WO2007024833A1 - Anthranilamides for controlling invertebrate pests - Google Patents

Anthranilamides for controlling invertebrate pests Download PDF

Info

Publication number
WO2007024833A1
WO2007024833A1 PCT/US2006/032726 US2006032726W WO2007024833A1 WO 2007024833 A1 WO2007024833 A1 WO 2007024833A1 US 2006032726 W US2006032726 W US 2006032726W WO 2007024833 A1 WO2007024833 A1 WO 2007024833A1
Authority
WO
WIPO (PCT)
Prior art keywords
compound
halogen
alkyl
chloro
invertebrate pest
Prior art date
Application number
PCT/US2006/032726
Other languages
French (fr)
Other versions
WO2007024833B1 (en
Inventor
Bruce Lawrence Finkelstein
Stephen Frederick Mccann
Original Assignee
E. I. Du Pont De Nemours And Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by E. I. Du Pont De Nemours And Company filed Critical E. I. Du Pont De Nemours And Company
Priority to AU2006283181A priority Critical patent/AU2006283181A1/en
Priority to US11/989,348 priority patent/US8012499B2/en
Priority to JP2008528057A priority patent/JP5039703B2/en
Priority to EP06802052A priority patent/EP1924575A1/en
Priority to BRPI0617046-3A priority patent/BRPI0617046A2/en
Priority to MX2008002236A priority patent/MX2008002236A/en
Publication of WO2007024833A1 publication Critical patent/WO2007024833A1/en
Publication of WO2007024833B1 publication Critical patent/WO2007024833B1/en

Links

Classifications

    • 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
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with 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
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • 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
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Definitions

