AR097998A1 - Compuestos plaguicidas - Google Patents
Compuestos plaguicidasInfo
- Publication number
- AR097998A1 AR097998A1 ARP140103791A ARP140103791A AR097998A1 AR 097998 A1 AR097998 A1 AR 097998A1 AR P140103791 A ARP140103791 A AR P140103791A AR P140103791 A ARP140103791 A AR P140103791A AR 097998 A1 AR097998 A1 AR 097998A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halogen
- halogen atoms
- haloalkyl
- atoms
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 108
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 77
- 229910052736 halogen Inorganic materials 0.000 abstract 58
- 125000000217 alkyl group Chemical group 0.000 abstract 53
- 150000002367 halogens Chemical class 0.000 abstract 41
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 37
- 229910052739 hydrogen Inorganic materials 0.000 abstract 35
- 239000001257 hydrogen Substances 0.000 abstract 35
- 150000002431 hydrogen Chemical class 0.000 abstract 33
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 28
- -1 nitro, cyano, hydroxy, amino Chemical group 0.000 abstract 25
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 21
- 125000000623 heterocyclic group Chemical group 0.000 abstract 21
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 15
- 125000003545 alkoxy group Chemical group 0.000 abstract 14
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 7
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 7
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 6
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 6
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 5
- 125000004429 atom Chemical group 0.000 abstract 5
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 5
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 4
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 229910052731 fluorine Inorganic materials 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 abstract 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000001054 5 membered carbocyclic group Chemical group 0.000 abstract 1
- 125000004008 6 membered carbocyclic group Chemical group 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 239000005645 nematicide Substances 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
- A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
- A01N43/30—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered 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
- A01N43/72—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
- A01N43/84—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/04—Amoebicides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
- A61P33/12—Schistosomicides
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/10—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 two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catching Or Destruction (AREA)
- Pyridine Compounds (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Compuestos que poseen propiedades plaguicidas, en especial nematicidas. También se reivindica al compuesto intermediario de la fórmula (32) donde R¹, R² e Yₘ se definen en la reivindicación 1. Reivindicación 1: Un compuesto de fórmula (1) en el que B¹, B² representan C-X o N, en el que al menos B¹ o B² es N; n es 0, 1, 2, 3 ó 4, limitado por el número de posiciones disponibles en el anillo al que se puede conectar un sustituyente X; cada X se selecciona de modo independiente del grupo constituido por hidrógeno, halógeno, nitro, ciano, hidroxi, amino, -SH, -SF₅, -CHO, -OCHO, -NHCHO, -COOH, -CONH₂, -CONH(OH), -OCONH₂, (hidroxiimino)-alquilo C₁₋₆, alquilo C₁₋₈, haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, alquenilo C₂₋₈, alquinilo C₂₋₈, alquil C₁₋₈amino, di-(alquil C₁₋₈)amino, alcoxi C₁₋₈, haloalcoxi C₁₋₈ que tiene 1 a 5 átomos de halógeno, alqueniloxi C₂₋₈, haloalqueniloxi C₂₋₈ que tiene 1 a 5 átomos de halógeno, alquiniloxi C₃₋₈, haloalquiniloxi C₃₋₈ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈ que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carbonilo, haloalquil C₁₋₈carbonilo que tiene 1 a 5 átomos de halógeno, -CONH(alquilo C₁₋₈), -CON(alquilo C₁₋₈)₂, -CONH(O-alquilo C₁₋₈), -CON(O-alquilo C₁₋₈)(alquilo C₁₋₈), alcoxi C₁₋₈carbonilo, haloalcoxi C₁₋₈carbonilo