AR106165A1 - Derivados heterocíclicos condensados sustituidos por 2-(het)arilo como pesticidas - Google Patents
Derivados heterocíclicos condensados sustituidos por 2-(het)arilo como pesticidasInfo
- Publication number
- AR106165A1 AR106165A1 ARP160102944A ARP160102944A AR106165A1 AR 106165 A1 AR106165 A1 AR 106165A1 AR P160102944 A ARP160102944 A AR P160102944A AR P160102944 A ARP160102944 A AR P160102944A AR 106165 A1 AR106165 A1 AR 106165A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- alkylsulfinyl
- alkylsulfonyl
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 75
- -1 C2−6 cyanoalkenyl Chemical group 0.000 abstract 36
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 13
- 125000005089 alkenylaminocarbonyl group Chemical group 0.000 abstract 11
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 abstract 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 10
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 9
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical group 0.000 abstract 9
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 8
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 8
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 8
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 8
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 8
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 8
- 125000001072 heteroaryl group Chemical group 0.000 abstract 8
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 7
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 7
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 7
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 7
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 7
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 7
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 7
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 7
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 abstract 6
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 6
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 6
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 6
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 6
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 6
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 6
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000005103 alkyl silyl group Chemical group 0.000 abstract 6
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 6
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 6
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 6
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 6
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 229920006395 saturated elastomer Polymers 0.000 abstract 6
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 6
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 4
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Reivindicaciones 1: Compuestos de la fórmula (1), en la que A¹ representa nitrógeno, =N⁺(O⁻)- o =C(R⁴)-; R¹ representa C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₁₋₆ haloalcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alqueniloxi-C₁₋₆ alquilo, C₂₋₆ haloalqueniloxi-C₁₋₆ alquilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ alquiniloxi-C₁₋₆ alquilo, C₂₋₆ haloalquiniloxi-C₁₋₆ alquilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquilo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo-C₃₋₈ cicloalquilo, halógeno-C₃₋₈ cicloalquilo, amino, C₁₋₆ alquilamino, di-C₁₋₆ alquil-amino, C₃₋₈ cicloalquilamino, C₁₋₆ alquilcarbonilo-amino, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ haloalquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ haloalquilsulfinil-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ haloalquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alquilcarbonilo-C₁₋₆ alquilo, C₁₋₆ haloalquilcarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ haloalcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilamino, aminosulfonil-C₁₋₆ alquilo, C₁₋₆ alquilaminosulfonil-C₁₋₆ alquilo, di-C₁₋₆ alquil-aminosulfonil-C₁₋₆ alquilo, o representa C₁₋₆ alquilo, C₁₋₆ alcoxi, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₃₋₈ cicloalquilo sustituido en cada caso opcionalmente en forma simple o múltiple, idéntico o distinto, por arilo, hetarilo o heterociclilo, donde arilo, hetarilo o heterociclilo en cada caso opcionalmente en forma simple o múltiple, idéntico o distinto pueden estar sustituidos por halógeno, ciano, nitro, hidroxi, amino, carboxi, carbamoil, aminosulfonilo, C₁₋₆ alquilo, C₃₋₆ cicloalquilo, C₁₋₆ alcoxi, C₁₋₆ haloalquilo, C₁₋₆ haloalcoxi, C₁₋₆ alquiltio, C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfimino, C₁₋₆ alquilsulfimino-C₁₋₆ alquilo, C₁₋₆ alquilsulfimino-C₂₋₆ alquilcarbonilo, C₁₋₆ alquilsulfoximino, C₁₋₆ alquilsulfoximino-C₁₋₆ alquilo, C₁₋₆ alquilsulfoximino-C₂₋₆ alquilcarbonilo, C₁₋₆ alcoxicarbonilo, C₁₋₆ alquilcarbonilo, C₃₋₆ trialquilsililo o bencilo, o R¹ representa arilo, hetarilo o heterociclilo sustituidos en cada caso opcionalmente en forma simple o múltiple, idéntico o distinto por halógeno, ciano, nitro, hidroxi, amino, carboxi, carbamoil, C₁₋₆ alquilo, C₃₋₈ cicloalquilo, C₁₋₆ -alcoxi, C₁₋₆ haloalquilo, C₁₋₆ haloalcoxi, C₁₋₆ alquiltio, C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfimino, C₁₋₆ alquilsulfimino-C₁₋₆ alquilo, C₁₋₆ alquilsulfimino-C₂₋₆ alquilcarbonilo, C₁₋₆ alquilsulfoximino, C₁₋₆ alquilsulfoximino-C₁₋₆ alquilo, C₁₋₆ alquilsulfoximino-C₂₋₆ alquilcarbonilo, C₁₋₆ alcoxicarbonilo, C₁₋₆ alquilcarbonilo, C₃₋₆ trialquilsililo, (=O) (sólo en el caso de heterociclilo) o (=O)₂ (sólo en el caso de heterociclilo); R² representa un anillo opcionalmente sustituido en forma simple o múltiple, idéntico o distinto saturado, parcialmente saturado o heteroaromático, en el que al menos un átomo C está sustituido por un heteroátomo, donde al menos puede estar contenido un grupo carbonilo y/o donde como sustituyentes se consideran: ciano, carboxilo, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsilil, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonilo-C₁₋₆ -alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₃₋₆ cicloalquilo, C₃₋₆ cicloalquilo-C₃₋₆ cicloalquilo, C₁₋₄ alquilo-C₃₋₆ cicloalquilo C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alcoxiimino, -N=C(H)-OC₁₋₆ alquilo, -C(H)=N-OC₁₋₆ alquilo, C₁₋₆ haloalquilo-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquilaminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquilaminotiocarbonilo, C₃₋₈ cicloalquilamino, C₁₋₆ alquilcarbonilamino; V representa un anillo opcionalmente sustituido en forma simple o múltiple, idéntico o distinto, saturado, parcialmente saturado o heteroaromático, en el que al menos un átomo C está sustituido por un heteroátomo o representa un anillo aromático sustituido en forma simple o múltiple, idéntico o distinto, donde al menos puede estar contenido un grupo carbonilo y/o donde como sustituyentes se consideran: ciano, carboxilo, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsilil, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonilo-C₁₋₆ alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₃₋₆ cicloalquilo, C₃₋₆ cicloalquilo-C₃₋₆ cicloalquilo, C₁₋₄ alquilo-C₃₋₆ cicloalquilo C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alcoxiimino, -N=C(H)-OC₁₋₆ alquilo, -C(H)=N-OC₁₋₆ alquilo, C₁₋₆ haloalquilo-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquilaminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquilaminotiocarbonilo, C₃₋₈ cicloalquilamino, C₁₋₆ alquilcarbonilamino; R³ representa hidrógeno, ciano, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsilil, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquilo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo-C₃₋₈ cicloalquilo, halógeno-C₃₋₈ cicloalquilo, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonilo-C₁₋₆ alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alquilhidroxiimino, C₁₋₆ alcoxiimino, C₁₋₆ alquilo-C₁₋₆ alcoxiimino, C₁₋₆ haloalquilo-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ alquiltiocarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquil-aminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₃₋₈ cicloalquilamino, NHCO-C₁₋₆ alquilo-(C₁₋₆ alquilcarbonilamino), representa en cada caso opcionalmente en forma simple o múltiple, idéntico o distinto, en forma independiente arilo o hetarilo sustituido, donde (en el caso de hetarilo) opcionalmente puede contener al menos un grupo carbonilo y/o donde como sustituyentes se consideran: ciano, carboxilo, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsilil, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquilo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo-C₃₋₈ cicloalquilo, halógeno-C₃₋₈ cicloalquilo, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonilo-C₁₋₆ alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alquilhidroxiimino, C₁₋₆ alcoxiimino, C₁₋₆ alquilo-C₁₋₆ alcoxiimino, C₁₋₆ haloalquilo-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquilaminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquilaminotiocarbonilo, C₃₋₈ cicloalquilamino, C₁₋₆ alquilcarbonilamino; R⁴ representa