AR089297A1 - Uso de derivados de diamida antranilicos con sustituyentes heteroaromaticos y heterociclicos en combinacion con un agente de control biologico - Google Patents
Uso de derivados de diamida antranilicos con sustituyentes heteroaromaticos y heterociclicos en combinacion con un agente de control biologicoInfo
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- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/20—Bacteria; Substances produced thereby or obtained therefrom
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- A01N63/30—Microbial fungi; Substances produced thereby or obtained therefrom
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- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/30—Microbial fungi; Substances produced thereby or obtained therefrom
- A01N63/32—Yeast
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- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/40—Viruses, e.g. bacteriophages
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- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
- A01N65/08—Magnoliopsida [dicotyledons]
- A01N65/10—Apiaceae or Umbelliferae [Carrot family], e.g. parsley, caraway, dill, lovage, fennel or snakebed
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- A—HUMAN NECESSITIES
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- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
- A01N65/08—Magnoliopsida [dicotyledons]
- A01N65/38—Solanaceae [Potato family], e.g. nightshade, tomato, tobacco or chilli pepper
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Abstract
Reivindicación 1: Una composición que comprende un derivado diamida de ácido antranílico con sustituyentes heteroaromáticos y heterocíclicos de fórmula (1) en 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 cuales está no sustituido o sustituido una o más veces con sustituyentes idénticos o diferentes que se pueden seleccionar de modo independiente uno de otro de entre halógeno, ciano, nitro, hidroxilo, alcoxi C₁₋₄, alquiltio C₁₋₄, alquil C₁₋₄sulfinilo, alquil C₁₋₄sulfonilo, (alcoxi C₁₋₄)carbonilo, alquil C₁₋₄amino, di(alquil C₁₋₄)amino, cicloalquil C₃₋₆amino o (alquil C₁₋₄)cicloalquil C₃₋₆amino; R² representa hidrógeno, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₄, alquil C₁₋₄amino, di(alquil C₁₋₄)amino, cicloalquil C₃₋₆amino, alcoxi C₂₋₆carbonilo o alquil C₂₋₆carbonilo; R³ representa hidrógeno o representa alquilo C₁₋₆, alcoxi C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆ cada uno de los cuales está opcionalmente sustituido una o más veces con sustituyentes idénticos o diferentes que se pueden seleccionar de modo independiente uno de otro de entre halógeno, ciano, nitro, hidroxilo, alquilo C₁₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquiltio C₁₋₄, alquil C₁₋₄sulfinilo, alquil C₁₋₄sulfonilo, alquil C₁₋₄sulfimino, alquil C₁₋₄sulfimino-alquilo C₁₋₄, alquil C₁₋₄sulfimino-alquil C₂₋₅carbonilo, alquil C₁₋₄sulfoximino, alquil C₁₋₄sulfoximino-alquilo C₁₋₄, alquil C₁₋₄sulfoximino-alquil C₂₋₅carbonilo, alcoxi C₂₋₆carbonilo, alquil C₂₋₆carbonilo o trialquil C₃₋₆sililo, R³ también representa alquilo C₁₋₆, alcoxi C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆ cada uno de los cuales está opcionalmente sustituido una o más veces con sustituyentes idénticos o diferentes que se pueden seleccionar de modo independiente uno de otro de entre amino, cicloalquil C₃₋₆amino o un anillo heteroaromático