AR111684A1 - Compuestos plaguicidas bicíclicos - Google Patents
Compuestos plaguicidas bicíclicosInfo
- Publication number
- AR111684A1 AR111684A1 ARP180101215A ARP180101215A AR111684A1 AR 111684 A1 AR111684 A1 AR 111684A1 AR P180101215 A ARP180101215 A AR P180101215A AR P180101215 A ARP180101215 A AR P180101215A AR 111684 A1 AR111684 A1 AR 111684A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- substituted
- cycloalkyl
- unsubstituted
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 18
- 229910052736 halogen Inorganic materials 0.000 abstract 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 10
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 10
- 125000005843 halogen group Chemical group 0.000 abstract 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 8
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- -1 tri -C1−6-alkylsilyl Chemical group 0.000 abstract 4
- 125000006570 (C5-C6) heteroaryl 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
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—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
- A01N43/90—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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pest Control & Pesticides (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Insects & Arthropods (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Reivindicación 1: Un compuesto caracterizado por la fórmula (1), en donde X es O ó S; Rˣ se selecciona del grupo que consiste en C₁₋₆-alquilo, C₁₋₆-alcoxi, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₁₋₆-alcoxi-C₁₋₄-alcoxi, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, C(O)-ORᵃ, NRᵇRᶜ, C₁₋₆-alquilen-NRᵇRᶜ, O-C₁₋₆-alquilen-NRᵇRᶜ, C₁₋₆-alquilen-CN, NH-C₁₋₆-alquilen-NRᵇRᶜ, C(O)-NRᵇRᶜ, C(O)-Rᵈ, SO₂NRᵇRᶜ, S(=O)ₘRᵉ, fenilo y bencilo, en donde el anillo de fenilo es no sustituido o sustituido con radicales Rᶠ; R¹ es H, C₁₋₆-alquilo, C₁₋₆-alcoxi, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalcoxi, C₁₋₆-alquilsulfenilo, C₁₋₆-alquilsulfinilo o C₁₋₆-alquilsulfonilo que son sustituidos o no sustituidos con halógeno; R², R³ se seleccionan, independientemente entre sí, del grupo que consiste en H, halógeno, N₃, CN, NO₂, -SCN, -SF₅, C₁₋₆-alquilo, C₁₋₆-alcoxi, C₂₋₆-alquenilo, tri-C₁₋₆-alquilsililo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₁₋₆-alcoxi-C₁₋₄-alcoxi, C₃₋₆-cicloalquilo, C₃₋₆-cicloalcoxi, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, C(O)-ORᵃ, NRᵇRᶜ, C₁₋₆-alquilen-NRᵇRᶜ, O-C₁₋₆-alquilen-NRᵇRᶜ, C₁₋₆-alquilen-CN, NH-C₁₋₆-alquilen-NRᵇRᶜ, C(O)-NRᵇRᶜ, C(O)-Rᵈ, SO₂NRᵇRᶜ y S(=O)ₘRᵉ, un radical también puede ser fenilo, fenoxi, fenilcarbonilo, feniltio o bencilo, en donde el anillo de fenilo es no sustituido o sustituido con radicales Rᶠ; Ar es fenilo o heteroarilo de 5 ó 6 miembros; RAʳ se seleccionan, independientemente entre sí, del grupo que consiste en halógeno, N₃, OH, CN, NO₂, -SCN, -SF₅, C₁₋₆-alquilo, C₁₋₆-alcoxi, C₂₋₆-alquenilo, tri-C₁₋₆-alquilsililo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₁₋₆-alcoxi-C₁₋₄-alcoxi, C₃₋₆-cicloalquilo, C₃₋₆-cicloalcoxi, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, C(O)-ORᵃ, NRᵇRᶜ, C₁₋₆-alquilan-NRᵇRᶜ, O-C₁₋₆-alquilen-NRᵇRᶜ, C₁₋₆-alquilen-CN, NH-C₁₋₆-alquilen-NRᵇRᶜ, C(O)-NRᵇRᶜ, C(O)-Rᵈ, SO₂NRᵇRᶜ y S(=O)ₘRᵉ, un radical también puede ser fenilo, fenoxi, fenilcarbonilo, feniltio o bencilo, en donde el anillo de fenilo es no sustituido o sustituido con radicales Rᶠ; Het es heteroarilo de 5 ó 6 miembros o heterociclilo de 5 ó 6 miembros, que es no sustituido o sustituido con R; R es halógeno, oxo (=O), N₃, OH, CN, NO₂, SCN, SF₅, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄,-alquilo, C₁₋₆-alcoxi-C₁₋₄-alcoxi, C₁₋₆-alcoxicarbonilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalcoxi, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄ alquilo, fenilo, heteroarilo de 5 ó 6 miembros o heterociclilo de 5 ó 6 miembros, en donde los grupos cíclicos de R son no sustituidos o sustituidos con radicales Rᶠ; siempre que RAʳ y Het no estén ambos presentes en el mismo átomo de Ar; cada Rᵃ se selecciona de H, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, C₁₋₆-alquilen-NRᵇRᶜ, C₁₋₆-alquilen-CN, fenilo y bencilo, en donde el anillo de fenilo es no sustituido o sustituido con radicales Rᶠ; cada Rᵇ se selecciona de H, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, (C=O)R, -C(=O)OR