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 Qₒ

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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
Application number
ARP190102142A
Other languages
Spanish (es)
Inventor
Hidekatsu Tobita
Yuichi Matsuzaki
Original Assignee
Sumitomo Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co filed Critical Sumitomo Chemical Co
Publication of AR115871A1 publication Critical patent/AR115871A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/36Biocides, 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
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/44Biocides, 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.

ARP190102142A 2018-07-31 2019-07-30 METHOD FOR CONTROLLING SOYBEAN ROY FUNGUS THAT HAS RESISTANCE TO SITE INHIBITOR Qₒ AR115871A1 (en)

Applications Claiming Priority (1)

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JP2018143529A JP2021176818A (en) 2018-07-31 2018-07-31 CONTROL METHOD FOR SOYBEAN RUST DISEASE FUNGUS HAVING RESISTANCE TO Qo INHIBITOR

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AR115871A1 true AR115871A1 (en) 2021-03-10

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JP (1) JP2021176818A (en)
AR (1) AR115871A1 (en)
BR (1) BR112021000153A2 (en)
WO (1) WO2020027216A1 (en)

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* Cited by examiner, † Cited by third party
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
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
KR20230022864A (en) * 2020-06-10 2023-02-16 바스프 에스이 Use of strobilurin-type compounds to combat phytopathogenic fungi containing the amino acid substitution F129L in the mitochondrial cytochrome B protein conferring resistance to the QO inhibitor V
US20230337672A1 (en) * 2020-06-30 2023-10-26 Sumitomo Chemical Company, Limited METHOD OF CONTROLLING SOYBEAN RUST FUNGUS HAVING RESISTANCE TO QoI FUNGICIDE
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

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Publication number Priority date Publication date Assignee Title
DE68928783T2 (en) * 1988-11-21 1998-12-24 Zeneca Ltd Intermediate compounds for the production of fungicides
ES2110421T5 (en) * 1990-06-27 2004-12-01 Basf Aktiengesellschaft O-BENCIL-OXIMETERES AND THE PROTECTIVE AGENTS OF THE 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
EP1893024B1 (en) * 2005-06-09 2010-10-13 Bayer CropScience AG Active substance combinations
CN101637157B (en) * 2008-07-30 2013-03-06 中国中化股份有限公司 Fungicide composition

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