AR059035A1 - Insecticidas derivados de antranilamida - Google Patents
Insecticidas derivados de antranilamidaInfo
- Publication number
- AR059035A1 AR059035A1 ARP070100150A ARP070100150A AR059035A1 AR 059035 A1 AR059035 A1 AR 059035A1 AR P070100150 A ARP070100150 A AR P070100150A AR P070100150 A ARP070100150 A AR P070100150A AR 059035 A1 AR059035 A1 AR 059035A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- alkoxy
- cycloalkyl
- haloalkoxy
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 30
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 25
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 19
- 125000000217 alkyl group Chemical group 0.000 abstract 13
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 12
- 150000002367 halogens Chemical class 0.000 abstract 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract 10
- 150000002431 hydrogen Chemical class 0.000 abstract 10
- 239000001257 hydrogen Substances 0.000 abstract 10
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 9
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 9
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 8
- 125000004414 alkyl thio group Chemical group 0.000 abstract 8
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 7
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 7
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 7
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 7
- -1 nitro, hydroxy Chemical group 0.000 abstract 7
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 6
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 6
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 abstract 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 5
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- 239000011593 sulfur Substances 0.000 abstract 5
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 abstract 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 abstract 4
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 4
- 125000003282 alkyl amino group Chemical group 0.000 abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 4
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 3
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000005202 dialkylaminocarbonyloxy group Chemical group 0.000 abstract 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 abstract 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 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
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl 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
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 229910003870 O—Li Inorganic materials 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings 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
- C07D223/12—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D331/00—Heterocyclic compounds containing rings of less than five members, having one sulfur atom as the only ring hetero atom
- C07D331/04—Four-membered rings
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- 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
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- 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
- C07D405/14—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 three or more hetero rings
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- 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
