AR109140A1 - Compuestos herbicidas de pirimidina - Google Patents

Compuestos herbicidas de pirimidina

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Publication number
AR109140A1
AR109140A1 ARP170102070A ARP170102070A AR109140A1 AR 109140 A1 AR109140 A1 AR 109140A1 AR P170102070 A ARP170102070 A AR P170102070A AR P170102070 A ARP170102070 A AR P170102070A AR 109140 A1 AR109140 A1 AR 109140A1
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AR
Argentina
Prior art keywords
alkyl
carbonyl
alkoxy
amino
haloalkoxy
Prior art date
Application number
ARP170102070A
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English (en)
Original Assignee
Basf Se
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Publication date
Priority to EP16180948 priority Critical
Application filed by Basf Se filed Critical Basf Se
Publication of AR109140A1 publication Critical patent/AR109140A1/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • 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
    • A01N43/541,3-Diazines; Hydrogenated 1,3-diazines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

Reivindicación 1: Los compuestos de pirimidina caracterizados por la fórmula (1), en donde la línea punteada (- - - - -) es un enlace simple o un enlace doble; R¹ es C₁₋₆-alquilo, C₁₋₆-haloalquilo, OH-C₁₋₆-alquilo, C₃₋₆-alquenilo, C₃₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₆-alcoxi-C₁₋₆-alquilo, C₁₋₆-alcoxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₁₋₆-haloalcoxi, C₃₋₆-cicloalcoxi, C₃₋₆-halocicloalcoxi, C₃₋₆-cicloalqueniloxi, C₃₋₆-halocicloalqueniloxi, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, C₁₋₆-alquilsulfinilo, C₁₋₆-alquilsulfonilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquenilo, C₃₋₆-halocicloalquilo, C₃₋₆-halocicloalquenilo, [1-(C₁₋₆-alquil)]-C₃₋₆-cicloalquilo, [1-(C₃₋₆-alquenil)]-C₃₋₆-cicloalquilo, [1-(C₂₋₆-alquinil)]-C₃₋₆-cicloalquilo, [1-(C₁₋₆-haloalquil)]-C₃₋₆-cicloalquilo, [1-(C₃₋₆-haloalquenil)]-C₃₋₆-cicloalquilo, [1-(C₃₋₆-haloalquinil)]-C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alquilo, C₃₋₆-cicloalquil-C₁₋₆-haloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alcoxi, C₃₋₆-cicloalquil-C₁₋₆-haloalcoxi, fenilo, heteroarilo de 5 ó 6 miembros, o heterociclilo de 3 a 6 miembros; en donde los grupos cíclicos de R¹ son no sustituidos o sustituidos con Rᵃ; R² es H, halógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonil-C₁₋₆-alquilo, C₁₋₆-alcoxicarbonil-C₁₋₆-alquilo, C₁₋₆-haloalquilcarbonil-C₁₋₆-alquilo, C₁₋₆-haloalcoxicarbonil-C₁₋₆-alquilo, C₁₋₆-alquilcarbonil-C₁₋₆-haloalquilo, C₁₋₆-alcoxicarbonil-C₁₋₆-haloalquilo, C₁₋₆-haloalquilcarbonil-C₁₋₆-haloalquilo, C₁₋₆-haloalcoxicarbonil-C₁₋₆-haloalquilo, OH, C₁₋₆-alcoxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi, C₁₋₆-haloalcoxi-C₁₋₆-alcoxi, C₁₋₆-alcoxi-C₁₋₆-haloalcoxi, C₁₋₆-haloalcoxi-C₁₋₆-haloalcoxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi-C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₁₋₆-cianoalcoxi, C₁₋₆-hidroxialcoxi, C₃₋₆-alqueniloxi, C₃₋₆-alqueniloxi-C₁₋₆-alcoxi, C₃₋₆-haloalqueniloxi-C₁₋₆-haloalcoxi, C₃₋₆-alqueniloxi-C₁₋₆-haloalcoxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₃₋₆-alquiniloxi-C₁₋₆-alcoxi, C₃₋₆-haloalquiniloxi-C₁₋₆-haloalcoxi, C₃₋₆-alquiniloxi-C₁₋₆-haloalcoxi, C₃₋₆-alquiniloxi-C₃₋₆-alqueniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-alqueniloxi, C₃₋₆-alquiniloxi-C₃₋₆-haloalqueniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi-C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-alquiniloxi, C₃₋₆-alquiniloxi-C₃₋₆-haloalquiniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-haloalquiniloxi, (C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alcoxi)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alcoxi)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