AR109076A1 - Derivados de heterociclos bicíclicos condensados como pesticidas - Google Patents
Derivados de heterociclos bicíclicos condensados como pesticidasInfo
- Publication number
- AR109076A1 AR109076A1 ARP170101988A ARP170101988A AR109076A1 AR 109076 A1 AR109076 A1 AR 109076A1 AR P170101988 A ARP170101988 A AR P170101988A AR P170101988 A ARP170101988 A AR P170101988A AR 109076 A1 AR109076 A1 AR 109076A1
- Authority
- AR
- Argentina
- Prior art keywords
- 6alkyl
- 4alkyl
- 6alkoxy
- halogen
- 6haloalkyl
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title 1
- -1 C1−6cianoalkyl Chemical group 0.000 abstract 17
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 12
- 125000000623 heterocyclic group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 8
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 5
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 4
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 3
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 abstract 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 2
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004122 cyclic group 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
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 2
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 239000000642 acaricide Substances 0.000 abstract 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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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
- A01N43/90—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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Su uso como acaricidas y/o insecticidas para el control de plagas animales y procedimientos e intermedios para su producción. Reivindicación 1: Los compuestos de la fórmula (1) en donde Aₐ es nitrógeno o =C(R⁷)-; Aᵇ es =N-, -S(O)ₘ-, -O-, -N(R¹⁵)-, =C(R²)-, -C(=O)- o -C(R⁹)(R¹⁰)-; Aᶜ es =N-, -S(O)ₘ-, -O-, =C(R³)-, -C(=O)- o -C(R¹¹)(R¹²)-; Aᵈ es =N-, -S(O)ₘ-, -O-, -N(R¹⁵)-, =C(R⁸)-, -C(=O)- o -C(R¹³)(R¹⁴)-, donde uno solo de los sustituyentes Aᵇ, Aᶜ o Aᵈ puede ser oxígeno, -S(O)ₘ- o -C(=O)-; R¹ es C₁₋₆alquilo, C₁₋₆haloalquilo, C₁₋₆cianoalquilo, C₁₋₆hidroxialquilo, C₁₋₆alcoxi-C₁₋₆alquilo, C₁₋₆haloalcoxi-C₁₋₆alquilo, C₂₋₆alquenilo, C₂₋₆alqueniloxi-C₁₋₆alquilo, C₂₋₆haloalqueniloxi-C₁₋₆alquilo, C₂₋₆haloalquenilo, C₂₋₆cianoalquenilo, C₂₋₆alquinilo, C₂₋₆alquiniloxi-C₁₋₆alquilo, C₂₋₆haloalquiniloxi-C₁₋₆alquilo, C₂₋₆haloalquinilo, C₂₋₆cianoalquinilo, C₃₋₈cicloalquilo, C₃₋₈cicloalquilo-C₃₋₈cicloalquilo, C₁₋₆alquilo-C₃₋₈cicloalquilo, halógeno-C₃₋₈cicloalquilo, amino, C₁₋₆alquilamino, di-C₁₋₆alquilo-amino, C₃₋₈cicloalquilamino, C₁₋₆alquilcarbonil-amino, C₁₋₆alquiltio-C₁₋₆alquilo, C₁₋₆haloalquiltio-C₁₋₆alquilo, C₁₋₆alquilsulfinil-C₁₋₆