AR127913A1 - Compuestos de piridazinona activos como pesticidas - Google Patents
Compuestos de piridazinona activos como pesticidasInfo
- Publication number
- AR127913A1 AR127913A1 ARP220103379A ARP220103379A AR127913A1 AR 127913 A1 AR127913 A1 AR 127913A1 AR P220103379 A ARP220103379 A AR P220103379A AR P220103379 A ARP220103379 A AR P220103379A AR 127913 A1 AR127913 A1 AR 127913A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- substituted
- alkoxy
- cycloalkyl
- haloalkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000000575 pesticide Substances 0.000 title 1
- 125000001424 substituent group Chemical group 0.000 abstract 16
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 11
- 125000001188 haloalkyl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 8
- -1 oxetan-3-yl-CH2- Chemical group 0.000 abstract 7
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 3
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 3
- 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 2
- 125000004770 (C1-C4) haloalkylsulfanyl group Chemical group 0.000 abstract 2
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 abstract 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 abstract 2
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000006528 (C2-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006660 (C3-C4) halocycloalkyl group Chemical group 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- SXZIXHOMFPUIRK-UHFFFAOYSA-N diphenylmethanimine Chemical compound C=1C=CC=CC=1C(=N)C1=CC=CC=C1 SXZIXHOMFPUIRK-UHFFFAOYSA-N 0.000 abstract 1
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004971 nitroalkyl group Chemical group 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Chemical group O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
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- 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
- C07D403/14—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 three or more hetero 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
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
-
- 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
- A01N43/713—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
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
- A01P7/02—Acaricides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
- A01P7/04—Insecticides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Organic Chemistry (AREA)
- Insects & Arthropods (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto de fórmula (1) donde: A¹, A² y A³ son, independientemente entre sí, N o CRY; o A¹=A²-A³, tomados juntos, son NR-C(=X)-N; donde X es O o S; A⁴ y A⁵ son, independientemente entre sí, N o CRY; Q es Qᵃ o Qᵇ, de fórmula (2) o (3), donde la línea escalonada representa la conexión de Q al resto de compuesto de fórmula (1); R es hidrógeno, alquilo C₁-C₃, haloalquilo C₁-C₃, alcoxilo C₁-C₃, o haloalcoxilo C₁-C₃; R¹ es hidrógeno, alquilo C₁-C₆, cianoalquilo C₁-C₆, aminocarbonil-alquilo C₁-C₆, hidroxicarbonil-alquilo C₁-C₆, nitroalquilo C₁-C₆, trimetilsilano-alquilo C₁-C₆, alcoxi C₁-C₃-alquilo C₁-C₆, haloalquilo C₁-C₆, alquenilo C₂-C₆, haloalquenilo C₂-C₆, alquinilo C₂-C₆, haloalquinilo C₂-C₆, cicloalquil C₃-C₄-alquil C₁-C₂-, cicloalquil C₃-C₄-alquil C₁-C₂- donde el grupo cicloalquilo C₃-C₄ está sustituido con 1 o 2 átomos de halógeno, oxetan-3-ilo-CH₂-, alquilcarbonilo C₁-C₆, alcoxicarbonilo C₁-C₆, feniloxicarbonilo, benciloxicarbonilo, bencilo o bencilo sustituido con de 1 a 3 sustituyentes seleccionados independientemente de halógeno, alcoxilo C₁-C₆ y haloalquilo C₁-C₆; R²ᵃ y R²ᵇ se seleccionan cada uno independientemente de hidrógeno, alquilo C₁-C₃, haloalquilo C₁-C₃, haloalquilsulfanilo C₁-C₃, alcoxilo C₁-C₃, haloalcoxilo C₁-C₃, halógeno, NO₂, SF₅, CN, C(O)NH₂, C(O)OH, C(S)NH₂, cicloalquilo C₃-C₆, cicloalquilo C₃-C₆ sustituido con de uno a tres sustituyentes seleccionados independientemente de Rˣ, cicloalquilcarbonilo C₃-C₆, fenilo, fenilo sustituido con de uno a tres sustituyentes seleccionados independientemente de Rˣ, heteroarilo, heteroarilo sustituido con de uno a tres sustituyentes seleccionados independientemente de Rˣ, OR⁶, piperidin-2-ona-1-ilo, piperidin-2-ona-1-ilo sustituido con de uno a dos sustituyentes seleccionados independientemente de Rˣ, piridin-2-ona-1-ilo, piridin-2-ona-1-ilo sustituido con de uno a dos sustituyentes seleccionados independientemente de Rˣ, azetidin-1-ilo, azetidin-1-ilo sustituido con de uno a dos sustituyentes