AR064401A1 - Composicion insecticida para semillas o granos cosechados y metodo para usar la misma - Google Patents
Composicion insecticida para semillas o granos cosechados y metodo para usar la mismaInfo
- Publication number
- AR064401A1 AR064401A1 ARP070105677A AR064401A1 AR 064401 A1 AR064401 A1 AR 064401A1 AR P070105677 A ARP070105677 A AR P070105677A AR 064401 A1 AR064401 A1 AR 064401A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- alkyl
- substituted
- halogen atom
- isoindolyl
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title 1
- -1 nitro, hydroxy Chemical group 0.000 abstract 36
- 125000005843 halogen group Chemical group 0.000 abstract 9
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 8
- 125000002837 carbocyclic group Chemical group 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 8
- 125000006595 (C1-C3) alkylsulfinyl group Chemical group 0.000 abstract 7
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 abstract 7
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 abstract 7
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 7
- 125000003282 alkyl amino group Chemical group 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 7
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 7
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 7
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 7
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 7
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 7
- 125000001424 substituent group Chemical group 0.000 abstract 7
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 6
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 6
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 6
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 6
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 6
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 abstract 6
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 6
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 6
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 6
- 125000000335 thiazolyl group Chemical group 0.000 abstract 6
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 abstract 5
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 abstract 5
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 abstract 5
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 abstract 4
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract 4
- 125000005043 dihydropyranyl group Chemical group O1C(CCC=C1)* 0.000 abstract 4
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 abstract 4
- 125000002541 furyl group Chemical group 0.000 abstract 4
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 abstract 4
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000002883 imidazolyl group Chemical group 0.000 abstract 4
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 abstract 4
- 125000001041 indolyl group Chemical group 0.000 abstract 4
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 abstract 4
- 125000005956 isoquinolyl group Chemical group 0.000 abstract 4
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 4
- 125000001624 naphthyl group Chemical group 0.000 abstract 4
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 abstract 4
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 4
- 125000002971 oxazolyl group Chemical group 0.000 abstract 4
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 4
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 4
- 125000005495 pyridazyl group Chemical group 0.000 abstract 4
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 4
- 125000005493 quinolyl group Chemical group 0.000 abstract 4
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 abstract 4
- 125000001412 tetrahydropyranyl group Chemical group 0.000 abstract 4
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 4
- 125000001544 thienyl group Chemical group 0.000 abstract 4
- 125000001425 triazolyl group Chemical group 0.000 abstract 4
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 3
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 3
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 230000000749 insecticidal effect Effects 0.000 abstract 3
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000004076 pyridyl group Chemical group 0.000 abstract 3
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 3
- 241000238631 Hexapoda Species 0.000 abstract 2
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 2
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 2
- ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- ABADUMLIAZCWJD-UHFFFAOYSA-N 1,3-dioxole Chemical compound C1OC=CO1 ABADUMLIAZCWJD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000000101 thioether group Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/713—Biocides, 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Furan Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Pyrane Compounds (AREA)
- Pyrrole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
La presente provee una composicion insecticida para semillas o granos cosechados y un método para prevenir dano de varios insectos en semillas o granos cosechados de una planta para agricultura. Se revela una composicion insecticida, en la cual los compuestos representados por la formula general (1) o (5) están contenidos como ingredientes activos y un método para prevenir dano de un insecto, en el cual la composicion se aplica a las semillas o granos cosechados de una planta para agricultura. Reivindicacion 1: Una composicion insecticida para semillas o granos cosechados caracterizada porque contiene uno o dos o más compuestos seleccionados de compuestos representados por la formula general (1) como ingredientes activos, en donde, en la formula, A1, A2, A3 y A4 de manera independiente representan un átomo de carbono, un átomo de nitrogeno o un átomo de nitrogeno oxidado; R1 y R2 cada uno de manera independiente representan un átomo de hidrogeno, un grupo alquilo C1-4 o un grupo alquilcarbonilo C1-4; G1 y G2 cada uno de manera independiente representan un átomo de oxígeno o un átomo de sulfuro; Xs pueden ser iguales o diferentes y representan un átomo de hidrogeno, un átomo de halogeno, un grupo alquilo C1-3 o un grupo trifluorometilo; n representa un entero de 0 a 4; Q1 representa un grupo fenilo, fenilo sustituido que tiene uno o más sustituyentes que pueden ser iguales o diferentes y están seleccionados de un átomo de halogeno, alquilo C1-4, haloalquilo C1-4, alquilo sustituido C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2-4, haloalquinilo C2-4, cicloalquilo C3-8, halocicloalquilo C3-8, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfinilo C1-3, haloalquilsulfinilo C1- 3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, alquilamino C1-4, dialquilamino C1-4, amino, ciano, nitro, hidroxi, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alquilcarboniloxi C1-4, haloalquilcarboniloxi C1-4, alcoxicarbonilo C1-4, haloalcoxicarbonilo C1-4, alquilcarbonilamino C1-4, haloalquilcarbonilamino C1-4, alquilsulfoniloxi C1-4, haloalquilsulfoniloxi C1-4, arilsulfoniloxi, pentafluorosulfanilo, fenilalquinilo y fenilo, un grupo carbocíclico (el grupo carbocíclico en la presente representa un grupo naftilo, tetrahidronaftilo, indanilo, fluorenilo, 9-oxofluorenilo, adamantilo, antracenilo o norbornilo), un grupo carbocíclico sustituido que tiene uno o más sustituyentes que pueden ser iguales o diferentes y están seleccionados de un átomo de halogeno, alquilo C1-4, haloalquilo C1-4, alquilo sustituido C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2-4, haloalquinilo C2-4, cicloalquilo C3-8, halocicloalquilo C3-8, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfinilo C1-3, haloalquilsulfinilo C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, alquilamino C1-4, dialquilamino C1-4, amino, ciano, nitro, hidroxi, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alquilcarboniloxi C1-4, haloalquilcarboniloxi C1-4, alcoxicarbonilo C1-4, haloalcoxicarbonilo C1-4, alquilcarbonilamino C1-4, haloalquilcarbonilamino C1-4, alquilsulfoniloxi C1-4, haloalquilsulfoniloxi C1-4, arilsulfoniloxi, pentafluorosulfanilo, fenilalquinilo y un grupo fenilo (el grupo carbocíclico en la presente representa un grupo naftilo, tetrahidronaftilo, indanilo, fluorenilo, 9-oxofluorenilo, adamantilo, antracenilo o norbornilo), un grupo heterocíclico (el grupo heterocíclico en la presente representa un grupo pirazinilo, piridilo, piridin-N-oxido, pirimidinilo, piridazilo, furilo, tienilo, oxazolilo, isoxazolilo, oxadiazolilo, tiazolilo, isotiazolilo, tiadiazolilo, pirrolo, imidazolilo, triazolilo, pirazolilo, tetrazolilo, benzotiazolilo, benzoxazolilo, benzofuranilo, benzotiofenilo, quinolilo, isoquinolilo, indolilo, isoindolilo, 1H-isoindolilo, 2,3-dihidro-benzo[1,4]dioxinilo, benzo[1,3]dioxolilo, tetrahidropiranilo, acridinilo o dihidropiranilo), o un grupo heterocíclico sustituido que tiene uno o más sustituyentes que pueden ser iguales o diferentes y están seleccionados de un átomo de halogeno, alquilo C1-4, haloalquilo C1-4, alquilo sustituido C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2- 4, haloalquinilo C2-4, cicloalquilo C3-8, halocicloalquilo