alquilo, C₁₋₆haloalquilsulfinil-C₁₋₆alquilo, C₁₋₆alquilsulfonil-C₁₋₆alquilo, C₁₋₆haloalquilsulfonil-C₁₋₆alquilo, C₁₋₆alcoxi-C₁₋₆alquiltio-C₁₋₆alquilo, C₁₋₆alcoxi-C₁₋₆alquilsulfinil-C₁₋₆alquilo, C₁₋₆alcoxi-C₁₋₆alquilsulfonil-C₁₋₆alquilo, C₁₋₆alquilcarbonil-C₁₋₆alquilo, C₁₋₆haloalquilcarbonil-C₁₋₆alquilo, C₁₋₆alcoxicarbonil-C₁₋₆alquilo, C₁₋₆haloalcoxicarbonil-C₁₋₆alquilo, C₁₋₆alquilsulfonilamino, aminosulfonil-C₁₋₆alquilo, C₁₋₆alquilaminosulfonil-C₁₋₆alquilo, di-C₁₋₆alquilo-aminosulfonil-C₁₋₆alquilo, o C₁₋₆alquilo, C₁₋₆alcoxi, C₂₋₆alquenilo, C₂₋₆alquinilo, C₃₋₈cicloalquilo cada uno opcionalmente mono- o polisustituido de manera idéntica o diferente con arilo, hetarilo o heterociclilo, donde arilo, hetarilo o heterociclilo puede estar cada uno opcionalmente mono- o polisustituido de manera idéntica o diferente con halógeno, ciano, nitro, hidroxi, amino, carboxi, carbamoil, aminosulfonil, C₁₋₆alquilo, C₃₋₆cicloalquilo, C₁₋₆alcoxi, C₁₋₆haloalquilo, C₁₋₆haloalcoxi, C₁₋₆alquiltio, C₁₋₆alquilsulfinil, C₁₋₆alquilsulfonil, C₁₋₆alquilsulfimino, C₁₋₆alquilsulfimino-C₁₋₆alquilo, C₁₋₆alquilsulfimino-C₂₋₆alquilcarbonilo, C₁₋₆alquilsulfoximino, C₁₋₆alquilsulfoximino-C₁₋₆alquilo, C₁₋₆alquilsulfoximino-C₂₋₆alquilcarbonilo, C₁₋₆alcoxicarbonil, C₁₋₆alquilcarbonil, C₃₋₆trialquilsililo o bencilo, o R¹ es arilo, hetarilo o heterociclilo, cada uno opcionalmente mono- o polisustituido de manera idéntica o diferente con halógeno, ciano, nitro, hidroxi, amino, carboxi, carbamoil, C₁₋₆alquilo, C₃₋₈cicloalquilo, C₁₋₆alcoxi, C₁₋₆haloalquilo, C₁₋₆haloalcoxi, C₁₋₆alquiltio, C₁₋₆alquilsulfinil, C₁₋₆alquilsulfonil, C₁₋₆alquilsulfimino, C₁₋₆alquilsulfimino-C₁₋₆alquilo, C₁₋₆alquilsulfimino-C₂₋₆alquilcarbonilo, C₁₋₆alquilsulfoximino, C₁₋₆alquilsulfoximino-C₁₋₆alquilo, C₁₋₆alquilsulfoximino-C₂₋₆alquilcarbonilo, C₁₋₆alcoxicarbonil, C₁₋₆alquilcarbonil, C₃₋₆trialquilsililo, (=O) (en el caso de heterociclilo solamente) o (=O)₂ (en el caso de heterociclilo solamente); R², R³, R⁸ son en forma independiente hidrógeno, ciano, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆alquilsililo, C₃₋₈cicloalquilo, C₃₋₈cicloalquilo-C₃₋₈cicloalquilo, C₁₋₆alquilo-C₃₋₈cicloalquilo, halógeno-C₃₋₈cicloalquilo, C₁₋₆alquilo, C₁₋₆haloalquilo, C₁₋₆cianoalquilo, C₁₋₆hidroxialquilo, hidroxicarbonilo-C₁₋₆alcoxi, C₁₋₆alcoxicarbonil-C₁₋₆alquilo, C₁₋₆alcoxi-C₁₋₆alquilo, C₂₋₆alquenilo, C₂₋₆haloalquenilo, C₂₋₆cianoalquenilo, C₂₋₆alquinilo, C₂₋₆haloalquinilo, C₂₋₆cianoalquinilo, C₁₋₆alcoxi, C₁₋₆haloalcoxi, C₁₋₆cianoalcoxi, C₁₋₆alcoxicarbonil-C₁₋₆alcoxi, C₁₋₆alcoxi-C₁₋₆alcoxi, C₁₋₆alquilhidroxiimino, C₁₋₆alcoxiimino, C₁₋₆alquilo-C₁₋₆alcoxiimino, C₁₋₆haloalquilo-C₁₋₆alcoxiimino, C₁₋₆alquiltio, C₁₋₆haloalquiltio, C₁₋₆alcoxi-C₁₋₆alquiltio, C₁₋₆alquiltio-C₁₋₆alquilo, C₁₋₆alquilsulfinil, C₁₋₆haloalquilsulfinil, C₁₋₆alcoxi-C₁₋₆alquilsulfinil, C₁₋₆alquilsulfinil-C₁₋₆alquilo, C₁₋₆alquilsulfonil, C₁₋₆haloalquilsulfonil, C₁₋₆alcoxi-C₁₋₆alquilsulfonil, C₁₋₆alquilsulfonil-C₁₋₆alquilo, C₁₋₆alquilsulfoniloxi, C₁₋₆alquilcarbonil, C₁₋₆alquiltiocarbonilo, C₁₋₆haloalquilcarbonil, C₁₋₆alquilcarboniloxi, C₁₋₆alcoxicarbonil, C₁₋₆haloalcoxicarbonil, aminocarbonilo, C₁₋₆alquilaminocarbonil, C₁₋₆alquilaminotiocarbonil, di-C₁₋₆alquilo-aminocarbonil, di-C₁₋₆alquilo-aminotiocarbonil, C₂₋₆alquenilaminocarbonil, di-C₂₋₆alquenilaminocarbonil, C₃₋₈cicloalquilaminocarbonil, C₁₋₆alquilsulfonilamino, C₁₋₆alquilamino, di-C₁₋₆alquilamino, aminosulfonil, C₁₋₆alquilaminosulfonil, di-C₁₋₆alquilo-aminosulfonil, C₁₋₆alquilsulfoximino, aminotiocarbonil, C₁₋₆alquilaminotiocarbonil, di-C₁₋₆alquilo-aminotiocarbonil, C₃₋₈cicloalquilamino o NHCO-C₁₋₆alquilo(C₁₋₆alquilcarboniloamino); R⁷ es hidrógeno, ciano, halógeno, acetilo, hidroxi, amino, C₃₋₈cicloalquilo, halógeno-C₃₋₈cicloalquilo, C₁₋₆alquilo, C₁₋₆haloalquilo, C₁₋₆cianoalquilo, C₂₋₆alquenilo, C₂₋₆haloalquenilo, C₂₋₆alquinilo, C₂₋₆haloalquinilo, C₁₋₆alcoxi, C₁₋₆haloalcoxi, C₁₋₆alquiltio, C₁₋₆haloalquiltio, C₁₋₆alquilsulfinil, C₁₋₆haloalquilsulfinil, C₁₋₆alquilsulfonil o C₁₋₆haloalquilsulfonil; R⁹, R¹⁰, R¹¹, R¹², R¹³, R¹⁴ son en forma independiente hidrógeno, halógeno, C₁₋₆alquilo o C₁₋₆haloalquilo; R¹⁵ es hidrógeno, acetilo, C₁₋₄alquilo, C₁₋₄hidroxialquilo, C₁₋₄haloalquilo, C₁₋₄cianoalquilo, C₁₋₄alcoxi-C₁₋₄alquilo, C₁₋₄haloalcoxi-C₁₋₄alquilo, C₂₋₄alquenilo, C₂₋₄alqueniloxi-C₁₋₄alquilo, C₂₋₄haloalqueniloxi-C₁₋₄alquilo, C₂₋₄haloalquenilo, C₂₋₄cianoalquenilo, C₂₋₄alquinilo, C₂₋₄alquiniloxi-C₁₋₄alquilo, C₂₋₄haloalquiniloxi-C₁₋₄alquilo, C₂₋₄haloalquinilo, C₂₋₄cianoalquinilo, C₃₋₆cicloalquilo, C₁₋₄alquilo-C₃₋₆cicloalquilo, halógeno-C₃₋₆cicloalquilo, C₁₋₄alquiltio-C₁₋₄alquilo, C₁₋₄haloalquiltio-C₁₋₄alquilo, C₁₋₄alquilsulfinil-C₁₋₄alquilo, C₁₋₄haloalquilsulfinil-C₁₋₄alquilo, C₁₋₄alquilsulfonil-C₁₋₄alquilo, C₁₋₄alquilcarbonil-C₁₋₄alquilo, C₁₋₄haloalquilcarbonil-C₁₋₄alquilo, o es C₁₋₄alquilo, C₁₋₄alquenilo, C₂₋₄alquinilo cada uno opcionalmente mono- o disustituido de manera idéntica o diferente por arilo o heterociclilo, donde arilo o heterociclilo opcionalmente pueden estar mono- o disustituido de manera idéntica o diferente por halógeno, ciano, C₁₋₄alquilo, C₃₋₄cicloalquilo, C₁₋₄alcoxi, C₁₋₄haloalquilo, C₁₋₄haloalcoxi, C₁₋₄alquiltio, C₁₋₄alquilsulfinil o C₁₋₄alquilsulfonil, o R¹⁵ es arilo o heterociclilo cada uno opcionalmente mono- o disustituido de manera idéntica o diferente por halógeno, ciano, C₁₋₄alquilo, C₃₋₆cicloalquilo, C₁₋₄alcoxi, C₁₋₄haloalquilo, C₁₋₄haloalcoxi, C₁₋₄alquiltio, C₁₋₄alquilsulfinil, C₁₋₄alquilsulfonil, C₁₋₄alquilsulfoximino, C₁₋₄alquilcarbonil, (=O) (en el caso de