
- Table 2 individualises 47 compounds of formula (I) wherein for each row of Table A, R 1 is as defined in Table 2; and so on for Tables 3 to 22.
- Table A discloses 47 sets of meanings of the variables R 2 , R 3 , R 4 , R 5 and R 6 in a compound of formula I.
- the invention is further illustrated by making available the following individual compounds of formula (la) listed below in Tables 23 to 44.
- Tables 23 to 44 make available 47 compounds of the formula (la) in which R 2 , R 3 , R 4 , R 5 and R 6 are the substituents defined in Table A and R 1 is the substituent defined in the relevant Table 23 to 44.
- Table 23 individualises 47 compounds of formula (la) wherein for each row of Table A, R 1 is as defined in Table 23.
- Table 24 individualises 47 compounds of formula (la) wherein for each row of Table A, R 1 is as defined in Table 24; and so on for Tables 25 to 44.
- Table A discloses 47 sets of meanings of the variables R 2 , R 3 , R 4 , R 5 and R 6 in a compound of formula la.
- Tables 45 to 66 which follow Table A below, make available 47 compounds of the formula (lb) in which R 2 , R 3 , R 4 , R 5 and R 6 are the substituents defined in Table A and R 1 is the substituent defined in the relevant Table 45 to 66.
- Table 45 individualises 47 compounds of formula (lb) wherein for each row of Table A, R 1 is as defined in Table 45.
- R 1 is as defined in Table 46; and so on for Tables 47 to 66.
- Table A discloses 47 sets of meanings of the variables R 2 , R 3 , R 4 , R 5 and R 6 in a compound of formula lb.
- Tables 1 , 23 and 45 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is hydrogen and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given the corresponding row of Table A. For example;
- compound 23.1.043 has the following structure:
- compound 45.1.043 has the following structure:
- Tables 2, 24 and 46 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is chloro and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 3, 25 and 47 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is bromo and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 4, 26 and 48 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is iodo and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 5, 27 and 49 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is methyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 6, 28 and 50 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is ethyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 7, 29 and 51 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is cyclopropyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 8, 30 and 52 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is trifluoromethyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 9, 31 and 53 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is difluoromethyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 10, 32 and 54 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is ethynyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 1 1 , 33 and 55 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is methoxy and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 12, 34 and 56 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is difluoromethoxy and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 13, 35 and 57 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is methylamino and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 14, 36 and 58 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is dimethylamino and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 15, 37 and 59 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is N- methylsulfonamide, wherein the broken line below indicates the point of attachment of the group R 1 to the remainder of the compound and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 16, 38 and 60 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is N,N- dimethylsulfonamide, wherein the broken line below indicates the point of attachment of the group R 1 to the remainder of the compound and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 17, 39 and 61 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is fluoro and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 18, 40 and 62 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is acetyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 19, 41 and 63 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is methoxyformyl wherein the broken line below indicates the point of attachment of the group R 1 to the remainder of the compound and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 20, 42 and 64 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is hydroxy and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 21 , 43 and 65 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is fluoromethyl and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- Tables 22, 44 and 66 disclose 47 compounds of formula (I), 47 compounds of formula (la) and 47 compounds of formula (lb) respectively wherein R 1 is cyano and each of the variables R 2 , R 3 , R 4 , R 5 and R 6 has the specific meaning given in the corresponding row of Table A.
- the compounds of formula (I) according to the invention have, for practical purposes, a very advantageous spectrum of activities for protecting useful plants against diseases that are caused by phytopathogenic microorganisms, such as fungi, bacteria or viruses, in particular against diseases that are caused by fungi.
- the invention therefore also relates to a method of controlling or preventing infestation of useful plants by phytopathogenic microorganisms, wherein a compound of formula (I) is applied as active ingredient to the plants, to parts thereof or the locus thereof.
- plants refers to all physical parts of a plant, including seeds, seedlings, saplings, roots, tubers, stems, stalks, foliage, and fruits.
