US20220104496A1 - Pesticidally active bi- or tricyclic heterocycles with sulfur containing substituents - Google Patents

Pesticidally active bi- or tricyclic heterocycles with sulfur containing substituents Download PDF

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US20220104496A1
US20220104496A1 US17/551,910 US202117551910A US2022104496A1 US 20220104496 A1 US20220104496 A1 US 20220104496A1 US 202117551910 A US202117551910 A US 202117551910A US 2022104496 A1 US2022104496 A1 US 2022104496A1
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alkyl
cycloalkyl
haloalkyl
spp
alkynyl
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Andrew Edmunds
Michel Muehlebach
Andre Stoller
Olivier Loiseleur
Anke Buchholz
Ottmar Franz Hueter
Roger Graham Hall
Daniel EMERY
Pierre Joseph Marcel Jung
Long Lu
Yaming Wu
Aurelien Bigot
Ruifang Chen
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Syngenta Participations AG
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Syngenta Participations AG
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems

Definitions

  • the present invention relates to insecticidally active heterocyclic sulfur containing derivatives, to processes for their preparation, to compositions comprising those compounds, and to their use for controlling animal pests (including arthropods and in particular insects or representatives of the order Acarina).
  • Heterocyclic compounds with pesticidal action are known and described, for example, in WO 2009/131237, WO 2011/043404, WO 2011/040629, WO 2010/125985, WO 2012/086848, WO 2013/018928, WO 2013/191113, WO 2013/180193 and WO 2013/180194.
  • the present invention accordingly relates to compounds of formula I,
  • A is a radical selected from the group consisting of formulae A 1 to A 8 :
  • B is a radical selected from the group consisting of formulae B 1 to B 11 :
  • L 1 is methylene or a direct bond; V 0 nitrogen or CR 5 ; V 1 is nitrogen or CR 20 ; V 2 is nitrogen or CR 21 ; V 3 is nitrogen or CR 22 ; V 4 is nitrogen or CR 23 ; V 5 is nitrogen or CR 24 ; V 6 is nitrogen or CR 25 ; V 7 is nitrogen or CR 26 ; V 8 is nitrogen or CR 27 ; V 9 is nitrogen, or CR 28 V 10 is nitrogen or CR 29 ; V 11 is nitrogen or CR 30 ; G 1 is nitrogen or CR 31 ; G 2 is nitrogen or CR 32 ; G 3 is —NR 35 , an oxygen atom or a sulfur atom; G 4 is nitrogen or CR 33 ; G 5 is nitrogen or CR 34 ; J 1 , J 2 , J 3 together form together a 5 membered heterocyclic ring, which can be saturated or unsaturated, containing one or two atoms selected from the
  • Compounds of formula I which have at least one basic centre can form, for example, acid addition salts, for example with strong inorganic acids such as mineral acids, for example perchloric acid, sulfuric acid, nitric acid, nitrose acid, a phosphorus acid or a hydrohalic acid, with strong organic carboxylic acids, such as C 1 -C 4 alkanecarboxylic acids which are unsubstituted or substituted, for example by halogen, for example acetic acid, such as saturated or unsaturated dicarboxylic acids, for example oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid or phthalic acid, such as hydroxycarboxylic acids, for example ascorbic acid, lactic acid, malic acid, tartaric acid or citric acid, or such as benzoic acid, or with organic sulfonic acids, such as C 1 -C 4 alkane- or arylsulfonic acids which are unsubstituted or substitute
  • Compounds of formula I which have at least one acidic group can form, for example, salts with bases, for example mineral salts such as alkali metal or alkaline earth metal salts, for example sodium, potassium or magnesium salts, or salts with ammonia or an organic amine, such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower-alkylamine, for example ethyl-, diethyl-, triethyl- or dimethylpropylamine, or a mono-, di- or trihydroxy-lower-alkylamine, for example mono-, di- or triethanolamine.
  • bases for example mineral salts such as alkali metal or alkaline earth metal salts, for example sodium, potassium or magnesium salts
  • salts with ammonia or an organic amine such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower-alkylamine, for example ethyl-, diethy
  • alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl, hexyl, nonyl, decyl and their branched isomers.
  • Alkoxy, alkenyl and alkynyl radicals are derived from the alkyl radicals mentioned.
  • the alkenyl and alkynyl groups can be mono- or polyunsaturated.
  • Halogen is generally fluorine, chlorine, bromine or iodine. This also applies, correspondingly, to halogen in combination with other meanings, such as haloalkyl or halophenyl.
  • Haloalkyl groups preferably have a chain length of from 1 to 6 carbon atoms.
  • Haloalkyl is, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, pentafluoroethyl, 1,1-difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl and 2,2,2-trichloroethyl; preferably trichloromethyl, difluorochloromethyl, difluoromethyl, trifluoromethyl and dichlorofluoromethyl.
  • Alkoxy groups preferably have a preferred chain length of from 1 to 6 carbon atoms.
  • Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy and also the isomeric pentyloxy and hexyloxy radicals; preferably methoxy and ethoxy.
  • Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferably methoxycarbonyl or ethoxycarbonyl.
  • Haloalkoxy groups preferably have a chain length of from 1 to 6 carbon atoms.
  • Haloalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferably difluoromethoxy, 2-chloroethoxy and trifluoromethoxy.
  • Alkylthio groups preferably have a chain length of from 1 to 6 carbon atoms.
  • Alkylthio is, for example, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio or tert-butylthio, preferably methylthio and ethylthio.
  • Alkylsulfinyl is, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl, tert-butylsulfinyl; preferably methylsulfinyl and ethylsulphinyl.
  • Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl or tert-butylsulfonyl; preferably methylsulfonyl or ethylsulfonyl.
  • Alkylamino is, for example, methylamino, ethylamino, n-propylamino, isopropylamino or the isomeric butylamines.
  • Dialkylamino is, for example, dimethylamino, methylethylamino, diethylamino, n-propylmethylamino, dibutylamino and diisopropylamino.
  • Preference is given to alkylamino groups having a chain length of from 1 to 4 carbon atoms.
  • Alkoxyalkyl groups preferably have a chain length of 1 to 6 carbon atoms.
  • Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl or isopropoxyethyl.
  • the cycloalkyl groups preferably have from 3 to 6 ring carbon atoms, for example cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
  • Phenyl also as part of a substituent such as phenoxy, benzyl, benzyloxy, benzoyl, phenylthio, phenylalkyl, phenoxyalkyl, may be substituted.
  • the substituents can be in ortho, meta and/or para position.
  • the preferred substituent positions are the ortho and para positions to the ring attachment point.
  • “mono- to polysubstituted” in the definition of the substituents means typically, depending on the chemical structure of the substituents, monosubstituted to seven-times substituted, preferably monosubstituted to five-times substituted, more preferably mono-, double- or triple-substituted.
  • “5-membered heterocyclic” in the present invention means a 5-membered aromatic heterocyclic group or 5-membered non-aromatic heterocyclic group
  • the “6-membered heterocyclic” means a 6-membered aromatic heterocyclic group or a. 6-membered non-aromatic heterocyclic group
  • a “5- or 6-membered heterocyclic group” in the present invention means a 5- or 6-membered aromatic heterocyclic group, or a 5- or 6-membered non-aromatic heterocyclic group.
  • “5- or 6-membered heterocyclic group, which can be substituted” in the present invention means a heterocyclic group, wherein the hydrogen atom(s) bound to the carbon atom(s), nitrogen atom(s) and/or sulfur atom(s) is/are optionally substituted by one or more atoms or groups selected from a pre-defined list, wherein the group has two or more atoms or groups selected from a pre-defined list, these atoms or groups are the same or different from each other.
  • an N atom or S atom when it's oxidized to form an N oxide or sulfone and sulfoxide respectively, the oxidised analog is not substituted; however, such an analog is within the scope of the invention.
  • Examples of 5- or 6-membered heterocyclic group, which can be substituted include pyrrolidin-1-yl group, a 3,3,4,4-tetrafluoropyrrolidin-1-yl group, a tetrahydrofuran-2-yl group, a piperidyl group, a morpholyl group, a thiomorpholyl group, and the like.
  • Examples of a 5- or 6-membered aromatic heterocyclic groups, which can be substituted, are 2-pyrroly, 2-furyl group, 3-furyl, 5-pyrazolyl, a 4-pyrazolyl, 1-pyrroly, I-methyl-2-pyrroly, 2-methylsulfanyl-1-pyrroly, 2-methylsulfinyl-1-pyrroly, 2-methylsulfonyl-1-pyrroly, a 2-methylamino-1-pyrroly group, a 2-dimethylamino-1-pyrroly group, a 5-bromo-2-furyl, a 5-nitro-2-furyl group, a 5-cyano-2-furyl group, a 5-methoxy-2-furyl group, a 5-acetyl-2-furyl, a 5-methoxycarbonyl-2-furyl group, a 2-methyl-3-furyl group, a 2,5-dimethyl-3-furyl group, a 2,4-dimethyl-3-furyl
  • R 35 is C 1 -C 6 alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 2 -C 6 alkenyloxy, C 2 -C 6 haloalkenyloxy, C 2 -C 6 alkynyloxy, C 2 -C 6 haloalkynyloxy, C 1 -C 6 alkylsulfanyl, C 1 -C 6 haloalkylsulfanyl, C 1 -C 6 alkylsulfinyl, C 1 -C 6 haloalkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 haloalkylsulfonyl, C 2 -C 6 alkylcarbonyl, C 2 -C 6 alkoxycarbonyl, cyano
  • R 4 , R 5 , R 20 , R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 27 , R 28 , R 29 , and R 30 are the same or different and represents cyano, nitro, halogen, hydroxy, —C(O)R 36 or hydrogen; or
  • C 1 -C 6 alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of cyano, halogen, hydroxy, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 2 -C 6 alkenyloxy, C 2 -C 6 haloalkenyloxy, C 2 -C 6 alkynyloxy, C 2 -C 6 haloalkynyloxy, C 1 -C 6 alkylsulphanyl, C 1 -C 6 haloalkylsulphanyl, C 1 -C 6 alkylsulphinyl, C 1 -C 6 haloalkylsulphinyl, C 1 -C 6 alkylsulphonyl, C 1 -C 6 haloalkylsulphonyl, C 2 -C 6 alkylcarbonyl, C 2 -C 6 haloalkylcarbonyl, C 2 -C 6
  • Compounds of formula (I) are made up of a combination of a radical selected from group A and a radical selected from group B.
  • the compound of formula (I) is a radical selected from A and any one radical selected from group B, such as
  • the compound of formula (I) is a radical selected from B and any one radical selected from group A, such as
  • radical A is selected from any one of the following more specific radicals Q 1 to Q 11 from A 1 to A 8 , wherein R 1 is as defined in the first aspect:
  • Embodiment E A group B group E1 A 1 B 1 E2 A 1 B 2 E3 A 1 B 3 E4 A 1 B 4 E5 A 1 B 5 E6 A 1 B 6 E7 A 1 B 7 E8 A 1 B 8 E9 A 1 B 9 E10 A 1 B 10 E11 A 1 B 11 E12 A 2 B 1 E13 A 2 B 2 E14 A 2 B 3 E15 A 2 B 4 E16 A 2 B 5 E17 A 2 B 6 E18 A 2 B 7 E19 A 2 B 8 E20 A 2 B 9 E21 A 2 B 10 E22 A 2 B 11 E23 A 3 B 1 E24 A 3 B 2 E25 A 3 B 3 E26 A 3 B 4 E27 A 3 B 5 E28 A 3 B 6 E29 A 3 B 7 E30 A 3 B 8 E31 A 3 B 9 E32 A 3 B 10 E33 A 3 B 11 E34 A 4 B 1 E35 A 4 B 2 E36 A 4 B 3 E37 A 4 B 4 E38 A 4 B 5 E39 A 4
  • a preferred radical A is A 1 , A 6 , or A 4 ; especially preferred is A 1 and A 6 ; in particular A 1 .
  • a preferred radical B is B 1 , B 2 , B 11 , B 7 , B 8 , B 9 , B 10 , B 3 or B 6 ; especially preferred is B 1 , B 2 , B 11 , B 7 , B 8 , B 9 , or B 10 , in particular B 1 , B 2 , B 11 , B 7 , B 8 or B 9 ; such as B 1 , B 2 or B 11 .
  • formula (I) preferably consists of the following combinations of radicals A and B:
  • V 0 in B 1 is CR 5
  • A is different from A 1 .
  • V 0 in B 1 is CR 5 and A is selected from A 2 , A 3 , A 4 , A 5 and A 6 , especially selected from A 4 and A 6 .
  • L 1 in reference to each of B, is a direct bond.
