AR105460A1 - Derivados sustituidos de 2-pirimidina furano / tienocicloalquilamino y su uso para el control del crecimiento de plantas no deseables - Google Patents
Derivados sustituidos de 2-pirimidina furano / tienocicloalquilamino y su uso para el control del crecimiento de plantas no deseablesInfo
- Publication number
- AR105460A1 AR105460A1 ARP160102251A ARP160102251A AR105460A1 AR 105460 A1 AR105460 A1 AR 105460A1 AR P160102251 A ARP160102251 A AR P160102251A AR P160102251 A ARP160102251 A AR P160102251A AR 105460 A1 AR105460 A1 AR 105460A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- cycloalkyl
- alkoxy
- cycloalkenyl
- Prior art date
Links
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 47
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical class 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 8
- 125000005915 C6-C14 aryl group Chemical group 0.000 abstract 7
- 229910052760 oxygen Inorganic materials 0.000 abstract 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 4
- -1 hydroxy, nitro, amino Chemical group 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 125000005974 C6-C14 arylcarbonyl group Chemical group 0.000 abstract 3
- 125000005914 C6-C14 aryloxy group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 2
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000006621 (C3-C8) cycloalkyl-(C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000006636 (C3-C8) cycloalkylcarbonyl group Chemical group 0.000 abstract 2
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 2
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 235000019256 formaldehyde Nutrition 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
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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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-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
- A01N43/90—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
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- 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
- C07D405/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
- C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Derivados sustituidos de 2-pirimidina furano / tienocicloalquilamino, su uso para el control del crecimiento de plantas no deseables y, en el campo de la protección fitosanitaria, así como los procesos para su preparación. Reivindicación 1: Compuestos de la fórmula general (1) y sus sales agroquímicamente aceptables, donde A¹, A² y A³ se seleccionan cada uno independientemente de O, S, CR⁹, CR¹⁰ o CR¹¹, donde exactamente un átomo es de A¹, A² y A³ O ó S; R⁹, R¹⁰ y R¹¹ se seleccionan cada uno independientemente del grupo compuesto por