que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carboniloxi, haloalquil C₁₋₈carboniloxi que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carbonilamino, haloalquil C₁₋₈carbonilamino que tiene 1 a 5 átomos de halógeno, -OCONH(alquilo C₁₋₈), -OCON(alquilo C₁₋₈)₂, -OCONH(O-alquilo C₁₋₈), -OCO(O-alquilo C₁₋₈), -S-alquilo C₁₋₈, -S-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -S(O)-alquilo C₁₋₈, -S(O)-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -S(O)₂-alquilo C₁₋₈, -S(O)₂-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, (alcoxi C₁₋₆imino)-alquilo C₁₋₆, (alqueniloxi C₂₋₆imino)-alquilo C₁₋₆, (alquiniloxi C₃₋₆imino)-alquilo C₁₋₆, (benciloxiimino)-alquilo C₁₋₆, benciloxi, -S-bencilo, bencilamino, fenoxi, -S-fenilo y fenilamino; m es 0, 1, 2, 3, 4 ó 5, y cada Y se selecciona de modo independiente del grupo constituido por hidrógeno, halógeno, nitro, ciano, hidroxi, amino, -SH, -SF₅, -CHO, -OCHO, -NHCHO, -COOH, -CONH₂, -CONH(OH), -OCONH₂, (hidroxiimino)-alquilo C₁₋₆, alquilo C₁₋₈, haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, alquenilo C₂₋₈, alquinilo C₂₋₈, alquil C₁₋₈amino, di-(alquil C₁₋₈)amino, en el que ambos residuos alquilo pueden formar un heterociclo de 4 a 7 miembros que incorporan el nitrógeno unido al sistema fenilo del compuesto, alcoxi C₁₋₈, haloalcoxi C₁₋₈ que tiene 1 a 5 átomos de halógeno, alqueniloxi C₂₋₈, haloalqueniloxi C₂₋₈ que tiene 1 a 5 átomos de halógeno, alquiniloxi C₃₋₈, haloalquiniloxi C₃₋₈ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈ que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carbonilo, haloalquil C₁₋₈carbonilo que tiene 1 a 5 átomos de halógeno, -CONH(alquilo C₁₋₈), -CON(alquilo C₁₋₈)₂, -CONH(O-alquilo C₁₋₈), -CON(O-alquilo C₁₋₈)(alquilo C₁₋₈), alcoxi C₁₋₈carbonilo, haloalcoxi C₁₋₈carbonilo que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carboniloxi, haloalquil C₁₋₈carboniloxi que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carbonilamino, haloalquil C₁₋₈carbonilamino que tiene 1 a 5 átomos de halógeno, -OCONH(alquilo C₁₋₈), -OCON(alquilo C₁₋₈)₂, -OCONH(O-alquilo C₁₋₈), -OCO(O-alquilo C₁₋₈), -S-alquilo C₁₋₈, -S-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -S(O)-alquilo C₁₋₈, -S(O)-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -S(O)₂-alquilo C₁₋₈, -S(O)₂-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -CH₂-S-alquilo C₁₋₈, -CH₂-S(O)-alquilo C₁₋₈, -CH₂-S(O)₂-alquilo C₁₋₈, (alcoxi C₁₋₆imino)-alquilo C₁₋₆, (alqueniloxi C₂₋₆imino)-alquilo C₁₋₆, (alquiniloxi C₃₋₆imino)-alquilo C₁₋₆, (benciIoxiimino)-alquilo C₁₋₆, benciloxi, -S-bencilo, bencilamino, fenoxi, -S-fenilo y fenilamino; o m es 2, 3, 4 ó 5, y al menos dos sustituyentes Y son vecinos y, junto con los átomos de carbono al que están unidos, forma un carbociclo de 5 ó 6 miembros condensado o un heterociclo de 5 ó 6 miembros con uno o dos heteroátomos seleccionados del grupo que consiste en oxígeno y nitrógeno, en el que dos átomos de oxigeno no están directamente no conectados, el carbociclo o el heterociclo está sustituido de modo independiente con 0 a 4 átomos de halógeno, 0 a 2 grupos oxo, 0 a 8 alquilo C₁₋₈, 0 a 8 alcoxi C₁₋₈ o 0 a 4 haloalquilo C₁₋₈ que tienen 1 a 5 átomos de halógeno, y los restantes sustituyentes Y se seleccionan de modo independiente del grupo que consiste en hidrógeno, halógeno, nitro, ciano, hidroxi, amino, -SH, -SF₅, -CHO, -OCHO, -NHCHO, -COOH, -CONH₂, -CONH(OH), -OCONH₂, (hidroxiimino)-alquilo C₁₋₆, alquilo C₁₋₈, haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, alquenilo C₂₋₈, alquinilo C₂₋₈, alquil C₁₋₈amino, di-(alquil C₁₋₈)amino, alcoxi C₁₋₈, haloalcoxi C₁₋₈ que tiene 1 a 5 átomos de halógeno, alqueniloxi C₂₋₈, haloalqueniloxi C₂₋₈ que tiene 1 a 5 átomos de halógeno, alquiniloxi C₃₋₈, haloalquiniloxi C₃₋₈ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈ que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carbonilo, haloalquil C₁₋₈carbonilo que tiene 1 a 5 átomos de halógeno, -CONH(alquilo C₁₋₈), -CON(alquilo C₁₋₈)₂, -CONH(O-alquilo C₁₋₈), -CON(O-alquilo C₁₋₈)(alquilo C₁₋₈), alcoxi C₁₋₈carbonilo, haloalcoxi C₁₋₈carbonilo que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carboniloxi, haloalquil C₁₋₈carboniloxi que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carbonilamino, haloalquil