  • R 1 in reference to each of A, is the same or different and each represents hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably hydrogen, bromine, chlorine, methyl, difluoromethyl or trifluoromethyl.
  • R 2 in reference to each of A, is the same or different and each represents, hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably hydrogen.
  • R 3 in reference to each of B, is the same or different and each represents C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably methyl or ethyl.
  • R 4 in reference to each of B, is the same or different and each represents, hydrogen or C 1 -C 3 alkyl; preferably hydrogen or methyl.
  • n in reference to each of B, is the same or different and each represents 0, 1 or 2; preferably 2.
  • R 6 and R 7 in reference to each of B, is the same or different and each represents C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably methyl.
  • R 10 and R 11 in reference to each of B, is the same or different and each represents, hydrogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably hydrogen or methyl.
  • R 11 is hydrogen and R 10 is methyl.
  • R 12 , R 13 , and R 14 in reference to each of B, is the same or different and each represents, hydrogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably hydrogen or methyl.
  • R 13 , and R 14 are each hydrogen and R 12 is methyl.
  • R 15 , R 16 , R 17 and R 18 in reference to each of B, is the same or different and each represents, hydrogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably hydrogen or methyl.
  • R 15 , R 16 , R 17 and R 18 are each hydrogen.
  • R 19 in reference to each of B, is the same or different and represents, hydrogen, C 1 -C 4 alkyl or C 1 -C 4 haloalkyl; preferably hydrogen or tert-butyl.
  • V 1 in reference to each of B, is the same or different and represents CH or N.
  • V 0 in reference to each of B, is the same or different and represents CH or N.
  • V 2 in reference to each of B, is the same or different and represents, CR 21′ , where R 21′ , in reference to each of B, is the same or different and represents, hydrogen, halogen, C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, or phenyl or 4-trifluoromethylphenyl, preferably hydrogen, chlorine, bromine or trifluoromethyl.
  • V 3 in reference to each of B, is the same or different and represents, CR 22′ , where R 22′ , in reference to each of B, is the same or different and represents, hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl, preferably hydrogen, chlorine, bromine or trifluoromethyl.
  • V 4 in reference to each of B, is the same or different and represents, N or CR 23′ , where R 23′ , in reference to each of B, is the same or different and represents, hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably V 4 represents N or CH.
  • V 5 in reference to each of B, is the same or different and represents, N or CR 24′ , where R 24 , in reference to each of B, is the same or different and represents, hydrogen, halogen, C 1 -C 6 alkyl or C 1 -C 6 haloalkyl; preferably V 5 represents CH.
  • V 6 in reference to each of B, is the same or different and represents, N or CR 25′ , where R 25 , in reference to each of B, is the same or different and represents, hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably V 5 represents N or CH.
  • V 7 in reference to each of B, is the same or different and represents, N or CR 26′ , where R 26′ , in reference to each of B, is the same or different and represents, hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably V 7 represents N, CH, C-chlorine, C-bromine or C—CF 3 .
  • V 8 in reference to each of B, is the same or different and represents, N or CR 27 , where R 27′ , in reference to each of B, is the same or different and represents hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably V 8 represents CH.
  • V 9 in reference to each of B, is the same or different and represents, N or CR 28 , where R 28′ , in reference to each of B, is the same or different and represents hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably V 9 represents N or CH.
  • V 10 in reference to each of B, is the same or different and represents, N or CR 29′ , where R 29′ , in reference to each of B, is the same or different and represents hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably V 9 represents N or CH.
  • V 11 in reference to each of B, is the same or different and represents N or CR 30 , where R 30 , in reference to each of B, is the same or different and represents hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably V 9 represents N or CH.
  • G 1 in reference to each of A, is the same or different and represents N or CR 31′ , where R 31′ , in reference to each of A, is the same or different and represents hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably G 1 represents N or CH.
  • G 2 in reference to each of A, is the same or different and represents N or CR 32′ , where R 32′ , in reference to each of A, is the same or different and represents hydrogen, halogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably G 2 represents N or CH.
  • G 3 in reference to each of A, is the same or different and represents oxygen, sulfur or NR 35 , where R 35 is N-methyl, in reference to each of A, is the same or different and represents C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably G 3 represents oxygen, sulfur, or N—CH 3 .
  • G 4 in reference to each of A, is the same or different and represents N or CR 33′ , where R 33′ , in reference to each of A, is the same or different and represents C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably G 4 represents N or N—CH 3 .
  • G 5 in reference to each of A, is the same or different and represents N or CR 34′ , where R 34′ , in reference to each of A, is the same or different and represents hydrogen, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl; preferably G 5 represents N or N—CH 3 .
  • J 1 in reference to each of radical A 4 , is N.
  • J 2 in reference to each of radical A 4 , is CH, C 1 -C 3 alkyl or C 1 -C 3 haloalkyl, such as CH, C—CH 3 , or C—CF 3 .
  • J 3 in reference to each of radical A 4 , is oxygen or sulfur.
  • Q is the radical B 1 , B 2 , B 3 , B 4 , B 5 , B 6 , B 7 , B 8 , B 9 and B 11 , wherein R 3 , R 4 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , V 0 , V 1 , V 2 , V 3 , V 4 , V 5 , V 6 , V 7 , V 8 and L 1 are as described in formula I, and the arrows in the radicals B 1 -B 9 and B 11 show the point of attachment to the carbonyl atom of the carboxyl group In formula II, with a compounds of formula III, IV, or V;
  • R 1 , R 2 , G 1 , G 2 , and G 5 are as described in formula (I) and M 1 is oxygen, sulfur, or NR 35 , in the presence of a dehydrating agent such as polyphosphoric acid at temperature between 150° C. to 200° C., to yield compounds of formula Ia, Ib, and Ic, wherein the substituents are as described for formula (I).
  • a dehydrating agent such as polyphosphoric acid at temperature between 150° C. to 200° C.
  • compounds of formula VI can be prepared by treatment of compounds of formula II with dicyclohexyl carbodiimide (DCC) or 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) to give the activated species IIa, wherein X 0 is X 01 and X 02 respectively, in an inert solvent, e.g. pyridine, or THF optionally in the presence of a base, e.g. triethylamine, at temperatures between 50-180° C.
  • DCC dicyclohexyl carbodiimide
  • EDC 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide
  • compounds of formula (I) can be prepared by reacting compounds of formula IX, X, XI, XII, and XIII;
  • V 0 , V 1 , V 2 , V 3 , V 4 , V 5 , V 6 , V 7 , V 8 and R 4 are as defined for formula (I) and X 04 is halogen, with compounds of formula III, IV and V as described in schemes 2 and 3 to give compounds of formula XIV, XV, XVI, XVII, XVIII, XIX, XX, XXI, XXII, XXIII, XIV, XV, XVI, XVII, and XVIII;
  • R 1 , R 2 , R 4 , G 1 , G 2 , G 5 , V 0 , V 1 , V 2 , V 3 , V 4 , V 5 , V 6 , V 7 , V 3 , J 1 , J 2 and J 3 are as defined in formula I, M 1 is oxygen, sulfur, or NR 35 , and X 04 is halogen.
  • R 3 is as described in formula I, in the presence of a suitable base, such as alkali metal carbonates, for example sodium carbonate and potassium carbonate or alkali metal hydrides such as sodium hydride, in a suitable solvent, at temperatures between 25-120° C. to give compounds of formula Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ip, Iq and Ir:
  • a suitable base such as alkali metal carbonates, for example sodium carbonate and potassium carbonate or alkali metal hydrides such as sodium hydride
  • solvent to be used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butylmethyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile. Similar chemistry has been previously described, as for example in WO 2013018928.
  • the reaction can be carried out in the presence of a palladium catalyst, such as tris(dibenzylideneacetone)dipalladium(0), in the presence of a phosphor ligand, such as xanthphos, in an inert solvent, for example, xylene at temperatures between 100-160° C., preferably 140° C., as described by Perrio et al in Tetrahedron, 61, 5253-5259, 2005.
  • a palladium catalyst such as tris(dibenzylideneacetone)dipalladium(0)
  • a phosphor ligand such as xanthphos
  • inert solvent for example, xylene
  • Compounds represented by the formula (I) wherein m is 1 or 2 can be produced by oxidizing the compounds of formula Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ip, Iq and Ir.
  • the oxidation reaction is generally conducted in the presence of a solvent.
  • a solvent examples include aliphatic halogenated hydrocarbons such-as dichloromethane and chloroform; alcohols such as methanol and ethanol; acetic acid; water; and mixtures thereof.
  • the oxidant to be used in the reaction include sodium periodate and m-chloroperbenzoic acid.
  • Q 1 is A 1 , A 2 , A 3 , A 4 , and A 8 and X 05 is a halogen or a leaving group OSO 2 R 38
  • the arrows in the substituents in A 1 , A 2 , A 3 , A 4 , and A 6 show the point attachment of the radical A to the substituent X 04
  • R 38 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or phenyl optionally substituted by nitro or C 1 -C 3 alkyl, with a compound of formula XXXI;
  • V 9 , V 10 , and V 11 are as described in formula I, in the presence of a suitable base, such as sodium hydride or cesium carbonate, in an inert solvent such as dimethyl formamide, N-methylpyrollidine, or acetonitrile, at temperatures between 20-150° C., to yield compounds of formula XXXII:
  • a suitable base such as sodium hydride or cesium carbonate
  • an inert solvent such as dimethyl formamide, N-methylpyrollidine, or acetonitrile
  • compounds of formula XXXII can be obtained by reacting compounds of formula XXX with compounds of formula XXXI in an inert solvent such as dioxane, in the presence of a catalytic amount of copper iodide and catalytic amount of a diamine, for example N,N-dimethylethylenediamine or racemic trans-N,N-dimethylcyclohexanediamine, with a base, for example potassium carbonate or potassium phosphate at temperatures between 50-120° C., preferably 90-110° C.
  • a base for example potassium carbonate or potassium phosphate
  • halogenating reagent such as phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide, or thionyl chloride, optionally in an inert solvent at temperatures between 25-120° C., to give compounds of formula XXXIII, wherein X 0s is halogen:
  • R 3 is as described in formula I, in the presence of a suitable base, such as an alkaline earth metal hydride, for example sodium hydride and a polar aprotic solvent, such as dimethyl formamide, at temperatures between 25-120° C. to give compounds of formula Is:
  • a suitable base such as an alkaline earth metal hydride, for example sodium hydride and a polar aprotic solvent, such as dimethyl formamide
  • MCPBA meta-chloroperbenozoic
  • R 1 , R 2 , G 1 , G 2 and G 4 are as described in formula (I) and R 34 is C 1 -C 6 alkyl or C 1 -C 6 haloalkyl can be prepared by reacting a compound of formula XXXIV
  • X 07 is a halogen or a leaving group OSO 2 R 38 and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • a further process to prepare compounds of formula Iu involves reacting a compound of formula XXXIV with a compound of XXXVa
  • M 0 is a boronic acid
  • the reaction is usually carried out in the presence of a base, for example potassium carbonate, cesium carbonate, or potassium phosphate, in an inert solvent, such as dioxane, optionally in the presence of water, with a palladium(0) catalyst, for example tetrakis(triphenylphosphine)palladium, at a temperature between 80-120° C.
  • a base for example potassium carbonate, cesium carbonate, or potassium phosphate
  • an inert solvent such as dioxane
  • a palladium(0) catalyst for example tetrakis(triphenylphosphine)palladium
  • an acyl halide of formula IIa is converted to a Weinreb amide Ib upon reaction with N, O-Dimethylhydroxylamine by methods known to those skilled in the art and described for example in C. Ferri, “Restrokeen der Organischen Synthese”, Georg Thieme Verlag, Stuttgart, 1978, page 223ff.
  • the Weinreb amide of formula Ib is then reacted with a Grignard reagent of formula R 35 CH 2 MgHal according to the method of Weinreb ( Tetrahedron Letters 1981, 22, 3815-3818) to give compounds of formula XXXVb and XXXVa.
  • Compounds of formula XXXVa and XXXVb can also be prepared by treatment of nitrile compounds of formula IIc, wherein Q is as described in formula I, with a Grignard reagent of formula R 35 CH 2 MgHal, followed by acidic hydrolysis (as described in C. Ferri, “Restrokeen der Organischen Synthese”, Georg Thieme Verlag, Stuttgart, 1978, page 223ff.).
  • Compounds of formula XXXVa and XXXVb can be halogenated to compounds of formula XXXV, with for example mixtures of bromine and hydrobromic acid in acetic acid (as described in Phosphorus, Sulfur and Silicon and the Related Elements, 2013, 188(12), 1835-1844) or with, for example, copper(II)bromide in an inert solvent, for example chloroform, ethyl acetate and the like, as described in J. Med. Chem., 2013, 56(1), 84-96.