hidrógeno, halógeno, ciano, C(O)OH, C(O)NH₂, C₁₋₆-alquilo, C₁₋₆-alquilcarbonilo, C₁₋₆-alquiloxicarbonilo, C₁₋₆-alquilaminocarbonilo, C₁₋₆-di-alquilaminocarbonilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₂₋₆-haloalquinilo, C₂₋₆-alquinilcarbonilo, C₂₋₆-haloalquinilcarbonilo, C₂₋₆-alquiniloxi, C₂₋₆-haloalquiniloxi, C₂₋₆-alquiniloxicarbonilo, C₂₋₆-haloalquiniloxicarbonilo y nitro; R¹ y R² se selecciona cada uno independientemente del grupo compuesto por halógeno, hidroxi, nitro, amino, ciano, C(O)NH₂; C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonilo, C₁₋₆-haloalquilcarbonilo, C₁₋₆-alquilcarboniloxi, C₁₋₆-haloalquilcarboniloxi, C₁₋₆-alquilcarbonilo-C₁₋₄-alquilo; C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₁₋₆-alcoxicarbonilo, C₁₋₆-haloalcoxicarbonilo, C₁₋₆-alcoxicarbonilo-C₁₋₆-alquilo, C₁₋₆-haloalcoxicarbonilo-C₁₋₆-alquilo, C₁₋₆-alcoxicarbonilo-C₁₋₆-haloalquilo, C₁₋₆-haloalcoxicarbonilo-C₁₋₆-haloalquilo; C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquenilcarbonilo, C₂₋₆-haloalquenilcarbonilo, C₂₋₆-alqueniloxi, C₂₋₆-haloalqueniloxi, C₂₋₆-alqueniloxicarbonilo, C₂₋₆-haloalqueniloxicarbonilo; C₂₋₆-alquinilo, C₂₋₆-haloalquinilo, C₂₋₆-alquinilcarbonilo, C₂₋₆-haloalquinilcarbonilo, C₂₋₆-alquiniloxi, C₂₋₆-haloalquiniloxi, C₂₋₆-alquiniloxicarbonilo, C₂₋₆-haloalquiniloxicarbonilo; tri-C₁₋₆-alquilsililo-C₂₋₆-alquinilo, di-C₁₋₆-alquilsililo-C₂₋₆-alquinilo, mono-C₁₋₆-alquilsililo-C₂₋₆-alquinilo; fenilsililo-C₂₋₆-alquinilo; C₆₋₁₄-arilo, C₆₋₁₄-ariloxi, C₆₋₁₄-arilcarbonilo y C₆₋₁₄-ariloxicarbonilo, que pueden estar sustituidos respectivamente en la parte arilo con halógeno, C₁₋₆-alquilo y/o C₁₋₆-haloalquilo; C₆₋₁₄-arilo-C₁₋₆-alquilo, C₆₋₁₄-arilo-C₁₋₆-alcoxi, C₆₋₁₄-arilo-C₁₋₆-alquilcarbonilo, C₆₋₁₄-arilo-C₁₋₆-alquilcarboniloxi, C₆₋₁₄-arilo-C₁₋₆-alcoxicarbonilo, C₆₋₁₄-arilo-C₁₋₆-alcoxicarboniloxi; aminocarbonilo-C₁₋₆-alquilo, di-C₁₋₆-alquilaminocarbonilo-C₁₋₆-alquilo; N-(C₁₋₆-haloalcanoilo)-aminocarbonilo, mono-(C₆₋₁₄-aril)-aminocarbonilo, di-(C₆₋₁₄-aril)-aminocarbonilo; C₁₋₆-alcoxi-C₁₋₆-alquilo, C₁₋₆-alcoxi-C₁₋₆-alcoxi, C₁₋₆-alcoxicarbonilo-C₁₋₆-alcoxi; C₃₋₈-cicloalquilo, opcionalmente sustituido en el radical cicloalquilo por C₁₋₆-alquilo y/o halógeno; C₃₋₈-cicloalcoxi, C₃₋₈-cicloalquilo-C₁₋₆-alquilo, C₃₋₈-cicloalquilo-C₁₋₆-haloalquilo, C₃₋₈-cicloalquilo-C₁₋₆-alcoxi, C₃₋₈-cicloalquilo-C₁₋₆-haloalcoxi, C₃₋₈-cicloalquilcarbonilo, C₃₋₈-cicloalcoxicarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-alquilcarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-haloalquilcarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-alcoxicarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-haloalcoxicarbonilo, C₃₋₈-cicloalquilcarboniloxi, C₃₋₈-cicloalcoxicarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-alquilcarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-haloalquilcarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-alcoxicarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-haloalcoxicarboniloxi; C₃₋₈-cicloalquenilo, C₃₋₈-cicloalqueniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-alquilo, C₃₋₈-cicloalquenilo-C₁₋₆-haloalquilo, C₃₋₈-cicloalquenilo-C₁₋₆-alcoxi, C₃₋₈-cicloalquenilo-C₁₋₆-haloalcoxi, C₃₋₈-cicloalquenilcarbonilo, C₃₋₈-cicloalqueniloxicarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-alquilcarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-haloalquilcarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-alcoxicarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-haloalcoxicarbonilo, C₃₋₈-cicloalquenilcarboniloxi, C₃₋₈-cicloalqueniloxicarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-alquilcarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-haloalquilcarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-alcoxicarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-haloalcoxicarboniloxi; hidroxi-C₁₋₆-alquilo, hidroxi-C₁₋₆-alcoxi, ciano-C₁₋₆-alcoxi, ciano-C₁₋₆-alquilo; y C₁₋₆-alquilsulfonilo, C₁₋₆-alquiltio, C₁₋₆-alquilsulfinilo, C₁₋₆-haloalquilsulfonilo, C₁₋₆-haloalquiltio, C₁₋₆-haloalquilsulfinilo, C₁₋₆-alquilsulfonilo-C₁₋₆-alquilo, C₁₋₆-alquiltio-C₁₋₆-alquilo, C₁₋₆-alquilsulfinilo-C₁₋₆-alquilo, C₁₋₆-haloalquilsulfonilo-C₁₋₆-alquilo, C₁₋₆-haloalquiltio-C₁₋₆-alquilo, C₁₋₆-haloalquilsulfinilo-C₁₋₆-alquilo, C₁₋₆-alquilsulfonilo-C₁₋₆-haloalquilo, C₁₋₆-alquiltio-C₁₋₆-haloalquilo, C₁₋₆-alquilsulfinilo-C₁₋₆-haloalquilo, C₁₋₆-haloalquilsulfonilo-C₁₋₆-haloalquilo, C₁₋₆-haloalquiltio-C₁₋₆-haloalquilo, C₁₋₆-haloalquilsulfinilo-C₁₋₆-haloalquilo, C₁₋₆-alquilsulfoniloxi, C₁₋₆-haloalquilsulfoniloxi, C₁₋₆-alquiltiocarbonilo, C₁₋₆-haloalquiltiocarbonilo, C₁₋₆-alquiltiocarboniloxi, C₁₋₆-haloalquiltiocarboniloxi, C₁₋₆-alquiltio-C₁₋₆-alquilo, C₁₋₆-alquiltio-C₁₋₆-alcoxi, C₁₋₆-alquiltio-C₁₋₆-alquilcarbonilo, C₁₋₆-alquiltio-C₁₋₆-alquilcarboniloxi; C₄₋₁₄-arilsulfonilo, C₆₋₁₄-ariltio, C₆₋₁₄-arilsulfinilo, C₃₋₈-cicloalquiltio, C₃₋₈-alqueniltio, C₃₋₈-cicloalquenilotio y C₃₋₆-alquiniltio; R³ se selecciona del grupo compuesto por hidrógeno, halógeno, hidroxi, nitro, amino, ciano, C(O)OH, C(O)NH₂; C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonilo, C₁₋₆-haloalquilcarbonilo, C₁₋₆-alquilcarboniloxi, C₁₋₆-haloalquilcarboniloxi, C₁₋₆-alquilcarbonilo-C₁₋₄-alquilo; C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₁₋₆-alcoxicarbonilo, C₁₋₆-haloalcoxicarbonilo, C₁₋₆-alcoxicarbonilo-C₁₋₆-alquilo, C₁₋₆-haloalcoxicarbonilo-C₁₋₆-alquilo, C₁₋₆-alcoxicarbonilo-C₁₋₆-haloalquilo, C₁₋₆-haloalcoxicarbonilo-C₁₋₆-haloalquilo; C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquenilcarbonilo, C₂₋₆-haloalquenilcarbonilo, C₂₋₆-alqueniloxi, C₂₋₆-haloalqueniloxi, C₂₋₆-alqueniloxicarbonilo, C₂₋₆-haloalqueniloxicarbonilo; C₂₋₆-alquinilo, C₂₋₆-haloalquinilo, C₂₋₆-alquinilcarbonilo, C₂₋₆-haloalquinilcarbonilo, C₂₋₆-alquiniloxi, C₂₋₆-haloalquiniloxi, C₂₋₆-alquiniloxicarbonilo, C₂₋₆-haloalquiniloxicarbonilo; tri-C₁₋₆-alquilsililo-C₂₋₆-alquinilo, di-C₁₋₆-alquilsililo-C₂₋₆-alquinilo, mono-C₁₋₆-alquilsililo-C₂₋₆-alquinilo; finilsililo-C₂₋₆-alquinilo; C₆₋₁₄-arilo, C₆₋₁₄-ariloxi, C₆₋₁₄-arilcarbonilo