AR085324A1 - Composiciones de moleculas pesticidas y proceso de aplicacion de dichas composiciones para controlar acaros, insectos y otras plagas - Google Patents

Composiciones de moleculas pesticidas y proceso de aplicacion de dichas composiciones para controlar acaros, insectos y otras plagas

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AR085324A1
AR085324A1 ARP120100398A AR085324A1 AR 085324 A1 AR085324 A1 AR 085324A1 AR P120100398 A ARP120100398 A AR P120100398A AR 085324 A1 AR085324 A1 AR 085324A1
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Argentina
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alkyl
haloalkyl
cycloalkyl
alkenyl
substituted
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Dow Agrosciences Llc
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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    • A01N43/86—Biocides, 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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
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Abstract

Reivindicación 1: Una composición que comprende una molécula de acuerdo con las fórmulas (1), (2) ó (3) en donde: (a) Ar1 es (i) furanilo, fenilo, piridazinilo, piridilo, pirimidinilo, tienilo o (ii) furanilo sustituido, fenilo sustituido, piridazinilo sustituido, piridilo sustituido, pirimidinilo sustituido o tienilo sustituido, en donde dicho furanilo sustituido, fenilo sustituido, piridazinilo sustituido, piridilo sustituido, pirimidinilo sustituido y tienilo sustituido tienen uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO2, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo, fenoxi, fenilo sustituido y fenoxi sustituido, en donde dicho fenilo sustituido y fenoxi sustituido tienen uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO2, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo y fenoxi; (b) Het es un anillo heterocíclico saturado o insaturado de 5 ó 6 miembros, que contiene uno o varios heteroátomos seleccionado, de modo independiente, de nitrógeno, azufre u oxígeno y donde Ar1 y Ar2 no son orto entre sí (pero pueden ser meta o para, tales como, para un anillo de cinco miembros son 1,3 y para un anillo de 6 miembros son 1,3 ó 1,4) y donde dicho anillo heterocíclico también puede estar sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO2, oxo, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo, fenoxi, fenilo sustituido y fenoxi sustituido, en donde dicho fenilo sustituido y fenoxi sustituido tienen uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO2, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)H, C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo y fenoxi; (c) Ar2 es (i) furanilo, fenilo, piridazinilo, piridilo, pirimidinilo, tienilo o (ii) furanilo sustituido, fenilo sustituido, piridazinilo sustituido, piridilo sustituido, pirimidinilo sustituido o tienilo sustituido, en donde dicho furanilo sustituido, fenilo sustituido, piridazinilo sustituido, piridilo sustituido, pirimidinilo sustituido y tienilo sustituido, tienen uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO2, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo, fenoxi, fenilo sustituido y fenoxi sustituido, en donde dicho fenilo sustituido y fenoxi sustituido tienen uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO2, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)H, C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(haloalquilo C1-6), C(=O) (alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo y fenoxi; (d) R1 está seleccionado de H, CN, F, Cl, Br, I, alquilo C1-6, cicloalquilo C3-6, cicloalcoxi C3-6, alcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), OSO2(alquilo C1-6), C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo o fenoxi, en donde cada alquilo, cicloalquilo, cicloalcoxi, alcoxi, alquenilo, alquinilo, fenilo y fenoxi están opcionalmente sustituidos con uno o varios sustituyentes seleccionados, de modo independiente, de F, Cl, Br, I, CN, NO2, oxo, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo y fenoxi; (e) R2 es H, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, alquinilo C2-6, C(=O)H, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo, alquil C1-6-fenilo, alquil C1-6-O-fenilo, C(=O)Het-1, Het-1, alquil C1-6-Het-1 o alquil C1-6-O-Het-1, en donde cada alquilo, cicloalquilo, alquenilo, alquinilo, fenilo y Het-1 están opcionalmente sustituidos con uno o varios sustituyentes seleccionados, de modo independiente, de F, Cl, Br, I, CN, NO2, NRxRy, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalcoxi C3-6, halocicloalcoxi C3-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, cicloalquenilo C3-6, alquinilo C2-6, S(=O)n(alquilo C1-6), S(=O)n(haloalquilo C1-6), OSO2(alquilo C1-6), OSO2(haloalquilo C1-6), C(=O)H, C(=O)NRxRy, (alquil C1-6)NRxRy, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(haloalquilo C1-6), C(=O)O(haloalquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo, fenoxi y Het-1; (f) R3 es alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, alquinilo C2-6, C(=O)H, C(=O)(alquilo C1-6), C(=O)O(alquilo C1-6), C(=O)(cicloalquilo C3-6), C(=O)O(cicloalquilo C3-6), C(=O)(alquenilo C2-6), C(=O)O(alquenilo C2-6), (alquil C1-6)O(alquilo C1-6), (alquil C1-6)S(alquilo C1-6), C(=O)(alquil C1-6)C(=O)O(alquilo C1-6), fenilo, alquil C1-6-fenilo, alquil C1-6-O-fenilo, C(=O)Het-1, Het-1, alquil C1-6-Het-1, alquil C1-6-O-C(=O)alquil C1-6-O-alquilo C1-6, alquil C1-6-O-C(=O)alquil C1-6-O-alquil C1-6-O-alquilo C1-6, alquil C1-6-O-C(=O)alquil C1-6-O-haloalquilo C1-6, alquil C1-6-O-C(=O)alquil C1-6-N(Rx)C(=O)-O-fenilo, alquil C1-6-O-C(=O)alquil C1-6-N(Rx)C(=O)-O-alquil C1-6-fenilo, alquil C1-6-C(=O)N(Rx)alquilo C1-6, alquil C1-6-C(=O)N(Rx)alquil C1-6-Het-1C(=O)-O-alquilo C1-6, alquil C1-6-C(=O)N(Rx)alquil C1-6-Het-1, alquil C1-6-C(=O)Het-1, alquil C1-6-C(=O)N(Rx)alquil C1-6-(N(Rx)(Ry))(C(=O)OH), alquil C1-6-C(=O)N(Rx)alquil C1-6-N(Rx)(Ry), alquil C1-6-C(=O)N(Rx)alquil C1-6-N(Rx)C(=O)-O-alquilo C1-6, alquil C1-6-C(=O)N(Rx)alquil C1-6-(N(Rx)C(=O)-O-alquil C1-6)(C(=O)OH), alquil C1-6-C(=O)Het-1C(=O)-O-alquilo C1-6, alquil C1-6-O-C(=O)-O-alquilo C1-6, alquil C1-6-O-C(=O)alquilo C1-6, alquil C1-6-O-C(=O)cicloalquilo C3-6, alquil C1-6-O-C(=O) Het-1, alquil C1-6-O-C(=O)alquil C1-6-N(Rx)C(=O)-O-alquilo C1-6, alquil C1-6-NRxRy o alquil C1-6-O-Het-1, en donde cada alquilo, cicloalquilo, alquenilo, alquinilo, fenilo y Het-1 están opcionalmente sustituidos con uno o varios sustituyentes seleccionados, de modo independiente, de F, Cl, Br, I, CN, NO2,
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BR102012008089A2 (pt) 2015-11-10
EP2672819A4 (en) 2014-09-10
IL227767A0 (en) 2013-09-30
US9018136B2 (en) 2015-04-28
KR20140048089A (ko) 2014-04-23
RU2597421C2 (ru) 2016-09-10
IL227767A (en) 2017-02-28
US9107413B2 (en) 2015-08-18
CO6741214A2 (es) 2013-08-30
AU2012214724B2 (en) 2015-09-24
AP2013007062A0 (en) 2013-08-31
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EP2672819B1 (en) 2017-11-29
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CA2826146A1 (en) 2012-08-16
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AP3447A (en) 2015-10-31
CN103458687A (zh) 2013-12-18
RU2013141202A (ru) 2015-03-20
UA112428C2 (uk) 2016-09-12
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US8815922B2 (en) 2014-08-26
TWI537264B (zh) 2016-06-11
TW201309686A (zh) 2013-03-01
US20140315721A1 (en) 2014-10-23
MA34950B1 (fr) 2014-03-01
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