AR075321A1 - Compuestos de amidina sustituida para combatir plagas de animales - Google Patents
Compuestos de amidina sustituida para combatir plagas de animalesInfo
- Publication number
- AR075321A1 AR075321A1 ARP090105077A ARP090105077A AR075321A1 AR 075321 A1 AR075321 A1 AR 075321A1 AR P090105077 A ARP090105077 A AR P090105077A AR P090105077 A ARP090105077 A AR P090105077A AR 075321 A1 AR075321 A1 AR 075321A1
- Authority
- AR
- Argentina
- Prior art keywords
- independently selected
- optionally substituted
- nitrogen
- substituents
- heterocyclic ring
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 32
- 229920006395 saturated elastomer Polymers 0.000 abstract 18
- 229910052757 nitrogen Inorganic materials 0.000 abstract 17
- 229910052717 sulfur Inorganic materials 0.000 abstract 14
- 125000001424 substituent group Chemical group 0.000 abstract 13
- 125000004432 carbon atom Chemical group C* 0.000 abstract 10
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 9
- 229910052760 oxygen Inorganic materials 0.000 abstract 9
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004434 sulfur atom Chemical group 0.000 abstract 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 125000005842 heteroatom Chemical group 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 239000001301 oxygen Substances 0.000 abstract 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 7
- 239000011593 sulfur Substances 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical group 0.000 abstract 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 4
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- -1 amidine compounds Chemical class 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 4
- HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 abstract 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 3
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 3
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000002837 carbocyclic group Chemical group 0.000 abstract 2
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 101100073357 Streptomyces halstedii sch2 gene Proteins 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 1
- 150000001409 amidines Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000004970 halomethyl group Chemical group 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 abstract 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—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
- A01N43/80—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 five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- 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
- A01N43/72—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
- A01N43/82—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 five-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/18—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/22—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having nitrogen atoms of amidino groups further bound to nitrogen atoms, e.g. hydrazidines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/12—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines
- C07C259/18—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines having carbon atoms of hydroxamidine groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Tropical Medicine & Parasitology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Composiciones que comprenden dichos compuestos. También el uso de los compuestos de amidina sustituida, sus sales o composiciones que los comprenden para combatir plagas de animales. Además métodos para aplicar dichos compuestos de amidina sustituida. Reivindicacion 1: Compuestos de amidina sustituida caracterizados porque tienen la formula general (1) en donde A1, A2, A3 y A4 son N o CH, en donde el átomo de carbono puede opcionalmente ser sustituido con R4, y siempre que no haya más de dos nitrogenos en el anillo; B1, B2, B3 son N o CH, en donde el átomo de carbono puede opcionalmente ser sustituido con R5, y siempre que no haya más de dos nitrogenos en al anillo; X se selecciona del grupo que consiste en alquilo C1-4, haloalquilo C1-4, alcoxialquilo