  • This invention relates to certain anthranilamides, their N-oxides, salts and compositions suitable for agronomic and nonagronomic uses, and methods of their use for controlling invertebrate pests such as arthropods in both agronomic and nonagronomic environments.
  • invertebrate pests The control of invertebrate pests is extremely important in achieving high crop efficiency. Damage by invertebrate pests to growing and stored agronomic crops can cause significant reduction in productivity and thereby result in increased costs to the consumer.
  • invertebrate pests in forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, turf, wood products, and public and animal health is also important. Many products are commercially available for these purposes, but the need continues for new compounds which are more effective, less costly, less toxic, environmentally safer or have different modes of action.
  • WO 03/015519 discloses N-acyl anthranilic acid derivatives of Formula i as anthropodicides
  • R 1 is CH 3 , F, Cl or Br
  • R 2 is F, Cl, Br, I or CF 3
  • R 3 is CF 3 , Cl, Br or OCH 2 CF 3
  • R 4a is C 1 -C 4 alkyl
  • R 4b is H or CH 3
  • R5 is Cl or Br.
  • This invention is directed to compounds of Formula 1 including all geometric isomers and stereoisomers, iV-oxides, and salts thereof, agricultural and nonagricultural compositions containing them and their use for controlling invertebrate pests:
  • X is O or S
  • J is a phenyl optionally substituted with one to four substituents independently selected from R 5 ; or J is a heterocyclic ring selected from the group consisting of
  • R 1 is C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, C 2 -C 6 haloalkenyl, C 2 -C 6 haloalkynyl, C 3 -C 6 halocycloalkyl, halogen, -CN, -CHO, -NO 2 , C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 1 -C 4 haloalkylthio, C 1 -C 4 haloalkylsulfinyl, C 1 -C 4 haloalkylsulfonyl, C 2 -C 4 alkylcarbon
  • R 2 is H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 6 cycloalkyl, C 1 -C - 0 6 haloalkyl, C 2 -C 6 haloalkenyl, C 2 -C 6 haloalkynyl, C 3 -C 6 halocycloalkyl, halogen, -CN, -CHO, -NO 2 , C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 1 -C 4 haloalkylthio, C 1 -C 4 haloalkylsulfinyl, C 1 -C 4 haloalkylsulfonyl, C 2 -
  • R 4 is H; or C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl or C 3 -C 6 cycloalkyl, each optionally substituted with one or more substituents selected from the group consisting of halogen, -CN, -NO 2 , hydroxy, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 2 -C 4 alkoxycarbonyl, C 1 -C 4 alkylamino, C 2 -Cg dialkylamino and C 3 -C 6 cycloalkylamino; or
  • R 4 is C 2 -C 6 alkylcarbonyl, C 2 -C 6 alkoxycarbonyl, C 2 -C 6 alkylaminocarbonyl or
  • each R 5 is independently C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, halogen, -CN, C 1 -C 4 alkoxy, C 1 -C 4 alkylthio, C 1 -C 4 haloalkoxy, C 1 -C 4 haloalkylthio, C 1 -C 4 haloalkylsulfinyl or C 1 -C 4 haloalkylsulfonyl; or phenyl or pyridyl, each optionally substituted with one to three R 9 ;
  • R 6 is H, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, halogen, -CN, C 1 -C 4 alkoxy, C 2 -C 4 alkoxycarbonyl, C 1 -C 4 alkylthio, C 1 -C 4 haloalkoxy, C 1 -C 4 haloalkylthio, C 1 -C 4 haloalkylsulfinyl or C 1 -C 4 haloalkylsulfonyl;
  • R 7 is C 1 -C 6 alkyl optionally substituted with one or more substituents selected from the group consisting of halogen, -CN, -NO 2 , hydroxy, C 1 -C 4 alkoxy, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C
  • R 7 is phenyl or pyridyl, each optionally substituted with one to three substituents selected from R 9 ;
  • R 8 is H, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 6 alkenyl, C 3 -C 6 haloalkenyl, C 3 -C 6 alkynyl or C 3 -C 6 haloalkynyl; each R 9 is independently C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, halogen, -CN, C 1 -C 4 alkoxy, C 1 -C 4 alkylthio, C 1 -C 4 haloalkoxy, C 1 -C 4 haloalkylthio, C 1 -C 4 haloalkylsulfinyl or C 1 -C 4 haloalkylsulfonyl;
  • R 11 and R 12 are independently H; halogen; -CN; OR 13 ; or C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl or C 3 -C 6 cycloalkyl, each optionally substituted with one or more halogen;
  • B is O, NR 13 , NOR 13 or NNR 14 R 15 ;
  • L is OH or NR 14 R 15 ;
  • R 13 is H; or C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl or C 3 -C 6 cycloalkyl, each optionally substituted with one or more halogen;
  • R 14 and R 15 are independently H; G; or C 1 -C 6 alkyl, C 2 -C 6 alkenyl or C 2 -C 6 alkynyl, each optionally substituted with one or more substituents selected from the group consisting of G, halogen, -CN, -NO 2 , hydroxy, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 2 -C 4 alkylcarbonyl, C 2 -C 4 alkoxycarbonyl, C 1 -C 4 alkylamino
  • R 14 and R 15 are taken together with the nitrogen to which they are attached to form a ring containing 2 to 6 atoms of carbon and optionally one additional atom of nitrogen, sulfur or oxygen, said ring 1 optionally substituted with 1 to 4 substituents selected from the group consisting of C 1 -C 2 alkyl, halogen, -CN,
  • This invention also provides a composition comprising a compound of Formula 1 and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent.
  • this invention also provides a composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula 1 and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent.
  • This invention further provides a spray composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula 1 or the composition described in the embodiment above and a propellant.
  • This invention also provides a bait composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula 1 or the composition described in the embodiment above, one or more food materials, optionally an attractant, and optionally a humectant.
  • This invention further provides a trap device for controlling an invertebrate pest comprising said bait composition and a housing adapted to receive said bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to said bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
  • This invention also provides a method for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of Formula 1 (e.g., as a composition described herein).
  • a biologically effective amount of a compound of Formula 1 e.g., as a composition described herein.
  • This invention also relates to such method wherein the invertebrate pest or its environment is contacted with a composition comprising a biologically effective amount of a compound of Formula 1 and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent.
  • compositions comprising, “comprising,” “includes,” “including,” “has,” “having,” “contains” or “containing,” or any other variation thereof, are intended to cover a non-exclusive inclusion.
  • a composition, a mixture, process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, mixture, process, method, article, or apparatus.
  • “or” refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).
  • compositions of the present invention comprises a biologically effective amount of "a" compound of Formula 1 which should be read that the composition includes one or at least one compound of Formula 1.
  • alkyl used either alone or in compound words such as “alkylthio” or “haloalkyl” includes straight-chain or branched alkyl, such as, methyl, ethyl, H-propyl, /-propyl, or the different butyl, pentyl or hexyl isomers.
  • 1-2 alkyl indicates that one or two of the available positions for that substituent may be alkyl which are independently selected.
  • Alkenyl includes straight-chain or branched alkenes such as ethenyl, 1-propenyl, 2-propenyl, and the different butenyl, pentenyl and hexenyl isomers.
  • Alkenyl also includes polyenes such as 1,2-propadienyl and 2,4-hexadienyl.
  • Alkynyl includes straight-chain or branched alkynes such as ethynyl, 1-propynyl, 2-propynyl and the different butynyl, pentynyl and hexynyl isomers.
  • Alkynyl can also include moieties comprised of multiple triple bonds such as 2,5-hexadiynyl.
  • Cycloalkyl includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
  • Alkoxy includes, for example, methoxy, ethoxy, n-propyloxy, isopropyloxy and the different butoxy, pentoxy and hexyloxy isomers.
  • Alkylthio includes branched or straight-chain alkylthio moieties such as methylthio, ethylthio, and the different propylthio and butylthio isomers.
  • Alkylsulfinyl includes both enantiomers of an alkylsulfinyl group.
  • alkylsulfinyl examples include CH 3 S(O), CH 3 CH 2 S(O), CH 3 CH 2 CH 2 S(O), (CH 3 ) 2 CHS(O) and the different butylsulfinyl isomers.
  • alkylsulfonyl examples include CH 3 S(O) 2 , CH 3 CH 2 S(O) 2 , CH 3 CH 2 CH 2 S(O) 2 , (CH 3 ) 2 CHS(O) 2 and the different butylsulfonyl isomers.
  • Alkylamino dialkylamino
  • cycloalkylamino and the like, are defined analogously to the above examples.
  • halogen either alone or in compound words such as “haloalkyl”, includes fluorine, chlorine, bromine or iodine.
  • 1-2 halogen indicates that one or two of the available positions for that substituent may be halogen which are independently selected. Further, when used in compound words such as “haloalkyl”, said alkyl may be partially or fully substituted with halogen atoms which may be the same or different. Examples of “haloalkyl” include F 3 C, ClCH 2 , CF 3 CH 2 and CF 3 CCl 2 .
  • haloalkynyl examples include HC ⁇ CCHCl, CF 3 C ⁇ C, CC1 3 C ⁇ C and FCH 2 C ⁇ CCH 2 .
  • haloalkoxy examples include CF 3 O, CCl 3 CH 2 O, HCF 2 CH 2 CH 2 O and CF 3 CH 2 O.
  • haloalkylthio examples include CCl 3 S, CF 3 S, CCl 3 CH 2 S and ClCH 2 CH 2 CH 2 S.
  • haloalkylsulfinyl examples include CF 3 S(O), CCl 3 S(O), CF 3 CH 2 S(O) and CF 3 CF 2 S(O).
  • haloalkylsulfonyl examples include CF 3 S(O) 2 , CCl 3 S(O) 2 , CF 3 CH 2 S(O) 2 and CF 3 CF 2 S(O) 2 .
  • (CH 3 ) 2 CHNHC( O)- and the different butylamino- or pentylaminocarbonyl isomers.
  • the total number of carbon atoms in a substituent group is indicated by the "Cj-C j " prefix where i and j are numbers from 1 to 8.
  • C1-C4 alkylsulfonyl designates methylsulfonyl through butylsulfonyl.
  • nonaromatic carbocyclic ring denotes fully saturated carbocyclic rings as well as partially or fully unsaturated carbocyclic rings where the H ⁇ ckel rule is not satisfied.
  • nonaromatic heterocyclic ring denotes fully saturated heterocyclic rings as well as partially or fully unsaturated heterocyclic rings where the H ⁇ ckel rule is not satisfied.
  • the heterocyclic ring systems can be attached through any available carbon or nitrogen by replacement of a hydrogen on said carbon or nitrogen.
  • optionally substituted in connection with aromatic ring groups refers to groups that are unsubstituted or have at least one non-hydrogen substituent. Commonly, the number of optional substituents (when present) ranges from one to four. In the above recitations, when a compound of Formula 1 is comprised of one or more heterocyclic rings, all substituents are attached to these rings through any available carbon or nitrogen by replacement of a hydrogen on said carbon or nitrogen.
  • pyridinyl and pyridyl are equivalent alternative names for an organic radical formed by removing a hydrogen atom from a pyridine ring to form an attachment point; accordingly "pyridinyl” and “pyridyl” are used herein as synonyms.
  • Compounds of this invention can exist as one or more stereoisomers.
  • the various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers.
  • one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or to selectively prepare said stereoisomers.
  • the compounds of the invention may be present as a mixture of stereoisomers, individual stereoisomers, or as an optically active form.
  • nitrogen-containing heterocycles can form N-oxides since the nitrogen requires an available lone pair for oxidation to the oxide; one skilled in the art will recognize those nitrogen-containing heterocycles which can form N-oxides.
  • nitrogen-containing heterocycles which can form N-oxides.
  • tertiary amines can form N-oxides.
  • N-oxides of heterocycles and tertiary amines are very well known by one skilled in the art including the oxidation of heterocycles and tertiary amines with peroxy acids such as peracetic and m-chloroperbenzoic acid (MCPBA), hydrogen peroxide, alkyl hydroperoxides such as t-butyl hydroperoxide, sodium perborate, and dioxiranes such as dimethyldioxirane.
  • MCPBA peroxy acids
  • alkyl hydroperoxides such as t-butyl hydroperoxide
  • sodium perborate sodium perborate
  • dioxiranes such as dimethyldioxirane
  • the salts of the compounds of the invention include acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids.
  • inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids.
  • the salts of the compounds of the invention also include those formed with organic bases (e.g., pyridine, ammonia, or triethylamine) or inorganic bases (e.g., hydrides, hydroxides, or carbonates of sodium, potassium, lithium, calcium, magnesium or barium) when the compound contains an acidic group such as a carboxylic acid.
  • organic bases e.g., pyridine, ammonia, or triethylamine
  • inorganic bases e.g., hydrides, hydroxides, or carbonates of sodium, potassium, lithium, calcium, magnesium or barium
  • the present invention comprises compounds selected from Formula 1, iV-oxides and agriculturally suitable salts thereof.
  • 3- to 6-membered nonaromatic carbocyclic or heterocyclic rings include those illustrated as G-I through G-45 in Exhibit 1. Note that the attachment point on these G groups is illustrated as floating; the G group can be attached to the remainder of Formula 1 through any available carbon or nitrogen of the G group by replacement of a hydrogen atom.
  • the optional substituents can be attached to any carbon or nitrogen by replacement of a hydrogen atom (said substituents are not illustrated in Exhibit 1 since they are optional substituents).
  • Q 2 may be selected from O, S, NH or substituted N.
  • Embodiment IA A compound of Formula 1 wherein R 1 is C 1 -C 4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or C1-C4 haloalkoxy.
  • Embodiment IB A compound of Embodiment IA wherein R 1 is CH3, CF3, OCF3, OCHF 2 , -CN or halogen.
  • Embodiment 1C A compound of Embodiment IB wherein R 1 is CH3, F, Cl, Br or I.
  • Embodiment ID A compound of Embodiment 1C wherein R 1 is CH3, Cl, Br or I.
  • Embodiment IE A compound of Embodiment ID wherein R 1 is CH3 or Cl.
  • Embodiment 2A A compound of Formula 1 wherein R 2 is H, C 1 - ⁇ alkyl, C1-C4 haloalkyl, halogen, -CN, -CHO, -NO 2 , C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 1 -C 4 haloalkylthio, C 1 -C 4 haloalkylsulfinyl, C 1 -C 4 haloalkylsulfonyl or C 2 -C 4 alkoxycarbonyl.
  • Embodiment 2B A compound of Embodiment 2A wherein R 2 is H, CH 3 , CF 3 , OCF 3 ,
  • Embodiment 2C A compound of Embodiment 2B wherein R 2 is H, CH 3 , CF 3 , -CN, F,
  • Embodiment 2D A compound of Embodiment 2C wherein R 2 is CH 3 , -CN, F, Cl, Br or I.
  • Embodiment 2E A compound of Embodiment 2D wherein R 2 is Cl, Br or -CN.
  • Embodiment 2F A compound of Embodiment 2E wherein R 2 is Cl or Br.
  • Embodiment 2G A compound of Embodiment 2E wherein R 2 is -CN.
  • Embodiment 3D A compound of Embodiment 3C wherein R 3 is
  • Embodiment 4A A compound of Formula 1 wherein R 4 is H, C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C 3 -C6 cycloalkyl, C 2 -Cg alkylcarbonyl or C 2 -Cg alkoxycarbonyl.
  • Embodiment 4B A compound of Embodiment 4A wherein R 4 is H.
  • Embodiment 6A A compound of Formula 1 wherein each R 5 is independently C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or C1-C4 haloalkoxy.
  • Embodiment 6B. A compound of Embodiment 6 A wherein each R 5 is independently
  • Embodiment 6C A compound of Embodiment 6B wherein each R 5 is independently
  • Embodiment 6D A compound of Embodiment 6C wherein each R 5 is independently CF 3 , OCF 3 or OCHF 2 .
  • Embodiment 7A A compound of Formula 1 wherein each R 6 is independently C1-C4 haloalkyl, halogen, -CN or C1-C4 haloalkoxy.
  • Embodiment 7B A compound of Embodiment 7 A wherein each R 6 is independently halogen, C 1 -C 2 fluoroalkoxy or C 1 -C 2 fluoroalkyl.
  • Embodiment 7C A compound of Embodiment 7B wherein each R 6 is independently halogen, OCH 2 CF 3 , OCHF 2 or CF 3 .
  • Embodiment 7D A compound of Embodiment 7C wherein each R 6 is independently
  • Embodiment 8A A compound of Formula 1 wherein R 7 is a phenyl ring optionally substituted with one to three substituents independently selected from R 9 - Embodiment 8B.
  • R 9 is independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, halogen or -CN.
  • Embodiment 8C A compound of Embodiment 8B wherein each R 9 is independently
  • Embodiment 9A A compound of Formula 1 wherein R 7 is
  • n 0, 1, 2 or 3.
  • Embodiment 9B A compound of Embodiment 9 A wherein each R 9 is independently
  • Embodiment 9C A compound of Embodiment 9B wherein each R 9 is independently
  • Embodiment 1OA A compound of Formula 1 wherein each R 8 is C 1 -C 4 alkyl or C 1 -C 4 haloalkyl.
  • Embodiment 1OB A compound of Embodiment 1OA wherein R 8 is C 1 -C 4 haloalkyl.
  • Embodiment 1OC A compound of Embodiment 1OB wherein R 8 is C 1 -C 2 fluoroalkyl.
  • Embodiment 1OD A compound of Embodiment 1OC wherein R 8 is CH 2 CF 3 or CHF 2 .
  • Embodiment HA A compound of Formula 1 wherein R ⁇ and R* 2 are independently
  • Embodiment HB A compound of Embodiment HA wherein R* 1 and R 12 are independently H or CH 3 .
  • Embodiment 12A A compound of Formula 1 wherein R 13 is H or C 1 -C 4 alkyl.
  • Embodiment 12B. A compound of Embodiment 12A wherein R 13 is H or CH 3 .
  • Embodiment 13A A compound of Formula 1 wherein R 14 and R 15 are independently
  • Embodiment 13B A compound of Embodiment 13A wherein R 14 and R 15 are independently H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl or C 3 -C 6 cycloalkyl.
  • Embodiment 14A A compound of Formula 1 wherein J is a heterocyclic ring selected from the group consisting of J-I, J-2 and J-3.
  • Embodiment 14B A compound of Formula 1 wherein J is J-I or J-2.
  • Embodiment 14C A compound of Formula 1 wherein J is J-I or J-3.
  • Embodiment 14D A compound of Formula 1 wherein J is J-2 or J-3.
  • Embodiment 14E A compound of Formula 1 wherein J is J-I.
  • Embodiment 14F A compound of Formula 1 wherein J is J-2.
  • Embodiment 14G A compound of Formula 1 wherein J is J-3.
  • Embodiment 14H A compound of Formula 1 wherein J is J-4.
  • Embodiment 141 A compound of Formula 1 wherein J is J-5.
  • Embodiment 14J A compound of Formula 1 wherein J is J-6.
  • Embodiment 14K A compound of Formula 1 wherein J is J-7.
  • Embodiment 14L A compound of Formula 1 wherein J is J-8. Combinations of Embodiments 1A-14L are illustrated by: Embodiment A. A compound of Formula 1 wherein
  • R 1 is C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, halogen, -CN, C 1 -C 4 alkoxy or C 1 -C 4 haloalkoxy;
  • R 4 is H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkylcarbonyl or C 2 -C 6 alkoxycarbonyl; or
  • Embodiment B A compound of Embodiment A wherein R 1 is CH 3 , CF 3 , OCF 3 , OCHF 2 , -CN or halogen;
  • R 2 is H, CH 3 , CF 3 , OCF 3 , OCHF 2 , S(O) p CF 3 , S(O) p CHF 2 , -CN or halogen;
  • R 4 is H; and p is 0, 1 or 2.
  • Embodiment C A compound of Embodiment B wherein each R 5 is independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, halogen, -CN, C 1 -C 4 alkoxy or C 1 -C 4 haloalkoxy; each R 6 is independently C 1 -C 4 haloalkyl, halogen, -CN or C 1 -C 4 haloalkoxy;
  • R 7 is phenyl optionally substituted with one to three substituents independently selected from R 9 ; or R7 is
  • each R 9 is independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, halogen or -CN;
  • R 8 is CH 2 CF 3 or CHF 2 ; and
  • n is 0, 1 or 2.
  • Embodiment D A compound of Embodiment C wherein each R 6 is independently halogen, OCH 2 CF 3 , OCHF 2 or CF 3 ; and each R 9 is independently CH 3 , CF 3 , -CN or halogen.
  • Embodiment E A compound of Embodiment D wherein J is a heterocyclic ring selected from the group consisting of J-I, J-2 and J-3.
  • Embodiment F A compound of Embodiment E wherein RMs CH 31 F 5 Cl 5 Br Or I;
  • R 2 is H, CH 3 , CF 3 , -CN, F, Cl, Br or I; and each R 6 is independently Cl, Br, OCH 2 CF 3 or CF 3 .
  • Specific embodiments include compounds of Formula 1 selected from the group consisting of:
  • compositions comprising a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising at least one additional biologically active compound or agent.
  • compositions for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent.
  • Embodiments of the invention further include methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof (e.g., as a composition described herein).
  • Embodiments of the invention also include a composition comprising a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, in the form of a soil drench liquid formulation.
  • Embodiments of the invention further include methods for controlling an invertebrate pest comprising contacting the soil with a liquid composition as a soil drench comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof.
  • Embodiments of the invention also include a spray composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof and a propellant.
  • Embodiments of the invention further include a bait composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, one or more food materials, optionally an attractant, and optionally a humectant.
  • Embodiments of the invention also include a device for controlling an invertebrate pest comprising said bait composition and a housing adapted to receive said bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to said bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
  • Compounds of Formula Ia wherein B is NR 13 , NOR 13 or NNRl 4 Rl 5 , can be prepared by the reaction of compounds of Formula Ic with corresponding amines, alkoxylamines or hydrazines of Formula 2 as outlined in Scheme 1.
  • This reaction can be run neat or in a variety of suitable solvents including water, methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent.
  • the general reaction of ketones with amines to produce imines, oximes and hydrazones is well documented in the chemical literature. For examples of this type see A. Franke, Liebigs Ami. Chem. 1982, (4), 794-804.
  • amides of Formula Ia can be converted to thioamides of Formula Ib using a variety of standard thio transfer reagents including phosphorus pentasulfide and 2,4-bis ⁇ (4-methoxyphenyl)-l,3- dithia-2,4-diphosphetane 2,4-disulfide (Lawesson's reagent).
  • Compounds of Formula Ib, where X is S and B is O, can be prepared from imines of Formula Ib, where X is S and B is NRI 3 , by hydrolysis of the imine group using aqueous acid such as hydrochloric acid, sulfuric acid or acetic acid, optionally with co-solvent such as methanol or tetrahydrofuran.
  • aqueous acid such as hydrochloric acid, sulfuric acid or acetic acid
  • co-solvent such as methanol or tetrahydrofuran.
  • Compounds of Formulae Id and Ie can be prepared by the reaction of compounds of Formulae Ig or Ih with aqueous base, such as potassium carbonate or sodium hydroxide, or with an amine of Formula 3 as outlined in Scheme 2.
  • aqueous base such as potassium carbonate or sodium hydroxide
  • an amine of Formula 3 as outlined in Scheme 2.
  • Rl 5 is H
  • Imines of Formula If can be converted to compounds of Formula Ie wherein R 4 and Rl 5 are H by treatment with aqueous acids such as hydrochloric acid, sulfuric acid or acetic acid, optionally with co-solvent such as methanol or tetrahydrofuran.
  • This reaction can be run neat or in a variety of suitable solvents including methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent.
  • suitable solvents including methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent.
  • Preparation of compounds of Formulae Id, Ie or If, wherein R 4 is other than H can be accomplished by standard alkylation or acylation of the amide by treatment with a base (such as sodium hydride in iV,N-dimethylformamide) and the alkylating or acylating reagent.
  • a base such as sodium hydride in iV,N-dimethylformamide
  • Compounds of Formula Ig can be prepared by acylation of isatins of Formula 4 with acid chlorides or mixed anhydrides of Formula 5 in the presence of a base such as triethylamine, pyridine or 3-picoline as outlined in Scheme 3.
  • This reaction can be run in a variety of suitable solvents including acetonitrile, dichloromethane, chloroform or tetrahydrofuran with optimum temperatures ranging from 0 0 C to the reflux temperature of the solvent.
  • the acylation of isatins is well documented in the chemical literature. For example see T. L. Jacobs et al., Organic Syntheses 1948, 28, 70-2 and A. Ferranti et al., Arch. Phartn. 1985, 318(5) 415-421.
  • amides of Formula Ig can be converted to thioamides of Formula Ih using a variety of standard thio transfer reagents including phosphorus pentasulfide and Lawesson's reagent.
  • Isatins of Formula 4 are well known and can be prepared from aniline derivatives following literature procedures such as those described by F. D. Popp, Adv. Heterocycl. Chem. 1975, 18, 1-58 and J. F. M. Da Silva et al., Journal of the Brazilian Chemical Society. 2001, 12(3), 273-324.
  • the acid chlorides of Formula 5 are available from the corresponding acids of Formula 6 by known methods such as chlorination with thionyl chloride or oxalyl chloride as outlined in Scheme 4.
  • the mixed anhydrides can be prepared in situ from the corresponding acids by treatment with an alkyl chloroformate or alkylsulfonyl chloride in the presence of a base such as triethylamine, pyridine or 3-picoline by well known methods.
  • the acids of Formula 6 can be prepared as disclosed in WO 03/016283 and US 6,747,047.
  • Anilines of Formula 7, wherein R 4 is H, can be prepared by reaction of isatins of Formula 4 with amines of Formula 3 as outlined in Scheme 6.
  • This reaction can be run neat or in a variety of suitable solvents including water, methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent.
  • suitable solvents including water, methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent.
  • Ij Anilines of Formula 8 wherein R 4 is H can be prepared by reduction of nitro compounds of Formula 9 as outlined in Scheme 8.
  • a variety of methods can be used for this transformation including catalytic hydrogenation, or treatment with iron in acetic acid or stannic chloride.
  • Compounds of Formula 8 wherein R 4 is alkyl, alkenyl, alkynyl or substituted derivatives thereof can be prepared by treatment of the aniline 8 wherein R 4 is H with an appropriate aldehyde in the presence of a reducing agent such as sodium cyanoborohydride.
  • R 4 is alkyl, substituted alkyl, etc.
  • Nitro compounds of Formula 9 wherein R 11 and R 12 are independently C ⁇ alkyl, C2-Cg alkenyl, C2-Cg alkynyl or C ⁇ -Cg cycloalkyl can be prepared by alkylation of nitro compounds of Formula 9a with the appropriate alkyl (or alkenyl, alkynyl or cycloalkyl) halides of Formulae 10a and 10b as outlined in Scheme 9. Particularly useful halides are bromides and iodides. This reaction can be run with a variety of bases including potassium t-butoxide, potassium carbonate and sodium hydride in a variety of suitable solvents including acetonitrile, ether or tetrahydrofuran.
  • Either the mono or dialkylation products can be obtained by adjusting the stoichiometry of the reagents.
  • stoichiometry for reactions of this type see T. J. Greshock and R. L. Funk, J. Amer. Chem. Soc, 2002, 124(5), 754-755, R. A. Bunce et al., J. Org. Chem., 2001, 66(8), 2822-2827 and M. Somei et al., Heterocycles, 1985, 23(5), 1101-1106.
  • R and R 12 are independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl or C 3 -C 6 cycloalkyl
  • Nitro compounds of Formula 9 wherein R 11 and R 12 are independently halogen can be prepared by halogenation of nitro compounds of Formula 9a as outlined in Scheme 10.
  • halogenating reagents can be employed such as a TV-halosuccmimide, bromine (for R 11 is bromine), chlorine (for R 11 is chlorine) or SelectfluorTM (i.e. l-chloromethyl-4-fluoro-l,4-diazoniabicyclo[2,2,2]octane bis(tetrafluoroborate)) (for R 11 is fluorine) in a variety of suitable solvents including carbon tetrachloride, chloroform, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent.
  • suitable solvents including carbon tetrachloride, chloroform, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent.
  • Nitro compounds of Formula 9b can be prepared from nitro compounds of Formula 9c by amination with amines of Formula 3 as outlined in Scheme 11.
  • the reaction can be performed by a variety of standard methods such as forming the acid chloride of the compound of Formula 9c and then reacting with the amine of Formula 3 or treating the compound of Formula 9c with a variety of coupling reagents such as 1,3-dicyclohexylcarbodiimide or l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride in the presence of the amine of Formula 3.
  • coupling reagents such as 1,3-dicyclohexylcarbodiimide or l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride in the presence of the amine of Formula 3.
  • Nitro compounds of Formula 9c can be prepared by acylation of ⁇ rt/i ⁇ -nitrotoluene compounds of Formula 11 with dimethyl or diethyl oxalate in the presence of base, followed by oxidation with basic hydrogen peroxide as outlined in Scheme 12.
  • An example of this procedure can be found in H. Rapoport et al., J. Org. Chem., 1954, 77, 670-675. ort/io-Nitro toluene compounds of Formula 11 are commercially available or are known in the art.
  • Scheme 12
  • Step A Preparation of 3-methyl-N-(l-methylethyl)-2-nitrobenzeneacetamide To a slurry of 3-methyl-2-nitrobenzeneacetic acid (prepared by the method of
  • reaction mixture was stirred overnight at room temperature. Saturated sodium bicarbonate solution was added, and the reaction mixture was passed through a Celite ® diatomaceous filter aid cartridge. The solvent was removed with a rotary evaporator to afford the title compound as an orange solid (0.4O g).
  • Step C Preparation of l-(3-chloro-2-pyridinyl)-N-r2-methyl-
  • the solvent was removed with a rotary evaporator.
  • the residue was purified by MPLC (40 ⁇ 60% ethyl acetate in hexanes as eluant) to afford the title compound plus an impurity.
  • the material was purified further by MPLC (20 ⁇ 30% ethyl acetate in 1-chlorobutane as eluant) to afford the title product, a compound of the present invention, as a white solid (0.12 g), m.p. 206-207 0 C.
  • Step B Preparation of l-(3-chloro-2-pyridinyl)-N-r2-r(diethylamino)oxoacetyll-4,6- dimethylphenyn-3-(trifluoromethyl)-lH-pyrazole-5-carboxamide
  • Compounds of this invention will generally be used as a formulation or composition with a suitable carrier comprising at least one of a liquid diluent, a solid diluent or a surfactant.
  • a suitable carrier comprising at least one of a liquid diluent, a solid diluent or a surfactant.
  • the formulation or composition ingredients are selected to be consistent with the physical properties of the active ingredient, mode of application and environmental factors such as soil type, moisture and temperature.
  • Useful formulations include liquids such as solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like which optionally can be thickened into gels.
  • Useful formulations further include solids such as dusts, powders, granules, pellets, tablets, films (including seed coatings), and the like which can be water-dispersible ("wettable") or water-soluble.
  • Active ingredient can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or "overcoated”). Encapsulation can control or delay release of the active ingredient.
  • Sprayable formulations can be extended in suitable media and used at spray volumes from about one to several hundred liters per hectare. High-strength compositions are primarily used as intermediates for further formulation.
  • the formulations will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.
  • Typical solid diluents are described in Watkins, et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, New Jersey. Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon's Detergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, New Jersey, as well as Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964, list surfactants and recommended uses.
  • All formulations can contain minor amounts of additives to reduce foam, caking, corrosion, microbiological growth and the like, or thickeners to increase viscosity.
