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AR089299A1 - Uso de derivados de diamida de acido antranilico para el control de plagas en cultivos transgenicos - Google Patents

Uso de derivados de diamida de acido antranilico para el control de plagas en cultivos transgenicos

Info

Publication number
AR089299A1
AR089299A1 ARP120104791A ARP120104791A AR089299A1 AR 089299 A1 AR089299 A1 AR 089299A1 AR P120104791 A ARP120104791 A AR P120104791A AR P120104791 A ARP120104791 A AR P120104791A AR 089299 A1 AR089299 A1 AR 089299A1
Authority
AR
Argentina
Prior art keywords
alkyl
alkoxy
cycloalkyl
halogen
amino
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
ARP120104791A
Other languages
English (en)
Inventor
Dr Fischer Rdiger
Hungenberg Heike
Striegel Bill
Riniker Steven
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer CropScience AG
Bayer Intellectual Property GmbH
Original Assignee
Bayer CropScience AG
Bayer Intellectual Property GmbH
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 Bayer CropScience AG, Bayer Intellectual Property GmbH filed Critical Bayer CropScience AG
Publication of AR089299A1 publication Critical patent/AR089299A1/es
Pending legal-status Critical Current

Links

Classifications

    • 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
    • A01N43/713Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
    • 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
    • A01N43/561,2-Diazoles; Hydrogenated 1,2-diazoles
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
    • Y02A40/146Genetically Modified [GMO] plants, e.g. transgenic plants

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

Abstract

Reivindicación 1: Uso de un compuesto de la fórmula (1) en la que R¹ representa hidrógeno, amino o hidroxilo o representa alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆ o cicloalquilo C₃₋₆ cada uno de los que está no sustituido o sustituido una o más veces con sustituyentes idénticos o diferentes seleccionables independientemente uno de otro de entre halógeno, ciano, nitro, hidroxilo, alcoxi C₁₋₄, alquiltio C₁₋₄, alquilsulfinilo C₁₋₄, alquilsulfonilo C₁₋₄, (alcoxi C₁₋₄)carbonilo, alquilamino C₁₋₄, di(alquil C₁₋₄)amino, cicloalquilamino C₃₋₆ o (alquil C₁₋₄)cicloalquilamino C₃₋₆; R² representa hidrógeno, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₄, alquilamino C₁₋₄, di(alquil C₁₋₄)amino, cicloalquilamino C₃₋₆, alcoxicarbonilo C₂₋₆ o alquilcarbonilo C₂₋₆; R³ representa hidrógeno o representa alquilo C₁₋₆, alcoxi C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆ cada uno de los que está opcionalmente sustituido una o más veces con sustituyentes idénticos o diferentes seleccionables independientemente uno de otro de entre halógeno, ciano, nitro, hidroxilo, alquilo C₁₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquiltio C₁₋₄, alquilsulfinilo C₁₋₄, alquilsulfonilo C₁₋₄, alquilsulfimino C₁₋₄, alquilsulfimino C₁₋₄-alquilo C₁₋₄, alquilsulfimino C₁₋₄-alquilcarbonilo C₂₋₅, alquilsulfoximino C₁₋₄, alquilsulfoximino C₁₋₄-alquilo C₁₋₄, alquilsulfoximino C₁₋₄-alquilcarbonilo C₂₋₅, alcoxicarbonílo C₂₋₆, alquilcarbonilo C₂₋₆ o trialquilsililo C₃₋₆, R³ además representa alquilo C₁₋₆, alcoxi C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆ cada uno de los que está opcionalmente sustituido una o más veces con sustituyentes idénticos o diferentes seleccionables independientemente uno de otro de entre amino, cicloalquilamino C₃₋₆ o un anillo heteroaromático de 5 ó 6 miembros, R³ asimismo además representa cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂-alquilo C₁₋₆ y bicicloalquilo C₄₋₁₂, siendo los sustituyentes seleccionables independientemente uno de otro de entre halógeno, ciano, nitro, hidroxilo, amino, alquilo C₁₋₆, cicloalquilo C₃₋₆, cicloalquilamino C₃₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquiltio C₁₋₄, alquilsulfinilo C₁₋₄, alquilsulfonilo C₁₋₄, alquilsulfimino C₁₋₄, alquilsulfimino C₁₋₄-alquilo C₁₋₄, alquilsulfimino C₁₋₄-alquilcarbonilo C₂₋₅, alquilsulfoximino C₁₋₄, alquilsulfoximino C₁₋₄-alquilo C₁₋₄, alquilsulfoximino C₁₋₄-alquilcarbonilo C₂₋₅, alcoxicarbonilo C₂₋₆, alquilcarbonilo C₂₋₆, trialquilsililo C₃₋₆ o un anillo heteroaromático de 5 ó 6 miembros, R² y R³ pueden unirse uno con otro a través de dos a seis átomos de carbono y formar un anillo que cuando corresponda adicionalmente contiene un átomo adicional de nitrógeno, azufre u oxígeno y cuando corresponda puede estar sustituido una a cuatro veces con alquilo C₁₋₂, halógeno, ciano, amino o alcoxi C₁₋₂, R² y R³ además juntos representan =S(alquilo C₁₋₄)₂ o =S(O)(alquilo C₁₋₄)₂; R⁴ representa hidrógeno, halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquinilo C₂₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄, SF₅, alquiltio C₁₋₄, alquilsulfinilo C₁₋₄, alquilsulfonilo C₁₋₄, haloalquiltio C₁₋₄, haloalquilsulfinilo C₁₋₄, haloalquilsulfonilo C₁₋₄, alquilamino C₁₋₄, di(alquil C₁₋₄)amino, cicloalquilamino C₃₋₆, (alcoxi C₁₋₄)imino, (alquil C₁₋₄)(alcoxi C₁₋₄)imino, (haloalquilo C₁₋₄)(alcoxi C₁₋₄)imino o trialquilsililo C₃₋₆, o dos R⁴ a través de átomos de carbono adyacentes, forman un anillo que representa -(CH₂)₃-, -(CH₂)₄-, -(CH₂)₅-, -(CH=CH-)₂-, -OCH₂O-, -O(CH₂)₂O-, -OCF₂O-, -(CF₂)₂O-, -O(CF₂)₂O-, -(CH=CH-CH=N)- o -(CH=CH-N=CH)-, dos R⁴ además, a través de átomos de carbono adyacentes, forman los siguientes anillos condensados, que cuando corresponda son sustituidos una o más veces con sustituyentes idénticos o diferentes seleccionables independientemente uno de otro de entre hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆, haloalquilo C₁₋₆, halocicloalquilo C₃₋₆, halógeno, alcoxi C₁₋₆, alquiltio C₁₋₄(alquilo C₁₋₆), alquilsulfinilo C₁₋₄(alquilo C₁₋₆), alquilsulfonilo C₁₋₄(alquilo C₁₋₆), alquilamino C₁₋₄, di(alquil C₁₋₄)amino o cicloalquilamino C₃₋₆, o un resto del grupo de fórmulas (2); n representa 0 a 3; R⁵ representa alquilo C₁₋₆, cicloalquilo C₃₋₆, haloalquilo C₁₋₆, halocicloalquilo C₁₋₆, alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquinilo C₂₋₆, haloalquinilo C₂₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquiltio C₁₋₄, alquilsulfinilo C₁₋₄, alquilsulfonilo C₁₋₄, haloalquiltio C₁₋₄, haloalquilsulfinilo C₁₋₄, haloalquilsulfonilo C₁₋₄, halógeno, ciano, nitro o trialquilsililo C₃₋₆; R⁶ representa hidrógeno, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆ o un resto de fórmula (3), R⁶ además representa cicloalcoxi C₃₋₆; R⁷ representa independientemente en cada aparición hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆, haloalquilo C₁₋₆, halógeno, ciano, nitro, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquiltio C₁₋₄ o haloalquiltio C₁₋₄; m representa 0 a 4; X representa N, CH, CF, CCI, CBr o Cl; A representa -CH₂-, -CH₂O-, -CH₂OCH₂-, -CH₂S-, -CH₂SCH₂-, -CH₂N(alquilo C₁₋₆)-, -CH₂N(alquilo C₁₋₆)CH₂-, -CH[CO₂(alquilo C₁₋₆)]-, -CH(CN)-, -CH(alquilo C₁₋₆)-, -C(di-alquilo C₁₋₆)-, -CH₂CH₂- o -C=NO(alquilo C₁₋₆)-; Q representa un anillo heteroaromático de 5 ó 6 miembros o un sistema anular heterobicíclico condensado aromático de 8, 9 ó 10 miembros, estando el sistema anular no sustituido o sustituido una o más veces con sustituyentes idénticos o diferentes seleccionables independientemente uno de otro de entre hidrógeno, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆, haloalquilo C₁₋₆, haloalquenilo C₂₋₆, haloalquinilo C₂₋₆, halocicloalquilo C₃₋₆, halógeno, CN, CO₂H, CO₂NH₂, NO₂, OH, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquiltio C₁₋₄, alquilsulfinilo C₁₋₄, alquilsulfonilo C₁₋₄, haloalquiltio C₁₋₄, haloalquilsulfinilo C₁₋₄, haloalquilsulfonilo C₁₋₄, alquilamino C₁₋₄, di(alquil C₁₋₄)amino, cicloalquilamino C₃₋₆, (alquil C₁₋₆)carbonilo, (alcoxi C₁₋₆)carbonilo, (alquil C₁₋&#x20
ARP120104791A 2011-12-19 2012-12-18 Uso de derivados de diamida de acido antranilico para el control de plagas en cultivos transgenicos Pending AR089299A1 (es)

