AR052254A1 - 1-alquinil-2-ariloxialquilamidas y su uso como fungicidas - Google Patents
1-alquinil-2-ariloxialquilamidas y su uso como fungicidasInfo
- Publication number
- AR052254A1 AR052254A1 ARP050104986A ARP050104986A AR052254A1 AR 052254 A1 AR052254 A1 AR 052254A1 AR P050104986 A ARP050104986 A AR P050104986A AR P050104986 A ARP050104986 A AR P050104986A AR 052254 A1 AR052254 A1 AR 052254A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- halo
- alkoxy
- atom
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 abstract 36
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 24
- 125000001072 heteroaryl group Chemical group 0.000 abstract 15
- 125000000217 alkyl group Chemical group 0.000 abstract 14
- 125000003118 aryl group Chemical group 0.000 abstract 13
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 10
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 9
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 9
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 8
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract 8
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 125000004104 aryloxy group Chemical group 0.000 abstract 7
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 125000004429 atom Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 4
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 4
- 125000005114 heteroarylalkoxy group Chemical group 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 4
- XSXHWVKGUXMUQE-UHFFFAOYSA-N osmium dioxide Inorganic materials O=[Os]=O XSXHWVKGUXMUQE-UHFFFAOYSA-N 0.000 abstract 4
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 4
- 125000004434 sulfur atom Chemical group 0.000 abstract 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 3
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 3
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- -1 cyano, hydroxy Chemical group 0.000 abstract 2
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 1
- 125000004011 3 membered carbocyclic group Chemical group 0.000 abstract 1
- 125000001845 4 membered carbocyclic group Chemical group 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004849 alkoxymethyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000005160 aryl oxy alkyl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 abstract 1
- 125000005326 heteroaryloxy alkyl group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 125000000464 thioxo group Chemical group S=* 0.000 abstract 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/91—Dibenzofurans; Hydrogenated dibenzofurans
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
-
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides
-
- 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
- A01N43/04—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 one hetero atom
- A01N43/06—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 one hetero atom five-membered rings
- A01N43/12—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 one hetero atom five-membered rings 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
- A01N43/02—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
- A01N43/42—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 condensed with carbocyclic 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
- A01N43/72—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
- A01N43/74—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 five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
- C07D327/04—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/76—Dibenzothiophenes
Abstract
Proceso, composicion fungicida y método para combatir o controlar hongos fitopatogenos. Reivindicacion 1: Un compuesto de formula general (1) donde Ar es un grupo de la formula (A) donde A1 es arilo, ariloxi, arilalquilo C1-6, arilalcoxi C1-6, heteroarilo, heteroariloxi, heteroarilalquilo C1-6 o heteroarilalcoxi C1-6 en el cual la porcion arilo o heteroarilo está opcionalmente sustituida con 1, 2 o 3 sustituyentes independientemente seleccionados de halo, ciano, hidroxi, alquilo C1-4, alcoxi C1-4 y alquiltio C1-4, y A2 y A3 son independientemente H, halo, ciano, nitro, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, cicloalquil C3-6- alquilo C1-4, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, alcoxi C1- 6, haloalcoxi C1-6, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiniloxi C2-6, haloalquiniloxi C2-6, arilo, ariloxi, arilalquilo C1-6 o arilalcoxi C1-6, heteroarilo, heteroariloxi, heteroarilalquilo C1-6 o heteroarilalcoxi C1-6, -SF5, -S(O)palquilo C1-4 donde p es 0, 1 o 2 y el grupo alquilo está opcionalmente substituido con halo, -OSO2 alquilo C1-4, donde el grupo alquilo está opcionalmente substituido con halo, -CONRpRq, CORp, -CO2Rp, - CRp=NRq, -NRpRq, -NRpCORq, -NRpCO2Rq, -SO2NRpRq o - NRpSO2Ro donde Ro es alquilo C1-4 opcionalmente substituido con halogeno y Rp y Rq son independientemente H o alquilo C1-4 opcionalmente substituido con halogeno o, en el caso de -CONRpRq o -SO2NRpRq, pueden unirse para formar un anillo de 5 o 6 miembros que contiene un solo átomo de N, un solo átomo de S, átomos de C saturados y opcionalmente un solo átomo de O; donde cualquiera de los grupos o porciones alquilo, cicloalquilo, alquenilo, alquinilo, arilo, o heteroarilo precedentes están opcionalmente sustituidos; o A1 y A2 forman un anillo saturado o insaturado de 5 miembros o un anillo saturado de 6, 7 u 8 miembros que está opcionalmente substituido con halo, alquilo C1-6, alcoxi C1-6, oxo, tioxo, arilo, ariloxi, arilalquilo C1-6, arilalcoxi C1-6, heteroarilo, heteroariloxi, heteroarilalquilo C1-6 o heteroarilalcoxi C1-6, donde si el anillo es un anillo saturado de 5 miembros, opcionalmente uno o dos de los átomos de C se reemplazan con un átomo de O o S, o si el anillo es un anillo insaturado de 5 miembros, opcionalmente un átomo de C se reemplaza con un átomo de O o S y el anillo de 5 miembros insaturado se fusiona opcionalmente con un anillo benceno o piridina, que puede estar opcionalmente substituido con halo o alquilo C1-4, o el anillo es un anillo insaturado de 6, 7 u 8 miembros, y A3 es H, halo, ciano, nitro, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, cicloalquil C3-6-alquilo C1-4, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, alcoxi C1-6, haloalcoxi C1-6, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiniloxi C2-6, haloalquiniloxi C2-6, arilo, ariloxi, arilalquilo C1-6, arilalcoxi C1-6, heteroarilo, heteroariloxi, heteroarilalquilo C1-6, heteroarilalcoxi C1-6, -SF5, -S(O)palquilo C1-4 donde p es 0, 1 o 2 y el grupo alquilo está opcionalmente substituido con halo, -OSO2 alquilo C1-4, donde el grupo alquilo está opcionalmente substituido con halo, -CONRpRq, CORp, -CO2Rp, -CRp=NRq, -NRpRq, -NRpCORq, - NRpCO2Rq, -SO2NRpRq o -NRpSO2Ro donde Ro es alquilo C1-4 opcionalmente substituido con halogeno y Rp y Rq son independientemente H o alquilo C1-4 opcionalmente substituido con halogeno o, en el caso de -CONRpRq o -SO2NRpRq, pueden unirse para formar un anillo de 5 o 6 miembros que contiene un solo átomo de N, un solo átomo de S, átomos de C saturados y opcionalmente un solo átomo de O; donde cualquiera de los grupos o porciones alquilo, cicloalquilo, alquenilo, alquinilo, arilo, o heteroarilo precedentes están opcionalmente sustituidos; o Ar es un grupo de la formula (B1) o (B2); en las cuales L y M son ambos CQ o L es N o N-oxido y M es CQ, o L es CQ y M es N o N-oxido; Ka y Kb son independientemente H o F; V es H, halo, ciano, nitro, alquilo C1-6 opcionalmente substituido con halo o alcoxi C1-4, cicloalquilo C3-6 opcionalmente substituido con halo o alcoxi C1-4, cicloalquilC3-6-alquilo C1-4 opcionalmente substituido con halo o alcoxi C1-4, alqueniloC2-4 opcionalmente substituido con halo, alquinilo C2-4 opcionalmente substituido con halo, alcoxi C1-6 opcionalmente substituido con halo o alcoxi C1-4, alqueniloxi C2-4 opcionalmente substituido con halo, alquiniloxi C2-4 opcionalmente substituido con halo, arilo, ariloxi, arilalquilo C1-6, arilalcoxi C1-6, heteroarilo, heteroariloxi, heteroarilalquilo C1-6, heteroarilalcoxi C1-6, -SF5, -S(O)p alquilo C1-4 donde p es 0, 1 o 2 y el grupo alquilo está opcionalmente substituido con halo, -OSO2 alquilo C1-4 donde el grupo alquilo está opcionalmente substituido con halo, -CONRpRq, CORp, -CO2Rp, - CRp=NRq, -NRpRq, -NRpCORq, -NRpCO2Rq, -SO2NRpRq o -NRpSO2Ro donde Ro es alquilo C1-4 opcionalmente substituido con halogeno y Rp y Rq son independientemente H o alquilo C1-4 opcionalmente substituido con halogeno o, en el caso de -CONRpRq o -SO2NRpRq, pueden unirse para formar un anillo de 5 o 6 miembros que contiene un solo átomo de N, un solo átomo de S, átomos de C saturados y opcionalmente un solo átomo de O; donde cualquiera de los grupos o porciones alquilo, cicloalquilo, alquenilo, alquinilo, arilo, o heteroarilo precedentes están opcionalmente sustituidos; Q es arilo, ariloxi, arilalquilo C1-6, arilalcoxi C1-6, heteroarilo, heteroariloxi, heteroarilalquilo C16 o heteroarilalcoxi C!-6, en el cual la porcion arilo o heteroarilo está opcionalmente substituido con 1, 2 o 3 sustituyentes independientemente seleccionados de halo, ciano, alquilo C1-4, alcoxi C1-4 y alquiltio C1-4; R1 es alquilo C1-4, haloalquilo C1-4 o cicloalquilo C3-4; R2 es H, alquilo C1-4, alcoximetilo C1-4 o benciloximetilo donde el anillo fenilo de la porcion bencilo está opcionalmente substituido con 1, 2 o 3 grupos alcoxi C1-4; R3 y R4 son independientemente H, alquilo C1-6, alquenilo C2-6 o alquinilo C2-6 opcionalmente substituidos con halo, alcoxi C1-4, ciano o -S(O)m alquilo C1-4 donde m es 0, 1 o 2 y el grupo alquilo C1-4 está opcionalmente substituido con halo con la condicion de que ambos no representen H, o R3 y R4 se unen con el átomo de C al cual están adheridos para formar un anillo carbocíclico de 3 o 4 miembros, que contiene opcionalmente un átomo de O, S o N y están opcionalmente substituidos con halo, alquilo C1-4, alcoxi C1-4 o ciano; R5 es H, alquilo C1-8, cicloalquilo C3-6 o cicloalquil C3-6-alquilo C1-4 en el cual el grupo alquilo o cicloalquilo está opcionalmente substituido con halo, hidroxi, alcoxi C16, alcoxi C1-3-alcoxi C1-3, ciano, alquilcarbonilo C1-4, alcoxicarbonilo C1-4, arilcarbonilo, heteroarilcarbonilo, alquilcarboniloxi C14, aminocarboniloxi o mono- o di-alquil C1-4-aminocarboniloxi, trialquilsililoxi C1-4, -S(O)r alquilo C1-6 donde r es 0, 1 o 2, o R5 es arilo opcionalmente substituido, arilalquilo C1-4, opcionalmente substituido, ariloxialquilo C1-4 opcionalmente substituido, arilalcoxi C1-4alqulo C1-4 opcionalmente substituido, heteroarilo opcionalmente substituido, heteroarilalquilo C14 opcionalmente substituido, heteroariloxialquilo C1-4 opcionalmente substituido o heteroarilalcoxi C1-4 alquilo C1-4 opcionalmente substituido, donde los anillos o porciones arilo y heteroarilo opcionalmente substituidos de los valores R5 están opcionalmente substituidos con 1, 2 o 3 substituyentes independientemente seleccionados de halo, ciano, nitro, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, cicloalquilC3-6-alquilo C1-4, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, alcoxi C1-6, haloalcoxi C1-6, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiniloxi C2-6, haloalquiniloxi C2-6, arilo, ariloxi, arilalquilo C1-6, arilalcoxi C1-6, heteroarilo, heteroariloxi, heteroarilalquilo C1-6, heteroarilalcoxi C1-6, -SF5, -S(O)r alquilo C1-4, donde r es 0, 1 o 2 y el alquilo está opcionalmente substituido con halo, -OSO2 alquilo C1-4 donde el grupo alquilo está opcionalmente substituido con halo, -CONRsRt, CORs, -CO2Rs, -CRs=NRt, -NRsRt, -NRsCORt, -NRsCO2Rt, -SO2NRsRt o -NRsSO2Rr donde Rr es alquilo C1- 6 opcionalmente substituido con halogeno y Rs y Rt son independientemente H o alquilo C1-6 opcionalmente substituido con halogeno o, en el caso de -CONRsRt o -SO2NRsRt, pueden unirse para formar un anillo de 5 o 6 miembros que contiene un solo átomo de N, un solo átomo de S, átomos de C saturados y opcionalmente un solo átomo de O; donde cualquiera de los grupos o porciones alquilo, cicloalquilo, alquenilo, alquinilo, arilo, o heteroarilo precedentes están opcionalmente sustituidos; y n es 0, 1 o 2.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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GBGB0426372.9A GB0426372D0 (en) | 2004-12-01 | 2004-12-01 | Fungicides |
Publications (1)
Publication Number | Publication Date |
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AR052254A1 true AR052254A1 (es) | 2007-03-07 |
Family
ID=34043872
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP050104986A AR052254A1 (es) | 2004-12-01 | 2005-11-29 | 1-alquinil-2-ariloxialquilamidas y su uso como fungicidas |
Country Status (21)
Country | Link |
---|---|
US (1) | US8193361B2 (es) |
EP (1) | EP1819689B1 (es) |
JP (1) | JP2008521850A (es) |
KR (1) | KR20070085656A (es) |
CN (1) | CN101065372B (es) |
AR (1) | AR052254A1 (es) |
AT (1) | ATE440093T1 (es) |
AU (1) | AU2005311491A1 (es) |
BR (1) | BRPI0518752A2 (es) |
CA (1) | CA2583335A1 (es) |
CR (1) | CR9124A (es) |
DE (1) | DE602005016142D1 (es) |
ES (1) | ES2329816T3 (es) |
GB (1) | GB0426372D0 (es) |
IL (1) | IL183180A0 (es) |
MX (1) | MX2007005932A (es) |
PL (1) | PL1819689T3 (es) |
PT (1) | PT1819689E (es) |
RU (1) | RU2394024C2 (es) |
TW (1) | TW200637837A (es) |
WO (1) | WO2006058699A1 (es) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0227554D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227555D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227556D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227551D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0312863D0 (en) | 2003-06-04 | 2003-07-09 | Syngenta Ltd | Fungicides |
GB0426373D0 (en) * | 2004-12-01 | 2005-01-05 | Syngenta Ltd | Fungicides |
CN102892756A (zh) * | 2010-05-21 | 2013-01-23 | 先正达参股股份有限公司 | 新颖的作为杀真菌剂的酰胺 |
EP2397467A1 (en) * | 2010-06-10 | 2011-12-21 | Syngenta Participations AG | Quinoline derivatives as fungicides |
TWI504350B (zh) | 2010-09-01 | 2015-10-21 | Du Pont | 殺真菌吡唑及其混合物 |
TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
WO2013126283A1 (en) | 2012-02-20 | 2013-08-29 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
EP2864293B1 (en) | 2012-06-22 | 2016-04-27 | E. I. du Pont de Nemours and Company | Fungicidal 4-methylanilino pyrazoles |
WO2014130409A2 (en) | 2013-02-21 | 2014-08-28 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazole mixtures |
AU2014254262B2 (en) | 2013-04-15 | 2018-08-23 | Fmc Corporation | Fungicidal carboxamides |
AU2014254261B2 (en) | 2013-04-15 | 2017-11-09 | Fmc Corporation | Fungicidal amides |
WO2015123193A1 (en) | 2014-02-12 | 2015-08-20 | E. I. Du Pont De Nemours And Company | Fungicidal benzodipyrazoles |
WO2015157005A1 (en) | 2014-04-10 | 2015-10-15 | E I Du Pont De Nemours And Company | Substituted tolyl fungicide mixtures |
US20170037014A1 (en) | 2014-05-06 | 2017-02-09 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
CA2978066A1 (en) | 2015-03-19 | 2016-09-22 | E I Du Pont De Nemours And Company | Fungicidal pyrazoles |
EP3558984B1 (en) | 2016-12-20 | 2023-08-02 | FMC Corporation | Fungicidal oxadiazoles |
WO2018170067A1 (en) * | 2017-03-14 | 2018-09-20 | Dana-Farber Cancer Institute, Inc. | Small molecule sensitization of bax activation for induction of cell death |
TWI829634B (zh) | 2017-04-06 | 2024-01-21 | 美商富曼西公司 | 殺真菌之噁二唑 |
AR112221A1 (es) | 2017-07-05 | 2019-10-02 | Fmc Corp | Oxadiazoles fungicidas, composición que los comprende y un método para controlar fitoenfermedades que los emplea |
TW202400547A (zh) | 2018-09-06 | 2024-01-01 | 美商富曼西公司 | 殺真菌之經硝苯胺基取代之吡唑 |
TW202024029A (zh) | 2018-09-14 | 2020-07-01 | 美商富曼西公司 | 殺真菌劑鹵甲基酮及水合物 |
AR116978A1 (es) | 2018-11-06 | 2021-06-30 | Fmc Corp | Fungicidas de tolilo sustituido |
CA3167647A1 (en) | 2020-01-15 | 2021-07-22 | Fmc Corporation | Fungicidal amides |
EP4103554A1 (en) | 2020-02-14 | 2022-12-21 | Fmc Corporation | Substituted 5,6-diphenyl-3(2h)-pyridazinones for use as fungicides |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2856840B2 (ja) * | 1990-05-15 | 1999-02-10 | 株式会社トクヤマ | チエニルオキシフェノキシカルボン酸誘導体 |
GB0129267D0 (en) * | 2001-12-06 | 2002-01-23 | Syngenta Ltd | Fungicides |
AU2003226929A1 (en) * | 2002-11-25 | 2004-06-18 | 7Tm Pharma A/S | Novel benzamide compounds for use in mch receptor related disorders |
GB0227556D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227554D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227551D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227558D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227557D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227555D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0312863D0 (en) * | 2003-06-04 | 2003-07-09 | Syngenta Ltd | Fungicides |
GB0312864D0 (en) * | 2003-06-04 | 2003-07-09 | Syngenta Ltd | Fungicides |
GB0426373D0 (en) * | 2004-12-01 | 2005-01-05 | Syngenta Ltd | Fungicides |
-
2004
- 2004-12-01 GB GBGB0426372.9A patent/GB0426372D0/en not_active Ceased
-
2005
- 2005-11-29 JP JP2007543759A patent/JP2008521850A/ja active Pending
- 2005-11-29 US US11/720,200 patent/US8193361B2/en not_active Expired - Fee Related
- 2005-11-29 WO PCT/EP2005/012734 patent/WO2006058699A1/en active Application Filing
- 2005-11-29 CA CA002583335A patent/CA2583335A1/en not_active Abandoned
- 2005-11-29 MX MX2007005932A patent/MX2007005932A/es active IP Right Grant
- 2005-11-29 PL PL05810902T patent/PL1819689T3/pl unknown
- 2005-11-29 RU RU2007124679/04A patent/RU2394024C2/ru not_active IP Right Cessation
- 2005-11-29 PT PT05810902T patent/PT1819689E/pt unknown
- 2005-11-29 DE DE602005016142T patent/DE602005016142D1/de active Active
- 2005-11-29 BR BRPI0518752-4A patent/BRPI0518752A2/pt not_active Application Discontinuation
- 2005-11-29 ES ES05810902T patent/ES2329816T3/es active Active
- 2005-11-29 AR ARP050104986A patent/AR052254A1/es not_active Application Discontinuation
- 2005-11-29 KR KR1020077012454A patent/KR20070085656A/ko not_active Application Discontinuation
- 2005-11-29 EP EP05810902A patent/EP1819689B1/en not_active Not-in-force
- 2005-11-29 CN CN2005800400643A patent/CN101065372B/zh not_active Expired - Fee Related
- 2005-11-29 AU AU2005311491A patent/AU2005311491A1/en not_active Abandoned
- 2005-11-29 AT AT05810902T patent/ATE440093T1/de not_active IP Right Cessation
- 2005-11-29 TW TW094141906A patent/TW200637837A/zh unknown
-
2007
- 2007-05-14 IL IL183180A patent/IL183180A0/en unknown
- 2007-05-15 CR CR9124A patent/CR9124A/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
IL183180A0 (en) | 2007-09-20 |
ATE440093T1 (de) | 2009-09-15 |
GB0426372D0 (en) | 2005-01-05 |
CR9124A (es) | 2007-10-04 |
MX2007005932A (es) | 2007-06-20 |
JP2008521850A (ja) | 2008-06-26 |
US20080096917A1 (en) | 2008-04-24 |
PL1819689T3 (pl) | 2010-02-26 |
CA2583335A1 (en) | 2006-06-08 |
EP1819689A1 (en) | 2007-08-22 |
EP1819689B1 (en) | 2009-08-19 |
RU2007124679A (ru) | 2009-01-10 |
AU2005311491A1 (en) | 2006-06-08 |
CN101065372A (zh) | 2007-10-31 |
US8193361B2 (en) | 2012-06-05 |
CN101065372B (zh) | 2011-05-18 |
KR20070085656A (ko) | 2007-08-27 |
WO2006058699A1 (en) | 2006-06-08 |
BRPI0518752A2 (pt) | 2008-12-02 |
RU2394024C2 (ru) | 2010-07-10 |
ES2329816T3 (es) | 2009-12-01 |
PT1819689E (pt) | 2009-11-20 |
DE602005016142D1 (de) | 2009-10-01 |
TW200637837A (en) | 2006-11-01 |
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