C1-4, haloalcoxialquilo C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2-4, haloalquinilo C2-4, cicloalquilo C3-6, halocicloalquilo C3-6; Y es O, N-R8 o una union química, p es 0, 1, 2, 3 o 4, q es 0,1, 2, 3, 4 o 5, R1 se selecciona del grupo que consiste de hidrogeno, ciano, aIquilo C1-10, cicloalquilo C3-8, alquenilo C2-10, alquinilo C2-10, en donde los átomos de carbono de los radicales alifáticos y cicloalifáticos antes mencionados, pueden ser opcionalmente sustituidos con uno o más R6, que se seleccionan independientemente entre si, Si(R11)2R12, S(O)nR7, S(O)nNR9aR9b, C(=O)R6, C(=O)NR9aR9b, C(=O)OR7, C(=S)R6, C(=S)NR9aR9b, C(=S)OR7, C(=S)SR7, fenilo, opcionalmente sustituido con uno o más sustituyentes R10; que se seleccionan independientemente entre sí, un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3, 4, 5, 6 o 7 miembros, que comprende 1, 2 o 3 heteroátomos seleccionados de oxígeno, nitrogeno y/o azufre, opcionalmente sustituidos con sustituyentes k R10, independientemente seleccionados entre sí, y en donde el/los átomo/s de nitrogeno y/o de azufre del anillo heterocíclico pueden estar opcionalmente oxidados, o R1 puede estar junto con R2 una union CH2CH2 o CH2, formando un anillo heterocíclico de 5 o 6 miembros junto con la unidad de amidina sustituida a la cual están unidos; R2, R3 se seleccionan, independientemente entre sí, del grupo que consiste en hidrogeno, ciano, aIquilo C1-10, cicloalquilo C3-8, alquenilo C2-10, alquinilo C2-10, en donde los átomos de carbono de los radicales alifáticos y cicloalifáticos antes mencionados, pueden ser opcionalmente sustituidos con uno o más R6, que se seleccionan independientemente entre si, NR9aRb, Si(R11)2R12, OR7, S(O)nR7, C(=O)R6, C(=O)NR9aR9b, C(=O)OR7, C(=S)R6, C(=S)NR9aR9b, C(=S)SR7, C(=NR9a)R6; fenilo, opcionalmente sustituido con uno o más sustituyentes R10; que se seleccionan independientemente entre sí, un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3, 4, 5, 6 o 7 miembros, que comprende 1, 2 o 3 heteroátomos seleccionados de oxígeno, nitrogeno y/o azufre, opcionalmente sustituidos con sustituyentes k R10, independientemente seleccionados entre sí, y en donde el/los átomo/s de nitrogeno y/o de azufre del anillo heterocíclico pueden estar opcionalmente oxidados, siempre que R2 y R3 no sean ambos hidrogeno al mismo tiempo, o R2 y R3 en conjunto pueden ser =CR13R14, =S(O)nR7; =S(O)nNR9aR9b, =NR9a o =NOR7; o R2 y R3 en conjunto pueden ser una cadena alquileno C2-7, formando un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3 a 8 miembros junto con el átomo de nitrogeno al cual están unidos, en donde la cadena de alquileno también puede contener 1 o 2 átomos de oxígeno, átomos de azufre o átomos de nitrogeno, y en donde la cadena alquileno puede, opcionalmente, ser sustituida con halogeno, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, haloalquiltio C1-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, fenilo, opcionalmente sustituido con uno o más sustituyentes R10, que se seleccionan independientemente entre sí, un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3, 4, 5, 6 o 7 miembros, que comprende 1, 2 o 3 heteroátomos seleccionados de oxígeno, nitrogeno y/o azufre, opcionalmente sustituidos con sustituyentes k R10, independientemente seleccionados entre sí, y en donde el/los átomos de nitrogeno y/o de azufre del anillo heterocíclico pueden estar opcionalmente oxidados, R4 se selecciona, independientemente de p, del grupo que consiste en hidrogeno, halogeno, ciano, azido, nitro, -SCN, SF5, aIquilo C1-6, cicloalquilo C3-8, alquenilo C2-6, alquinilo C2-6, en donde los átomos de carbono de los radicales alifáticos y cicloalifáticos antes mencionados, pueden ser opcionalmente sustituidos con uno o más R6, que se seleccionan independientemente entre si, Si(R11)2R12, OR7, -OS(O)nR7, S(O)nR7, NR9aRb, N(R9a)C(=O)R6, C(=O)R6, C(=O)OR7, C(=NR9a)R6, C(=S)R6, fenilo, opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente de R10; que se seleccionan independientemente entre sí, un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3, 4, 5, 6 o 7 miembros, que comprende 1, 2 o 