heterociclilo solamente) o (=O)₂ (en el caso de heterociclilo solamente); Q es un sistema de anillos bicíclicos o tricíclicos fusionados de 8, 9, 10, 11 ó 12 miembros heterocíclicos o heteroaromáticos saturados o parcialmente saturados, donde al menos un grupo carbonilo puede estar presente opcionalmente y/o donde el sistema de anillos puede estar opcionalmente mono- o polisustituido de manera idéntica o diferente, y donde los sustituyentes se pueden seleccionar de manera independiente entre ciano, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆alquilsililo, C₃₋₈cicloalquilo, C₃₋₈cicloalquilo-C₃₋₈cicloalquilo, C₁₋₆alquilo-C₃₋₈cicloalquilo, halógeno-C₃₋₈cicloalquilo, C₁₋₆alquilo, C₁₋₆haloalquilo, C₁₋₆cianoalquilo, C₁₋₆hidroxialquilo, hidroxicarbonilo-C₁₋₆alcoxi, C₁₋₆alcoxicarbonil-C₁₋₆alquilo, C₁₋₆alcoxi-C₁₋₆alquilo, C₂₋₆alquenilo, C₂₋₆haloalquenilo, C₂₋₆cianoalquenilo, C₂₋₆alquinilo, C₂₋₆alquiniloxi-C₁₋₄alquilo, C₂₋₆haloalquinilo, C₂₋₆cianoalquinilo, C₁₋₆alcoxi, C₁₋₆haloalcoxi, C₁₋₆haloalcoxi-C₁₋₆alquilo, C₂₋₆alqueniloxi-C₁₋₆alquilo, C₂₋₆haloalqueniloxi-C₁₋₆alquilo, C₁₋₆cianoalcoxi, C₁₋₆alcoxicarbonil-C₁₋₆alcoxi, C₁₋₆alcoxi-C₁₋₆alcoxi, C₁₋₆alquilhidroxiimino, C₁₋₆alcoxiimino, C₁₋₆alquilo-C₁₋₆alcoxiimino, C₁₋₆haloalquilo-C₁₋₆alcoxiimino, C₁₋₆alquiltio, C₁₋₆haloalquiltio, C₁₋₆alcoxi-C₁₋₆alquiltio, C₁₋₆alquiltio-C₁₋₆alquilo, C₁₋₆alquilsulfinil, C₁₋₆haloalquilsulfinil, C₁₋₆alcoxi-C₁₋₆alquilsulfinil, C₁₋₆alquilsulfinil-C₁₋₆alquilo, C₁₋₆alquilsulfonil, C₁₋₆haloalquilsulfonil, C₁₋₆alcoxi-C₁₋₆alquilsulfonil, C₁₋₆alquilsulfonil-C₁₋₆alquilo, C₁₋₆alquilsulfoniloxi, C₁₋₆alquilcarbonil, C₁₋₆alquilcarbonil-C₁₋₆alquilo, C₁₋₆alquiltiocarbonilo, C₁₋₆haloalquilcarbonil, C₁₋₆alquilcarboniloxi, C₁₋₆alcoxicarbonil, C₁₋₆haloalcoxicarbonil, aminocarbonilo, C₁₋₆alquilaminocarbonil, C₁₋₆alquilaminotiocarbonil, di-C₁₋₆alquilo-aminocarbonil, di-C₁₋₆alquilo-aminotiocarbonil, C₂₋₆alquenilaminocarbonil, di-C₂₋₆alquenilaminocarbonil, C₃₋₈cicloalquilaminocarbonil, C₁₋₆alquilsulfonilamino, C₁₋₆alquilamino, di-C₁₋₆alquilamino, aminosulfonil, C₁₋₆alquilaminosulfonil, di-C₁₋₆alquilo-aminosulfonil, C₁₋₆alquilsulfoximino, aminotiocarbonil, C₁₋₆alquilaminotiocarbonil, di-C₁₋₆alquilo-aminotiocarbonil, C₃₋₈cicloalquilamino, NHCO-C₁₋₆alquilo(C₁₋₆alquilcarboniloamino), o donde los sustituyentes se pueden seleccionar de manera independiente entre fenilo o un anillo heteroaromático de 5 ó 6 miembros, donde el fenilo o el anillo puede estar opcionalmente mono- o polisustituido de manera idéntica o diferente con C₁₋₆alquilo, C₂₋₆alquenilo, C₂₋₆alquinilo, C₃₋₆cicloalquilo, C₁₋₆haloalquilo, C₂₋₆haloalquenilo, C₂₋₆haloalquinilo, C₃₋₆halocicloalquilo, halógeno, CN, NO₂, C₁₋₄alcoxi, C₁₋₄haloalcoxi; m es 0, 1 ó 2; n es 0, 1 ó 2; salvo el compuesto de fórmula (2).
