AR085318A1 - TRIAZOL DERIVATIVES THAT HAVE INSECTICIATED ACTIVITY - Google Patents
TRIAZOL DERIVATIVES THAT HAVE INSECTICIATED ACTIVITYInfo
- Publication number
- AR085318A1 AR085318A1 ARP120100392A ARP120100392A AR085318A1 AR 085318 A1 AR085318 A1 AR 085318A1 AR P120100392 A ARP120100392 A AR P120100392A AR P120100392 A ARP120100392 A AR P120100392A AR 085318 A1 AR085318 A1 AR 085318A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- substituted
- haloalkyl
- alkoxy
- substituents
- Prior art date
Links
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
- 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
- A01N43/647—Triazoles; Hydrogenated triazoles
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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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La presente se refiere a derivados de triazol de fórmula (1) que tienen actividad insecticida, a procesos e intermediarios para prepararlos, a composiciones insecticidas, acaricidas, nematicidas o molusquicidas que los comprenden y a métodos de utilización de los mismos para combatir y controlar plagas de insectos, de ácaros, de nemátodos o de moluscos.Reivindicación 1: Un compuesto de fórmula (1) en donde A1, A2, A3 y A4 son cada uno independientemente C-X o nitrógeno, en donde cada X puede ser igual o diferente; R1 es hidrógeno, alquilo C1-4, H2NC(O)-alquilo C1-4 o alquil C1-4-carbonilo; R2 es hidrógeno, halógeno, alquilo C1-4, haloalquilo C1-6 o ciano; G1 es oxígeno o azufre; X es hidrógeno, halógeno, ciano, alquil C1-4oxi, alquilo C1-4 o haloalquilo C1-4; Q1 es arilo o heterociclilo, cada uno opcionalmente sustituido por uno a cinco sustituyentes R3, que pueden ser iguales o diferentes; o Q1 es alquilo C1-8 o alquilo C1-8 sustituido por uno a cinco R4, alquenilo C2-8, alquenilo C2-8 sustituido por uno a cinco R4, alquinilo C2-8, alquinilo C2-8 sustituido por uno a cinco R4, cicloalquilo C3-10, cicloalquilo C3-10 sustituido por uno a cinco R4 o alquil C1-8-(CO)-N-alquilo C1-8 o alquil C1-8-(CO)-N-alquilo C1-8 sustituido por uno a cinco R4; R3 se selecciona de ciano, amino, nitro, hidroxi, oxo, halógeno, alquilo C1-4, haloalquilo C1-4, alquenilo C2-4, haloalquenilo C2-4, alquinilo C2-4, haloalquinilo C2-4, cicloalquilo C3-6, halocicloalquilo C3-6, alcoxi C1-3, haloalcoxi C1-3, alquil C1-3tio, haloalquil C1-3tio, alquil C1-3sulfinilo, haloalquil C1-3sulfinilo, alquil C1-3sulfonilo, haloalquil C1-3sulfonilo, alquil C1-4amino, di-(alquil C1-4)-amino, alquil C1-4-carbonilo, alquil C1-4-carboniloxi, alcoxi C1-4carbonilo, alquil C1-4-carbonilamino y fenilo; cada R4 es independientemente halógeno, ciano, nitro, hidroxi, cicloalquilo C3-10, cicloalquilo C3-10 sustituido por uno a cinco R3, di(alquil C1-8)amino, alcanoil C1-8amino, alquilo C1-8, alquinilo C2-8, alcoxi C1-8, haloalcoxi C1-8, alquil C1-8tio, haloalquil C1-8tio, alquil C1-8sulfinilo, haloalquil C1-8sulfinilo, alquil C1-8sulfonilo, haloalquil C1-8sulfonilo, alquil C1-8carbonilo, alcoxi C1-8carbonilo, arilo o arilo sustituido por uno a cinco R3, ariloxi o ariloxi sustituido por uno a cinco R3 o heterociclilo o heterociclilo sustituido por uno a cinco R3; Q2 es un resto de fórmula (2) en donde R7 y R6 son independientemente entre sí hidrógeno, ciano, halógeno, alquilo C1-6, haloalquilo C1-6, alcoxi C1-4-alquilo C1-4, alquil C1-6tio, haloalquil C1-6tio, alquil C1-6sulfinilo, haloalquil