AR073356A1 - ANILINOPIRIMIDINAS HETEROCíCLICAMENTE SUSTITUíDAS, MÉTODO E INTERMEDIARIO PARA SU SíNTESIS Y SU USO EN COMPOSICIONES Y EN PROCEDIMIENTOS DE CONTROL DE HONGOS FITOPAToGENOS. - Google Patents
ANILINOPIRIMIDINAS HETEROCíCLICAMENTE SUSTITUíDAS, MÉTODO E INTERMEDIARIO PARA SU SíNTESIS Y SU USO EN COMPOSICIONES Y EN PROCEDIMIENTOS DE CONTROL DE HONGOS FITOPAToGENOS.Info
- Publication number
- AR073356A1 AR073356A1 ARP090103353A ARP090103353A AR073356A1 AR 073356 A1 AR073356 A1 AR 073356A1 AR P090103353 A ARP090103353 A AR P090103353A AR P090103353 A ARP090103353 A AR P090103353A AR 073356 A1 AR073356 A1 AR 073356A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- branched
- optionally branched
- alkoxy
- unsubstituted
- Prior art date
Links
- 241000233866 Fungi Species 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 3
- 239000000203 mixture Substances 0.000 title abstract 2
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- -1 morpholin-4-ylmethyl Chemical group 0.000 abstract 37
- 229910052739 hydrogen Inorganic materials 0.000 abstract 15
- 239000001257 hydrogen Substances 0.000 abstract 15
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 15
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 12
- 125000001424 substituent group Chemical group 0.000 abstract 12
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 9
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 6
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 235000019256 formaldehyde Nutrition 0.000 abstract 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 229910052731 fluorine Inorganic materials 0.000 abstract 5
- 239000011737 fluorine Substances 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 229910052794 bromium Inorganic materials 0.000 abstract 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 4
- 239000011593 sulfur Substances 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 3
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- 125000001188 haloalkyl group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 101100495923 Schizosaccharomyces pombe (strain 972 / ATCC 24843) chr2 gene Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000006299 oxetan-3-yl group Chemical group [H]C1([H])OC([H])([H])C1([H])* 0.000 abstract 2
- 230000003032 phytopathogenic effect Effects 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 abstract 1
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 abstract 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 abstract 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005079 alkoxycarbonylmethyl 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
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 238000003898 horticulture Methods 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- 125000004014 thioethyl group Chemical group [H]SC([H])([H])C([H])([H])* 0.000 abstract 1
- ZBZJXHCVGLJWFG-UHFFFAOYSA-N trichloromethyl(.) Chemical compound Cl[C](Cl)Cl ZBZJXHCVGLJWFG-UHFFFAOYSA-N 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
- C07D405/10—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 aromatic rings
-
- 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
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Procedimientos y composiciones para controlar hongos daninos fitopatogenos en y/o sobre plantas o en y/o sobre semillas de plantas y también su uso para controlar hongos daninos fitopatogenos en la agricultura, horticultura y silvicultura, en la proteccion de materiales y en el sector doméstico y en el de la higiene. Además un procedimiento para preparar anilinopirimidinenos heterocíclicamente sustituidos de formula (1). Reivindicacion 1: Compuestos de formula (1) donde uno o más de los símbolos tienen uno de los siguientes significados, R1 a R5 independientemente entre sí representan hidrogeno, OH, halogeno, ciano, alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, alcoxi C1-4-carbonilo, NMe2, SCF3, SCH3, OCF2H o OCF3, donde exactamente uno de los radicales R2 y R3 representa un grupo de formula E1, E2 o E3, en las que uno o más de los símbolos tienen uno de los