de 5 ó 6 miembros, R³ asimismo también representa cicloalquilo C₃₋₁₂, cicloalquil C₃₋₁₂-alquilo C₁₋₆ y bicicloalquilo C₄₋₁₂, los sustituyentes que se pueden seleccionar de modo independiente uno de otro de entre halógeno, ciano, nitro, hidroxilo, amino, alquilo C₁₋₆, cicloalquilo C₃₋₆, cicloalquil C₃₋₆amino, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquiltio C₁₋₄, alquil C₁₋₄sulfinilo, alquil C₁₋₄sulfonilo, alquil C₁₋₄sulfimino, alquil C₁₋₄sulfimino-alquilo C₁₋₄, alquil C₁₋₄sulfimino-alquil C₂₋₅carbonilo, alquil C₁₋₄sulfoximino, alquil C₁₋₄sulfoximino-alquilo C₁₋₄, alquil C₁₋₄sulfoximino-alquil C₂₋₅carbonilo, alcoxi C₂₋₆carbonilo, alquil C₂₋₆carbonilo, trialquilsililo C₃₋₆ o un anillo heteroaromático de 5 ó 6 miembros, R² y R³ se pueden unir entre sí por medio de dos a seis átomos de carbono y forman un anillo que cuando sea apropiado contiene adicionalmente otro átomo de nitrógeno, azufre u oxígeno y cuando sea apropiado se puede sustituir una a cuatro veces con alquilo C₁₋₂, halógeno, ciano, amino o alcoxi C₁₋₂, R² y R³ juntos también representan =S(alquil C₁₋₄)₂ o =S(O)(alquil 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, alquil C₁₋₄sulfinilo, alquil C₁₋₄sulfonilo, haloalquiltio C₁₋₄, haloalquil C₁₋₄sulfinilo, haloalquil C₁₋₄sulfonilo, alquil C₁₋₄amino, di(alquil C₁₋₄)amino, cicloalquil C₃₋₆amino, (alcoxi C₁₋₄)imino, (alquil C₁₋₄)(alcoxi C₁₋₄)imino, (haloalquil C₁₋₄)(alcoxi C₁₋₄)imino o trialquilsililo C₃₋₆, o dos R⁴, por medio 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 adicionalmente, por medio de átomos de carbono adyacentes, forman los siguientes anillos condensados, que cuando sea apropiado están sustituidos una o más veces con sustituyentes idénticos o diferentes que se pueden seleccionar de modo independiente 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), alquil C₁₋₄sulfinil(alquilo C₁₋₆), alquil C₁₋₄sulfonil(alquilo C₁₋₆), alquil C₁₋₄amino, di(alquil C₁₋₄)amino o cicloalquil C₃₋₆amino, 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, alquil C₁₋₄sulfinilo, alquil C₁₋₄sulfonilo, haloalquiltio C₁₋₄, haloalquil C₁₋₄sulfinilo, haloalquil C₁₋₄sulfonilo, 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 también representa cicloalcoxi C₃₋₆; R⁷ representa de modo independiente 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 de 8, 9 ó 10 miembros, estando el sistema anular no sustituido o sustituido una o más veces con sustituyentes idénticos o diferentes que se pueden seleccionar de modo independiente 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, alquil C₁₋₄sulfinilo, alquil C₁₋₄sulfonilo, haloalquiltio C₁₋₄, haloalquil C₁₋₄sulfinilo, haloalquil C₁₋₄sulfonilo, alquil C₁₋₄amino, di(alquil C₁₋&
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11194336.1A EP2606732A1 (en) | 2011-12-19 | 2011-12-19 | Use of an anthranilic diamide derivatives with heteroaromatic and heterocyclic substituents in combination with a biological control agent |
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| Publication Number | Publication Date |
|---|---|
| AR089297A1 true AR089297A1 (es) | 2014-08-13 |
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| Application Number | Title | Priority Date | Filing Date |
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| ARP120104789A AR089297A1 (es) | 2011-12-19 | 2012-12-18 | Uso de derivados de diamida antranilicos con sustituyentes heteroaromaticos y heterociclicos en combinacion con un agente de control biologico |
