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AR105544A1 - Compuestos de n-carboxamida cíclica útiles como herbicidas - Google Patents

Compuestos de n-carboxamida cíclica útiles como herbicidas

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Publication number
AR105544A1
AR105544A1 ARP160102329A ARP160102329A AR105544A1 AR 105544 A1 AR105544 A1 AR 105544A1 AR P160102329 A ARP160102329 A AR P160102329A AR P160102329 A ARP160102329 A AR P160102329A AR 105544 A1 AR105544 A1 AR 105544A1
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AR
Argentina
Prior art keywords
ring
independently
ring members
alkyl
alkoxy
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ARP160102329A
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English (en)
Inventor
Duncan Satterfield Andrew
Original Assignee
Du Pont
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Publication of AR105544A1 publication Critical patent/AR105544A1/es

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    • 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/38Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2632-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/272-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • C07D233/38One oxygen atom with acyl radicals or hetero atoms directly attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/18Oxygen atoms
    • C07D263/20Oxygen atoms attached in position 2
    • C07D263/26Oxygen atoms attached in position 2 with hetero atoms or acyl radicals directly attached to the ring nitrogen atom

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pyrrole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Reivindicación 1: Un compuesto seleccionado de la fórmula (1), N-óxidos y sales de estos, en donde: Q¹ es un anillo fenilo o un sistema de anillo naftalenilo; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁶; o un anillo heterocíclico de 4 a 7 miembros o un sistema de anillo bicíclico de 8 a 10 miembros, cada anillo o sistema de anillo que contiene miembros de anillo seleccionados de átomos de carbono y de 1 a 4 heteroátomos seleccionados, independientemente, de hasta 2 átomos de O, hasta 2 átomos de S y hasta 4 átomos de N, en donde hasta 3 miembros de anillo que son carbono se seleccionan, independientemente, de C(=O) y C(=S), y los miembros de anillo que son átomos de azufre se seleccionan, independientemente, de S(=O)ᵘ(=NR⁷)ᵛ; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁶ en miembros de anillo que son átomos de carbono y seleccionados de R⁸ en miembros de anillo que son átomos de nitrógeno; Q² es un anillo fenilo o un sistema de anillo naftalenilo; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁹; o un anillo heterocíclico de 4 a 7 miembros o un sistema de anillo bicíclico de 8 a 10 miembros, cada anillo o sistema de anillo que contiene miembros de anillo seleccionados de átomos de carbono y de 1 a 4 heteroátomos seleccionados, independientemente, de hasta 2 átomos de O, hasta 2 átomos de S y hasta 4 átomos de N, en donde hasta 3 miembros de anillo que son carbono se seleccionan, independientemente, de C(=O) y C(=S), y los miembros de anillo que son átomos de azufre se seleccionan, independientemente, de S(=O)ᵘ(=NR⁷)ᵛ; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁹ en miembros de anillo que son átomos de carbono y seleccionados de R¹⁰ en miembros de anillo que son átomos de nitrógeno; J es -CR²R³- o -CR²R³-CR²ᵃR³ᵃ- (en donde el enlace que se proyecta a la izquierda se conecta a G); G es -O-, -N(R¹)- o -C(R¹⁸)(R¹⁹)-; Y¹ es O, S o NR¹¹; Y² es O ó S; R¹ es H, hidroxi, amino, ciano, formilo, alquilcarbonilalquilo C₃₋₈, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆, cianoalquilo C₂₋₆, cicloalquilo C₃₋₆, cicloalquilalquilo C₄₋₈, alcoxialquilo C₂₋₈, haloalcoxialquilo C₂₋₈, haloalquenilalquilo C₂₋₈, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, cicloalquilcarbonilalquilo