AR115871A1 - METHOD FOR CONTROLLING SOYBEAN ROY FUNGUS THAT HAS RESISTANCE TO SITE INHIBITOR Qₒ - Google Patents
METHOD FOR CONTROLLING SOYBEAN ROY FUNGUS THAT HAS RESISTANCE TO SITE INHIBITOR QₒInfo
- Publication number
- AR115871A1 AR115871A1 ARP190102142A ARP190102142A AR115871A1 AR 115871 A1 AR115871 A1 AR 115871A1 AR P190102142 A ARP190102142 A AR P190102142A AR P190102142 A ARP190102142 A AR P190102142A AR 115871 A1 AR115871 A1 AR 115871A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- optionally substituted
- substituents selected
- hydrocarbon chain
- halogen atom
- Prior art date
Links
Classifications
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Reivindicación 1: Un método para controlar un hongo de la roya de la soja que tiene una sustitución de aminoácidos de F129L en la proteína de citocromo b mitocondrial, caracterizado porque comprende la aplicación de una cantidad eficaz de un compuesto representado por la fórmula (1), [en donde Q representa un grupo representado por los compuestos Q1 ó Q2 del grupo de fórmulas (2) (en las fórmulas, · representa un sitio de unión con el anillo benceno), R¹ representa un grupo de cadena hidrocarbonada C₁₋₃, n es 1, 2, 3, 4 ó 5, cuando n es 2, 3, 4 ó 5, un plural de R² puede ser igual o diferente entre sí, R² representa un grupo de cadena hidrocarbonada C₁₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo A, un grupo cicloalquilo C₃₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo B, OR³, S(O)ₘR⁵, OS(O)₂R⁵, C(O)R³, C(O)OR³, NR³R⁴, C(O)NR³R⁴, S(O)₂NR³R⁴, NR⁴C(O)R³, NR⁴C(O)OR⁵, NR⁴S(O)₂R⁵, CR⁴=N-OR³, un grupo ciano, un grupo nitro o un átomo de halógeno, cuando R² está unido en la posición 2, R¹ y R² se combinan entre sí con el átomo de carbono al que están unidos y el átomo de carbono en la posición 1, para formar un carbociclo de cinco, seis o siete miembros {el carbociclo puede estar opcionalmente sustituido con uno o más R⁶ y cuando un plural de R⁶ está presente, el plural de R⁶ puede ser igual o diferente entre sí}, cuando dos R² son adyacentes entre sí, dos de los R² se pueden combinar junto con el átomo de carbono al que están unidos para formar un anillo parcialmente insaturado o aromático de cinco, seis o siete miembros {el anillo parcialmente insaturado o aromático puede estar opcionalmente sustituido con uno o más R⁷ y cuando un plural de R⁷ está presente, un plural del R⁷ puede ser igual o diferente entre sí y además el anillo parcialmente insaturado o aromático puede ser un carbociclo o un heterociclo y los átomos del anillo en el heterociclo pueden contener, además de los átomos de carbono, uno, dos o tres heteroátomos seleccionados del grupo que consiste en N, O y S}, R³ y R⁴ son iguales o diferentes entre sí y representan un grupo de cadena hidrocarbonada C₁₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo A, un grupo cicloalquilo C₃₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo B o un átomo de hidrógeno, R⁵ representa un grupo de cadena hidrocarbonada C₁₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo A o un grupo cicloalquilo C₃₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo B, R⁶ y R⁷ son iguales o diferentes entre sí y representan un grupo de cadena hidrocarbonada C₁₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo A, un grupo cicloalquilo C₃₋₆ opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo B, un átomo de halógeno, un grupo ciano o un grupo nitro, Grupo A: un grupo seleccionado del grupo que consiste en un átomo de halógeno, un grupo cicloalquilo C₃₋₆, un grupo de alcoxi C₁₋₄, un grupo alquil C₁₋₄-tio {el grupo cicloalquilo C₃₋₆, el grupo alcoxi C₁₋₄ y el grupo alquil C₁₋₄-tio puede estar cada uno opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo que consiste en un átomo de halógeno y un grupo ciano}, un grupo ciano, un grupo nitro y un grupo hidroxi, Grupo B: un grupo que consiste en un átomo de halógeno, un grupo de cadena hidrocarbonada C₁₋₆, un grupo cicloalquilo C₃₋₆, un grupo alcoxi C₁₋₄, un grupo alquil C₁₋₄-tio {el grupo de cadena hidrocarbonada C₁₋₆, el grupo cicloalquilo C₃₋₆, el grupo alcoxi C₁₋₄ y el grupo alquil C₁₋₄-tio puede estar cada uno opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo que consiste en un átomo de halógeno y un grupo ciano}, un grupo ciano, un grupo nitro y un grupo hidroxi] a la soja o al suelo donde crece la soja. Reivindicación 5: Uso del compuesto representado por la fórmula (1) descrito en cualquiera de las reivindicaciones 1 a 4, caracterizado porque es para controlar un hongo de la roya de la soja que tenía una sustitución de aminoácidos de F129L en la proteína de citocromo b mitocondrial.Claim 1: A method for controlling a soybean rust fungus that has an amino acid substitution of F129L in the mitochondrial cytochrome b protein, characterized in that it comprises the application of an effective amount of a compound represented by the formula (1) , [where Q represents a group represented by the compounds Q1 or Q2 of the group of formulas (2) (in the formulas, · represents a binding site with the benzene ring), R¹ represents a group of hydrocarbon chain C₁₋₃, n is 1, 2, 3, 4 or 5, when n is 2, 3, 4 or 5, a plural of R² may be the same or different from each other, R² represents a C₁₋₆ hydrocarbon chain group optionally substituted with one or plus substituents selected from group A, a C₃₋₆ cycloalkyl group optionally substituted with one or more substituents selected from group B, OR³, S (O) ₘR⁵, OS (O) ₂R⁵, C (O) R³, C (O) OR³ , NR³R⁴, C (O) NR³R⁴, S (O) ₂NR³R⁴, NR⁴C (O) R³, NR⁴C (O) OR⁵, NR⁴S (O) ₂R⁵, CR⁴ = N-OR³, a cyano group, a nitro group or a halogen atom, when R² is attached at position 2, R¹ and R² combine with each other with the carbon atom to which they are attached and the carbon atom at position 1, to form a carbocycle of five, six, or seven members {the carbocycle can be optionally substituted with one or more R⁶ and when a plural of R⁶ is present, the plural of R⁶ can be the same or different from each other}, when two R² are adjacent to each other, two of the R² can be combined together with the carbon atom to which they are attached to form a five-, six- or seven-membered aromatic or partially unsaturated ring {the aromatic or partially unsaturated ring may be optionally substituted with one or more R⁷ and when a plural of R⁷ is present, a plural of R⁷ may be the same or different from each other and furthermore the partially unsaturated or aromatic ring may be a carbocycle or a heterocycle and the ring atoms in the heterocycle may contain, in addition to the carbon atoms, one, two or three heteroatoms selected from the group consisting of N, O and S}, R³ and R⁴ are the same or different from each other and represent a C₁₋₆ hydrocarbon chain group optionally substituted with one or more substituents selected from group A, a cycloalkyl group C₃₋₆ optionally substituted with one or more substituents selected from group B or a hydrogen atom, R⁵ represents a C₁₋₆ hydrocarbon chain group optionally substituted with one or more substituents selected from group A or an optionally substituted C₃₋₆ cycloalkyl group with one or more substituents selected from group B, R⁶ and R⁷ are the same or different from each other and represent a C₁₋₆ hydrocarbon chain group optionally substituted with one or more substituents selected from group A, a C₃₋₆ cycloalkyl group optionally substituted with one or more substituents selected from group B, a halogen atom, a cyano group, or a nitro group, Group A: a group selected from the group that consists of a halogen atom, a C₃₋₆ cycloalkyl group, a C₁₋₄ alkoxy group, a C₁₋₄ alkyl-thio group {the C₃₋₆ cycloalkyl group, the C₁₋₄ alkoxy group and the C₁₋ alkyl group ₄-thio may each be optionally substituted with one or more substituents selected from the group consisting of a halogen atom and a cyano group}, a cyano group, a nitro group, and a hydroxy group, Group B: a group consisting of a halogen atom, a C₁₋₆ hydrocarbon chain group, a C₃₋₆ cycloalkyl group, a C₁₋₄ alkoxy group, a