AR098105A1 - Composiciones plaguicidas y métodos relacionados - Google Patents

Composiciones plaguicidas y métodos relacionados

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Publication number
AR098105A1
AR098105A1 ARP140103911A ARP140103911A AR098105A1 AR 098105 A1 AR098105 A1 AR 098105A1 AR P140103911 A ARP140103911 A AR P140103911A AR P140103911 A ARP140103911 A AR P140103911A AR 098105 A1 AR098105 A1 AR 098105A1
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Argentina
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Dow Agrosciences Llc
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8261Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield
    • C12N15/8271Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance
    • C12N15/8279Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance for biotic stress resistance, pathogen resistance, disease resistance
    • C12N15/8286Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance for biotic stress resistance, pathogen resistance, disease resistance for insect resistance
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    • A01N43/80Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
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    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
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    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G3/00Mixtures of one or more fertilisers with additives not having a specially fertilising activity
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  • Life Sciences & Earth Sciences (AREA)
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Abstract

Composiciones y compuestos con utilidad nematicida, acaricida, plaguicida, insecticida, miticida y/o molusquicida. Reivindicación 1: Una composición pesticida, que comprende un compuesto de la fórmula (1) o cualquiera de sus sales aceptables en agricultura, en donde: (a) R¹, R² y R⁴ están seleccionados, de modo independiente, de hidrógeno, F, Cl, Br, I, alquilo C₁₋₆ sustituido o no sustituido o haloalquilo C₁₋₆ sustituido o no sustituido, en donde cada uno de dichos R¹, R², y R⁴, cuando están sustituidos, tiene uno o varios sustituyentes seleccionados de F, Cl, Br, I. CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₀ o halocicloalquilo C₃₋₁₀, (cada uno de los cuales que puede estar sustituido, puede estar opcionalmente sustituido con R¹⁰); (b) R³ está seleccionado de hidrógeno, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alcoxi C₁₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, haloalquilo C₁₋₆ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, OR¹⁰, C(=X¹)R¹⁰, C(=X¹)OR¹⁰, C(=X¹)N(R¹⁰)₂, N(R¹⁰)₂, N(R¹⁰)C(=X¹)R¹⁰, SR¹⁰, S(O)ₙOR¹⁰ o R¹⁰S(O)ₙR¹⁰, en donde cada uno de dichos R³, cuando están sustituidos, tiene uno o varios sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquil C₁₋₆-oxi, haloalquenil C₂₋₆-oxi, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR¹⁰, S(O)ₙOR¹⁰, arilo C₆₋₂₀ o heterociclilo C₁₋₂₀, (cada uno de los cuales que puede estar sustituido, puede estar opcionalmente sustituido con R¹⁰); (c) R⁵ está seleccionado de H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alcoxi C₁₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, OR¹⁰, C(=X¹)R¹⁰, C(=X¹)OR¹⁰, C(=X¹)N(R¹⁰)₂, N(R¹⁰)₂, N(R¹⁰)C(=X¹)R¹⁰, SR¹⁰, S(O)ₙOR¹⁰ o R¹⁰S(O)ₙR¹⁰, en donde cada uno de dichos R⁵, cuando están sustituidos, tiene uno o varios sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquil C₁₋₆-oxi, haloalquenil C₂₋₆-oxi, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR¹⁰, S(O)ₙOR¹⁰, arilo C₆₋₂₀ o heterociclilo C₁₋₂₀, (cada uno de los cuales que puede estar sustituido, puede estar opcionalmente sustituido con R¹⁰); (d) R⁶ es H, F, Cl, Br, I, alquilo C₁₋₆ sustituido o no sustituido o haloalquilo C₁₋₆, en donde cada uno de dichos R⁶, cuando están sustituidos, tiene uno o varios sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquil, C₁₋₆-oxi, haloalquenil C₂₋₆-oxi, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀ o halocicloalquenilo C₃₋₁₀; (e) R⁷ está seleccionado de hidrógeno, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alquinilo C₂₋₆ sustituido o no sustituido, alcoxi C₁₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, alquil C₁₋₆-alquinilo C₂₋₆ en donde el alquilo y el alquinilo está sustituido o no sustituido de modo independiente, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, alquil C₁₋₆-arilo C₆₋₂₀, en donde el alquilo y el arilo están sustituidos o no sustituidos de modo independiente), alquil C₁₋₆-(ciclohaloalquilo C₃₋₁₀) en donde el alquilo y el ciclohaloalquilo están sustituidos o no sustituidos de modo independiente o alquil C₁₋₆-(cicloalquilo C₃₋₁₀) en donde el alquilo y el cicloalquilo están sustituidos o no sustituidos de modo independiente, en donde cada uno de dichos R⁷, cuando están sustituidos, tiene uno o varios sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, C₂₋₆ alquinil haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquil C₁₋₆-oxi, haloalquenil C₂₋₆-oxi, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR¹⁰, S(O)ₙOR¹⁰, arilo C₆₋₂₀ o heterociclilo C₁₋₂₀, R¹⁰-arilo, (cada uno de los cuales que puede estar sustituido, puede estar opcionalmente sustituido con R¹⁰); (f) R⁸ está seleccionado de alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alcoxi C₁₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, halocicloalquilo C₃₋₁₀ sustituido o no sustituido cicloalquenilo C₃₋₁₀ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido o heterociclilo C₁₋₂₀ sustituido o no sustituido, en donde cada uno de dichos R⁸, cuando están sustituidos, tiene uno o varios sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, haloalquilo C₁₋₆ sustituido o no sustituido, haloalquenilo C₂₋₆ sustituido o no sustituido, haloalquil C₁₋₆-oxi sustituido o no: sustituido, haloalquenil C₂₋₆-oxi sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, halocicloalquilo C₃₋₁₀ sustituido o no sustituido, halocicloalquenilo C₃₋₁₀ sustituido o no sustituido, oxo, OR¹⁰, S(O)ₙR¹⁰, arilo C₆₋₂₀ sustituido o no sustituido o heterociclilo C₁₋₂₀ sustituido o no sustituido, (cada uno de los cuales, cuando están sustituidos, está sustituido con R¹⁰); (g) L está seleccionado de a bond, R⁹, O, S, N(R⁹), N(R⁹)C(=X¹), C(R⁹)₂, o C(R⁹)(R¹¹); (h) Lₐ está seleccionado de R⁹, OR⁹, N(R⁹)₂, N(R⁹)(R¹¹), N(R⁹)(OR¹¹), N(R⁹)C(=X¹)R⁹, N(R⁹)C(=X¹)(R¹¹), C(R⁹)₃, C(R⁹)(R¹¹)(R¹²) o SR⁹; opcionalmente L y Lₐ, están conectados en una disposición cíclica, que forma heterociclos o carbociclos de 3 - 8 miembros que incluyen L y Lₐ, en donde la disposición cíclica no contiene ninguno o contiene al menos uno de heteroátomos de O, S o N y la disposición cíclica no está sustituida o está sustituida, en donde, cuando están sustituidos, la disposición cíclica tiene uno o varios sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alquinilo C₂₋₆ sustituido o no sustituido, haloalquilo C₁₋₆ sustituido o no sustituido, haloalquenilo C₂₋₆ sustituido o no sustituido, haloalquil C₁₋₆-oxi sustituido o no sustituido, haloalquenil C₂₋₆-oxi sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, halocicloalquilo
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KR20160077113A (ko) 2016-07-01
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US9295260B2 (en) 2016-03-29
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US20160208281A1 (en) 2016-07-21
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