C₅₋₁₀, haloalcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, cicloalquilaminocarbonilo C₄₋₁₀, alcoxi C₁₋₆, alquiltio C₁₋₆, haloalquiltio C₁₋₆, cicloalquiltio C₃₋₈, alquilsulfinilo C₁₋₆, haloalquilsulfinilo C₁₋₆, cicloalquilsulfinilo C₃₋₈, alquilsulfonilo C₁₋₆, haloalquilsulfonilo C₁₋₆, cicloalquilsulfonilo C₃₋₈, alquilaminosulfonilo C₁₋₆, dialquilaminosulfonilo C₂₋₈ o trialquilsililo C₃₋₁₀; o Q³; o -W¹Q³; R² y R³ son, cada uno, independientemente, H, halógeno, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄ o alcoxi C₁₋₄; R²ᵃ y R³ᵃ son, cada uno, independientemente, H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆ o alcoxi C₁₋₆; R⁴ es H, halógeno, hidroxi, alcoxi C₁₋₄, haloalquilo C₁₋₄ o alquilo C₁₋₄; R⁵ es H, hidroxi, amino, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆, alcoxialquilo C₂₋₈, haloalcoxialquilo C₂₋₈, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, alcoxicarbonilo C₂₋₈, haloalcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, cicloalquilaminocarbonilo C₄₋₁₀, alcoxi C₁₋₆, alquiltio C₁₋₆, haloalquiltio C₁₋₆, cicloalquiltio C₃₋₈, alquilsulfinilo C₁₋₆, haloalquilsulfinilo C₁₋₆, cicloalquilsulfinilo C₃₋₈, alquilsulfonilo C₁₋₆, haloalquilsulfonilo C₁₋₆, cicloalquilsulfonilo C₃₋₈; alquilaminosulfonilo C₁₋₆, dialquilaminosulfonilo C₂₋₈ o trialquilsililo C₃₋₁₀; o Q⁴; o -W²Q⁴; cada R⁶ y R⁹ es, independientemente, halógeno, hidroxi, ciano, nitro, amino, alquilo C₁₋₈, cianoalquilo C₁₋₈, cianoalcoxi C₁₋₈, haloalquilo C₁₋₈, nitroalquilo C₁₋₈, alquenilo C₂₋₈, haloalquenilo C₂₋₈, nitroalquenilo C₂₋₈, alquinilo C₂₋₈, haloalquinilo C₂₋₈, alcoxialquilo C₂₋₈, alcoxialcoxialquilo C₃₋₈, haloalcoxialquilo C₂₋₈, haloalcoxihaloalcoxi C₂₋₈, cicloalquilalquilo C₄₋₁₀, halocicloalquilalquilo C₄₋₁₀, alquilcicloalquilalquilo C₅₋₁₂, cicloalquilalquenilo C₅₋₁₂, cicloalquilalquinilo C₅₋₁₂, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈, alquilcicloalquilo C₄₋₁₀, cicloalquilcicloalquilo C₆₋₁₂, cicloalquenilo C₃₋₈, halocicloalquenilo C₃₋₈, haloalcoxialcoxi C₂₋₈, alcoxialcoxi C₂₋₈, cicloalcoxialquilo C₄₋₁₀, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alquilamino C₂₋₈, dialquilamino C₂₋₈, halodialquilamino C₂₋₈, alquilaminoalquilo C₂₋₈, haloalquilaminoalquilo C₂₋₈, cicloalquilaminoalquilo C₄₋₁₀, dialquilaminoalquilo C₃₋₁₀, -CHO, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, -C(=O)OH, alcoxicarbonilo C₂₋₈, haloalcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, cicloalquilalcoxicarbonilo C₅₋₁₂, -C(=O)NH₂, alquilaminocarbonilo C₂₋₈, cicloalquilaminocarbonilo C₄₋₁₀, dialquilaminocarbonilo C₃₋₁₀, alcoxi C₁₋₈, haloalcoxi C₁₋₈, alcoxialcoxi C₂₋₈, alqueniloxi C₂₋₈, haloalqueniloxi C₂₋₈, alquiniloxi C₃₋₈, haloalquiniloxi C₃₋₈, cicloalcoxi C₃₋₈, halocicloalcoxi C₃₋₈, cicloalquilalcoxi C₄₋₁₀, alquilcarbonilalcoxi C₃₋₁₀, alquilcarboniloxi C₂₋₈, haloalquilcarboniloxi C₂₋₈, cicloalquilcarboniloxi C₄₋₁₀, alquilsulfoniloxi C₁₋₈, haloalquilsulfoniloxi C₁₋₈, alquiltio C₁₋₈, haloalquiltio C₁₋₈, cicloalquiltio C₃₋₈, alquilsulfinilo C₁₋₈, haloalquilsulfinilo C₁₋₈, alquilsulfonilo C₁₋₈, haloalquilsulfonilo C₁₋₈, cicloalquilsulfonilo C₃₋₈, formilamino, alquilcarbonilamino C₂₋₈, haloalquilcarbonilamino C₂₋₈, cicloalquilamino C₃₋₈, alcoxicarbonilamino C₂₋₈, alquilsulfonilamino C₁₋₆, haloalquilsulfonilamino C₁₋₆, -SF₅, -SCN, SO₂NH₂, trialquilsililo C₃₋₁₂, trialquilsililalquilo C₄₋₁₂ o trialquilsililalcoxi C₄₋₁₂; o Q⁵; o -W³Q⁵; cada R⁷ es, independientemente, H, ciano, alquilcarbonilo C₂₋₃ o haloalquilcarbonilo C₂₋₃; cada R⁸ y R¹⁰ es, independientemente, ciano, alquilo C₁₋₃, alquenilo C₂₋₃, alquinilo C₂₋₃, cicloalquilo C₃₋₆, alcoxialquilo C₂₋₃, alcoxilo C₁₋₃, alquilcarbonilo C₂₋₃, alcoxicarbonilo C₂₋₃, alquilaminoalquilo C₂₋₃ o dialquilaminoalquilo C₃₋₄; cada R¹¹ es, independientemente, H, ciano, hidroxi, CHO, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄, alquilcarbonilo