3 heteroátomos seleccionados de oxígeno, nitrogeno y/o azufre, opcionalmente sustituidos con sustituyentes k R10, independientemente seleccionados entre sí, y en donde el/los átomo/s de nitrogeno y/o de azufre del anillo heterocíclico pueden estar opcionalmente oxidados, o, cuando p es 2 o más y dos de R4 son adyacentes, los dos R4 adyacentes pueden ser una union seleccionada del grupo que consiste en CH2CH2CH2CH2, CH=CH-CH=CH, N=CH-CH=CH, CH=N-CH=CH, N=CH-N=CH, OCH2CH2CH2, OCH=CHCH2, CH2OCH2CH2, OCH2CH2O, OCH2OCH2, CH2CH2CH2, CH=CHCH2, CH2CH2O, CH=CHO, CH2OCH2, CH2C(=O)O, C(=O)OCH2, O(CH2)O, SCH2CH2CH2, SCH=CHCH2, CH2SCH2CH2, SCH2CH2S, SCH2SCH2, CH2CH2S, CH=CHS, CH2SCH2, CH2C(=S)S, C(=S)SCH2, S(CH2)S, CH2CH2NR9a, CH2CH=N, OCH=N, SCH=N, CH=CH-NR9a, cuya union puede formar, junto con los átomos de carbono a los cuales los dos R4 adyacentes están unidos, un anillo heterocíclico o carbocíclico aromático parcialmente saturado o no saturado de 5 o 6 miembros, en donde los átomos de carbono de la union pueden ser opcionalmente sustituidos con uno o dos sustituyentes seleccionados del grupo que consiste en =O, OH, CH3, OCH3, halogeno, halometilo o halometoxi; R5 se selecciona, independientemente de q, del grupo que consiste en hidrogeno, halogeno, ciano, azido, nitro, -SCN, SF5, aIquilo C1-6, cicloalquilo C3-8, alquenilo C2-6, alquinilo C2-6, en donde los átomos de carbono de los radicales alifáticos y cicloalifáticos antes mencionados, pueden ser opcionalmente sustituidos con uno o más R6, que se seleccionan independientemente entre si, Si(R12)2R13, OR7, -OS(O)nR7, S(O)nR7, NR9aRb, N(=R9a)C(=O)R6, C(=O)R6, C(=O)OR7, C(=NR9a)R6, C(=S)R6, fenilo, opcionalmente sustituido con uno o más sustituyentes R10; que se seleccionan independientemente entre sí, un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3, 4, 5, 6 o 7 miembros, que comprende 1, 2 o 3 heteroátomos seleccionados de oxígeno, nitrogeno y/o azufre, opcionalmente sustituidos con sustituyentes k R10, independientemente seleccionados entre sí, y en donde el/los átomo/s de nitrogeno y/o de azufre del anillo heterocíclico pueden estar opcionalmente oxidados, R6 se selecciona del grupo que consiste en hidrogeno, halogeno, ciano, azido, nitro, -SCN, SF5, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, Si(R12)2R13, OR16, OSO2R16, S(O)nR16, S(O)nNR17aR17b2, NR17aR17b, C(=O)NR17aR17b, C(=S)NR17aR17b, C(=O)OR16, fenilo, opcionalmente sustituido con uno o más sustituyentes R18, que se seleccionan independientemente entre sí, un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3, 4, 5, 6 o 7 miembros, que comprende 1, 2 o 3 heteroátomos seleccionados de oxígeno, nitrogeno y/o azufre, opcionalmente sustituidos con sustituyentes k R18, seleccionados independientemente entre sí, y en donde el nitrogeno y/o el(los) átomo(s) de azufre del anillo heterocíclico pueden estar opcionalmente oxidados, o dos R6 presente en un átomo de carbono pueden formar, en forma conjunta, =O, =CR13R14, =S(O)nR16, =S(O)nNR17aR17b, =NR17a, =NOR16, =NNR17a; o dos R6 pueden formar un anillo heterocíclico o carbocíclico saturado o parcialmente no saturado de 3, 4, 5, 6, 7 u 8 miembros junto con !os átomos de carbono a los cuales están unidos los dos R6; R7 se selecciona independientemente entre sí, del grupo que consiste en hidrogeno, ciano, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, cicloalquilo C3-8, alquilcicloalquilo C4-8, halocicloalquilo C3-8, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, Si(R11)2R12, S(O)nR16, S(O)nNR17aR17b, NR17aR17b, -N=CR13R14, -C(=O)R16, C(=O)NR17aR17b, C(=S)NR17aR17b, C(=O)OR16, fenilo, opcionalmente sustituido con uno o más sustituyentes R18, que se seleccionan independientemente entre sí, un anillo heterocíclico aromático saturado, parcialmente saturado o no saturado de 3, 4, 5, 6 o 7 miembros, que comprende 1, 2 o 3 heteroátomos seleccionados de oxígeno, nitrogeno y/o azufre, opcionalmente sustituidos con sustituyentes k R18, seleccionados independientemente entre sí, y en donde el nitrogeno y/o el(los) átomo(s) de azufre del anillo heterocíclico pueden estar opcionalmente oxidados, R8 se selecciona del grupo que consiste en hidrogeno, ciano, aIquilo C1-10, cicloalquilo C3-8, alquenilo C2-10, alquinilo C2-10, en donde los átomos de carbono de los radicales alifáticos y cicloalifáticos antes mencionados, pueden ser opcionalmente sustituidos con uno o más R15, que se seleccionan independientemente entre si, NR17aR17b, Si(