  • compounds of formula XXXV where R 35 is hydrogen can be prepared directly from compounds of formula IIa by treatment with diazomethane or trimethyl silyl diazomethane and subsequent treatment with an halogen acid, for example, hydrobromic acid or hydrochloric acid in an inert solvent such as diethyl ether.
  • an halogen acid for example, hydrobromic acid or hydrochloric acid in an inert solvent such as diethyl ether.
  • R 1 , G 1 , G 2 are as described in formula (I), and G 5 is CR 34 can be prepared by reacting compounds of formula (XXXIVa),
  • R 1 , R 2 , G 1 , G 2 and G 4 are as described in formula I, can be prepared by reacting a compound of formula XXXVI;
  • R 1 , R 2 , G 1 and G 2 are as described in formula (I) and in which X 00 is a halide ion or an anion of the formula —OSO 2 R 38 with a compound of formula IIa
  • X 0 is a halogen and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • R 1 , R 2 , G 1 and G 2 are as described in formula (I) and in which X 0s is a halogen or a leaving group OSO 2 R 38 , with ammonia (either gaseous or aqueous) as a nucleophile.
  • Ammonia may be used in equimolar amounts or in large excess in an appropriate inert solvent, optionally in a pressurised vessel. The reaction may be performed between 0 and 200° C., optionally with microwave irradiation.
  • Ammonia equivalents such as, for example, ammonium hydroxide NH 4 OH, ammonium acetate NH 4 OAc, ammonium carbonate (NH4)2CO3 may also be used as a nitrogen source.
  • R 1 , R 2 , G 1 and G 2 are as described in formula (I) with reagents such as, for example, phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide in an inert solvent.
  • reagents such as, for example, phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide in an inert solvent.
  • Compounds of the formula XXXVI can be prepared via N-amination by reacting a compound of formula XXXIV above with O-mesitylenesulfonylhydroxylamine (MSH) as amination reagent, as described for example by Y. Tamura et al., J. Heterocyclic Chem. 1975, 12, 107-110.
  • MSH is also known in form of a precursor as its ethyl-acetohydroxamate; a pre-treatment with for example perchloric acid HClO 4 in tetrahydrofurane liberates the required amination reagent MSH.
  • O-mesitylenesulfonyl-hydroxylamine and related aminating reagents have been reviewed: Y. Tamura et al., Synthesis, 1-17, 1977.
  • Q is one of the radical B 1 , B 2 , B 3 , B 4 , B 5 , B 6 , B 7 , B 8 , B 9 or B 11 , and wherein R 1 , R 2 , G 1 , G 2 and G 4 are as described in formula I.
  • X 10 is a halogen or a leaving group OSO 2 R 38 and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • R 1 , R 2 , G 1 and G 2 are as described in formula (I) and in which X 11 ⁇ is a halide ion or an anion of the formula ⁇ OSO 2 R 38 with a compound of formula IIa
  • X 0 is a halogen and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • R 1 , R 2 , G 1 and G 2 are as described in formula (I) and in which X 12 is a halogen or a leaving group OSO 2 R 38 with ammonia (either gaseous or aqueous) as a nucleophile.
  • Ammonia may be used in equimolar amounts or in large excess in an appropriate inert solvent, optionally in a pressurized vessel. The reaction may be performed between 0 and 200° C., optionally with microwave irradiation. Ammonia equivalents such as, for example, ammonium hydroxide NH 4 OH, ammonium acetate NH 4 OAc, and ammonium carbonate (NH 4 ) 2 CO 3 may also be used as a nitrogen source.
  • R 1 , R 2 , G 1 and G 2 are as described in formula (I) with reagents such as, for example, phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide or thionyl chloride in an inert solvent.
  • reagents such as, for example, phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide or thionyl chloride in an inert solvent.
  • Compounds of the formula XLI can be prepared via N-amination by reacting a compound of formula XXXIX above with O-mesitylenesulfonylhydroxylamine (MSH)—or one of its equivalent—as amination reagent, as described previously for the preparation of compounds of the formula XXXVI.
  • MSH O-mesitylenesulfonylhydroxylamine
  • Q is one of the radical B 1 , B 2 , B 3 , B 4 , B 5 , B 6 , B 7 , B 8 , B 9 or B 11 , and wherein R 1 , R 2 , G 1 and G 2 are as described in formula I.
  • X 13 is a halogen or a leaving group OSO 2 R 38 and Q is as defined above, where the arrows in the radicals B 1 , B 2 , B 3 , B 4 , B 5 , B 6 , B 7 , B 8 , B 9 or B 11 show the point of attachment of the substituent X 13 , optionally in the presence of a suitable base in an inert solvent, for example sodium hydride in dimethylformamide, in analogy to, for example, WO10/038081.
  • a suitable base for example sodium hydride in dimethylformamide
  • compounds of the formula Ix can be prepared by reacting a compound of formula XLIV, with a compound of formula XLV under palladium-catalyzed N-arylation conditions as described, for example, in S. L. Buchwald et al., Angew. Chem. Int. Ed., 50, 8944-8947, 2011.
  • Compounds of the formula XLIV above can be prepared through diazotization by treating a compound of formula XLVI
  • R 1 , R 2 , G 1 and G 2 are as described in formula I, with either sodium nitrite and hydrohalic acid in water or with an alkyl nitrite (such as, for example, tert-butyl nitrite or isoamyl nitrite) under anhydrous conditions, optionally in presence of an acid (such as, for example, acetic acid) in an inert solvent (such as, for example, tetrahydrofurane) at temperatures between 0 and 130° C.
  • an acid such as, for example, acetic acid
  • an inert solvent such as, for example, tetrahydrofurane
  • the obtained product XLIX is then treated with a mineral acid, for example aqueous hydrochloric acid, in the presence of an organic co-solvent, for example methanol, acetone, ethanol, THF, etc. to give the product of formula 1y, where the substituents R 1 , R 2 , G 1 , G 2 , L 1 , R 3 , R 4 , V 1 , V 0 and R 39 are as previously described.
  • a mineral acid for example aqueous hydrochloric acid
  • an organic co-solvent for example methanol, acetone, ethanol, THF, etc.
  • Analogous chemistry can be used to introduce such a substituent in R 4 , R 5 , R 20 , R 22 , R 23 , R 24 , R 25 , R 26 , R 27 , R 28 , R 29 , and R 30 .
  • the reactants can be reacted in the presence of a base.
  • suitable bases are alkali metal or alkaline earth metal hydroxides, alkali metal or alkaline earth metal hydrides, alkali metal or alkaline earth metal amides, alkali metal or alkaline earth metal alkoxides, alkali metal or alkaline earth metal acetates, alkali metal or alkaline earth metal carbonates, alkali metal or alkaline earth metal dialkylamides or alkali metal or alkaline earth metal alkylsilylamides, alkylamines, alkylenediamines, free or N-alkylated saturated or unsaturated cycloalkylamines, basic heterocycles, ammonium hydroxides and carbocyclic amines.
  • Examples which may be mentioned are sodium hydroxide, sodium hydride, sodium amide, sodium methoxide, sodium acetate, sodium carbonate, potassium tert-butoxide, potassium hydroxide, potassium carbonate, potassium hydride, lithium diisopropylamide, potassium bis(trimethylsilyl)amide, calcium hydride, triethylamine, diisopropylethylamine, triethylenediamine, cyclohexylamine, N-cyclohexyl-N,N-dimethylamine, N,N-diethylaniline, pyridine, 4-(N,N-dimethylamino)pyridine, quinuclidine, N-methylmorpholine, benzyltrimethylammonium hydroxide and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).
  • DBU 1,8-diazabicyclo[5.4.0]undec-7-ene
  • the reactants can be reacted with each other as such, i.e. without adding a solvent or diluent. In most cases, however, it is advantageous to add an inert solvent or diluent or a mixture of these. If the reaction is carried out in the presence of a base, bases which are employed in excess, such as triethylamine, pyridine, N-methylmorpholine or N,N-diethylaniline, may also act as solvents or diluents.
  • the reaction is advantageously carried out in a temperature range from approximately ⁇ 80° C. to approximately +140° C., preferably from approximately ⁇ 30° C. to approximately +100° C., in many cases in the range between ambient temperature and approximately +80° C.
  • a compound of formula I can be converted in a manner known per se into another compound of formula I by replacing one or more substituents of the starting compound of formula I in the customary manner by (an)other substituent(s) according to the invention.
  • Salts of compounds of formula I can be prepared in a manner known per se.
  • acid addition salts of compounds of formula I are obtained by treatment with a suitable acid or a suitable ion exchanger reagent and salts with bases are obtained by treatment with a suitable base or with a suitable ion exchanger reagent.
  • Salts of compounds of formula I can be converted in the customary manner into the free compounds I, acid addition salts, for example, by treatment with a suitable basic compound or with a suitable ion exchanger reagent and salts with bases, for example, by treatment with a suitable acid or with a suitable ion exchanger reagent.
  • Salts of compounds of formula I can be converted in a manner known per se into other salts of compounds of formula I, acid addition salts, for example, into other acid addition salts, for example by treatment of a salt of inorganic acid such as hydrochloride with a suitable metal salt such as a sodium, barium or silver salt, of an acid, for example with silver acetate, in a suitable solvent in which an inorganic salt which forms, for example silver chloride, is insoluble and thus precipitates from the reaction mixture.
  • a salt of inorganic acid such as hydrochloride
  • a suitable metal salt such as a sodium, barium or silver salt
  • the compounds of formula I which have salt-forming properties, can be obtained in free form or in the form of salts.
  • the compounds of formula I and, where appropriate, the tautomer's thereof, in each case in free form or in salt form, can be present in the form of one of the isomers which are possible or as a mixture of these, for example in the form of pure isomers, such as antipodes and/or diastereomers, or as isomer mixtures, such as enantiomer mixtures, for example racemates, diastereomer mixtures or racemate mixtures, depending on the number, absolute and relative configuration of asymmetric carbon atoms which occur in the molecule and/or depending on the configuration of non-aromatic double bonds which occur in the molecule; the invention relates to the pure isomers and also to all isomer mixtures which are possible and is to be understood in each case in this sense hereinabove and hereinbelow, even when stereochemical details are not mentioned specifically in each case.
  • Diastereomer mixtures or racemate mixtures of compounds of formula I, in free form or in salt form, which can be obtained depending on which starting materials and procedures have been chosen can be separated in a known manner into the pure diasteromers or racemates on the basis of the physicochemical differences of the components, for example by fractional crystallization, distillation and/or chromatography.
  • Enantiomer mixtures such as racemates, which can be obtained in a similar manner can be resolved into the optical antipodes by known methods, for example by recrystallization from an optically active solvent, by chromatography on chiral adsorbents, for example high-performance liquid chromatography (HPLC) on acetyl cellulose, with the aid of suitable microorganisms, by cleavage with specific, immobilized enzymes, via the formation of inclusion compounds, for example using chiral crown ethers, where only one enantiomer is complexed, or by conversion into diastereomeric salts, for example by reacting a basic end-product racemate with an optically active acid, such as a carboxylic acid, for example camphor, tartaric or malic acid, or sulfonic acid, for example camphorsulfonic acid, and separating the diastereomer mixture which can be obtained in this manner, for example by fractional crystallization based on their differing solubilities, to give the di
  • Pure diastereomers or enantiomers can be obtained according to the invention not only by separating suitable isomer mixtures, but also by generally known methods of diastereoselective or enantioselective synthesis, for example by carrying out the process according to the invention with starting materials of a suitable stereochemistry.
  • N-oxides can be prepared by reacting a compound of the formula I with a suitable oxidizing agent, for example the H 2 O 2 /urea adduct in the presence of an acid anhydride, e.g. trifluoroacetic anhydride.
  • a suitable oxidizing agent for example the H 2 O 2 /urea adduct
  • an acid anhydride e.g. trifluoroacetic anhydride
  • the compounds of formula I and, where appropriate, the tautomers thereof, in each case in free form or in salt form, can, if appropriate, also be obtained in the form of hydrates and/or include other solvents, for example those which may have been used for the crystallization of compounds which are present in solid form.
  • the compounds of formula I according to the invention are preventively and/or curatively valuable active ingredients in the field of pest control, even at low rates of application, which have a very favorable biocidal spectrum and are well tolerated by warm-blooded species, fish and plants.
  • the active ingredients according to the invention act against all or individual developmental stages of normally sensitive, but also resistant, animal pests, such as insects or representatives of the order Acarina.
  • the insecticidal or acaricidal activity of the active ingredients according to the invention can manifest itself directly, i. e.