C₂₋₆, haloalquilcarbonilo C₂₋₆, -(C=O)CH₃ o -(C=O)CF₃; W¹ es -O-, -OS(=O)₂-, -C(=O)-, alcanodiilo C₁₋₃, alquenodiilo C₂₋₃, alquinodiilo C₂₋₃, -C(=O)(alquilo C₁₋₃)-, -C(=O)(alquenilo C₂₋₃)-, -C(=O)(alquinilo C₁₋₄)-; W² es -O-, -OS(=O)₂-, -C(=O)- o alcanodiilo C₁₋₃; W³ es -O-, -OS(=O)₂-, -C(=O)- o alcanodiilo C₁₋₃; cada Q³ es fenilo de -CPh=N-O(alquilo C₁₋₄) sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹²; o un anillo heteroaromático de 5 ó 6 miembros, cada uno sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹² y en miembros de anillo que son nitrógeno con hasta 2 sustituyentes seleccionados, independientemente, de R¹⁵; cada Q⁴ es fenilo sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹³; o un anillo heteroaromático de 5 ó 6 miembros, cada uno sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹³ y en miembros de anillo que son nitrógeno con hasta 2 sustituyentes seleccionados, independientemente, de R¹⁶; cada Q⁵ es fenilo sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹⁴; o un anillo heteroaromático de 5 ó 6 miembros, cada uno sustituido opcionalmente en miembros de anillo que son carbono con hasta 5 sustituyentes seleccionados, independientemente, de R¹⁴ y en miembros de anillo que son nitrógeno con hasta 2 sustituyentes seleccionados, independientemente, de R¹⁷; cada R¹², R¹³ y R¹⁴ es, independientemente, halógeno, ciano, hidroxi, amino, nitro, -CHO, -C(=O)OH, -C(=O)NH₂, -SO₂NH₂, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, alcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, cicloalquilalcoxicarbonilo C₅₋₁₂, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquilcarboniloxi C₂₋₈, alquiltio C₁₋₆, haloalquiltio C₁₋₆, alquilsulfinilo C₁₋₆, haloalquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, haloalquilsulfonilo C₁₋₆, alquilaminosulfonilo C₁₋₆, dialquilaminosulfonilo C₂₋₈, trialquilsililo C₃₋₁₀, alquilamino C₁₋₆, dialquilamino C₂₋₈, alquilcarbonilamino C₂₋₈, alquilsulfonilamino C₁₋₆, fenilo, piridinilo o tienilo; cada R¹⁵, R¹⁶ y R¹⁷ es, independientemente, H o alquilo C₁₋₆; cada R¹⁸ y R¹⁹ es, independientemente, H, halógeno, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄ o alcoxi C₁₋₄; y cada u y v es, independientemente, 0, 1 ó 2 en cada instancia de S(=O)ᵘ(=NR⁷)ᵛ, siempre que la suma de u y v sea 0, 1 ó 2; siempre que cuando Q¹ sea un anillo fenilo sustituido por R⁶ en la posición 4, G sea -C(R¹⁸)(R¹⁹)-, Y¹ sea O, Y² sea O, J sea -CR²R³-, R² sea H, R³ sea H, R⁴ sea H, R⁵ sea H, R⁶ sea Cl, R¹⁸ sea H y R¹⁹ sea H, entonces Q² es distinto de 2-fluorofenilo; y siempre que el compuesto de la fórmula (1) sea distinto de trans-N-(3-clorofenil)-5-(1-metiletil)-2-oxo-4-fenil-3-oxazolidinacarboxamida (CA núm. 158323-70-7), 2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-N-fenil-1-pirrolidincarboxamida (CA núm. 182815-19-6), N-(4-clorofenil)-2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-1-pirrolidincarboxamida (CA núm. 182815-21-0), N-(3,4-diclorofenil)-2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-1-pirrolidincarboxamida (CA núm. 182815-22-1), 2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-N-[3-(trifluorometil)fenil]-1-pirrolidincarboxamida (CA núm. 182815-23-2) o 2-oxo-N,6-difenil-1-piperidincarboxamida (CA núm. 111422-82-3).
ARP160102329A 2015-07-31 2016-07-29 Compuestos de n-carboxamida cíclica útiles como herbicidas AR105544A1 (es)

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EP (1) EP3328836B1 (es)
JP (1) JP6937290B2 (es)
CN (1) CN108137512B (es)
AR (1) AR105544A1 (es)
AU (1) AU2016303209B2 (es)
BR (1) BR112018001964B1 (es)
CA (1) CA2993000C (es)
RU (1) RU2720994C2 (es)
WO (1) WO2017023515A1 (es)

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US11589583B2 (en) 2013-12-03 2023-02-28 Fmc Corporation Pyrrolidinones herbicides
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