  • Surfactants include, for example, polyethoxylated alcohols, polyethoxylated alkylphenols, polyethoxylated sorbitan fatty acid esters, dialkyl sulfosuccinates, alkyl sulfates, alkylbenzene sulfonates, organosilicones, iV,./V-dialkyltaurates, lignin sulfonates, naphthalene sulfonate formaldehyde condensates, polycarboxylates, glycerol esters, poly- oxyethylene/polyoxypropylene block copolymers, and alkylpolyglycosides where the number of glucose units, referred to as degree of polymerization (D.P.), can range from 1 to 3 and the alkyl units
  • Solid diluents include, for example, clays such as bentonite, montmorillonite, attapulgite and kaolin, starch, sugar, silica, talc, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarbonate, and sodium sulfate.
  • Liquid diluents include, for example, water, N,N-dimethylformamide, dimethyl sulfoxide, JV-alkylpyrrolidone, ethylene glycol, polypropylene glycol, propylene carbonate, dibasic esters, paraffins, alkylbenzenes, alkylnaphthalenes, glycerine, triacetine, oils of olive, castor, linseed, tung, sesame, corn, peanut, cotton-seed, soybean, rape-seed and coconut, fatty acid esters, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxy-4-methyl-2-pentanone, acetates such as hexyl acetate, heptyl acetate and octyl acetate, and alcohols such as methanol, cyclohexanol, decanol, benzyl and tetrahydrofurfury
  • Useful formulations of this invention may also contain materials well known to those skilled in the art as formulation aids such as antifoams, film formers and dyes.
  • Antifoams can include water dispersible liquids comprising polyorganosiloxanes like Rhodorsil® 416.
  • the film formers can include polyvinyl acetates, polyvinyl acetate copolymers, polyvinylpyrrolidone- vinyl acetate copolymer, polyvinyl alcohols, polyvinyl alcohol copolymers and waxes.
  • Dyes can include water dispersible liquid colorant compositions like Pro-lzed® Colorant Red.
  • formulation aids include those listed herein and those listed in McCutcheon's 2001, Volume 2: Functional Materials published by MC Publishing Company and PCT Publication WO 03/024222.
  • Solutions can be prepared by simply mixing the ingredients. Dusts and powders can be prepared by blending and, usually, grinding as in a hammer mill or fluid-energy mill. Suspensions are usually prepared by wet-milling; see, for example, U.S. 3,060,084. Granules and pellets can be prepared by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, "Agglomeration", Chemical Engineering, December 4, 1967, pp 147—48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and following, and WO 91/13546. Pellets can be prepared as described in U.S.
  • Water-dispersible and water-soluble granules can be prepared as taught in U.S. 4,144,050, U.S. 3,920,442 and DE 3,246,493. Tablets can be prepared as taught in U.S. 5,180,587, U.S. 5,232,701 and U.S. 5,208,030. Films can be prepared as taught in GB 2,095,558 and U.S. 3,299,566.
  • Compound 1 65.0% dodecylphenol polyethylene glycol ether 2.0% sodium ligninsulfonate 4.0% sodium silicoaluminate 6.0% montmorillonite (calcined) 23.0%
  • Compound 3 25.0% anhydrous sodium sulfate 10.0% crude calcium ligninsulfonate 5.0% sodium alkylnaphthalenesulfonate 1.0% calcium/magnesium bentonite 59.0%
  • Compound 8 20.0% blend of oil soluble sulfonates and polyoxyethylene ethers 10.0% isophorone 70.0%
  • Compound 14 20.00% polyvinylpyrrolidone- vinyl acetate copolymer 5.00% montan acid wax 5.00% calcium ligninsulfonate 1.00% polyoxyethylene/polyoxypropylene block copolymers 1.00% stearyl alcohol (POE 20) 2.00% polyorganosilane 0.20% colorant red dye 0.05% water 65.75%
  • invertebrate pest control means inhibition of invertebrate pest development (including mortality, feeding reduction, and/or mating disruption) and as a result significant reduction in feeding or injury to an agronomic crop or damage to a building structure caused by the invertebrate pest; related expressions are defined analogously.
  • agronomic refers to the production of field crops such as for food and fiber and includes the growth of corn, soybeans and other legumes, rice, cereal (e.g., wheat, oats, barley, rye, rice, maize), leafy vegetables (e.g., lettuce, cabbage, and other cole crops), fruiting vegetables (e.g., tomatoes, pepper, eggplant, crucifers and cucurbits), potatoes, sweet potatoes, grapes, cotton, tree fruits (e.g., pome, stone and citrus), small fruit (berries, cherries) and other specialty crops (e.g., canola, sunflower, olives).
  • agronomic also refers to the production of such crops that contain genetic material introduced by genetic engineering (i.e.
  • transgenic or modified by mutagenesis to provide advantageous traits.
  • traits include tolerance to herbicides, resistance to phytophagous pests (e.g., insects, mites, aphids, spiders, nematodes, snails, plant-pathogenic fungi, bacteria and viruses), improved plant growth, increased tolerance of adverse growing conditions such as high and low temperatures, low or high soil moisture, and high salinity, increased flowering or fruiting, greater harvest yields, more rapid maturation, higher quality and/or nutritional value of the harvested product, and improved storage or process properties of the harvested products.
  • Transgenic plants can be modified to express multiple traits.
  • plants containing traits provided by genetic engineering or mutagenesis include varieties of corn, cotton, soybean and potato expressing an insecticidal Bacillus thuringiensis toxin such as YIELD GARD®, KNOCKOUT ® , STARLINK ® , BOLLGARD ® , NuCOTN ® and NEWLEAF , and herbicide-tolerant varieties of corn, cotton, soybean and rapeseed such as ROUNDUP READY ® , LIBERTY LINK ® , IMI ® , STS ® and CLEARFIELD ® , as well as crops expressing N-acetyltransferase (GAT) to provide resistance to glyphosate herbicide, or crops containing the HRA gene providing resistance to herbicides inhibiting acetylactate synthase (ALS).
  • GAT N-acetyltransferase
  • nonagronomic refers to other horticultural crops (e.g., greenhouse, nursery or ornamental plants not grown in a field), residential and commercial structures in urban and industrial settings, turf (commercial, golf, residential, recreational, etc.), wood products, stored product, agro-forestry and vegetation management, public health (human) and animal health (domestical animals, pets, livestock, poultry, undomestical animals such as wildlife) applications.
  • turf commercial, golf, residential, recreational, etc.
  • wood products stored product
  • agro-forestry and vegetation management public health (human) and animal health (domestical animals, pets, livestock, poultry, undomestical animals such as wildlife) applications.
  • protection of agronomic crops from damage or injury caused by invertebrate pests by controlling invertebrate pests are embodiments of the invention.
  • the term “invertebrate pest” includes arthropods, gastropods and nematodes of economic importance as pests.
  • arthropod includes insects, mites, spiders, scorpions, centipedes, millipedes, pill bugs and symphylans.
  • gastropod includes snails, slugs and other Stylommatophora.
  • nematode includes all of the helminths, such as: roundworms, heartworms, and phytophagous nematodes (Nematoda), flukes (Tematoda), Acanthocephala, and tapeworms (Cestoda).
  • Compounds of this invention exhibit activity against a wide spectrum of foliar-feeding, fruit-feeding, stem or root feeding, seed-feeding, aquatic and soil-inhabiting invertebrate pests which are pests of growing and stored agronomic crops, forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, public health and animal health.
  • Agronomic or nonagronomic pests include eggs, larvae and adults of the order
  • Lepidoptera such as armyworms, cutworms, loopers, and heliothines in the family Noctuidae (e.g., fall armyworm (Spodoptera fugiperda J. E. Smith), beet armyworm (Spodoptera exigua H ⁇ bner), black cutworm (Agrotis ipsilon Hufnagel), cabbage looper ⁇ Trichoplusia ni H ⁇ bner), tobacco budworm ⁇ Heliothis virescens Fabricius)); borers, casebearers, webworms, coneworms, cabbageworms and skeletonizers from the family Pyralidae (e.g., European corn borer ⁇ Ostrinia nubilalis H ⁇ bner), navel orangeworm ⁇ Amyelois transitella Walker), corn root webworm ⁇ Crambus caliginosellus Clemens), sod webworms (Pyralidae: Crambinae) such as sod
  • agronomic and nonagronomic pests include: eggs, adults and larvae of the order Dermaptera including earwigs from the family Forficulidae (e.g., European earwig ⁇ Forficula auricularia Linnaeus), black earwig ⁇ Chelisoches mono Fabricius)); eggs, immatures, adults and nymphs of the orders Hemiptera and Homoptera such as, plant bugs from the family Miridae, cicadas from the family Cicadidae, leafhoppers (e.g.
  • eggs, larvae, nymphs and adults of the order Acari such as spider mites and red mites in the family Tetranychidae (e.g., European red mite ⁇ Panonychus ulmi Koch), two spotted spider mite ⁇ Tetranychus urticae Koch), McDaniel mite ⁇ Tetranychus mcdanieli McGregor)); flat mites in the family Tenuipalpidae (e.g., citrus flat mite ⁇ Brevipalpus lewisi McGregor)); rust and bud mites in the family Eriophyidae and other foliar feeding mites and mites important in human and animal health, i.e.
  • Tetranychidae e.g., European red mite ⁇ Panonychus ulmi Koch
  • two spotted spider mite ⁇ Tetranychus urticae Koch McDaniel mite ⁇ Tetranychus
  • femoralis Stein stable flies (e.g., Stomoxys calcitrans Linnaeus), face flies, horn flies, blow flies (e.g., Chrysomya spp., Phormia spp.), and other muscoid fly pests, horse flies (e.g., Tabanus spp.), bot flies (e.g., Gastrophilus spp., Oestrus spp.), cattle grubs (e.g., Hypoderma spp.), deer flies (e.g., Chrysops spp.), keds (e.g., Melophagus ovinus Linnaeus) and other Brachycera, mosquitoes (e.g., Aedes spp., Anopheles spp., Culex spp.), black flies (e.g., Prosimulium spp., Simulium s
  • insect pests of the order Isoptera including termites in the Termitidae (ex. Macrotermes sp.), Kalotermitidae (ex. Cryptotermes sp.), and Rhinotermitidae (ex.
  • Reticulitermes sp., Coptotermes sp.) families the eastern subterranean termite (Reticulitermes flavipes Kollar), western subterranean termite (Reticulitermes hesperus Banks), Formosan subterranean termite (Coptotermes formosanus Shiraki), West Indian drywood termite (Incisitermes immigrans Snyder), powder post termite (Cryptotermes brevis Walker), drywood termite (Incisitermes snyderi Light), southeastern subterranean termite (Reticulitermes virginicus Banks), western drywood termite (Incisitermes minor Hagen), arboreal termites such as Nasutitermes sp.
  • insect pests of the order Thysanura such as silverfish (Lepisma saccharina Linnaeus) and firebrat (Thermobia domestica Packard); insect pests of the order Mallophaga and including the head louse (Pediculus humanus capitis De Geer), body louse (Pediculus humanus Linnaeus), chicken body louse (Menacanthus stramineus Nitszch), dog biting louse (Trichodectes canis De Geer), fluff louse (Goniocotes gallinae De Geer), sheep body louse (Bovicola ovis Schrank), short-nosed cattle louse (Haematopinus eurysternus Nitzsch), long-nosed cattle louse (Linognathus vituli Linnaeus) and other sucldng and chewing parasitic lice that attack man and animals; insect pests of the order Siphonoptera including the oriental
  • Additional arthropod pests covered include: spiders in the order Araneae such as the brown recluse spider (Loxosceles reclusa Gertsch & Mulaik) and the black widow spider (Latrodectus mactans Fabricius), and centipedes in the order Scutigeromorpha such as the house centipede (Scutigera coleoptrata Linnaeus).
  • spiders in the order Araneae such as the brown recluse spider (Loxosceles reclusa Gertsch & Mulaik) and the black widow spider (Latrodectus mactans Fabricius)
  • centipedes in the order Scutigeromorpha such as the house centipede (Scutigera coleoptrata Linnaeus).
  • Compounds of the present invention also have activity on members of the Classes Nematoda, Cestoda, Trematoda, and Acanthocephala including economically important members of the orders Strongylida, Ascaridida, Oxyurida, Rhabditida, Spirurida, and Enoplida such as but not limited to economically important agricultural pests (i.e. root knot nematodes in the genus Meloidogyne, lesion nematodes in the genus Pratylenchus, stubby root nematodes in the genus Trichodorus, etc.) and animal and human health pests (i.e.
  • Compounds of the invention show particularly high activity against pests in the order Lepidoptera (e.g., Alabama argillacea Hubner (cotton leaf worm), Archips argyrospila Walker (fruit tree leaf roller), A. rosana Linnaeus (European leaf roller) and other Archips species, Ch ⁇ lo suppressalis Walker (rice stem borer), Cnaphalocrosis medinalis Guenee (rice leaf roller), Crambus caliginosellus Clemens (corn root webworm), Crambus teterrellus Zincken (bluegrass webworm), Cydia pomonella Linnaeus (codling moth), Earias insulana Boisduval (spiny bollworm), Earias vittella Fabricius (spotted bollworm), Helicoverpa armigera Hubner (American bollworm), Helicoverpa zea Boddie (corn earworm), Heliothis virescens Fabricius (tobacco budworm), Her
  • Compounds of the invention also have significant activity on members from the order Homoptera including: Acyrthisiphon pisum Harris (pea aphid), Aphis craccivora Koch (cowpea aphid), Aphis fabae Scopoli (black bean aphid), Aphis gossypii Glover (cotton aphid, melon aphid), Aphis pomi De Geer (apple aphid), Aphis spiraecola Patch (spirea aphid), Aulacorthum solani Kaltenbach (foxglove aphid), Chaetosiphon fragaefolii Cockerell (strawberry aphid), Diuraphis noxia Kurdjumov/Mordvilko (Russian wheat aphid), Dysaphis plantaginea Paaserini (rosy apple aphid), Eriosoma lanigerum Hausmann (woolly apple aphid), Hyalopterus
  • Compounds of this invention also have activity on members from the order Hemiptera including: Acrosternum hilare Say (green stink bug), Anasa tristis De Geer (squash bug), Blissus leucopterus leucopterus Say (chinch bug), Corythuca gossypii Fabricius (cotton lace bug), Cyrtopeltis modesta Distant (tomato bug), Dysdercus suturellus He ⁇ ich-Schaffer (cotton stainer), Euchistus servus Say (brown stink bug), Euchistus variolarius Palisot de Beauvois (one-spotted stink bug), Graptosthetus spp.
  • Thysanoptera e.g., Frankliniella occidentalis Pergande (western flower thrip), Scirthothrips citri Moulton (citrus thrip), Sericothrips variabilis Beach (soybean thrip), and Thrips tabaci Lindeman (onion thrip); and the order Coleoptera (e.g., Leptinotarsa decemlineata Say (Colorado potato beetle), Epilachna varivestis Mulsant (Mexican bean beetle) and wireworms of the genera Agriotes, Athous or Limonius).
  • Thysanoptera e.g., Frankliniella occidentalis Pergande (western flower thrip), Scirthothrips citri Moulton (citrus thrip), Sericothrips variabilis Beach (soybean thrip), and Thrips tabaci Lindeman (onion thrip
  • Coleoptera e.g.
  • Compounds of this invention can also be mixed with one or more other biologically active compounds or agents including insecticides, fungicides, nematocides, bactericides, acaricides, herbicides, growth regulators such as rooting stimulants, chemosterilants, semiochemicals, repellents, attractants, pheromones, feeding stimulants, other biologically active compounds or entomopathogenic bacteria, virus or fungi to form a multi-component pesticide giving an even broader spectrum of agronomic and nonagronomic utility.
  • the present invention also pertains to a composition
  • a composition comprising a biologically effective amount of a compound of Formula 1 and an effective amount of at least one additional biologically active compound or agent and can further comprise at least one of a surfactant, a solid diluent or a liquid diluent.
  • the other biologically active compounds or agents can be formulated in compositions comprising at least one of a surfactant, solid or liquid diluent.
  • the other biologically active compounds or agents can be formulated together with the present compounds, including the compounds of Formula 1, to form a premix, or the other biologically active compounds or agents can be formulated separately from the present compounds, including the compounds of Formula 1, and the two formulations combined together before application (e.g., in a spray tank) or, alternatively, applied in succession.
  • insecticides such as abamectin, acephate, acetamiprid, amidoflumet (S-1955), avermectin, azadirachtin, azinphos-methyl, bifenthrin, bifenazate, buprofezin, carbofuran, cartap, chlorfenapyr, chlorfluazuron, chlorpyrifos, chlorpyrifos- methyl, chromafenozide, clothianidin, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, cype ⁇ nethrin, cyromazine, deltamethrin, diafenthiuron, diazinon, dieldrin, diflubenzuron, dimefluthrin, dimetho
  • Bacillus thuringiensis subsp. Kurstaki and the encapsulated delta-endotoxins of Bacillus thuringiensis (e.g., Cellcap, MPV, MPVII); entomopathogenic fungi, such as green muscardine fungus; and entomopathogenic virus including baculovirus, nucleopolyhedro virus (NPV) such as HzNPV, AfNPV; and granulosis virus (GV) such as CpGV.
  • NPV nucleopolyhedro virus
  • GV granulosis virus
  • Compounds of this invention and compositions thereof can be applied to plants genetically transformed to express proteins toxic to invertebrate pests (such as Bacillus thuringiensis delta-endotoxins).
  • the effect of the exogenously applied invertebrate pest control compounds of this invention may be synergistic with the expressed toxin proteins.
  • compositions of the present invention can further comprise a biologically effective amount of at least one additional invertebrate pest control compound or agent having a similar spectrum of control but a different mode of action.
  • a plant protection compound e.g., protein
  • a biologically effective amount of a compound of this invention can also provide a broader spectrum of plant protection and be advantageous for resistance management.
  • combinations of a compound of this invention with other invertebrate pest control compounds or agents can result in a greater-than-additive (i.e.
  • synergistic effect and/or a less-than-additive effect i.e. antagonistic. It is always desirable to reduce the quantity of chemical agents released in the environment while ensuring effective pest control.
  • synergism of invertebrate pest control agents is found at application rates giving agronomically satisfactory levels of pest control, such combinations can be advantageous for lowering crop production cost and reducing environmental load.
  • Table A lists specific combinations of a compound of Formula 1 with other invertebrate pest control agents illustrative of the mixtures, compositions and methods of the present invention.
  • the first column of Table A lists the specific invertebrate pest control agents (e.g., "Abamectin" in the first line).
  • the second column of Table A lists the mode of action (if known) of the invertebrate pest control agents.
  • the third column of Table A lists embodiment(s) of ranges of weight ratios for rates at which the invertebrate pest control agent can be applied relative to a compound of Formula 1, an iV-oxide, or a salt thereof, (e.g., "50:1 to 1:50" of abamectin relative to a compound of Formula 1 by weight).
  • the first line of Table A specifically discloses the combination of a compound of Formula 1 with abamectin can be applied in a weight ratio between 50:1 to 1:50.
  • the remaining lines of Table A are to be construed similarly.
  • Table A lists specific combinations of a compound of Formula 1 with other invertebrate pest control agents illustrative of the mixtures, compositions and methods of the present invention and includes additional embodiments of weight ratio ranges for application rates.
  • insecticides and acaricides for mixing with compounds of this invention include sodium channel modulators such as cypermethrin, cyhalothrin, cyfluthrin, beta-cyfluthrin, esfenvalerate, fenvalerate, indoxacarb and tralomethrin; cholinesterase inhibitors such as methomyl, oxamyl and thiodicarb; neonicotinoids such as acetamiprid, clothianidin, imidacloprid, thiacloprid and thiamethoxam; neuronal sodium channel blockers such as indoxacarb; insecticidal macrocyclic lactones such as spinosad, abamectin, avermectin and emamectin; GABA ( ⁇ -aminobutyric acid)-regulated chloride channel blockers such as endosulfan, ethiprole and fipron
  • biological agents for mixing with compounds of this invention include Bacillus thuringiensis and Bacillus thuringiensis delta-endotoxin as well as naturally occurring and genetically modified viral insecticides including members of the family Baculoviridae as well as entomophagous fungi.
  • the weight ratios of a compound, including a compound of Formula 1, an N-oxide or a salt thereof, to the additional invertebrate pest control agent typically are between 1000:1 and 1:1000, with one embodiment being between 500:1 and 1:500, another embodiment being between 250:1 and 1:200 and another embodiment being between 100:1 and 1:50.
  • Table B Listed below in Table B are embodiments of specific compositions comprising a compound of Formula 1 (compound numbers refer to compounds in Index Table A) and an additional invertebrate pest control agent.
  • A-47 1 and NPV e.g., Gemstar
  • B-47 11 and NPV e.g., Gemstar
  • Invertebrate pests are controlled in agronomic and nonagronomic applications by applying a composition comprising a compound of this invention, in a biologically effective amount, to the environment of the pests, including the agronomic and/or nonagronomic locus of infestation, to the area to be protected, or directly on the pests to be controlled.
  • Agronomic applications include protecting a field crop from invertebrate pests typically by applying a composition or a mixture of the invention to the seed of the crop before the planting, to the foliage, stems, flowers and/or fruit of crop plants, or to the soil or other growth medium before or after the crop is planted.
  • Nonagronomic applications refer to invertebrate pest control in the areas other than fields of crop plants.
  • Nonagronomic applications include control of invertebrate pests in stored grains, beans and other foodstuffs, and in textiles such as clothing and carpets.
  • Nonagronomic applications also include invertebrate pest control in ornamental plants, forests, in yards, along roadsides and railroad rights of way, and on turf such as lawns, golf courses and pastures.
  • Nonagronomic applications also include invertebrate pest control in houses and other buildings which may be occupied by humans and/or companion, farm, ranch, zoo or other animals.
  • Nonagronomic applications also include the control of pests such as termites that can damage wood or other structural materials used in buildings.
  • Nonagronomic applications also include protecting human and animal health by controlling invertebrate pests that are parasitic or transmit infectious diseases.
  • the controlling of animal parasites includes controlling external parasites that are parasitic to the surface of the body of the host animal (e.g., shoulders, armpits, abdomen, inner part of the thighs) and internal parasites that are parasitic to the inside of the body of the host animal (e-g-j stomach, intestine, lung, veins, under the skin, lymphatic tissue).
  • External parasitic or disease transmitting pests include, for example, chiggers, ticks, lice, mosquitoes, flies, mange, mites and fleas.
  • Internal parasites include heartworms, hookworms and helminths.
  • Compounds and compositions of the present invention are particular suitable for combating external parasitic or disease transmitting pests.
  • Compounds and compositions of the present invention are suitable for combating parasites that infest agricultural working animals, such as cattle, sheep, goats, horses, pigs, donkeys, camels, buffalos, rabbits, hens, turkeys, ducks, geese and bees; pet animals and domestic animals such as dogs, cats, pet birds and aquarium fish; as well as so-called experimental animals, such as hamsters, guinea pigs, rats and mice.
  • fatalities and performance reduction in term of meat, milk, wool, skins, eggs, honey, etc.
  • applying a composition comprising a compound of the present invention is intended to allow more economic and simple husbandry of animals.
  • Nonagronomic applications in the veterinary sector takes place in the known manner, by enteral administration in the form of, for example, tablets, capsules, drinks, drenching preparations, granulates, pastes, boli, feed-through procedures, suppositories; by parenteral administration, such as by injection (including intramuscular, subcutaneous, intravenous, intraperitoneal), implants; by nasal administration; by dermal administration, for example, in the form of immersion or dipping, spraying, pouring, washing, coating with powder, and through bodied devices such as neck collars, ear marks, tail marks, limb measuring tapes or halters which comprise compounds or compositions of the present invention.
  • the present invention further comprises a method for controlling an invertebrate pest in agronomic and/or nonagronomic applications, comprising contacting the invertebrate pest or its environment with a biologically effective amount of one or more of the compounds of the invention, or with a composition comprising at least one such compound or a composition comprising at least one such compound and a biologically effective amount of at least one additional biologically active compound or agent.
  • suitable compositions comprising a compound of the invention and a biologically effective amount of at least one additional biologically active compound or agent include granular compositions wherein the additional active compound is present on the same granule as the compound of the invention or on granules separate from those of the compound of the invention.
  • a method of contact is by spraying.
  • a granular composition comprising a compound of the invention can be applied to the plant foliage or the soil.
  • Compounds of this invention can also be effectively delivered through plant uptake by contacting the plant with a composition comprising a compound of this invention applied as a soil drench of a liquid formulation, a granular formulation to the soil, a nursery box treatment or a dip of transplants.
  • a method for controlling an invertebrate pest comprising contacting the soil environment of the invertebrate pest with a biologically effective amount of a compound of the present invention.
  • compounds of this invention also effective by topical application to the locus of infestation.
  • Other methods of contact include application of a compound or a composition of the invention by direct and residual sprays, aerial sprays, gels, seed coatings, microencapsulations, systemic uptake, baits, ear tags, boluses, foggers, fumigants, aerosols, dusts and many others.
  • One embodiment of a method of contact is a dimensionally stable fertilizer granule, stick or tablet comprising a mixture or composition of the invention.
  • the compounds of this invention can also be impregnated into materials for fabricating invertebrate control devices (e.g., insect netting).
  • Seed coatings can be applied to all types of seeds, including those from which plants genetically transformed to express specialized traits will germinate.
  • Representative examples include those expressing proteins toxic to invertebrate pests, such as Bacillus thuringiensis toxin or those expressing herbicide resistance, such as "Roundup Ready” seed.
  • the compounds of this invention can be incorporated into a bait composition that is consumed by an invertebrate pest or used within a device such as a trap, bait station, and the like.
  • a bait composition can be in the form of granules which comprise (a) active ingredients, namely a biologically effective amount of a compound of Formula 1, an N-oxide, or salt thereof; (b) one or more food materials; optionally (c) an attractant, and optionally (d) one or more humectants.
  • granules or bait compositions which comprise between about 0.001-5% active ingredients, about 40-99% food material and/or attractant; and optionally about 0.05-10% humectants, which are effective in controlling soil invertebrate pests at very low application rates, particularly at doses of active ingredient that are lethal by ingestion rather than by direct contact.
  • Some food materials can function both as a food source and an attractant.
  • Food materials include carbohydrates, proteins and lipids. Examples of food materials are vegetable flour, sugar, starches, animal fat, vegetable oil, yeast extracts and milk solids.
  • attractants are odorants and flavorants, such as fruit or plant extracts, perfume, or other animal or plant component, pheromones or other agents known to attract a target invertebrate pest.
  • humectants i.e. moisture retaining agents, are glycols and other polyols, glycerine and sorbitol.
  • a bait composition (and a method utilizing such a bait composition) used to control at least one invertebrate pest selected from the group consisting of ants, termites and cockroaches.
  • a device for controlling an invertebrate pest can comprise the present bait composition and a housing adapted to receive the bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to the bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
  • the compounds of this invention can be applied without other adjuvants, but most often application will be of a formulation comprising one or more active ingredients with suitable carriers, diluents, and surfactants and possibly in combination with a food depending on the contemplated end use.
  • One method of application involves spraying a water dispersion or refined oil solution of a compound of the present invention. Combinations with spray oils, spray oil concentrations, spreader stickers, adjuvants, other solvents, and synergists such as piperonyl butoxide often enhance compound efficacy.
  • Such sprays can be applied from spray containers such as a can, a bottle or other container, either by means of a pump or by releasing it from a pressurized container, e.g., a pressurized aerosol spray can.
  • Such spray compositions can take various forms, for example, sprays, mists, foams, fumes or fog.
  • Such spray compositions thus can further comprise propellants, foaming agents, etc. as the case may be.
  • a spray composition comprising a biologically effective amount of a compound or a composition of the present invention and a carrier.
  • a spray composition comprises a biologically effective amount of a compound or a composition of the present invention and a propellant.
  • propellants include, but are not limited to, methane, ethane, propane, butane, isobutane, butene, pentane, isopentane, neopentane, pentene, hydrofluorocarbons, chlorofluorocarbons, dimethyl ether, and mixtures of the foregoing.
  • a spray composition (and a method utilizing such a spray composition dispensed from a spray container) used to control at least one invertebrate pest selected from the group consisting of mosquitoes, black flies, stable flies, deer flies, horse flies, wasps, yellow jackets, hornets, ticks, spiders, ants, gnats, and the like, including individually or in combinations.
  • the rate of application required for effective control (i.e. "biologically effective amount") will depend on such factors as the species of invertebrate to be controlled, the pest's life cycle, life stage, its size, location, time of year, host crop or animal, feeding behavior, mating behavior, ambient moisture, temperature, and the like. Under normal circumstances, application rates of about 0.01 to 2 kg of active ingredients per hectare are sufficient to control pests in agronomic ecosystems, but as little as 0.0001 kg/hectare may be sufficient or as much as 8 kg/hectare may be required. For nonagronomic applications, effective use rates will range from about 1.0 to 50 mg/square meter but as little as 0.1 mg/square meter may be sufficient or as much as 150 mg/square meter may be required.
  • One skilled in the art can easily determine the biologically effective amount necessary for the desired level of invertebrate pest control.
  • Control efficacy represents inhibition of invertebrate pest development (including mortality) that causes significantly reduced feeding.
  • the pest control protection afforded by the compounds is not limited, however, to these species. See Index Tables A-E for compound descriptions. The following abbreviations are used in the Index Tables which follow: i is iso, Me is methyl, Et is ethyl and f-Pr is isopropyl.
  • (d) means melts with apparent decomposition.
  • the abbreviation “Ex.” stands for "Example” and is followed by a number indicating in which example the compound is prepared.