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2017
- 2017-07-14 MX MX2019000793A patent/MX2019000793A/es unknown
- 2017-07-14 BR BR112019001135-8A patent/BR112019001135B1/pt not_active IP Right Cessation
- 2017-07-14 PE PE2019000225A patent/PE20190206A1/es unknown
- 2017-07-14 CN CN201780054877.0A patent/CN109689662B/zh not_active Expired - Fee Related
- 2017-07-14 EP EP17739984.7A patent/EP3487860B1/de active Active
- 2017-07-14 CA CA3031139A patent/CA3031139A1/en not_active Abandoned
- 2017-07-14 AU AU2017298972A patent/AU2017298972B2/en not_active Ceased
- 2017-07-14 KR KR1020197004746A patent/KR102435080B1/ko active Active
- 2017-07-14 US US16/318,592 patent/US10561145B2/en not_active Expired - Fee Related
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- 2017-07-14 WO PCT/EP2017/067838 patent/WO2018015289A1/de not_active Ceased
- 2017-07-14 ES ES17739984T patent/ES2877571T3/es active Active
- 2017-07-14 JP JP2019502171A patent/JP6967064B2/ja not_active Expired - Fee Related
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2019
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- 2019-01-16 CL CL2019000125A patent/CL2019000125A1/es unknown
- 2019-01-18 PH PH12019500139A patent/PH12019500139A1/en unknown
- 2019-01-18 CO CONC2019/0000503A patent/CO2019000503A2/es unknown
- 2019-02-18 ZA ZA2019/01024A patent/ZA201901024B/en unknown
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| AU2017298972A1 (en) | 2019-01-31 |
| JP6967064B2 (ja) | 2021-11-17 |
| PH12019500139A1 (en) | 2019-10-28 |
| IL264204B (en) | 2022-03-01 |
| ES2877571T3 (es) | 2021-11-17 |
| CL2019000125A1 (es) | 2019-06-14 |
| RU2019104378A (ru) | 2020-08-19 |
| KR20190027919A (ko) | 2019-03-15 |
| MX2019000793A (es) | 2019-06-20 |
| US10561145B2 (en) | 2020-02-18 |
| ZA201901024B (en) | 2022-07-27 |
| EP3487860A1 (de) | 2019-05-29 |
| CN109689662B (zh) | 2022-03-15 |
| BR112019001135A2 (pt) | 2019-04-30 |
| IL264204A (en) | 2019-02-28 |
| CN109689662A (zh) | 2019-04-26 |
| BR112019001135B1 (pt) | 2022-11-01 |
| KR102435080B1 (ko) | 2022-08-22 |
| CA3031139A1 (en) | 2018-01-25 |
| TW201811804A (zh) | 2018-04-01 |
| EP3487860B1 (de) | 2021-04-14 |
| CO2019000503A2 (es) | 2019-04-30 |
| JP2019527221A (ja) | 2019-09-26 |
| UY37327A (es) | 2018-02-28 |
| AU2017298972B2 (en) | 2021-03-04 |
| TWI747924B (zh) | 2021-12-01 |
| PE20190206A1 (es) | 2019-02-07 |
| US20190239510A1 (en) | 2019-08-08 |
| WO2018015289A1 (de) | 2018-01-25 |
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