y C₆₋₁₄-ariloxicarbonilo, que pueden estar sustituidos respectivamente en la parte arilo con halógeno, C₁₋₆-alquilo y/o C₁₋₆-haloalquilo; C₆₋₁₄-arilo-C₁₋₆-alquilo, C₆₋₁₄-arilo-C₁₋₆-alcoxi, C₆₋₁₄-arilo-C₁₋₆-alquilcarbonilo, C₆₋₁₄-arilo-C₁₋₆-alquilcarboniloxi, C₆₋₁₄-arilo-C₁₋₆-alcoxicarbonilo, C₆₋₁₄-arilo-C₁₋₆-alcoxicarboniloxi; aminocarbonilo-C₁₋₆-alquilo, di-C₁₋₆-alquilaminocarbonilo-C₁₋₆-alquilo; N-(C₁₋₆-haloalcanoilo)-aminocarbonilo, mono-(C₆₋₁₄-aril)-aminocarbonilo, di-(C₆₋₁₄-aril)-aminocarbonilo; C₁₋₆-alcoxi-C₁₋₆-alquilo, C₁₋₆-alcoxi-C₁₋₆-alcoxi, C₁₋₆-alcoxicarbonilo-C₁₋₆-alcoxi; C₃₋₈-cicloalquilo, opcionalmente sustituido en el radical cicloalquilo por C₁₋₆-alquilo y/o halógeno; C₃₋₈-cicloalcoxi, C₃₋₈-cicloalquilo-C₁₋₆-alquilo, C₃₋₈-cicloalquilo-C₁₋₆-haloalquilo, C₃₋₈-cicloalquilo-C₁₋₆-alcoxi, C₃₋₈-cicloalquilo-C₁₋₆-haloalcoxi, C₃₋₈-cicloalquilcarbonilo, C₃₋₈-cicloalcoxicarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-alquilcarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-haloalquilcarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-alcoxicarbonilo, C₃₋₈-cicloalquilo-C₁₋₆-haloalcoxicarbonilo, C₃₋₈-cicloalquilcarboniloxi, C₃₋₈-cicloalcoxicarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-alquilcarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-haloalquilcarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-alcoxicarboniloxi, C₃₋₈-cicloalquilo-C₁₋₆-haloalcoxicarboniloxi; C₃₋₈-cicloalquenilo, C₃₋₈-cicloalqueniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-alquilo, C₃₋₈-cicloalquenilo-C₁₋₆-haloalquilo, C₃₋₈-cicloalquenilo-C₁₋₆-alcoxi, C₃₋₈-cicloalquenilo-C₁₋₆-haloalcoxi, C₃₋₈-cicloalquenilcarbonilo, C₃₋₈-cicloalqueniloxicarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-alquilcarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-haloalquilcarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-alcoxicarbonilo, C₃₋₈-cicloalquenilo-C₁₋₆-haloalcoxicarbonilo, C₃₋₈-cicloalquenilcarboniloxi, C₃₋₈-cicloalqueniloxicarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-alquilcarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-haloalquilcarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-alcoxicarboniloxi, C₃₋₈-cicloalquenilo-C₁₋₆-haloalcoxicarboniloxi; hidroxi-C₁₋₆-alquilo, hidroxi-C₁₋₆-alcoxi, ciano-C₁₋₆-alcoxi, ciano-C₁₋₆-alquilo; y