Abstract

Disclosed are compounds of Formula (1), including all geometric and stereoisomers, N-oxides, and salts thereof, wherein R3 is -C(=B)C(=O)L or -C(R11R12)C(=O)L; R4 is, inter alia, H, C1-C4 alkyl or C2-C6 alkoxycarbonyl; or R3 and R4 are taken together as -C(=O)C(=O)-, -C(=NR13)C(=O)- or -C(R11R12)C(=O)-. B is O, NR13, NOR13 Or NNR14 R15; L is OH or NR14 R15; and X, Rl, R2, R11, R12, R13, R14, R15 and J are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula (1) and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.

Description

ANTHRANILAMIDES FOR CONTROLLING INVERTEBRATE PESTS
FIELD OF THE INVENTION
This invention relates to certain anthranilamides, their N-oxides, salts and compositions suitable for agronomic and nonagronomic uses, and methods of their use for controlling invertebrate pests such as arthropods in both agronomic and nonagronomic environments.
BACKGROUND OF THE INVENTION
The control of invertebrate pests is extremely important in achieving high crop efficiency. Damage by invertebrate pests to growing and stored agronomic crops can cause significant reduction in productivity and thereby result in increased costs to the consumer.
The control of invertebrate pests in forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, turf, wood products, and public and animal health is also important. Many products are commercially available for these purposes, but the need continues for new compounds which are more effective, less costly, less toxic, environmentally safer or have different modes of action.
WO 03/015519 discloses N-acyl anthranilic acid derivatives of Formula i as anthropodicides
Figure imgf000002_0001
wherein, inter alia, R1 is CH3, F, Cl or Br; R2 is F, Cl, Br, I or CF3; R3 is CF3, Cl, Br or OCH2CF3; R4a is C1-C4 alkyl; R4b is H or CH3; and R5 is Cl or Br.
SUMMARY OF THE INVENTION
This invention is directed to compounds of Formula 1 including all geometric isomers and stereoisomers, iV-oxides, and salts thereof, agricultural and nonagricultural compositions containing them and their use for controlling invertebrate pests:
Figure imgf000003_0001
wherein:
X is O or S;
J is a phenyl optionally substituted with one to four substituents independently selected from R5; or J is a heterocyclic ring selected from the group consisting of
Figure imgf000003_0002
J-5 J-6 J-7 J-8
R1 is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkenyl, C2-C6 haloalkynyl, C3-C6 halocycloalkyl, halogen, -CN, -CHO, -NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C2-C4 alkylaminocarbonyl, C3-C5 dialkylaminocarbonyl, C1-C4 alkylamino or C2-C6 dialkylamino;
R2 is H, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C -06 haloalkyl, C2-C6 haloalkenyl, C2-C6 haloalkynyl, C3-C6 halocycloalkyl, halogen, -CN, -CHO, -NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C2-C4 alkylaminocarbonyl, C3-C5 dialkylaminocarbonyl, C1-C4 alkylamino or C2-C6 dialkylamino;
R3 is -C(=B)C(=O)L or -C(R11R1^CC=O)L; R4 is H; or C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each optionally substituted with one or more substituents selected from the group consisting of halogen, -CN, -NO2, hydroxy, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C2-C4 alkoxycarbonyl, C1-C4 alkylamino, C2-Cg dialkylamino and C3-C6 cycloalkylamino; or
R4 is C2-C6 alkylcarbonyl, C2-C6 alkoxycarbonyl, C2-C6 alkylaminocarbonyl or
C3-Cg dialkylaminocarbonyl; or R3 and R4 are taken together as -C(=B)C(=O)- or -C(R11R12JCC=O)-, wherein the left-hand of these moieties is bonded as R3 and the right-hand as R4; each R5 is independently C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, -CN, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 haloalkoxy, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl or C1-C4 haloalkylsulfonyl; or phenyl or pyridyl, each optionally substituted with one to three R9;
R6 is H, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, -CN, C1-C4 alkoxy, C2-C4 alkoxycarbonyl, C1-C4 alkylthio, C1-C4 haloalkoxy, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl or C1-C4 haloalkylsulfonyl; R7 is C1-C6 alkyl optionally substituted with one or more substituents selected from the group consisting of halogen, -CN, -NO2, hydroxy, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C2-C4 alkoxycarbonyl, C1-C4 alkylamino, C2-Cg dialkylamino and C3-C6 cycloalkylamino; or
R7 is phenyl or pyridyl, each optionally substituted with one to three substituents selected from R9; R8 is H, C1-C6 alkyl, C1-C6 haloalkyl, C3-C6 alkenyl, C3-C6 haloalkenyl, C3-C6 alkynyl or C3-C6 haloalkynyl; each R9 is independently C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, -CN, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 haloalkoxy, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl or C1-C4 haloalkylsulfonyl;
R11 and R12 are independently H; halogen; -CN; OR13; or C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each optionally substituted with one or more halogen;
B is O, NR13, NOR13 or NNR14R15;
L is OH or NR14R15;
R13 is H; or C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each optionally substituted with one or more halogen; R14 and R15 are independently H; G; or C1-C6 alkyl, C2-C6 alkenyl or C2-C6 alkynyl, each optionally substituted with one or more substituents selected from the group consisting of G, halogen, -CN, -NO2, hydroxy, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C1-C4 alkylamino, C2-C8 dialkylamino and C3-C6 cycloalkylamino; or
R14 and R15 are taken together with the nitrogen to which they are attached to form a ring containing 2 to 6 atoms of carbon and optionally one additional atom of nitrogen, sulfur or oxygen, said ring1 optionally substituted with 1 to 4 substituents selected from the group consisting of C1-C2 alkyl, halogen, -CN,
-NO2 and C1-C2 alkoxy; and each G is independently a 3- to 6-membered nonaromatic carbocyclic or heterocyclic ring, optionally including one or two ring members selected from the group consisting of C(=O), S(O) or S(O)2 and optionally substituted with 1 to 4 substituents selected from the group consisting of C1-C2 alkyl, halogen, -CN, -NO2 and C1-
C2 alkoxy.
This invention also provides a composition comprising a compound of Formula 1 and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent. In one embodiment, this invention also provides a composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula 1 and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent.
This invention further provides a spray composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula 1 or the composition described in the embodiment above and a propellant. This invention also provides a bait composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula 1 or the composition described in the embodiment above, one or more food materials, optionally an attractant, and optionally a humectant.
This invention further provides a trap device for controlling an invertebrate pest comprising said bait composition and a housing adapted to receive said bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to said bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
This invention also provides a method for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of Formula 1 (e.g., as a composition described herein). This invention also relates to such method wherein the invertebrate pest or its environment is contacted with a composition comprising a biologically effective amount of a compound of Formula 1 and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent.
DETAILS OF THE INVENTION
As used herein, the terms "comprises," "comprising," "includes," "including," "has," "having," "contains" or "containing," or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a composition, a mixture, process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, mixture, process, method, article, or apparatus. Further, unless expressly stated to the contrary, "or" refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).
Also, the indefinite articles "a" and "an" preceding an element or component of the invention are intended to be nonrestrictive regarding the number of instances (i.e. occurrences) of the element or component. Therefore "a" or "an" should be read to include one or at least one, and the singular word form of the element or component also includes the plural unless the number is obviously meant to be singular. For example, a composition of the present invention comprises a biologically effective amount of "a" compound of Formula 1 which should be read that the composition includes one or at least one compound of Formula 1.
In the above recitations, the term "alkyl", used either alone or in compound words such as "alkylthio" or "haloalkyl" includes straight-chain or branched alkyl, such as, methyl, ethyl, H-propyl, /-propyl, or the different butyl, pentyl or hexyl isomers. The term "1-2 alkyl" indicates that one or two of the available positions for that substituent may be alkyl which are independently selected. "Alkenyl" includes straight-chain or branched alkenes such as ethenyl, 1-propenyl, 2-propenyl, and the different butenyl, pentenyl and hexenyl isomers. "Alkenyl" also includes polyenes such as 1,2-propadienyl and 2,4-hexadienyl. "Alkynyl" includes straight-chain or branched alkynes such as ethynyl, 1-propynyl, 2-propynyl and the different butynyl, pentynyl and hexynyl isomers. "Alkynyl" can also include moieties comprised of multiple triple bonds such as 2,5-hexadiynyl. "Cycloalkyl" includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. "Alkoxy" includes, for example, methoxy, ethoxy, n-propyloxy, isopropyloxy and the different butoxy, pentoxy and hexyloxy isomers. "Alkylthio" includes branched or straight-chain alkylthio moieties such as methylthio, ethylthio, and the different propylthio and butylthio isomers. "Alkylsulfinyl" includes both enantiomers of an alkylsulfinyl group. Examples of "alkylsulfinyl" include CH3S(O), CH3CH2S(O), CH3CH2CH2S(O), (CH3)2CHS(O) and the different butylsulfinyl isomers. Examples of "alkylsulfonyl" include CH3S(O)2, CH3CH2S(O)2, CH3CH2CH2S(O)2, (CH3)2CHS(O)2 and the different butylsulfonyl isomers. "Alkylamino", "dialkylamino", "cycloalkylamino" , and the like, are defined analogously to the above examples.
The term "halogen", either alone or in compound words such as "haloalkyl", includes fluorine, chlorine, bromine or iodine. The term "1-2 halogen" indicates that one or two of the available positions for that substituent may be halogen which are independently selected. Further, when used in compound words such as "haloalkyl", said alkyl may be partially or fully substituted with halogen atoms which may be the same or different. Examples of "haloalkyl" include F3C, ClCH2, CF3CH2 and CF3CCl2. The terms "haloalkenyl", "haloalkynyl", "haloalkoxy", "haloalkylthio", and the like, are defined analogously to the term "haloalkyl". Examples of "haloalkenyl" include (Cl)2C=CHCH2 and CF3CH2CH=CHCH2. Examples of "haloalkynyl" include HC≡CCHCl, CF3C≡C, CC13C≡C and FCH2C≡CCH2. Examples of "haloalkoxy" include CF3O, CCl3CH2O, HCF2CH2CH2O and CF3CH2O. Examples of "haloalkylthio" include CCl3S, CF3S, CCl3CH2S and ClCH2CH2CH2S. Examples of "haloalkylsulfinyl" include CF3S(O), CCl3S(O), CF3CH2S(O) and CF3CF2S(O). Examples of "haloalkylsulfonyl" include CF3S(O)2, CCl3S(O)2, CF3CH2S(O)2 and CF3CF2S(O)2. "Alkylcarbonyl" denotes a straight-chain or branched alkyl moieties bonded to a C(=0) moiety. Examples of "alkylcarbonyl" include CH3C(=O)-, CH3CH2CH2CC=O)- and (CH3)2CHC(=O)-. Examples of "alkoxycarbonyl" include CH30C(=0)-, CH3CH2OC(=O)-, CH3CH2CH2OC(=O)-, (CH3)2CHOC(=O)- and the different butoxy- or pentoxycarbonyl isomers. Examples of "alkylaminocarbonyl" include CH3NHC(=0)-, CH3CH2NHC(=O)-, CH3CH2CH2NHC(=O)-,
(CH3)2CHNHC(=O)- and the different butylamino- or pentylaminocarbonyl isomers. Examples of "dialkylaminocarbonyl" include (CH3)2NC(=O)-, (CH3CH2)2NC(=O)-, CH3CH2(CH3)NC(=O)-, (CH3)2CHN(CH3)C(=O)- and CH3CH2CH2(CH3)NC(=O)-. The total number of carbon atoms in a substituent group is indicated by the "Cj-Cj" prefix where i and j are numbers from 1 to 8. For example, C1-C4 alkylsulfonyl designates methylsulfonyl through butylsulfonyl.
The term "nonaromatic carbocyclic ring" denotes fully saturated carbocyclic rings as well as partially or fully unsaturated carbocyclic rings where the Hϋckel rule is not satisfied. The term "nonaromatic heterocyclic ring" denotes fully saturated heterocyclic rings as well as partially or fully unsaturated heterocyclic rings where the Hϋckel rule is not satisfied. The heterocyclic ring systems can be attached through any available carbon or nitrogen by replacement of a hydrogen on said carbon or nitrogen. The term "optionally substituted" in connection with aromatic ring groups refers to groups that are unsubstituted or have at least one non-hydrogen substituent. Commonly, the number of optional substituents (when present) ranges from one to four. In the above recitations, when a compound of Formula 1 is comprised of one or more heterocyclic rings, all substituents are attached to these rings through any available carbon or nitrogen by replacement of a hydrogen on said carbon or nitrogen.
When a compound is substituted with a substituent bearing a subscript that indicates the number of said substituents can exceed 1, said substituents (when they exceed 1) are independently selected from the group of defined substituents. Further, when the subscript indicates a range, e.g. (R5)^, then the number of substituents may be selected from the integers between 1 and 4 inclusive. When a group contains a substituent which can be hydrogen, for example R2 or R6, then, when this substituent is taken as hydrogen, it is recognized that this is equivalent to said group being unsubstituted.
One skilled in the art recognizes that "pyridinyl" and "pyridyl" are equivalent alternative names for an organic radical formed by removing a hydrogen atom from a pyridine ring to form an attachment point; accordingly "pyridinyl" and "pyridyl" are used herein as synonyms. Compounds of this invention can exist as one or more stereoisomers. The various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers. One skilled in the art will appreciate that one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or to selectively prepare said stereoisomers. The compounds of the invention may be present as a mixture of stereoisomers, individual stereoisomers, or as an optically active form.
One skilled in the art will appreciate that not all nitrogen-containing heterocycles can form N-oxides since the nitrogen requires an available lone pair for oxidation to the oxide; one skilled in the art will recognize those nitrogen-containing heterocycles which can form N-oxides. One skilled in the art will also recognize that tertiary amines can form N-oxides. Synthetic methods for the preparation of N-oxides of heterocycles and tertiary amines are very well known by one skilled in the art including the oxidation of heterocycles and tertiary amines with peroxy acids such as peracetic and m-chloroperbenzoic acid (MCPBA), hydrogen peroxide, alkyl hydroperoxides such as t-butyl hydroperoxide, sodium perborate, and dioxiranes such as dimethyldioxirane. These methods for the preparation of N-oxides have been extensively described and reviewed in the literature; see for example: T. L. Gilchrist in Comprehensive Organic Synthesis, vol. 7, pp 748-750, S. V. Ley, Ed., Pergamon Press; M. Tisler and B. Stanovnik in Comprehensive Heterocyclic Chemistry, vol. 3, pp 18-20, A. J. Boulton and A. McKillop, Eds., Pergamon Press; M. R. Grimmett and B. R. T. Keene in Advances in Heterocyclic Chemistry, vol. 43, pp 149-161, A. R. Katritzky, Ed., Academic Press; M. Tisler and B. Stanovnik in Advances in Heterocyclic Chemistry, vol. 9, pp 285-291, A. R. Katritzky and A. J. Boulton, Eds., Academic Press; and G. W. H. Cheeseman and E. S. G. Werstiuk in Advances in Heterocyclic Chemistry, vol. 22, pp 390-392, A. R. Katritzky and A. J. Boulton, Eds., Academic Press.
The salts of the compounds of the invention include acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids. The salts of the compounds of the invention also include those formed with organic bases (e.g., pyridine, ammonia, or triethylamine) or inorganic bases (e.g., hydrides, hydroxides, or carbonates of sodium, potassium, lithium, calcium, magnesium or barium) when the compound contains an acidic group such as a carboxylic acid. Accordingly, the present invention comprises compounds selected from Formula 1, iV-oxides and agriculturally suitable salts thereof.
As noted above, G is a 3- to 6-membered nonaromatic carbocyclic or heterocyclic ring, optionally including one or two ring members selected from the group consisting of C(=O), S(O) or S(O)2 and optionally substituted with 1 to 4 substituents selected from the group consisting of C1-C2 alkyl, halogen, -CN, -NO2 and C1-C2 alkoxy. Examples of 3- to 6-membered nonaromatic carbocyclic or heterocyclic rings include those illustrated as G-I through G-45 in Exhibit 1. Note that the attachment point on these G groups is illustrated as floating; the G group can be attached to the remainder of Formula 1 through any available carbon or nitrogen of the G group by replacement of a hydrogen atom. The optional substituents can be attached to any carbon or nitrogen by replacement of a hydrogen atom (said substituents are not illustrated in Exhibit 1 since they are optional substituents). Note that when G comprises a ring selected from G-24 through G-31, G-34 and G-35, Q2 may be selected from O, S, NH or substituted N.
Exhibit 1
Figure imgf000009_0001
G-6 G-7 G-8 G-9 G-IO
Figure imgf000009_0002
G-Il G-12 G-13 G-14 G-15
Figure imgf000010_0001
G-26 G-27 G-28 G-29 G-30
Figure imgf000010_0002
-31 G-32. G-33 G-34 G-35
Figure imgf000010_0003
G-36 G-37 G-38 G-39 G-40
Figure imgf000010_0004
G-41 G-42 G-43 G-44 G-45
Embodiments of the present invention include:
Embodiment IA. A compound of Formula 1 wherein R1 is C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or C1-C4 haloalkoxy.
Embodiment IB. A compound of Embodiment IA wherein R1 is CH3, CF3, OCF3, OCHF2, -CN or halogen.
Embodiment 1C. A compound of Embodiment IB wherein R1 is CH3, F, Cl, Br or I.
Embodiment ID. A compound of Embodiment 1C wherein R1 is CH3, Cl, Br or I.
Embodiment IE. A compound of Embodiment ID wherein R1 is CH3 or Cl.
Embodiment 2A. A compound of Formula 1 wherein R2 is H, C1-^ alkyl, C1-C4 haloalkyl, halogen, -CN, -CHO, -NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl or C2-C4 alkoxycarbonyl. Embodiment 2B. A compound of Embodiment 2A wherein R2 is H, CH3, CF3, OCF3,
OCHF2, S(O)pCF3, S(O)pCHF2, -CN or halogen; and p is 0, 1 or 2. Embodiment 2C. A compound of Embodiment 2B wherein R2 is H, CH3, CF3, -CN, F,
Cl, Br or I. Embodiment 2D. A compound of Embodiment 2C wherein R2 is CH3, -CN, F, Cl, Br or I.
Embodiment 2E. A compound of Embodiment 2D wherein R2 is Cl, Br or -CN. Embodiment 2F. A compound of Embodiment 2E wherein R2 is Cl or Br. Embodiment 2G. A compound of Embodiment 2E wherein R2 is -CN. Embodiment 3 A. A compound of Formula 1 wherein R3 is -C(=O)C(=O)OH,
-C(=NR13)C(=O)OH or -C(R11R12^=O)OH.
Embodiment 3B. A compound of Embodiment 3 A wherein R3 is -C(=O)C(=O)OH. Embodiment 3C. A compound of Formula 1 wherein R3 is -C(=O)C(=O)NR14R15,
-C(=NR13)C(=O)NR14R15 or -C(R11R1^CC=O)NR14R15. Embodiment 3D. A compound of Embodiment 3C wherein R3 is
-C(=O)C(=O)NR14R15. Embodiment 3E. A compound of Formula 1 wherein R3 is -C(=O)C(=O)OH, -
C(R11R1^CC=O)OH, -C(=O)C(=O)NR14R15 or
-C(R11R12XX=O)NR14R15. Embodiment 4A. A compound of Formula 1 wherein R4 is H, C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C3-C6 cycloalkyl, C2-Cg alkylcarbonyl or C2-Cg alkoxycarbonyl.
Embodiment 4B. A compound of Embodiment 4A wherein R4 is H. Embodiment 5 A. A compound of Formula 1 wherein R3 and R4 are taken together as -C(=O)C(=O)-, -C(=NR13)C(=O)- or -C(RnR12)C(=O)-.
Embodiment 5B. A compound of Embodiment 5 A wherein R3 and R4 are taken together as -C(=O)C(=O)-. Embodiment 6A. A compound of Formula 1 wherein each R5 is independently C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or C1-C4 haloalkoxy. Embodiment 6B. A compound of Embodiment 6 A wherein each R5 is independently
CH3, CF3, halogen, -CN, OCH3, OCF3 or OCHF2. Embodiment 6C. A compound of Embodiment 6B wherein each R5 is independently
CF3 F, Cl, Br, -CN, OCF3 or OCHF2.
Embodiment 6D. A compound of Embodiment 6C wherein each R5 is independently CF3, OCF3 or OCHF2.
Embodiment 7A. A compound of Formula 1 wherein each R6 is independently C1-C4 haloalkyl, halogen, -CN or C1-C4 haloalkoxy. Embodiment 7B. A compound of Embodiment 7 A wherein each R6 is independently halogen, C1-C2 fluoroalkoxy or C1-C2 fluoroalkyl. Embodiment 7C. A compound of Embodiment 7B wherein each R6 is independently halogen, OCH2CF3, OCHF2 or CF3. Embodiment 7D. A compound of Embodiment 7C wherein each R6 is independently
Cl, Br, OCH2CF3 or CF3. Embodiment 8A. A compound of Formula 1 wherein R7 is a phenyl ring optionally substituted with one to three substituents independently selected from R9- Embodiment 8B. A compound of Embodiment 8 A wherein each R9 is independently C1-C4 alkyl, C1-C4 haloalkyl, halogen or -CN.
Embodiment 8C. A compound of Embodiment 8B wherein each R9 is independently
CH3, CF3, -CN or halogen. Embodiment 9A. A compound of Formula 1 wherein R7 is
Figure imgf000012_0001
n is 0, 1, 2 or 3.
Embodiment 9B. A compound of Embodiment 9 A wherein each R9 is independently
C1-C4 alkyl, C1-C4 haloalkyl, halogen or -CN; and n is 0, 1 or 2. Embodiment 9C. A compound of Embodiment 9B wherein each R9 is independently
CH3, CF3, -CN or halogen. Embodiment 1OA. A compound of Formula 1 wherein each R8 is C1-C4 alkyl or C1-C4 haloalkyl.
Embodiment 1OB. A compound of Embodiment 1OA wherein R8 is C1-C4 haloalkyl. Embodiment 1OC. A compound of Embodiment 1OB wherein R8 is C1-C2 fluoroalkyl. Embodiment 1OD. A compound of Embodiment 1OC wherein R8 is CH2CF3 or CHF2. Embodiment HA. A compound of Formula 1 wherein R^ and R*2 are independently
H or C1-C4 alkyl. Embodiment HB. A compound of Embodiment HA wherein R*1 and R12 are independently H or CH3.
Embodiment 12A. A compound of Formula 1 wherein R13 is H or C1-C4 alkyl. Embodiment 12B. A compound of Embodiment 12A wherein R13 is H or CH3.
Embodiment 13A. A compound of Formula 1 wherein R14 and R15 are independently
H; or C1-Cg alkyl, C2-Cg alkenyl, C2-Cg alkynyl or C3-Cg cycloalkyl, each optionally substituted with one or more halogen or -CN. Embodiment 13B. A compound of Embodiment 13A wherein R14 and R15 are independently H, C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl or C3-C6 cycloalkyl.
Embodiment 14A. A compound of Formula 1 wherein J is a heterocyclic ring selected from the group consisting of J-I, J-2 and J-3.
Embodiment 14B. A compound of Formula 1 wherein J is J-I or J-2. Embodiment 14C. A compound of Formula 1 wherein J is J-I or J-3. Embodiment 14D. A compound of Formula 1 wherein J is J-2 or J-3. Embodiment 14E. A compound of Formula 1 wherein J is J-I. Embodiment 14F. A compound of Formula 1 wherein J is J-2.
Embodiment 14G. A compound of Formula 1 wherein J is J-3. Embodiment 14H. A compound of Formula 1 wherein J is J-4. Embodiment 141. A compound of Formula 1 wherein J is J-5. Embodiment 14J. A compound of Formula 1 wherein J is J-6. Embodiment 14K. A compound of Formula 1 wherein J is J-7.
Embodiment 14L. A compound of Formula 1 wherein J is J-8. Combinations of Embodiments 1A-14L are illustrated by: Embodiment A. A compound of Formula 1 wherein
R1 is C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or C1-C4 haloalkoxy;
R2 is H, C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, -CHO, -NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl or C2-C4 alkoxycarbonyl; R3 is -C(=O)C(=O)OH, -C(R11R12^=O)OH, -C(=O)C(=O)NR14R15 or
-C(R11R12XX=O)NR14R15; and R4 is H, C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C3-C6 cycloalkyl, C2-C6 alkylcarbonyl or C2-C6 alkoxycarbonyl; or
R3 and R4 are taken together as -C(=O)C(=O)-, -C(=NR13)C(=O)- or -C(R11R^)CC=O)-.
Embodiment B. A compound of Embodiment A wherein R1 is CH3, CF3, OCF3, OCHF2, -CN or halogen;
R2 is H, CH3, CF3, OCF3, OCHF2, S(O)pCF3, S(O)pCHF2, -CN or halogen; R4 is H; and p is 0, 1 or 2.
Embodiment C. A compound of Embodiment B wherein each R5 is independently C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or C1-C4 haloalkoxy; each R6 is independently C1-C4 haloalkyl, halogen, -CN or C1-C4 haloalkoxy;
R7 is phenyl optionally substituted with one to three substituents independently selected from R9; or R7 is
Figure imgf000014_0001
each R9 is independently C1-C4 alkyl, C1-C4 haloalkyl, halogen or -CN; R8 is CH2CF3 or CHF2; and n is 0, 1 or 2.
Embodiment D. A compound of Embodiment C wherein each R6 is independently halogen, OCH2CF3, OCHF2 or CF3; and each R9 is independently CH3, CF3, -CN or halogen. Embodiment E. A compound of Embodiment D wherein J is a heterocyclic ring selected from the group consisting of J-I, J-2 and J-3. Embodiment F. A compound of Embodiment E wherein RMs CH31 F5 Cl5 Br Or I;
R2 is H, CH3, CF3, -CN, F, Cl, Br or I; and each R6 is independently Cl, Br, OCH2CF3 or CF3.
Embodiment G. A compound of Embodiment F wherein R3 is -C(=O)C(=O)OH. Embodiment H. A compound of Embodiment F wherein R3 is -C(=O)C(=O)NR14R15. Specific embodiments include compounds of Formula 1 selected from the group consisting of:
1 -(3 -chloro-2-pyridinyl)-iV- [2-methyl-6- [2- [( 1 -methylethyl)amino] -
2-oxoethyl]phenyl]-3-(trifluoromethyl)-lH-pyrazole-5-carboxamide; l-(3-chloro-2-pyridinyl)-N-[2-[(diethylamino)oxoacetyl]-4,6-dimethylphenyl]-
3-(trifluoromethyl)-lH-pyrazole-5-carboxamide; l-(3-chloro-2-pyridinyl)-N-[2-[(lZ)-2-(diethylamino)-l-(hydroxyimino)-
2-oxoethyl]-4,6-dimethylphenyl]-3-(trifluoromethyl)-lH-pyrazole-5-carboxamide;
2- [ [ [3 -bromo- 1 -(3 -chloro-2-pyridinyl)- lH-pyrazol-5-yl] carbonyl] amino] -
S-chloro-S-methyl-α-oxobenzeneacetic acid; l-[[3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazol-5-yl]carbonyl]-5-chloro-
7-methyl-lH-indole-2,3-dione;
3-bromo-N-[4-chloro-2-methyl-6-[(lE)-2-(methylamino)-l-(methylimino)-
2-oxoethyl]phenyl]-l-(3-chloro-2-pyridinyl)-lH-ρyrazole-5-carboxamide; and
3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)oxoacetyl]phenyl]-l-(3-chloro-
2-pyridinyl)-lH-pyrazole-5-carboxamide. Further specific embodiments include any combination of the compounds of Formula 1 selected from the group immediately above.
Also noteworthy as embodiments of the present invention are compositions comprising a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising at least one additional biologically active compound or agent.
Also noteworthy as embodiments of the present invention are compositions for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent. Embodiments of the invention further include methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof (e.g., as a composition described herein). Embodiments of the invention also include a composition comprising a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, in the form of a soil drench liquid formulation. Embodiments of the invention further include methods for controlling an invertebrate pest comprising contacting the soil with a liquid composition as a soil drench comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof.
Embodiments of the invention also include a spray composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof and a propellant. Embodiments of the invention further include a bait composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, one or more food materials, optionally an attractant, and optionally a humectant. Embodiments of the invention also include a device for controlling an invertebrate pest comprising said bait composition and a housing adapted to receive said bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to said bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
Compounds of Formula 1 can be prepared by one or more of the following methods and variations as described in Schemes 1-12. The definitions of X, J, B, L, R1, R2, R3, R4, R5, R6, R7, R8, R9, RlO, RlI, Rl2, Rl3, R14 and R15 m the compounds of Formulae 1-11 below are as defined above in the Summary of the Invention unless indicated otherwise. Formulae Ia-Ij are subsets of Formula 1, and Formulae 9a-9c are subsets of Formula 9.
Compounds of Formula Ia, wherein B is NR13, NOR13 or NNRl4Rl5, can be prepared by the reaction of compounds of Formula Ic with corresponding amines, alkoxylamines or hydrazines of Formula 2 as outlined in Scheme 1. This reaction can be run neat or in a variety of suitable solvents including water, methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent. The general reaction of ketones with amines to produce imines, oximes and hydrazones is well documented in the chemical literature. For examples of this type see A. Franke, Liebigs Ami. Chem. 1982, (4), 794-804. In a subsequent step, amides of Formula Ia can be converted to thioamides of Formula Ib using a variety of standard thio transfer reagents including phosphorus pentasulfide and 2,4-bis~(4-methoxyphenyl)-l,3- dithia-2,4-diphosphetane 2,4-disulfide (Lawesson's reagent). Compounds of Formula Ib, where X is S and B is O, can be prepared from imines of Formula Ib, where X is S and B is NRI3, by hydrolysis of the imine group using aqueous acid such as hydrochloric acid, sulfuric acid or acetic acid, optionally with co-solvent such as methanol or tetrahydrofuran.
Scheme 1
Figure imgf000016_0001
Compounds of Formulae Id and Ie can be prepared by the reaction of compounds of Formulae Ig or Ih with aqueous base, such as potassium carbonate or sodium hydroxide, or with an amine of Formula 3 as outlined in Scheme 2. When Rl5 is H, it is possible to obtain compounds of Formula If wherein R3 is -C(=NRl4)C(=O)NHRl4 directly. Imines of Formula If can be converted to compounds of Formula Ie wherein R4 and Rl5 are H by treatment with aqueous acids such as hydrochloric acid, sulfuric acid or acetic acid, optionally with co-solvent such as methanol or tetrahydrofuran. Scheme 2
i:.s H
Figure imgf000017_0001
H
Figure imgf000017_0002
If wherein R is H
This reaction can be run neat or in a variety of suitable solvents including methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent. For examples of reactions of isatins with amines see A. Franke, Liebigs Ann. Chem. 1982, (4), 794-804. For examples of reactions of isatins with aqueous base see B. A. Johnson and K. Undheim, Acta Chemica Scand., Series B 1984, B 38(2), 109-112. Preparation of compounds of Formulae Id, Ie or If, wherein R4 is other than H (e.g., alkyl, alkylcarbonyl, etc.), can be accomplished by standard alkylation or acylation of the amide by treatment with a base (such as sodium hydride in iV,N-dimethylformamide) and the alkylating or acylating reagent.
Compounds of Formula Ig can be prepared by acylation of isatins of Formula 4 with acid chlorides or mixed anhydrides of Formula 5 in the presence of a base such as triethylamine, pyridine or 3-picoline as outlined in Scheme 3. This reaction can be run in a variety of suitable solvents including acetonitrile, dichloromethane, chloroform or tetrahydrofuran with optimum temperatures ranging from 0 0C to the reflux temperature of the solvent. The acylation of isatins is well documented in the chemical literature. For example see T. L. Jacobs et al., Organic Syntheses 1948, 28, 70-2 and A. Ferranti et al., Arch. Phartn. 1985, 318(5) 415-421. In a subsequent step, amides of Formula Ig can be converted to thioamides of Formula Ih using a variety of standard thio transfer reagents including phosphorus pentasulfide and Lawesson's reagent.
Scheme 3
Figure imgf000018_0001
Ig (X is O) Ih (X is S)
Ra is Cl, -OC(=O)alkyl or -OS(=O)2alkyl
Isatins of Formula 4 are well known and can be prepared from aniline derivatives following literature procedures such as those described by F. D. Popp, Adv. Heterocycl. Chem. 1975, 18, 1-58 and J. F. M. Da Silva et al., Journal of the Brazilian Chemical Society. 2001, 12(3), 273-324.