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- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65681—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a (thio)phosphinic acid or ester thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Reivindicacion 1: Un compuesto de formula (1), donde D es fenilo, 2-piridilo, 3-piridilo o 4-piridilo; o fenilo, 2-piridilo, 3-piridilo o 4-piridilo mono-, di- o trisubstituido con alquilo C1-6, cicloalquilo C3-6, haloalquilo C1-6, halogeno, ciano, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, haloalquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalquilsulfinilo C1-4 o haloalquilsulfonilo C1-4; o D es un radical seleccionado del grupo de formulas (2); R4, R4', R10, R17 y R19 independientemente entre sí, son hidrogeno, alquilo C1-6, cicloalquilo C3-6, haloalquilo C1-6, halogeno, ciano, alcoxi C1-4, haloalcoxi C1-4, alcoxicarbonilo C2-4, alquiltio C1-4, haloalquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalquilsulfinilo C1-4 o haloalquilsulfonilo C1-4; R5, R6, R8, R11, R12, R15. R16 y R18 independientemente entre sí, son alquilo C1-6, o alquilo C1-6 mono-, di- o trisubstituido con halogeno, ciano, nitro, hidroxi, alcoxi C1-4, alcoxicarbonilo C2- 4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, alquilamino C1-4, dialquilamino C2-4 o cicloalquilamino C3-6; o son fenilo, 2-piridilo, 3-piridilo, 4-piridilo; o son fenilo, 2-piridilo, 3-piridilo o 4-piridilo mono-, di- o trisubstituido con alquilo C1-6, cicloalquilo C3-6, haloalquilo C1-6, halogeno, ciano, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, haloalquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalquilsulfinilo C1-4 o haloalquilsulfonilo C1-4; R7, R9, R13 y R14 independientemente entre sí, son hidrogeno, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquenilo C3-6 o haloalquenilo ; cada R1 es independientemente halogeno, nitro, ciano, hidroxi, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, halocicloalquilo C3-6, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, haloalquiltio C1-4, haloalquilsulfinilo C1-4, haloalquilsulfonilo C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, alquilamino C1-4, dialquilamino C2-4, cicloalquilamino C3-6, alquil C1-6-cicloalquilamino C3-6, alquilcarbonilo C2-4, alcoxicarbonilo C2-6, alquilaminocarbonilo C2-6, dialquilaminocarbonilo C3-6, alcoxicarboniloxi C2-6, dialquilaminocarboniloxi C2-6 o trialquilsililo C3-6, fenilo, bencilo o fenoxi, o fenilo, bencilo o fenoxi mono-, di- o trisubstituido con halogeno, ciano, nitro, halogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, halocicloalquilo C3-6, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, haloalquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, alquilamino C1-4, dialquilamino C2-4, cicloalquilamino C3-6, alquil C1-6-cicloalquilamino C3-6, alquilcarbonilo C2-4, alcoxicarbonilo C2-6, alquilaminocarbonilo C2-6, dialquilaminocarbonilo C3-6, alcoxicarboniloxi C2-6, alquilaminocarboniloxi C2-6, dialquilaminocarboniloxi C3-6 o trialquilsililo C3-6; n es 0, 1, 2 o 3; cada uno de R2 y R3, los cuales pueden ser iguales o diferentes, representa hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o cicloalquilo C3-8; o alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o cicloalquilo C3-8 substituido con uno o más substituyentes seleccionados entre halogeno nitro, ciano, hidroxi, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, haloalquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, alquilamino C1-4, dialquilamino C2-4, cicloalquilamino C3-6 y alquil C1-6-cicloalquilamino C3-6; cada uno de E1 y E2, los cuales pueden ser iguales o diferentes, representa oxígeno o azufre; A es oxígeno, azufre, SO, SO2, S(O)p=N-R, C=N-OR36, N-R0, C=O o P(X)t-R33; R33 es hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo , haloalquilo C1-6, alcoxi C1-6, hidroxi, cicloalquilo C3-6, cicloalquil C3-6-alquilo C1-6, bencilo o fenilo; donde fenilo y bencilo por su parte pueden ser mono- di- o trisubstituidos con alquilo C1-6, haloalquilo C1-6, halogeno, ciano o nitro; o R33 es O-Na+, O-Li+ o O-K+; R36 es hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, alcoxi C1-6-alquilo C1-6, haloalcoxi C1- 6-alquilo C1-6 o bencilo; X es oxígeno o azufre; p es 0 o 1 ; t es 0 o 1; cada