  • the compounds of formula I can be used to combat and control infestations of insect pests such as Lepidoptera, Diptera, Hemiptera, Thysanoptera, Orthoptera, Dictyoptera, Coleoptera, Siphonaptera, Hymenoptera and Isoptera and also other invertebrate pests, for example, acarine, nematode and mollusc pests. Insects, acarines, nematodes and molluscs are hereinafter collectively referred to as pests.
  • the pests which may be combated and controlled by the use of the invention compounds include those pests associated with agriculture (which term includes the growing of crops for food and fibre products), horticulture and animal husbandry, companion animals, forestry and the storage of products of vegetable origin (such as fruit, grain and timber); those pests associated with the damage of man-made structures and the transmission of diseases of man and animals; and also nuisance pests (such as flies).
  • pest species which may be controlled by the compounds of formula I include: Myzus persicae (aphid), Aphis gossypii (aphid), Aphis fabae (aphid), Lygus spp. (capsids), Dysdercus spp. (capsids), Nilaparvata lugens (planthopper), Nephotettixc incticeps (leafhopper), Nezara spp. (stinkbugs), Euschistus spp. (stinkbugs), Leptocorisa spp. (stinkbugs), Frankliniella occidentalis (thrip), Thrips spp.
  • Acarina for example, Acalitus spp, Aculus spp, Acaricalus spp, Aceria spp, Acarus siro, Amblyomma spp., Argas spp., Boophilus spp., Brevipalpus spp., Bryobia spp, Calipitrimerus spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides spp, Eotetranychus spp, Eriophyes spp., Hemitarsonemus spp, Hyalomma spp., Ixodes spp., Olygonychus spp, Ornithodoros spp., Polyphagotarsone latus, Panonychus spp., Phyllocoptruta oleivora, Phytonemus spp, Polyphagotarsonemus spp, Psorop
  • Tetranychus spp. from the order Anoplura , for example, Haematopinus spp., Linognathus spp., Pediculus spp., Pemphigus spp. and Phylloxera spp.; from the order Coleoptera, for example, Agriotes spp., Amphimallon majale, Anomala orientalis, Anthonomus spp., Aphodius spp, Astylus atromaculatus, Ataenius spp, Atomaria linearis, Chaetocnema tibialis, Cerotoma spp, Conoderus spp, Cosmopolites spp., Cotinis nitida, Curculio spp., Cyclocephala spp, Dermestes spp., Diabrotica spp., Diloboderus abderus, Epilachna spp., Eremnus,
  • Trogoderma spp. from the order Diptera, for example, Aedes spp., Anopheles spp, Antherigona soccata, Bactrocea oleae, Bibio hortulanus, Bradysia spp, Calliphora erythrocephala, Ceratitis spp., Chrysomyia spp., Culex spp., Cuterebra spp., Dacus spp., Delia spp, Drosophila melanogaster, Fannia spp., Gastrophilus spp., Geomyza tripunctata, Glossina spp., Hypoderma spp., Hyppobosca spp., Liriomyza spp., Lucilia spp., Melanagromyza spp., Musca spp., Oestrus spp., Orseolia spp., Oscinella fri
  • Hemiptera for example, Acanthocoris scabrator, Acrosternum spp, Adelphocoris lineolatus, Amblypelta nitida, Bathycoelia thalassina, Blissus spp, Cimex spp., Clavigralla tomentosicollis, Creontiades spp, Distantiella theobroma, Dichelops furcatus, Dysdercus spp., Edessa spp, Euchistus spp., Eurydema pulchrum, Eurygaster spp., Halyomorpha halys, Horcias nobilellus, Leptocorisa spp., Lygus spp, Margarodes spp, Murgantia histrionic, Neomegalotomus spp, Nesidiocoris tenuis, Nezara spp., Nysius simul
  • Triatoma spp. from the order Homoptera, for example, Aleurothrixus floccosus, Aleyrodes brassicae, Aonidiella spp., Aphididae, Aphis spp., Aspidiotus spp., Bemisia tabaci, Ceroplaster spp., Chrysomphalus aonidium, Chrysomphalus dictyospermi, Coccus hesperidum, Empoasca spp., Eriosoma larigerum, Erythroneura spp., Gascardia spp., Laodelphax spp., Lecanium corni, Lepidosaphes spp., Macrosiphus spp., Myzus spp., Nephotettix spp., Nilaparvata spp., Parlatoria spp., Pemphigus spp., Planococc
  • Vespa spp. from the order Isoptera, for example, Coptotermes spp, Corniternes cumulans, Incisitermes spp, Macrotermes spp, Mastotermes spp, Microtermes spp, Reticulitermes spp.; Solenopsis geminate; from the order Lepidoptera, for example, Acleris spp., Adoxophyes spp., Aegeria spp., Agrotis spp., Alabama argillaceae, Amylois spp., Anticarsia gemmatalis, Archips spp., Argyresthia spp, Argyrotaenia spp., Autographa spp., Bucculatrix thurberiella, Busseola fusca, Cadra cautella, Carposina nipponensis, Chilo spp., Choristoneura spp., Chrysoteuchia topiaria, C
  • Orthoptera for example, Blatta spp., Blattella spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Neocurtilla hexadactyla, Periplaneta spp., Scapteriscus spp, and Schistocerca spp.; from the order Psocoptera, for example, Liposcelis spp.; from the order Siphonaptera, for example, Ceratophyllus spp., Ctenocephalides spp.
  • Orthoptera for example, Blatta spp., Blattella spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Neocurtilla hexadactyla, Periplaneta spp., Scapteriscus spp, and Schistocerca spp.
  • Psocoptera for
  • Thysanoptera for example, Calliothrips phaseoli, Frankliniella spp., Heliothrips spp, Hercinothrips spp., Parthenothrips spp, Scirtothrips aurantii, Sericothrips variabilis, Taeniothrips spp., Thrips spp; and from the order Thysanura, for example, Lepisma saccharina.
  • the active ingredients according to the invention can be used for controlling, i. e. containing or destroying, pests of the abovementioned type which occur in particular on plants, especially on useful plants and ornamentals in agriculture, in horticulture and in forests, or on organs, such as fruits, flowers, foliage, stalks, tubers or roots, of such plants, and in some cases even plant organs which are formed at a later point in time remain protected against these pests.
  • Suitable target crops are, in particular, cereals, such as wheat, barley, rye, oats, rice, maize or sorghum; beet, such as sugar or fodder beet; fruit, for example pomaceous fruit, stone fruit or soft fruit, such as apples, pears, plums, peaches, almonds, cherries or berries, for example strawberries, raspberries or blackberries; leguminous crops, such as beans, lentils, peas or soya; oil crops, such as oilseed rape, mustard, poppies, olives, sunflowers, coconut, castor, cocoa or ground nuts; cucurbits, such as pumpkins, cucumbers or melons; fibre plants, such as cotton, flax, hemp or jute; citrus fruit, such as oranges, lemons, grapefruit or tangerines; vegetables, such as spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes or bell peppers; Lauraceae, such as avocado, Cinnamonium or camphor; and also tobacco, nuts,
  • the invention may also relate to a method of controlling damage to plant and parts thereof by plant parasitic nematodes (Endoparasitic-, Semiendoparasitic- and Ectoparasitic nematodes), especially plant parasitic nematodes such as root knot nematodes, Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, Meloidogyne arenaria and other Meloidogyne species; cyst-forming nematodes, Globodera rostochiensis and other Globodera species; Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii , and other Heterodera species; Seed gall nematodes, Anguina species; Stem and foliar nematodes, Aphelenchoides species; Sting nematodes, Belonola
  • the compounds of the invention may also have activity against the molluscs.
  • Examples of which include, for example, Ampullariidae; Arion ( A. ater, A. circumscriptus, A. hortensis, A. rufus ); Bradybaenidae ( Bradybaena fruticum ); Cepaea ( C. hortensis, C. Nemoralis ); ochlodina; Deroceras ( D. agrestis, D. empiricorum, D. laeve, D. reticulatum ); Discus ( D. rotundatus ); Euomphalia; Galba ( G. trunculata ); Helicelia ( H. itala, H.
  • H. aperta Limax ( L. cinereoniger, L. flavus, L. marginatus, L. maximus, L. tenellus ); Lymnaea; Milax ( M. gagates, M. marginatus, M. sowerbyi ); Opeas; Pomacea ( P. canaticulata ); Vallonia and Zanitoides.
  • crops is to be understood as including also crops that have been rendered tolerant to herbicides like bromoxynil or classes of herbicides (such as, for example, HPPD inhibitors, ALS inhibitors, for example primisulfuron, prosulfuron and trifloxysulfuron, EPSPS (5-enol-pyrovyl-shikimate-3-phosphate-synthase) inhibitors, GS (glutamine synthetase) inhibitors) as a result of conventional methods of breeding or genetic engineering.
  • herbicides like bromoxynil or classes of herbicides
  • ALS inhibitors for example primisulfuron, prosulfuron and trifloxysulfuron
  • EPSPS 5-enol-pyrovyl-shikimate-3-phosphate-synthase
  • GS glutamine synthetase
  • imazamox by conventional methods of breeding (mutagenesis) is Clearfield® summer rape (Canola).
  • crops that have been rendered tolerant to herbicides or classes of herbicides by genetic engineering methods include glyphosate- and glufosinate-resistant maize varieties commercially available under the trade names RoundupReady® and LibertyLink®.
  • crops is also to be understood as including also crop plants which have been so transformed by the use of recombinant DNA techniques that they are capable of synthesising one or more selectively acting toxins, such as are known, for example, from toxin-producing bacteria, especially those of the genus Bacillus.
  • Toxins that can be expressed by such transgenic plants include, for example, insecticidal proteins, for example insecticidal proteins from Bacillus cereus or Bacillus popliae; or insecticidal proteins from Bacillus thuringiensis , such as ⁇ -endotoxins, e.g. CryIA(b), CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c, or vegetative insecticidal proteins (VIP), e.g. VIP1, VIP2, VIP3 or VIP3A; or insecticidal proteins of bacteria colonising nematodes, for example Photorhabdus spp.
  • insecticidal proteins for example insecticidal proteins from Bacillus cereus or Bacillus popliae
  • Bacillus thuringiensis such as ⁇ -endotoxins, e.g. CryIA(b), CryIA(c), CryIF, Cry
  • Xenorhabdus spp. such as Photorhabdus luminescens, Xenorhabdus nematophilus ; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins and other insect-specific neurotoxins; toxins produced by fungi, such as Streptomycetes toxins, plant lectins, such as pea lectins, barley lectins or snowdrop lectins; agglutinins; proteinase inhibitors, such as trypsine inhibitors, serine protease inhibitors, patatin, cystatin, papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroidoxidase, ecdysteroid-UDP-glycosyl-transferase, cholesterol oxidases, ec
  • ⁇ -endotoxins for example CryIA(b), CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c, or vegetative insecticidal proteins (VIP), for example VIP1, VIP2, VIP3 or VIP3A
  • VIP vegetative insecticidal proteins
  • Hybrid toxins are produced recombinantly by a new combination of different domains of those proteins (see, for example, WO 02/15701).
  • Truncated toxins for example a truncated CryIA(b), are known.
  • modified toxins one or more amino acids of the naturally occurring toxin are replaced.
  • amino acid replacements preferably non-naturally present protease recognition sequences are inserted into the toxin, such as, for example, in the case of CryIIIA055, a cathepsin-D-recognition sequence is inserted into a CryIIIA toxin (see WO 03/018810).
  • Examples of such toxins or transgenic plants capable of synthesising such toxins are disclosed, for example, in EP-A-0 374 753, WO 93/07278, WO 95/34656, EP-A-0 427 529, EP-A-451 878 and WO 03/052073.
  • the toxin contained in the transgenic plants imparts to the plants tolerance to harmful insects.
  • insects can occur in any taxonomic group of insects, but are especially commonly found in the beetles (Coleoptera), two-winged insects (Diptera) and butterflies (Lepidoptera).
  • Transgenic plants containing one or more genes that code for an insecticidal resistance and express one or more toxins are known and some of them are commercially available. Examples of such plants are: YieldGard® (maize variety that expresses a CryIA(b) toxin); YieldGard Rootworm® (maize variety that expresses a CryIIIB(b1) toxin); YieldGard Plus® (maize variety that expresses a CryIA(b) and a CryIIIB(b1) toxin); Starlink® (maize variety that expresses a Cry9(c) toxin); Herculex I® (maize variety that expresses a CryIF(a2) toxin and the enzyme phosphinothricine N-acetyltransferase (PAT) to achieve tolerance to the herbicide glufosinate ammonium); NuCOTN 33B® (cotton variety that expresses a CryIA(c) toxin
  • transgenic crops are:
  • This toxin is Cry3A055 modified by insertion of a cathepsin-D-protease recognition sequence.