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| TWI649303B (zh) | 2007-08-17 | 2019-02-01 | 杜邦股份有限公司 | 製備4-乙醯基-n-〔2-側氧基-2-〔(2,2,2-三氟乙基)胺基〕乙基〕-1-萘甲醯胺之化合物及方法 |
| WO2009035004A1 (ja) | 2007-09-10 | 2009-03-19 | Nissan Chemical Industries, Ltd. | 置換イソキサゾリン化合物および有害生物防除剤 |
| MX2010003557A (es) | 2007-10-03 | 2010-04-12 | Du Pont | Compuestos de isoxazolina de naftaleno para el control de plagas de invertebrados. |
| JP2009108046A (ja) | 2007-10-10 | 2009-05-21 | Nissan Chem Ind Ltd | 殺虫、殺ダニ、殺線虫、殺軟体動物、殺菌又は殺バクテリア組成物及び病害虫の防除方法 |
| GB0720232D0 (en) | 2007-10-16 | 2007-11-28 | Syngenta Participations Ag | Insecticidal compounds |
| BRPI0821086A2 (pt) | 2007-12-19 | 2014-10-07 | Syngenta Participations Ag | Compostos inseticidas |
| JP2009286773A (ja) | 2008-03-14 | 2009-12-10 | Bayer Cropscience Ag | 殺虫性縮環式アリール類 |
| TWI583664B (zh) | 2008-04-09 | 2017-05-21 | 杜邦股份有限公司 | 羰基化合物及其製備方法 |
| EP2306837B2 (en) | 2008-07-09 | 2023-10-25 | Basf Se | Pesticidal active mixtures comprising isoxazoline compounds i |
| US8597688B2 (en) | 2008-07-09 | 2013-12-03 | Basf Se | Pesticidal mixtures comprising isoxazoline compounds II |
| WO2010020522A1 (en) | 2008-08-22 | 2010-02-25 | Syngenta Participations Ag | Insecticidal compounds |
| CN105294668A (zh) | 2008-08-22 | 2016-02-03 | 先正达参股股份有限公司 | 杀虫化合物 |
| CN102325758A (zh) | 2008-12-23 | 2012-01-18 | 巴斯夫欧洲公司 | 用于防治无脊椎动物害虫的亚胺化合物 |
| EP2414353A1 (en) | 2009-04-01 | 2012-02-08 | Basf Se | Isoxazoline compounds for combating invertebrate pests |
| BR112012014944A2 (pt) | 2009-12-18 | 2015-09-15 | Basf Se | compostos de azolina substituída , composição , uso de um composto , e, métodos para controlar pragas invertebradas e para tratar , controlar , prevenir ou proteger animais contra infestação ou infecção por parasitas. |
| CN101927860A (zh) * | 2010-08-27 | 2010-12-29 | 成都新志实业有限公司 | 新型饮料袋 |
-
2009
- 2009-12-14 US US13/141,264 patent/US8633134B2/en not_active Expired - Fee Related
- 2009-12-14 CN CN2009801572679A patent/CN102325759A/zh active Pending
- 2009-12-14 JP JP2011541373A patent/JP5715065B2/ja not_active Expired - Fee Related
- 2009-12-14 BR BRPI0918305-1A patent/BRPI0918305A2/pt not_active Application Discontinuation
- 2009-12-14 EP EP09768530A patent/EP2382195A1/en not_active Withdrawn
- 2009-12-14 MX MX2011006736A patent/MX2011006736A/es active IP Right Grant
- 2009-12-14 KR KR1020117017300A patent/KR20110099139A/ko not_active Withdrawn
- 2009-12-14 AU AU2009331664A patent/AU2009331664A1/en not_active Abandoned
- 2009-12-14 WO PCT/EP2009/067037 patent/WO2010072602A1/en not_active Ceased
- 2009-12-14 CA CA2747986A patent/CA2747986A1/en not_active Abandoned
- 2009-12-14 EA EA201100980A patent/EA201100980A1/ru unknown
- 2009-12-22 TW TW98144290A patent/TWI468404B/zh not_active IP Right Cessation
- 2009-12-23 UY UY0001032366A patent/UY32366A/es unknown
- 2009-12-23 AR ARP090105077A patent/AR075321A1/es unknown
-
2011
- 2011-06-19 IL IL213635A patent/IL213635A0/en unknown
- 2011-06-22 CR CR20110354A patent/CR20110354A/es unknown
- 2011-07-21 ZA ZA2011/05378A patent/ZA201105378B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP5715065B2 (ja) | 2015-05-07 |
| WO2010072602A1 (en) | 2010-07-01 |
| UY32366A (es) | 2010-06-30 |
| EA201100980A1 (ru) | 2012-01-30 |
| IL213635A0 (en) | 2011-07-31 |
| AU2009331664A1 (en) | 2011-07-14 |
| KR20110099139A (ko) | 2011-09-06 |
| CA2747986A1 (en) | 2010-07-01 |
| CN102325759A (zh) | 2012-01-18 |
| TW201028405A (en) | 2010-08-01 |
| US20110257011A1 (en) | 2011-10-20 |
| ZA201105378B (en) | 2012-10-31 |
| JP2012513376A (ja) | 2012-06-14 |
| EP2382195A1 (en) | 2011-11-02 |
| US8633134B2 (en) | 2014-01-21 |
| TWI468404B (zh) | 2015-01-11 |
| BRPI0918305A2 (pt) | 2015-08-11 |
| MX2011006736A (es) | 2011-11-18 |
| CR20110354A (es) | 2011-08-24 |
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