siguientes significados; Y representa un enlace directo o una cadena de alquilo C1-3 opcionalmente sustituida con alquilo C1-4, haloalquilo C1-3 o alcoxi C1-3-alquilo; Z representa azufre u oxígeno, con la condicion de que si R2 o R3 representan un grupo E3, ambos Z representan oxígeno o azufre; L1 representa una cadena de alquileno C2-4 sin sustituir o sustituida o CH2CH=CHCH2, donde los átomos de carbono individuales de la cadena de alquileno pueden llevar uno o más sustituyentes, independientemente entre sí seleccionados de la siguiente lista: hidrogeno, OH, CH2OH, halogeno, CN, NMe2, SCH3, NO2, alquilo C1-6 opcionalmente ramificado, cicloalquilo C3-6 opcionalmente ramificado, alcoxi C1-4 opcionalmente ramificado, alcoxi C1-4-carbonilo opcionalmente ramificado, alcoxi C1-4-alquilo C1-4 opcionalmente ramificado, fenilo o bencilo opcionalmente sustituidos, haloalquilo C1-4 opcionalmente ramificado, alquil C1-4-mercaptoalquilo C1-4 opcionalmente ramificado, alquil C1-4-carbonilo, CH2O(CO)CH3, morfolin-4-ilmetilo, pirrolidin-1-ilmetilo, (4-metoxifenoxi)metilo, (dietilamino)metilo, (prop-2-en-1-iloxi)metilo, (2-etoxietoxi)metilo, CH2CN, CH2CH2CN, CHSiMe3, 2,2-difluorociclopropilo o metilideno, o dos sustituyentes unidos a un átomo de carbono junto con este átomo de carbono forman un carbociclo saturado de 3 a 6 miembros sin sustituir o sustituido, donde los sustituyentes independientemente entre si se seleccionan de la siguiente lista: hidrogeno, fluor, alquilo C1-4 opcionalmente ramificado, alcoxi C1-4 opcionalmente ramificado o haloalquilo C1-4 opcionalmente ramificado, o dos sustituyentes unidos a dos átomos de carbono adyacentes junto con estos dos átomos de carbono forman un carbociclo saturado de 5 a 8 miembros sin sustituir o sustituido, donde los sustituyentes independientemente entre sí se seleccionan de la siguiente lista: hidrogeno, fluor, alquilo C1-4 opcionalmente ramificado, alcoxi C1-4 opcionalmente ramificado o haloalquilo C1-4 opcionalmente ramificado, o un heterociclo saturado de 5 o 6 miembros sin sustituir o sustituido que contiene un átomo de oxigeno o un átomo de azufre, donde los sustituyentes independientemente entre si se seleccionan de la siguiente lista: hidrogeno, fluor, alquilo C1-4 opcionalmente ramificado, alcoxi C1-4 opcionalmente ramificado o haloalquilo C1-4 opcionalmente ramificado, o un anillo de fenilo sin sustituir o sustituido, donde los sustituyentes independientemente entre sí se seleccionan de la siguiente lista: hidrogeno, halogeno, CN, SCH3, NO2, alquilo C1-4 opcionalmente ramificado, alcoxi C1-4 opcionalmente ramificado, alquil C1-4carbonilo opcionalmente ramificado, haloalquilo C1-4 opcionalmente ramificado, haloalcoxi C1-4 opcionalmente ramificado; L2 es una cadena de alquileno C2 a C3 sin sustituir o sustituida donde los átomos de carbono individuales pueden llevar uno o más sustituyentes independientemente entre si seleccionados de la siguiente lista: hidrogeno, CH2OH, alquilo C1-4 opcionalmente ramificado, alcoxi C1-4 opcionalmente ramificado, alcoxi C1-4-alquilo C1-4 opcionalmente ramificado, carboniloxi C1-4-alquilo C1-4 opcionalmente ramificado, alcoxi C1-4-carbonilo opcionalmente ramificado, haloalquilo C1-4 ramificado, CH2O(CO)CH3, CH2O(CO)CH2CH3, fenilo o bencilo; R11 representa hidrogeno, CH2OH, alquilo C1-4 opcionalmente ramificado, alcoxi C1-4-alquilo C1-4 opcionalmente ramificado, haloalquilo C1-4 opcionalmente ramificado, alcoxi C1-4-carbonilmetilo, cicloalquilo C3-6 opcionalmente ramificado, CH2CN, CH2CH2CN, (2-metil-3-dioxan-2-il)metilo, tiofen-2-ilo, CH2CH2OH, fenilo o CH2Ph; R12 representa alquilo C1-5 ramificado o de cadena lineal, CH2CH2SH, prop-2-en-1-ilo, COCH3, COCH2CH3 o CH2Ph; R6 representa hidrogeno, metilo, alquil C1-4-carbonilo, CHO, alcoxi C1-4-alquil C1-4-carbonilo, alcoxi C1-4-alquilo C1-4, alcoxi C1-4-carbonilo opcionalmente ramificado, haloalquil C1-4-carbonilo, alquenilo C1-3, alquinilo C1-3, alquil C1-4-sulfinilo, alquil C1-4-sulfonilo, bencilo opcionalmente sustituido, trialquil C1-4-sililo, trialquil C1-4-sililetilo o dialquil C1-4-monofenilsililo, donde los sustituyentes independientemente entre si se seleccionan del grupo que está constituido por hidrogeno, metilo, fluor, cloro o bromo, alquilo C1-4, alcoxi C1-4, hidroxilo, haloalquilo C1-4 y ciano; R7 representa hidrogeno, ciano, alquilo C1-3 o haloalquilo C1-3; R8 representa halogeno, ciano, CF3, metilo, CFH2, CF2H, CCl3, SMe, S(O)Me o SO2Me; R9 representa hidrogeno, alquilo C1-3 de cadena lineal o ramificado, 2-metoxietan-1-ilo, prop-2-en-1-ilo, alcoxi C1-4-alquilo C1-4, alquil C1-4carbonilo de cadena lineal o ramificado, haloalquil C1-4carbonilo, bencilo sin sustituir o sustituido, trialquil C1-6-sililo, trialquil C1-4-sililetilo, dialquil C1-4-monofenilsililo, alcoxi C1-4carbonilo, alquil C1-6-sulfinilo, alquil C1-6-sulfonilo, haloalquil C1-6-sulfinilo o haloalquil C1-6-sulfonilo, donde los sustituyentes independientemente entre sí se seleccionan del grupo que está constituido por hidrogeno, halogeno, nitro, alquilo C1-4, alcoxi C1-4, hidroxilo, haloalquilo C1-4 y ciano; R10 representa alquilo C1-7 sin sustituir o sustituido de cadena lineal o ramificado, haloalquilo C2-7 sin sustituir o sustituido de cadena lineal o ramificado, cicloalquilo C3-7 sin sustituir o sustituido, cicloalquil C3-7-alquilo C1-3 sin sustituir o sustituido de cadena lineal o ramificado, alquenilo C3-7 sin sustituir o sustituido de cadena lineal o ramificado, alquinilo C3-7 sin sustituir o sustituido de cadena lineal o ramificado, alcoxi C1-4-alquilo C1-4 sin sustituir o sustituido de cadena lineal o ramificado, haloalcoxi C1-4-alquilo C1-4 sin sustituir o sustituido de cadena lineal o ramificado, 2-metil-1-(metilsulfanil)propan-2-ilo u oxetan-3-ilo; o R9 y R10 junto con el átomo de nitrogeno al que están unidos forman un ciclo saturado de 3 a 7 miembros sin sustituir o sustituido que puede contener hasta un heteroátomo adicional seleccionado del grupo que está constituido por oxígeno, azufre y nitrogeno, donde los sustituyentes R10 independientemente entre sí se seleccionan del grupo que está constituido por metilo, etilo, isopropilo, ciclopropilo, átomos de fluor, cloro y/o bromo, metoxi, etoxi, metilmercapto, etilmercapto, ciano, hidroxilo y CF3; y también sales agroquímicamente activas de los mismos. Reivindicacion 15: Compuestos de formula (2) en la que R7 representa hidrogeno, y, si R8 representa CF3, CFH2, o OCF2H, Hal representa F, CI, Br o I; R9 representa hidrogeno, etilo, propilo, propan-2-ilo, 2-metoxetan-1-ilo, prop-2-en-1-ilo, CH2OCH3, COMe, COOMe, COOEt, COOtercBu, COCF3 o bencilo; R10 representa etilo, propilo, ciclopropilo, ciclopropilmetilo, 1-ciclopropilet-1-ilo, 2-metilciclopropilo, 2,2-dimetilciclopropilo, 2,2-dimetilprop-1-ilo, terc-butilo, ciclobutilo, 2-metilciclobut-1-ilo, 3-metilciclobut-1-ilo, butilo, 3-metilbut-1-ilo, 2-metilbut-1-ilo, 2-metilprop-1-ilo, 1-fluoroprop-2-ilo, ciclopentilo, propan-2-ilo, pentan-3-ilo, pentan-2-ilo, pentilo, prop-2-en-1-ilo, butan-2-ilo, 2,2,2-trifluoroetilo, 2,2-difluoroetilo, 2-metoxietan-1-ilo, 2-metilmercaptoetan-1-ilo, 2-fluoroetan-1-ilo, 2-cloroetan-1-ilo, 2-cianoetan-1-ilo, 1-metoxipropan-2-ilo, 3-metoxipropan-1-ilo, 1-metilmercaptopropan-2-ilo, 2-metil-1-(metilsulfanil)propan-2-ilo, oxetan-3-ilo, 1,1,1-trifluoropropan-2-ilo, 2,2,3,3,3-pentafluoropropilo, 1,1,1-trifIuoropropan-3-ilo, 1,1,1-trifluorobutan-2-ilo, 1,1,1-trifluorobutan-3-ilo, 2-metilprop-2-en-1-ilo o 1-fluoropropan-2-ilo, o R9 y R10 junto con el átono de nitrogeno al que están unidos forman un ciclo saturado de 3 a 7 miembros sin sustituir o sustituido que puede contener hasta un heteroátomo adicional, donde los sustituyentes independientemente entre si se seleccionan del grupo que está constituido por metilo, átomos de fluor, cloro y/o bromo, ciano, hidroxilo, metoxi o CF3, y donde los heteroátomos se seleccionan del grupo que está constituido por oxígeno, azufre y nitrogeno.
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| CN102203087A (zh) | 2011-09-28 |
| EP2331533A1 (de) | 2011-06-15 |
| BRPI0918293A2 (pt) | 2019-09-24 |
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| TW201021703A (en) | 2010-06-16 |
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