C₁₋₈carbonilamino que tiene 1 a 5 átomos de halógeno, -OCONH(alquilo C₁₋₈), -OCON(alquilo C₁₋₈)₂, -OCONH(O-alquilo C₁₋₈), -OCO(O-alquilo C₁₋₈), -S-alquilo C₁₋₈, -S-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -S(O)-alquilo C₁₋₈, -S(O)-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -S(O)₂-alquilo C₁₋₈, -S(O)₂-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -CH₂-S-alquilo C₁₋₈, -CH₂-S(O)-alquilo C₁₋₈, -CH₂-S(O)₂-alquilo C₁₋₈, (alcoxi C₁₋₆imino)-alquilo C₁₋₆, (alqueniloxi C₂₋₆imino)-alquilo C₁₋₆, (alquiniloxi C₃₋₆imino)-alquilo C₁₋₆, (benciloxiimino)-alquilo C₁₋₆, benciloxi, -S-bencilo, bencilamino, fenoxi, -S-fenilo y fenilamino; R¹, R², R³ y R⁴ son iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, ciano, hidroxi, amino, -SH, -CHO, -OCHO, -NHCHO, -COOH, -CONH₂, -CONH(OH), -OCONH₂, un grupo (hidroxiimino)-alquilo C₁₋₆, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, alquil C₁₋₆amino, di-(alquilo C₁₋₆)amino, alcoxi C₁₋₆, hidroxi-alquilo C₁₋₄, alcoxi C₁₋₄-alquilo C₁₋₃, haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, haloalcoxi C₁₋₆ que tiene 1 a 5 átomos de halógeno, alqueniloxi C₂₋₆, haloalqueniloxi C₂₋₆ que tiene 1 a 5 átomos de halógeno, alquiniloxi C₃₋₆, haloalquiniloxi C₃₋₆ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₆, halocicloalquilo C₃₋₆ que tiene 1 a 5 átomos de halógeno, cicloalquil C₃₋₆-alquilo C₁₋₆, halocicloalquil C₃₋₆-alquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, alquil C₁₋₆carbonilo, haloalquil C₁₋₆carbonilo que tiene 1 a 5 átomos de halógeno, -CONH(alquilo C₁₋₆), -CON(alquilo C₁₋₆)₂, -CONH(O-alquilo C₁₋₆), -CON(O-alquilo C₁₋₆)(alquilo C₁₋₆), alcoxi C₁₋₆carbonilo, un haloalcoxi C₁₋₆carbonilo que tiene 1 a 5 átomos de halógeno, -OC(O)-alquilo C₁₋₆, -OC(O)-haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, -NHC(O)-alquilo C₁₋₆, -NHC(O)-haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, -OCONH(alquilo C₁₋₆), -OCON(alquilo C₁₋₆)₂, -OCONH(O-alquilo C₁₋₆), OCO(O-alquilo C₁₋₆), -S-alquilo C₁₋₆, -S-haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, -S(O)-alquilo C₁₋₆, -S(O)-haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, -S(O)₂-alquilo C₁₋₆, -S(O)₂-haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, bencilo, benciloxi, -S-bencilo, -S(O)-bencilo, -S(O)₂-bencilo, bencilamino, fenoxi, -S-fenilo, -S(O)-fenilo, -S(O)₂-fenilo, fenilamino, fenilcarbonilamino y fenilo, con la condición de que R¹ es flúor y/o R² es flúor; R⁵ se selecciona del grupo que consiste en hidrógeno, ciano, -CHO, -OH, alquilo C₁₋₆, haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₆, haloalcoxi C₁₋₆ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₇, halocicloalquilo C₃₋₇ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₇-alquilo C₁₋₆, -CONH(alquilo C₁₋₆), alquenilo C₂₋₆, alquinilo C₂₋₆, alcoxi C₁₋₆-alquilo C₁₋₆, cicloalquilo C₃₋₇-alquilo C₁₋₆, ciano-alquilo C₁₋₆, amino-alquilo C₁₋₆, alquil C₁₋₆amino-alquilo C₁₋₆, di-(alquilo C₁₋₆)amino-alquilo C₁₋₆, alquil C₁₋₆carbonilo, haloalquil C₁₋₆carbonilo que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₆carbonilo, C₁₋₆-benciloxicarbonilo, alcoxi C₁₋₆-alquil C₁₋₆carbonilo, -S-alquilo C₁₋₆, -S-haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno, -S(O)₂-alquilo C₁₋₆, y -S(O)₂-haloalquilo C₁₋₆ que tiene 1 a 5 átomos de halógeno; A representa un grupo fenilo de la formula (2) en la que o es 0, 1, 2, 3, 4 ó 5, y cada R se selecciona de modo independiente del grupo constituido por halógeno, nitro, -OH, NH₂, SH, SF₅, CHO, OCHO, NHCHO, COOH, ciano, alquilo C₁₋₈, haloalquilo C₁₋₈ que tiene 1 a 9 átomos de halógeno, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₆, -S-alquil C₁₋₈, -S-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₈, haloalcoxi C₁₋₈ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₈-alquenilo C₂₋₈, alcoxi C₁₋₈carbonilo, haloalcoxi C₁₋₈carbonilo que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈carboniloxi, haloalquil C₁₋₈carboniloxi que tiene 1 a 5 átomos de halógeno, -S(O)-alquilo C₁₋₈, -S(O)-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, -S(O)₂-alquilo C₁₋₈, -S(O)₂-haloalquilo C₁₋₈ que tiene 1 a 5 átomos de halógeno, alquil C₁₋₈sulfonamida, -NH(alquilo C₁₋₈), N(alquilo