  • the preparation of such transgenic maize plants is described in WO 03/018810.
  • MON 863 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/DE/02/9.
  • MON 863 expresses a CryIIIB(b1) toxin and has resistance to certain Coleoptera insects.
  • NK603 ⁇ MON 810 Maize transgenically expresses the protein CP4 EPSPS, obtained from Agrobacterium sp. strain CP4, which imparts tolerance to the herbicide Roundup® (contains glyphosate), and also a CryIA(b) toxin obtained from Bacillus thuringiensis subsp. kurstaki which brings about tolerance to certain Lepidoptera, include the European corn borer.
  • crops is to be understood as including also crop plants which have been so transformed by the use of recombinant DNA techniques that they are capable of synthesising antipathogenic substances having a selective action, such as, for example, the so-called “pathogenesis-related proteins” (PRPs, see e.g. EP-A-0 392 225).
  • PRPs pathogenesis-related proteins
  • Examples of such antipathogenic substances and transgenic plants capable of synthesising such antipathogenic substances are known, for example, from EP-A-0 392 225, WO 95/33818, and EP-A-0 353 191.
  • the methods of producing such transgenic plants are generally known to the person skilled in the art and are described, for example, in the publications mentioned above.
  • Antipathogenic substances which can be expressed by such transgenic plants include, for example, ion channel blockers, such as blockers for sodium and calcium channels, for example the viral KP1, KP4 or KP6 toxins; stilbene synthases; bibenzyl synthases; chitinases; glucanases; the so-called “pathogenesis-related proteins” (PRPs; see e.g. EP-A-0 392 225); antipathogenic substances produced by microorganisms, for example peptide antibiotics or heterocyclic antibiotics (see e.g. WO 95/33818) or protein or polypeptide factors involved in plant pathogen defence (so-called “plant disease resistance genes”, as described in WO 03/000906).
  • ion channel blockers such as blockers for sodium and calcium channels
  • the viral KP1, KP4 or KP6 toxins stilbene synthases; bibenzyl synthases; chitinases; glucanases; the so-called “pathogenesis
  • Crops may also be modified for enhanced resistance to fungal (for example Fusarium, Anthracnose , or Phytophthora ), bacterial (for example Pseudomonas ) or viral (for example potato leafroll virus, tomato spotted wilt virus, cucumber mosaic virus) pathogens.
  • fungal for example Fusarium, Anthracnose , or Phytophthora
  • bacterial for example Pseudomonas
  • viral for example potato leafroll virus, tomato spotted wilt virus, cucumber mosaic virus pathogens.
  • Crops also include those that have enhanced resistance to nematodes, such as the soybean cyst nematode.
  • Crops that are tolerance to abiotic stress include those that have enhanced tolerance to drought, high salt, high temperature, chill, frost, or light radiation, for example through expression of NF-YB or other proteins known in the art.
  • Crops that exhibit enhanced yield or quality include those with improved flowering or fruit ripening properties (such as delayed ripening); modified oil, starch, amino acid, fatty acid, vitamin, phenolic or other content (such as VistiveTM soybean variety); enhanced nutrient utilisation (such as improved nitrogen assimilation); and enhanced quality plant product (such as higher quality cotton fibre).
  • improved flowering or fruit ripening properties such as delayed ripening
  • modified oil, starch, amino acid, fatty acid, vitamin, phenolic or other content such as VistiveTM soybean variety
  • enhanced nutrient utilisation such as improved nitrogen assimilation
  • enhanced quality plant product such as higher quality cotton fibre.
  • compositions according to the invention are the protection of stored goods and storerooms and the protection of raw materials, such as wood, textiles, floor coverings or buildings, and also in the hygiene sector, especially the protection of humans, domestic animals and productive livestock against pests of the mentioned type.
  • the present invention also provides a method for controlling pests (such as mosquitoes and other disease vectors; see also http://www.who.int/malaria/vector_control/irs/en/).
  • the method for controlling pests comprises applying the compositions of the invention to the target pests, to their locus or to a surface or substrate by brushing, rolling, spraying, spreading or dipping.
  • an IRS (indoor residual spraying) application of a surface such as a wall, ceiling or floor surface is contemplated by the method of the invention.
  • the method for controlling such pests comprises applying a pesticidally effective amount of the compositions of the invention to the target pests, to their locus, or to a surface or substrate so as to provide effective residual pesticidal activity on the surface or substrate.
  • a pesticidally effective amount of the compositions of the invention to the target pests, to their locus, or to a surface or substrate so as to provide effective residual pesticidal activity on the surface or substrate.
  • Such application may be made by brushing, rolling, spraying, spreading or dipping the pesticidal composition of the invention.
  • an IRS application of a surface such as a wall, ceiling or floor surface is contemplated by the method of the invention so as to provide effective residual pesticidal activity on the surface.
  • it is contemplated to apply such compositions for residual control of pests on a substrate such as a fabric material in the form of (or which can be used in the manufacture of) netting, clothing, bedding, curtains and tents.
  • Substrates including non-woven, fabrics or netting to be treated may be made of natural fibres such as cotton, raffia, jute, flax, sisal, hessian, or wool, or synthetic fibres such as polyamide, polyester, polypropylene, polyacrylonitrile or the like.
  • the polyesters are particularly suitable.
  • the methods of textile treatment are known, e.g. WO 2008/151984, WO 2003/034823, U.S. Pat. No. 5,631,072, WO 2005/64072, WO2006/128870, EP 1724392, WO2005113886 or WO 2007/090739.
  • compositions according to the invention are the field of tree injection/trunk treatment for all ornamental trees as well all sort of fruit and nut trees.
  • the compounds according to the present invention are especially suitable against wood-boring insects from the order Lepidoptera as mentioned above and from the order Coleoptera, especially against woodborers listed in the following tables AA and BB:
  • the compounds and compositions according to the invention are active against ectoparasites such as hard ticks, soft ticks, mange mites, harvest mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, bird lice and fleas.
  • ectoparasites such as hard ticks, soft ticks, mange mites, harvest mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, bird lice and fleas.
  • Anoplurida Haematopinus spp., Linognathus spp., Pediculus spp. and Phtirus spp., Solenopotes spp.
  • Nematocerina and Brachycerina for example Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Glossina spp., Calliphora spp., Glossina spp., Call
  • Siphonaptrida for example Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp.
  • Heteropterida for example Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp.
  • Actinedida Prostigmata
  • Acaridida Acaridida
  • Acarapis spp. Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp. and Laminosioptes spp.
  • the compounds and compositions according to the invention are also suitable for protecting against insect infestation in the case of materials such as wood, textiles, plastics, adhesives, glues, paints, paper and card, leather, floor coverings and buildings.
  • compositions according to the invention can be used, for example, against the following pests: beetles such as Hylotrupes bajulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinuspecticornis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubescens, Trogoxylon aequale, Minthesrugicollis, Xyleborus spec., Tryptodendron spec., Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec.
  • hymenopterans such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus and Urocerus augur , and termites such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis and Coptotermes formosanus , and bristletails such as Lepisma saccharina.
  • the present invention therefore provides an insecticidal, acaricidal, nematicidal or molluscicidal composition, preferably an insecticidal or acaricidal composition comprising an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a compound of formula I and a suitable carrier or diluent therefor.
  • the invention provides a method of combating and controlling pests which comprises applying an insecticidally, acaricidally, nematicidally or molluscicidally effective amount, preferably an insecticidally and acaricidally effective amount of a compound of formula I or a composition comprising a compound of formula I, to a pest, a locus of pest, or to a plant susceptible to attack by a pest, with the exception of a method for treatment of the human or animal body by surgery or therapy and diagnostic methods practised on the human or animal body.
  • the compounds of formula I are preferably used against insects or acarines.
  • plant as used herein includes seedlings, bushes and trees.
  • the invention also relates to a pesticidal composition, which, in addition to comprising the compound of formula I, comprises formulation adjuvants.
  • the invention therefore also relates to pesticidal compositions such as emulsifiable concentrates, suspension concentrates, directly sprayable or dilutable solutions, spreadable pastes, dilute emulsions, soluble powders, dispersible powders, wettable powders, dusts, granules or encapsulations in polymeric substances, which comprise—at least—one of the active ingredients according to the invention and which are to be selected to suit the intended aims and the prevailing circumstances.
  • pesticidal compositions such as emulsifiable concentrates, suspension concentrates, directly sprayable or dilutable solutions, spreadable pastes, dilute emulsions, soluble powders, dispersible powders, wettable powders, dusts, granules or encapsulations in polymeric substances, which comprise—at least—one of the active ingredients according to the invention and which are to be selected to suit the intended aims and the prevailing circumstances.
  • the active ingredient is employed in pure form, a solid active ingredient for example in a specific particle size, or, preferably, together with—at least—one of the auxiliaries conventionally used in the art of formulation, such as extenders, for example solvents or solid carriers, or such as surface-active compounds (surfactants).
  • auxiliaries conventionally used in the art of formulation, such as extenders, for example solvents or solid carriers, or such as surface-active compounds (surfactants).
  • Suitable solvents are: unhydrogenated or partially hydrogenated aromatic hydrocarbons, preferably the fractions C8 to C12 of alkylbenzenes, such as xylene mixtures, alkylated naphthalenes or tetrahydronaphthalene, aliphatic or cycloaliphatic hydrocarbons, such as paraffins or cyclohexane, alcohols such as ethanol, propanol or butanol, glycols and their ethers and esters such as propylene glycol, dipropylene glycol ether, ethylene glycol or ethylene glycol monomethyl ether or ethylene glycol monoethyl ether, ketones, such as cyclohexanone, isophorone or diacetone alcohol, strongly polar solvents, such as N-methylpyrrolid-2-one, dimethyl sulfoxide or N,N-dimethylformamide, water, unepoxidized or epoxidized vegetable oils, such as unexpodized or e
  • Solid carriers which are used for example for dusts and dispersible powders are, as a rule, ground natural minerals such as calcite, talc, kaolin, montmorillonite or attapulgite.
  • ground natural minerals such as calcite, talc, kaolin, montmorillonite or attapulgite.
  • highly disperse silicas or highly disperse absorbtive polymers are also possible to add highly disperse silicas or highly disperse absorbtive polymers.
  • Suitable particulate adsorptive carriers for granules are porous types, such as pumice, brick grit, sepiolite or bentonite, and suitable non-sorptive carrier materials are calcite or sand.
  • a large number of granulated materials of inorganic or organic nature can be used, in particular dolomite or comminuted plant residues.
  • Suitable surface-active compounds are, depending on the type of the active ingredient to be formulated, non-ionic, cationic and/or anionic surfactants or surfactant mixtures which have good emulsifying, dispersing and wetting properties.
  • the surfactants mentioned below are only to be considered as examples; a large number of further surfactants which are conventionally used in the art of formulation and suitable according to the invention are described in the relevant literature.
  • Suitable non-ionic surfactants are, especially, polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, of saturated or unsaturated fatty acids or of alkyl phenols which may contain approximately 3 to approximately 30 glycol ether groups and approximately 8 to approximately 20 carbon atoms in the (cyclo)aliphatic hydrocarbon radical or approximately 6 to approximately 18 carbon atoms in the alkyl moiety of the alkyl phenols.
  • water-soluble polyethylene oxide adducts with polypropylene glycol, ethylenediaminopo ⁇ lypropylene glycol or alkyl polypropylene glycol having 1 to approximately 10 carbon atoms in the alkyl chain and approximately 20 to approximately 250 ethylene glycol ether groups and approximately 10 to approximately 100 propylene glycol ether groups.
  • the abovementioned compounds contain 1 to approximately 5 ethylene glycol units per propy ⁇ lene glycol unit.
  • nonylphenoxypolyethoxyethanol castor oil polyglycol ether, polypropylene glycol/polyethylene oxide adducts, tributylpheno ⁇ xypolyethoxyethanol, polyethylene glycol or octylphenoxypolyethoxyethanol.
  • fatty acid esters of polyoxyethylene sorbitan such as polyoxyethylene sorbitan trioleate.
  • the cationic surfactants are, especially, quarternary ammonium salts which generally have at least one alkyl radical of approximately 8 to approximately 22 C atoms as substituents and as further substituents (unhalogenated or halogenated) lower alkyl or hydroxyalkyl or benzyl radicals.
  • the salts are preferably in the form of halides, methylsulfates or ethylsulfates. Examples are stearyltrimethylammonium chloride and benzylbis(2-chloroethyl)ethyl ⁇ ammonium bromide.