-halo-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alquiltio)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalquiltio)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquiltio)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalquiltio)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-halo-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)-carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, C₃₋₆-cicloalcoxi, C₃₋₆-halocicloalcoxi, (C₃₋₆-cicloalquil)C₁₋₆-alcoxi, (C₃₋₆-halocicloalquil)C₁₋₆-alcoxi, (C₃₋₆-cicloalquil)C₁₋₆-haloalcoxi, C₁₋₆-alquilcarbonilmino, [(C₁₋₆-alquil)carbonil](C₁₋₆-alquil)amino, C₁₋₆-haloalquilcarbonilamino, [(C₁₋₆-haloalquil)carbonil](C₁₋₆-alquil)amino, C₃₋₆-cicloalquilcarbonilamino, [(C₃₋₆-ciclo-alquil)carbonil](C₁₋₆-alquil)amino, fenilcarbonilamino, (fenilcarbonil)(C₁₋₆-alquil)amino, heterociclilcarbonilamino, (heterociclilcarbonil)(C₁₋₆-alquil)-amino, heteroarilcarbonilamino, (heteroarilcarbonil)(C₁₋₆-alquil)amino, [(C₁₋₆-alquil)-carbonil](C₁₋₆-alcoxi)amino, [(C₁₋₆-haloalquil)carbonil](C₁₋₆-alcoxi)amino, [(C₃₋₆-cicloalquil)carbonil](C₁₋₆-alquiloxi)amino, (fenilcarbonil)(C₁₋₆-alcoxi)-amino, (heterociclilcarbonil)(C₁₋₆-alcoxi)amino, (heteroarilcarbonil)(C₁₋₆-alcoxi)-amino, [(C₁₋₆-alquil)carbonil](C₂₋₆-alquenil)amino, [(C₁₋₆-haloalquil)carbonil](C₂₋₆-alquenil)amino, [(C₃₋₆-cicloalquil)carbonil](C₂₋₆-alquenil)amino, (fenil-carbonil)(C₂₋₆-alquenil)amino, (heterociclilcarbonil)(C₂₋₆-alquenil)amino, (heteroarilcarbonil)(C₂₋₆-alquenil)amino, [(C₁₋₆-alquil)carbonil](C₃₋₆-alquinil)amino, [(C₁₋₆-haloalquil)carbonil](C₃₋₆-alquinil)amino, [(C₃₋₆-cicloalquil)(C₃₋₆-alquinil)amino, (fenilcarbonil)(C₃₋₆-alquinil)amino, (heterociclilcarbonil)(C₃₋₆-alquinil)amino, (heteroarilcarbonil)(C₃₋₆-alquinil)amino, [(C₂₋₆-alquenil)carbonil]-amino, [(C₂₋₆-alquenil)carbonil](C₁₋₆-alquil)amino, [(C₂₋₆-alquenil)carbonil](C₁₋₆-alcoxi)amino, [(C₃₋₆-alquinil)carbonil]amino, [(C₃₋₆-alquinil)carbonil](C₁₋₆-alquil)amino, [(C₃₋₆-alquinil)carbonil](C₁₋₆-alcoxi)amino, [di(C₁₋₆-alquil)amino]carbonilamino, [di(C₁₋₆-alquil)aminocarbonil](C₁₋₆-alquil)amino, [di(C₁₋₆-alquil)aminocarbonil](C₁₋₆-alcoxi)amino, aminocarbonil-C₁₋₆-alcoxi, (C₃₋₆-halocicloalquil)C₁₋₆-haloalcoxi, aminocarbonil-C₁₋₆-haloalcoxi, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alcoxi, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalcoxi, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alcoxi, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalcoxi, (difenil)C=N-O, (C₁₋₆-alquil)(fenil)C=N-O, [di(C₁₋₆-alquil)]C=N-O, (C₁₋₆-alquil)₃-silil-C₁₋₆-alcoxi, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, C₁₋₆-alcoxi-C₁₋₆-alquiltio, C₁₋₆-haloalcoxi-C₁₋₆-alquiltio, C₁₋₆-alcoxi-C₁₋₆-haloalquiltio, C₁₋₆-haloalcoxi-C₁₋₆-haloalquiltio, C₁₋₆-alcoxi-C₁₋₆-alcoxi-C₁₋₆-alquiltio, C₁₋₆-cianoalquiltio, C₃₋₆-alqueniltio, C₃₋₆-haloalqueniltio, C₃₋₆-alqueniloxi-C₁₋₆-alquiltio, C₃₋₆-haloalqueniloxi-C₁₋₆-alquiltio, C₃₋₆-alqueniloxi-C₁₋₆-haloalquiltio, C₃₋₆-haloalqueniloxi-C₁₋₆-haloalquiltio, C₃₋₆-alquiniltio, C₃₋₆-haloalquiniltio, C₃₋₆-alquiniloxi-C₁₋₆-alquiltio, C₃₋₆-haloalquiniloxi-C₁₋₆-haloalquiltio, C₃₋₆-alquiniloxi-C₁₋₆-haloalquiltio, C₃₋₆-alquiniloxi-C₃₋₆-alqueniltio, C₃₋₆-haloalquiniloxi-C₃₋₆-alqueniltio, C₃₋₆-alquiniloxi-C₃₋₆-haloalqueniltio, C₃₋₆-haloalquiniloxi-C₃₋₆-haloalqueniltio, C₃₋₆-alquiniloxi-C₂₋₆-alquiniltio, C₃₋₆-haloalquiniloxi-C₃₋₆-alquiniltio, C₃₋₆-alquiniloxi-C₃₋₆-haloalquiniltio, C₃₋₆-haloalquiniloxi-C₃₋₆-haloalquiniltio, (C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alcoxi)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alcoxi)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alquiltio)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalquiltio)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquiltio)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquiltio)carbonil-C₁₋₆-haloalquiltio (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, C₃₋₆-cicloalquiltio, C₃₋₆-halocicloalquiltio, (C₃₋₆-cicloalquil)C₁₋₆-alquiltio, (C₃₋₆-cicloalquil)C₁₋₆-haloalquiltio, (C₃₋₆-halocicloalquil)C₁₋₆ alquiltio, (C₃₋₆-halocicloalquil)C₁₋₆-haloalquiltio, aminocarbonil-C₁₋₆-alquiltio, aminocarbonil-C₁₋₆-haloalquiltio, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alquiltio, N-(C₁₋₆-haloalquil)-aminocarbonil-C₁₋₆-alquiltio, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalquiltio, N-(C₁₋₆-haloalquil)-aminocarbonil-C₁₋₆-haloalquiltio, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alquiltio, N,N-di(C₁₋₆-haloalquil)-aminocarbonil-C₁₋₆-alquiltio, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalquiltio, N,N-di(C₁₋₆-haloalquil)-aminocarbonil-C₁₋₆-haloalquiltio, NH₂, (C₁₋₆-alquil)amino, hidroxiamino, (C₁₋₆-alcoxi)amino, (C₃₋₆-cicloalcoxi)amino, (C₁₋₆-alquil)sulfinilamino, (C₁₋₆-alquil)sulfonilamino, (amino)sulfinilamino, [(C₁₋₆-alquil)amino]sulfinilamino, (amino)sulfonilamino, [(C₁₋₆-alquil)amino]sulfonilamino, [di(C₁₋₆-alquil)amino]sulfonilamino, di(C₁₋₆-alquil)amino, (hidroxi)(C₁₋₆-alquil)amino, (hidroxi)(C₁₋₆-cicloalquil)amino, (C₁₋₆-alcoxi)(C₁₋₆-alquil)amino, (C₁₋₆-alcoxi)(C₃₋₆-cicloalquil)amino, (C₃₋₆-cicloalcoxi)(C₁₋₆-alquil)amino, (C₃₋₆-cicloalcoxi)(C₃₋₆-cicloalquil)amino, [(C₁₋₆-alquil)sulfinil](C₁₋₆-alquil)amino, [(C₁₋₆-alquil)sulfonil](C₁₋₆-alquil)amino, [di(C₁₋₆-alquil)amino]sulfinilamino, [di(C₁₋₆-alquil)amino]sulfonilamino, feniloxi, fenil-C₁₋₆-alcoxi, feniltio, fenil-C₁₋₆-alquiltio, fenilamino, (C₁₋₆-alquil)(fenil)amino, (heteroaril)oxi, heteroaril-C₁₋₆-alcoxi (heterociclil)oxi o heterociclil-C₁₋₆-alcoxi; en donde los grupos cíclicos de R² son no sustituidos o sustituidos con Rᵃ; A es CR³ o NR³A; Z es un anillo de heteroarilo de 5 ó 6 miembros que comprende A; R³ es halógeno, CN, NO₂, CHO, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonilo, C₃₋₆-alquenilo, C₃₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi, hidroxicarbonilo, C₁₋₆-alcoxicarbonilo, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, NH₂, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, (C₁₋₆-alquil)sulfinilo, (C₁₋₆-alquil)sulfonilo, C₃₋₆-cicloalquilo, (C₃₋₆-cicloalquil)oxi o fenilo; en donde los grupos cíclicos de R³ son no sustituidos o sustituidos con sustituyentes Rᵃ; R³A es H, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonilo, C₃₋₆-alquenilo, C₃₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi, hidroxicarbonilo, C₁₋₆-alcoxicarbonilo, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, NH₂, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, (C₁₋₆-alquil)sulfinilo, (C₁₋₆-alquil)sulfonilo, C₃₋₆-cicloalquilo, (C₃₋₆-cicloalquil)oxi o fenilo; en donde los grupos cíclicos de R³A son no sustituidos o sustituidos con Rᵃ; R⁴ es halógeno, CN, NO₂, CHO, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquil-carbonilo, C₃₋₆-alquenilo, C₃₋₆-haloalquenilo, C₃₋₆-alquenilo, C₃₋₆-haloalquenilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi, hidroxicarbonilo, C₁₋₆-alcoxicarbonilo, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, NH₂, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, (C₁₋₆-alquil)sulfinilo, [C₁₋₆-alquil)sulfonilo, C₃₋₆-cicloalquilo, (C₃₋₆-cicloalquil)oxi o fenilo; en donde los grupos cíclicos de R⁴ son no sustituidos o sustituidos con Rᵃ; Rᵃ es halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi o C₁₋₆-haloalcoxi; m es 0, 1, 2 ó 3; y derivados o sales aceptables en la agricultura de los compuestos de la fórmula (1) que tienen una funcionalidad ácida.
ARP170102070A 2016-07-25 2017-07-24 Compuestos herbicidas de pirimidina AR109140A1 (es)

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