seleccionados independientemente de Rˣ, pirrolidin-1-ilo, pirrolidin-1-ilo sustituido con de uno a dos sustituyentes seleccionados independientemente de Rˣ, cicloalquil C₃-C₆-alquilo C₁-C₄, cicloalquil C₃-C₆-alquilo C₁-C₄ sustituido con de uno a dos sustituyentes seleccionados independientemente de Rᶻ, cicloalquil C₃-C₆-alcoxilo C₁-C₃, cicloalquil C₃-C₆-alcoxilo C₁-C₃ sustituido con de uno a dos sustituyentes seleccionados independientemente de Rˣ, cianoalquilo C₁-C₅, cianoalcoxilo C₁-C₅, alquilsulfanilo C₁-C₄, alquilsulfanilo C₁-C₄ sustituido con de uno a tres sustituyentes seleccionados independientemente de Rˣ, alquilsulfonilo C₁-C₄, alquilsulfonilo C₁-C₄ sustituido con de uno a tres sustituyentes seleccionados independientemente de Rˣ, alquilsulfinilo C₁-C₄, y alquilsulfinilo C₁-C₄ sustituido con de uno a tres sustituyentes seleccionados independientemente de Rˣ; R³ es alquilo C₁-C₃ o haloalquilo C₁-C₃; R⁴ es R⁴ᵃ o R⁴ᵇ, de fórmula (4) o (5), donde la línea escalonada representa la conexión de R⁴ a Qᵃ o Qᵇ; A¹⁴, A²⁴, y A³⁴ son, independientemente entre sí, N o CH; R⁴ᶜ es alquilo C₁-C₃, haloalquilo C₁-C₃, alilo, propargilo, o cicloalquil C₃-C₆-alquilo C₁-C₄; R⁵ es hidrógeno, alquilo C₁-C₃, haloalquilo C₁-C₃, cicloalquilo C₃-C₄, alcoxilo C₁-C₃, alcoxi C₃-C₄-C(O)-, (alcoxi C₁-C₃)₂CH-, halógeno, CN, NH₂C(O), amino (es decir, NH₂), (alquil C₁-C₃)amino, di(alquil C₁-C₃)amino, hidroxilo, halocicloalquilo C₃-C₄, cianocicloalquilo C₃-C₄, alquenilo C₂-C₆, haloalquenilo C₂-C₆, alquinilo C₂-C₆, haloalquinilo C₂-C₆, haloalquilsulfanilo C₁-C₄, haloalquilsulfinilo C₁-C₄, haloalquilsulfonilo C₁-C₄, alquilsulfanilo C₁-C₄, alquilsulfinilo C₁-C₄, alquilsulfonilo C₁-C₄, alcoxi C₁-C₃-alquilo C₁-C₃, alcoxi C₁-C₃-alcoxi C₁-C₃-alquilo C₁-C₃, (alquil C₁-C₃)sulfonilamino, (alquil C₁-C₃)sulfonil(alquil C₁-C₃)amino, (alquil C₁-C₃)NHC(O), (alquil C₁-C₃)₂NC(O), (cicloalquil C₁-C₃)NHC(O), (cicloalquil C₁-C₃)(alquil C₁-C₃)NC(O), (alquilo C₁-C₃)C(O)(alquilo C₁-C₃)N, (alquilo C₁-C₃)C(O)NH, (alquilo C₁-C₃)C(O), (alcoxilo C₁-C₃)C(O), HC(O), difenilmetanimina, haloalcoxilo C₁-C₃, fenilo, o un anillo heteroaromático de 5 miembros; o R⁵ es fenilo sustituido con de uno a tres sustituyentes seleccionados de alquilo C₁-C₃, haloalquilo C₁-C₃, alcoxilo C₁-C₃, cicloalquilo C₃-C₄, halógeno, CN e hidroxilo; o R⁵ es un anillo heteroaromático de 5 miembros sustituido con de uno a tres sustituyentes seleccionados de alquilo C₁-C₃, haloalquilo C₁-C₃, alcoxilo C₁-C₃, cicloalquilo C₃-C₄, halógeno, CN e hidroxilo; R⁵ᵃ y R⁵ᵇ son, independientemente entre sí, seleccionados de hidrógeno, halógeno, CN, alquilo C₁-C₃, haloalquilo C₁-C₃, cicloalquilo C₃-C₄, alcoxilo C₁-C₃, y haloalcoxilo C₁-C₃; R⁶ es fenilo, bencilo, heteroarilo, o cicloalquilo C₃-C₆; o R⁶ es fenilo, bencilo, heteroarilo, o cicloalquilo C₃-C₆, cada uno de los cuales, independientes entre sí, está sustituido con de uno a tres sustituyentes seleccionados independientemente de Rˣ; Rˣ se selecciona independientemente de halógeno, alquilo C₁-C₃, haloalquilo C₁-C₃, alcoxilo C₁-C₃, haloalcoxilo C₁-C₃, NO₂, SF₅, CN, C(O)NH₂, C(S)NH₂, haloalquilsulfanilo C₁-C₄, haloalquilsulfinilo C₁-C₄, haloalquilsulfonilo C₁-C₄, alquilsulfanilo C₁-C₄, alquilsulfinilo C₁-C₄ y alquilsulfonilo C₁-C₄; RY se selecciona de hidrógeno, alquilo C₁-C₃, haloalquilo C₁-C₃, hidroxilo, alcoxilo C₁-C₃, haloalcoxilo C₁-C₃, halógeno, CN y ciclopropilo; y Rᶻ se selecciona de oxo, halógeno, alquilo C₁-C₃, haloalquilo C₁-C₃, alcoxilo C₁-C₃, haloalcoxilo C₁-C₃ y CN; o una sal, estereoisómero, enantiómero, tautómero y N-óxido agroquímicamente aceptables del compuesto de fórmula (1).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN202111057521 | 2021-12-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR127913A1 true AR127913A1 (es) | 2024-03-06 |
Family
ID=84627238
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP220103379A AR127913A1 (es) | 2021-12-10 | 2022-12-08 | Compuestos de piridazinona activos como pesticidas |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR127913A1 (es) |
| TW (1) | TW202342459A (es) |
| WO (1) | WO2023104714A1 (es) |
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-
2022
- 2022-12-05 WO PCT/EP2022/084409 patent/WO2023104714A1/en unknown
- 2022-12-08 TW TW111147215A patent/TW202342459A/zh unknown
- 2022-12-08 AR ARP220103379A patent/AR127913A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2023104714A1 (en) | 2023-06-15 |
| TW202342459A (zh) | 2023-11-01 |
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