C₁₋₈)₂, fenilo (opcionalmente sustituido con alcoxi C₁₋₆) y fenoxi, o dos R unidos a los átomos de carbono adyacentes entre si representan -O(CH₂)ₚO-, en donde p representa 1 ó 2, o A representa un heterociclo de la fórmula (3) en la que R⁶ y R⁷ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, amino, nitro, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R⁸ se selecciona del grupo que consiste en hidrógeno, halógeno, nitro, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (4) en la que R⁹ se selecciona del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R¹⁰ y R¹¹ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, amino, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno y fenilo (opcionalmente sustituido con halógeno o alquilo C₁₋₄), o A representa un heterociclo de la fórmula (5) en la que R¹² se selecciona del grupo que consiste en halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R¹³ se selecciona del grupo que consiste en hidrógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (6) en la que R¹⁴ y R¹⁵ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, -S-alquilo C₁₋₄, -S(O)₂-alquilo C₁₋₄, fenilo opcionalmente sustituido con halógeno o alquilo C₁₋₄ y piridilo (opcionalmente sustituido con halógeno o alquilo C₁₋₄), y R¹⁶ se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno y haloalcoxi C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (7) en la que R¹⁷ y R¹⁸ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄, alquil C₁₋₄oxi y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R¹⁹ se selecciona del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos, o A representa un heterociclo de la fórmula (8) en la que R²⁰ se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R²¹ y R²³ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R²² se selecciona del grupo que consiste en hidrógeno, ciano, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₄-alquilo C₁₋₄, hidroxil-alquilo C₁₋₄, -S(O)₂-alquilo C₁₋₄, -S(O)₂-N(alquilo C₁₋₄)₂, alquil C₁₋₆carbonilo, -S(O)₂-fenilo (opcionalmente sustituido con halógeno o alquilo C₁₋₄) y benzoílo (opcionalmente sustituido con halógeno o alquilo C₁₋₄), o A representa un heterociclo de la fórmula (9) en la que R²⁴ se selecciona del grupo que consiste en hidrógeno, ciano, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₄-alquilo C₁₋₄, hidroxi-alquilo C₁₋₄, -S(O)₂-alquilo C₁₋₄, -S(O)₂-N(alquilo C₁₋₄)₂, alquil C₁₋₆carbonilo, -S(O)₂-fenilo (opcionalmente sustituido con halógeno o alquilo C₁₋₄) y benzoílo (opcionalmente sustituido con halógeno o un alquilo C₁₋₄), y R²⁵, R²⁶ y R²⁷ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, ciano, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno y alquil C₁₋₄carbonilo, o A representa un heterociclo de la fórmula (10) en la que R²⁸ se selecciona del grupo que consiste en hidrógeno y alquilo C₁₋₄, y R²⁹ se selecciona del grupo que consiste en halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (11) en la que R³⁰ se selecciona del grupo que consiste en hidrógeno y alquilo C₁₋₄, y R³¹ se selecciona del grupo que consiste en halógeno, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno y fenilo (opcionalmente sustituido con halógeno o alquilo C₁₋₄), o A representa un heterociclo de la fórmula (12) en la que R³² se selecciona del grupo que consiste en hidrógeno, halógeno, amino, ciano, alquil C₁₋₄amino, di-(alquilo C₁₋₄)amino, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno y fenilo (opcionalmente sustituido con halógeno o alquilo C₁₋₄), y R³³ se selecciona del grupo que consiste en halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, haloalcoxi C₁₋₅ que tiene 1 a 9 átomos de halógeno, amino, alquilamino C₁₋₅ sustituido o no sustituido o di-(alquilo C₁₋₅)-amino sustituido o no sustituido, o A representa un heterociclo de la fórmula (13) en la que R³⁴ se selecciona del grupo que consiste en hidrógeno, halógeno, amino, ciano, alquil C₁₋₄amino, di-(alquilo C₁₋₄)amino, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R³⁵ se selecciona del grupo que consiste en halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (14) en la que R³⁶ se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄ que tiene 1 a 5 átomos de halógeno, -S-alquilo