The acid chlorides of Formula 5 are available from the corresponding acids of Formula 6 by known methods such as chlorination with thionyl chloride or oxalyl chloride as outlined in Scheme 4. The mixed anhydrides can be prepared in situ from the corresponding acids by treatment with an alkyl chloroformate or alkylsulfonyl chloride in the presence of a base such as triethylamine, pyridine or 3-picoline by well known methods. The acids of Formula 6 can be prepared as disclosed in WO 03/016283 and US 6,747,047.
Scheme 4
Figure imgf000018_0002
base ► Ra is -OC(=O)alkyl or -OS(=O)2alkyl alkyl chloroformate or alkylsulfonyl chloride
Alternatively compounds of Formula Ie (i.e. Formula 1 wherein R3 is -C(=O)C(=O)- NR14R15) can be prepared by acylation of anilines of Formula 7 with acid chlorides or other activated derivatives of carboxylic acids of Formula 6 in the presence of base such as triethylamine, pyridine or 3-picoline as outlined in Scheme 5. This reaction can be run in a variety of suitable solvents including acetonitrile, dichloromethane, chloroform or tetrahydrofuran with optimum temperatures ranging from 0 0C to the reflux temperature of the solvent. Scheme 5
Figure imgf000019_0001
X is O
Anilines of Formula 7, wherein R4 is H, can be prepared by reaction of isatins of Formula 4 with amines of Formula 3 as outlined in Scheme 6.
Scheme 6
Figure imgf000019_0002
7
(R4 is H)
This reaction can be run neat or in a variety of suitable solvents including water, methanol, ethanol, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent. For examples of this procedure see J. EQavac et al., /. Ret. Chem., 2004, 41(4), 633-636 and J. Bergman et al. Acta Chemica Second., 1997, 51 (6/7), 753-759.
Compounds of Formula Ij (i.e. Formula 1 wherein R3 is -C(RnR12)C(=O)L) can be prepared by acylation of anilines of Formula 8 with acid chlorides of Formula 5 in the presence of a base such as triethylamine, pyridine or 3-picoline as outlined in Scheme 7. This reaction can be run in a variety of suitable solvents including acetonitrile, dichloromethane, chloroform or tetrahydrofuran with optimum temperatures ranging from
0 0C to the reflux temperature of the solvent.
Scheme 7
Figure imgf000019_0003
Ij Anilines of Formula 8 wherein R4 is H can be prepared by reduction of nitro compounds of Formula 9 as outlined in Scheme 8. A variety of methods can be used for this transformation including catalytic hydrogenation, or treatment with iron in acetic acid or stannic chloride.
Compounds of Formula 8 wherein R4 is alkyl, alkenyl, alkynyl or substituted derivatives thereof can be prepared by treatment of the aniline 8 wherein R4 is H with an appropriate aldehyde in the presence of a reducing agent such as sodium cyanoborohydride.
Scheme 8
(R4 is alkyl, substituted alkyl, etc.)
Figure imgf000020_0001
Nitro compounds of Formula 9 wherein R11 and R12 are independently C^^ alkyl, C2-Cg alkenyl, C2-Cg alkynyl or Cβ-Cg cycloalkyl can be prepared by alkylation of nitro compounds of Formula 9a with the appropriate alkyl (or alkenyl, alkynyl or cycloalkyl) halides of Formulae 10a and 10b as outlined in Scheme 9. Particularly useful halides are bromides and iodides. This reaction can be run with a variety of bases including potassium t-butoxide, potassium carbonate and sodium hydride in a variety of suitable solvents including acetonitrile, ether or tetrahydrofuran. Either the mono or dialkylation products can be obtained by adjusting the stoichiometry of the reagents. For reactions of this type see T. J. Greshock and R. L. Funk, J. Amer. Chem. Soc, 2002, 124(5), 754-755, R. A. Bunce et al., J. Org. Chem., 2001, 66(8), 2822-2827 and M. Somei et al., Heterocycles, 1985, 23(5), 1101-1106.
Scheme 9
Figure imgf000020_0002
wherein R and R12 are independently C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C6 cycloalkyl
Nitro compounds of Formula 9 wherein R11 and R12 are independently halogen can be prepared by halogenation of nitro compounds of Formula 9a as outlined in Scheme 10. Scheme 10
halogenating agent
Figure imgf000021_0002
Figure imgf000021_0001
9a
1 1 19 wherein R and R are halogen
A variety of halogenating reagents can be employed such as a TV-halosuccmimide, bromine (for R11 is bromine), chlorine (for R11 is chlorine) or Selectfluor™ (i.e. l-chloromethyl-4-fluoro-l,4-diazoniabicyclo[2,2,2]octane bis(tetrafluoroborate)) (for R11 is fluorine) in a variety of suitable solvents including carbon tetrachloride, chloroform, acetonitrile or tetrahydrofuran with optimum temperatures ranging from room temperature to the reflux temperature of the solvent. For an example see K. Schaper et al., EMr. J. Org. Chem., 2002, (6), 1037-1046.
Nitro compounds of Formula 9b can be prepared from nitro compounds of Formula 9c by amination with amines of Formula 3 as outlined in Scheme 11. The reaction can be performed by a variety of standard methods such as forming the acid chloride of the compound of Formula 9c and then reacting with the amine of Formula 3 or treating the compound of Formula 9c with a variety of coupling reagents such as 1,3-dicyclohexylcarbodiimide or l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride in the presence of the amine of Formula 3.
Scheme 11
Figure imgf000021_0003
Nitro compounds of Formula 9c can be prepared by acylation of ørt/iø-nitrotoluene compounds of Formula 11 with dimethyl or diethyl oxalate in the presence of base, followed by oxidation with basic hydrogen peroxide as outlined in Scheme 12. An example of this procedure can be found in H. Rapoport et al., J. Org. Chem., 1954, 77, 670-675. ort/io-Nitro toluene compounds of Formula 11 are commercially available or are known in the art. Scheme 12
Figure imgf000022_0001
It is recognized that some reagents and reaction conditions described above for preparing compounds of Formula 1 may not be compatible with certain functionalities present in the intermediates. In these instances, the incorporation of protection/deprotection sequences or functional group interconversions into the synthesis will aid in obtaining the desired products. The use and choice of the protecting groups will be apparent to one skilled in chemical synthesis (see, for example, Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 2nd ed.; Wiley: New York, 1991). One skilled in the art will recognize that, in some cases, after the introduction of a given reagent as it is depicted in any individual scheme, it may be necessary to perform additional routine synthetic steps not described in detail to complete the synthesis of compounds of Formula 1. One skilled in the art will also recognize that it may be necessary to perform a combination of the steps illustrated in the above schemes in an order other than that implied by the particular sequence presented to prepare the compounds of Formula 1.
One skilled in the art will also recognize that compounds of Formula 1 and the intermediates described herein can be subjected to various electrophilic, nucleophilic, radical, organometallic, oxidation, and reduction reactions to add substituents or modify existing substituents. Without further elaboration, it is believed that one skilled in the art using the preceding description can utilize the present invention to its fullest extent. The following Examples are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Percentages are by weight except for chromatographic solvent mixtures or where otherwise indicated. Parts and percentages for chromatographic solvent mixtures are by volume unless otherwise indicated. 1H NMR spectra are reported in ppm downfield from tetramethylsilane; s means singlet, d means doublet, t means triplet, q means quartet, m means multiplet, dd means doublet of doublets, dt means doublet of triplets, br s means broad singlet. EXAMPLE 1
Preparation of l-(3-chloro-2-pyridinyl)-N-r2-methyl-6-r2-rfl-methylethvπaminol- 2-oxoethyl1phenyl1-3-(trifluoromethylMH-pyrazole-5-carboxainide
Step A: Preparation of 3-methyl-N-(l-methylethyl)-2-nitrobenzeneacetamide To a slurry of 3-methyl-2-nitrobenzeneacetic acid (prepared by the method of
Η. Rapoport et al, J. Org. Chem., 1954, 77, 670-675 from l,3-dimethyl-2-nitrobenzene, 0.70 g, 3.6 mmol) in 10 mL of dichloromethane was added oxalyl chloride (0.41 mL, 4.7 mmol) and two drops of Λ^N-dimethylformamide. The reaction mixture was stirred for 20 minutes, resulting in a solution. The volatiles were removed with a rotary evaporator. The residue was dissolved in 10 mL of dichloromethane. Half of this material was added dropwise at 0 °C to isopropylamine (1 mL) in 5 mL of dichloromethane. The reaction mixture was stirred overnight at room temperature. Saturated sodium bicarbonate solution was added, and the reaction mixture was passed through a Celite® diatomaceous filter aid cartridge. The solvent was removed with a rotary evaporator to afford the title compound as an orange solid (0.4O g).
1H NMR (CDCl3) 67.35 (m, 2H), 7.23 (d, IH), 5.48 (br s, IH), 4.03 (m, IH), 3.44 (s, 2H), 2.36 (s, 3H), 1.10 (d, 6H).
Step B: Preparation of 2-amino-3-methyl-Ar-(l-methylethyl)benzeneacetamide
To 3-methyl-Λ/'-(l-methylethyl)-2-nitrobenzeneacetamide (i.e. the title product of Step A) (0.40 g, 1.7 mmol) and 10% palladium on carbon (0.13 g) was added 20 mL of ethanol. The reaction mixture was placed under a balloon of nitrogen overnight. Then the reaction mixture was filtered through Celite® diatomaceous filter aid. The solvent was removed with a rotary evaporator to afford the title compound as a tan solid (0.29 g). 1H NMR (CDCl3) δ 7.00 (d, IH), 6.90 (d, IH), 6.66 (dd, IH), 5.40 (br s, IH), 4.16 (br s, 2H) 4.04 (m, IH), 3.44 (s, 2H), 2.19 (s, 3H), 1.08 (d, 6H).
Step C: Preparation of l-(3-chloro-2-pyridinyl)-N-r2-methyl-
6-r2-r(l-methylethyl)aminol-2-oxoethyllphenyl1-3-(trifluoromethylVlH-pyrazole- 5-carboxamide
To a slurry of l-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-lH-pyrazole-5-carboxylic acid (for preparation see WO 02/48115, 0.19 g, 0.66 mmol) in 10 mL of dichloromethane was added oxalyl chloride (0.087 mL, 1.0 mmol) and two drops of N,N-dimethylformamide. The reaction mixture was stirred for 15 minutes, resulting in a solution. The volatiles were removed with a rotary evaporator. The residue was dissolved in 10 mL of tetrahydrofuran, and the solution was added dropwise at 0 °C to 2-amino-3-methyl-iV-(l-methylethyl)- benzeneacetamide (i.e. the title product of Step B) (0.14 g, 0.66 mmol), iV,N-diisopropyl- ethylamine, (0.23 mL, 1.3 mmol) and 4-(dimethylamino)pyridine (5 mg) in 5 mL of tetrahydrofuran. The reaction mixture was stirred overnight at room temperature. Dichloromethane was added and the mixture was washed with water and dried (sodium sulfate). The solvent was removed with a rotary evaporator. The residue was purified by MPLC (40→60% ethyl acetate in hexanes as eluant) to afford the title compound plus an impurity. The material was purified further by MPLC (20→30% ethyl acetate in 1-chlorobutane as eluant) to afford the title product, a compound of the present invention, as a white solid (0.12 g), m.p. 206-207 0C. lH NMR (CDCl3) δ 10.78 (br s, IH), 8.48 (dd, IH), 8.70 (dd, IH), 7.40 (dd, IH), 7.34 (s, 3H), 7.11 (m, 2H), 6.97 (m, IH), 5.65 (br d, IH), 4.05 (m, IH), 3.44 (s, 2H), 2.22 (s, 3H), 1.15 (d, 6H). EXAMPLE 2
Preparation of l-(3-chloro-2-pyridinyl)-N-r2-r(diethylamino)oxoacetyll- 4,6-dimethylphenyll-3-(trifluoromethyD-lH-pyrazole-5-carboxamide
Step A: Preparation of 2-amino-N,N-diethyl-3,5-dimethyl-α-oxobenzeneacetamide
A mixture of 5,7-dimethyl-lH-indole-2,3-dione (1.0 g, 5.7 mmol), diethylamine (2.9 mL, 29 mmol), water (1.7 mL) and methanol (5.7 mL) was heated at 60 °C for 15 h. The resulting mixture was diluted with acetonitrile (100 mL) and concentrated onto silica gel (3 g). The resulting material was purified by MPLC on a silica gel column eluted with a gradient of 30% to 50% ethyl acetate in hexanes to afford 1.31 g of the title compound as a tacky solid. 1H NMR (CDCl3) 5 7.11 (d, IH), 7.08 (d, IH), 6.25 (br s, 2H), 3.56 (q, 2H), 3.23 (q, 2H), 2.19 (s, 3H), 2.15 (s, 3H), 1.29 (t, 3H), 1.15 (t, 3H).
Step B: Preparation of l-(3-chloro-2-pyridinyl)-N-r2-r(diethylamino)oxoacetyll-4,6- dimethylphenyn-3-(trifluoromethyl)-lH-pyrazole-5-carboxamide A suspension of l-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-lH-pyrazole- 5-carboxylic acid (1.5 g, 5.1 mmol) and dichloromethane (15 mL) was treated successively with oxalyl chloride (0.67 mL, 7.7 mmol) and iV,N-dimethylformamide (1 drop) with stirring at 25°C. Gas evolution occurred over ca. 30 minutes and the mixture gradually became homogeneous. After stirring for 2 h at 25 °C the brown solution was concentrated, the residue was dissolved in 1,2-dichloroethane (20 mL) and the resulting solution was concentrated. The residue was dissolved in 1,2-dichloroethane (13 mL), and an aliquot (3.3 mL) of this solution was added to 2-amino-N,N-diethyl-3,5-dimethyl-α-oxobenzene- acetamide (i.e. the title product of Step A) (266 mg, 1.1 mmol). The resulting solution was cooled in an ice-water bath and treated with N, TV-diisopropylethylamine (0.28 mL, 1.6 mmol). The resulting mixture was stirred at 25 0C for 15 h and then partitioned between ethyl acetate and 0.2 N aqueous hydrochloric acid. The organic layer was washed with saturated aqueous sodium bicarbonate, dried (MgSC^) and concentrated onto 1 g of silica gel. Flash chromatography of the residue on silica gel eluted with 50% ethyl acetate in hexanes gave 470 mg of the title product, a compound of the present invention, as a tacky solid.
IH NMR (CDCl3) δ 9.98 (br s, IH), 8.48 (d, IH), 7.85 (d, IH), 7.43 (s, IH), 7.43-7.39 (m, IH), 7.33 (s, IH), 7.29 (s, IH), 3.50 (q, 2H), 3.18 (q, 2H), 2.33 (s, 3H), 2.19 (s, 3H), 1.24 (t, 3H), 1.11 (t, 3H).
EXAMPLE 3
Preparation of l-(3-chloro-2-pyridinyl)-N-r2-r(lZ)-2-(diethylamino')-l-(hvdroxyimino)- 2-oxoethyll-4,6-dimethylphenyll-3--(trifluoiOmethyl)-lH-pyrazole-5-carboxamide
A solution of hydroxylamine hydrochloride (50 mg, 0.71 mmol) in water (0.5 mL) was added to a solution of l-(3-chloro-2-pyridinyl)-N-[2-[(diethylamino)oxoacetyl]- 4,6-dimethylphenyl]-3-(trifluoromethyl)-lH-pyrazole-5-carboxamide (i.e. the title product of Example 2, 124 mg, 0.24 mmol) in ethanol (5 mL) at 25°C. The resulting mixture was treated with a solution of sodium acetate (200 mg) in water (2 mL). The resulting mixture was heated at reflux for 3 days and then cooled to 25°C, diluted with ethanol (30 mL) and concentrated onto silica gel (0.5 g). The residue was purified by flash chromatography on silica gel eluted with 35% ethyl acetate in hexanes to give 50 mg of the title product, a compound of the present invention, as a yellow glassy solid.
1H NMR (CDCl3) δ 9.64 (s, IH), 8.40 (d, IH), 7.83 (d, IH), 7.39 (dd, IH), 7.31 (s, IH), 6.98 (s, IH), 6.91 (s, IH), 3.52 (q, 2H), 3.15 (q, 2H), 2.22 (s, 3H), 2.11 (s, 3H), 1.28-1.18 (m, 6H) .
EXAMPLE 4
Preparation of 2-rrr3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazol-5-yllcarbonynamino1- S-chloro-S-methyl-α-oxobenzeneacetic acid
To a suspension of 3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazole-5-carboxylic acid (see PCT Patent Publication WO 03/015519 for preparation) (97.6% purity, 3.25 g, 10.5 mmol) and 5-chloro-7-methylindoline-2,3-dione (K. Tsuji et al., Bioorg. Med. Chem. Letters, 2002, 12(17), pp 2427-2430) (1.96 g, 10.0 mmol) in dry acetonitrile (12 mL) was added 3-picoline (2.60 g, 28 mmol). The mixture was cooled to 0 °C, and then methanesulfonyl chloride (1.48 g, 12.9 mmol) was added dropwise at 0-10 °C. After stirring 5 minutes at this temperature, the mixture was warmed to room temperature for 2 hours. Then additional quantities of 3-picoline (0.37 g, 4.0 mmol) and methanesulfonyl chloride (0.24 g, 2.1 mmol) were added, and stirring was continued at room temperature for 3 hours. The mixture was cooled to 0 °C, water (6 mL) was added dropwise, and stirring at 0-5 0C was continued for 1 hour. Then the mixture was filtered, and the solids were washed with 2:1 acetonitrile-water (3 x 3 mL), and dried under nitrogen to afford the 3-picoline salt of the title compound as a light green solid, 1.23 g. The isolated solid was suspended in acetonitrile (3 mL) and IN aqueous hydrochloric acid (3 mL) was added dropwise. The solids dissolved, and then a new precipitate formed. The mixture was stirred at room temperature for 1 hour, and the precipitate was filtered, washed with 1 : 1 acetonitrile-water (3 x 2 mL), and dried under nitrogen to afford the title product, a compound of the present invention, as an off-white solid, 0.27 g (5.6% yield), m.p. 139-142 0C.
1H NMR (DMSO-^6) δ 2.22 (s, 3H), 7.29 (s, IH), 7.58 (d, J = 2.4 Hz, IH), 7.61 (dd, J = 8.2, 4.6 Hz, IH), 7.71 (d, J = 2.4 Hz, IH), 8.17 (dd, / = 8.2, 1.4 Hz, IH), 8.49 (dd, J = 4.6, 1.4 Hz, IH), 10.57 (br s, IH). EXAMPLE 5
Preparation of l-rr3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazol-5-yllcarbonyl1-5-chloro- 7-methyl- lH-indole-2,3-dione
To a suspension of 3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazole-5-carboxylic acid (see PCT Patent Publication WO 03/015519 for preparation) (97.6% purity, 13.02 g, 42 mmol) and 5-chloro-7-methylindoline-2,3-dione (K. Tsuji et al., Bioorg. Med. Chem. Letters, 2002, 72(17), pp 2427-2430) (7.82 g, 40 mmol) in dry acetonitrile (50 mL) was added 3-picoline (11.9 g, 127 mmol). The mixture was cooled to 0 °C, and then methanesulfonyl chloride (6.87 g, 60 mmol) was added dropwise at 0-10 0C. After stirring 5 minutes at this temperature, the mixture was warmed to room temperature for 20 hours. The precipitated solids were filtered, washed with acetonitrile (3 x 5 mL), and dried under nitrogen to afford the title product, a compound of the present invention, as a yellow powder, 14.90 g (77.6% yield), m.p. 173-177 0C (decomp.).
1H NMR (CDCl3) δ 2.16 (s, 3H), 7.14 (s, IH), 7.38 (dd, J = 8.1, 4.8 Hz, IH), 7.53 (d, /= 2.1 Hz, IH), 7.60 (d, /= 2.1 Hz, IH), 7.89 (dd, /= 8.1, 1.5 Hz, IH), 8.39 (dd, / = 4.8, 1.5 Hz, IH). The NMR spectrum also showed that some 3-picoline salts were present in the crude product.
EXAMPLE 6
Preparation of 3-bromo-N-r4-chloro-2-methyl-6-r(lE)-2-(methylamino)-l-(methylimino)- 2-oxoethyl1phenyll-l-(3-chloro-2-pyridinylVlH-pyrazole-5-carboxamide A suspension of l-[[3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazol-5-yl]carbonyl]-
5-chloro-7-methyl-lH-indole-2,3-dione (i.e. the crude product of Example 5) (4.80 g,
10 mmol) in acetonitrile (15 mL) was cooled to -10 °C, and liquefied methylamine (0.35 g,
11 mmol) was added. The mixture was stirred for 1 hour at -10 °C, then warmed to 0 0C, and three more portions of liquefied methylamine (each 0.35 g, 11 mmol) were added periodically. Finally the reaction mass was filtered, and the solids were washed with acetonitrile (3 x 2 mL) and dried under nitrogen to afford the title product, a compound of the present invention, as off-white solids, 1.09 g. Almost immediately, more solids began to precipitate from the filtrate. These were filtered, washed with acetonitrile (3 x 2 mL), and dried under nitrogen to afford a second crop of the title product as light yellow crystals, 2.91 g, m.p. 230-234 0C (decomp.). The total isolated yield from both crops was 4.00 g (76.3%). 1H NMR (CDCl3) δ 2.08 (s, 3H), 2.92 (d, J = 5.1 Hz, IH), 3.11 (s, 3H), 6.85 (d, J = 2.4 Hz, IH), 7.05 (s, IH), 7.21 (dd, J = 2.4, 0.6 Hz, IH), 7.36 (dd, J = 8.0, 4.8 Hz, IH), 7.64 (br quartet, J= 5.1 Hz, IH), 7.83 (dd, J = 8.0, 1.5 Hz, IH), 8.45 (dd, J = 4.8, 1.5 Hz, IH).
EXAMPLE 7
Preparation of 3-bromo-A^-r4-chloro-2-methyl-6-r(methylamino)oxoacetyl1phenyl1- l-(3-chloro-2-pyridinyl)-lH-pyrazole-5-carboxamide To a suspension of 3~bromo-N-[4-chloro-2-methyl-6-[(lE)-2-(methylamino)-
1 -(methylimino)-2-oxoethyl]phenyl] - 1 -(3-chloro-2-pyridinyl)- lH-pyrazole-5-carboxamide (i.e. the product of Example 6) (0.52 g, 1.0 mmol) in acetonitrile (8 mL) was added IN aqueous hydrochloric acid (2.0 mL, 2.0 mmol), and the mixture was stirred for 2 hours at room temperature. Then the mixture was filtered, and the solids were washed with 2:1 acetonitrile-water (3 x 1 mL), and dried under nitrogen to afford the title product, a compound of the present invention, as off-white solids, 0.42 g (83% yield), m.p. 246-247 °C. 1H NMR (DMSO-^6) δ 2.22 (s, 3H), 2.62 (d, J = 4.8 Hz, IH), 7.28 (s, IH), 7.52 (d, / = 2.6 Hz, IH), 7.61 (dd, J = 8.1, 4.8 Hz, IH), 7.65 (d, J = 2.6 Hz, IH), 8.17 (dd, J= 8.1, 1.5 Hz, IH), 8.50 (dd, J = 4.8, 1.5 Hz, IH), 8.57 (br quartet, J = 4.8 Hz, IH). EXAMPLE 8
Alternative method for the preparation of 3-bromo-N-r4-chloro-2-methyl- 6-r(methylamino)oxoacetyllphenyl]-l-(3-chloro-2-pyridinyl)-lH-pyrazole-5-carboxamide
A suspension of l-[[3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazol-5-yl]carbonyl]- 5-chloro-7-methyl-lH-indole-2,3-dione (i.e. the crude product of Example 5) (4.80 g, 10 mmol) in acetonitrile (18 mL) was cooled to -10 0C and liquefied methylamine (1.05 g, 34 mmol) was added. The mixture was stirred for 5 minutes at -10 0C and then for 1 hour at room temperature. Then the mixture was cooled to 0 °C, 6N aqueous hydrochloric acid (6.0 mL, 36 mmol) was added dropwise at 0-10 °C, and the mixture was stirred for 1 hour at 0 0C. The mixture was then filtered, and the solids were washed with 3:1 acetonitrile-water 1H ΝMR (DMSO-^6) δ 2.22 (s, 3H), 2.62 (d, J = 4.8 Hz, IH), 7.28 (s, IH), 7.52 (d, J = 2.6 (3 x 3 mL), then with acetonitrile (3 x 3 mL), and dried under nitrogen to afford the title product, a compound of the present invention, as off-white solids, 3.66 g (71.6% yield).Hz, IH), 7.61 (dd, J = 8.1, 4.8 Hz, IH), 7.65 (d, J = 2.6 Hz, IH), 8.17 (dd, J = 8.1, 1.5 Hz, IH), 8.50 (dd, J = 4.8, 1.5 Hz, IH), 8.57 (br quartet, J = 4.8 Hz, IH). By the procedures described herein together with methods known in the art, the following compounds of Tables 1 to 6 can be prepared. The following abbreviations are used in the Tables which follow: t means tertiary, i means iso, Me means methyl, Et means ethyl, Pr means propyl, /-Pr means isopropyl, Bu means butyl, Ph means phenyl, OMe means methoxy, CN means cyano, 3-Cl-2-Py means 3-chloro-2-pyridinyl.
Figure imgf000028_0001
Rl R2 R6 X R14 R15 B
Me Cl CF3 CH Me H 0
Me Cl Br CH Me H 0
Me Cl Cl CH Me H O
Me Br CF3 CH Me H 0
Me Br Br CH Me H O
Me Br Cl CH Me H 0
Me CN CF3 CH Me H O
Me CN Br CH Me H 0
Me CN Cl CH Me H O
Cl Cl CF3 CH Me H 0
Cl Cl Br CH Me H O
Cl Cl Cl CH Me H O
Br Br CF3 CH Me H O
Br Br Br CH Me H 0
Br Br Cl CH Me H 0
Me Cl CF3 N Me H O
Me Cl Br N Me H O
Me Cl Cl N Me H O
Me Br CF3 N Me H 0
Me Br Br N Me H 0
Me Br Cl N Me H O
Me CN CF3 N Me H 0
Me CN Br N Me H O
Me CN Cl N Me H O R2 R6 X R14 B
Cl Cl CF3 N Me H O
Cl Cl Br N Me H O
Cl Cl Cl N Me H O
Br Br CF3 N Me H O
Br Br Br N Me H O
Br Br Cl N Me H O
Me Cl CF3 CH Et H O
Me Cl Br CH Et H O
Me Cl Cl CH Et H O
Me Br CF3 CH Et H O
Me Br Br CH Et H O
Me Br Cl CH Et H O
Me CN CF3 CH Et H O
Me CN Br CH Et H O
Me CN Cl CH Et H O
Cl Cl CF3 CH Et H O
Cl Cl Br CH Et H O
Cl Cl Cl CH . Et H O
Br Br CF3 CH Et H O
Br Br Br CH Et H O
Br Br Cl CH Et H O
Me Cl CF3 N Et H O
Me Cl Br N Et H O
Me Cl Cl N Et H O
Me Br CF3 N Et H O
Me Br Br N Et H O
Me Br Cl N Et H O
Me CN CF3 N Et H O
Me CN Br N Et H O
Me CN Cl N Et H O
Cl Cl CF3 N Et H O
Cl Cl Br N Et H O
Cl Cl Cl N Et H O
Br Br CF3 N Et H O
Br Br Br N Et H O
Br Br , Cl N Et H O
Me Cl CF3 CH i-Pr H O R2 R6 X R14 R15 B
Me Cl Br CH z-Pr H O
Me Cl Cl CH /-Pr H O
Me Br CF3 CH z-Pr H O
Me Br Br CH /-Pr H O
Me Br Cl CH /-Pr H O
Me CN CF3 CH /-Pr H O
Me CN Br CH i-Pr H O
Me CN Cl CH j-Pr H O
Cl Cl CF3 CH /-Pr H O
Cl Cl Br CH /-Pr H O
Cl Cl Cl CH /-Pr H O
Br Br CF3 CH /-Pr H O
Br Br Br CH /-Pr H O
Br Br Cl CH /-Pr H O
Me Cl CF3 N /-Pr H O
Me Cl Br N /-Pr H O
Me Cl Cl N /-Pr H O
Me Br CF3 N /-Pr H O
Me Br Br N /-Pr H O
Me Br Cl N /-Pr H O
Me CN CF3 N /-Pr H O
Me CN Br N /-Pr H O
Me CN Cl N /-Pr H O
Cl Cl CF3 N /-Pr H O
Cl Cl Br N /-Pr H O
Cl Cl Cl N /-Pr H O
Br Br CF3 N /-Pr H O
Br Br Br N /-Pr H O
Br Br Cl N /-Pr H O
Me Cl CF3 CH t-Bu H O
Me Cl Br CH t-Bu H O
Me Cl Cl CH t-Bu H O
Me Br CF3 CH J-Bu H O
Me Br Br CH t-Bu H O
Me Br Cl CH t-Bu H O
Me CN CF3 CH t-Bu H O
Me CN Br CH t-Bu H O R2 R6 X R14 R15 B
Me CN Cl CH t-Bu H O
Cl Cl CF3 CH t-Bu H O
Cl Cl Br CH f-Bu H O
Cl Cl Cl CH t-Bu H O
Br Br CF3 CH t-Bu H O
Br Br Br CH f-Bu H O
Br Br Cl CH t-Bu H O
Me Cl CF3 N t-Bu H O
Me Cl Br N • t-Bu H O
Me Cl Cl N t-Bu H O
Me Br CF3 N t-Bu H O
Me Br Br N t-Bu H O
Me Br Cl N t-Bu H O
Me CN CF3 N t-Bu H O
Me CN Br N t-Bu H O
Me CN Cl N t-Bu H O
Cl Cl CF3 N t-Bu H O
Cl Cl Br N t-Bu H O
Cl Cl Cl N t-Bu H O
Br Br CF3 N t-Bu H O
Br Br Br N t-Bu H O
Br Br Cl N t-Bu H O
Me Cl CF3 CH Me Me O
Me Cl Br CH Me Me O
Me Cl Cl CH Me Me O
Me Br CF3 CH Me Me O
Me Br Br CH Me Me O
Me Br Cl CH Me Me O
Me CN CF3 CH Me Me O
Me CN Br CH Me Me O
Me CN Cl CH Me Me O
Cl Cl CF3 CH Me Me O
Cl Cl Br CH Me Me O
Cl Cl Cl CH Me Me O
Br Br CF3 CH Me Me O
Br Br Br CH Me Me O
Br Br Cl CH Me Me O Rl R2 R6 X R 14 R15 B
Me Cl CF3 N Me Me O
Me Cl Br N Me Me O
Me Cl Cl N Me Me O
Me Br CF3 N Me Me O
Me Br Br N Me Me O
Me Br Cl N ■ Me Me O
Me CN CF3 N Me Me O
Me CN Br N Me Me O
Me CN Cl N Me Me O
Cl Cl CF3 N Me Me O
Cl Cl Br N Me Me O
Cl Cl Cl N Me Me O
Br Br CF3 N Me Me O
Br Br Br N Me Me O
Br Br Cl N Me Me O
Me Cl CF3 N Me H NMe
Me Cl Br N Me H NMe
Me Cl Cl N Me H NMe
Me Br CF3 N Me H NMe
Me Br Br N Me H NMe
Me Br Cl N Me H NMe
Me CN CF3 N Me H NMe
Me CN Br N Me H NMe
Me CN Cl N Me H NMe
Me Cl CF3 N Me H NOMe
Me Cl Br N Me H NOMe
Me Cl Cl N Me H NOMe
Me Br CF3 N Me H NOMe
Me Br Br N Me H NOMe
Me Br Cl N Me H NOMe
Me CN CF3 N Me H NOMe
Me CN Br N Me H NOMe
Me CN Cl N Me H NOMe
Me Cl CF3 N Me H NNMe2
Me Cl Br N Me H NNMe2
Me Cl Cl N Me H NNMe2
Me Br CF3 N Me H NNMe2 Rl R^ R6 X R14 RlS B
Me Br Br N Me H NNMe2
Me Br Cl N Me H NNMe2
Me CN CF3 N Me H NNMe2
Me CN Br N Me H NNMe2
Me CN Cl N Me H NNMe2
Table 2
Figure imgf000033_0001
J-2 J-3 J-5 J-6
J Rl R2 R7 R8 R14
J-2 Me Cl 2-Cl-Ph CH2CF3 Me
J-2 Me Cl 2-Cl-Ph CHF2 Me
J-2 Me Cl 3-Cl-2-Py CH2CF3 Me
J-2 Me Cl 3-Cl-2-Py CHF2 Me
J-2 Me CN 2-Cl-Ph CH2CF3 Me
J-2 Me CN 2-Cl-Ph CHF2 Me
J-2 Me CN 3-Cl-2-Py CH2CF3 Me
J-2 Me CN 3-Cl-2-Py CHF2 Me
J-2 Cl Cl 2-Cl-Ph CH2CF3 Me
J-2 Cl Cl 2-Cl-Ph CHF2 Me
J-2 Cl Cl 3-Cl-2-Py CH2CF3 Me
J-2 Cl Cl 3-Cl-2-Py CHF2 Me
J-2 Br Br 2-Cl-Ph CH2CF3 Me
J-2 Br Br 2-Cl-Ph CHF2 Me
J-2 Br Br 3-Cl-2-Py CH2CF3 Me
J-2 Br Br 3-Cl-2-Py CHF2 Me J Rl R2 R7 R8 R14
J-3 Me Cl 2-Cl-Ph CH2CF3 Me
J-3 Me Cl 2-Cl-Ph CHF2 Me
J-3 Me Cl 3-Cl-2-Py CH2CF3 Me
J-3 Me Cl 3-Cl-2-Py CHF2 Me
J-3 Me CN 2-Cl-Ph CH2CF3 Me
J-3 Me CN 2-Cl-Ph CHF2 Me
J-3 Me CN 3-Cl-2-Py CH2CF3 Me
J-3 Me CN 3-Cl-2-Py CHF2 Me
J-3 Cl Cl 2-Cl-Ph CH2CF3 Me
J-3 Cl Cl 2-Cl-Ph CHF2 Me
J-3 Cl Cl 3-Cl-2-Py CH2CF3 Me
J-3 Cl Cl 3-Cl-2-Py CHF2 Me
J-3 Br Br 2-Cl-Ph CH2CF3 Me
J-3 Br Br 2-Cl-Ph CHF2 Me
J-3 Br Br 3-Cl-2-Py CH2CF3 Me
J-3 Br Br 3-Cl-2-Py CHF2 Me
J-5 Me Cl 2-Cl-Ph CH2CF3 Me
J-5 Me Cl 2-Cl-Ph CHF2 Me
J-5 Me Cl 3-Cl-2-Py CH2CF3 Me
J-5 Me Cl 3-Cl-2-Py CHF2 Me
J-5 Me CN 2-Cl-Ph CH2CF3 Me
J-5 Me CN 2-Cl-Ph CHF2 Me
J-5 Me CN 3-Cl-2-Py CH2CF3 Me
J-5 Me CN 3-Cl-2-Py CHF2 Me
J-5 Cl Cl 2-Cl-Ph CH2CF3 Me
J-5 Cl Cl 2-Cl-Ph CHF2 Me
J-5 Cl Cl 3-Cl-2-Py CH2CF3 Me
J-5 Cl Cl 3-Cl-2-Py CHF2 Me
J-5 Br Br 2-Cl-Ph CH2CF3 Me
J-5 Br Br 2-Cl-Ph CHF2 Me
J-5 Br Br 3-Cl-2-Py CH2CF3 Me
J-5 Br Br 3-Cl-2-Py CHF2 Me
J-6 Me Cl 2-Cl-Ph CH2CF3 Me
J-6 Me Cl 2-Cl-Ph CHF2 Me
J-6 Me Cl 3-Cl-2-Py CH2CF3 Me
J-6 Me Cl 3-Cl-2-Py CHF2 Me
J-6 Me CN 2-Cl-Ph CH2CF3 Me J Rl R2 R7 R8 R!4
J-6 Me CN 2-Cl-Ph CHF2 Me
J-6 Me CN 3-Cl-2-Py CH2CF3 Me
J-6 Me CN 3-Cl-2-Py CHF2 Me
J-6 Cl Cl 2-Cl-Ph CH2CF3 Me
J-6 Cl Cl 2-Cl-Ph CHF2 Me
J-6 Cl Cl 3-Cl-2-Py CH2CF3 Me
J-6 Cl Cl 3-Cl-2-Py CHF2 Me
J-6 Br Br 2-Cl-Ph CH2CF3 Me
J-6 Br Br 2-Cl-Ph CHF2 Me
J-6 Br Br 3-Cl-2-Py CH2CF3 Me
J-6 Br Br 3-Cl-2-Py CHF2 Me
J-2 Me Cl 2-Cl-Ph CH2CF3 J-Pr
J-2 Me Cl 2-Cl-Ph CHF2 /-Pr
J-2 Me Cl 3-Cl-2-Py CH2CF3 /-Pr
J-2 Me Cl 3-Cl-2-Py CHF2 /-Pr
J-2 Me CN 2-Cl-Ph CH2CF3 /-Pr
J-2 Me CN 2-Cl-Ph CHF2 /-Pr
J-2 Me CN 3-Cl-2-Py CH2CF3 /-Pr
J-2 Me CN 3-Cl-2-Py CHF2 /-Pr
J-2 Cl Cl 2-Cl-Ph CH2CF3 /-Pr
J-2 Cl Cl 2-Cl-Ph CHF2 /-Pr
J-2 Cl Cl 3-Cl-2-Py CH2CF3 /-Pr
J-2 Cl Cl 3-Cl-2-Py CHF2 /-Pr
J-2 Br Br 2-Cl-Ph CH2CF3 /-Pr
J-2 Br Br 2-Cl-Ph CHF2 /-Pr
J-2 Br Br 3-Cl-2-Py CH2CF3 /-Pr
J-2 Br Br 3-Cl-2-Py CHF2 /-Pr
J-3 Me Cl 2-Cl-Ph CH2CF3 /-Pr
J-3 Me Cl 2-Cl-Ph CHF2 /-Pr
J-3 Me Cl 3-Cl-2-Py CH2CF3 /-Pr
J-3 Me Cl 3-Cl-2-Py CHF2 /-Pr
J-3 Me CN 2-Cl-Ph CH2CF3 /-Pr
J-3 Me CN 2-Cl-Ph CHF2 /-Pr
J-3 Me CN 3-Cl-2-Py CH2CF3 /-Pr
J-3 Me CN 3-Cl-2-Py CHF2 /-Pr
J-3 Cl Cl 2-Cl-Ph CH2CF3 /-Pr
J-3 Cl Cl 2-Cl-Ph CHF2 /-Pr J Rl R2 R7 R8 Rl4
J-3 Cl Cl 3-Cl-2-Py CH2CF3 i-Pr
J-3 Cl Cl 3-Cl-2-Py CHF2 i-Pr
J-3 Br Br 2-Cl-Ph CH2CF3 i-Pr
J-3 Br Br 2-Cl-Ph CHF2 j-Pr
J-3 Br Br 3-Cl-2-Py CH2CF3 j-Pr
J-3 Br Br 3-Cl-2-Py CHF2 (-Pr
J-5 Me Cl 2-Cl-Ph CH2CF3 i-Pr
J-5 Me Cl 2-Cl-Ph CHF2 i-Pr
J-5 Me Cl 3-Cl-2-Py CH2CF3 i-Pr
J-5 Me Cl 3-Cl-2-Py CHF2 j-Pr
J-5 Me CN 2-Cl-Ph CH2CF3 j-Pr
J-5 Me CN 2-Cl-Ph CHF2 i-Pr
J-5 Me CN 3-Cl-2-Py CH2CF3 i-Pr
J-5 Me CN 3-Cl-2-Py CHF2 /-Pr
J-5 Cl Cl 2-Cl-Ph CH2CF3 i-Pr
J-5 Cl Cl 2-Cl-Ph CHF2 J-Pr
J-5 Cl Cl 3-Cl-2-Py CH2CF3 J-Pr
J-5 Cl Cl 3-Cl-2-Py CHF2 J-Pr
J-5 Br Br 2-Cl-Ph CH2CF3 i-Pr
J-5 Br Br 2-Cl-Ph CHF2 i-Pr
J-5 Br Br 3-Cl-2-Py CH2CF3 i-Pr
J-5 Br Br 3-Cl-2-Py CHF2 i-Pr
J-6 Me Cl 2-Cl-Ph CH2CF3 j-Pr
J-6 Me Cl 2-Cl-Ph CHF2 j-Pr
J-6 Me Cl 3-Cl-2-Py CH2CF3 j-Pr
J-6 Me Cl 3-Cl-2-Py CHF2 j-Pr
J-6 Me CN 2-Cl-Ph CH2CF3 j-Pr
J-6 Me CN 2-Cl-Ph CHF2 j-Pr
J-6 Me CN 3-Cl-2-Py CH2CF3 z-Pr
J-6 Me CN 3-Cl-2-Py CHF2 /-Pr
J-6 Cl Cl 2-Cl-Ph CH2CF3 j-Pr
J-6 Cl Cl 2-Cl-Ph CHF2 j-Pr
J-6 Cl Cl 3-Cl-2-Py CH2CF3 j-Pr
J-6 Cl Cl 3-Cl-2-Py CHF2 j-Pr
J-6 Br Br 2-Cl-Ph CH2CF3 j-Pr
J-6 Br Br 2-Cl-Ph CHF2 j-Pr
J-6 Br Br 3-Cl-2-Py CH2CF3 j-Pr J Rl R2 R7 R8 R14
J-6 Br Br 3-Cl-2-Py CHF2 j-Pr
Table 3
Figure imgf000037_0001
Rl R2 R7 R6 Rl4
J-4 Me Cl 2-Cl-Ph 4-Br Me
J-4 Me Cl 2-Cl-Ph 5-Br Me
J-4 Me Cl 3-Cl-2-Py 4-Br Me
J-4 Me Cl 3-Cl-2-Py 5-Br Me
J-4 Me CN 2-Cl-Ph 4-Br Me
J-4 Me CN 2-Cl-Ph 5-Br Me
J-4 Me CN 3-Cl-2-Py 4-Br Me
J-4 Me CN 3-Cl-2-Py 5-Br Me
J-4 Cl Cl 2-Cl-Ph 4-Br Me
J-4 Cl Cl 2-Cl-Ph 5-Br Me
J-4 Cl Cl 3-Cl-2-Py 4-Br Me
J-4 Cl Cl 3-Cl-2-Py 5-Br Me
J-4 Br Br 2-Cl-Ph 4-Br Me
J-4 Br Br 2-Cl-Ph 5-Br Me
J-4 Br Br 3-Cl-2-Py 4-Br Me
J-4 Br Br 3-Cl-2-Py 5-Br Me
J-7 Me Cl 2-Cl-Ph CF3 Me
J-7 Me Cl 3-Cl-2-Py CF3 Me
J-7 Me CN 2-Cl-Ph CF3 Me
J-7 Me CN ' 3-Cl-2-Py CF3 Me
J-7 Cl Cl 2-Cl-Ph CF3 Me J R1 R2 R7 R6 R14
J-7 Cl Cl 3-Cl-2-Py CF3 Me
J-7 Br Br 2-Cl-Ph CF3 Me
J-7 Br Br 3-Cl-2-Py CF3 Me
J-8 Me Cl 2-Cl-Ph CF3 Me
J-8 Me Cl 3-Cl-2-Py CF3 Me
J-8 Me CN 2-Cl-Ph CF3 Me
J-8 Me CN 3-Cl-2-Py CF3 Me
J-8 Cl Cl 2-Cl-Ph CF3 Me
J-8 Cl Cl 3-Cl-2-Py CF3 Me
J-8 Br Br 2-Cl-Ph CF3 Me
J-8 Br Br 3-Cl-2-Py CF3 Me
J-4 Me Cl 2-Cl-Ph 4-Br /-Pr
J-4 Me Cl 2-Cl-Ph 5-Br /-Pr
J-4 Me Cl 3-Cl-2-Py 4-Br j-Pr
J-4 Me Cl 3-Cl-2-Py 5-Br /-Pr
J-4 Me CN 2-Cl-Ph 4-Br /-Pr
J-4 Me CN 2-Cl-Ph 5-Br /-Pr
J-4 Me CN 3-Cl-2-Py 4-Br J-Pr
J-4 Me CN 3-Cl-2-Py 5-Br /-Pr
J-4 Cl Cl 2-Cl-Ph 4-Br /-Pr
J-4 Cl Cl 2-Cl-Ph 5-Br J-Pr
J-4 Cl Cl 3-Cl-2-Py 4-Br /-Pr
J-4 Cl Cl 3-Cl-2-Py 5-Br /-Pr
J-4 Br Br 2-Cl-Ph 4-Br /-Pr
J-4 Br Br 2-Cl-Ph 5-Br /-Pr
J-4 Br Br 3-Cl-2-Py 4-Br /-Pr
J-4 Br Br 3-Cl-2-Py 5-Br /-Pr
J-7 Me Cl 2-Cl-Ph CF3 /-Pr
J-7 Me Cl 3-Cl-2-Py CF3 /-Pr
J-7 Me CN 2-Cl-Ph CF3 /-Pr
J-7 Me CN 3-Cl-2-Py CF3 /-Pr
J-7 Cl Cl 2-Cl-Ph CF3 /-Pr
J-7 Cl Cl 3-Cl-2-Py CF3 /-Pr
J-7 Br Br 2-Cl-Ph CF3 /-Pr
J-7 Br Br 3-Cl-2-Py CF3 /-Pr
J-8 Me Cl 2-Cl-Ph CF3 /-Pr
J-8 Me Cl 3-Cl-2-Py CF3 /-Pr Rl R2 R7 R6 R14
J-8 Me CN 2-Cl-Ph CF3 j-Pr
J-8 Me CN 3-Cl-2-Py CF3 /-Pr
J-8 Cl Cl 2-Cl-Ph CF3 i-Pr
J-8 Cl Cl 3-Cl-2-Py CF3 /-Pr
J-8 Br Br 2-Cl-Ph CF3 /-Pr
J-8 Br Br 3-Cl-2-Py CFc1 /-Pr
Table 4
Figure imgf000039_0001
Rl R2 R6 X RH Rl2 R14 Rl5
Me Cl CF3 CH H H Me H
Me Cl Br CH H H Me H
Me Cl Cl CH H H Me H
Me Br CF3 CH H H Me H
Me Br Br CH H H Me H
Me Br Cl CH H H Me H
Me CN CF3 CH H H Me H
Me CN Br CH H H Me H
Me CN Cl CH H H Me H
Cl Cl CF3 CH H H Me H
Cl Cl Br CH H H Me H
Cl Cl Cl CH H H Me H
Br Br CF3 CH H H Me H
Br Br Br CH H H Me H
Br Br Cl CH H H Me H
Me Cl CF3 N H H Me H
Me Cl Br N H H Me H
Me Cl Cl N H H Me H
Me Br CF3 N H H Me H Rl R2 R6 X RH R12 R14 R15
Me Br Br N H H Me H
Me Br Cl N H H Me H
Me CN CF3 N H H Me H
Me CN Br N H H Me H
Me CN Cl N H H Me H
Cl Cl CF3 N H H Me H
Cl Cl Br N H H Me H
Cl Cl Cl N H H Me H
Br Br CF3 N H H Me H
Br Br Br N H H Me H
Br Br Cl N H H Me H
Me Cl CF3 CH H H Et H
Me Cl Br CH H H Et H
Me Cl Cl CH H H Et H
Me Br CF3 CH H H Et H
Me Br Br CH H H Et H
Me Br Cl CH H H Et H
Me CN CF3 CH H H Et H
Me CN Br CH H H Et H
Me CN Cl CH H H Et H
Cl Cl CF3 CH H H Et H
Cl Cl Br CH H H Et H
Cl Cl Cl CH H H Et H
Br Br CF3 CH H H Et H