  • suitable anionic surfactants are water-soluble soaps or water-soluble synthetic surface-active compounds.
  • soaps are the alkali, alkaline earth or (unsubstituted or substituted) ammonium salts of fatty acids having approximately 10 to approximately 22 C atoms, such as the sodium or potassium salts of oleic or stearic acid, or of natural fatty acid mixtures which are obtainable for example from coconut or tall oil; mention must also be made of the fatty acid methyl taurates.
  • synthetic surfactants are used more frequently, in particular fatty sulfonates, fatty sulfates, sulfonated benzimidazole derivatives or alkylaryl sulfonates.
  • the fatty sulfonates and fatty sulfates are present as alkali, alkaline earth or (substituted or unsubstituted) ammonium salts and they generally have an alkyl radical of approximately 8 to approximately 22 C atoms, alkyl also to be understood as including the alkyl moiety of acyl radicals; examples which may be mentioned are the sodium or calcium salts of lignosulfonic acid, of the dodecylsulfuric ester or of a fatty alcohol sulfate mixture prepared from natural fatty acids. This group also includes the salts of the sulfuric esters and sulfonic acids of fatty alcohol/ethylene oxide adducts.
  • the sulfonated benzimidazole derivatives preferably contain 2 sulfonyl groups and a fatty acid radical of approximately 8 to approximately 22 C atoms.
  • alkylarylsulfonates are the sodium, calcium or triethanolammonium salts of decylbenzenesulfonic acid, of dibutyl ⁇ naphthalenesulfonic acid or of a naphthalenesulfonic acid/formaldehyde condensate.
  • suitable phosphates such as salts of the phosphoric ester of a p-nonylphenol/(4-14)ethylene oxide adduct, or phospholipids.
  • Suitable phosphates are tris-esters of phosphoric acid with aliphatic or aromatic alcohols and/or bis-esters of alkyl phosphonic acids with aliphatic or aromatic alcohols, which are a high performance oil-type adjuvant.
  • tris-esters have been described, for example, in WO 01/47356, WO 00/56146, EP-A-0579052 or EP-A-1018299 or are commercially available under their chemical name.
  • Preferred tris-esters of phosphoric acid for use in the new compositions are tris-(2-ethylhexyl) phosphate, tris-n-octyl phosphate and tris-butoxyethyl phosphate, where tris-(2-ethylhexyl) phosphate is most preferred.
  • Suitable bis-ester of alkyl phosphonic acids are bis-(2-ethylhexyl)-(2-ethylhexyl)-phosphonate, bis-(2-ethylhexyl)-(n-octyl)-phosphonate, dibutyl-butyl phosphonate and bis(2-ethylhexyl)-tripropylene-phosphonate, where bis-(2-ethylhexyl)-(n-octyl)-phosphonate is particularly preferred.
  • compositions according to the invention can preferably additionally include an additive comprising an oil of vegetable or animal origin, a mineral oil, alkyl esters of such oils or mixtures of such oils and oil derivatives.
  • the amount of oil additive used in the composition according to the invention is generally from 0.01 to 10%, based on the spray mixture.
  • the oil additive can be added to the spray tank in the desired concentration after the spray mixture has been prepared.
  • Preferred oil additives comprise mineral oils or an oil of vegetable origin, for example rapeseed oil such as ADIGOR® and MERO®, olive oil or sunflower oil, emulsified vegetable oil, such as AMIGO® (Rhône-Poulenc Canada Inc.), alkyl esters of oils of vegetable origin, for example the methyl derivatives, or an oil of animal origin, such as fish oil or beef tallow.
  • a preferred additive contains, for example, as active components essentially 80% by weight alkyl esters of fish oils and 15% by weight methylated rapeseed oil, and also 5% by weight of customary emulsifiers and pH modifiers.
  • Especially preferred oil additives comprise alkyl esters of C 8 -C 22 fatty acids, especially the methyl derivatives of C 12 -C 18 fatty acids, for example the methyl esters of lauric acid, palmitic acid and oleic acid, being important.
  • Those esters are known as methyl laurate (CAS-111-82-0), methyl palmitate (CAS-112-39-0) and methyl oleate (CAS-112-62-9).
  • a preferred fatty acid methyl ester derivative is Emery® 2230 and 2231 (Cognis GmbH).
  • Those and other oil derivatives are also known from the Compendium of Herbicide Adjuvants, 5th Edition, Southern Illinois University, 2000.
  • alkoxylated fatty acids can be used as additives in the inventive compositions as well as polymethylsiloxane based additives, which have been described in WO 2008/037373.
  • the application and action of the oil additives can be further improved by combining them with surface-active substances, such as non-ionic, anionic or cationic surfactants.
  • surface-active substances such as non-ionic, anionic or cationic surfactants.
  • suitable anionic, non-ionic and cationic surfactants are listed on pages 7 and 8 of WO 97/34485.
  • Preferred surface-active substances are anionic surfactants of the dodecylbenzylsulfonate type, especially the calcium salts thereof, and also non-ionic surfactants of the fatty alcohol ethoxylate type. Special preference is given to ethoxylated C 12 -C 22 fatty alcohols having a degree of ethoxylation of from 5 to 40.
  • Examples of commercially available surfactants are the Genapol types (Clariant AG).
  • silicone surfactants especially polyalkyl-oxide-modified heptamethyltrisiloxanes, which are commercially available e.g. as Silwet L-77®, and also perfluorinated surfactants.
  • concentration of surface-active substances in relation to the total additive is generally from 1 to 30% by weight.
  • oil additives that consist of mixtures of oils or mineral oils or derivatives thereof with surfactants are Edenor ME SU®, Turbocharge® (Syngenta AG, CH) and Actipron® (BP Oil UK Limited, GB).
  • the said surface-active substances may also be used in the formulations alone, that is to say without oil additives.
  • an organic solvent to the oil additive/surfactant mixture can contribute to a further enhancement of action.
  • Suitable solvents are, for example, Solvesso® (ESSO) and Aromatic Solvent® (Exxon Corporation).
  • the concentration of such solvents can be from 10 to 80% by weight of the total weight.
  • Such oil additives which may be in admixture with solvents, are described, for example, in U.S. Pat. No. 4,834,908.
  • a commercially available oil additive disclosed therein is known by the name MERGE® (BASF Corporation).
  • a further oil additive that is preferred according to the invention is SCORE® (Syngenta Crop Protection Canada.)
  • alkylpyrrolidones e.g. Agrimax®
  • formulations of alkylpyrrolidones such as, for example, Agrimax®
  • synthetic latices such as, for example, polyacrylamide, polyvinyl compounds or poly-1-p-menthene (e.g. Bond®, Courier® or Emerald®)
  • propionic acid for example Eurogkem Pen-e-trate®
  • active ingredient refers to one of the compounds of formula I, especially the compounds of formula I specifically disclosed in the tables. It also refers to mixtures of the compound of formula I, in particular a compound selected from said Table 1, with other insecticides, fungicides, herbicides, safeners, adjuvants and the like, which mixtures are specifically disclosed below.
  • compositions can also comprise further solid or liquid auxiliaries, such as stabilizers, for example unepoxidized or epoxidized vegetable oils (for example epoxidized coconut oil, rapeseed oil or soya oil), antifoams, for example silicone oil, preservatives, viscosity regulators, binders and/or tackifiers; fertilizers, in particular nitrogen containing fertilizers such as ammonium nitrates and urea as described in WO 2008/017388, which can enhance the efficacy of the inventive compounds; or other active ingredients for achieving specific effects, for example ammonium or phosphonium salts, in particular halides, (hydrogen)sulphates, nitrates, (hydrogen)carbonates, citrates, tartrates, formiates and acetates, as described in WO 2007/068427 and WO 2007/068428, which also can enhance the efficacy of the inventive compounds and which can be used in combination with penetration enhancers such as alkox
  • compositions according to the invention are prepared in a manner known per se, in the absence of auxiliaries for example by grinding, screening and/or compressing a solid active ingredient and in the presence of at least one auxiliary for example by intimately mixing and/or grinding the active ingredient with the auxiliary (auxiliaries).
  • compositions that is the methods of controlling pests of the abovementioned type, such as spraying, atomizing, dusting, brushing on, dressing, scattering or pouring—which are to be selected to suit the intended aims of the prevailing circumstances—and the use of the compositions for controlling pests of the abovementioned type are other subjects of the invention.
  • Typical rates of concentration are between 0.1 and 1000 ppm, preferably between 0.1 and 500 ppm, of active ingredient.
  • a preferred method of application in the field of crop protection is application to the foliage of the plants (foliar application), it being possible to select frequency and rate of application to match the danger of infestation with the pest in question.
  • the active ingredient can reach the plants via the root system (systemic action), by drenching the locus of the plants with a liquid composition or by incorporating the active ingredient in solid form into the locus of the plants, for example into the soil, for example in the form of granules (soil application). In the case of paddy rice crops, such granules can be metered into the flooded paddy-field.
  • compositions according to the invention are also suitable for the protection of plant propagation material, for example seeds, such as fruit, tubers or kernels, or nursery plants, against pests of the abovementioned type.
  • the propagation material can be treated with the compositions prior to planting, for example seed can be treated prior to sowing.
  • the compositions can be applied to seed kernels (coating), either by soaking the kernels in a liquid composition or by applying a layer of a solid composition. It is also possible to apply the compositions when the propagation material is planted to the site of application, for example into the seed furrow during drilling.
  • compositions according to the invention comprise drip application onto the soil, dipping of parts of plants such as roots bulbs or tubers, drenching the soil, as well as soil injection. These methods are known in the art.
  • a compound of formula I is usually formulated into a composition which includes, in addition to the compound of formula I, a suitable inert diluent or carrier and, optionally, a formulation adjuvant in form of a surface active agent (SFA) as described herein or, for example, in EP-B-1062217.
  • SFA surface active agent
  • SFAs are chemicals which are able to modify the properties of an interface (for example, liquid/solid, liquid/air or liquid/liquid interfaces) by lowering the interfacial tension and thereby leading to changes in other properties (for example dispersion, emulsification and wetting).
  • an interface for example, liquid/solid, liquid/air or liquid/liquid interfaces
  • the compositions comprise 0.1 to 99%, especially 0.1 to 95%, of active ingredient of the formula I and 1 to 99.9%, especially 5 to 99.9%, of at least one solid or liquid adjuvant, it being possible as a rule for 0 to 25%, especially 0.1 to 20%, of the composition to be surfactants (% in each case meaning percent by weight).
  • surfactants % in each case meaning percent by weight.
  • Typical rates of concentration are between 0.1 and 1000 ppm, preferably between 0.1 and 500 ppm, of active ingredient.
  • the rate of application per hectare is generally 1 to 2000 g of active ingredient per hectare, in particular 10 to 1000 g/ha, preferably 10 to 600 g/ha.
  • a compound of formula I When used in a seed dressing, a compound of formula I is used at a rate of 0.0001 g to 10 g (for example 0.001 g or 0.05 g), preferably 0.005 g to 10 g, more preferably 0.005 g to 4 g, per kilogram of seed.
  • Preferred seed treatment pre-mix formulations are aqueous suspension concentrates.
  • the formulation can be applied to the seeds using conventional treating techniques and machines, such as fluidized bed techniques, the roller mill method, rotostatic seed treaters, and drum coaters. Other methods, such as spouted beds may also be useful.
  • the seeds may be presized before coating. After coating, the seeds are typically dried and then transferred to a sizing machine for sizing. Such procedures are known in the art.
  • compositions can be chosen from a number of formulation types, including dustable powders (DP), soluble powders (SP), water soluble granules (SG), water dispersible granules (WG), wettable powders (WP), granules (GR) (slow or fast release), soluble concentrates (SL), oil miscible liquids (OL), ultra low volume liquids (UL), emulsifiable concentrates (EC), dispersible concentrates (DC), emulsions (both oil in water (EW) and water in oil (EO)), micro-emulsions (ME), suspension concentrates (SC), oil-based suspension concentrate (OD), aerosols, fogging/smoke formulations, capsule suspensions (CS) and seed treatment formulations.
  • the formulation type chosen in any instance will depend upon the particular purpose en-visaged and the physical, chemical and biological properties of the compound of formula I.
  • Dustable powders may be prepared by mixing a compound of formula I with one or more solid diluents (for example natural clays, kaolin, pyrophyllite, bentonite, alumina, montmorillonite, kieselguhr, chalk, diatomaceous earths, calcium phosphates, calcium and magnesium carbonates, sulphur, lime, flours, talc and other organic and inorganic solid carriers) and mechanically grinding the mixture to a fine powder.
