AR094169A1 - Compuestos y composiciones pesticidas y procesos relacionados con las mismas - Google Patents

Compuestos y composiciones pesticidas y procesos relacionados con las mismas

Info

Publication number
AR094169A1
AR094169A1 ARP130104897A ARP130104897A AR094169A1 AR 094169 A1 AR094169 A1 AR 094169A1 AR P130104897 A ARP130104897 A AR P130104897A AR P130104897 A ARP130104897 A AR P130104897A AR 094169 A1 AR094169 A1 AR 094169A1
Authority
AR
Argentina
Prior art keywords
alkyl
substituted
haloalkyl
alkoxy
substituents selected
Prior art date
Application number
ARP130104897A
Other languages
English (en)
Inventor
C Lo William
E Hunter James
B Watson Gerald
Patny Akshay
S Iyer Pravin
Boruwa Joshodeep
Original Assignee
Dow Agrosciences Llc
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 Dow Agrosciences Llc filed Critical Dow Agrosciences Llc
Publication of AR094169A1 publication Critical patent/AR094169A1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
    • C07C63/68—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings containing halogen
    • C07C63/70—Monocarboxylic 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
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
    • 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
    • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/02—Amines; Quaternary ammonium compounds
    • A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
    • 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
    • A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
    • 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
    • A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
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    • A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
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    • A01N37/34—Nitriles
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    • 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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    • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/10—Sulfones; Sulfoxides
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    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Reivindicación 1: Una composición que contiene una molécula de acuerdo con la fórmula {1} en la que: (a) R¹ está seleccionada desde (1) H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, S-alquilo C₁₋₈, S(haloalquilo C₁₋₈), S(O)alquilo C₁₋₈, S(O)(haloalquilo C₁₋₈), S(O)₂alquilo C₁₋₈, S(O)₂(haloalquilo C₁₋₈), N(R¹⁴)(R¹⁵), (2) alquilo C₁₋₈ substituido, en donde dicho alquilo C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, (3) haloalquil C₁₋₈arilo substituido, en donde dicho haloalquil C₁₋₈arilo substituido, tiene uno o más sustituyentes seleccionados desde CN y NO₂, (4) alcoxi C₁₋₈ substituido, en donde dicho alcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, y (5) haloalcoxi C₁₋₈ substituido, en donde dicho haloalcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂; (b) R² está seleccionada desde (1) H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, S-alquilo C₁₋₈, S(haloalquilo C₁₋₈), S(O)alquilo C₁₋₈, S(O)(haloalquilo C₁₋₈), S(O)₂alquilo C₁₋₈, S(O)₂(haloalquilo C₁₋₈), N(R¹⁴)(R¹⁵), (2) alquilo C₁₋₈ substituido, en donde dicho alquilo C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, (3) haloalquil C₁₋₈arilo substituido, en donde dicho haloalquil C₁₋₈arilo substituido, tiene uno o más sustituyentes seleccionados desde CN y NO₂, (4) alcoxi C₁₋₈ substituido, en donde dicho alcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, y (5) halo alcoxi C₁₋₈ substituido, en donde dicho haloalcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂; (c) R³ está seleccionada desde (1) H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, S-alquilo C₁₋₈, S(haloalquilo C₁₋₈), S(O)alquilo C₁₋₈, S(O)(haloalquilo C₁₋₈), S(O)₂alquilo C₁₋₈, S(O)₂(haloalquilo C₁₋₈), N(R¹⁴)(R¹⁵), (2) alquilo C₁₋₈ substituido, en donde dicho alquilo C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, (3) haloalquil C₁₋₈arilo substituido, en donde dicho haloalquil C₁₋₈arilo substituido, tiene uno o más sustituyentes seleccionados desde CN y NO₂, (4) alcoxi C₁₋₈ substituido, en donde dicho alcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, y (5) haloalcoxi C₁₋₈ substituido, en donde dicho haloalcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂; (d) R⁴ está seleccionada desde (1) H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, S-alquilo C₁₋₈, S(haloalquilo C₁₋₈), S(O)alquilo C₁₋₈, S(O)(haloalquilo C₁₋₈), S(O)₂alquilo C₁₋₈, S(O)₂(haloalquilo C₁₋₈), N(R¹⁴)(R¹⁵), (2) alquilo C₁₋₈ substituido, en donde dicho alquilo C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, (3) haloalquil C₁₋₈arilo substituido, en dond dicho haloalquil C₁₋₈arilo substituido, tiene uno o más sustituyentes seleccionados desde CN y NO₂, (4) alcoxi C₁₋₈ substituido, en donde dicho alcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, y (5) haloalcoxi C₁₋₈ substituido, en donde dicho haloalcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂; (e) R⁵ está seleccionada desde (1) H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, S-alquilo C₁₋₈, S(haloalquilo C₁₋₈), S(O)alquilo C₁₋₈, S(O)(haloalquilo C₁₋₈), S(O)₂alquilo C₁₋₈, S(O)₂(haloalquilo C₁₋₈), N(R¹⁴)(R¹⁵), (2) alquilo C₁₋₈ substituido, en donde dicho alquilo C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, (3) haloalquil C₁₋₈arilo substituido, en donde dicho haloalquil C₁₋₈arilo substituido, tiene uno o más sustituyentes seleccionados desde CN y NO₂, (4) alcoxi C₁₋₈ substituido, en donde dicho alcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂, y (5) haloalcoxi C₁₋₈ substituido, en donde dicho haloalcoxi C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde CN y NO₂; (f) R⁶ es a haloalquil C₁₋₈; (g) R⁷ está seleccionada desde H, F, Cl, Br, I, OH, alcoxi C₁₋₈, y haloalcoxi C₁₋₈; (h) R⁸ está seleccionada desde H, alquilo C₁₋₈, haloalquilo C₁₋₈, OR¹⁴, y N(R¹⁴)(R¹⁵); (i) R⁹ está seleccionada desde H, F, Cl, Br, I, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, OR¹⁴, y N(R¹⁴)(R¹⁵); (j) R¹⁰ está seleccionada desde (1) H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, cicloalquilo C₃₋₆, S-alquilo C₁₋₈, S(haloalquilo C₁₋₈), S(O)alquilo C₁₋₈, S(O)(haloalquilo C₁₋₈), S(O)₂alquilo C₁₋₈, S(O)₂(haloalquilo C₁₋₈), NR¹⁴R¹⁵ C(=O)H, C(=O)N(R¹⁴)(R¹⁵), CN(R¹⁴)(R¹⁵)(=NOH), (C=O)O-alquilo C₁₋₈, (C=O)OH, heterociclilo, alquenilo C₂₋₈, haloalquenilo C₂₋₈, alquinilo C₂₋₈, (2) alquilo C₁₋₈ substituido, en donde dicho alquilo C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde OH, alcoxi C₁₋₈, S-alquilo C₁₋₈, S(O)alquilo C₁₋₈, S(O)₂alquilo C₁₋₈, NR¹⁴R¹⁵, y (3) haloalquil C₁₋₈arilo substituido, en donde dicho haloalquil C₁₋₈arilo substituido, tiene uno o más sustituyentes seleccionados desde alcoxi C₁₋₈, S-alquilo C₁₋₈, S(O)alquilo C₁₋₈, S(O)₂alquilo C₁₋₈, y N(R¹⁴)(R¹⁵); (k) R¹¹ es C(=X⁵)N(H)(alquil C₀₋₈)N(R¹¹ᵃ)(C(=X⁵)(R¹¹ᵇ)) en donde cada X⁵ está independientemente seleccionada desde O ó S, y en donde cada R¹¹ᵃ está independientemente seleccionada desde H, alquilo C₁₋₈, alquilo C₁₋₈ substituido, haloalquilo C₁₋₈, haloalquil C₁₋₈arilo substituido, cicloalquilo C₃₋₈, y cicloalquilo C₃₋₈ substituido, en donde cada una de dicho alquilo C₁₋₈ substituido tiene uno o más sustituyentes seleccionados desde F, Cl, Br, I, CN, NO₂, OC(=O)H, OH, S-alquilo C₁₋₈, S(O)alquilo C₁₋₈, S(O)₂alquilo C₁₋₈, OS(O)₂arilo, N(alquil C₁₋₈)₂ (en donde cada alquilo C₁₋₈ es independientemente seleccionado), arilo, arilo substituido, heterociclilo, heterociclilo substituido, en donde cada una de dicho arilo substituido tiene uno o más sustituyentes seleccionados desde F, Cl, Br, I, CN, NO₂, alquilo C₁₋₈, haloalquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, S-alquilo C₁₋₈, S(haloalquilo C₁₋₈), N(alquil C₁₋₈)₂ (en donde cada alquilo C₁₋₈ es independientemente seleccionado), y oxo, en donde cada una de dicho heterociclilo substit
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TWI667224B (zh) * 2014-06-09 2019-08-01 美商陶氏農業科學公司 殺蟲組成物及與其相關之方法

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US9211280B2 (en) 2015-12-15
RU2638043C2 (ru) 2017-12-11
CN105025715A (zh) 2015-11-04
CA2894206A1 (en) 2014-06-26
NZ708823A (en) 2018-08-31
EP2934135A4 (en) 2016-08-10
HK1211426A1 (en) 2016-05-27
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US20140171311A1 (en) 2014-06-19
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