uno de R34 y R35, los cuales pueden ser iguales o diferentes, representa hidrogeno, COOH, halogeno, nitro, ciano, hidroxi, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquenilo C2-6, haloalquinilo C2-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, haloalquilsulfinilo C1-6, haloalquilsulfonilo C1-6, alcoxicarbonilo C1-6, alquilcarbonilo C1-6, alquilaminocarbonilo C3-6, dialquilaminocarbonilo C3-6, alcoxi C1-6-alquilo C1-6, haloalcoxi C1-6-alquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquilamino C1-6, dialquilamino C2-6, trialquilsililo C3-8, bencilo o fenilo; donde fenilo y bencilo por su parte pueden ser mono- di- o trisubstituido con alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, halogeno, ciano, hidroxilo o nitro; m es 0, 1, 2, 3 o 4; R es hidrogeno, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquiltio C1-6, haloalquiltio C1-6, alcoxi C1-6-alquilo C1-6 o haloalcoxi C1-6-alquilo C1-6; o R es alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquiltio C1-6, haloalquiltio C1-6, alcoxi C1-6- alquilo C1-6 o haloalcoxi C1-6-alquilo C1-6 substituido con alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alcoxi C1-6, o haloalcoxi C1-6; o R es ciano, nitro, -C(O)R26, -C(O)OR27, -CONR28R29, -SO2R30 o -P(O)(OR31)(OR32); R0 es hidrogeno, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquiltio C1-6, haloalquiltio C1-6, alcoxi C1-6-alquilo C1-6 o haloalcoxi C1-6-alquilo C1-6; o R0 es alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquiltio C1-6, haloalquiltio C1-6, alcoxi C1-6-alquilo C1-6 o haloalcoxi C1-6-alquilo C1-6 substituido con alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alcoxi C1-6, o haloalcoxi C1-6; o R0 es ciano, nitro, -C(O)R026, -C(O)OR027, -CONR028R029, -SO2R030 o -P(O)(OR031)(OR032); o R0 es fenilo o bencilo, o fenilo o bencilo mono-, di- o trisubstituido con substituyentes seleccionados entre alquilo C1-6, cicloalquilo C3-6, haloalquilo C1-6, halogeno, ciano, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, haloalquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalquilsulfinilo C1-4 y haloalquilsulfonilo C1-4; cada uno de R26 y R026. los cuales pueden ser iguales o diferentes, representa hidrogeno, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquiltio C1-6, haloalquiltio C1-6, alcoxicarbonilo C1-6, alquilcarbonilo C1-6 o alcoxi C1-6-alquilo C1-6; o alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquiltio C1-6, haloalquiltio C1-6, alcoxicarbonilo C1-6, alquilcarbonilo C1-6 o alcoxi C1-6-alquilo C1-6 substituido con alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alcoxi C1-6, o haloalcoxi C1-6; cada uno de R27, R28, R29, R30, R31, R32, R027, R028, R029, R030, R031 y R032 los cuales pueden ser iguales o diferentes, representa alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6 o halocicloalquilo C3-6; o alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6 o halocicloalquilo C3-6 substituido con alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, halocicloalquilo C3-6, alcoxi C1-6 o haloalcoxi C1-6; con la condicion de que E1 o E2 sea azufre si A es oxígeno, azufre o N-R0, donde R0 es hidrogeno, alquilo C1-3, haloalquilo C1-3, alquilcarbonilo C2-4, haloalquilcarbonilo C2-4, alcoxicarbonilo C2-4 o alquilsulfonilo C1-3; y las sales, isomeros, diasteromeros, enantiomeros, tautomeros, N-oxidos aceptables para agronomía de esos compuestos.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06000826 | 2006-01-16 | ||
| EP06002803 | 2006-02-13 |
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| US (2) | US8084474B2 (es) |
| EP (2) | EP1976385A2 (es) |
| JP (1) | JP5215190B2 (es) |
| KR (1) | KR101342875B1 (es) |
| AR (1) | AR059035A1 (es) |
| AU (1) | AU2007204417B2 (es) |
| BR (1) | BRPI0707882A2 (es) |
| CA (1) | CA2635827C (es) |
| ES (1) | ES2430419T3 (es) |
| IL (2) | IL192470A (es) |