Br Br Br CH H H Et H
Br Br Cl CH H H Et H
Me Cl CF3 N H H Et H
Me Cl Br N H H Et H
Me Cl Cl N H H Et H
Me Br CF3 N H H Et H
Me Br Br N H H Et H
Me Br Cl N H H Et H
Me CN CF3 N H H Et H
Me CN Br N H H Et H
Me CN Cl N H H Et H
Cl Cl CF3 N H H Et H
Cl Cl Br N H H Et H Rl R2 R6 X RH Rl2 R14 R15
Cl Cl Cl N H H Et H
Br Br CF3 N H H Et H
Br Br Br N H H Et H
Br Br Cl N H H Et H
Me Cl CF3 CH H H j-Pr H
Me Cl Br CH H H i-Pr H
Me Cl Cl CH H H i-Pr H
Me Br CF3 CH H H i-Pr H
Me Br Br CH H H i-Pr H
Me Br Cl CH H H i-Pr H
Me CN CF3 CH H H i-Pr H
Me CN Br CH H H i-Pr H
Me CN Cl CH H H z-Pr H
Cl Cl CF3 CH H H i-Pr H
Cl Cl Br CH H H i-Pr H
Cl Cl Cl CH H H i-Pr H
Figure imgf000041_0001
Br Br Br CH H H i-Pr H
Br Br Cl CH H H i-Pr H
Me Cl CF3 N H H i-Pr H
Me Cl Br N H H i-Pr H
Me Cl Cl N H H /-Pr H
Me Br CF3 N H H i-Pr H
Me Br Br N H H i-Pr H
Figure imgf000041_0002
Me CN CF3 N H H i-Pr H
Me CN Br N H H i-Pr H
Me CN Cl N H H i-Pr H
Cl Cl CF3 N H H i-Pr H
Cl Cl Br N H H i-Pr H
Cl Cl Cl N H H i-Pr H
Br Br CF3 N H H i-Pr H
Br Br Br N H H i-Pr H
Br Br Cl N H H i-Pr H
Me Cl CF3 CH H H t-Bu H
Me Cl Br CH H H f-Bu H
Me Cl Cl CH H H t-Bu H Rl R2 R6 X RH Rl2 Rl4 RlS
Me Br CF3 CH H H t-Bu H
Me Br Br CH H H f-Bu H
Me Br Cl CH H H t-Bu H
Me CN CF3 CH H H t-Bu H
Me CN Br CH H H t-Bu H
Me CN Cl CH H H t-Bu H
Cl Cl CF3 CH H H t-Bu H
Cl Cl Br CH H H t-Bu H
Cl Cl Cl CH H H t-Bu H
Br Br CF3 CH H H t-Bu H
Br Br Br CH H H t-Bu H
Br Br Cl CH H H t-Bu H
Me Cl CF3 N H H t-Bu H
Me Cl Br N H H t-Bu H
Me Cl Cl N H H t-Bu H
Me Br CF3 N H H t-Bu H
Me Br Br N H H t-Bu H
Me Br Cl N H H t-Bu H
Me CN CF3 N H H t-Bu H
Me CN Br N H H t-Bu H
Me CN Cl N H H t-Bu H
Cl Cl CF3 N H H t-Bu H
Cl Cl Br N H H t-Bu H
\
Cl Cl Cl N H H *-Bu H
Br Br CF3 N H H *-Bu H
Br Br Br N H H *-Bu H
Br Br Cl N H H t-Bu H
Me Cl CF3 CH H H Me Me
Me Cl Br CH H H Me Me
Me Cl Cl CH H H Me Me
Me Br CF3 CH H H Me Me
Me Br Br CH H H Me Me
Me Br Cl CH H H Me Me
Me CN CF3 CH H H Me Me
Me CN Br CH H H Me Me
Me CN Cl CH H H Me Me
Cl Cl CF3 CH H H Me Me Rl R2 R6 X RH R12 R14 Rl5
Cl Cl Br CH H H Me Me
Cl Cl Cl CH H H Me Me
Br Br CF3 CH H H Me Me
Br Br Br CH H H Me Me
Br Br Cl CH H H Me Me
Me Cl CF3 N H H Me Me
Me Cl Br N H H Me Me
Me Cl Cl N H H Me Me
Me Br CF3 N H H Me Me
Me Br Br N H H Me Me
Me Br Cl N H H Me Me
Me CN CF3 N H H Me Me
Me CN Br N H H Me Me
Me CN Cl N H H Me Me
Cl Cl CF3 N H H Me Me
Cl Cl Br N H H Me Me
Cl Cl Cl N H H Me Me
Br Br CF3 N H H Me Me
Br Br Br N H H Me Me
Br Br Cl N H H Me Me
Me Cl CF3 N OH H Me H
Me Cl Br N OH H Me H
Me Cl Cl N OH H Me H
Me Br CF3 N OH H Me H
Me Br Br N OH H Me H
Me Br Cl N OH H Me H
Me CN CF3 N OH H Me H
Me CN Br N OH H Me H
Me CN Cl N OH H Me H
Me Cl CF3 N OMe H Me H
Me Cl Br N OMe H Me H
Me Cl Cl N OMe H Me H
Me Br CF3 N OMe H Me H
Me Br Br N OMe H Me H
Me Br Cl N OMe H Me H
Me CN CF3 N OMe H Me H
Me CN Br N OMe H Me H Rl R^ R0 X RH Rl2 R 14 Rl5
Me CN Cl N OMe H Me H
Me Cl CF3 N Me H Me H
Me Cl Br N Me H Me H
Me Cl Cl N Me H Me H
Me Br CF3 N Me H Me H
Me Br Br N Me H Me H
Me Br Cl N Me H Me H
Me CN CF3 N Me H Me H
Me CN Br N Me H Me H
Me CN Cl N Me H Me H
Me Cl CF3 N Me Me Me H
Me Cl Br N Me Me Me H
Me Cl Cl N Me Me Me H
Me Br CF3 N Me Me Me H
Me Br Br N Me Me Me H
Me Br Cl N Me Me Me H
Me CN CF3 N Me Me Me H
Me CN Br N Me Me Me H
Me CN Cl N Me Me Me H
Table 5
Figure imgf000044_0001
R2 R6 X Rl R2 R6 X
Me CN CF3 CH Me CN CF3 N
Me CN Br CH Me CN Br N
Me CN Cl CH Me CN Cl N
Cl Cl CF3 CH Cl Cl CF3 N
Cl Cl Br CH Cl Cl Br N
Cl Cl Cl CH Cl Cl Cl N
Br Br CF3 CH Br Br CF3 N
Br Br Br CH Br Br Br N
Br Br Cl CH Br Br Cl N
Table 6
Figure imgf000045_0001
Rl R2 R6 X Rl R2 R6 X
Me Cl CF3 CH Me Cl CF3 N
Me Cl Br CH Me Cl Br N
Me Cl Cl CH Me Cl Cl N
Me Br CF3 CH Me Br CF3 N
Me Br Br CH Me Br Br N
Me Br Cl CH Me Br Cl N
Me CN CF3 CH Me CN CF3 N
Me CN Br CH Me CN Br N
Me CN Cl CH Me CN Cl N
Cl Cl CF3 CH Cl Cl CF3 N
Cl Cl Br CH Cl Cl Br N
Cl Cl Cl CH Cl Cl Cl N
Br Br CF3 CH Br Br CF3 N
Br Br Br CH Br Br Br N
Br Br Cl CH Br Br Cl N Formulation/Utility
Compounds of this invention will generally be used as a formulation or composition with a suitable carrier comprising at least one of a liquid diluent, a solid diluent or a surfactant. The formulation or composition ingredients are selected to be consistent with the physical properties of the active ingredient, mode of application and environmental factors such as soil type, moisture and temperature. Useful formulations include liquids such as solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like which optionally can be thickened into gels. Useful formulations further include solids such as dusts, powders, granules, pellets, tablets, films (including seed coatings), and the like which can be water-dispersible ("wettable") or water-soluble. Active ingredient can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or "overcoated"). Encapsulation can control or delay release of the active ingredient. Sprayable formulations can be extended in suitable media and used at spray volumes from about one to several hundred liters per hectare. High-strength compositions are primarily used as intermediates for further formulation.
The formulations will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.
Weight Percent Active Ingredient Diluent Surfactant
Water-Dispersible and Water-soluble 0.001-90 0-99.999 0-15
Granules, Tablets and Powders.
Suspensions, Emulsions, Solutions 1-50 40-99 0-50
(including Emulsifiable Concentrates)
Dusts 1-25 70-99 0-5
Granules and Pellets 0.001-99 5-99.999 0-15
High Strength Compositions 90-99 0-10 0-2
Typical solid diluents are described in Watkins, et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, New Jersey. Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon's Detergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, New Jersey, as well as Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964, list surfactants and recommended uses. All formulations can contain minor amounts of additives to reduce foam, caking, corrosion, microbiological growth and the like, or thickeners to increase viscosity. Surfactants include, for example, polyethoxylated alcohols, polyethoxylated alkylphenols, polyethoxylated sorbitan fatty acid esters, dialkyl sulfosuccinates, alkyl sulfates, alkylbenzene sulfonates, organosilicones, iV,./V-dialkyltaurates, lignin sulfonates, naphthalene sulfonate formaldehyde condensates, polycarboxylates, glycerol esters, poly- oxyethylene/polyoxypropylene block copolymers, and alkylpolyglycosides where the number of glucose units, referred to as degree of polymerization (D.P.), can range from 1 to 3 and the alkyl units can range from Cg to C^ (see Pure and Applied Chemistry 72, 1255— 1264). Solid diluents include, for example, clays such as bentonite, montmorillonite, attapulgite and kaolin, starch, sugar, silica, talc, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarbonate, and sodium sulfate. Liquid diluents include, for example, water, N,N-dimethylformamide, dimethyl sulfoxide, JV-alkylpyrrolidone, ethylene glycol, polypropylene glycol, propylene carbonate, dibasic esters, paraffins, alkylbenzenes, alkylnaphthalenes, glycerine, triacetine, oils of olive, castor, linseed, tung, sesame, corn, peanut, cotton-seed, soybean, rape-seed and coconut, fatty acid esters, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxy-4-methyl-2-pentanone, acetates such as hexyl acetate, heptyl acetate and octyl acetate, and alcohols such as methanol, cyclohexanol, decanol, benzyl and tetrahydrofurfuryl alcohol.
Useful formulations of this invention may also contain materials well known to those skilled in the art as formulation aids such as antifoams, film formers and dyes. Antifoams can include water dispersible liquids comprising polyorganosiloxanes like Rhodorsil® 416. The film formers can include polyvinyl acetates, polyvinyl acetate copolymers, polyvinylpyrrolidone- vinyl acetate copolymer, polyvinyl alcohols, polyvinyl alcohol copolymers and waxes. Dyes can include water dispersible liquid colorant compositions like Pro-lzed® Colorant Red. One skilled in the art will appreciate that this is a non-exhaustive list of formulation aids. Suitable examples of formulation aids include those listed herein and those listed in McCutcheon's 2001, Volume 2: Functional Materials published by MC Publishing Company and PCT Publication WO 03/024222.
Solutions, including emulsifiable concentrates, can be prepared by simply mixing the ingredients. Dusts and powders can be prepared by blending and, usually, grinding as in a hammer mill or fluid-energy mill. Suspensions are usually prepared by wet-milling; see, for example, U.S. 3,060,084. Granules and pellets can be prepared by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, "Agglomeration", Chemical Engineering, December 4, 1967, pp 147—48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and following, and WO 91/13546. Pellets can be prepared as described in U.S. 4,172,714. Water-dispersible and water-soluble granules can be prepared as taught in U.S. 4,144,050, U.S. 3,920,442 and DE 3,246,493. Tablets can be prepared as taught in U.S. 5,180,587, U.S. 5,232,701 and U.S. 5,208,030. Films can be prepared as taught in GB 2,095,558 and U.S. 3,299,566.
For further information regarding the art of formulation, see T. S. Woods, "The Formulator's Toolbox - Product Forms for Modern Agriculture" in Pesticide Chemistry and Bioscience, The Food-Environment Challenge, T. Brooks and T. R. Roberts, Eds., Proceedings of the 9th International Congress on Pesticide Chemistry, The Royal Society of Chemistry, Cambridge, 1999, pp. 120-133. See also U.S. 3,235,361, Col. 6, line 16 through Col. 7, line 19 and Examples 10-41; U.S. 3,309,192, Col. 5, line 43 through Col. 7, line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138-140, 162-164, 166, 167 and 169-182; U.S. 2,891,855, Col. 3, line 66 through Col. 5, line 17 and Examples 1-4; Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, pp 81-96; Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989; and Developments in formulation technology, PJB Publications, Richmond, UK, 2000.
In the following Examples, all percentages are by weight and all formulations are prepared in conventional ways. Compound numbers refer to compounds in Index
Tables A-E. Without further elaboration, it is believed that one skilled in the art using the preceding description can utilize the present invention to its fullest extent. The following
Examples are, therefore, to be constructed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Percentages are by weight except where otherwise indicated.
Example A Wettable Powder
Compound 1 65.0% dodecylphenol polyethylene glycol ether 2.0% sodium ligninsulfonate 4.0% sodium silicoaluminate 6.0% montmorillonite (calcined) 23.0%
Example B
Granule
Compound 11 10.0% attapulgite granules (low volatile matter, 0.71/0.30 mm; 90.0%
U.S. S. No. 25-50 sieves)
Example C
Extruded Pellet
Compound 3 25.0% anhydrous sodium sulfate 10.0% crude calcium ligninsulfonate 5.0% sodium alkylnaphthalenesulfonate 1.0% calcium/magnesium bentonite 59.0%
Example D
Emulsifiable Concentrate
Compound 8 20.0% blend of oil soluble sulfonates and polyoxyethylene ethers 10.0% isophorone 70.0%
Example E
Microemulsion
Compound 12 5.0% polyvinylpyrrolidone- vinyl acetate copolymer 30.0% alkylpolyglycoside 30.0% glyceryl monooleate 15.0% water 20.0%
Example F
Seed Treatment
Compound 14 20.00% polyvinylpyrrolidone- vinyl acetate copolymer 5.00% montan acid wax 5.00% calcium ligninsulfonate 1.00% polyoxyethylene/polyoxypropylene block copolymers 1.00% stearyl alcohol (POE 20) 2.00% polyorganosilane 0.20% colorant red dye 0.05% water 65.75%
Example G
Fertilizer Stick
Compound 1 2.50% pyrrolidone-styrene copolymer 4.80% tristyrylphenyl 16-ethoxylate 2.30% talc 0.80% corn starch 5.00%
Nitrophoska® Permanent 15-9-15 slow-release fertilizer 36.00%
(BASF) kaolin 38.00% water 10.60%
Compounds of this invention are characterized by favorable metabolic and/or soil residual patterns and exhibit activity controlling a spectrum of agronomic and nonagronomic invertebrate pests. Compounds of this invention are also characterized by favorable foliar and or soil-applied systemicity in plants exhibiting translocation to protect foliage and other plant parts not directly contacted with invertebrate pest control compositions comprising the present compounds. In the context of this disclosure "invertebrate pest control" means inhibition of invertebrate pest development (including mortality, feeding reduction, and/or mating disruption) and as a result significant reduction in feeding or injury to an agronomic crop or damage to a building structure caused by the invertebrate pest; related expressions are defined analogously.
The term "agronomic" refers to the production of field crops such as for food and fiber and includes the growth of corn, soybeans and other legumes, rice, cereal (e.g., wheat, oats, barley, rye, rice, maize), leafy vegetables (e.g., lettuce, cabbage, and other cole crops), fruiting vegetables (e.g., tomatoes, pepper, eggplant, crucifers and cucurbits), potatoes, sweet potatoes, grapes, cotton, tree fruits (e.g., pome, stone and citrus), small fruit (berries, cherries) and other specialty crops (e.g., canola, sunflower, olives). The term "agronomic" also refers to the production of such crops that contain genetic material introduced by genetic engineering (i.e. transgenic) or modified by mutagenesis to provide advantageous traits. Examples of such traits include tolerance to herbicides, resistance to phytophagous pests (e.g., insects, mites, aphids, spiders, nematodes, snails, plant-pathogenic fungi, bacteria and viruses), improved plant growth, increased tolerance of adverse growing conditions such as high and low temperatures, low or high soil moisture, and high salinity, increased flowering or fruiting, greater harvest yields, more rapid maturation, higher quality and/or nutritional value of the harvested product, and improved storage or process properties of the harvested products. Transgenic plants can be modified to express multiple traits. Examples of plants containing traits provided by genetic engineering or mutagenesis include varieties of corn, cotton, soybean and potato expressing an insecticidal Bacillus thuringiensis toxin such as YIELD GARD®, KNOCKOUT®, STARLINK®, BOLLGARD®, NuCOTN® and NEWLEAF , and herbicide-tolerant varieties of corn, cotton, soybean and rapeseed such as ROUNDUP READY®, LIBERTY LINK®, IMI®, STS® and CLEARFIELD®, as well as crops expressing N-acetyltransferase (GAT) to provide resistance to glyphosate herbicide, or crops containing the HRA gene providing resistance to herbicides inhibiting acetylactate synthase (ALS).
The term "nonagronomic" refers to other horticultural crops (e.g., greenhouse, nursery or ornamental plants not grown in a field), residential and commercial structures in urban and industrial settings, turf (commercial, golf, residential, recreational, etc.), wood products, stored product, agro-forestry and vegetation management, public health (human) and animal health (domestical animals, pets, livestock, poultry, undomestical animals such as wildlife) applications. For reasons of invertebrate pest control spectrum and economic importance, protection of agronomic crops from damage or injury caused by invertebrate pests by controlling invertebrate pests are embodiments of the invention.
As referred to in this disclosure, the term "invertebrate pest" includes arthropods, gastropods and nematodes of economic importance as pests. The term "arthropod" includes insects, mites, spiders, scorpions, centipedes, millipedes, pill bugs and symphylans. The term "gastropod" includes snails, slugs and other Stylommatophora. The term "nematode" includes all of the helminths, such as: roundworms, heartworms, and phytophagous nematodes (Nematoda), flukes (Tematoda), Acanthocephala, and tapeworms (Cestoda). Compounds of this invention exhibit activity against a wide spectrum of foliar-feeding, fruit-feeding, stem or root feeding, seed-feeding, aquatic and soil-inhabiting invertebrate pests which are pests of growing and stored agronomic crops, forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, public health and animal health. Those skilled in the art will appreciate that not all compounds are equally effective against all growth stages of all pests. Agronomic or nonagronomic pests include eggs, larvae and adults of the order
Lepidoptera, such as armyworms, cutworms, loopers, and heliothines in the family Noctuidae (e.g., fall armyworm (Spodoptera fugiperda J. E. Smith), beet armyworm (Spodoptera exigua Hϋbner), black cutworm (Agrotis ipsilon Hufnagel), cabbage looper {Trichoplusia ni Hϋbner), tobacco budworm {Heliothis virescens Fabricius)); borers, casebearers, webworms, coneworms, cabbageworms and skeletonizers from the family Pyralidae (e.g., European corn borer {Ostrinia nubilalis Hϋbner), navel orangeworm {Amyelois transitella Walker), corn root webworm {Crambus caliginosellus Clemens), sod webworms (Pyralidae: Crambinae) such as sod worm {Herpeto gramma licarsisalis Walker)); leafrollers, budworms, seed worms, and fruit worms in the family Tortricidae (e.g., codling moth {Cydia pomonella Linnaeus), grape berry moth (Endopiza viteana Clemens), oriental fruit moth (Grapholita molesta Busck)); and many other economically important lepidoptera (e.g., diamondback moth (Plutella xylostella Linnaeus), pink bollworm {Pectinophora gossypiella Saunders), gypsy moth {Lymantria dispar Linnaeus)); eggs, nymphs and adults of the order Blattodea including cockroaches from the families Blattellidae and Blattidae (e.g., oriental cockroach {Blatta orientalis Linnaeus), Asian cockroach {Blatella asahinai Mizukubo), German cockroach {Blattella germanica Linnaeus), brownbanded cockroach (Supella longipalpa Fabricius), American cockroach {Periplaneta americana Linnaeus), brown cockroach (Periplaneta brunnea Burmeister), Madeira cockroach {Leucophaea maderae Fabricius)), smoky brown cockroach {Periplaneta fuliginosa Service), Australian cockroach {Periplaneta australasiae Fabr.), lobster cockroach {Nauphoeta cinerea Olivier) and smooth cockroach {Symploce pollens Stephens)); eggs, foliar feeding, fruit feeding, root feeding, seed feeding and vesicular tissue feeding larvae and adults of the order Coleoptera including weevils from the families Anthribidae, Bruchidae, and Curculionidae (e.g., boll weevil (Anthonomus grandis Boheman), rice water weevil {Lissorhoptrus oryzophilus Kuschel), granary weevil {Sitophilus granarius Linnaeus), rice weevil (Sitophilus oryzae Linnaeus)), annual bluegrass weevil (Listronotus maculicollis Dietz), bluegrass billbug {Sphenophorus parvulus Gyllenhal), hunting billbug {Sphenophorus venatus vestitus), Denver billbug {Sphenophorus cicatristriatus Fahraeus)); flea beetles, cucumber beetles, rootworms, leaf beetles, potato beetles, and leafminers in the family Chrysomelidae (e.g., Colorado potato beetle {Leptinotarsa decemlineata Say), western corn rootworm {Diabrotica virgifera virgifera LeConte)); chafers and other beetles from the family Scaribaeidae (e.g., Japanese beetle {Popillia japonica Newman), oriental beetle {Anomala orientalis Waterhouse), northern masked chafer {Cyclocephala borealis Arrow), southern masked chafer {Cyclocephala immaculata Olivier), black turfgrass ataenius {Ataenius spretulus Haldeman), green June beetle {Cotinis nitida Linnaeus), Asiatic garden beetle {Maladera castanea Arrow), May/June beetles {Phyllophaga spp.) and European chafer {Rhizotrogus majalis Razoumowsky)); carpet beetles from the family Dermestidae; wireworms from the family Elateridae; bark beetles from the family Scolytidae and flour beetles from the family Tenebrionidae. In addition, agronomic and nonagronomic pests include: eggs, adults and larvae of the order Dermaptera including earwigs from the family Forficulidae (e.g., European earwig {Forficula auricularia Linnaeus), black earwig {Chelisoches mono Fabricius)); eggs, immatures, adults and nymphs of the orders Hemiptera and Homoptera such as, plant bugs from the family Miridae, cicadas from the family Cicadidae, leafhoppers (e.g. Empoasca spp.) from the family Cicadellidae, planthoppers from the families Fulgoroidae and Delphacidae, treehoppers from the family Membracidae, psyllids from the family Psyllidae, whiteflies from the family Aleyrodidae, aphids from the family Aphididae, phylloxera from the family Phylloxeridae, mealybugs from the family Pseudococcidae, scales from the families Coccidae, Diaspididae and Margarodidae, lace bugs from the family Tingidae, stink bugs from the family Pentatomidae, chinch bugs (e.g., hairy chinch bug {Blissus leucopterus hirtus Montandon) and southern chinch bug {Blissus insularis Barber)) and other seed bugs from the family Lygaeidae, spittlebugs from the family Cercopidae squash bugs from the family Coreidae, and red bugs and cotton stainers from the family Pyrrhocoridae. Also included are eggs, larvae, nymphs and adults of the order Acari (mites) such as spider mites and red mites in the family Tetranychidae (e.g., European red mite {Panonychus ulmi Koch), two spotted spider mite {Tetranychus urticae Koch), McDaniel mite {Tetranychus mcdanieli McGregor)); flat mites in the family Tenuipalpidae (e.g., citrus flat mite {Brevipalpus lewisi McGregor)); rust and bud mites in the family Eriophyidae and other foliar feeding mites and mites important in human and animal health, i.e. dust mites in the family Epidermoptidae, follicle mites in the family Demodicidae, grain mites in the family Glycyphagidae, ticks in the order Ixodidae (e.g., deer tick {Ixodes scapularis Say), Australian paralysis tick {Ixodes holocyclus Neumann), American dog tick (Dermacentor variabilis Say), lone star tick (Amblyomma americanum Linnaeus)) and scab and itch mites in the families Psoroptidae, Pyemotidae, and Sarcoptidae; eggs, adults and immatures of the order Orthoptera including grasshoppers, locusts and crickets (e.g., migratory grasshoppers (e.g., Melanoplus sanguinipes Fabricius, M. differentialis Thomas), American grasshoppers (e.g., Schistocerca americana Drury), desert locust (Schistocerca gregaria Forskal), migratory locust (Locusta migratoria Linnaeus), bush locust {Zonocerus spp.), house cricket (Acheta domesticus Linnaeus), mole crickets (e.g., tawny mole cricket {Scapteriscus vicinus Scudder) and southern mole cricket (Scapteriscus borellii Giglio-Tos)); eggs, adults and immatures of the order Diptera including leafminers, midges, fruit flies (Tephritidae), frit flies (e.g., Oscinella frit Linnaeus), soil maggots, house flies (e.g., Musca domestica Linnaeus), lesser house flies (e.g., Fannia canicularis Linnaeus, F. femoralis Stein), stable flies (e.g., Stomoxys calcitrans Linnaeus), face flies, horn flies, blow flies (e.g., Chrysomya spp., Phormia spp.), and other muscoid fly pests, horse flies (e.g., Tabanus spp.), bot flies (e.g., Gastrophilus spp., Oestrus spp.), cattle grubs (e.g., Hypoderma spp.), deer flies (e.g., Chrysops spp.), keds (e.g., Melophagus ovinus Linnaeus) and other Brachycera, mosquitoes (e.g., Aedes spp., Anopheles spp., Culex spp.), black flies (e.g., Prosimulium spp., Simulium spp.), biting midges, sand flies, sciarids, and other Nematocera; eggs, immatures and adults of the order Thysanoptera including onion thrips (Thrips tabaci Lindeman), flower thrips (Frankliniella spp.), and other foliar feeding thrips; insect pests of the order Hymenoptera including ants (e.g., red carpenter ant (Camponotus ferrugineus Fabricius), black carpenter ant (Camponotus pennsylvanicus De Geer), Pharaoh ant (Monornorium pharaonis Linnaeus), little fire ant (Wasmannia auropunctata Roger), fire ant (Solenopsis geminata Fabricius), red imported fire ant (Solenopsis invicta Buren), Argentine ant (Iridomyrmex humilis Mayr), crazy ant (Paratrechina longicornis Latreille), pavement ant (Tetramorium caespitum Linnaeus), cornfield ant (Lasius alienus Forster), odorous house ant (Tapinoma sessile Say), bees (including carpenter bees), hornets, yellow jackets, wasps, and sawflies (Neodiprion spp.; Cephus spp.); insect pests of the Family Formicidae including the Florida carpenter ant (Camponotus floridanus Buckley), white-footed ant (Technomyrmex albipes fr. Smith), big headed ants (Pheidole sp.) and ghost ant (Tapinoma melanocephalum Fabricius); insect pests of the order Isoptera including termites in the Termitidae (ex. Macrotermes sp.), Kalotermitidae (ex. Cryptotermes sp.), and Rhinotermitidae (ex. Reticulitermes sp., Coptotermes sp.) families, the eastern subterranean termite (Reticulitermes flavipes Kollar), western subterranean termite (Reticulitermes hesperus Banks), Formosan subterranean termite (Coptotermes formosanus Shiraki), West Indian drywood termite (Incisitermes immigrans Snyder), powder post termite (Cryptotermes brevis Walker), drywood termite (Incisitermes snyderi Light), southeastern subterranean termite (Reticulitermes virginicus Banks), western drywood termite (Incisitermes minor Hagen), arboreal termites such as Nasutitermes sp. and other termites of economic importance; insect pests of the order Thysanura such as silverfish (Lepisma saccharina Linnaeus) and firebrat (Thermobia domestica Packard); insect pests of the order Mallophaga and including the head louse (Pediculus humanus capitis De Geer), body louse (Pediculus humanus Linnaeus), chicken body louse (Menacanthus stramineus Nitszch), dog biting louse (Trichodectes canis De Geer), fluff louse (Goniocotes gallinae De Geer), sheep body louse (Bovicola ovis Schrank), short-nosed cattle louse (Haematopinus eurysternus Nitzsch), long-nosed cattle louse (Linognathus vituli Linnaeus) and other sucldng and chewing parasitic lice that attack man and animals; insect pests of the order Siphonoptera including the oriental rat flea (Xenopsylla cheopis Rothschild), cat flea (Ctenocephalides felis Bouche), dog flea (Ctenocephalides canis Curtis), hen flea (Ceratophyllus gallinae Schrank), sticktight flea {Echidnophaga gallinacea Westwood), human flea (Pulex irritans Linnaeus) and other fleas afflicting mammals and birds. Additional arthropod pests covered include: spiders in the order Araneae such as the brown recluse spider (Loxosceles reclusa Gertsch & Mulaik) and the black widow spider (Latrodectus mactans Fabricius), and centipedes in the order Scutigeromorpha such as the house centipede (Scutigera coleoptrata Linnaeus). Compounds of the present invention also have activity on members of the Classes Nematoda, Cestoda, Trematoda, and Acanthocephala including economically important members of the orders Strongylida, Ascaridida, Oxyurida, Rhabditida, Spirurida, and Enoplida such as but not limited to economically important agricultural pests (i.e. root knot nematodes in the genus Meloidogyne, lesion nematodes in the genus Pratylenchus, stubby root nematodes in the genus Trichodorus, etc.) and animal and human health pests (i.e. all economically important flukes, tapeworms, and roundworms, such as Strongylus vulgaris in horses, Toxocara canis in dogs, Haemonchus contortus in sheep, Dirofilaria immitis Leidy in dogs, Anoplocephala perfoliata in horses, Fasciola hepatica Linnaeus in ruminants, etc.).
Compounds of the invention show particularly high activity against pests in the order Lepidoptera (e.g., Alabama argillacea Hubner (cotton leaf worm), Archips argyrospila Walker (fruit tree leaf roller), A. rosana Linnaeus (European leaf roller) and other Archips species, Chϊlo suppressalis Walker (rice stem borer), Cnaphalocrosis medinalis Guenee (rice leaf roller), Crambus caliginosellus Clemens (corn root webworm), Crambus teterrellus Zincken (bluegrass webworm), Cydia pomonella Linnaeus (codling moth), Earias insulana Boisduval (spiny bollworm), Earias vittella Fabricius (spotted bollworm), Helicoverpa armigera Hubner (American bollworm), Helicoverpa zea Boddie (corn earworm), Heliothis virescens Fabricius (tobacco budworm), Herpeto gramma licarsisalis Walker (sod webworm), Lobesia botrana Denis & Schiffermϋller (grape berry moth), Pectinophora gossγpiella Saunders (pink bollworm), Phyllocnistis citrella Stainton (citrus leafminer), Pieris brassicae Linnaeus (large white butterfly), Pieris rapae Linnaeus (small white butterfly), Plutella xylostella Linnaeus (diamondback moth), Spodoptera exigua Hubner (beet armyworm), Spodoptera litura Fabricius (tobacco cutworm, cluster caterpillar), Spodoptera frugiperda J. E. Smith (fall armyworm), Trichoplusia ni Hϋbner (cabbage looper) and Tula absoluta Meyrick (tomato leafminer)).
Compounds of the invention also have significant activity on members from the order Homoptera including: Acyrthisiphon pisum Harris (pea aphid), Aphis craccivora Koch (cowpea aphid), Aphis fabae Scopoli (black bean aphid), Aphis gossypii Glover (cotton aphid, melon aphid), Aphis pomi De Geer (apple aphid), Aphis spiraecola Patch (spirea aphid), Aulacorthum solani Kaltenbach (foxglove aphid), Chaetosiphon fragaefolii Cockerell (strawberry aphid), Diuraphis noxia Kurdjumov/Mordvilko (Russian wheat aphid), Dysaphis plantaginea Paaserini (rosy apple aphid), Eriosoma lanigerum Hausmann (woolly apple aphid), Hyalopterus pruni Geoffroy (mealy plum aphid), Lipaphis erysimi Kaltenbach (turnip aphid), Metopolophium dirrhodum Walker (cereal aphid), Macrosipum euphorbiae Thomas (potato aphid), Myzus persicae Sulzer (peach-potato aphid, green peach aphid), Nasonovia ribisnigri Mosley (lettuce aphid), Pemphigus spp. (root aphids and gall aphids), Rhopalosiphum maidis Fitch (corn leaf aphid), Rhopalosiphum padi Linnaeus (bird cherry-oat aphid), Schizaphis graminum Rondani (greenbug), Sitobion avenae Fabricius (English grain aphid), Therioaphis maculata Buckton (spotted alfalfa aphid), Toxoptera aurantii Boyer de Fonscolombe (black citrus aphid), and Toxoptera citricida Kirkaldy (brown citrus aphid); Adelges spp. (adelgids); Phylloxera devastatrix Pergande (pecan phylloxera); Bemisia tabaci Gennadius (tobacco whitefly, sweetpotato whitefly), Bemisia argentifolii Bellows & Perring (silverleaf whitefly), Dialeurodes citri Ashmead (citrus whitefly) and Trialeurodes vaporariorum Westwood (greenhouse whitefly); Empoasca fabae Harris (potato leafhopper), Laodelphax striatellus Fallen (smaller brown planthopper), Macrolestes quadrilineatus Forbes (aster leafhopper), Nephotettix cinticeps Uhler (green leafhopper), Nephotettix nigropictus Stal (rice leafhopper), Nilaparvata lugens Stal (brown planthopper), Peregrinus maidis Ashmead (corn planthopper), Sogatella furcifera Horvath (white-backed planthopper), Sogatodes orizicola Muir (rice delphacid), Typhlocyba pomaria McAtee white apple leafhopper, Erythroneoura spp. (grape leafhoppers); Magicidada septendecim Linnaeus (periodical cicada); Icerya purchasi Maskell (cottony cushion scale), Quadraspidiotus perniciosus Comstock (San Jose scale);( Planococcus citri Risso (citrus mealybug); Pseudococcus spp. (other mealybug complex); Cacopsylla pyricola Foerster (pear psylla), Trioza diospyri Ashmead (persimmon psylla).
Compounds of this invention also have activity on members from the order Hemiptera including: Acrosternum hilare Say (green stink bug), Anasa tristis De Geer (squash bug), Blissus leucopterus leucopterus Say (chinch bug), Corythuca gossypii Fabricius (cotton lace bug), Cyrtopeltis modesta Distant (tomato bug), Dysdercus suturellus Heπich-Schaffer (cotton stainer), Euchistus servus Say (brown stink bug), Euchistus variolarius Palisot de Beauvois (one-spotted stink bug), Graptosthetus spp. (complex of seed bugs), Leptoglossus corculus Say (leaf-footed pine seed bug), Lygus lineolaris Palisot de Beauvois (tarnished plant bug), Nezara viridula Linnaeus (southern green stink bug), Oebalus pugnca Fabricius (rice stink bug), Oncopeltus fasciatus Dallas (large milkweed bug), Pseudatomoscelis seriatus Reuter (cotton fleahopper). Other insect orders controlled by compounds of the invention include Thysanoptera (e.g., Frankliniella occidentalis Pergande (western flower thrip), Scirthothrips citri Moulton (citrus thrip), Sericothrips variabilis Beach (soybean thrip), and Thrips tabaci Lindeman (onion thrip); and the order Coleoptera (e.g., Leptinotarsa decemlineata Say (Colorado potato beetle), Epilachna varivestis Mulsant (Mexican bean beetle) and wireworms of the genera Agriotes, Athous or Limonius). Of note is use of compounds of this invention for controlling silverleaf whitefly