C₁₋₄, -S(O)-alquilo C₁₋₄, -S(O)₂-alquilo C₁₋₄, -S-haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, aminocarbonilo y aminocarbonil-alquilo C₁₋₄, y R³⁷ se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, nitro, alquilo C₁₋₄, alcoxi C₁₋₄, -S-alquilo C₁₋₄, -S(O)-alquilo C₁₋₄ y -S(O)₂-alquilo C₁₋₄, y R³⁸ se selecciona del grupo que consiste en hidrógeno, fenilo, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, hidroxi-alquilo C₁₋₄, alquenilo C₂₋₆, cicloalquilo C₃₋₆, alquiltio C₁₋₄-alquilo C₁₋₄, alquil C₁₋₄-S(O)-alquilo C₁₋₄, alquil C₁₋₄-S(O)₂-alquilo C₁₋₄, haloalquiltio C₁₋₄-alquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₄-alquilo C₁₋₄ y haloalcoxi C₁₋₄-alquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (15) en la que R³⁹ se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄ que tiene 1 a 5 átomos de halógeno, -S-alquilo C₁₋₄, S(O)-alquilo C₁₋₄, -S(O)₂-alquilo C₁₋₄, -S-haloalquilo C₁₋₄ que tiene 1 a 5 átomos, aminocarbonilo y aminocarbonil-alquilo C₁₋₄, y R⁴⁰ se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, alquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄ que tiene 1 a 5 átomos de halógeno, -S-alquil C₁₋₄-S(O)-alquilo C₁₋₄, y -S(O)₂-alquilo C₁₋₄, y R⁴¹ se selecciona del grupo que consiste en hidrógeno, alquilo C₁₋₄,haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, hidroxi-alquilo C₁₋₄, alquenilo C₂₋₆, cicloalquilo C₃₋₆, alquiltio C₁₋₄-alquilo C₁₋₄, alquil C₁₋₄-S(O)-alquilo C₁₋₄, alquil C₁₋₄-S(O)₂-alquilo C₁₋₄, haloalquiltio C₁₋₄-alquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₄-alquilo C₁₋₄, haloalcoxi C₁₋₄-alquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno y fenilo (opcionalmente sustituido con halógeno, alquilo C₁₋₄, alcoxi C₁₋₄-alquilo C₁₋₄ o nitro), o A representa un heterociclo de la fórmula (16) en la que R⁴² se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, cicloalquilo C₃₋₆, alcoxi C₁₋₄, haloalcoxi C₁₋₄ que tiene 1 a 5 átomos de halógeno, -S-alquilo C₁₋₄, S(O)-alquilo C₁₋₄, -S(O)₂-alquilo C₁₋₄, -S-haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, aminocarbonilo y aminocarbonil-alquilo C₁₋₄, y R⁴³ se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, alquilo C₁₋₄, alcoxi C₁₋₄, -S-alquilo C₁₋₄, S(O)-alquilo C₁₋₄, -S(O)₂-alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, y R⁴⁴ se selecciona del grupo que consiste en hidrógeno, fenilo, bencilo, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, hidroxi-alquilo C₁₋₄, alquenilo C₂₋₆, cicloalquilo C₃₋₆, alquiltio C₁₋₄-alquilo C₁₋₄, alquil C₁₋₄-S(O)-alquilo C₁₋₄, alquil C₁₋₄-S(O)₂-alquilo C₁₋₄, haloalquiltio C₁₋₄-alquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, alcoxi C₁₋₄-alquilo C₁₋₄ y haloalcoxi C₁₋₄-alquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (17) en la que R⁴⁵ y R⁴⁶ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de la fórmula (18) en la que R⁴⁷ y R⁴⁸ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄, haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, fenilo (opcionalmente sustituido con halógeno o un alquilo C₁₋₄), y heterociclilo como piridilo, pirimidinilo y tiadiazolilo (cada uno opcionalmente sustituido con halógeno o alquilo C₁₋₄), o A representa un heterociclo de la fórmula (19) en la que R⁴⁹ y R⁵⁰ pueden ser iguales o diferentes y se seleccionan del grupo que consiste en hidrógeno, halógeno, alquilo C₁₋₄ y haloalquilo C₁₋₄ que tiene 1 a 5 átomos de halógeno, o A representa un heterociclo de
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13188513 | 2013-10-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR097998A1 true AR097998A1 (es) | 2016-04-27 |
Family
ID=49356287
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP140103791A AR097998A1 (es) | 2013-10-14 | 2014-10-10 | Compuestos plaguicidas |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US9776967B2 (es) |
| EP (1) | EP3057939A1 (es) |
| JP (1) | JP2016540035A (es) |
| CN (1) | CN106061946A (es) |
| AR (1) | AR097998A1 (es) |
| AU (1) | AU2014336360A1 (es) |
| CA (1) | CA2926981A1 (es) |
| CL (1) | CL2016000795A1 (es) |
| MX (1) | MX2016004393A (es) |
| RU (1) | RU2016118655A (es) |
| TW (1) | TW201607924A (es) |
| UY (1) | UY35772A (es) |
| WO (1) | WO2015055535A1 (es) |