- locus means fields in or on which plants are growing, or where seeds of cultivated plants are sown, or where seed will be placed into the soil. It includes soil, seeds, and seedlings, as well as established vegetation.
- the compounds of formula I can be used in the agricultural sector and related fields of use e.g. as active ingredients for controlling plant pests or on non-living materials for control of spoilage microorganisms or organisms potentially harmful to man.
- the compounds of formula (I) according to the invention are distinguished by excellent activity at low rates of application, by being well tolerated by plants and by being
- the compounds of formula (I) can be used to inhibit or destroy the diseases that occur on plants or parts of plants of different crops of useful plants, while at the same time protecting also those parts of the plants that grow later from phytopathogenic micro-organisms.
- fungicide as used herein means a compound that controls, modifies, or prevents the growth of fungi.
- fungicidally effective amount means the quantity of such a compound or combination of such compounds that is capable of producing an effect on the growth of fungi. Controlling or modifying effects include all deviation from natural development, such as killing, retardation and the like, and prevention includes barrier or other defensive formation in or on a plant to prevent fungal infection.
- a preferred method of applying a compound of formula (I) is foliar application.
- the frequency of application and the rate of application will depend on the risk of infestation by the corresponding pathogen.
- the compounds of formula (I) may also penetrate the plant through the roots via the soil (systemic action) by drenching the locus of the plant with a liquid formulation, or by applying the compounds in solid form to the soil, e.g. in granular form (soil application). In crops of water rice such granulates can be applied to the flooded rice field.
- compounds of formula (I) as dressing agents for the treatment of plant propagation material, in particular of seeds and plant cuttings (e.g. rice), for the protection against fungal infections as well as against phytopathogenic fungi occurring in the soil.
- the propagation material can be treated with a composition comprising a compound of formula I before planting: seed, for example, can be dressed before being sown.
- the active ingredients according to the invention can also be applied to grains (coating), either by impregnating the seeds in a liquid formulation or by coating them with a solid formulation.
- the composition can also be applied to the planting site when the propagation material is being planted, for example, to the seed furrow during sowing.
- the invention relates also to such methods of treating plant propagation material and to the plant propagation material so treated.
- plant propagation material denotes all generative parts of a plant, for example seeds or vegetative parts of plants such as cuttings and tubers. It includes seeds in the strict sense, as well as roots, fruits, tubers, bulbs, rhizomes, and parts of plants.
- the compounds of formula (I) according to the invention may be used for controlling fungi in related areas, for example in the protection of technical materials, including wood and wood related technical products, in food storage or in hygiene management.
- the invention could be used to protect non-living materials from fungal attack, e.g. lumber, wall boards and paint.
- the compounds of formula I are for example, effective against Fungi and fungal vectors of disease as well as phytopathogenic bacteria and viruses.
- These Fungi and fungal vectors of disease as well as phytopathogenic bacteria and viruses are for example:
- Absidia corymbifera Alternaria spp, Aphanomyces spp, Ascochyta spp, Aspergillus spp. including A. flavus, A. fumigatus, A. nidulans, A. niger, A. terrus, Aureobasidium spp. including A. pullulans, Blastomyces dermatitidis, Blumeria graminis, Bremia lactucae, Botryosphaeria spp. including B. dothidea, B. obtusa, Botrytis spp. comprising B. cinerea, Candida spp. including C. albicans, C. glabrata, C. krusei, C. lusitaniae, C. parapsilosis, C. tropicalis, Cephaloascus fragrans, Ceratocystis spp, Cercospora spp. including C.
- Cryptococcus neoformans Diaporthe spp, Didymella spp, Drechslera spp, Elsinoe spp, Epidermophyton spp, Erwinia amylovora, Erysiphe spp. including E. cichoracearum, Eutypa lata, Fusarium spp. including F. culmorum, F. graminearum, F. langsethiae, F. moniliforme, F. oxysporum, F. proliferatum, F. subglutinans, F.