  • solid diluents for example natural clays, kaolin, pyrophyllite, bentonite, alumina, montmorillonite, kieselguhr, chalk, diatomaceous earths, calcium phosphates, calcium and magnesium carbonates, sulphur, lime, flours, talc and other organic and inorganic solid carriers
  • Soluble powders may be prepared by mixing a compound of formula I with one or more water-soluble inorganic salts (such as sodium bicarbonate, sodium carbonate or magnesium sulphate) or one or more water-soluble organic solids (such as a polysaccharide) and, optionally, one or more wetting agents, one or more dispersing agents or a mixture of said agents to improve water dispersibility/solubility. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water soluble granules (SG).
  • water-soluble inorganic salts such as sodium bicarbonate, sodium carbonate or magnesium sulphate
  • water-soluble organic solids such as a polysaccharide
  • wetting agents such as sodium bicarbonate, sodium carbonate or magnesium sulphate
  • dispersing agents such as sodium bicarbonate, sodium carbonate or magnesium sulphate
  • SG water soluble granules
  • WP Wettable powders
  • WG Water dispersible granules
  • Granules may be formed either by granulating a mixture of a compound of formula I and one or more powdered solid diluents or carriers, or from pre-formed blank granules by absorbing a compound of formula I (or a solution thereof, in a suitable agent) in a porous granular material (such as pumice, attapulgite clays, fuller's earth, kieselguhr, diatomaceous earths or ground corn cobs) or by adsorbing a compound of formula I (or a solution thereof, in a suitable agent) on to a hard core material (such as sands, silicates, mineral carbonates, sulphates or phosphates) and drying if necessary.
  • a hard core material such as sands, silicates, mineral carbonates, sulphates or phosphates
  • Agents which are commonly used to aid absorption or adsorption include solvents (such as aliphatic and aromatic petroleum solvents, alcohols, ethers, ketones and esters) and sticking agents (such as polyvinyl acetates, polyvinyl alcohols, dextrins, sugars and vegetable oils).
  • solvents such as aliphatic and aromatic petroleum solvents, alcohols, ethers, ketones and esters
  • sticking agents such as polyvinyl acetates, polyvinyl alcohols, dextrins, sugars and vegetable oils.
  • One or more other additives may also be included in granules (for example an emulsifying agent, wetting agent or dispersing agent).
  • DC Dispersible Concentrates
  • a compound of formula I may be prepared by dissolving a compound of formula I in water or an organic solvent, such as a ketone, alcohol or glycol ether.
  • organic solvent such as a ketone, alcohol or glycol ether.
  • surface active agent for example to improve water dilution or prevent crystallisation in a spray tank.
  • Emulsifiable concentrates or oil-in-water emulsions (EW) may be prepared by dissolving a compound of formula I in an organic solvent (optionally containing one or more wetting agents, one or more emulsifying agents or a mixture of said agents).
  • organic solvents for use in ECs include aromatic hydrocarbons (such as alkylbenzenes or alkylnaphthalenes, exemplified by SOLVESSO 100, SOLVESSO 150 and SOLVESSO 200; SOLVESSO is a Registered Trade Mark), ketones (such as cyclohexanone or methylcyclohexanone) and alcohols (such as benzyl alcohol, furfuryl alcohol or butanol),
  • N-alkylpyrrolidones such as N-methylpyrrolidone or N-octylpyrrolidone
  • dimethyl amides of fatty acids such as C 8 -C 10 fatty acid dimethylamide
  • chlorinated hydrocarbons such as C 8 -C 10 fatty acid dimethylamide
  • Preparation of an EW involves obtaining a compound of formula I either as a liquid (if it is not a liquid at room temperature, it may be melted at a reasonable temperature, typically below 70° C.) or in solution (by dissolving it in an appropriate solvent) and then emulsifiying the resultant liquid or solution into water containing one or more SFAs, under high shear, to produce an emulsion.
  • Suitable solvents for use in EWs include vegetable oils, chlorinated hydrocarbons (such as chlorobenzenes), aromatic solvents (such as alkylbenzenes or alkylnaphthalenes) and other appropriate organic solvents which have a low solubility in water.
  • Microemulsions may be prepared by mixing water with a blend of one or more solvents with one or more SFAs, to produce spontaneously a thermodynamically stable isotropic liquid formulation.
  • a compound of formula I is present initially in either the water or the solvent/SFA blend.
  • Suitable solvents for use in MEs include those hereinbefore described for use in in ECs or in EWs.
  • An ME may be either an oil-in-water or a water-in-oil system (which system is present may be determined by conductivity measurements) and may be suitable for mixing water-soluble and oil-soluble pesticides in the same formulation.
  • An ME is suitable for dilution into water, either remaining as a microemulsion or forming a conventional oil-in-water emulsion.
  • SC Suspension concentrates
  • SCs may comprise aqueous or non-aqueous suspensions of finely divided insoluble solid particles of a compound of formula I.
  • SCs may be prepared by ball or bead milling the solid compound of formula I in a suitable medium, optionally with one or more dispersing agents, to produce a fine particle suspension of the compound.
  • One or more wetting agents may be included in the composition and a suspending agent may be included to reduce the rate at which the particles settle.
  • a compound of formula I may be dry milled and added to water, containing agents hereinbefore described, to produce the desired end product.
  • Oil-based suspension concentrate may be prepared similarly by suspending finely divided insoluble solid particles of a compound of formula I in an organic fluid (for example at least one mineral oil or vegetable oil).
  • ODs may further comprise at least one penetration promoter (for example an alcohol ethoxylate or a related compound), at least one non-ionic surfactants and/or at least one anionic surfactant, and optionally at least one additive from the group of emulsifiers, foam-inhibiting agents, preservatives, anti-oxidants, dyestuffs, and/or inert filler materials.
  • An OD is intended and suitable for dilution with water before use to produce a spray solution with sufficient stability to allow spray application through appropriate equipment.
  • Aerosol formulations comprise a compound of formula I and a suitable propellant (for example n-butane).
  • a compound of formula I may also be dissolved or dispersed in a suitable medium (for example water or a water miscible liquid, such as n-propanol) to provide compositions for use in non-pressurised, hand-actuated spray pumps.
  • a compound of formula I may be mixed in the dry state with a pyrotechnic mixture to form a composition suitable for generating, in an enclosed space, a smoke containing said compound.
  • Capsule suspensions may be prepared in a manner similar to the preparation of EW formulations but with an additional polymerisation stage such that an aqueous dispersion of oil droplets is obtained, in which each oil droplet is encapsulated by a polymeric shell and contains a compound of formula I and, optionally, a carrier or diluent therefor.
  • the polymeric shell may be produced by either an interfacial polycondensation reaction or by a coacervation procedure.
  • the compositions may provide for controlled release of the compound of formula I and they may be used for seed treatment.
  • a compound of formula I may also be formulated in a biodegradable polymeric matrix to provide a slow, controlled release of the compound.
  • a compound of formula I may also be formulated for use as a seed treatment, for example as a powder composition, including a powder for dry seed treatment (DS), a water soluble powder (SS) or a water dispersible powder for slurry treatment (WS), or as a liquid composition, including a flowable concentrate (FS), a solution (LS) or a capsule suspension (CS).
  • DS powder for dry seed treatment
  • SS water soluble powder
  • WS water dispersible powder for slurry treatment
  • CS capsule suspension
  • the preparations of DS, SS, WS, FS and LS compositions are very similar to those of, respectively, DP, SP, WP, SC, OD and DC compositions described above.
  • Compositions for treating seed may include an agent for assisting the adhesion of the composition to the seed (for example a mineral oil or a film-forming barrier).
  • a composition of the present invention may include one or more additives to improve the biological performance of the composition (for example by improving wetting, retention or distribution on surfaces; resistance to rain on treated surfaces; or uptake or mobility of a compound of formula I).
  • additives include surface active agents (SFAs), spray additives based on oils, for example certain mineral oils, vegetable oils or natural plant oils (such as soy bean and rape seed oil), and blends of these with other bio-enhancing adjuvants (ingredients which may aid or modify the action of a compound of formula I).
  • Increasing the effect of a compound of formula I may for example be achieved by adding ammonium and/or phosphonium salts, and/or optionally at least one penetration promotor such as fatty alcohol alkoxylates (for example rape oil methyl ester) or vegetable oil esters.
  • fatty alcohol alkoxylates for example rape oil methyl ester
  • vegetable oil esters for example rape oil methyl ester
  • Wetting agents, dispersing agents and emulsifying agents may be surface active agents (SFAs) of the cationic, anionic, amphoteric or non-ionic type.
  • Suitable SFAs of the cationic type include quaternary ammonium compounds (for example cetyltrimethyl ammonium bromide), imidazolines and amine salts.
  • Suitable anionic SFAs include alkali metals salts of fatty acids, salts of aliphatic monoesters of sulphuric acid (for example sodium lauryl sulphate), salts of sulphonated aromatic compounds (for example sodium dodecylbenzenesulphonate, calcium dodecylbenzenesulphonate, butylnaphthalene sulphonate and mixtures of sodium di-isopropyl- and tri-isopropyl-naphthalene sulphonates), ether sulphates, alcohol ether sulphates (for example sodium laureth-3-sulphate), ether carboxylates (for example sodium laureth-3-carboxylate), phosphate esters (products from the reaction between one or more fatty alcohols and phosphoric acid (predominately mono-esters) or phosphorus pentoxide (predominately di-esters), for example the reaction between lauryl alcohol and tetraphosphoric acid; additionally
  • Suitable SFAs of the amphoteric type include betaines, propionates and glycinates.
  • Suitable SFAs of the non-ionic type include condensation products of alkylene oxides, such as ethylene oxide, propylene oxide, butylene oxide or mixtures thereof, with fatty alcohols (such as oleyl alcohol or cetyl alcohol) or with alkylphenols (such as octylphenol, nonylphenol or octylcresol); partial esters derived from long chain fatty acids or hexitol anhydrides; condensation products of said partial esters with ethylene oxide; block polymers (comprising ethylene oxide and propylene oxide); alkanolamides; simple esters (for example fatty acid polyethylene glycol esters); amine oxides (for example lauryl dimethyl amine oxide); and lecithins.
  • alkylene oxides such as ethylene oxide, propylene oxide, butylene oxide or mixtures thereof
  • fatty alcohols such as oleyl alcohol or cetyl alcohol
  • alkylphenols such as octylphenol, nonyl
  • Suitable suspending agents include hydrophilic colloids (such as polysaccharides, polyvinylpyrrolidone or sodium carboxymethylcellulose) and swelling clays (such as bentonite or attapulgite).
  • hydrophilic colloids such as polysaccharides, polyvinylpyrrolidone or sodium carboxymethylcellulose
  • swelling clays such as bentonite or attapulgite
  • a compound of formula I may be applied by any of the known means of applying pesticidal compounds. For example, it may be applied, formulated or unformulated, to the pests or to a locus of the pests (such as a habitat of the pests, or a growing plant liable to infestation by the pests) or to any part of the plant, including the foliage, stems, branches or roots, to the seed before it is planted or to other media in which plants are growing or are to be planted (such as soil surrounding the roots, the soil generally, paddy water or hydroponic culture systems), directly or it may be sprayed on, dusted on, applied by dipping, applied as a cream or paste formulation, applied as a vapour or applied through distribution or incorporation of a composition (such as a granular composition or a composition packed in a water-soluble bag) in soil or an aqueous environment.
  • a locus of the pests such as a habitat of the pests, or a growing plant liable to infestation by the pests
  • any part of the plant
  • a compound of formula I may also be injected into plants or sprayed onto vegetation using electrodynamic spraying techniques or other low volume methods, or applied by land or aerial irrigation systems.
  • compositions for use as aqueous preparations are generally supplied in the form of a concentrate containing a high proportion of the active ingredient, the concentrate being added to water before use.
  • These concentrates which may include DCs, SCs, ODs, ECs, EWs, MEs SGs, SPs, WPs, WGs and CSs, are often required to withstand storage for prolonged periods and, after such storage, to be capable of addition to water to form aqueous preparations which remain homogeneous for a sufficient time to enable them to be applied by conventional spray equipment.
  • Such aqueous preparations may contain varying amounts of a compound of formula I (for example 0.0001 to 10%, by weight) depending upon the purpose for which they are to be used.
  • a compound of formula I may be used in mixtures with fertilisers (for example nitrogen-, potassium- or phosphorus-containing fertilisers, and more particularly ammonium nitrate and/or urea fertilizers).
  • fertilisers for example nitrogen-, potassium- or phosphorus-containing fertilisers, and more particularly ammonium nitrate and/or urea fertilizers.
  • Suitable formulation types include granules of fertiliser.
  • the mixtures suitably contain up to 25% by weight of the compound of formula I.