| ZA (1) | ZA201602507B (es) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX374120B (es) | 2014-03-05 | 2025-03-05 | Univ Tokyo | Compuestos derivados de carboxamida y el uso de los mismos para controlar endoparásitos en mamíferos. |
| CN106543167B (zh) * | 2015-09-17 | 2021-12-03 | 沈阳中化农药化工研发有限公司 | 一种异噻唑类化合物及其用途 |
| CN106083787B (zh) * | 2016-06-21 | 2018-05-04 | 济南川成医药科技开发有限公司 | 一种4-(2-氨乙基)四氢吡喃的合成方法 |
| CN106323893B (zh) * | 2016-07-28 | 2019-03-19 | 山东师范大学 | 一种钯离子多通道响应探针及其合成方法与应用 |
| AU2018240031B2 (en) | 2017-03-20 | 2022-07-14 | President And Fellows Of Harvard College | Compounds and methods for the treatment of parasitic diseases |
| CN115215793A (zh) * | 2022-08-11 | 2022-10-21 | 南开大学 | 氟吡菌酰胺的合成方法 |
| CN120240473B (zh) * | 2025-06-05 | 2025-08-26 | 中国农业科学院烟草研究所(中国烟草总公司青州烟草研究所) | 一种胆碱类烟草根结线虫抑制剂及其制备方法 |
Family Cites Families (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4885026A (en) | 1986-05-12 | 1989-12-05 | Monsanto Company | Certain 3-amino-5-carboxy (or thio carboxy) pyridine herbicides |
| DE69624728T2 (de) | 1995-12-29 | 2003-07-10 | Boehringer Ingelheim (Canada) Ltd., Laval | Phenyl thiazol derivate mit antiherpesvirus eigenschaften |
| US6034106A (en) | 1996-06-07 | 2000-03-07 | Merck & Co., Inc. | Oxadiazole benzenesulfonamides as selective β3 Agonist for the treatment of Diabetes and Obesity |
| MY153569A (en) | 1998-01-20 | 2015-02-27 | Mitsubishi Tanabe Pharma Corp | Inhibitors of ?4 mediated cell adhesion |
| DE69919436T2 (de) | 1998-04-16 | 2005-09-15 | Pfizer Products Inc., Groton | N-Acyl und N-Aroyl Aralkylamide |
| ATE264328T1 (de) | 1999-04-21 | 2004-04-15 | Wyeth Corp | Substituierte 3-cyano-(1.7), (1.5) und (1.8)naphthyridininhibitoren von tyrosin kinasen |
| EP1204323B1 (en) | 1999-08-18 | 2004-07-14 | Aventis CropScience GmbH | Fungicides |
| US6388084B1 (en) | 1999-12-06 | 2002-05-14 | Hoffmann-La Roche Inc. | 4-pyridinyl-n-acyl-l-phenylalanines |
| JP4186484B2 (ja) | 2002-03-12 | 2008-11-26 | 住友化学株式会社 | ピリミジン化合物およびその用途 |
| GB0213715D0 (en) | 2002-06-14 | 2002-07-24 | Syngenta Ltd | Chemical compounds |
| EP1449841A1 (en) | 2003-02-19 | 2004-08-25 | Bayer CropScience SA | New fungicidal compounds |
| TWI312272B (en) | 2003-05-12 | 2009-07-21 | Sumitomo Chemical Co | Pyrimidine compound and pests controlling composition containing the same |
| US20040242644A1 (en) | 2003-05-27 | 2004-12-02 | Buckley Michael J. | (IS-5S)-3-(5,6-dichloro-3-pyridinyl-)-3,6-diazabicyclo[3.2.0]heptane is an effective analgesic agent |
| WO2005007627A1 (ja) | 2003-07-18 | 2005-01-27 | Nihon Nohyaku Co., Ltd. | フェニルピリジン誘導体、その中間体及びこれを有効成分とする除草剤 |
| EP1500651A1 (en) | 2003-07-25 | 2005-01-26 | Bayer CropScience S.A. | N-[2-(2-Pyridinyl)ethyl]benzamide compounds and their use as fungicides |
| TWI368482B (en) | 2003-12-19 | 2012-07-21 | Bayer Sas | New 2-pyridinylethylbenzamide derivatives |
| EP1548007A1 (en) | 2003-12-19 | 2005-06-29 | Bayer CropScience S.A. | 2-Pyridinylethylcarboxamide derivatives and their use as fungicides |
| AU2005212424A1 (en) | 2004-02-10 | 2005-08-25 | Janssen Pharmaceutica, N.V. | Pyridazinones as antagonists of a4 integrins |
| EP1717237B1 (en) | 2004-02-18 | 2010-12-29 | Ishihara Sangyo Kaisha, Ltd. | Anthranilamides, process for the production thereof, and pest controllers containing the same |
| EP1574511A1 (en) | 2004-03-03 | 2005-09-14 | Bayer CropScience S.A. | 2-Pyridinylethylcarboxamide derivatives and their use as fungicides |
| AU2005219788B2 (en) | 2004-03-05 | 2010-06-03 | Nissan Chemical Corporation | Isoxazoline-substituted benzamide compound and noxious organism control agent |
| PL1740544T3 (pl) | 2004-04-26 | 2007-11-30 | Bayer Ip Gmbh | Pochodne 2-pirydynylocykloalkilokarboksamidowe użyteczne jako fungicydy |
| EP1591442A1 (en) | 2004-04-26 | 2005-11-02 | Bayer CropScience S.A. | 2-Pyridinycycloalkylbenzamide derivatives and their use as fungicides |
| US7795448B2 (en) | 2004-05-06 | 2010-09-14 | Cytokinetics, Incorporated | Imidazoyl-benzamide anti-cancer agents |
| US7504413B2 (en) | 2004-05-06 | 2009-03-17 | Cytokinetics, Inc. | N-(4-(imidazo[1,2A]pyridin-YL)phenethyl)benzamide inhibitors of the mitotic kinesin CENP-E for treating certain cellular proliferation diseases |
