AR031243A1 - Piridincetonas herbicidamente activas, procedimiento para su preparacion, agentes herbicidas y para inhibir el desarrollo de las plantas, procedimiento para combatir el crecimiento no deseado de plantas, procedimiento para inhibir el crecimiento no deseado de plantas y compuestos utiles como interme - Google Patents
Piridincetonas herbicidamente activas, procedimiento para su preparacion, agentes herbicidas y para inhibir el desarrollo de las plantas, procedimiento para combatir el crecimiento no deseado de plantas, procedimiento para inhibir el crecimiento no deseado de plantas y compuestos utiles como intermeInfo
- Publication number
- AR031243A1 AR031243A1 ARP010102734A ARP010102734A AR031243A1 AR 031243 A1 AR031243 A1 AR 031243A1 AR P010102734 A ARP010102734 A AR P010102734A AR P010102734 A ARP010102734 A AR P010102734A AR 031243 A1 AR031243 A1 AR 031243A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- thio
- sulfinyl
- sulfonyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title 3
- -1 amino, formyl Chemical group 0.000 abstract 24
- 229910052736 halogen Inorganic materials 0.000 abstract 18
- 150000002367 halogens Chemical class 0.000 abstract 14
- 125000000217 alkyl group Chemical group 0.000 abstract 13
- 125000002947 alkylene group Chemical group 0.000 abstract 12
- 125000001188 haloalkyl group Chemical group 0.000 abstract 12
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 11
- 125000003545 alkoxy group Chemical group 0.000 abstract 10
- 229910052739 hydrogen Inorganic materials 0.000 abstract 10
- 239000001257 hydrogen Substances 0.000 abstract 10
- 229910052760 oxygen Inorganic materials 0.000 abstract 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 9
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 9
- 239000001301 oxygen Substances 0.000 abstract 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 8
- 125000003342 alkenyl group Chemical group 0.000 abstract 8
- 125000000304 alkynyl group Chemical group 0.000 abstract 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 4
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 4
- 229910052717 sulfur Chemical group 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 239000011593 sulfur Chemical group 0.000 abstract 3
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002950 monocyclic group Chemical group 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- AZWFNQKHHGQCET-UHFFFAOYSA-N 2-(2-methylphenyl)acetamide Chemical compound CC1=CC=CC=C1CC(N)=O AZWFNQKHHGQCET-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000005193 alkenylcarbonyloxy group Chemical group 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000005136 alkenylsulfinyl group Chemical group 0.000 abstract 1
- 125000005137 alkenylsulfonyl group Chemical group 0.000 abstract 1
- 150000001345 alkine derivatives Chemical class 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005198 alkynylcarbonyloxy group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000005109 alkynylthio group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003396 thiol group Chemical class [H]S* 0.000 abstract 1
Classifications
-
- 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
- C07D401/06—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 only aliphatic carbon atoms
-
- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/50—Ketonic radicals
-
- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D409/06—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 carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Piridincetonas herbicidamente activas, que tienen la formula (1), en la cual: p significa 0 o 1; R1 representa una cadena de alquileno C1-6, alquenileno C3-6 o alquinileno C3-6, que puede estar substituida de forma sencilla o multiple por halogeno o R5, no estando los enlaces no saturados de la cadena unidos directamente a los substituyentes X1; X1 significa oxígeno, -O(CO)-, -(CO)O-, -O(CO)O-, -N(R6)-O-, -ONR51-, tio, sulfinilo, sulfonilo, -SO2NR7-, -NR52SO2- o -NR8-; R2 representa un grupo alquilo C1-8, alquenilo C3-6 o alquinilo C3-6, que están substituidos de forma sencilla o multiple por halogeno, hidroxilo, amino, formilo, nitro, ciano, mercapto, carbamoílo, alcoxilo C1-6, alcoxi C1-6-carbonilo, alquenilo C2-6, halogenoalquenilo C2-6, alquinilo C2-6, halogenoalquinilo C2-6, cicloalquilo C3-6, cicloalquilo C3-6 substituido por halogeno, o por alqueniloxilo C3-6, alquiniloxilo C3-6, halogenoalcoxilo C1-6, halogenoalquenil-oxilo C3-6, cianoalcoxilo C1-6, alcoxi C1-6-alcoxilo C1-6, alcoxi C1-6-alcoxi C1-6-alcoxilo C1-6, alquil C1-6-tio-alcoxilo C1-6, alquil C1-6-sulfinil-alcoxilo C1-6, alquil C1-6-sulfonil-alcoxilo C1-6, alcoxi C1-6-carbonil-alcoxilo C1-6, alcoxi C1-6-carbonilo, alquil C1-6-carbonilo, alquil C1-6-tio, alquil C1-6-sulfinilo, alquil C1-6-sulfonilo, halogenoalquil C1-6-tio, halogenoalquil C1-6-sulfinilo, halogenoalquil C1-6-sulfonilo, oxiranilo, que a su vez puede estar substituido por alquilo C1-6 o por (3-oxetanil)-oxilo, que a su vez puede estar substituido por alquilo C1-6, o por benciltio, bencilsulfinilo, bencilsulfonilo, alquil C1-6-amino, di-(alquil C1-6)-amino, R9S(O)2O, R10N(R11)SO2, rodano, fenilo, fenoxilo, feniltio, fenilsulfinilo o fenilsulfonilo; pudiendo estar los grupos que contienen fenilo o bencilo a su vez substituidos por uno o más grupos alquilo C1-6, halogenoalquilo C1-6, alcoxilo C1-6, halogenoalcoxilo C1-6, halogeno, ciano, hidroxilo o nitro; o R2 representa fenilo, que puede estar substituido una o varias veces por alquilo C1-6, halogenoalquilo C1-6, alcoxilo C1-6, halogenoalcoxilo C1-6, halogeno, ciano, hidroxilo o nitro; o R2 representa cicloalquilo C3-6, cicloalquilo C3-6 substituido por alcoxilo C1-6 o alquilo C1-6, 3-oxetanilo o 3-oxetanilo substituido por alquilo C1-6; o cuando Q representa Q2 o Q3 o cuando representa Q1, en los cuales R14 y R22 significan una cadena de alquileno C2-3, R2 representa adicionalmente también un sistema anular monocíclico o bicíclico condensado de 5 a 10 miembros, que puede ser aromático, saturado o parcialmente saturado y que puede contener de 1 a 4 heteroátomos seleccionados del grupo formado por nitrogeno, oxígeno y azufre, estando unido el sistema anular directamente o por medio de un grupo alquileno C1-4, alquenil C2-4-alquileno C1-4, alquinil C2-4-alquileno C1-4, -N(R12)-alquileno C1-4, -SO-alquileno C1-4 o -SO2-alquileno C1-4 a los substituyentes X1, no pudiendo contener cada sistema anular más de 2 átomos de oxígeno ni más de 2 átomos de azufre, estando el sistema anular mismo sustituido una, dos o tres veces por alquilo C1-6, halogenoalquilo C1-6, alquenilo C2-6, halogenoalquenilo C2-6, alquinilo C2-6, halogenoalquinilo C2-6, alcoxilo C1-6, hidroxilo, halogenoalcoxilo C1-6, alqueniloxilo C3-6, alquiniloxilo