C1-6sulfinilo, alquil C1-6sulfonilo o haloalquil C1-6sulfonilo; R5 es independientemente hidrógeno, hidroxilo, amino, N-alquil C1-6amino, N,N-di(alquil C1-6)-amino, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, alquinilo C2-6, alquilo C1-6 sustituido por uno a cinco sustituyentes R9, cicloalquilo C3-6 sustituido por uno a cinco sustituyentes R9, alquinilo C2-6 sustituido por uno a cinco sustituyentes R9, alquenilo C2-6 sustituido por uno a cinco sustituyentes R9, arilo o arilo sustituido por uno a cinco sustituyentes R10, heteroarilo o heteroarilo sustituido por uno a cinco sustituyentes R10; cada R9 es independientemente ciano, nitro, amino, hidroxi, halógeno, N-alquil C1-6amino, N,N-di-(alquil C1-6)-amino, alcoxi C1-6, alquil C1-6tio, alquil C1-6sulfinilo, arilo o arilo que está sustituido por uno a cinco sustituyentes que se seleccionan independientemente de ciano, nitro, hidroxilo, halógeno, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6 o haloalcoxi C1-6 o heteroarilo o heteroarilo que está sustituido por uno a cinco sustituyentes que se seleccionan independientemente de ciano, nitro, hidroxi, halógeno, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6 o haloalcoxi C1-6; cada R10 es independientemente ciano, nitro, amino, hidroxi, halógeno, alquilo C1-6, haloalquilo C1-6, alcoxi C1-4-alquilo C1-4, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, cicloalquilo C3-6, halocicloalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, alcoxi C1-4-alcoxi C1-4, alquil C1-6tio, haloalquil C1-6tio, alquil C1-6sulfinilo, haloalquil C1-6sulfinilo, alquil C1-6sulfonilo, haloalquil C1-6sulfonilo, N-alquil C1-6amino, N,N-di-(alquil C1-6)-amino, N,N-di-(alquil C1-6)-aminocarbonilo, N,N-di-(alquil C1-6)-aminosulfonilo, alquil C1-6-carbonilo, alquil C1-6-carboniloxi, alcoxi C1-6-carbonilo, alquil C1-6carbonilamino; o una sal agroquímicamente aceptable o N-óxidos del mismo.This refers to triazole derivatives of formula (1) that have insecticidal activity, to processes and intermediates to prepare them, to insecticidal, acaricidal, nematicidal or molluscicidal compositions that comprise them and methods of using them to combat and control pests of insects, mites, nematodes or mollusks. Claim 1: A compound of formula (1) wherein A1, A2, A3 and A4 are each independently CX or nitrogen, wherein each X may be the same or different; R1 is hydrogen, C1-4 alkyl, H2NC (O) -C1-4 alkyl or C1-4 alkylcarbonyl; R2 is hydrogen, halogen, C1-4 alkyl, C1-6 haloalkyl or cyano; G1 is oxygen or sulfur; X is hydrogen, halogen, cyano, C 1-4 alkyl, C 1-4 alkyl or C 1-4 haloalkyl; Q1 is aryl or heterocyclyl, each optionally substituted by one to five R3 substituents, which may be the same or different; or Q1 is C1-8 alkyl or C1-8 alkyl substituted by one to five R4, C2-8 alkenyl, C2-8 alkenyl substituted by one to five R4, C2-8 alkynyl, C2-8 alkynyl substituted by one to five R4 , C3-10 cycloalkyl, C3-10 cycloalkyl substituted by one to five R4 or C1-8- (CO) -N-C1-8 alkyl or C1-8- (CO) -N-C1-8 alkyl substituted by one to five R4; R3 is selected from cyano, amino, nitro, hydroxy, oxo, halogen, C1-4 alkyl, C1-4 haloalkyl, C2-4 alkenyl, C2-4 haloalkenyl, C2-4 alkynyl, C2-4 haloalkynyl, C3-6 cycloalkyl , C3-6 halocycloalkyl, C1-3 alkoxy, C1-3 haloalkoxy, C1-3thio alkyl, C1-3 haloalkyl, C1-3sulfinyl alkyl, C1-3sulfinyl haloalkyl, C1-3sulfonyl alkyl, C1-3alkyl haloalkyl, C1-4amino alkyl , di- (C 1-4 alkyl) -amino, C 1-4 alkylcarbonyl, C 1-4 alkylcarbonyloxy, C 1-4 alkoxycarbonyl, C 1-4 alkylcarbonylamino and phenyl; each R4 is independently halogen, cyano, nitro, hydroxy, C3-10 cycloalkyl, C3-10 cycloalkyl substituted by one to five R3, di (C1-8 alkyl) amino, C1-8 alkanoyl, C1-8 alkyl, C2- alkynyl 8, C1-8 alkoxy, C1-8 haloalkoxy, C1-8thio alkyl, C1-8thio haloalkyl, C1-8sulfinyl alkyl, halo C1-8sulfinyl, C1-8sulfonyl alkyl, C1-8 haloalkyl sulfonyl, C1-8carbonyl alkyl, C1- alkoxy 8carbonyl, aryl or aryl substituted by one to five R3, aryloxy or aryloxy substituted by one to five R3 or heterocyclyl or heterocyclyl substituted by one to five R3; Q2 is a moiety of formula (2) wherein R7 and R6 are independently from each other hydrogen, cyano, halogen, C1-6 alkyl, C1-6 haloalkyl, C1-4 alkoxy-C1-4 alkyl, C1-6 alkyl, haloalkyl C1-6thio, C1-6sulfinyl alkyl, halo- C1-6sulfinyl alkyl, C1-6sulfonyl alkyl or halo- C1-6sulfonyl alkyl; R5 is independently hydrogen, hydroxy, amino, N-C 1-6 alkyl, N, N-di (C 1-6 alkyl) -amino, C 1-6 alkyl, C 3-6 cycloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, C1-6 alkyl substituted by one to five R9 substituents, C3-6 cycloalkyl substituted by one to five R9 substituents, C2-6 alkynyl substituted by one to five R9 substituents, C2-6 alkenyl substituted by one to five R9 substituents, aryl or aryl substituted by one to five R10 substituents, heteroaryl or heteroaryl substituted by one to five R10 substituents; each R9 is independently cyano, nitro, amino, hydroxy, halogen, N-C1-6 alkyl, N, N-di- (C1-6 alkyl) -amino, C1-6 alkoxy, C1-6thio alkyl, C1-6sulfinyl alkyl , aryl or aryl which is substituted by one to five substituents that are independently selected from cyano, nitro, hydroxyl, halogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy or C1-6 haloalkoxy or heteroaryl or heteroaryl which is substituted by one to five substituents that are independently selected from cyano, nitro, hydroxy, halogen, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy or C 1-6 haloalkoxy; each R 10 is independently cyano, nitro, amino, hydroxy, halogen, C 1-6 alkyl, C 1-6 haloalkyl, C 1-4 alkoxy-C 1-4 alkyl, C 2-6 alkenyl, C 2-6 haloalkenyl, C 2-6 alkynyl, haloalkynyl C2-6, C3-6 cycloalkyl, C3-6 halocycloalkyl, C1-6 alkoxy, C1-6 haloalkoxy, C1-4 alkoxy-C1-4 alkoxy, C1-6thio alkyl, haloC1-6thio alkyl, C1-6 alkyl sulfulyl, haloalkyl C1-6 sulfinyl, C1-6 alkyl sulfonyl, halo C1-6 alkyl sulfonyl, N-C1-6 alkyl, N, N-di- (C1-6 alkyl) -amino, N, N-di- (C1-6 alkyl) -aminocarbonyl , N, N-di- (C 1-6 alkyl) -aminosulfonyl, C 1-6 alkylcarbonyl, C 1-6 alkylcarbonyloxy, C 1-6 alkoxycarbonyl, C 1-6 alkylcarbonylamino; or an agrochemically acceptable salt or N-oxides thereof.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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EP11153820 | 2011-02-09 | ||
EP11167014 | 2011-05-23 | ||
EP11179995 | 2011-09-05 |
Publications (1)
Publication Number | Publication Date |
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AR085318A1 true AR085318A1 (en) | 2013-09-25 |
Family
ID=47108302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP120100392A AR085318A1 (en) | 2011-02-09 | 2012-02-07 | TRIAZOL DERIVATIVES THAT HAVE INSECTICIATED ACTIVITY |
Country Status (10)
Country | Link |
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EP (1) | EP2673270A1 (en) |
KR (1) | KR20140051835A (en) |