| GB0414438D0 (en) | 2004-06-28 | 2004-07-28 | Syngenta Participations Ag | Chemical compounds |
| WO2006008192A1 (en) | 2004-07-23 | 2006-01-26 | Bayer Cropscience Sa | N-[2-(4-pyridinyl)ethyl]benzamide derivatives as fungicides |
| WO2006008193A1 (en) | 2004-07-23 | 2006-01-26 | Bayer Cropscience Sa | 4-pyridinylethylcarboxamide derivatives useful as fungicides |
| WO2006008191A1 (en) | 2004-07-23 | 2006-01-26 | Bayer Cropscience Sa | 3-pyridinylethylbenzamide derivatives as fungicides |
| JP2008507494A (ja) | 2004-07-23 | 2008-03-13 | バイエル・クロツプサイエンス・エス・アー | 殺菌剤としての3−ピリジニルエチルカルボキサミド誘導体 |
| PE20060721A1 (es) | 2004-09-16 | 2006-08-24 | Basf Ag | Serinamidas sustituidas por heteroaroilo |
| WO2006043635A1 (ja) | 2004-10-20 | 2006-04-27 | Kumiai Chemical Industry Co., Ltd. | 3-トリアゾリルフェニルスルフィド誘導体及びそれを有効成分として含有する殺虫・殺ダニ・殺線虫剤 |
| ES2383903T3 (es) | 2004-12-21 | 2012-06-27 | Bayer Cropscience Ag | Procedimiento para la preparación de un derivado de 2-piridiletilcarboxamida |
| EP1674455A1 (en) | 2004-12-21 | 2006-06-28 | Bayer CropScience S.A. | Process for the preparation of a 2-ethylaminopyridine derivative |
| JP2008545637A (ja) | 2005-05-18 | 2008-12-18 | バイエル・クロツプサイエンス・エス・アー | 2−ピリジニルシクロアルキルベンズアミド誘導体及び殺菌剤としてのそれらの使用 |
| PT1885712E (pt) | 2005-05-18 | 2011-04-29 | Bayer Cropscience Ag | Novos derivados de 2-piridinilcicloalquilcrboxamida como fungicidas |
| US20090137601A1 (en) | 2005-11-23 | 2009-05-28 | Astrazeneca Ab | L-Phenylalanine Derivatives |
| TWI435863B (zh) | 2006-03-20 | 2014-05-01 | Nihon Nohyaku Co Ltd | N-2-(雜)芳基乙基甲醯胺衍生物及含該衍生物之蟲害防治劑 |
| EP2132203A1 (en) | 2007-04-10 | 2009-12-16 | Bristol-Myers Squibb Company | Thiazolyl compounds useful as kinase inhibitors |
| PL2132987T3 (pl) | 2007-04-12 | 2016-09-30 | Kompozycja środka nicieniobójczego oraz sposób jej zastosowania | |
| WO2008134969A1 (fr) | 2007-04-30 | 2008-11-13 | Sinochem Corporation | Composés benzamides et leurs applications |
| TWI430995B (zh) | 2007-06-26 | 2014-03-21 | Du Pont | 萘異唑啉無脊椎有害動物控制劑 |
| GB0720126D0 (en) | 2007-10-15 | 2007-11-28 | Syngenta Participations Ag | Chemical compounds |
| TWI411395B (zh) | 2007-12-24 | 2013-10-11 | Syngenta Participations Ag | 殺蟲化合物 |
| TWI401023B (zh) | 2008-02-06 | 2013-07-11 | Du Pont | 中離子農藥 |
| CN101337940B (zh) | 2008-08-12 | 2012-05-02 | 国家农药创制工程技术研究中心 | 具杀虫活性的含氮杂环二氯烯丙醚类化合物 |
| WO2010060231A1 (zh) | 2008-11-25 | 2010-06-03 | Qin Zhaohai | 硝基缩氨基胍类化合物及其制备方法与其作为杀虫剂的应用 |
| WO2010069502A2 (de) | 2008-12-18 | 2010-06-24 | Bayer Cropscience Ag | Tetrazolsubstituierte anthranilsäureamide als pestizide |
| CN101747320B (zh) | 2008-12-19 | 2013-10-16 | 华东理工大学 | 二醛构建的具有杀虫活性的含氮或氧杂环化合物及其制备方法 |
| TWI482771B (zh) | 2009-05-04 | 2015-05-01 | Du Pont | 磺醯胺殺線蟲劑 |
| EP2289880A1 (en) | 2009-07-08 | 2011-03-02 | Bayer CropScience AG | 2-Pyridinylcyclopropylbenzamide fungicides |
| PL2631235T3 (pl) | 2010-08-31 | 2016-05-31 | Meiji Seika Pharma Co Ltd | Środek do zwalczania szkodników |
| CN101935291B (zh) | 2010-09-13 | 2013-05-01 | 中化蓝天集团有限公司 | 一种含氰基的邻苯二甲酰胺类化合物、制备方法和作为农用化学品杀虫剂的用途 |
| CN102057925B (zh) | 2011-01-21 | 2013-04-10 | 陕西上格之路生物科学有限公司 | 一种含噻虫酰胺和生物源类杀虫剂的杀虫组合物 |
| UA114287C2 (uk) * | 2011-03-02 | 2017-05-25 | Дзе Юніверсіті Оф Токіо | Засіб для боротьби з ендопаразитами |
| PH12014500977A1 (en) * | 2011-11-02 | 2014-06-09 | Bayer Ip Gmbh | Compounds with nematicidal activity |
| MX2014004849A (es) | 2011-11-02 | 2014-08-27 | Bayer Ip Gmbh | Compuesto con actividad nematicida. |
| MX2014005197A (es) | 2011-11-04 | 2014-05-28 | Syngenta Participations Ag | Compuestos plaguicidas. |
| EP2773617B1 (en) | 2011-11-04 | 2018-08-22 | Syngenta Participations AG | Pesticidal compounds |
| US20140287916A1 (en) | 2011-11-04 | 2014-09-25 | Syngenta Participations Ag | Pesticidal compounds |
| BR112014010707A2 (pt) | 2011-11-04 | 2017-04-25 | Syngenta Participations Ag | compostos pesticidas |
| PL2782565T3 (pl) | 2011-11-25 | 2020-08-24 | Bayer Intellectual Property Gmbh | Zastosowanie arylo- i heteroarylokarboksyamidów jako środki endopasożytobójcze |
| WO2013120940A2 (en) | 2012-02-14 | 2013-08-22 | Syngenta Participations Ag | Novel compounds |
| EP2644595A1 (en) | 2012-03-26 | 2013-10-02 | Syngenta Participations AG. | N-Cyclylamides as nematicides |
| TWI654180B (zh) | 2012-06-29 | 2019-03-21 | 美商艾佛艾姆希公司 | 殺真菌之雜環羧醯胺 |