C3-6, mercapto, alquil C1-6-tio, halogenoalquil C1-6-tio, alquenil C3-6-tio, halogenoalquenil C3-6-tio, alquinil C3-6-tio, alcoxi C2-5-alquiltio, acetilalquil C3-5-tio, alcoxi C3-6-carbonilalquiltio, cianoalquil C2-4-tio, alquil C1-6-sulfinilo, halogenoalquil C1-6-sulfinilo, alquil C1-6-sulfonilo, halogenoalquil C1-6-sulfonilo, aminosulfonilo, alquil C1-2-aminosulfonilo, di(alquil C1-2)-aminosulfonilo, di-(alquil C1-4)-amino, halogeno, ciano, nitro, fenilo y benciltio, pudiendo estar sustituido a su vez el fenilo y el benciltio en el anillo fenolico por alquilo C1-3, halogenoalquilo C1-3, alcoxilo C1-3, halogenoalcoxilo C1-3, halogeno, ciano o nitro, siendo los sustituyentes en el nitrogeno en el anillo heterocíclico distintos de halogeno; o R2 representa hidrogeno o alquilo C1-8 sin sustituir, cuando: (a) R1 está sustituido por el grupo R5, o (b) Q representa el grupo Q2, o (c) Q representa el grupo Q3, en el cual X1 significa -O(CO)-, -(CO)O-, -N(R6)-O-, -ONR51-, -SO2NR7-, -NR52SO2- o -NR8-, o (d) Q representa el grupo Q1, en el cual X1 significa -N(R6)-O-, -ONR51-, -SO2NR7-, -NR52SO2- o -NR8-, o (e) Q representa el grupo Q1, en el cual R14 y R22 en Q1 significan una cadena de alquileno C2-3 y X1 -O(CO)- o -(CO)O-; R3 significa halogenoalquilo C1-3; R4 significa hidrogeno, halogeno, alquilo C1-3, halogenoalquilo C1-3, alcoxilo C1-3, alcoxi C1-3-alquilo C1-3 o alcoxi C1-3-alcoxilo C1-3; R5 representa hidroxilo, alcoxilo C1-6, cicloalcoxilo C3-6, alcoxi C1-6-alcoxilo C1-6, alcoxi C1-6-alcoxi C1-6-alcoxilo C1-6 o alquil C1-2-sulfoniloxilo; R6, R7, R8, R9, R10, R11, R12, R51 y R52 significan independientemente entre sí hidrogeno, alquilo C1-6, halogenoalquilo C1-6, alcoxi C1-6-carbonilo, alquil C1-6-carbonilo, alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alquilo C1-6 sustituido por alcoxilo C1-6, bencilo o fenilo, pudiendo estar sustituido a su vez el fenilo y bencilo una o varias veces por alquilo C1-6, halogenoalquilo C1-6, alcoxilo C1-6, halogenoalcoxilo C1-6, halogeno, ciano, hidroxilo o nitro, no representando al mismo tiempo R6 hidrogeno y R9 hidrogeno, alcoxi C1-6-carbonilo o alquil C1-6-carbonilo; Q representa Q1, en la cual: A1 significa C(R14R15), NR16 u oxígeno; A2 significa C(R17R18), C(O), -C=N-O-R19, oxígeno, tio, sulfinilo, sulfonilo, NR20 o etileno, con las condiciones de que A1 sea distinto de oxígeno cuando A2 representa oxígeno, C(O), tio, sulfinilo, -C=N-O-R19, NR20 o C(R17R18), significando R17 y R18, independientemente entre sí, alcoxilo C1-4, alquil C1-4-tio, alquil C1-4-sulfinilo, alquil C1-4-sulfonilo y de que A1 sea distinto de NR16 cuando A2 representa tio, sulfinilo o C(R17R18), significando R17 y R18, independientemente entre sí, alcoxilo C1-4, alquil C1-4-tio, alquil C1-4-sulfinilo, alquil C1-4-sulfonilo; R14 y R22 representan, independientemente entre sí, hidrogeno, alquilo C1-4, haloalquilo C1-4, alquenilo C3-4, alquinilo C3-4, alquil C1-4-tio, alquil C1-4-sulfinilo, alquil C1-4-sulfonilo, alquil C1-4-sulfoniloxilo, alcoxilo C1-4, alcoxi C1-4-carbonilo o alquil C1-4-carbonilo; R15 y R21 significan independientemente entre sí, hidrogeno, alquilo C1-4, halogenoalquilo C1-4, alquenilo C3-4 o alquinilo C3-4; R17 significa hidrogeno, alquilo C1-4, halogenoalquilo C1-4, alcoxilo C1-4, alquil C1-4-tio, alquil C1-4-sulfinilo o alquil C1-4-sulfonilo; R18 significa hidrogeno, alquilo C1-4, halogenoalquilo C1-4, alquenilo