C₁₋₄ alkyl-thio group {the C₁₋₆ hydrocarbon chain group, the C₃ cycloalkyl group ₋₆, the C₁₋₄ alkoxy group and the C₁₋₄ alkylthio group may each be optionally substituted with one or more substituents selected from the group consisting of a halogen atom and a cyano group}, a cyano group, a nitro group and a hydroxy group] to the soybean or the soil where the soybean grows. Claim 5: Use of the compound represented by formula (1) described in any of claims 1 to 4, characterized in that it is to control a soybean rust fungus that had an amino acid substitution of F129L in the cytochrome b protein mitochondrial.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018143529A JP2021176818A (en) | 2018-07-31 | 2018-07-31 | CONTROL METHOD FOR SOYBEAN RUST DISEASE FUNGUS HAVING RESISTANCE TO Qo INHIBITOR |
Publications (1)
Publication Number | Publication Date |
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AR115871A1 true AR115871A1 (en) | 2021-03-10 |
Family
ID=69231108
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP190102142A AR115871A1 (en) | 2018-07-31 | 2019-07-30 | METHOD FOR CONTROLLING SOYBEAN ROY FUNGUS THAT HAS RESISTANCE TO SITE INHIBITOR Qₒ |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP2021176818A (en) |
AR (1) | AR115871A1 (en) |
BR (1) | BR112021000153A2 (en) |
WO (1) | WO2020027216A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2023025308A (en) * | 2020-01-31 | 2023-02-22 | 住友化学株式会社 | Method for controlling qoi fungicide-resistant soybean rust fungi |
WO2021219390A1 (en) * | 2020-04-28 | 2021-11-04 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors iv |
EP4142497A1 (en) * | 2020-04-28 | 2023-03-08 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors i |
EP4142494A1 (en) * | 2020-04-28 | 2023-03-08 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ii |
AU2021262412A1 (en) * | 2020-04-28 | 2022-11-24 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution FT29L in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors III |
JP2023528961A (en) * | 2020-06-10 | 2023-07-06 | ビーエーエスエフ ソシエタス・ヨーロピア | Use of strobilurin-type compounds to combat phytopathogenic fungi containing the amino acid substitution F129L in the mitochondrial cytochrome b protein that confers resistance to the Qo inhibitor V |
EP3945089A1 (en) * | 2020-07-31 | 2022-02-02 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors v |
UY39302A (en) * | 2020-06-30 | 2021-12-31 | Sumitomo Chemical Co | METHOD TO CONTROL SOYBEAN RUST FUNGUS WHICH HAS RESISTANCE TO QOI FUNGICIDES. |
CN115836049A (en) * | 2020-07-08 | 2023-03-21 | 巴斯夫欧洲公司 | Use of strobilurin-type compounds to control phytopathogenic fungi containing the amino acid substitution F129L in the mitochondrial cytochrome b protein conferring tolerance to Qo inhibitor VI |
WO2023072670A1 (en) * | 2021-10-28 | 2023-05-04 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors x |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0370629B2 (en) * | 1988-11-21 | 1998-01-07 | Zeneca Limited | Fungicides |
ES2120100T3 (en) * | 1990-06-27 | 1998-10-16 | Basf Ag | O-BENCIL-OXIMETERES AND PROTECTIVE AGENTS OF PLANTS CONTAINING THESE COMPOUNDS. |
NZ242290A (en) * | 1991-04-15 | 1994-12-22 | Zeneca Ltd | Pyridyl and pyrimidinyl substituted oxime-o-benzyl ether derivatives; preparatory processes, fungicidal compositions and an intermediate |
ATE484194T1 (en) * | 2005-06-09 | 2010-10-15 | Bayer Cropscience Ag | ACTIVE INGREDIENTS COMBINATIONS |
CN101637157B (en) * | 2008-07-30 | 2013-03-06 | 中国中化股份有限公司 | Fungicide composition |
-
2018
- 2018-07-31 JP JP2018143529A patent/JP2021176818A/en active Pending
-
2019
- 2019-07-30 AR ARP190102142A patent/AR115871A1/en unknown
- 2019-07-31 BR BR112021000153-0A patent/BR112021000153A2/en unknown
- 2019-07-31 WO PCT/JP2019/030061 patent/WO2020027216A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
JP2021176818A (en) | 2021-11-11 |
WO2020027216A1 (en) | 2020-02-06 |
BR112021000153A2 (en) | 2021-04-06 |
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