- Penicillium spp. including P. digitatum, P. italicum, Petriellidium spp, Peronosclerospora spp. Including P. maydis, P. philippinensis and P. sorghi, Peronospora spp, Phaeosphaeria nodorum, Phakopsora pachyrhizi, Phellinus igniarus, Phialophora spp, Phoma spp,
- Crops of useful plants in which the composition according to the invention can be used include perennial and annual crops, such as berry plants for example blackberries, blueberries, cranberries, raspberries and strawberries; cereals for example barley, maize (corn), millet, oats, rice, rye, sorghum triticale and wheat; fibre plants for example cotton, flax, hemp, jute and sisal; field crops for example sugar and fodder beet, coffee, hops, mustard, oilseed rape (canola), poppy, sugar cane, sunflower, tea and tobacco; fruit trees for example apple, apricot, avocado, banana, cherry, citrus, nectarine, peach, pear and plum; grasses for example Bermuda grass, bluegrass, bentgrass, centipede grass, fescue, ryegrass, St.
- perennial and annual crops such as berry plants for example blackberries, blueberries, cranberries, raspberries and strawberries
- cereals for example barley, maize (corn), mille
- Augustine grass and Zoysia grass herbs such as basil, borage, chives, coriander, lavender, lovage, mint, oregano, parsley, rosemary, sage and thyme; legumes for example beans, lentils, peas and soya beans; nuts for example almond, cashew, ground nut, hazelnut, peanut, pecan, pistachio and walnut; palms for example oil palm; ornamentals for example flowers, shrubs and trees; other trees, for example cacao, coconut, olive and rubber;
- vegetables for example asparagus, aubergine, broccoli, cabbage, carrot, cucumber, garlic, lettuce, marrow, melon, okra, onion, pepper, potato, pumpkin, rhubarb, spinach and tomato; and vines for example grapes.
- Crops are to be understood as being those which are naturally occurring, obtained by conventional methods of breeding, or obtained by genetic engineering. They include crops which contain so-called output traits (e.g. improved storage stability, higher nutritional value and improved flavour).
- output traits e.g. improved storage stability, higher nutritional value and improved flavour.
- Crops are to be understood as also including those crops which have been rendered tolerant to herbicides like bromoxynil or classes of herbicides such as ALS-, EPSPS-, GS-, HPPD- and PPO-inhibitors.
- herbicides like bromoxynil or classes of herbicides such as ALS-, EPSPS-, GS-, HPPD- and PPO-inhibitors.
- An example of a crop that has been rendered tolerant to imidazolinones, e.g. imazamox, by conventional methods of breeding is Clearfield® summer canola.
- crops that have been rendered tolerant to herbicides by genetic engineering methods include e.g. glyphosate- and glufosinate-resistant maize varieties commercially available under the trade names RoundupReady®, Herculex I® and
- Crops are also to be understood as being those which naturally are or have been rendered resistant to harmful insects. This includes plants transformed by the use of recombinant DNA techniques, for example, to be capable of synthesising one or more selectively acting toxins, such as are known, for example, from toxin-producing bacteria. Examples of toxins which can be expressed include ⁇ -endotoxins, vegetative insecticidal proteins (Vip), insecticidal proteins of bacteria colonising nematodes, and toxins produced by scorpions, arachnids, wasps and fungi.
- Vip vegetative insecticidal proteins
- insecticidal proteins of bacteria colonising nematodes and toxins produced by scorpions, arachnids, wasps and fungi.
- An example of a crop that has been modified to express the Bacillus thuringiensis toxin is the Bt maize KnockOut® (Syngenta Seeds).
- An example of a crop comprising more than one gene that codes for insecticidal resistance and thus expresses more than one toxin is VipCot® (Syngenta Seeds).
- Crops or seed material thereof can also be resistant to multiple types of pests (so-called stacked transgenic events when created by genetic modification).
- a plant can have the ability to express an insecticidal protein while at the same time being herbicide tolerant, for example Herculex I® (Dow AgroSciences, Pioneer Hi-Bred International).
- the compounds of formula (I) can be used in unmodified form or, preferably, together with carriers and adjuvants conventionally employed in the art of formulation.