| NZ (1) | NZ569504A (es) |
| TW (1) | TWI389898B (es) |
| UY (1) | UY30090A1 (es) |
| WO (1) | WO2007080131A2 (es) |
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| GB0717189D0 (en) * | 2007-09-04 | 2007-10-17 | Syngenta Participations Ag | Novel processes and compounds |
| TWI411395B (zh) | 2007-12-24 | 2013-10-11 | Syngenta Participations Ag | 殺蟲化合物 |
| JP5468275B2 (ja) * | 2008-03-13 | 2014-04-09 | 石原産業株式会社 | 有害生物防除用組成物 |
| WO2010020522A1 (en) * | 2008-08-22 | 2010-02-25 | Syngenta Participations Ag | Insecticidal compounds |
| US8822502B2 (en) * | 2008-08-22 | 2014-09-02 | Syngenta Crop Protection Llc | Insecticidal compounds |
| MX2011002072A (es) * | 2008-09-04 | 2011-03-29 | Syngenta Participations Ag | Compuestos insecticidas. |
| BRPI1007878A2 (pt) * | 2009-01-29 | 2015-09-01 | Syngenta Participations Ag | "compostos inseticidas" |
| ES2502340T3 (es) | 2009-06-22 | 2014-10-03 | Syngenta Participations Ag | Compuestos insecticidas |
| TW201211057A (en) | 2010-06-11 | 2012-03-16 | Syngenta Participations Ag | Process for the preparation of dihydropyrrole derivatives |
| US8957058B2 (en) | 2010-10-05 | 2015-02-17 | Syngenta Participations Ag | Insecticidal pyrrolidin-yl-aryl-carboxamides |
| KR20140051835A (ko) | 2011-02-09 | 2014-05-02 | 신젠타 파티서페이션즈 아게 | 살곤충 화합물 |
| EP2688864A1 (en) | 2011-03-22 | 2014-01-29 | Syngenta Participations AG | Insecticidal compounds |
| WO2012175474A1 (en) | 2011-06-20 | 2012-12-27 | Syngenta Participations Ag | 1,2,3 triazole pesticides |
| JP6080846B2 (ja) * | 2011-07-08 | 2017-02-15 | シンジェンタ パーティシペーションズ アーゲー | チエタンアミンの製造方法 |
| WO2013026933A1 (en) | 2011-08-25 | 2013-02-28 | Syngenta Participations Ag | Isoxazoline derivatives as insecticidal compounds |
| WO2013026695A1 (en) | 2011-08-25 | 2013-02-28 | Syngenta Participations Ag | Isoxazoline derivatives as insecticidal compounds |
| AU2012298448A1 (en) | 2011-08-25 | 2014-03-06 | Syngenta Participations Ag | Isoxazoline derivatives as insecticidal compounds |
| WO2013026929A1 (en) | 2011-08-25 | 2013-02-28 | Syngenta Participations Ag | Dihydropyrrole derivatives as insecticidal compounds |
| EP2748157B1 (de) * | 2011-08-26 | 2015-10-07 | Bayer Intellectual Property GmbH | Verfahren zur herstellung von tetrazol-substituierten anthranilsäurediamid-derivaten durch umsetzung von benzoxazinonen mit aminen |
| BR122018069466B1 (pt) | 2011-09-13 | 2019-04-02 | Syngenta Participations Ag | Derivados isotiazolina como compostos inseticidas |
| AU2013265512A1 (en) * | 2012-05-24 | 2014-12-18 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
| WO2014128136A1 (en) * | 2013-02-20 | 2014-08-28 | Basf Se | Anthranilamide compounds and their use as pesticides |
| CN105189483B (zh) | 2013-03-06 | 2018-10-30 | 拜耳作物科学股份公司 | 作为农药的烷氧亚氨基取代的邻氨基苯甲酸二酰胺 |
| EP2873668A1 (en) | 2013-11-13 | 2015-05-20 | Syngenta Participations AG. | Pesticidally active bicyclic heterocycles with sulphur containing substituents |
| JPWO2016175017A1 (ja) * | 2015-04-28 | 2018-02-22 | アグロカネショウ株式会社 | 新規な4−ピリジンカルボキサマイド誘導体及びこれを有効成分として含む農園芸用薬剤 |
| CN109069475B (zh) | 2016-04-22 | 2022-01-28 | 受体控股公司 | 快速作用植物类医药化合物和营养补剂 |
| EA201892396A1 (ru) | 2016-12-02 | 2019-04-30 | Ресептор Лайф Сайенсиз, Инк. | Быстродействующие растительные лекарственные соединения и биологически активные добавки |
| JP7536656B2 (ja) | 2018-06-06 | 2024-08-20 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | スルホキシイミン含有置換基を有する殺有害生物的に活性な複素環式誘導体 |
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| WO2002015701A2 (en) | 2000-08-25 | 2002-02-28 | Syngenta Participations Ag | Bacillus thuringiensis crystal protein hybrids |
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| AU2002345250A1 (en) | 2001-06-22 | 2003-01-08 | Syngenta Participations Ag | Plant disease resistance genes |
| MY142967A (en) * | 2001-08-13 | 2011-01-31 | Du Pont | Method for controlling particular insect pests by applying anthranilamide compounds |