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| Country | Link |
|---|---|
| US (2) | US9572342B2 (es) |
| EP (2) | EP2606732A1 (es) |
| JP (1) | JP6088539B2 (es) |
| KR (1) | KR20140107494A (es) |
| CN (1) | CN104066329B (es) |
| AR (1) | AR089297A1 (es) |
| AU (1) | AU2012357893B2 (es) |
| BR (1) | BR112014014662A8 (es) |
| IN (1) | IN2014CN04480A (es) |
| MX (1) | MX2014006696A (es) |
| WO (1) | WO2013092516A1 (es) |
| ZA (1) | ZA201405315B (es) |
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| CN104902753A (zh) * | 2012-05-30 | 2015-09-09 | 拜耳农作物科学股份公司 | 包含生物防治剂和杀虫剂的组合物 |
| AR105480A1 (es) * | 2015-04-22 | 2017-10-11 | Monsanto Technology Llc | Beneficios de rendimiento de plantas por microbianos |
| WO2016176764A1 (en) | 2015-05-04 | 2016-11-10 | Green Advantage Technology Inc. | Methods and formulations for storing entomopathogenic nematodes |
| CN109475126A (zh) * | 2016-04-06 | 2019-03-15 | Fmc有限公司 | 控制蛛型纲物种生殖力的组合物和方法 |
| CU24557B1 (es) * | 2018-09-27 | 2021-12-08 | Ct Ingenieria Genetica Biotecnologia | Composición sólida de uso agrícola que comprende cepa bacteriana de brevibacterium celere |
| CN110161029A (zh) * | 2019-06-24 | 2019-08-23 | 南京林业大学 | 一种薄壳山核桃染色体核型分析方法 |
| CN111944699B (zh) * | 2020-07-27 | 2022-11-01 | 中国科学院成都生物研究所 | 一种角毛壳菌菌剂及其制备方法 |
| CN116584509A (zh) * | 2023-05-17 | 2023-08-15 | 湖南省林业科学院 | 含油茶皂素的抑制剂的制备方法及其在抑制蜡样芽孢杆菌催吐毒素表达中的应用 |
| CN118389317A (zh) * | 2024-03-01 | 2024-07-26 | 南京师范大学常州合成生物学产业研究院有限公司 | 枯草芽孢杆菌斯氏亚种、菌剂、生物制剂及其应用 |
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-
2011
- 2011-12-19 EP EP11194336.1A patent/EP2606732A1/en not_active Ceased
-
2012
- 2012-12-17 JP JP2014546574A patent/JP6088539B2/ja not_active Expired - Fee Related
- 2012-12-17 CN CN201280062902.7A patent/CN104066329B/zh not_active Expired - Fee Related
- 2012-12-17 AU AU2012357893A patent/AU2012357893B2/en not_active Ceased
- 2012-12-17 IN IN4480CHN2014 patent/IN2014CN04480A/en unknown
- 2012-12-17 KR KR1020147019921A patent/KR20140107494A/ko not_active Ceased
- 2012-12-17 US US14/366,110 patent/US9572342B2/en not_active Expired - Fee Related
- 2012-12-17 BR BR112014014662A patent/BR112014014662A8/pt active Search and Examination
- 2012-12-17 MX MX2014006696A patent/MX2014006696A/es unknown
- 2012-12-17 EP EP12806032.4A patent/EP2793584B1/en not_active Not-in-force
- 2012-12-17 WO PCT/EP2012/075840 patent/WO2013092516A1/en not_active Ceased
- 2012-12-18 AR ARP120104789A patent/AR089297A1/es unknown
-
2014
- 2014-07-18 ZA ZA2014/05315A patent/ZA201405315B/en unknown
-
2016
- 2016-12-21 US US15/386,496 patent/US9854802B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN104066329A (zh) | 2014-09-24 |
| BR112014014662A8 (pt) | 2017-07-04 |
| KR20140107494A (ko) | 2014-09-04 |
| EP2793584B1 (en) | 2017-08-16 |
| AU2012357893A1 (en) | 2014-06-19 |
| IN2014CN04480A (es) | 2015-09-04 |
| US20140364458A1 (en) | 2014-12-11 |
| US9854802B2 (en) | 2018-01-02 |
| AU2012357893B2 (en) | 2016-08-25 |
| US20170156328A1 (en) | 2017-06-08 |
| BR112014014662A2 (pt) | 2017-06-13 |
| CN104066329B (zh) | 2017-09-29 |
| US9572342B2 (en) | 2017-02-21 |
| MX2014006696A (es) | 2014-07-09 |
| JP2015507616A (ja) | 2015-03-12 |
| ZA201405315B (en) | 2016-04-28 |
| EP2606732A1 (en) | 2013-06-26 |
| WO2013092516A1 (en) | 2013-06-27 |
| EP2793584A1 (en) | 2014-10-29 |
| JP6088539B2 (ja) | 2017-03-01 |
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