- the invention also relates to compositions for controlling and protecting against phytopathogenic microorganisms, comprising a compound of formula (I) and an inert carrier, and to a method of controlling or preventing infestation of useful plants by
- phytopathogenic microorganisms wherein a composition, comprising a compound of formula (I) as active ingredient and an inert carrier, is applied to the plants, to parts thereof or the locus thereof.
- compounds of formula (I) and inert carriers are conveniently formulated in known manner to emulsifiable concentrates, coatable pastes, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granulates, and also encapsulations e.g. in polymeric substances.
- the methods of application such as spraying, atomising, dusting, scattering, coating or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances.
- the compositions may also contain further adjuvants such as stabilizers, antifoams, viscosity regulators, binders or tackifiers as well as fertilizers, micronutrient donors or other formulations for obtaining special effects.
- Suitable carriers and adjuvants can be solid or liquid and are substances useful in formulation technology, e.g. natural or regenerated mineral substances, solvents, dispersants, wetting agents, tackifiers, thickeners, binders or fertilizers. Such carriers are for example described in WO 97/33890.
- a formulation i.e. a composition comprising the compound of formula (I) and, if desired, a solid or liquid adjuvant, is prepared in a known manner, typically by intimately mixing and/or grinding the compound with extenders, for example solvents, solid carriers and, optionally, surface-active compounds (surfactants).
- extenders for example solvents, solid carriers and, optionally, surface-active compounds (surfactants).
- the agrochemical formulations will usually contain from 0.1 to 99% by weight, preferably from 0.1 to 95% by weight, of the compound of formula (I), 99.9 to 1 % by weight, preferably 99.8 to 5% by weight, of a solid or liquid adjuvant, and from 0 to 25% by weight, preferably from 0.1 to 25% by weight, of a surfactant.
- the end user will normally use dilute formulations.
- Advantageous rates of application are normally from 5g to 2kg of active ingredient (a.i.) per hectare (ha), preferably from 10g to 1 kg a.i./ha, most preferably from 20g to 600g a.i./ha.
- convenient rates of application are from 10mg to 1 g of active substance per kg of seeds.
- the rate of application for the desired action can be determined by experiments. It depends for example on the type of action, the developmental stage of the useful plant, and on the application (location, timing, application method) and can, owing to these parameters, vary within wide limits.
- agronomic chemicals include pesticides, such as acaricides, bactericides, fungicides, herbicides, insecticides, nematicides, as well as plant nutrients and plant fertilizers.
- the present invention provides a composition
- a composition comprising a compound of formula (I) according to the present invention together with one or more pesticides, plant nutrients or plant fertilizers.
- the combination may also encompass specific plant traits incorporated into the plant using any means, for example conventional breeding or genetic modification.
- Such compositions may also contain one or more inert carriers as described above.
- the invention also provides for the use of provides a composition comprising a compound of formula (I) according to the present invention together with one or more pesticides, plant nutrients or plant fertilizers.
- the combination may also encompass specific plant traits incorporated into the plant using any means, for example conventional breeding or genetic modification.
- Suitable examples of plant nutrients or plant fertilizers are calcium sulfate (CaS0 4 ), calcium nitrate (Ca(N0 3 ) 2 .4H 2 0), calcium carbonate (CaC0 3 ), potassium nitrate (KN0 3 ), magnesium sulfate (MgS0 4 ), potassium hydrogen phosphate (KH 2 P0 4 ), manganese sulfate (MnS0 4 ), copper sulfate (CuS0 4 ), zinc sulfate (ZnS0 4 ), nickel chloride (NiCI 2 ), cobalt sulfate (CoS0 4 ), potassium hydroxide (KOH), sodium chloride (NaCI), boric acid (H 3 B0 3 ) and metal salts thereof (Na 2 Mo0 4 ).
- CaS0 4 calcium sulfate
- Ca(N0 3 ) 2 .4H 2 0 calcium carbonate
- CaC0 3 calcium carbonate
- the nutrients may be present in an amount of 5% to 50% by weight, preferably of 10% to 25% by weight or of 15% to 20% by weight each.