C3-4, alquinilo C3-4, alcoxilo C1-4, alquil C1-4-tio, alquil C1-4-sulfinilo, alquil C1-4-sulfonilo o dialcoxialquil C1-4-alquilo C1-4; R20 significa alquilo C1-4, cicloalquilo C3-6, alquenilo C3-4, alquinilo C3-4, alquil C1-4-carbonilo, alquil C1-4-carboniloxilo, di-(alquil C1-4)-aminocarbonilo o bencilo, pudiendo estar el grupo fenilo sustituido una o varias veces por alquilo C1-6, halogenoalquilo C1-6, alcoxilo C1-6, halogenoalcoxilo C1-6, halogeno, ciano, hidroxilo o nitro; R19 y R16 significan, independientemente entre sí, hidrogeno, alquilo C1-4, cicloalquilo C3-6, alquenilo C3-4, alquinilo C3-4, bencilo o fenilo, pudiendo estar el grupo fenilo y bencilo a su vez sustituido una o varias veces por alquilo C1-6, halogenoalquilo C1-6, alcoxilo C1-6, halogenoalcoxilo C1-6, halogeno, ciano, hidroxilo o nitro; o R14 y R22 forman conjuntamente una cadena de alquileno C2-3; o R14 y R15 conjuntamente y/o R17 y R18 conjuntamente y/o R21 y R22 conjuntamente forman una cadena de alquileno C2-4, que puede estar interrumpida por oxígeno y/o carbonilo y/o azufre, con la condicion de que el átomo de oxígeno y el átomo de azufre estén separados por al menos un grupo metileno; o R14 y R18 forman conjuntamente una cadena de alquileno C2-4; o R22 y R18 forman conjuntamente una cadena de alquileno C2-4; o R18 forma conjuntamente con R22 o R14 un enlace directo; o R16 y R18 forman conjuntamente una cadena de alquileno C2-4; R13 significa hidroxilo, O-M+, en el cual M+ representa un cation de metal alcalino o un cation de amonio, halogeno, alquil C1-12-sulfoniloxilo, amino, alquil C1-4-tio, alquil C1-12-sulfinilo, alquil C1-12-sulfonilo, halogenoalquil C1-12-tio, halogenoalquil C1-12-sulfinilo, halogenoalquil C1-12-sulfonilo, alcoxi C1-6-alquil C1-6-tio, alcoxi C1-6-alquil C1-6-sulfinilo, alcoxi C1-6-alquil C1-6-sulfonilo, alquenil C3-12-tio, alquenil C3-12-sulfinilo, alquenil C3-12-sulfonilo, alquilnil C3-12-tio, alquinil C3-12-sulfinilo, alquinil C3-12-sulfonilo, alcoxi C1-4-carbonil-alquil C1-4-tio, alcoxi C1-4-carbonil-alquil C1-4-sulfinilo, alcoxi C1-4-carbonil-alquil C1-4-sulfonilo, (alcoxi C1-4)2P(O)O, alquil C1-4-(alcoxi C1-4)P(O)O, H-(alcoxi C1-4)P(O)O, R23R24N, R25R26NNH, R27R28NC(O)O-, R29R30NC(O)NH-, alquil C1-18-carboniloxilo, alquenil C2-18-carboniloxilo, alquinil C2-18-carboniloxilo, cicloalquil C3-6-carboniloxilo, alcoxi C1-12-carboniloxilo, alquil C1-12-tio-carboniloxilo, alquil C1-12-tiocarbamoílo, pudiendo los grupos alquilo, alquenilo y alquinilo estar substituidos por halogeno, alcoxilo C1-6, alquil C1-6-tio, alquil C1-6-sulfinilo, alquil C1-6-sulfonilo o ciano; o R13 representa fenoxilo, feniltio, fenilsulfinilo, fenilsulfonilo, fenilsulfonilamino, fenilsulfoniloxilo o benzoiloxilo, pudiendo estar los grupos fenilo substituidos a su vez por uno o varios grupos halogeno, nitro, ciano, alquilo C1-4, halogenoalquilo C1-4, alcoxilo C1-4 o halogenoalcoxilo C1-4; o R13 significa un grupo het1-tio, het2-sulfinilo, het3-sulfonilo, het4-(CO)O o het5-N(R33), en los cuales het1, het2, het3, het4 o het5 representan, independientemente entre sí, un sistema anular monocíclico o bicíclico condensado de 5 a 10 miembros, que puede ser aromático o parcialmente saturado y contener de 1 a 4 heteroátomos seleccionados del grupo formado por nitrogeno, oxígeno y azufre, no pudiendo contener cada sistema anular
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