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US (1) US9414595B2 (es)
CN (1) CN104270946B (es)
AR (1) AR089299A1 (es)
AU (1) AU2012357896B9 (es)
BR (1) BR112014015002A2 (es)
CA (1) CA2859467C (es)
IN (1) IN2014CN04325A (es)
WO (1) WO2013092519A1 (es)
ZA (1) ZA201405326B (es)

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CN106588870B (zh) * 2015-10-19 2024-02-13 海利尔药业集团股份有限公司 取代水杨酰胺类化合物及其应用
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CN113912698B (zh) * 2021-10-20 2023-07-04 河南农业大学 咖啡短体线虫Pc-CD蛋白、其编码基因及应用
CN116622760B (zh) * 2023-04-06 2024-04-23 西北农林科技大学 LuAccD基因用于调节植物脂肪酸合成和耐盐抗旱性的应用
CN116640761B (zh) * 2023-07-20 2023-09-22 隆平生物技术(海南)有限公司 转基因玉米事件lp018-1及其检测方法

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CN102057925B (zh) 2011-01-21 2013-04-10 陕西上格之路生物科学有限公司 一种含噻虫酰胺和生物源类杀虫剂的杀虫组合物

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CA2859467A1 (en) 2013-06-27
AU2012357896B9 (en) 2016-12-15
US20140329676A1 (en) 2014-11-06
IN2014CN04325A (es) 2015-09-04
AU2012357896A1 (en) 2014-07-03
ZA201405326B (en) 2016-05-25
US9414595B2 (en) 2016-08-16
CA2859467C (en) 2019-10-01
AU2012357896B2 (en) 2016-11-24

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