- Preferred additional nutrients are urea ((NH 2 ) 2 CO), melamine (C 3 H 6 N 6 ), potassium oxide (K 2 0), and inorganic nitrates.
- the most preferred additional plant nutrient is potassium oxide. Where the preferred additional nutrient is urea, it is present in an amount of generally 1 % to 20% by weight, preferably 2% to 10% by weight or of 3% to 7% by weight.
- Suitable examples of pesticides are acycloamino acid fungicides, aliphatic nitrogen fungicides, amide fungicides, anilide fungicides, antibiotic fungicides, aromatic fungicides, arsenical fungicides, aryl phenyl ketone fungicides, benzamide fungicides, benzanilide fungicides, benzimidazole fungicides, benzothiazole fungicides, botanical fungicides, bridged diphenyl fungicides, carbamate fungicides, carbanilate fungicides, conazole fungicides, copper fungicides, dicarboximide fungicides, , dinitrophenol fungicides, dithiocarbamate fungicides, dithiolane fungicides, furamide fungicides, furanilide fungicides, hydrazide fungicides, imidazole fungicides, mercury fungicides, morpholine
- diazodicarboxylate (0.24 ml_, 1 .21 mmol, 1.1 equiv) was added dropwise over 10 minutes while keeping the temperature below 40°C. The reaction mixture was stirred for 16h under heating at 60°C. After this time, triphenylphosphine (0.15 g, 0.55 mmol, 0.5 equiv) and DIAD (diisopropyl diazodicarboxylate) (0.1 1 ml_, 0.55 mmol, 0.5 equiv) were added again and the reaction mixture wasfurther stirred for 9 h. The reaction mixture was allowed to reach room temperature before quenching with water (10 mL) and 2M NaOH aqueous solution (2 ml_).
- Method 1 Mass spectra were recorded on a Mass Spectrometer from Waters (SQD or ZQ Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive or negative ions, Capillary: 3.00 kV, Cone range: 30-60 V, Extractor: 2.00 V, Source Temperature: 150°C, Desolvation Temperature: 350°C, Cone Gas Flow: 0 L/Hr, Desolvation Gas Flow: 650 L/Hr, Mass range: 100 to 900 Da) and an Acquity UPLC from Waters: Binary pump, heated column compartment and diode-array detector. Solvent degasser, binary pump, heated column compartment and diode-array detector.
- Method 2 Mass spectra were recorded on a Mass Spectrometer from Shimadzu (SQD or ZQ Single quadrupole mass spectrometer) equipped with an electrospray source
- Method 3 Mass spectra were recorded on a ZQ2000 Mass Spectrometer from Waters (Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive ions, Capillary (kV) 3.5, Cone (V) 60.00, Extractor (V) 3.00, Source Temperature (°C) 150, Desolvation Temperature (°C) 350, Cone Gas Flow (L/Hr) 50, Desolvation Gas Flow (L/Hr) 800, Mass range: 140 to 800 Da) DAD Wavelength range (nm): 210 to 400, Type of column: Waters ACQUITY UPLC HSS T3; Column length: 30 mm; Internal diameter of column: 2.1 mm; Particle Size: 1 .8 micron; Temperature: 60°C.
- Wheat leaf segments cv. Kanzler were placed on agar in a multiwell plate (24-well format) and sprayed with the formulated test compound diluted in water.
- the leaf disks were inoculated by shaking powdery mildew infected plants above the test plates 1 day after application.
- the inoculated leaf disks were incubated at 20°C and 60% rh under a light regime of 24 h darkness followed by 12 h light / 12 h darkness in a climate chamber and the activity of a compound was assessed as percent disease control compared to untreated when an appropriate level of disease damage appears on untreated check leaf segments (6 - 8 days after application).
- the following compounds gave at 200 ppm give at least 80% disease control in this test when compared to untreated control leaf disks under the same conditions, which show extensive disease development:
- Wheat leaf segments cv. Kanzler were placed on agar in multiwell plates (24-well format) and sprayed with the formulated test compound diluted in water.