y -C(=O)NR, C₁₋₆-alquilen-CN, fenilo y bencilo, en donde el fenilo es no sustituido o sustituido con radicales Rᶠ; cada Rᶜ se selecciona de H, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, C₁₋₆-alquilen-CN, fenilo y bencilo, en donde el anillo de fenilo es no sustituido o sustituido con radicales Rᶠ; cada porción NRᵇRᶜ también puede formar un heterociclo unido a N, saturado de 3 a 8 miembros, que además del átomo de nitrógeno, puede tener 1 ó 2 heteroátomos adicionales o porciones de heteroátomos seleccionadas de O, S(=O)ₘ y N-R, en donde R es H o C₁₋₆-alquilo y en donde el heterociclo unido a N es no sustituido o sustituido con radicales seleccionados de halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; cada Rᵈ se selecciona de H, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, fenilo y bencilo, en donde el anillo de fenilo es no sustituido o sustituido con radicales Rᶠ; cada Rᵉ se selecciona de C₁₋₆-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno, fenilo y bencilo, en donde el anillo de fenilo es no sustituido o sustituido con Rᶠ; cada Rᶠ se selecciona de halógeno, N₃, OH, CN, NO₂, SCN, SF₅, C₁₋₆-alquilo, C₁₋₆-alcoxi, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₁₋₆-alcoxi-C₁₋₄-alcoxi, C₃₋₆-cicloalquilo, C₃₋₆-cicloalcoxi, C₃₋₆-cicloalquil-C₁₋₄-alquilo, C₃₋₆-cicloalcoxi-C₁₋₄-alquilo, que son no sustituidos o sustituidos con halógeno; m es 0, 1 ó 2; n es 0 1 ó 2; y los N-óxidos, estereoisómeros, tautómeros y las sales aceptables en la agricultura o veterinaria de aquel.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17170404 | 2017-05-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR111684A1 true AR111684A1 (es) | 2019-08-07 |
Family
ID=58699069
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP180101215A AR111684A1 (es) | 2017-05-10 | 2018-05-09 | Compuestos plaguicidas bicíclicos |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US11591335B2 (es) |
| EP (1) | EP3621967B1 (es) |
| JP (1) | JP2020519607A (es) |
| KR (1) | KR102694625B1 (es) |
| CN (1) | CN110546152B (es) |
| AR (1) | AR111684A1 (es) |
| AU (1) | AU2018266990B2 (es) |
| CA (1) | CA3059282A1 (es) |
| CL (1) | CL2019003213A1 (es) |
| ES (1) | ES2910854T3 (es) |
| IL (1) | IL270403B (es) |
| MX (1) | MX2019013419A (es) |
| RU (1) | RU2019139232A (es) |
| UA (1) | UA125047C2 (es) |
| WO (1) | WO2018206479A1 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20252542A1 (es) | 2018-07-14 | 2025-10-27 | Fmc Corp | Compuestos derivados de 2-(3-piridinil)-2h-indazol-4-carboxamidas con actividad pesticida |
| AR119140A1 (es) | 2019-06-13 | 2021-11-24 | Pi Industries Ltd | Compuestos heterocíclicos fusionados y su uso como agentes de control de plagas |
| US20220411428A1 (en) * | 2019-11-22 | 2022-12-29 | Basf Se | Pyrimidone Derivatives Containing Two Fused Bicyclic Rings |
| AU2021251335A1 (en) | 2020-04-06 | 2022-10-27 | Basf Se | Imidazo-pyrimidone compounds as pesticides |
| WO2022128524A1 (en) | 2020-12-14 | 2022-06-23 | Basf Se | Sulfoximine pesticides |
| CA3211349A1 (en) | 2021-03-09 | 2022-09-15 | Basf Se | Tricyclic pesticidal compounds |
| EP4305033B1 (en) | 2021-03-09 | 2025-05-07 | Basf Se | Tricyclic pesticidal compounds |
| CN112979721B (zh) * | 2021-03-29 | 2023-05-09 | 江苏集萃分子工程研究院有限公司 | 一种高纯度抗肿瘤药曲氟胞苷的制备方法 |
| WO2025229111A1 (en) | 2024-05-01 | 2025-11-06 | Basf Se | Pyrimidinone derivatives as pesticidal compounds |
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- 2018-05-07 WO PCT/EP2018/061652 patent/WO2018206479A1/en not_active Ceased
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| JP2020519607A (ja) | 2020-07-02 |
| CN110546152A (zh) | 2019-12-06 |
| AU2018266990B2 (en) | 2022-01-27 |
| CA3059282A1 (en) | 2018-11-15 |
| RU2019139232A3 (es) | 2021-07-22 |
| US11591335B2 (en) | 2023-02-28 |
| KR20200005585A (ko) | 2020-01-15 |
| ES2910854T3 (es) | 2022-05-13 |
| IL270403B (en) | 2022-06-01 |
| AU2018266990A1 (en) | 2019-10-31 |
| US20200165255A1 (en) | 2020-05-28 |
| MX2019013419A (es) | 2020-02-07 |
| EP3621967A1 (en) | 2020-03-18 |
| UA125047C2 (uk) | 2021-12-29 |
| RU2019139232A (ru) | 2021-06-10 |
| KR102694625B1 (ko) | 2024-08-12 |
| WO2018206479A1 (en) | 2018-11-15 |
| EP3621967B1 (en) | 2022-01-19 |
| CN110546152B (zh) | 2023-09-08 |
| CL2019003213A1 (es) | 2020-01-31 |
| BR112019022316A2 (pt) | 2020-05-26 |
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