{Bemisia argentifolii). Of note is use of compounds of this invention for controlling western flower thrip {Frankliniella occidentalis). Of note is use of compounds of this invention for controlling potato leafhopper (Empoasca fabae). Of note is use of compounds of this invention for controlling corn planthopper {Peregrinus maidis). Of note is use of compounds of this invention for controlling cotton melon aphid {Aphis gossypii). Of note is use of compounds of this invention for controlling green peach aphid {Myzus persicae). Of note is use of compounds of this invention for controlling diamondback moth {Plutella xylostella). Of note is use of compounds of this invention for controlling fall armyworm {Spodopterafrugiperdά). Compounds of this invention can also be mixed with one or more other biologically active compounds or agents including insecticides, fungicides, nematocides, bactericides, acaricides, herbicides, growth regulators such as rooting stimulants, chemosterilants, semiochemicals, repellents, attractants, pheromones, feeding stimulants, other biologically active compounds or entomopathogenic bacteria, virus or fungi to form a multi-component pesticide giving an even broader spectrum of agronomic and nonagronomic utility. Thus the present invention also pertains to a composition comprising a biologically effective amount of a compound of Formula 1 and an effective amount of at least one additional biologically active compound or agent and can further comprise at least one of a surfactant, a solid diluent or a liquid diluent. The other biologically active compounds or agents can be formulated in compositions comprising at least one of a surfactant, solid or liquid diluent. For mixtures of the present invention, the other biologically active compounds or agents can be formulated together with the present compounds, including the compounds of Formula 1, to form a premix, or the other biologically active compounds or agents can be formulated separately from the present compounds, including the compounds of Formula 1, and the two formulations combined together before application (e.g., in a spray tank) or, alternatively, applied in succession.
Examples of such biologically active compounds or agents with which compounds of this invention can be formulated are: insecticides such as abamectin, acephate, acetamiprid, amidoflumet (S-1955), avermectin, azadirachtin, azinphos-methyl, bifenthrin, bifenazate, buprofezin, carbofuran, cartap, chlorfenapyr, chlorfluazuron, chlorpyrifos, chlorpyrifos- methyl, chromafenozide, clothianidin, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, cypeπnethrin, cyromazine, deltamethrin, diafenthiuron, diazinon, dieldrin, diflubenzuron, dimefluthrin, dimethoate, dinotefuran, diofenolan, emamectin, endosulfan, esfenvalerate, ethiprole, fenothiocarb, fenoxycarb, fenpropathrin, fenvalerate, fipronil, flonicamid, flubendiamide, flucythrinate, tau-fluvalinate, flufenerim (UR-50701), flufenoxuron, fonophos, halofenozide, hexaflumuron, hydramethylnon, imidacloprid, indoxacarb, isofenphos, lufenuron, malathion, metaflumizone, metaldehyde, methamidophos, methidathion, methoiriyl, methoprene, methoxychlor, metofluthrin, monocrotophos, methoxyfenozide, nitenpyram, nithiazine, novaluron, noviflumuron (XDE- 007), oxamyl, parathion, parathion-methyl, permethrin, phorate, phosalone, phosmet, phosphamidon, pirimicarb, profenofos, profluthrin, pymetrozine, pyrafluprole, pyrethrin, pyridalyl, pyriprole, pyriproxyfen, rotenone, ryanodine, spinosad, spirodiclofen, spiromesifen (BSN 2060), spirotetramat, sulprofos, tebufenozide, teflubenzuron, tefluthrin, terbufos, tetrachlorvinphos, thiacloprid, thiamethoxam, thiodicarb, thiosultap-sodium, txalomethrin, triazamate, trichlorfon and triflumuron; fungicides such as fungicides such as acibenzolar, aldimorph, amisulbrom, azaconazole, azoxystrobin, benalaxyl, benomyl, benthiavalicarb, benthiavalicarb-isopropyl, binomial, biphenyl, bitertanol, blasticidin-S, Bordeaux mixture (Tribasic copper sulfate), boscalid/nicobifen, bromuconazole, bupirimate, buthiobate, carboxin, carpropamid, captafol, captan, carbendazim, chloroneb, chlorothalonil, chlozolinate, clotrimazole, copper oxychloride, copper salts such as copper sulfate and copper hydroxide, cyazofamid, cyflunamid, cymoxanil, cyproconazole, cyprodinil, dichlofluanid, diclocymet, diclomezine, dicloran, diethofencarb, difenoconazole, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinocap, discostrobin, dithianon, dodemorph, dodine, econazole, etaconazole, edifenphos, epoxiconazole, ethaboxam, ethirimol, ethridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fencaramid, fenfuram, fenhexamide, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fentin acetate, fentin hydroxide, ferbam, ferfurazoate, ferimzone, fluazinam, fludioxonil, flumetover, fluopicolide, fluoxastrobin, fluquinconazole, fluquinconazole, flusilazole, flusulfamide, flutolanil, flutriafol, folpet, fosetyl-aluminum, fuberidazole, furalaxyl, furametapyr, hexaconazole, hymexazole, guazatine, imazalil, imibenconazole, iminoctadine, iodicarb, ipconazole, iprobenfos, iprodione, iprovalicarb, isoconazole, isoprothiolane, kasugamycin, kresoxim-methyl, mancozeb, mandipropamid, maneb, mapanipyrin, mefenoxam, mepronil, metalaxyl, metaminostrobin, metconazole, methasulfocarb, metiram- zink, metominostrobin/fenominostrobin, mepanipyrim, metiram, metrafenone, miconazole, myclobutanil, neo-asozin (ferric methanearsonate), nuarimol, octhilinone, ofurace, orysastrobin, oxadixyl, oxolinic acid, oxpoconazole, oxycarboxin, paclobutrazol, penconazole, pencycuron, penthiopyrad, perfurazoate, phosphonic acid, phthalide, picobenzamid, picoxystrobin, polyoxin, probenazole, prochloraz, procymidone, propamocarb, propamocarb-hydrochloride, propiconazole, propineb, proquinazid, prothioconazole, pyraclostrobin, pryazophos, pyrifenox, pyrimethanil, pyrifenox, pyrolni trine, pyroquilon, quinconazole, quinoxyfen, quintozene, silthiofam, simeconazole, spiroxamine, streptomycin, sulfur, tebuconazole, techrazene, tecloftalam, tecnazene, tetraconazole, thiabendazole, thifluzamide, thiophanate, thiophanate-methyl, thiram, tiadinil, tolclofos-methyl, tolyfluanid, triadimefon, triadimenol, triarimol, triazoxide, tridemorph, trimoprhamide tricyclazole, trifloxystrobin, triforine, triticonazole, uniconazole, validamycin, vinclozolin, zineb, ziram, and zoxamide; nematocides such as aldicarb, oxamyl and fenamiphos; bactericides such as streptomycin; acaricides such as amitraz, chinomethionat, chlorobenzilate, cyhexatin, dicofol, dienochlor, etoxazole, fenazaquin, fenbutatin oxide, fenpropathrin, fenpyroximate, hexythiazox, propargite, pyridaben and tebufenpyrad; and biological agents including entomopathogenic bacteria, such as Bacillus thuringiensis subsp. Aizawai, Bacillus thuringiensis subsp. Kurstaki, and the encapsulated delta-endotoxins of Bacillus thuringiensis (e.g., Cellcap, MPV, MPVII); entomopathogenic fungi, such as green muscardine fungus; and entomopathogenic virus including baculovirus, nucleopolyhedro virus (NPV) such as HzNPV, AfNPV; and granulosis virus (GV) such as CpGV. Compounds of this invention and compositions thereof can be applied to plants genetically transformed to express proteins toxic to invertebrate pests (such as Bacillus thuringiensis delta-endotoxins). The effect of the exogenously applied invertebrate pest control compounds of this invention may be synergistic with the expressed toxin proteins.
General references for these agricultural protectants (i.e. insecticides, fungicides, nematocides, acaricides, herbicides and biological agents) include The Pesticide Manual, 13th Edition, C. D. S. Tomlin, Ed., British Crop Protection Council, Farnham, Surrey, U.K., 2003 and The BioPesticide Manual, 2nd Edition, L. G. Copping, Ed., British Crop Protection Council, Farnham, Surrey, U.K., 2001.
In certain instances, combinations with other arthropodicides having a similar spectrum of control but a different mode of action will be particularly advantageous for resistance management. Thus, compositions of the present invention can further comprise a biologically effective amount of at least one additional invertebrate pest control compound or agent having a similar spectrum of control but a different mode of action. Contacting a plant genetically modified to express a plant protection compound (e.g., protein) or the locus of the plant with a biologically effective amount of a compound of this invention can also provide a broader spectrum of plant protection and be advantageous for resistance management. In certain instances, combinations of a compound of this invention with other invertebrate pest control compounds or agents can result in a greater-than-additive (i.e. synergistic) effect and/or a less-than-additive effect (i.e. antagonistic). It is always desirable to reduce the quantity of chemical agents released in the environment while ensuring effective pest control. When synergism of invertebrate pest control agents is found at application rates giving agronomically satisfactory levels of pest control, such combinations can be advantageous for lowering crop production cost and reducing environmental load.
Table A lists specific combinations of a compound of Formula 1 with other invertebrate pest control agents illustrative of the mixtures, compositions and methods of the present invention. The first column of Table A lists the specific invertebrate pest control agents (e.g., "Abamectin" in the first line). The second column of Table A lists the mode of action (if known) of the invertebrate pest control agents. The third column of Table A lists embodiment(s) of ranges of weight ratios for rates at which the invertebrate pest control agent can be applied relative to a compound of Formula 1, an iV-oxide, or a salt thereof, (e.g., "50:1 to 1:50" of abamectin relative to a compound of Formula 1 by weight). Thus, for example, the first line of Table A specifically discloses the combination of a compound of Formula 1 with abamectin can be applied in a weight ratio between 50:1 to 1:50. The remaining lines of Table A are to be construed similarly. Of further note Table A lists specific combinations of a compound of Formula 1 with other invertebrate pest control agents illustrative of the mixtures, compositions and methods of the present invention and includes additional embodiments of weight ratio ranges for application rates.
Table A
Figure imgf000059_0001
Figure imgf000060_0001
Figure imgf000061_0001
One embodiment of insecticides and acaricides for mixing with compounds of this invention include sodium channel modulators such as cypermethrin, cyhalothrin, cyfluthrin, beta-cyfluthrin, esfenvalerate, fenvalerate, indoxacarb and tralomethrin; cholinesterase inhibitors such as methomyl, oxamyl and thiodicarb; neonicotinoids such as acetamiprid, clothianidin, imidacloprid, thiacloprid and thiamethoxam; neuronal sodium channel blockers such as indoxacarb; insecticidal macrocyclic lactones such as spinosad, abamectin, avermectin and emamectin; GABA ( γ-aminobutyric acid)-regulated chloride channel blockers such as endosulfan, ethiprole and fipronil; chitin synthesis inhibitors such as flufenoxuron and triflumuron; juvenile hormone mimics such as diofenolan and pyriproxyfen; octopamine receptor ligands such as amitraz; ecdysone agonists such as methoxyfenozide and tebufenozide; ryanodine receptor ligands such as ryanodine, anthranilamides and flubendiamide; fenothiocarb; flonicamid; metaflumizone; pyridalyl; and pymetrozine. One embodiment of biological agents for mixing with compounds of this invention include Bacillus thuringiensis and Bacillus thuringiensis delta-endotoxin as well as naturally occurring and genetically modified viral insecticides including members of the family Baculoviridae as well as entomophagous fungi.
The weight ratios of a compound, including a compound of Formula 1, an N-oxide or a salt thereof, to the additional invertebrate pest control agent typically are between 1000:1 and 1:1000, with one embodiment being between 500:1 and 1:500, another embodiment being between 250:1 and 1:200 and another embodiment being between 100:1 and 1:50.
Listed below in Table B are embodiments of specific compositions comprising a compound of Formula 1 (compound numbers refer to compounds in Index Table A) and an additional invertebrate pest control agent.
Table B
Mixture Comp. and Invertebrate Pest Mixture Comp. and Invertebrate Pest Control
No. No. Control Agent No. No. Agent
A-I 1 and Abamectin B-I 11 and Abamectin
A-2 1 and Acetamiprid B-2 11 and Acetamiprid
A-3 1 and Amitraz B-3 11 and Amitraz
A-4 1 and Anthranilamides B-4 11 and Anthranilamides
A-5 1 and Avermectin B-5 11 and Avermectin
A-6 1 and Azadirachtin B-6 11 and Azadirachtin
A-7 1 and Beta-cyfluthrin B-7 11 and Beta-cyfluthrin
A-8 1 and Bifenthrin B-8 11 and Bifenthrin
A-9 1 and Buprofezin B-9 11 and Buprofezin
A-10 1 and Cartap B-10 11 and Cartap
A-I l 1 and Chlorfenapyr B-I l 11 and Chlorfenapyr
A-12 1 and Chlorpyrifos B-12 11 and Chlorpyrifos
A-13 1 and Clothianidin B-13 11 and Clothianidin
A-14 1 and Cyfluthrin B-14 11 and Cyfluthrin
A-15 1 and Cyhalothrin B-15 11 and Cyhalothrin
A-16 1 and Cypermethrin B-16 11 and Cypermethrin
A- 17 1 and Cyromazine B-17 11 and Cyromazine
A-18 1 and Deltamethrin B-18 11 and Deltamethrin
A-19 1 and Dieldrin B-19 11 and Dieldrin
A-20 1 and Dinotefuran B-20 11 and Dinotefuran
A-21 1 and Diofenolan B-21 11 and Diofenolan
A-22 1 and Emamectin B-22 11 and Emamectin
A-23 1 and Emamectin Benzoate B-23 11 and Emamectin Benzoate Mixture Comp. and Invertebrate Pest Mixture Comp. and Invertebrate Pest Control
No. No. Control Agent No. No. Agent
A-24 1 and Endosulfan B-24 11 and Endosulfan
A-25 1 and Esfenvalerate B-25 11 and Esfenvalerate
A-26 1 and Ethiprole B-26 11 and Ethiprole
A-27 1 and Fenothiocarb B-27 11 and Fenothiocarb
A-28 1 and Fenoxycarb B-28 11 and Fenoxycarb
A-29 1 and Fenvalerate B-29 11 and Fenvalerate
A-30 1 and Fipronil B-30 11 and Fipronil
A-31 1 and Flonicamid B-31 11 and Flonicamid
A-32 1 and Flubendiamide B-32 11 and Flubendiamide
A-33 1 and Flufenoxuron B-33 11 and Flufenoxuron
A-34 1 and Hexaflumuron B-34 11 and Hexaflumuron
A-35 1 and Hydramethylnon B-35 11 and Hydramethylnon
A-36 1 and Imidacloprid B-36 11 and Imidacloprid
A-37 1 and Indoxacarb B-37 11 and Indoxacarb
A-38 1 and Lambda-cyhalothrin B-38 11 and Lambda-cyhalothrin
A-39 1 and Lufenuron B-39 11 and Lufenuron
A-40 1 and Metaflumizone B-40 11 and Metaflumizone
A-41 1 and Methomyl B-41 11 and Methomyl
A-42 1 and Methoprene B-42 11 and Methoprene
A-43 1 and Methoxyfenozide B-43 11 and Methoxyfenozide
A-44 1 and Nitenpyram B-44 11 and Nitenpyram
A-45 1 and Nithiazine B-45 11 and Nithiazine
A-46 1 and Novaluron B-46 11 and Novaluron
A-47 1 and NPV (e.g., Gemstar) B-47 11 and NPV (e.g., Gemstar)
A-48 1 and Oxamyl 1 B-48 11 and Oxamyl
A-49 1 and Pymetrozine B-49 11 and Pymetrozine
A-50 1 and Pyrethrin B-50 11 and Pyrethrin
A-51 1 and Pyridaben B-51 11 and Pyridaben
A-52 1 and Pyridalyl B-52 11 and Pyridalyl
A-53 1 and Pyriproxyfen B-53 11 and Pyriproxyfen
A-54 1 and Ryanodine B-54 11 and Ryanodine
A-55 1 and Spinosad B-55 11 and Spinosad
A-56 1 and Spirodiclofen B-56 11 and Spirodiclofen
A-57 1 and Spiromesifen B-57 11 and Spiromesifen
A-58 1 and Tebufenozide B-58 11 and Tebufenozide
A-59 1 and Thiacloprid B-59 11 and Thiacloprid Mixture Comp. and Invertebrate Pest Mixture Comp. and Invertebrate Pest Control
No. No. Control Agent No. No. Agent
A-60 1 and Thiamethoxam B-60 11 and Thiamethoxam
A-61 1 and Thiodicarb B-61 11 and Thiodicarb
A-62 1 and Tralomethrin B-62 11 and Tralomethrin
A-63 1 and Triazamate B-63 11 and Triazamate
A-64 1 and Triflumuron B-64 11 and Triflumuron
A-65 1 and Bacillus thuringiensis B-65 11 and Bacillus thuringiensis
A-66 1 and Bacillus thuringiensis B-66 11 and Bacillus thuringiensis delta toxin delta toxin
A-67 1 and Beauvaria bassiana B-67 11 and Beauvaria bassiana
The specific mixtures listed in Table B typically combine a compound of Formula 1 with the other invertebrate pest agent in the ratios specified in Table A.
Invertebrate pests are controlled in agronomic and nonagronomic applications by applying a composition comprising a compound of this invention, in a biologically effective amount, to the environment of the pests, including the agronomic and/or nonagronomic locus of infestation, to the area to be protected, or directly on the pests to be controlled. Agronomic applications include protecting a field crop from invertebrate pests typically by applying a composition or a mixture of the invention to the seed of the crop before the planting, to the foliage, stems, flowers and/or fruit of crop plants, or to the soil or other growth medium before or after the crop is planted. Nonagronomic applications refer to invertebrate pest control in the areas other than fields of crop plants. Nonagronomic applications include control of invertebrate pests in stored grains, beans and other foodstuffs, and in textiles such as clothing and carpets. Nonagronomic applications also include invertebrate pest control in ornamental plants, forests, in yards, along roadsides and railroad rights of way, and on turf such as lawns, golf courses and pastures. Nonagronomic applications also include invertebrate pest control in houses and other buildings which may be occupied by humans and/or companion, farm, ranch, zoo or other animals. Nonagronomic applications also include the control of pests such as termites that can damage wood or other structural materials used in buildings. Nonagronomic applications also include protecting human and animal health by controlling invertebrate pests that are parasitic or transmit infectious diseases. The controlling of animal parasites includes controlling external parasites that are parasitic to the surface of the body of the host animal (e.g., shoulders, armpits, abdomen, inner part of the thighs) and internal parasites that are parasitic to the inside of the body of the host animal (e-g-j stomach, intestine, lung, veins, under the skin, lymphatic tissue). External parasitic or disease transmitting pests include, for example, chiggers, ticks, lice, mosquitoes, flies, mange, mites and fleas. Internal parasites include heartworms, hookworms and helminths. Compounds and compositions of the present invention are particular suitable for combating external parasitic or disease transmitting pests.
Compounds and compositions of the present invention are suitable for combating parasites that infest agricultural working animals, such as cattle, sheep, goats, horses, pigs, donkeys, camels, buffalos, rabbits, hens, turkeys, ducks, geese and bees; pet animals and domestic animals such as dogs, cats, pet birds and aquarium fish; as well as so-called experimental animals, such as hamsters, guinea pigs, rats and mice. By combating these parasites, fatalities and performance reduction (in term of meat, milk, wool, skins, eggs, honey, etc.) are to be reduced, so that applying a composition comprising a compound of the present invention is intended to allow more economic and simple husbandry of animals.
Nonagronomic applications in the veterinary sector takes place in the known manner, by enteral administration in the form of, for example, tablets, capsules, drinks, drenching preparations, granulates, pastes, boli, feed-through procedures, suppositories; by parenteral administration, such as by injection (including intramuscular, subcutaneous, intravenous, intraperitoneal), implants; by nasal administration; by dermal administration, for example, in the form of immersion or dipping, spraying, pouring, washing, coating with powder, and through bodied devices such as neck collars, ear marks, tail marks, limb measuring tapes or halters which comprise compounds or compositions of the present invention.
Therefore, the present invention further comprises a method for controlling an invertebrate pest in agronomic and/or nonagronomic applications, comprising contacting the invertebrate pest or its environment with a biologically effective amount of one or more of the compounds of the invention, or with a composition comprising at least one such compound or a composition comprising at least one such compound and a biologically effective amount of at least one additional biologically active compound or agent. Examples of suitable compositions comprising a compound of the invention and a biologically effective amount of at least one additional biologically active compound or agent include granular compositions wherein the additional active compound is present on the same granule as the compound of the invention or on granules separate from those of the compound of the invention. One embodiment of a method of contact is by spraying. Alternatively, a granular composition comprising a compound of the invention can be applied to the plant foliage or the soil. Compounds of this invention can also be effectively delivered through plant uptake by contacting the plant with a composition comprising a compound of this invention applied as a soil drench of a liquid formulation, a granular formulation to the soil, a nursery box treatment or a dip of transplants. Of note is a composition of the present invention in the form of a soil drench liquid formulation. Also of note is a method for controlling an invertebrate pest comprising contacting the soil environment of the invertebrate pest with a biologically effective amount of a compound of the present invention. Of further note are compounds of this invention also effective by topical application to the locus of infestation. Other methods of contact include application of a compound or a composition of the invention by direct and residual sprays, aerial sprays, gels, seed coatings, microencapsulations, systemic uptake, baits, ear tags, boluses, foggers, fumigants, aerosols, dusts and many others. One embodiment of a method of contact is a dimensionally stable fertilizer granule, stick or tablet comprising a mixture or composition of the invention. The compounds of this invention can also be impregnated into materials for fabricating invertebrate control devices (e.g., insect netting). Seed coatings can be applied to all types of seeds, including those from which plants genetically transformed to express specialized traits will germinate. Representative examples include those expressing proteins toxic to invertebrate pests, such as Bacillus thuringiensis toxin or those expressing herbicide resistance, such as "Roundup Ready" seed.
The compounds of this invention can be incorporated into a bait composition that is consumed by an invertebrate pest or used within a device such as a trap, bait station, and the like. Such a bait composition can be in the form of granules which comprise (a) active ingredients, namely a biologically effective amount of a compound of Formula 1, an N-oxide, or salt thereof; (b) one or more food materials; optionally (c) an attractant, and optionally (d) one or more humectants. Of note are granules or bait compositions which comprise between about 0.001-5% active ingredients, about 40-99% food material and/or attractant; and optionally about 0.05-10% humectants, which are effective in controlling soil invertebrate pests at very low application rates, particularly at doses of active ingredient that are lethal by ingestion rather than by direct contact. Some food materials can function both as a food source and an attractant. Food materials include carbohydrates, proteins and lipids. Examples of food materials are vegetable flour, sugar, starches, animal fat, vegetable oil, yeast extracts and milk solids. Examples of attractants are odorants and flavorants, such as fruit or plant extracts, perfume, or other animal or plant component, pheromones or other agents known to attract a target invertebrate pest. Examples of humectants, i.e. moisture retaining agents, are glycols and other polyols, glycerine and sorbitol. Of note is a bait composition (and a method utilizing such a bait composition) used to control at least one invertebrate pest selected from the group consisting of ants, termites and cockroaches. A device for controlling an invertebrate pest can comprise the present bait composition and a housing adapted to receive the bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to the bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
The compounds of this invention can be applied without other adjuvants, but most often application will be of a formulation comprising one or more active ingredients with suitable carriers, diluents, and surfactants and possibly in combination with a food depending on the contemplated end use. One method of application involves spraying a water dispersion or refined oil solution of a compound of the present invention. Combinations with spray oils, spray oil concentrations, spreader stickers, adjuvants, other solvents, and synergists such as piperonyl butoxide often enhance compound efficacy. For nonagronomic uses such sprays can be applied from spray containers such as a can, a bottle or other container, either by means of a pump or by releasing it from a pressurized container, e.g., a pressurized aerosol spray can. Such spray compositions can take various forms, for example, sprays, mists, foams, fumes or fog. Such spray compositions thus can further comprise propellants, foaming agents, etc. as the case may be. Of note is a spray composition comprising a biologically effective amount of a compound or a composition of the present invention and a carrier. One embodiment of such a spray composition comprises a biologically effective amount of a compound or a composition of the present invention and a propellant. Representative propellants include, but are not limited to, methane, ethane, propane, butane, isobutane, butene, pentane, isopentane, neopentane, pentene, hydrofluorocarbons, chlorofluorocarbons, dimethyl ether, and mixtures of the foregoing. Of note is a spray composition (and a method utilizing such a spray composition dispensed from a spray container) used to control at least one invertebrate pest selected from the group consisting of mosquitoes, black flies, stable flies, deer flies, horse flies, wasps, yellow jackets, hornets, ticks, spiders, ants, gnats, and the like, including individually or in combinations.
The rate of application required for effective control (i.e. "biologically effective amount") will depend on such factors as the species of invertebrate to be controlled, the pest's life cycle, life stage, its size, location, time of year, host crop or animal, feeding behavior, mating behavior, ambient moisture, temperature, and the like. Under normal circumstances, application rates of about 0.01 to 2 kg of active ingredients per hectare are sufficient to control pests in agronomic ecosystems, but as little as 0.0001 kg/hectare may be sufficient or as much as 8 kg/hectare may be required. For nonagronomic applications, effective use rates will range from about 1.0 to 50 mg/square meter but as little as 0.1 mg/square meter may be sufficient or as much as 150 mg/square meter may be required. One skilled in the art can easily determine the biologically effective amount necessary for the desired level of invertebrate pest control.
The following Tests demonstrates the control efficacy of compounds of this invention on specific pests. "Control efficacy" represents inhibition of invertebrate pest development (including mortality) that causes significantly reduced feeding. The pest control protection afforded by the compounds is not limited, however, to these species. See Index Tables A-E for compound descriptions. The following abbreviations are used in the Index Tables which follow: i is iso, Me is methyl, Et is ethyl and f-Pr is isopropyl. "(d)" means melts with apparent decomposition. The abbreviation "Ex." stands for "Example" and is followed by a number indicating in which example the compound is prepared.
INDEX TABLE A
Figure imgf000068_0001
Compound Rl R2 RH Rl2 R14 R6 X m.p. (0C)
1 (Ex. 1) Me H H H ϊ-Pr H CF3 N 206-207
2 Me H H H Me H CF3 N 223-227
INDEX TABLE B
3
Figure imgf000068_0002
Compound Rl R2 R4 Rl4 R5 m.p. (0C)
3 Me Me H z-Pr 4-CF3 180-192 INDEX TABTP, C
Figure imgf000069_0001
Compound R^ R2 B R14 R15 Re X m.p. (0C)
4 (Ex. 2) Me Me O Et Et CF3 N
5 Me Me O Me Me CF3 N *
6 (Ex. 3) Me Me N-OH Et Et CF3 N **
7 Me Cl 0 Me Me CF3 N *
8 Me Cl 0 Et Et CF3 N *
9 Me Me N-NHCO2Me Et Et CF3 N *
10 Me Me N-OMe Et Et CF3 N
11 (Ex. 7) Me Cl 0 Me H Br N 246-247
12 (Ex. 6) Me Cl (E)-N-Me Me H Br N 230-234 (d)
13 Me Cl (Z)-N-Me Me H Br N 239-241 (d)
*See Index Table F for 1H NMR data. **See Example! 3 for 1H NMR data.
INDEX TABLE D
Figure imgf000069_0002
Compound Rl R2 R4 R6 X m.p. (0C)
14 (Ex. 4) Me Cl H Br N 139-142 INDEXTABLEB
Figure imgf000070_0001
Compound Rl R2 R6 X m.p. (0C)
15 (Ex. 5) Me Cl Br N 173-177 (d)
INDEXTABLEF
Cmpd No. 1H NMR Data (CDCI3 solution unless indicated otherwise)*1
5 9.77 (br s, IH), 8.44 (d, IH), 7.85 (d, IH), 7.48 (apparent s, 2H), 7.40 (dd, IH), 7.26 (s,
IH), 2.96 (s, 3H), 2.84 (s, 3H), 2.32 (s, 3H), 2.14 (s, 3H).
7 9.72 (s, IH), 8.42 (d, IH), 7.87 (d, IH), 7.65 (d, IH), 7.57 (s, IH), 7.41 (dd, IH), 7.39 (s, IH), 2.94 (s, 3H), 2.85 (s, 3H), 2.12 (s, 3H).
8 9.94 (s, IH), 8.48 (d, IH), 7.90 (d, IH), 7.60 (d, IH), 7.44 (s, IH), 7.40 (dd, IH), 7.39 (s, IH), 3.49 (q, 2H), 3.18 (q, 2H), 2.19 (s, 3H), 1.22 (t, 3H), 1.13 (t, 3H).
9 10.04 (br s, IH), 8.79 (br s, IH), 8.45 (d, IH), 7.84 (d, IH), 7.40 (dd, IH), 7.08 (s, IH), 6.90 (s, IH), 3.87 (s, 3H), 3.48 (q, 2H), 2.91 (q, 2H), 2.26 (s, 3H), 2.21 (s, 3H), 1.20 (t, 3H), 0.74 (t, 3H).
10 major isomer: 9.99 (s, IH), 8.47 (d, IH), 7.86 (d, IH), 7.42-7.38 (m, 2H), 7.06 (s, IH), 7.02 (s, IH), 3.94 (s, 3H), 3.49 (q, 2H), 3.2-3.07 (m, 2H), 2.26 (s, 3H), 2.18 (s, 3H), 1.26 (t, 3H), 0.99 (t, 3H). Also showed a minor oxime isomer. a 1H NMR data are in ppm downfield from tetramethylsilane. Couplings are designated by (s)-singlet, (d)-doublet, (t)-triplet, (q)-quartet, (m)-multiplet, (dd)-doublet of doublets, (dt)-doublet of triplets, (br s)-broad singlet.
BIOLOGICAL EXAMPLES OF THE INVENTION
TEST A
For evaluating control of diamondback moth (Plutella xylostella) the test unit consisted of a small open container with a 12-14-day-old radish plant inside. This was pre-infested with 10-15 neonate larvae on a piece of insect diet by use of a core sampler to remove a plug from a sheet of hardened insect diet having many larvae growing on it and transfer the plug containing larvae and diet to the test unit. The larvae moved onto the test plant as the diet plug dried out. Test compounds were formulated using a solution containing 10% acetone, 90% water and 300 ppm X-77® Spreader Lo-Foam Formula non-ionic surfactant containing alkylarylpolyoxyethylene, free fatty acids, glycols and isopropanol (Loveland Industries, Inc. Greeley, Colorado, USA). The formulated compounds were applied in 1 mL of liquid through a SUJ2 atomizer nozzle with 1/8 JJ custom body (Spraying Systems Co. Wheaton, Illinois, USA) positioned 1.27 cm (0.5 inches) above the top of each test unit. Test compounds were sprayed at 50 ppm and replicated three times. After spraying of the formulated test compound, each test unit was allowed to dry for 1 hour and then a black, screened cap was placed on top. The test units were held for 6 days in a growth chamber at 25 0C and 70% relative humidity. Each test unit was visually assessed for insect mortality. Of the compounds tested, the following resulted in at least 80% insect mortality: 1, 3, 4, 7, 8, 11, 12 and 14.
TEST B
For evaluating control of fall armyworm (Spodoptera frugiperda) the test unit consisted of a small open container with a 4-5-day-old corn (maize) plant inside. This was pre-infested (using a core sampler) with 10-15 1-day-old larvae on a piece of insect diet. Test compounds were formulated and sprayed at 50 ppm as described for Test A.
The applications were replicated three times. After spraying, the test units were maintained in a growth chamber and then visually rated as described for Test A.
Of the compounds tested, the following resulted in at least 80% insect mortality: 1 and 11.

Claims

What is claimed is: 1. A compound of Formula 1, an N-oxide, or a salt thereof,
Λ.
Figure imgf000072_0001
wherein
X is O or S;
J is a phenyl optionally substituted with one to four substituents independently selected from R5; or J is a heterocyclic ring selected from the group consisting of
Figure imgf000072_0002
J-5 J-6 J-7 J-8
R1 is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkenyl, C2-C6 haloalkynyl, C3-C6 halocycloalkyl, halogen, -CN, - CHO, -NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C2-C4 alkylaminocarbonyl, C3-Cs dialkylaminocarbonyl, C1-C4 alkylamino or C2-C6 dialkylamino;
R2 is H, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkenyl, C2-C6 haloalkynyl, C3-C6 halocycloalkyl, halogen, -CN, -CHO, -NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C2-C4 alkylaminocarbonyl, C3-C5 dialkylaminocarbonyl, C1-C4 alkylamino or C2-C6 dialkylamino; R3 is -C(=B)C(=O)L or -C(R11R^)CC=O)L;
R4 is H; or C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each optionally substituted with one or more substituents selected from the group consisting of halogen, -CN, -NO2, hydroxy, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C2-C4 alkoxycarbonyl, C1- C4 alkylamino, C2-C8 dialkylamino and C3-C5 cycloalkylamino; or R4 is C2-C6 alkylcarbonyl, C2-C6 alkoxycarbonyl, C2-C6 alkylaminocarbonyl or C3-Cg dialkylaminocarbonyl; or
R3 and R4 are taken together as -C(=B)C(=O)- or -C(R11R^)CC=O)- wherein the left-hand of these moieties is bonded as R3 and the right-hand as R4; each R5 is independently C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl,1 halogen, -CN, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 haloalkoxy, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl or C1-C4 haloalkylsulfonyl; or phenyl or pyridyl, each optionally substituted with one to three R9;
R6 is H, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, -CN, C1-C4 alkoxy, C2-C4 alkoxycarbonyl, C1-C4 alkylthio, C1-C4 haloalkoxy, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl or C1-C4 haloalkylsulfonyl; R7 is C1-C6 alkyl optionally substituted with one or more substituents selected from the group consisting of halogen, -CN, -NO2, hydroxy, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C2-C4 alkoxycarbonyl, C1-C4 alkylamino, C2-Cg dialkylamino and C3-C6 cycloalkylamino; or R7 is phenyl or pyridyl, each optionally substituted with one to three substituents selected from R9;
R8 is H, C1-C6 alkyl, C1-C6 haloalkyl, C3-C6 alkenyl, C3-C6 haloalkenyl, C3-C6 alkynyl or C3-C6 haloalkynyl; each R9 is independently C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, halogen, -CN, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 haloalkoxy, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl or C1-C4 haloalkylsulfonyl;
R11 and R12 are independently H; halogen; -CN; OR13; or C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each optionally substituted with one or more halogen;
B is O, NR13, NOR13 or NNR14R15; L is OH or NR14R15;
R13 is H; or C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C6 cycloalkyl, each optionally substituted with one or more halogen; Rl4 and R15 are independently H; G; or C1-C6 alkyl, C2-C6 alkenyl or C2-C6 alkynyl, each optionally substituted with one or more substituents selected from the group consisting of G, halogen, -CN, -NO2, hydroxy, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C1-C4 alkylamino, C2-Cg dialkylamino and C3"C6 cycloalkylamino; or
R14 and R15 are taken together with the nitrogen to which they are attached to form a ring containing 2 to 6 atoms of carbon and optionally one additional atom of nitrogen, sulfur or oxygen, said ring optionally substituted with 1 to 4 substituents selected from the group consisting of C1-C2 alkyl, halogen, -CN,
-NO2 and C1-C2 alkoxy; and each G is independently a 3- to 6-membered nonaromatic carbocyclic or heterocyclic ring, optionally including one or two ring members selected from the group consisting of C(=O), S(O) or S(O)2 and optionally substituted with 1 to 4 substituents selected from the group consisting of C1-C2 alkyl, halogen, -CN, -NO2 and C1-
C2 alkoxy.
2. The compound of Claim 1 wherein R1 is C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or C1-C4 haloalkoxy; R2 is H, C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, -CHO, -NO2, C1-C4 alkoxy,
C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl or C2-C4 alkoxycarbonyl ;
R3 is -C(=0)C(=0)0H, -C(RnR12)C(=O)OH, -C(=O)C(=O)NR14R15 or -C(R11R12)C(=O)NR14R15; and
R4 is H, C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C3-C6 cycloalkyl, C2-C6 alkylcarbonyl or C2-C6 alkoxycarbonyl; or R3 and R4 are taken together as -C(=O)C(=O)-, -C(=NR13)C(=0)- or
-C(R11R12)C(=0)-.
3. The compound of Claim 2 wherein
R1 is CH3, CF3, OCF3, OCHF2, -CN or halogen;
R2 is H, CH3, CF3, OCF3, OCHF2, S(O)pCF3, S(O)pCHF2, -CN or halogen; R4 is H; and p is 0, 1 or 2.
4. The compound of Claim 3 wherein each R5 is independently C1-C4 alkyl, C1-C4 haloalkyl, halogen, -CN, C1-C4 alkoxy or
C1-C4 haloalkoxy; each R6 is independently C1-C4 haloalkyl, halogen, -CN or C1-C4 haloalkoxy; R7 is phenyl optionally substituted with one to three substituents independently selected from R9; or R? is
Figure imgf000075_0001
each R9 is independently C1-C4 alkyl, C1-C4 haloalkyl, halogen or -CN; R8 is CH2CF3 or CHF2; and n is 0, 1 or 2.
5. The compound of Claim 3 wherein each R6 is independently halogen, OCH2CF3, OCHF2 or CF3; each R9 is independently CH3, CF3, -CN or halogen.
6. The compound of Claim 5 wherein
J is a heterocyclic ring selected from the group consisting of J-I, J-2 and J-3.
7. The compound of Claim 6 wherein RMs CH35 F5 Cl5 Br Or I; R2 is H, CH3, CF3, -CN, F, Cl, Br or I; and each R6 is independently Cl, Br, OCH2CF3 or CF3.
8. The compound of Claim 7 wherein R3 is -C(=O)C(=O)OH.
9. The compound of Claim 7 wherein R3 is -C(=O)C(=O)NR14R15.
10. The compound of Claim 1 that is selected from the group consisting of: l-(3-chloro-2-pyridinyl)-N-[2-methyl-6-[2-(l-methylethyl)amino]-2- oxoethyljphenylJ-S-Ctrifluoromethy^-lH-pyrazole-S-carboxamide; 1 -(3 -chloro-2-pyridinyl)-iV- [2- [(diethylamino)oxoacetyl] -4,6-dimethylphenyl] -3 - (trifluoromethyl)-lH-pyrazole-5-carboxamide;
1 -(3-chloro-2-pyridinyl)-iV-[2- [( lZ)-2-(diethylamino)- 1 -(hydroxyimino)-2- oxoethyl]-4,6-dimethylphenyl]-3-(trifluoromethyl)-lH-pyrazole-5-carboxamide; 2-[[[3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazol-5-yl]carbonyl]amino]-5- chloro-3-methyl-α-oxobenzeneacetic acid; l-[[3-bromo-l-(3-chloro-2-pyridinyl)-lH-pyrazol-5-yl]carbonyl]-5-chloro-7- methyl-lH-indole-2,3-dione;
3-bromo-N-[4-chloro-2-methyl-6-(lE)-2-(methylamino)-l-(methylimino)-2- oxoethyl]phenyl]-l-(3-chloro-2-pyridinyl)-lΗ-pyrazole-5-carboxamide; and 3-bromo-iV- [4-chloro-2-methyl-6- [(methylamino)oxoacetyl] phenyl] - 1 -(3 -chloro- 2-pyridinyl)-lH-pyrazole-5-carboxamide.
11. A composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Claim 1 and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent.
12. The composition of Claim 11 in the form of a soil drench liquid formulation.
13. A bait composition for controlling an invertebrate pest, comprising:
(a) a biologically effective amount of the compound of Claim 1 or the composition of Claim 11;
(b) one or more food materials;
(c) optionally an attractant; and (d) optionally a humectant.
14. A trap device for controlling an invertebrate pest, comprising:
(a) the bait composition of Claim 13; and
(b) a housing adapted to receive the bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to the bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
15. A spray composition for controlling an invertebrate pest, comprising:
(a) a biologically effective amount of the compound of Claim 1 or the composition of Claim 11; and
(b) a propellant.
16. A method for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of the compound of Claim 1.
17. A method for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with the composition of Claim 11.
18. The method of Claim 17 wherein the environment is soil and the composition is applied to the soil as a soil drench formulation.
19. A method for controlling a cockroach, an ant or a termite, comprising contacting the cockroach, the ant, or the termite with the bait composition in the trap device of Claim
14.
20. A method for controlling a mosquito, a black fly, a stable, fly, a deer fly, a horse fly, a wasp, a yellow jacket, a hornet, a tick, a spider, an ant, or a gnat, comprising contacting the mosquito, the black fly, the stable fly, the deer fly, the horse fly, the wasp, the yellow jacket, the hornet, the tick, the spider, the ant, or the gnat with the spray composition of Claim 15 dispensed from a spray container.
PCT/US2006/032726 2005-08-24 2006-08-22 Anthranilamides for controlling invertebrate pests WO2007024833A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
AU2006283181A AU2006283181A1 (en) 2005-08-24 2006-08-22 Anthranilamides for controlling invertebrate pests
US11/989,348 US8012499B2 (en) 2005-08-24 2006-08-22 Anthranilamides for controlling invertebrate pests
JP2008528057A JP5039703B2 (en) 2005-08-24 2006-08-22 Anthranilamides for invertebrate pest control
EP06802052A EP1924575A1 (en) 2005-08-24 2006-08-22 Anthranilamides for controlling invertebrate pests
BRPI0617046-3A BRPI0617046A2 (en) 2005-08-24 2006-08-22 compound, invertebrate pest control composition, bait composition for invertebrate pest control, spray composition for invertebrate pest control, invertebrate pest control methods, cockroach, ant or termite control method and mosquito, fly control method black, stable flies, deer flies, horse flies, wasps, hornets, hornets, ticks, spiders, ants or mosquitoes
MX2008002236A MX2008002236A (en) 2005-08-24 2006-08-22 Anthranilamides for controlling invertebrate pests.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US71103005P 2005-08-24 2005-08-24
US60/711,030 2005-08-24

Publications (2)

Publication Number Publication Date
WO2007024833A1 true WO2007024833A1 (en) 2007-03-01
WO2007024833B1 WO2007024833B1 (en) 2007-04-19

Family

ID=37441930

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2006/032726 WO2007024833A1 (en) 2005-08-24 2006-08-22 Anthranilamides for controlling invertebrate pests

Country Status (9)

Country Link
US (1) US8012499B2 (en)
EP (1) EP1924575A1 (en)
JP (1) JP5039703B2 (en)
KR (1) KR20080038426A (en)
CN (1) CN101243067A (en)
AU (1) AU2006283181A1 (en)
BR (1) BRPI0617046A2 (en)
MX (1) MX2008002236A (en)
WO (1) WO2007024833A1 (en)

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007144100A1 (en) 2006-06-13 2007-12-21 Bayer Cropscience Ag Anthranilic acid diamide derivative with hetero-aromatic and hetero-cyclic substituents
WO2011098408A2 (en) 2010-02-09 2011-08-18 Bayer Cropscience Ag Hydrazine-substituted anthranilic acid derivatives
WO2011128329A1 (en) 2010-04-16 2011-10-20 Bayer Cropscience Ag Triazole-substituted anthranilic acid amides as pesticides
WO2011157653A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Anthranilic acid derivatives
WO2011157654A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Anthranilic acid diamide derivatives
WO2011157663A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Novel ortho-substituted aryl amide derivatives
WO2011157651A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Anthranilic acid diamide derivatives with cyclical side chains
WO2012004208A1 (en) 2010-07-09 2012-01-12 Bayer Cropscience Ag Anthranilic acid diamide derivative as a pesticide
EP2484676A2 (en) 2008-12-18 2012-08-08 Bayer CropScience AG Tetrazol-substituted anthranilic acid amides as pesticides
WO2013024008A1 (en) 2011-08-12 2013-02-21 Basf Se Aniline type compounds
WO2013024006A1 (en) * 2011-08-12 2013-02-21 Basf Se Anthranilamide compounds and their use as pesticides
EP2606732A1 (en) 2011-12-19 2013-06-26 Bayer CropScience AG Use of an anthranilic diamide derivatives with heteroaromatic and heterocyclic substituents in combination with a biological control agent
WO2013092519A1 (en) 2011-12-19 2013-06-27 Bayer Cropscience Ag Use of anthranilic acid diamide derivatives for pest control in transgenic crops
WO2014053395A1 (en) 2012-10-01 2014-04-10 Basf Se Use of n-thio-anthranilamide compounds on cultivated plants
WO2014053405A1 (en) 2012-10-01 2014-04-10 Basf Se Pesticidally active mixtures comprising anthranilamide compounds
WO2014053406A1 (en) 2012-10-01 2014-04-10 Basf Se Method of controlling ryanodine-modulator insecticide resistant insects
WO2014053404A1 (en) 2012-10-01 2014-04-10 Basf Se Pesticidally active mixtures comprising anthranilamide compounds
WO2014053403A1 (en) 2012-10-01 2014-04-10 Basf Se Method of controlling insecticide resistant insects
WO2014053407A1 (en) 2012-10-01 2014-04-10 Basf Se N-thio-anthranilamide compounds and their use as pesticides
WO2014053401A2 (en) 2012-10-01 2014-04-10 Basf Se Method of improving plant health
WO2014079820A1 (en) 2012-11-22 2014-05-30 Basf Se Use of anthranilamide compounds for reducing insect-vectored viral infections
US9044016B2 (en) 2011-08-12 2015-06-02 Basf Se N-thio-anthranilamide compounds and their use as pesticides
US9056853B2 (en) 2005-07-07 2015-06-16 Basf Se N-Thio-anthranilamid compounds and their use as pesticides
US9533968B2 (en) 2012-05-24 2017-01-03 Basf Se N-thio-anthranilamide compounds and their use as pesticides
US9609868B2 (en) 2013-03-06 2017-04-04 Bayer Cropscience Ag Alkoximino-substituted anthranilic acid diamides as pesticides
WO2019123194A1 (en) 2017-12-20 2019-06-27 Pi Industries Ltd. Anthranilamides, their use as insecticide and processes for preparing the same.
WO2019123195A1 (en) 2017-12-20 2019-06-27 Pi Industries Ltd. Pyrazolopyridine-diamides, their use as insecticide and processes for preparing the same.
WO2019150220A1 (en) 2018-01-30 2019-08-08 Pi Industries Ltd. Novel anthranilamides, their use as insecticide and processes for preparing the same.

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100031556A1 (en) * 2007-01-08 2010-02-11 Km Investors, Llc Device and method for controlling insect pests
GB0716414D0 (en) * 2007-08-22 2007-10-03 Syngenta Participations Ag Novel insecticides
JP5894928B2 (en) * 2009-12-28 2016-03-30 バイエル・クロップサイエンス・アクチェンゲゼルシャフト Fungicide hydroxymoyl-heterocyclic derivative
JP5676736B2 (en) * 2010-03-16 2015-02-25 ニサス・コーポレーション Wood-based termite bait system
WO2013069771A1 (en) * 2011-11-11 2013-05-16 Ｍｅｉｊｉ Ｓｅｉｋａファルマ株式会社 Anthranilic acid derivative and noxious organism control agent
CN104472500B (en) * 2014-12-15 2016-06-29 广西颐生园生态农业有限公司 Composition pesticide containing Aminothiocarbonylbenzene and triazole bactericidal agent
CA3002451A1 (en) 2015-11-18 2017-05-26 Monsanto Technology Llc Insecticidal compositions and methods

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003015519A1 (en) * 2001-08-13 2003-02-27 E.I. Du Pont De Nemours And Company Arthropodicidal anthranilamides
WO2003016300A1 (en) * 2001-08-15 2003-02-27 E. I. Du Pont De Nemours And Company Ortho-substituted aryl amides for controlling invertebrate pests
WO2003106427A2 (en) * 2002-06-13 2003-12-24 E.I. Du Pont De Nemours And Company Pyrazolecarboxamide insecticides

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1246847A (en) 1996-12-23 2000-03-08 杜邦药品公司 Nitrogen containing heteroaromatics as factor Xa inhibitors
PT991625E (en) 1997-06-19 2005-10-31 Bristol Myers Squibb Pharma Co XA FACTOR INHIBITORS WITH A P1 NEUTRAL SPECIFICITY GROUP
MY138097A (en) 2000-03-22 2009-04-30 Du Pont Insecticidal anthranilamides
US20040102324A1 (en) 2002-02-28 2004-05-27 Annis Gary David Heterocyclic diamide invertebrate pest control agents
AU2002305669B2 (en) 2001-05-21 2008-09-11 E.I. Du Pont De Nemours And Company Diamide invertebrate pest control agents containing a non-aromatic heterocyclic ring
TWI327566B (en) 2001-08-13 2010-07-21 Du Pont Novel substituted ihydro 3-halo-1h-pyrazole-5-carboxylates,their preparation and use
TWI325302B (en) 2001-08-13 2010-06-01 Du Pont Benzoxazinone compounds
DE60236600D1 (en) 2001-08-13 2010-07-15 Du Pont SUBSTITUTED 1H-DIHYDROPYRAZOLE, THEIR PREPARATION AND USE
ES2255624T3 (en) 2001-08-15 2006-07-01 E. I. Du Pont De Nemours And Company ARIL AMIDAS REPLACED WITH ORTO-HETEROCICLIC GROUPS FOR THE CONTROL OF INVERTEBRATE PESTS.
CN100453532C (en) 2001-08-16 2009-01-21 纳幕尔杜邦公司 Substituted anthranilamides for controlling invertebrate pests
CN1279038C (en) 2001-09-21 2006-10-11 杜邦公司 Arthropodicidal anthranilamides
JP2005504084A (en) 2001-09-21 2005-02-10 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Insecticidal diamide
TWI283164B (en) 2001-09-21 2007-07-01 Du Pont Anthranilamide arthropodicide treatment
US7148217B2 (en) 2001-10-15 2006-12-12 E. I. Du Pont De Nemours And Company Iminobenzoxazines, iminobenzthiazines and iminoquinazolines for controlling invertebrate pests
US20040110777A1 (en) 2001-12-03 2004-06-10 Annis Gary David Quinazolinones and pyridinylpyrimidinones for controlling invertebrate pests
EP1467985A1 (en) 2002-01-22 2004-10-20 E.I. Du Pont De Nemours And Company Diamide invertebrate pest control agents
EP1467988B1 (en) 2002-01-22 2013-07-17 E.I. Du Pont De Nemours And Company Quinazoline(di)ones for invertebrate pest control
EP1511385B1 (en) 2002-06-11 2005-11-30 E.I. Du Pont De Nemours And Company Insecticidal amides with nitrogen-containing benzo-fused bicyclic ring systems
TWI343376B (en) 2002-07-31 2011-06-11 Du Pont Method for preparing 3-halo-4, 5-dihydro-1h-pyrazoles
TWI326283B (en) 2002-07-31 2010-06-21 Du Pont Method for preparing fused oxazinones
US7211270B2 (en) 2002-10-04 2007-05-01 E. I. Du Pont De Nemours And Company Anthranilamide insecticides
US7666882B2 (en) 2002-11-15 2010-02-23 E.I. Du Pont De Nemours And Company Anthranilamide insecticides
US20040096102A1 (en) * 2002-11-18 2004-05-20 Xerox Corporation Methodology for scanned color document segmentation
PL209772B1 (en) 2003-01-28 2011-10-31 Du Pont Cyano anthranilamide insecticides
TWI367882B (en) 2003-03-26 2012-07-11 Du Pont Preparation and use of 2-substituted-5-oxo-3-pyrazolidinecarboxylates
JP4543043B2 (en) 2003-06-12 2010-09-15 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Process for producing condensed oxazinone
TWI336325B (en) 2004-01-23 2011-01-21 Du Pont Process for the manufacture of 2,3-dichloropyridine
WO2005118552A2 (en) 2004-04-13 2005-12-15 E.I. Dupont De Nemours And Company Anthranilamide insecticides
GT200500179BA (en) 2004-07-01 2008-10-29 SYNERGIST MIXTURES OF ANTRANILAMIDE AGENTS FOR THE CONTROL OF INVERTEBRATE PESTS
MY140912A (en) 2004-07-26 2010-01-29 Du Pont Mixtures of anthranilamide invertebrate pest control agents
AU2005277228A1 (en) 2004-08-17 2006-03-02 E.I. Dupont De Nemours And Company Novel anthranilamides useful for controlling invertebrate pests
EA012929B1 (en) 2004-11-18 2010-02-26 Е.И. Дюпон Де Немур Энд Компани Anthranilamide insecticides
TWI363756B (en) 2004-12-07 2012-05-11 Du Pont Method for preparing n-phenylpyrazole-1-carboxamides
PL1858878T3 (en) 2005-03-18 2012-09-28 Du Pont Conversion of 2-pyrazolines to pyrazoles using bromine
CA2539012C (en) * 2006-03-10 2013-07-09 John Flottvik Closed retort charcoal reactor system

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003015519A1 (en) * 2001-08-13 2003-02-27 E.I. Du Pont De Nemours And Company Arthropodicidal anthranilamides
WO2003016300A1 (en) * 2001-08-15 2003-02-27 E. I. Du Pont De Nemours And Company Ortho-substituted aryl amides for controlling invertebrate pests
WO2003106427A2 (en) * 2002-06-13 2003-12-24 E.I. Du Pont De Nemours And Company Pyrazolecarboxamide insecticides

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT [ABTEILUNG] B: ABHANDLUNGEN , 55B, 2681-97 CODEN: BDCBAD; ISSN: 0365-9488, 1922 *
DATABASE CAPLUS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; HELLER, GUSTAV: "New isomerisms in the isatin series. V", XP002409890, retrieved from STN Database accession no. 1923:5524 *

Cited By (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9056853B2 (en) 2005-07-07 2015-06-16 Basf Se N-Thio-anthranilamid compounds and their use as pesticides
US9365543B2 (en) 2005-07-07 2016-06-14 Basf Se N-Thio-anthranilamid compounds and their use as pesticides
US8101550B2 (en) 2006-06-13 2012-01-24 Bayer Cropscience Ag Anthranilic acid diamide derivative with hetero-aromatic and hetero-cyclic substituents
US8946236B2 (en) 2006-06-13 2015-02-03 Bayer Cropscience Ag Anthranilic acid diamide derivative with hetero-aromatic and hetero-cyclic substituents
US8536092B2 (en) 2006-06-13 2013-09-17 Bayer Cropscience Ag Anthranilic acid diamide derivative with hetero-aromatic and hetero-cyclic substituents
WO2007144100A1 (en) 2006-06-13 2007-12-21 Bayer Cropscience Ag Anthranilic acid diamide derivative with hetero-aromatic and hetero-cyclic substituents
US8324390B2 (en) 2008-12-18 2012-12-04 Bayer Cropscience Ag Tetrazole-substituted anthranilamides as pesticides
EP2484676A2 (en) 2008-12-18 2012-08-08 Bayer CropScience AG Tetrazol-substituted anthranilic acid amides as pesticides
US8410106B2 (en) 2010-02-09 2013-04-02 Bayer Cropscience Ag Hydrazine-substituted anthranilic acid derivatives
WO2011098408A2 (en) 2010-02-09 2011-08-18 Bayer Cropscience Ag Hydrazine-substituted anthranilic acid derivatives
US8536202B2 (en) 2010-04-16 2013-09-17 Bayer Cropscience Ag Triazole-substituted anthranilamides as pesticides
WO2011128329A1 (en) 2010-04-16 2011-10-20 Bayer Cropscience Ag Triazole-substituted anthranilic acid amides as pesticides
TWI486124B (en) * 2010-04-16 2015-06-01 Bayer Cropscience Ag Triazole-substituted anthranilamides as pesticides
US8658800B2 (en) 2010-06-15 2014-02-25 Bayer Cropscience Ag Ortho-substituted arylamide derivatives
WO2011157654A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Anthranilic acid diamide derivatives
WO2011157653A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Anthranilic acid derivatives
WO2011157663A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Novel ortho-substituted aryl amide derivatives
US8791143B2 (en) 2010-06-15 2014-07-29 Bayer Cropscience Ag Anthranilic diamide derivatives having cyclic side-chains
US8980886B2 (en) 2010-06-15 2015-03-17 Bayer Cropscience Ag Anthranilic acid derivatives
WO2011157651A1 (en) 2010-06-15 2011-12-22 Bayer Cropscience Ag Anthranilic acid diamide derivatives with cyclical side chains
US8791139B2 (en) 2010-06-15 2014-07-29 Bayer Cropscience Ag Anthranilic diamide derivatives
US9790202B2 (en) 2010-07-09 2017-10-17 Bayer Intellectual Property Gmbh Anthranilamide derivatives as pesticides
WO2012004208A1 (en) 2010-07-09 2012-01-12 Bayer Cropscience Ag Anthranilic acid diamide derivative as a pesticide
US9044016B2 (en) 2011-08-12 2015-06-02 Basf Se N-thio-anthranilamide compounds and their use as pesticides
WO2013024008A1 (en) 2011-08-12 2013-02-21 Basf Se Aniline type compounds
WO2013024006A1 (en) * 2011-08-12 2013-02-21 Basf Se Anthranilamide compounds and their use as pesticides
WO2013092519A1 (en) 2011-12-19 2013-06-27 Bayer Cropscience Ag Use of anthranilic acid diamide derivatives for pest control in transgenic crops
US9854802B2 (en) 2011-12-19 2018-01-02 Bayer Intellectual Property Gmbh Use of an anthranilic diamide derivatives with heteroaromatic and heterocyclic substituents in combination with a biological control agent
US9572342B2 (en) 2011-12-19 2017-02-21 Bayer Intellectual Property Gmbh Use of an anthranilic diamide derivatives with heteroaromatic and heterocyclic substituents in combination with a biologicalcontrol agent
US9414595B2 (en) 2011-12-19 2016-08-16 Bayer Cropscience Ag Use of anthranilic acid diamide derivatives for pest control in transgenic crops
EP2606732A1 (en) 2011-12-19 2013-06-26 Bayer CropScience AG Use of an anthranilic diamide derivatives with heteroaromatic and heterocyclic substituents in combination with a biological control agent
WO2013092516A1 (en) 2011-12-19 2013-06-27 Bayer Intellectual Property Gmbh Use of an anthranilic diamide derivatives with heteroaromatic and heterocyclic substituents in combination with a biological control agent
US9533968B2 (en) 2012-05-24 2017-01-03 Basf Se N-thio-anthranilamide compounds and their use as pesticides
WO2014053406A1 (en) 2012-10-01 2014-04-10 Basf Se Method of controlling ryanodine-modulator insecticide resistant insects
WO2014053395A1 (en) 2012-10-01 2014-04-10 Basf Se Use of n-thio-anthranilamide compounds on cultivated plants
WO2014053405A1 (en) 2012-10-01 2014-04-10 Basf Se Pesticidally active mixtures comprising anthranilamide compounds
WO2014053403A1 (en) 2012-10-01 2014-04-10 Basf Se Method of controlling insecticide resistant insects
WO2014053404A1 (en) 2012-10-01 2014-04-10 Basf Se Pesticidally active mixtures comprising anthranilamide compounds
WO2014053401A2 (en) 2012-10-01 2014-04-10 Basf Se Method of improving plant health
WO2014053407A1 (en) 2012-10-01 2014-04-10 Basf Se N-thio-anthranilamide compounds and their use as pesticides
WO2014079820A1 (en) 2012-11-22 2014-05-30 Basf Se Use of anthranilamide compounds for reducing insect-vectored viral infections
US9609868B2 (en) 2013-03-06 2017-04-04 Bayer Cropscience Ag Alkoximino-substituted anthranilic acid diamides as pesticides
WO2019123194A1 (en) 2017-12-20 2019-06-27 Pi Industries Ltd. Anthranilamides, their use as insecticide and processes for preparing the same.
WO2019123195A1 (en) 2017-12-20 2019-06-27 Pi Industries Ltd. Pyrazolopyridine-diamides, their use as insecticide and processes for preparing the same.
WO2019150220A1 (en) 2018-01-30 2019-08-08 Pi Industries Ltd. Novel anthranilamides, their use as insecticide and processes for preparing the same.

Also Published As

Publication number Publication date
MX2008002236A (en) 2008-03-27
AU2006283181A1 (en) 2007-03-01
US20090269300A1 (en) 2009-10-29
KR20080038426A (en) 2008-05-06
JP2009506039A (en) 2009-02-12
EP1924575A1 (en) 2008-05-28
CN101243067A (en) 2008-08-13
WO2007024833B1 (en) 2007-04-19
US8012499B2 (en) 2011-09-06
JP5039703B2 (en) 2012-10-03
BRPI0617046A2 (en) 2011-07-12

Similar Documents

Publication Publication Date Title
US8012499B2 (en) Anthranilamides for controlling invertebrate pests
EP1812421B1 (en) Anthranilamide insecticides
AU2003295491B2 (en) Novel anthranilamide insecticides
AU2003212811B2 (en) Quinazoline(di) ones for invertebrate pest control
EP1389190B1 (en) Diamide invertebrate pest control agents containing a non-aromatic heterocyclic ring
US20090143410A1 (en) Isoxazolines for Controlling Invertebrate Pests
WO2007123855A2 (en) Pyrazolines for controlling invertebrate pests
WO2003106427A2 (en) Pyrazolecarboxamide insecticides
WO2006023783A1 (en) Novel anthranilamides useful for controlling invertebrate pests
WO2005118552A2 (en) Anthranilamide insecticides
AU2003282711A1 (en) Anthranilamide insecticides
WO2007089455A1 (en) Fluoroalkenyl derivatives as insecticides and nematicides
EP3887354B1 (en) Meta-diamide compounds for controlling invertebrate pests
WO2013173218A1 (en) 1,3-diaryl-substituted heterocyclic pesticides
WO2013063282A1 (en) 1,3-diaryl-substituted heterocyclic pesticides
ZA200806394B (en) Anthranilamide insecticides
WO2012012366A1 (en) Pesticidal 3-(aryloxy)azacycloalkanes
US20190161487A1 (en) Heterocycle-substituted bicyclic azole pesticides
TWI381805B (en) Anthranilamide insecticides
MX2007005816A (en) Anthranilamide insecticides

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200680030538.0

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 11989348

Country of ref document: US

Ref document number: 2006283181

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 1054/DELNP/2008

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: MX/a/2008/002236

Country of ref document: MX

ENP Entry into the national phase

Ref document number: 2006283181

Country of ref document: AU

Date of ref document: 20060822

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2008528057

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2006802052

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: KR

ENP Entry into the national phase

Ref document number: PI0617046

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20080222