CN (1) | CN103354811A (en) |
AR (1) | AR085318A1 (en) |
BR (1) | BR112013020213A2 (en) |
CA (1) | CA2826059A1 (en) |
EA (1) | EA201300894A1 (en) |
MX (1) | MX2013009067A (en) |
UY (1) | UY33895A (en) |
WO (1) | WO2012107434A1 (en) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
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AU2014204978A1 (en) | 2013-01-10 | 2015-08-20 | Grünenthal GmbH | Pyrazolyl-based carboxamides I as CRAC channel inhibitors |
EA201500737A1 (en) | 2013-01-10 | 2016-04-29 | Грюненталь Гмбх | PYRAZOLILKARBOXAMIDA II AS CRAC CHANNEL INHIBITORS |
SI2953942T1 (en) * | 2013-02-06 | 2018-03-30 | Bayer Cropscience Ag | Halogen-substituted pyrazole derivatives as pesticides |
ES2616508T3 (en) * | 2013-03-04 | 2017-06-13 | Bayer Cropscience Aktiengesellschaft | Halogen-substituted 1H-pyrazole derivatives as insecticides |
EP3066083B1 (en) | 2013-11-05 | 2019-10-30 | Bayer Animal Health GmbH | Novel compounds for combating arthropods |
KR102400756B1 (en) | 2013-11-05 | 2022-05-20 | 바이엘 애니멀 헬스 게엠베하 | Substituted benzamides for treating arthropodes |
BR112016011899B1 (en) | 2013-11-27 | 2021-03-23 | Bayer Animal Health Gmbh | PROCESS FOR THE PREPARATION OF 5-FLUORO-1H-PIRAZÓIS |
KR102367319B1 (en) * | 2013-11-27 | 2022-02-23 | 바이엘 애니멀 헬스 게엠베하 | Process for the preparation of 5-fluoro-1h-pyrazoles |
RU2016131792A (en) * | 2014-01-03 | 2018-02-06 | Байер Энимэл Хельс ГмбХ | NEW PYRAZOLYL-HETEROARYL AMIDES AS PREVENTIVE AGENTS |
WO2015143654A1 (en) * | 2014-03-26 | 2015-10-01 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS,COMPOSITIONS AND METHODS THEREOF |
WO2015143652A1 (en) | 2014-03-26 | 2015-10-01 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS,COMPOSITIONS AND METHODS THEREOF |
WO2015143653A1 (en) | 2014-03-26 | 2015-10-01 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS,COMPOSITIONS AND METHODS THEREOF |
AR101816A1 (en) * | 2014-04-02 | 2017-01-18 | Bayer Cropscience Ag | DERIVATIVES OF 3 - [(PIRAZOL-5-IL) -HETEROARIL] -BENZAMIDAS AS PESTICIDE AGENTS |
EP3140298A1 (en) * | 2014-05-07 | 2017-03-15 | Pfizer Inc. | Tropomyosin-related kinase inhibitors |
AR100817A1 (en) * | 2014-06-18 | 2016-11-02 | Bayer Cropscience Ag | PIRAZOLES AND TETRAZOLES REPLACED WITH HALOGEN |
AR100821A1 (en) * | 2014-06-18 | 2016-11-02 | Bayer Cropscience Ag | PIRAZOLIL-TRIAZOLIL-PIRIDINAS AS PESTICID AGENTS |
RU2017104717A (en) * | 2014-07-15 | 2018-08-15 | Байер Энимэл Хельс ГмбХ | ARILTRIAZOLYLPYRIDINES AS MEANS FOR PEST CONTROL |
AR101401A1 (en) * | 2014-08-08 | 2016-12-14 | Bayer Cropscience Ag | BIPIRAZOL DERIVATIVES, REPLACED WITH HALOGEN |
AR101448A1 (en) * | 2014-08-08 | 2016-12-21 | Bayer Cropscience Ag | HALOGEN SUBSTITUTED COMPOUNDS |
PL3183237T3 (en) * | 2014-08-19 | 2020-03-31 | Bayer Animal Health Gmbh | Process for the preparation of 5-fluoro-1h-pyrazoles starting from hexafluoropropene |
WO2016161572A1 (en) | 2015-04-08 | 2016-10-13 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
WO2016174049A1 (en) | 2015-04-30 | 2016-11-03 | Bayer Animal Health Gmbh | Anti-parasitic combinations including halogen-substituted compounds |
US20180084782A1 (en) * | 2015-05-05 | 2018-03-29 | Syngenta Participations Ag | Method of control of stinkbugs |
CN108137509B (en) | 2015-08-13 | 2021-03-19 | 拜耳作物科学股份公司 | Pyrrole, oxadiazole, triazole or tetrazole derivatives suitable for controlling arthropods |