- the leaf disks were inoculated with a spore suspension of the fungus 1 day after application.
- the inoculated leaf segments were incubated at 19°C and 75% rh under a light regime of 12 h light / 12 h darkness in a climate cabinet and the activity of a compound was assessed as percent disease control compared to untreated when an appropriate level of disease damage appears in untreated check leaf segments (7 - 9 days after application).
- Wheat leaf segments cv. Kanzler are placed on agar in multiwell plates (24-well format). The leaf segments are inoculated with a spore suspension of the fungus. Plates were stored in darkness at 19°C and 75% rh. The formulated test compound diluted in water was applied 1 day after inoculation. The leaf segments were incubated at 19°C and 75% rh under a light regime of 12 h light / 12 h darkness in a climate cabinet and the activity of a compound was assessed as percent disease control compared to untreated when an appropriate level of disease damage appears in untreated check leaf segments (6 - 8 days after application).
- Phakopsora pachyrhizi on soybean, preventive treatment The compound activity was tested under 1 day preventive conditions. Soybean plants with a fully enfolded first trifoliate leaf were sprayed with a track sprayer and 50 l/ha spray volume with the test compounds, either solo or in tankmix as shown in the table below. 1 day after application leaf discs were cut from the first trifoliate leaf and placed in multiwell plates on water-agar. 5 leaf discs per treatment where infested with spores of a triazole tolerant soybean rust strain. The multiwell plates where sealed and placed in an incubator 48 h in darkness and 12 h light/dark cycle afterwards. Rust infestation on leaf discs was evaluated visually 1 1 days after application and average activity calculated in relation to disease severity on untreated check leaf discs.
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- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Description
Claims
Priority Applications (15)
Application Number | Priority Date | Filing Date | Title |
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UAA201611294A UA118788C2 (en) | 2014-04-11 | 2015-03-31 | Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture |
CA2945228A CA2945228C (en) | 2014-04-11 | 2015-03-31 | Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture |
SI201530613T SI3129355T1 (en) | 2014-04-11 | 2015-03-31 | Fungicidal n'-(2-methyl-6-(2-alkoxy-ethoxy)-3-pyridyl)-n-alkyl-formamidine derivatives for use in agriculture |
RU2016144197A RU2701370C2 (en) | 2014-04-11 | 2015-03-31 | Fungicidal derivatives of n'-[2-methyl-6 [2-alkoxyethoxy]-3-pyridyl]-n-alkylformamidine for use in agriculture |
US15/127,911 US10173983B2 (en) | 2014-04-11 | 2015-03-31 | Fungicidal pyridylamidines |
JP2016561738A JP6543269B2 (en) | 2014-04-11 | 2015-03-31 | Fungicidal and fungicidal N '-[2-methyl-6- [2-alkoxy-ethoxy] -3-pyridyl] -N-alkyl-formamidine derivatives used in agriculture |
BR112016023016-7A BR112016023016B1 (en) | 2014-04-11 | 2015-03-31 | COMPOUNDS DERIVED FROM N'-[2-METHYL-6-[2-ALKOXY-ETOXY]-3-PYRIDYL]-N-ALKYL-FORMAMIDINE, COMPOSITION INCLUDING SUCH COMPOUNDS AND METHOD OF CONTROL OR PREVENTION OF PHYTOPATHOGENIC DISEASES |
KR1020167027227A KR102369885B1 (en) | 2014-04-11 | 2015-03-31 | Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture |
DK15715205.9T DK3129355T3 (en) | 2014-04-11 | 2015-03-31 | FUNGICIDE N '- [2-METHYL-6- [2-ALCOXYETHOXY] -3-PYRIDYL] -N-ALKYL FORMAMIDE INGREDIENTS FOR AGRICULTURAL USE |
ES15715205T ES2711727T3 (en) | 2014-04-11 | 2015-03-31 | Derivatives of N '- [2-methyl-6- [2-alkoxy-ethoxy] -3-pyridyl] -N-alkyl-formamidine fungicides for use in agriculture |
CN201580019160.3A CN106164048B (en) | 2014-04-11 | 2015-03-31 | Fungicidal N' - [ 2-methyl-6- [ 2-alkoxy-ethoxy ] -3-pyridinyl ] -N-alkyl-formamidines for use in agriculture |
AU2015243632A AU2015243632C1 (en) | 2014-04-11 | 2015-03-31 | Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture |
EP15715205.9A EP3129355B1 (en) | 2014-04-11 | 2015-03-31 | Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture |
ZA2016/05977A ZA201605977B (en) | 2014-04-11 | 2016-08-29 | Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture |
US16/194,034 US11014889B2 (en) | 2014-04-11 | 2018-11-16 | Fungicidal pyridylamidines |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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EP14164464 | 2014-04-11 | ||
EP14164464.1 | 2014-04-11 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US15/127,911 A-371-Of-International US10173983B2 (en) | 2014-04-11 | 2015-03-31 | Fungicidal pyridylamidines |
US16/194,034 Division US11014889B2 (en) | 2014-04-11 | 2018-11-16 | Fungicidal pyridylamidines |
Publications (1)
Publication Number | Publication Date |
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WO2015155075A1 true WO2015155075A1 (en) | 2015-10-15 |
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ID=50473194
Family Applications (1)
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PCT/EP2015/057088 WO2015155075A1 (en) | 2014-04-11 | 2015-03-31 | Fungicidal n'-[2-methyl-6-[2-alkoxy-ethoxy]-3-pyridyl]-n-alkyl-formamidine derivatives for use in agriculture |
Country Status (17)
Country | Link |
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US (2) | US10173983B2 (en) |
EP (1) | EP3129355B1 (en) |
JP (1) | JP6543269B2 (en) |
KR (1) | KR102369885B1 (en) |
CN (1) | CN106164048B (en) |
AR (1) | AR099995A1 (en) |
AU (1) | AU2015243632C1 (en) |
BR (1) | BR112016023016B1 (en) |
CA (1) | CA2945228C (en) |
DK (1) | DK3129355T3 (en) |
ES (1) | ES2711727T3 (en) |
HU (1) | HUE042601T2 (en) |
RU (1) | RU2701370C2 (en) |
SI (1) | SI3129355T1 (en) |
UA (1) | UA118788C2 (en) |
WO (1) | WO2015155075A1 (en) |
ZA (1) | ZA201605977B (en) |
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AU2015243632A1 (en) | 2016-09-15 |
EP3129355B1 (en) | 2018-11-28 |
AR099995A1 (en) | 2016-08-31 |
JP6543269B2 (en) | 2019-07-10 |
US20190084936A1 (en) | 2019-03-21 |
SI3129355T1 (en) | 2019-03-29 |
RU2016144197A3 (en) | 2018-10-22 |
CN106164048B (en) | 2020-08-18 |
RU2701370C2 (en) | 2019-09-26 |
CN106164048A (en) | 2016-11-23 |
JP2017513832A (en) | 2017-06-01 |
CA2945228C (en) | 2023-03-14 |
KR20160144363A (en) | 2016-12-16 |
KR102369885B1 (en) | 2022-03-02 |
US11014889B2 (en) | 2021-05-25 |
AU2015243632B2 (en) | 2019-04-11 |
RU2016144197A (en) | 2018-05-11 |
ES2711727T3 (en) | 2019-05-07 |
US20170107181A1 (en) | 2017-04-20 |
BR112016023016B1 (en) | 2021-09-21 |
BR112016023016A2 (en) | 2017-10-10 |
CA2945228A1 (en) | 2015-10-15 |
AU2015243632C1 (en) | 2019-08-01 |
UA118788C2 (en) | 2019-03-11 |
HUE042601T2 (en) | 2019-07-29 |
DK3129355T3 (en) | 2019-03-11 |
US10173983B2 (en) | 2019-01-08 |
EP3129355A1 (en) | 2017-02-15 |
ZA201605977B (en) | 2019-04-24 |
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