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AR088534A1 - Composiciones plaguicidas y procesos relacionados con dichas composiciones - Google Patents

Composiciones plaguicidas y procesos relacionados con dichas composiciones

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AR088534A1
AR088534A1 ARP120104003A ARP120104003A AR088534A1 AR 088534 A1 AR088534 A1 AR 088534A1 AR P120104003 A ARP120104003 A AR P120104003A AR P120104003 A ARP120104003 A AR P120104003A AR 088534 A1 AR088534 A1 AR 088534A1
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Argentina
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substituted
unsubstituted
alkyl
alkenyl
nor9
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Dow Agrosciences Llc
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    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01MCATCHING, TRAPPING OR SCARING OF ANIMALS; APPARATUS FOR THE DESTRUCTION OF NOXIOUS ANIMALS OR NOXIOUS PLANTS
    • A01M1/00Stationary means for catching or killing insects
    • A01M1/20Poisoning, narcotising, or burning insects
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    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
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    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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    • A01N43/781,3-Thiazoles; Hydrogenated 1,3-thiazoles
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    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, 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
    • 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
    • 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/18Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
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    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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  • Chemical & Material Sciences (AREA)
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  • Organic Chemistry (AREA)
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  • Animal Behavior & Ethology (AREA)
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  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
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Abstract

Reivindicación 1: Una composición que comprende una molécula de acuerdo con la fórmula (1) en donde: (a) A es un compuesto de formula (2) ó (3); (b) R¹ es 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, alqueniloxi C₂₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, OR⁹, C(=X¹)R⁹, C(=X¹)OR⁹, C(=X¹)N(R⁹)₂, N(R⁹)₂, N(R⁹)C(=X¹)R⁹, SR⁹, S(O)ₙOR⁹, S(O)ₙN(R⁹)₂, o R⁹S(O)ₙR⁹, en donde cada R¹, que se encuentra sustituido, posee uno o más sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquiloxi C₁₋₆, haloalqueniloxi C₂₋₆, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR⁹, S(O)ₙOR⁹, arilo C₆₋₂₀, o heterociclilo C₁₋₂₀, (cada uno de los cuales que se puede sustituir, se puede sustituir opcionalmente con R⁹); (c) R² es 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, alqueniloxi C₂₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, OR⁹, C(=X¹)R⁹, C(=X¹)OR⁹, C(X¹)N(R⁹)₂, N(R⁹)₂, N(R⁹)C(=X¹)R⁹, SR⁹, S(O)ₙOR⁹, o R⁹S(O)ₙR⁹, en donde cada R², que está sustituido, posee uno o más sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquiloxi C₁₋₆, haloalqueniloxi C₂₋₆, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR⁹, S(O)ₙOR⁹, arilo C₆₋₂₀, o heterociclilo C₁₋₂₀, (cada uno de los cuales que se puede sustituir, se puede sustituir opcionalmente con R⁹); (d) R³ es 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, alqueniloxi C₂₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, OR⁹, C(=X¹)R⁹, C(=X¹)OR⁹, C(=X¹)N(R⁹)₂, N(R⁹)₂, N(R⁹)C(=X¹)R⁹, SR⁹, S(O)ₙOR⁹, o R⁹S(O)ₙR⁹, en donde cada R³, que está sustituido, posee uno o más sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquiloxi C₁₋₆, haloalqueniloxi C₂₋₆, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR⁹, S(O)ₙOR⁹, arilo C₆₋₂₀, o heterociclilo C₁₋₂₀, (cada uno de los cuales que se puede sustituir, se puede sustituir opcionalmente con R⁹); (e) cuando A es: (i) el compuesto de fórmula (2), entonces el compuesto de fórmula (2) es: (a) un compuesto de fórmula (4) en donde R⁴ es H, 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, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, C(=X¹)R⁹, C(=X¹)OR⁹, C(=X¹)N(R⁹)₂, N(R⁹)₂, N(R⁹)C(=X¹)R⁹, S(O)ₙOR⁹, o R⁹S(O)ₙR⁹, en donde cada uno de dicho R⁴, que está sustituido, posee uno o más sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquiloxi C₁₋₈, haloalqueniloxi C₂₋₆, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR⁹, S(O)ₙOR⁹, arilo C₆₋₂₀, o heterociclilo C₁₋₂₀, (cada uno de los cuales que se puede sustituir, se puede sustituir opcionalmente con R⁹), o (b) un compuesto de fórmula (5) en donde R⁴ es un alquilo C₁₋₆; (ii) el compuesto de fórmula (3), entonces R⁴ es 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, alqueniloxi C₂₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido, heterociclilo C₁₋₂₀ sustituido o no sustituido, OR⁹, C(=X¹)R⁹, C(=X¹)OR⁹, C(=X¹)N(R⁹)₂, N(R⁹)₂, N(R⁹)C(=X¹)R⁹, SR⁹, S(O)ₙOR⁹, o R⁹S(O)ₙR⁹, en donde cada uno de dichos R⁴, que está sustituido, posee uno o más sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquiloxi C₁₋₆, haloalqueniloxi C₂₋₆, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR⁹, S(O)ₙOR⁹, arilo C₆₋₂₀, o heterociclilo C₁₋₂₀, (cada uno de los cuales que se puede sustituir, se puede sustituir opcionalmente con R⁹); (f) R⁵ es 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, alqueniloxi C₂₋₆ sustituido o no sustituido, cicloalquilo C₃₋₁₀ sustituido o no sustituido, cicloalquenilo C₃₋₁₀ sustituido o no sustituido, arilo C₆₋₂₀ sustituido o no sustituido, OR⁹, C(=X¹)R⁹, C(=X¹)OR⁹, C(=X¹)N(R⁹)₂, N(R⁹)₂, N(R⁹)C(=X¹)R⁹, SR⁹, S(O)ₙOR⁹, o R⁹S(O)ₙR⁹, en donde cada R⁵, que está sustituido, posee uno o más sustituyentes seleccionados de F, Cl, Br, I, CN, NO₂, alquilo C₁₋₆, alquenilo C₂₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquiloxi C₁₋₆, haloalqueniloxi C₂₋₆, cicloalquilo C₃₋₁₀, cicloalquenilo C₃₋₁₀, halocicloalquilo C₃₋₁₀, halocicloalquenilo C₃₋₁₀, OR⁹, S(O)ₙOR⁹, o arilo C₆₋₂₀, (cada uno de los cuales que se puede sustituir, se puede sustituir opcionalmente con R⁹); (g) (i) cuando A es de fórmula (2), entonces R⁶ es R¹¹, y (ii) cuando A es de fórmula (3), entonces R⁶ es R¹¹; (h) R⁷ es O, S, NR⁹, o NOR⁹; (i) R⁸ es alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o
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