C3-8, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfinilo C1-3, haloalquilsulfinilo C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, alquilamino C1-4, dialquilamino C1-4, amino, ciano, nitro, hidroxi, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alquilcarboniloxi C1-4, haloalquilcarboniloxi C1-4, alcoxicarbonilo C1-4, haloalcoxicarbonilo C1-4, alquilcarbonilamino C1-4, haloalquilcarbonilamino C1-4, alquilsulfoniloxi C1-4, haloalquilsulfoniloxi C1-4, arilsulfoniloxi, pentafluorosulfanilo, fenilalquinilo y un grupo fenilo (el grupo heterocíclico en la presente representa un grupo pirazinilo, piridilo, piridin-N-oxido, pirimidinilo, piridazilo, furilo, tienilo, oxazolilo, isoxazolilo, oxadiazolilo, tiazolilo, isotiazolilo, tiadiazolilo, pirrolo, imidazolilo, triazolilo, pirazolilo, tetrazolilo, benzotiazolilo, benzoxazolilo, benzofuranilo, benzotiofenilo, quinolilo, isoquinolilo, indolilo, isoindolilo, 1H-isoindolilo, 2,3-dihidro-benzo[1,4]dioxinilo, benzo[1,4]dioxolilo, tetrahidropiranilo, acridinilo o un grupo dihidropiranilo); y Q2 representa un grupo carbocíclico (el grupo carbocíclico en la presente representa un grupo naftilo, tetrahidronaftilo, cicloalquilo C3-8, indanilo, fluorenilo, 9-oxofluorenilo, adamantilo o norbornilo), un grupo carbocíclico sustituido que tiene uno o más sustituyentes que pueden ser iguales o diferentes y están seleccionados de un átomo de halogeno, alquilo C1-4, haloalquilo C1-4, alquilo sustituido C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2-4, haloalquinilo C2-4, cicloalquilo C3-8, halocicloalquilo C3-8, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfinilo C1-3, haloalquilsulfinilo C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, alquilamino C1-4, dialquilamino C1-4, ciano, nitro, hidroxi, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alquilcarboniloxi C1-4, haloalquilcarboniloxi C1-4, alcoxicarbonilo C1-4, haloalcoxicarbonilo C1-4, alquilcarbonilamino C1-4, haloalquilcarbonilamino C1-4, alquilsulfoniloxi C1-4, haloalquilsulfoniloxi C1-4, arilsulfoniloxi, pentafluorosulfanilo y un grupo fenilo (el grupo carbocíclico en la presente representa un grupo naftilo, tetrahidronaftilo, cicloalquilo C3-8, indanilo, fluorenilo, 9-oxofluorenilo, adamantilo o un grupo norbornilo), un grupo heterocíclico (el grupo heterocíclico en la presente representa pirazinilo, piridilo, piridin-N-oxido, pirimidinilo, piridazilo, furilo, tienilo, oxazolilo, isoxazolilo, oxadiazolilo, tiazolilo, isotiazolilo, tiadiazolilo, pirrolo, imidazolilo, triazolilo, pirazolilo, tetrazolilo, benzotiazolilo, benzoxazolilo, benzofuranilo, benzotiofenilo, quinolilo, isoquinolilo, indolilo, isoindolilo, 1H-isoindolilo, 2,3-dihidro-benzo[1,4]dioxinilo, benzo[1,4]dioxolilo, tetrahidropiranilo, benzoimidazolilo o un grupo dihidropiranilo), un grupo heterocíclico sustituido que tiene uno o más sustituyentes que pueden ser iguales o diferentes y están seleccionados de un átomo de halogeno, un grupo alquilo C1-4, haloalquilo C1-4, alquilo sustituido C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2-4, haloalquinilo C2-4, cicloalquilo C3-8, halocicloalquilo C3-8, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfinilo C1-3, haloalquilsulfinilo C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, alquilamino C1-4, dialquilamino C1-4, ciano, nitro, hidroxi, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alquilcarboniloxi C1-4, haloalquilcarboniloxi C1-4, alcoxicarbonilo C1-4, haloalcoxicarbonilo C1-4, alquilcarbonilamino C1-4, haloalquilcarbonilamino C1-4, alquilsulfoniloxi C1- 4, haloalquilsulfoniloxi C1-4, arilsulfoniloxi, pentafluorosulfanilo y un grupo fenilo (el grupo heterocíclico en la presente representa un grupo pirazinilo, piridin-2-ilo, piridin-4-ilo, piridin-N-oxido, pirimidinilo, piridazilo, furilo, tienilo, oxazolilo, isoxazolilo, oxadiazolilo, tiazolilo, isotiazolilo, tiadiazolilo, pirrolo, imidazolilo, triazolilo, pirazolilo, tetrazolilo, benzotiazolilo, benzoxazolilo, benzofuranilo, benzotiofenilo, quinolilo, isoquinolilo, indolilo, isoindolilo, 1H- isoindolilo, 2,3-dihidro-benzo[1,4]dioxinilo, benzo[1,4]dioxolilo, tetrahidropiranilo, benzoimidazolilo o un grupo dihidropiranilo), un grupo alquilo C1-6, alquilo sustituido C1-6 que tiene uno o más sustituyentes que pueden ser iguales o diferentes y están seleccionados de un átomo de halogeno, haloalquilo C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2-4, haloalquinilo C2-4, cicloalquilo C3-8, halocicloalquilo C3-8, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfinilo C1-3, haloalquilsulfinilo