CA3006911A1 (en) * | 2015-12-22 | 2017-06-29 | Syngenta Participations Ag | Pesticidally active pyrazole derivatives |
BR112018016794B1 (en) * | 2016-02-18 | 2022-07-19 | Syngenta Participations Ag | ACTIVE PYRAZOLE DERIVATIVES IN TERMS OF PESTICIDES, PESTICIDE COMPOSITION, METHOD FOR CONTROL OF PESTS, METHOD FOR PROTECTING VEGETABLE PROPAGATION MATERIAL FROM PEST ATTACK AND VEGETABLE PROPAGATION MATERIAL |
CN105753795B (en) * | 2016-04-29 | 2018-04-13 | 济南大学 | A kind of alkaloid compound with 1,2,3 triazole structure fragments and application thereof |
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CN110475776B (en) | 2017-03-31 | 2024-03-19 | 拜耳作物科学股份公司 | Tricyclic carboxamides for combating arthropods |
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CN110770223B (en) * | 2017-06-19 | 2023-08-22 | 先正达参股股份有限公司 | Pesticidally active pyrazole derivatives |
AR112673A1 (en) | 2017-08-11 | 2019-11-27 | Syngenta Participations Ag | PYRAZOLE DERIVATIVES ACTIVE AS PESTICIDES |
AR112672A1 (en) | 2017-08-11 | 2019-11-27 | Syngenta Participations Ag | THIOPHENE DERIVATIVES ACTIVE AS PESTICIDES |
EP3665166A1 (en) | 2017-08-11 | 2020-06-17 | Syngenta Participations AG | Pesticidally active pyrazole derivatives |
EP3665167B1 (en) | 2017-08-11 | 2022-11-30 | Syngenta Participations AG | Pesticidally active pyrazole derivatives |
WO2019068819A1 (en) | 2017-10-06 | 2019-04-11 | Syngenta Participations Ag | Pesticidally active pyrrole derivatives |
US11384074B2 (en) | 2017-10-06 | 2022-07-12 | Syngenta Participations Ag | Pesticidally active pyrrole derivatives |
CN108934821A (en) * | 2018-06-28 | 2018-12-07 | 遵义天旺华胜种植有限公司 | The insect-pest cultural method of capsicum |
EP3590927A1 (en) | 2018-07-05 | 2020-01-08 | Bayer Animal Health GmbH | Novel compounds for controlling arthropods |
WO2020064565A1 (en) * | 2018-09-26 | 2020-04-02 | Syngenta Crop Protection Ag | Insecticidal compounds |
WO2020127345A1 (en) | 2018-12-21 | 2020-06-25 | Syngenta Participations Ag | Pesticidally active pyrazole derivatives |
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WO2020164994A1 (en) | 2019-02-13 | 2020-08-20 | Syngenta Crop Protection Ag | Pesticidally active pyrazole derivatives |
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- 2012-02-07 AR ARP120100392A patent/AR085318A1/en not_active Application Discontinuation
- 2012-02-07 WO PCT/EP2012/052027 patent/WO2012107434A1/en active Application Filing
- 2012-02-07 CA CA2826059A patent/CA2826059A1/en not_active Abandoned
- 2012-02-07 BR BR112013020213A patent/BR112013020213A2/en not_active IP Right Cessation
- 2012-02-07 EP EP12703298.5A patent/EP2673270A1/en not_active Withdrawn
- 2012-02-07 EA EA201300894A patent/EA201300894A1/en unknown
- 2012-02-07 UY UY0001033895A patent/UY33895A/en not_active Application Discontinuation
- 2012-02-07 MX MX2013009067A patent/MX2013009067A/en unknown
- 2012-02-07 CN CN2012800082636A patent/CN103354811A/en active Pending
- 2012-02-07 KR KR1020137023644A patent/KR20140051835A/en not_active Application Discontinuation
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CN103354811A (en) | 2013-10-16 |
CA2826059A1 (en) | 2012-08-16 |
BR112013020213A2 (en) | 2016-08-02 |
EA201300894A1 (en) | 2014-01-30 |
MX2013009067A (en) | 2013-10-01 |
WO2012107434A8 (en) | 2013-05-02 |
KR20140051835A (en) | 2014-05-02 |
UY33895A (en) | 2012-09-28 |
WO2012107434A1 (en) | 2012-08-16 |
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