C₁₋₆-alquilsulfonilo, C₁₋₆-alquiltio, C₁₋₆-alquilsulfinilo, C₁₋₆-haloalquilsulfonilo, C₁₋₆-haloalquiltio, C₁₋₆-haloalquilsulfinilo, C₁₋₆-alquilsulfonilo-C₁₋₆-alquilo, C₁₋₆-alquiltio-C₁₋₆-alquilo, C₁₋₆-alquilsulfinilo-C₁₋₆-alquilo, C₁₋₆-haloalquilsulfonilo-C₁₋₆-alquilo, C₁₋₆-haloalquiltio-C₁₋₆-alquilo, C₁₋₆-haloalquilsulfinilo-C₁₋₆-alquilo, C₁₋₆-alquilsulfonilo-C₁₋₆-haloalquilo, C₁₋₆-alquiltio-C₁₋₆-haloalquilo, C₁₋₆-alquilsulfinilo-C₁₋₆-haloalquilo, C₁₋₆-haloalquilsulfonilo-C₁₋₆-haloalquilo, C₁₋₆-haloalquiltio-C₁₋₆-haloalquilo, C₁₋₆-haloalquilsulfinilo-C₁₋₆-haloalquilo, C₁₋₆-alquilsulfoniloxi, C₁₋₆-haloalquilsulfoniloxi, C₁₋₆-alquiltiocarbonilo, C₁₋₆-haloalquiltiocarbonilo, C₁₋₆-alquiltiocarboniloxi, C₁₋₆-haloalquiltiocarboniloxi, C₁₋₆-alquiltio-C₁₋₆-alquilo, C₁₋₆-alquiltio-C₁₋₆-alcoxi, C₁₋₆-alquiltio-C₁₋₆-alquilcarbonilo, C₁₋₆-alquiltio-C₁₋₆-alquilcarboniloxi; C₄₋₁₄-arilsulfonilo, C₆₋₁₄-ariltio, C₆₋₁₄-arilsulfinilo, C₃₋₈-cicloalquiltio, C₃₋₈-alqueniltio, C₃₋₈-cicloalquenilotio y C₃₋₆-alquiniltio, o R¹ puede estar unido a R² mediante un enlace entre sí, de modo que resulta un carbociclo o un heterociclo parcialmente hidrogenados de 5 a 7 miembros, con al menos un heteroátomo seleccionado de N, O, S y P, que opcionalmente está sustituido por uno o varios sustituyentes seleccionados del grupo compuesto por hidroxi, =O, =N-O-H, =N-O-C₁₋₆-alquilo, =N-O-bencilo, =N-O-fenilo, fenilo, por un fenilo sustituido por uno o varios átomos de halógeno iguales o diferentes, C₁₋₆-alquilo, C₃₋₆-cicloalquilo y C₁₋₆-haloalquilo, y R³ se define como anteriormente, pero es preferiblemente hidrógeno, metilo o amino; R⁴ se selecciona del grupo compuesto por hidrógeno, C₁₋₆-alquilo, C₁₋₆-alcoxi, C₁₋₆-alcoxi-C₁₋₆-alquilo, C₁₋₆-alcoxicarbonilo y aminocarbonilo; R⁵ y R⁶ se seleccionan cada uno independientemente del grupo compuesto por hidrógeno, hidroxi, C₁₋₆-alquilo, C₁₋₆-alquilfenilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi y C₁₋₆-haloalcoxi; o los radicales R⁵ y R⁶ junto con el átomo de carbono al que están unidos, forman un anillo de 3 a 7 miembros; R⁷ y R⁸ se seleccionan cada uno independientemente del grupo compuesto por hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₆₋₁₄-arilo, C₆₋₁₄-ariloxi, C₆₋₁₄-arilcarbonilo y C₆₋₁₄-ariloxicarbonilo; o los radicales R⁷ y R⁸ juntos forman un grupo C₁₋₇-alquilo, que pueden contener uno o varios átomos de oxígeno y/o azufre, donde el grupo C₁₋₇-alquilo puede estar sustituido una o más veces por halógeno y los respectivos sustituyentes halógeno pueden ser idénticos o diferentes; X es un enlace (si n = 1 ó 2) o se selecciona del grupo compuesto por O, S, CH₂, C=O, NH, CR¹²R¹³, y NR¹⁴, CH₂O y CH₂S, en la que en los dos últimos grupos mencionados el átomo de carbono está unido a la parte aromática y el heteroátomo O ó S está unido a la parte parcialmente hidrogenada de la amina; R¹² y R¹³ se seleccionan cada uno independientemente del grupo compuesto por hidrógeno, C₁₋₆-alquilo y C₁₋₆-haloalquilo; R¹⁴ se selecciona del grupo compuesto por hidrógeno, C₁₋₆-alquilo y C₁₋₆-haloalquilo; y n es el número 0, 1 ó 2.
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