hidrógeno, ciano, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsilil, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquilo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo-C₃₋₈ cicloalquilo, halógeno-C₃₋₈ cicloalquilo, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonilo-C₁₋₆ -alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alquilhidroxiimino, C₁₋₆ alcoxiimino, C₁₋₆ alquilo-C₁₋₆ alcoxiimino, C₁₋₆ haloalquilo-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ alquiltiocarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquil-aminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₃₋₈ cicloalquilamino o -NHCO-C₁₋₆ alquilo-(C₁₋₆ alquilcarbonilamino); X representa un sistema de anillos condensados, bi- o tricíclico, parcialmente saturado o saturado, heterocíclico o heteroaromático de 8, 9 10, 11 ó 12 miembros, que puede contener al menos un grupo carbonilo y/o donde el sistema de anillos opcionalmente pueden estar sustituidos en forma simple o múltiple, idéntico o distinto y donde los sustituyentes pueden ser seleccionados independientemente de hidrógeno, ciano, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsilil, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquilo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo-C₃₋₈ cicloalquilo, halógeno-C₃₋₈ cicloalquilo, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonilo-C₁₋₆ alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ alquiniloxi-C₁₋₄ alquilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ haloalcoxi-C₁₋₆ alquilo, C₂₋₆ alqueniloxi-C₁₋₆ alquilo, C₂₋₆ haloalqueniloxi-C₁₋₆ alquilo, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alquilhidroxiimino, C₁₋₆ alcoxiimino, C₁₋₆ alquilo-C₁₋₆ alcoxiimino, C₁₋₆ haloalquilo-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonilo-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ alquilcarbonilo-C₁₋₆ alquilo, C₁₋₆ alquiltiocarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquil-aminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₃₋₈ cicloalquilamino, NHCO-C₁₋₆ alquilo-(C₁₋₆ alquilcarbonilamino), o donde los sustituyentes pueden ser seleccionados independientemente de fenilo o de un anillo heteroaromático de 5 ó 6 miembros, en el que el fenilo o el anillo opcionalmente pueden estar sustituidos en forma simple o múltiple, idéntico o distinto por C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₃₋₆ cicloalquilo, C₁₋₆ haloalquilo, C₂₋₆ haloalquenilo, C₂₋₆ haloalquinilo, C₃₋₆ halocicloalquilo, halógeno, CN, NO₂, C₁₋₄ alcoxi, C₁₋₄ haloalcoxi; n representa 0, 1 ó 2.
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| TWI762568B (zh) | 2017-02-06 | 2022-05-01 | 德商拜耳作物科學股份有限公司 | 製備鹵化咪唑並吡啶衍生物之方法 |
| TW201833107A (zh) | 2017-02-06 | 2018-09-16 | 德商拜耳廠股份有限公司 | 作為殺蟲劑之經２－（雜）芳基取代的稠合雜環衍生物 |
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| WO2015198859A1 (ja) | 2014-06-26 | 2015-12-30 | 住友化学株式会社 | 縮合複素環化合物 |
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| WO2016020286A1 (en) | 2014-08-07 | 2016-02-11 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| BR112017002598B1 (pt) | 2014-08-12 | 2022-03-03 | Syngenta Participations Ag | Derivados heterocíclicos ativos do ponto de vista pesticida com substituintes contendo enxofre |
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| WO2016046071A1 (en) | 2014-09-25 | 2016-03-31 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
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- 2016-09-23 EP EP16770499.8A patent/EP3356362B1/de active Active
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| JP6871917B2 (ja) | 2021-05-19 |
| ES2866911T3 (es) | 2021-10-20 |
| KR20180054680A (ko) | 2018-05-24 |
| KR102629107B1 (ko) | 2024-01-24 |
| EP3356362B1 (de) | 2021-02-03 |
| JP2018529702A (ja) | 2018-10-11 |
| TW201726672A (zh) | 2017-08-01 |
| UY36918A (es) | 2017-04-28 |
| US10745398B2 (en) | 2020-08-18 |
| IL258089A (en) | 2018-05-31 |
| AU2016330299A1 (en) | 2018-04-12 |
| CL2018000741A1 (es) | 2019-04-26 |
| EP3356362A1 (de) | 2018-08-08 |
| RU2018116054A (ru) | 2019-10-28 |
| US20180303097A1 (en) | 2018-10-25 |
| PH12018500638A1 (en) | 2018-10-01 |
| BR112018006198A2 (pt) | 2018-10-09 |
| PE20181094A1 (es) | 2018-07-09 |
| TWI720023B (zh) | 2021-03-01 |
| CN108290886B (zh) | 2020-11-03 |
| PH12018500638B1 (en) | 2022-06-03 |
| MX2018003761A (es) | 2018-07-06 |
| ZA201802797B (en) | 2020-01-29 |
| WO2017055185A1 (de) | 2017-04-06 |
| BR112018006198B1 (pt) | 2022-05-31 |
| CO2018003427A2 (es) | 2018-06-12 |
| AU2016330299B2 (en) | 2020-04-30 |
| CA2999790A1 (en) | 2017-04-06 |
| CN108290886A (zh) | 2018-07-17 |
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