C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, alquilamino C1-4, dialquilamino C1-4, ciano, nitro, hidroxi, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alquilcarboniloxi C1-4, haloalquilcarboniloxi C1-4, alcoxicarbonilo C1-4, haloalcoxicarbonilo C1-4, alquilcarbonilamino C1-4, haloalquilcarbonilamino C1-4, alquilsulfoniloxi C1-4, haloalquilsulfoniloxi C1-4, arilsulfoniloxi, pentafluorosulfanilo y un grupo fenilo, un grupo representado por la formula general (2), en donde, en la formula, Y1, Y2, Y3, Y4 e Y5 pueden ser iguales o diferentes y representan un átomo de hidrogeno, un átomo de halogeno o alquilo C1-6, alquilo sustituido C1-6 sustituido con uno o más sustituyentes que pueden ser iguales o diferentes y están seleccionados de un átomo de halogeno, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfinilo C1-3, haloalquilsulfinilo C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, alquilamino C1-4, dialquilamino C1-4, ciano, nitro, hidroxi, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alquilcarboniloxi C1-4
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| Application Number | Priority Date | Filing Date | Title |
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| JP2006340923A JP2010047480A (ja) | 2006-12-19 | 2006-12-19 | 虫害の予防方法 |
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| ARP070105677 AR064401A1 (es) | 2006-12-19 | 2007-12-18 | Composicion insecticida para semillas o granos cosechados y metodo para usar la misma |
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| JP (1) | JP2010047480A (es) |
| AR (1) | AR064401A1 (es) |
| CL (1) | CL2007003717A1 (es) |
| TW (1) | TW200836629A (es) |
| WO (1) | WO2008075465A1 (es) |
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| EP2072501A1 (en) * | 2007-12-21 | 2009-06-24 | Bayer CropScience AG | Aminobenzamide derivatives as useful agents for controlling animal parasites |
| BRPI0918022B1 (pt) | 2008-08-13 | 2017-12-26 | Mitsui Cheminicals Agro, Inc | Method for the production of amida derivatives |
| WO2010018714A1 (ja) * | 2008-08-13 | 2010-02-18 | 三井化学アグロ株式会社 | アミド誘導体、該アミド誘導体を含有する有害生物防除剤およびその使用方法 |
| CN102378754B (zh) | 2009-02-06 | 2014-06-25 | 阿格罗－金正株式会社 | 3-氨基乙二酰基氨基苯甲酰胺衍生物及以其作为有效成分的杀虫、杀螨剂 |
| CN104245665B (zh) * | 2012-04-03 | 2017-08-25 | 三井化学Agro株式会社 | 烷基化芳香族酰胺衍生物的制造方法 |
| CN102993054B (zh) * | 2012-10-24 | 2015-02-18 | 中化蓝天集团有限公司 | 苯甲酰胺类衍生物、其制备方法及应用 |
| EP3087052B1 (en) | 2013-12-23 | 2019-11-20 | Syngenta Participations AG | Insecticidal compounds |
| CN112479996B (zh) * | 2019-09-12 | 2023-05-26 | 上海济煜医药科技有限公司 | 吡啶氮氧化合物及其制备方法和用途 |
| CN115868499B (zh) * | 2022-12-12 | 2025-11-11 | 中农立华生物科技股份有限公司 | 一种含溴虫氟苯双酰胺的复配农用杀虫剂及其应用 |
| US12384773B2 (en) | 2023-11-02 | 2025-08-12 | Arcus Biosciences, Inc. | Thiazole compounds and methods of use thereof |
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| CA2554437C (en) * | 2004-01-28 | 2011-06-21 | Mitsui Chemicals, Inc. | Amide derivatives, process for preparation thereof and use thereof as insecticide |
| JP2006306771A (ja) * | 2005-04-28 | 2006-11-09 | Mitsui Chemicals Inc | 農園芸用殺虫剤 |
| JP5149003B2 (ja) * | 2005-06-21 | 2013-02-20 | 三井化学アグロ株式会社 | アミド誘導体ならびに該化合物を含有する殺虫剤 |
| TW200740370A (en) * | 2005-06-23 | 2007-11-01 | Mitsui Chemicals Inc | Amide derivative, pesticide containing such compound and use thereof |
| JP4580836B2 (ja) * | 2005-07-25 | 2010-11-17 | 三井化学アグロ株式会社 | 殺虫殺菌組成物 |
| BRPI0520441A2 (pt) * | 2005-07-27 | 2009-05-12 | Mitsui Chemicals Inc | composição para previnir organismos nocivos |
| JP2007031395A (ja) * | 2005-07-29 | 2007-02-08 | Bayer Cropscience Ag | 殺虫性３−アシルアミノベンズアニリド類 |
| JP2007099761A (ja) * | 2005-09-08 | 2007-04-19 | Mitsui Chemicals Inc | アミド誘導体ならびにその殺虫剤としての使用方法 |
| WO2007083394A1 (ja) * | 2006-01-19 | 2007-07-26 | Mitsui Chemicals, Inc. | ジアミン誘導体を含む有害生物防除組成物 |
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- 2006-12-19 JP JP2006340923A patent/JP2010047480A/ja active Pending
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2007
- 2007-12-17 TW TW96148242A patent/TW200836629A/zh unknown
- 2007-12-18 AR ARP070105677 patent/AR064401A1/es not_active Application Discontinuation
- 2007-12-19 CL CL2007003717A patent/CL2007003717A1/es unknown
- 2007-12-19 WO PCT/JP2007/001424 patent/WO2008075465A1/ja not_active Ceased
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| Publication number | Publication date |
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| WO2008075465A1 (ja) | 2008-06-26 |
| TW200836629A (en) | 2008-09-16 |
| JP2010047480A (ja) | 2010-03-04 |
| CL2007003717A1 (es) | 2008-04-18 |
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