| US9562034B2 (en) | 2012-08-30 | 2017-02-07 | The University Of Tokyo | Endoparasite control agent |
| MX356342B (es) | 2012-08-30 | 2018-05-23 | Univ Tokyo | Agente de control de endoparásitos y método para usarlo. |
-
2014
- 2014-10-03 UY UY0001035772A patent/UY35772A/es not_active Application Discontinuation
- 2014-10-09 TW TW103135140A patent/TW201607924A/zh unknown
- 2014-10-10 AR ARP140103791A patent/AR097998A1/es unknown
- 2014-10-10 EP EP14783623.3A patent/EP3057939A1/en not_active Withdrawn
- 2014-10-10 WO PCT/EP2014/071778 patent/WO2015055535A1/en not_active Ceased
- 2014-10-10 JP JP2016547235A patent/JP2016540035A/ja not_active Withdrawn
- 2014-10-10 RU RU2016118655A patent/RU2016118655A/ru not_active Application Discontinuation
- 2014-10-10 AU AU2014336360A patent/AU2014336360A1/en not_active Abandoned
- 2014-10-10 US US15/022,583 patent/US9776967B2/en active Active
- 2014-10-10 CN CN201480068427.3A patent/CN106061946A/zh active Pending
- 2014-10-10 MX MX2016004393A patent/MX2016004393A/es unknown
- 2014-10-10 CA CA2926981A patent/CA2926981A1/en not_active Abandoned
-
2016
- 2016-04-06 CL CL2016000795A patent/CL2016000795A1/es unknown
- 2016-04-13 ZA ZA2016/02507A patent/ZA201602507B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015055535A1 (en) | 2015-04-23 |
| CL2016000795A1 (es) | 2017-07-14 |
| ZA201602507B (en) | 2018-11-28 |
| RU2016118655A3 (es) | 2018-05-22 |
| JP2016540035A (ja) | 2016-12-22 |
| US20160221950A1 (en) | 2016-08-04 |
| TW201607924A (zh) | 2016-03-01 |
| CN106061946A (zh) | 2016-10-26 |
| US9776967B2 (en) | 2017-10-03 |
| UY35772A (es) | 2015-05-29 |
| AU2014336360A1 (en) | 2016-04-07 |
| MX2016004393A (es) | 2016-07-05 |
| RU2016118655A (ru) | 2017-11-22 |
| EP3057939A1 (en) | 2016-08-24 |
| CA2926981A1 (en) | 2015-04-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR097998A1 (es) | Compuestos plaguicidas | |
| AR098475A1 (es) | Compuestos pesticidas y usos | |
| AR111776A1 (es) | Heteroarilos inhibidores de las proteínas ras mutantes de g12c | |
| AR106299A1 (es) | Compuestos de piridona y fungicidas agrícolas y hortícolas que contienen dichos compuestos como ingrediente activo | |
| AR113905A1 (es) | Feniléteres herbicidas | |
| AR088014A1 (es) | Derivados de alcoholes 1-fenil-2-piridinil alquilicos como inhibidores de la fosfodiesterasa | |
| AR084444A1 (es) | Oxindolpirimidinas bencilicas y las preparaciones farmaceuticas que las contienen | |
| AR103297A1 (es) | Pirrolo y pirazolopirimidinas como inhibidores de la proteasa 7 específica de ubiquitina | |
| AR086983A1 (es) | Derivados de azetidinil fenil, piridil o pirazinil carboxamida como inhibidores de jak | |
| AR085283A1 (es) | Antagonistas de hepcidina a base de sulfonaminoquinolina | |
| AR096330A1 (es) | Derivados del bipirazol como inhibidores jak | |
| AR087984A1 (es) | Derivados biciclicos de dihidroquinolina-2-ona | |
| AR103561A1 (es) | Fenilpiridinas herbicidas | |
| AR098492A1 (es) | Derivados de purina | |
| AR102457A1 (es) | Compuestos para usarse en el tratamiento antihelmíntico | |
| AR091261A1 (es) | Derivados de alcoholes 1-fenil-2-piridinilalquilicos como inhibidores de la fosfodiesterasa | |
| AR092205A1 (es) | 4-piridonas sustituidas y su uso como inhibidores de la actividad de elastasa de neutrofilos | |
| AR110227A2 (es) | Derivados de pirazol con acción sobre fgf | |
| AR088886A1 (es) | Compuestos de 1,2,5-oxadiazol sustituido y su uso como herbicidas ii | |
| AR091464A1 (es) | Compuestos biciclicos de tiofenilamida | |
| AR094684A1 (es) | Triterpenoides de c-19 modificados, con actividad inhibidora de la maduración del vih | |
| AR090678A1 (es) | Derivados de fenil-tetrahidroisoquinolina como inhibidores de la aldosterona-sintasa y un metodo para su sintesis | |
| UA117007C2 (uk) | Заміщені біциклічні дигідропіримідинони і їх застосування як інгібіторів активності нейтрофільної еластази | |
| UY35357A (es) | Dihidropirimidinonas bicíclicas sustituidas y su uso como inhibidores de la actividad de elastasa n eutrofílica | |
| AR117006A1 (es) | Compuesto de 1,3-azol sustituido, composición farmacéutica que lo comprende y su uso para la fabricación de un medicamento |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |