AR045678A1 - Derivados ciclicos fenil substituidos - Google Patents
Derivados ciclicos fenil substituidosInfo
- Publication number
- AR045678A1 AR045678A1 ARP040101471A ARP040101471A AR045678A1 AR 045678 A1 AR045678 A1 AR 045678A1 AR P040101471 A ARP040101471 A AR P040101471A AR P040101471 A ARP040101471 A AR P040101471A AR 045678 A1 AR045678 A1 AR 045678A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- optionally substituted
- hydrogen
- alkoxy
- Prior art date
Links
- 229910052739 hydrogen Inorganic materials 0.000 abstract 13
- 239000001257 hydrogen Substances 0.000 abstract 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 13
- 229910052799 carbon Inorganic materials 0.000 abstract 9
- 229910052760 oxygen Inorganic materials 0.000 abstract 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 8
- 229910052717 sulfur Inorganic materials 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical group 0.000 abstract 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract 6
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 2
- 241000238631 Hexapoda Species 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract 2
- 125000005879 dioxolanyl group Chemical group 0.000 abstract 2
- 235000019256 formaldehyde Nutrition 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- -1 pentahalotio Chemical group 0.000 abstract 2
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 abstract 1
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 abstract 1
- 125000006698 (C1-C3) dialkylamino group Chemical group 0.000 abstract 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy 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
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004741 (C1-C6) haloalkylsulfonyl 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
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000002636 imidazolinyl group Chemical group 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000005968 oxazolinyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 abstract 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group 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
- A01N43/02—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
- A01N43/02—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
- A01N43/32—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 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/16—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof the nitrogen atom being part of a heterocyclic ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
-
- 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
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- 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
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans 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 carbon atoms of the hetero ring
- C07D307/83—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D495/10—Spiro-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (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)
- Health & Medical Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Hydrogenated Pyridines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Furan Compounds (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
- Fertilizers (AREA)
Abstract
Compuesto de fórmula (1) y composiciones que comprenden una cantidad insecticidamente efectiva de al menos un segundo compuesto, con al menos un vehículo insecticidamente compatible; junto con los métodos para controlar los insectos que comprenden aplicar dichas composiciones a un lugar donde los insectos están presentes o se espera que estén presentes Reivindicación 1: Un compuesto de fórmula (1), donde -R y R4 están independientemente seleccionados desde el hidrógeno, halógeno, hidroxi, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-5, alquinilo C2-5, haloalquilo C1-3, alcoxi C1-3, haloalcoxi C1-3, alquiltio C1-3, haloalquiltio C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, ciano, nitro; amino opcionalmente substituido donde el substituyente opcional está seleccionado desde alquilo C1-4,alquilcarbonilo C1-3 y alcoxicarbonilo C1-3; imidazolilo opcionalmente substituido, imidazolinilo opcionalmente substituido, oxazolinilo opcionalmente substituido, oxazolilo opcionalmente substituido, oxadiazolilo opcionalmente substituido, tiazolilo opcionalmente substituido, pirazolilo opcionalmente substituido, triazolilo opcionalmente substituido, furanilo opcionalmente substituido, tetrahidrofuranilo opcionalmente substituido, dioxolanilo opcionalmente substituido, dioxanilo opcionalmente substituido, -C(=E)-G, y -C(R10)-Q-R11, donde E está seleccionada desde O, S, NR12, y NOR12, donde R12 es hidrógeno, alquilo C1-4, haloalquilo C1-4, arilo y arilalquilo C1- 4; G está seleccionada desde hidrógeno, alquilo C1-3, haloalquilo C1-3, alcoxi C1-3, alquilamino C1-3 y dialquilamino C1-3; J está seleccionada desde O, S, y NR12, donde R12 es como se describiera previamente; R10 y R11 están independientemente seleccionados desde el hidrógeno, alquilo C1-4 y haloalquilo C1-4, y R10 y R11 pueden ser tomados juntos con -K(CHR12)e-, donde e es un entero de 2 a 4; K está seleccionada desde O, S, y NR12, donde R12 es como se describiera previamente; -R1 y R3 están independientemente seleccionados desde el hidrógeno, halógeno y alquilo C1-3; -L está seleccionada desde CH2, O, S y NR16 donde R16 está seleccionada desde hidrógeno, alquilo C1-3, alcoxi C1-3 alquilo C1-3, arilalquilo C1-3, alquenilo C2-4 alquilo C1-3, haloalquenilo C2-4 alquilo C1-3, dialquilfosfonato C1-3, alquilcarbonilo C1-3, halo(C1- C3) alquilcarbonilo C1-3, alcoxi C1-3 alquilcarbonilo C1-3, arilcarbonilo y alquilsulfonilo C1-3; -M está seleccionada desde O, S, CH2O* y (CH2)f donde el asterisco denota adjunto a L, y f es un entero seleccionado desde 1, 2 y 3, siempre que L y M no sean simultaneamente O ó S; -R13 es hidrógeno; -R14 y R15 están independientemente seleccionados desde halógeno; -a es un entero seleccionado desde 0 o 1;y cuando a es 1,-A es O, CH2, OCH2, CH2O, OCH=CH, C(=O), S(O)g, -CH=CH-, -OC(=O)-, -OC(=O)NH-, -NHC(=O)-, -NHSO2-, y -N=CH-, NR16 o N(óxido)R16 donde R16 es tal como se describiera previamente, y g es un entero seleccionado desde 0, 1 o 2; -b es un entero seleccionado desde 0, 1, 2, 3 o 4; -R5 y R6 están independientemente seleccionados desde el hidrógeno, halógeno, alquilo C1-4, ciclo C3-6alquilo, haloalquilo C1-4, o arilo; -B es un grupo puente cíclico de la estructura (2), donde Q y T están independientemente seleccionados desde, -CRa-, -N-, y -N(óxido)-; y U es -(CRaRb)j-, donde Ra y Rb en Q, T y U están independientemente seleccionados desde el hidrógeno, hidroxi, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, alquilcarboniloxi, alquilsulfonilo C1-4 alquilfosfinato C1-4 y alquilfosfonato C1-4; y j es un entero seleccionado desde 1 o 2; -c es un entero seleccionado desde 0, 1, 2, 3 o 4 y cuando c es 1 o más, R7 y R8 están independientemente seleccionados desde el hidrógeno, alquilo C1-4, haloalquilo C1-4 o alcoxi C1-4 o arilo;d es un entero seleccionado desde 0 o 1; y cuando d es 1, D está seleccionada desde O, CH=CH, S(O)g, HC=N, C(=O), OC(=O), C(=O)O, C(=O)NH, NR16, N(óxido)R16 y NR16C(=O), donde R16 y g son tal como se describiera previamente; R9 esta seleccionado desde alquilo C1-8, haloalquilo C1-6, alquiltio C1-4, alcoxi C1-4, arilalquilo C1-3, arilalcoxi C1-3, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquilalquilo C4-10, alquilamino C1-3, di(alquil C1-3)amino, arilalquilamino C1-3, y fenilamino, donde el fenilo está opcionalmente substituido con uno o más de ciano, halógeno, alquilo C1-3, alcoxi C1-3, haloalquilo C1-3, haloalcoxi C1- 3alquilo C1-3-S(O)g, donde g está previamente descripto, pentahalotio, trialquil C1-3sililo, y NR16 donde R16 es como se definiera previamente; y la fórmula (3), donde h es un entero seleccionado desde 0 o 1; A1 está seleccionada desde N, C y C=; V, W, X, Y y Z están independientemente seleccionados desde O, S, N, N=, C, C= o C(=O); siempre que cuando V, W, X, Y y Z están seleccionados desde N, C o C=, entonces R17 hasta R21, inclusive, están independientemente seleccionados desde el hidrógeno, halógeno, alquilo C1-6, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-6, hidroxialquilo C1-6, cicloalquilo C3-6, haloalquenilo C2-4, haloalquinilo C2-4, alcoxi C1-6, alcoxi C1-6alquilo C1-6, alqueniloxi C2-4, alquiniloxi C2-4, haloalcoxi C1-6, haloalqueniloxi C2-4, haloalquiniloxi C2-4, alquiltio C1-6, pentahalotio, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, haloalquilsulfinilo C1-6, haloalquilsulfonilo C1-6, ciano, nitro, NRcRd, donde Rc y Rd están independientemente seleccionados desde el hidrógeno, alquilo C1-6, haloalquilo C1-6alcoxi C1-6, alquilcarbonilo C1-6, alcoxicarbonilo C1-6, y donde Rc y Rd pueden ser tomados juntos para formar un anillo de 5 o 6 miembros saturado o no saturado conteniendo carbono,, O, N o S; alquilcarbonilo C1-6, alquilcarboniloxi C1-6, alcoxicarbonilo C1-6, alcoxicarboniloxi C1-6, alcoxicarbonilo C1-6, alcoxicarboniloxi C1-6, alquilaminocarbonilo C1-6, alquilaminocarboniloxi C1-6, trialquilsililo C1-6, di(alquil C1-6)fosfinoil, arilo, ariloxi, y arilalcoxi;cuando h es 1; y A1, W y Y son C= y V, X y Z son CR17 y R18 o R18 y R19 pueden ser tomados juntos con -CR22=CR23CR24=CR25-, -OCR22R23CH2-, -CH2CR22R23O-, -OCR22R23O-, -OCR22R23CR24R25O-, - OCR22R23CH=CH-, -OCR22R23CH2CH2-, -OCR22=N-, -N=CR22O-, -ON=CR22-, -ONR22C(=O)-, -CH2-NR22C(=O)-, -C3H6-, -C2H4(C=O)-, -SCR22=N-, -OCR22R23C(=O)-, -CR22=CR23NR24-, -CR22=NNR23u-, -N=NNR22-, y -N=CR22N=N-, para formar un anillo fusionado, donde R22 hasta R25, inclusive, están independientemente seleccionados desde el hidrógeno, halógeno, alquilo C1-3, haloalquilo C1-3 y arilo; y las sales agrícolamente aceptables de las mismas.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US46667403P | 2003-04-30 | 2003-04-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR045678A1 true AR045678A1 (es) | 2005-11-09 |
Family
ID=33418411
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040101474A AR044138A1 (es) | 2003-04-30 | 2004-04-29 | Derivados plaguicidas de benzodioxol y benzodioxolano sustituidos con (dihalopropenilo) fenilalquilo |
| ARP040101471A AR045678A1 (es) | 2003-04-30 | 2004-04-29 | Derivados ciclicos fenil substituidos |
| ARP040101472A AR045679A1 (es) | 2003-04-30 | 2004-04-29 | Derivados insecticidas de dihidrobenzopiran y dihidrobenzofuran sustituidos con (dihalopropenil)fenilalquilo |
| ARP040101473A AR044137A1 (es) | 2003-04-30 | 2004-04-29 | Derivados plaguicidas de benzotiazol y benzoxazol sustituidos con (dihalopropenil) fenilalquilo |
Family Applications Before (1)
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| ARP040101474A AR044138A1 (es) | 2003-04-30 | 2004-04-29 | Derivados plaguicidas de benzodioxol y benzodioxolano sustituidos con (dihalopropenilo) fenilalquilo |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040101472A AR045679A1 (es) | 2003-04-30 | 2004-04-29 | Derivados insecticidas de dihidrobenzopiran y dihidrobenzofuran sustituidos con (dihalopropenil)fenilalquilo |
| ARP040101473A AR044137A1 (es) | 2003-04-30 | 2004-04-29 | Derivados plaguicidas de benzotiazol y benzoxazol sustituidos con (dihalopropenil) fenilalquilo |
Country Status (16)
| Country | Link |
|---|---|
| US (5) | US6987194B2 (es) |
| EP (4) | EP1620401A4 (es) |
| JP (4) | JP2006525335A (es) |
| KR (4) | KR20060006065A (es) |
| CN (4) | CN1780818A (es) |
| AR (4) | AR044138A1 (es) |
| AT (2) | ATE434612T1 (es) |
| AU (4) | AU2004237745A1 (es) |
| BR (4) | BRPI0409685A (es) |
| CA (4) | CA2523085A1 (es) |
| DE (2) | DE602004021689D1 (es) |
| MX (4) | MXPA05011336A (es) |
| TW (4) | TW200512203A (es) |
| UA (1) | UA82875C2 (es) |
| WO (4) | WO2004099145A2 (es) |
| ZA (4) | ZA200508621B (es) |
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| EP1863783A4 (en) * | 2005-03-23 | 2008-06-18 | Bayer Cropscience Ag | IMPROVED PROCESS FOR THE PREPARATION OF INSECTICIDAL PHENYL ALKYL SUBSTITUTED DIHYDROBENZOFURANES |
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- 2004-04-29 AR ARP040101474A patent/AR044138A1/es not_active Application Discontinuation
- 2004-04-29 AR ARP040101471A patent/AR045678A1/es not_active Application Discontinuation
- 2004-04-29 AR ARP040101472A patent/AR045679A1/es not_active Application Discontinuation
- 2004-04-29 TW TW093112060A patent/TW200509793A/zh unknown
- 2004-04-29 TW TW093112058A patent/TW200508198A/zh unknown
- 2004-04-29 AR ARP040101473A patent/AR044137A1/es not_active Application Discontinuation
-
2005
- 2005-10-24 ZA ZA200508621A patent/ZA200508621B/en unknown
- 2005-10-24 ZA ZA200508619A patent/ZA200508619B/en unknown
- 2005-10-24 ZA ZA200508622A patent/ZA200508622B/en unknown
- 2005-10-24 ZA ZA200508624A patent/ZA200508624B/en unknown
- 2005-12-01 US US11/292,023 patent/US7576224B2/en not_active Expired - Lifetime
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