| ATE417829T1 (de) | 2001-08-16 | 2009-01-15 | Du Pont | Substituierte anthranilamide und ihre verwendung als pesticide |
| US7230167B2 (en) | 2001-08-31 | 2007-06-12 | Syngenta Participations Ag | Modified Cry3A toxins and nucleic acid sequences coding therefor |
| WO2003052073A2 (en) | 2001-12-17 | 2003-06-26 | Syngenta Participations Ag | Novel corn event |
| BR0308230B1 (pt) | 2002-03-05 | 2014-05-20 | Syngenta Participations Ag | O-ciclopropil-carboxanilida, composição e método de controle ou prevenção de infestação de plantas cultivadas por microorganismos fitopatogênicos |
| US7211270B2 (en) | 2002-10-04 | 2007-05-01 | E. I. Du Pont De Nemours And Company | Anthranilamide insecticides |
| GB0224316D0 (en) | 2002-10-18 | 2002-11-27 | Syngenta Participations Ag | Chemical compounds |
| GB0230155D0 (en) | 2002-12-24 | 2003-02-05 | Syngenta Participations Ag | Chemical compounds |
| IN243219B (es) | 2003-01-28 | 2010-10-01 | Du Pont | |
| KR20060008336A (ko) | 2003-06-12 | 2006-01-26 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 융합된 옥사지논 제조 방법 |
| AU2005306363B2 (en) | 2004-11-18 | 2012-08-09 | E. I. Du Pont De Nemours And Company | Anthranilamide insecticides |
| GB0427008D0 (en) | 2004-12-09 | 2005-01-12 | Syngenta Participations Ag | Novel insecticides |
| EP1871760B1 (en) * | 2005-04-20 | 2010-08-11 | Syngenta Participations AG | Cyano anthranilamide insecticides |
| TW201345908A (zh) * | 2006-07-05 | 2013-11-16 | Mitsubishi Tanabe Pharma Corp | 吡唑并〔1,5-a〕嘧啶化合物 |
-
2007
- 2007-01-12 UY UY30090A patent/UY30090A1/es not_active Application Discontinuation
- 2007-01-12 AR ARP070100150A patent/AR059035A1/es unknown
- 2007-01-15 AU AU2007204417A patent/AU2007204417B2/en not_active Ceased
- 2007-01-15 TW TW096101442A patent/TWI389898B/zh not_active IP Right Cessation
- 2007-01-15 ES ES10160989T patent/ES2430419T3/es active Active
- 2007-01-15 NZ NZ569504A patent/NZ569504A/en not_active IP Right Cessation
- 2007-01-15 EP EP07711342A patent/EP1976385A2/en not_active Withdrawn
- 2007-01-15 JP JP2008549849A patent/JP5215190B2/ja not_active Expired - Fee Related
- 2007-01-15 BR BRPI0707882-0A patent/BRPI0707882A2/pt not_active Application Discontinuation
- 2007-01-15 CA CA2635827A patent/CA2635827C/en not_active Expired - Fee Related
- 2007-01-15 WO PCT/EP2007/000302 patent/WO2007080131A2/en not_active Ceased
- 2007-01-15 EP EP10160989.9A patent/EP2213167B1/en not_active Not-in-force
- 2007-01-15 US US12/160,794 patent/US8084474B2/en not_active Expired - Fee Related
-
2008
- 2008-06-26 IL IL192470A patent/IL192470A/en not_active IP Right Cessation
- 2008-08-14 KR KR1020087020082A patent/KR101342875B1/ko not_active Expired - Fee Related
-
2011
- 2011-12-08 US US13/314,564 patent/US8278464B2/en not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| WO2007080131A2 (en) | 2007-07-19 |
| BRPI0707882A2 (pt) | 2011-05-10 |
| CA2635827C (en) | 2014-04-08 |
| EP2213167B1 (en) | 2013-07-31 |
| TWI389898B (zh) | 2013-03-21 |
| CA2635827A1 (en) | 2007-07-19 |
| EP1976385A2 (en) | 2008-10-08 |
| IL219104A0 (en) | 2012-05-31 |
| WO2007080131A3 (en) | 2008-03-20 |
| AU2007204417B2 (en) | 2012-02-02 |
| US20120077991A1 (en) | 2012-03-29 |
| NZ569504A (en) | 2010-07-30 |
| KR20080099268A (ko) | 2008-11-12 |
| KR101342875B1 (ko) | 2013-12-20 |
| US20100168066A1 (en) | 2010-07-01 |
| IL219104A (en) | 2013-11-28 |
| JP2009523715A (ja) | 2009-06-25 |
| UY30090A1 (es) | 2007-08-31 |
| AU2007204417A1 (en) | 2007-07-19 |
| ES2430419T3 (es) | 2013-11-20 |
| JP5215190B2 (ja) | 2013-06-19 |
| IL192470A (en) | 2013-12-31 |
| IL192470A0 (en) | 2009-08-03 |
| US8084474B2 (en) | 2011-12-27 |
| EP2213167A1 (en) | 2010-08-04 |
| TW200800939A (en) | 2008-01-01 |
| US8278464B2 (en) | 2012-10-02 |
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