  • active ingredient 1 to 95%, preferably 5 to 20% surfactant: 1 to 30%, preferably 10 to 20% solvent: 5 to 98%, preferably 70 to 85%
  • active ingredient 0.1 to 10%, preferably 0.1 to 1% solid carrier: 99.9 to 90%, preferably 99.9 to 99%
  • active ingredient 5 to 75%, preferably 10 to 50% water: 94 to 24%, preferably 88 to 30% surfactant: 1 to 40%, preferably 2 to 30%
  • active ingredient 0.5 to 90%, preferably 1 to 80% surfactant: 0.5 to 20%, preferably 1 to 15% solid carrier: 5 to 99%, preferably 15 to 98%
  • active ingredient 0.5 to 30%, preferably 3 to 15% solid carrier: 99.5 to 70%, preferably 97 to 85%
  • Melt means melting point in ° C. Free radicals represent methyl groups.
  • Spectra were recorded on a Mass Spectrometer from Waters (SQD Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive or negative ions, Capillary: 3.00 kV, Cone range: 30-60 V, Extractor: 2.00 V, Source Temperature: 150° C., Desolvation Temperature: 350° C., Cone Gas Flow: 0 L/Hr, Desolvation Gas Flow: 650 L/Hr, Mass range: 100 to 900 Da) and an Acquity UPLC from Waters: Binary pump, heated column compartment and diode-array detector. Solvent degasser, binary pump, heated column compartment and diode-array detector.
  • Spectra were recorded on a Mass Spectrometer from Waters (ZQ Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive or negative ions, Capillary: 3.00 kV, Cone range: 30-60 V, Extractor: 2.00 V, Source Temperature: 150° C., Desolvation Temperature: 350° C., Cone Gas Flow: 0 L/Hr, Desolvation Gas Flow: 650 L/Hr, Mass range: 100 to 900 Da) and an Acquity UPLC from Waters: Binary pump, heated column compartment and diode-array detector. Solvent degasser, binary pump, heated column compartment and diode-array detector.
  • Spectra were recorded on a Mass Spectrometer from Waters (ZQ Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive or negative ions, Capillary: 3.00 kV, Cone range: 30-60 V, Extractor: 2.00 V, Source Temperature: 150° C., Desolvation Temperature: 350° C., Cone Gas Flow: 0 L/Hr, Desolvation Gas Flow: 650 L/Hr, Mass range: 100 to 900 Da) and an Acquity UPLC from Waters: Binary pump, heated column compartment and diode-array detector. Solvent degasser, binary pump, heated column compartment and diode-array detector.
  • Type of column Waters ACQUITY UPLC HSS T3; Column length: 30 mm; Internal diameter of column: 2.1 mm; Particle Size: 1.8 micron; Temperature: 60° C.
  • Electrospray Polarity positive and negative ions
  • Step A 2-methyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-1,1-dioxo-4-(trifluoromethyl)-2,3-dihydrobenzothiophene-7-carboxamide
  • Step B 2-methyl-7-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-4-(trifluoromethyl)-2,3-dihydrobenzothiophene 1,1-dioxide (Compound A1.014-B2.022)
  • Example P2 4-bromo-2-methyl-7-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-2,3-dihydrobenzothiophene 1,1-dioxide (Compound A1.014-B2.023)
  • Step A 4-bromo-2-methyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-1,1-dioxo-2,3-dihydrobenzothiophene-7-carboxamide
  • Step B 4-bromo-2-methyl-7-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-2,3-dihydrobenzothiophene 1,1-dioxide (A1.014-B2.023)
  • Example P3 2-[4-ethylsulfonyl-6-(trifluoromethyl) pyridazin-3-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine (A1.014-B1.058)
  • Step A 5-ethylsulfanyl-3-(trifluoromethyl)-1H-pyridazin-6-one
  • EtSNa (100 mg, 1.2 mmol) was added to a solution of 5-bromo-3-(trifluoromethyl)-1H-pyridazin-6-one (243 mg, 1 mmol, Prepared as described in WO 2008128995) in 10 ml of DMF. After the addition, the mixture was stirred at room temperature for 2 hours. Then the mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give 5-ethylsulfanyl-3-(trifluoromethyl)-1H-pyridazin-6-one (182 mg, 81%).
  • Step B 3-chloro-4-ethylsulfanyl-6-(trifluoromethyl)Pyridazine
  • Step C methyl 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylate
  • Carbon monoxide gas was introduced to a mixture of 3-chloro-4-ethylsulfanyl-6-(trifluoromethyl)pyridazine (2.5 g, 10 mmol), Pd(OAc) 2 (232 mg, 0.1 mmol), dppf (572 mg, 0.1 mmol) and Et 3 N (3.1 g, 30 mmol) in 30 ml of MeOH, and the internal pressure was increased to 1.5 MPa. Then, the reaction was stirred at 80° C. for 16 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure.
  • Step D 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylic acid
  • Step E 4-ethylsulfanyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-6-(trifluoromethyl)pyridazine-3-carboxamide
  • Step D 2-[4-Ethylsulfanyl-6-(Trifluoromethyl)Pyridazin-3-Yl]-3-Methyl-6-(Trifluoromethyl)Imidazo[4,5-b]Pyridine (Compound A1.014-B1.050)
  • Step E 2-[4-ethylsulfonyl-6-(trifluoromethyl)pyridazin-3-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine (A1.014-B1.058)
  • Step B 5-ethylsulfanylthiazole-4-carboxylic acid
  • Step C tert-butyl N-[4-amino-6-(trifluoromethyl)-3-pyridyl]carbamate:
  • Step D tert-butyl N-[4-amino-6-(trifluoromethyl)-3-pyridyl]-N-methyl-carbamate
  • N3-methyl-6-(trifluoromethyl)pyridine-3,4-diamine can be obtained by the following procedure:
  • Step F 5-ethylsulfanyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]thiazole (Compound A6.002-B7.037)
  • reaction mixture was concentrated in vacuo and purified by column chromatography on silica gel to give title compound (120 mg), 5-ethylsulfanyl-N-[5-(methylamino)-2-(trifluoromethyl)-4-pyridyl]thiazole-4-carboxamide (51 mg and), and N-[4-amino-6-(trifluoromethyl)-3-pyridyl]-5-ethylsulfanyl-N-methyl-thiazole-4-carboxamide (162 mg). The latter two compounds were dissolved in 10 ml of AcOH and refluxed for 16 h.
  • Step G 5-ethylsulfonyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]thiazole (V13.05
  • Step A 2,3-Dichloro-5-[(4-methoxyphenyl)methoxy]pyridine
  • Step B Ethyl 3-chloro-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylate
  • Step C Ethyl 3-ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylate
  • Step D 3-Ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylic acid
  • Step E 3-Ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]-N-[5-(methylamino)-2-(trifluoromethyl)-4-pyridyl]pyridine-2-carboxamide
  • Step F 5-ethylsulfanyl-6-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]pyridin-3-ol
  • Step G 2-[5-(difluoromethoxy)-3-ethylsulfanyl-2-pyridyl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine
  • CHCIF 2 gas was introduced to a mixture of 5-ethylsulfanyl-6-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]pyridin-3-ol (100 mg, 0.28 mmol) and Cs 2 CO 3 (460 mg, 1.41 mmol) in 10 ml of DMF for 2 hours. Then, the mixture was poured into water, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title product (94 mg, 82%).
  • Step H 2-[5-(difluoromethoxy)-3-ethylsulfonyl-2-pyridyl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine (Compound V12.19)
  • Example P6 6-(2-Ethanesulfonyl-6-trifluoromethyl-pyridin-3-yl)-3-methyl-2-trifluoromethyl-3,5-dihydro-diimidazo[4,5-b;4′,5′-e]pyridine (Compound V26.03)
  • Step B 3-methyl-6-nitro-4-oxido-2-(trifluoromethyl)imidazo[4,5-b]pyridin-4-ium
  • Step D N5,3-dimethyl-6-nitro-2-(trifluoromethyl)imidazo[4,5-b]pyridin-5-amine
  • Step E N5,3-dimethyl-2-(trifluoromethyl)imidazo[4,5-b]pyridine-5,6-diamine
  • Step F 3-bromo-2-chloro-6-(trifluoromethyl)pyridine
  • Step G 3-bromo-2-ethylsulfanyl-6-(trifluoromethyl)pyridine
  • Step H ethyl 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carboxylate
  • Carbon monoxide gas was introduced to a mixture of 3-bromo-2-ethylsulfanyl-6-(trifluoromethyl)pyridine (572 mg, 2 mmol), Pd(OAc) 2 (90 mg, 0.4 mmol), dppf (444 mg, 0.8 mmol) and Et 3 N (1.01 g, 10 mmol) in 10 ml of EtOH and 10 ml of DMF and the internal pressure was raised to 2.7 MPa. The mixture was heated at 90° C. for 6 h and cooled to room temperature. Then, it was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo.
  • Step J 2-ethylsulfanyl-N-[3-methyl-5-(methylamino)-2-(trifluoromethyl)imidazo[4,5-b]pyridin-6-yl]-6-(trifluoromethyl) pyridine-3-carboxamide
  • Step K 6-(2-Ethylsulfanyl-6-trifluoromethyl-pyridin-3-yl)-3-methyl-2-trifluoromethyl-3,5-dihydro-diimidazo[4,5-;4′,5′-e]pyridine
  • Step L 6-(2-Ethanesulfonyl-6-trifluoromethyl-pyridin-3-yl)-3-methyl-2-trifluoromethyl-3,5-dihydro-diimidazo[4,5-b;4′,5′-e]pyridine (Compound V26.03)
  • Step A 4-bromo-2-(trifluoromethyl)thiazole
  • Step B 4-bromo-2-(trifluoromethyl)thiazole-5-carboxylic acid
  • n-BuLi 2.5M in hexane, 62 mmol
  • i-Pr 2 NH 6 g, 59 mmol
  • anhydrous THF 150 ml
  • 4-bromo-2-(trifluoromethyl)thiazole (12 g, 52.0 mmol) was slowly added to the above mixture and stirring was continued for 20 min.
  • the mixture was poured into dry ice and stirred for a further hour.
  • reaction mixture was allowed to warm to ambient temperature, diluted with ethyl acetate and the organic phase washed successively with water and saturated brine, dried over sodium sulfate, filtered and concentrated under vacuum to give the title product (10.1 g, 71%).
  • Step C 4-bromo-2-(trifluoromethyl)thiazole-5-carbonyl chloride
  • Step D 4-bromo-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole
  • Step E 4-Ethylsulfanyl-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole
  • EtSNa (123 mg, 1.5 mmol) was added to a mixture of 4-bromo-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole (315 mg, 0.7 mmol) in 10 ml of DMF. After the addition, the mixture was stirred at room temperature for 2 hours. Then the mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel to give the title compound (176 mg, 58%).
  • Step F 4-ethylsulfonyl-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole (Compound V14.05)
  • Example P8 4-ethylsulfonyl-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole (Compound V2.11)
  • Step A 4-bromo-N-methoxy-N-methyl-2-(trifluoromethyl)thiazole-5-carboxamide
  • Step B 1-[4-bromo-2-(trifluoromethyl)thiazol-5-yl]ethanone
  • Step C 4-bromo-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole
  • Step D 4-ethylsulfanyl-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole
  • EtSNa (157 mg, 1.9 mmol) was added to a mixture of 4-bromo-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole (389 mg, 0.9 mmol) in 15 ml of DMF. After the addition, the mixture was stirred at ambient temperature for 2 hours. The reaction mixture was then poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (281 mg, 76%).
  • Step E 4-ethylsulfonyl-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole (Compound V2.11)
  • Step A 3-methylsulfonyl-5-(trifluoromethyl)pyridine-2-carbonyl chloride
  • Step B N-[5-(methylamino)-2-(trifluoromethyl)-4-pyridyl]-3-methylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxamide
  • Step C 3-methyl-2-[3-methylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)imidazo[4,5-c]pyridine (Compound V12.18)
  • Step B 2-ethylsulfanyl-N-methoxy-N-methyl-6-(trifluoromethyl)pyridine-3-carboxamide
  • Step D 2-[2-ethylsulfanyl-6-(trifluoromethyl)-3-pyridyl]-7-(trifluoromethyl)imidazo[1,2-a]pyridine
  • Step E 2-[2-ethylsulfonyl-6-(trifluoromethyl)-3-pyridyl]-7-(trifluoromethyl)imidazo[1,2-a]pyridine (Compound V3.05)
  • Step A ethyl (2Z)-2-cyano-2-hydroxyimino-acetate
  • H 3 PO 4 (1.83 mL, 27 mmol) was added to a mixture of ethyl cyanacetate (5 g, 44.2 mmol) and NaNO 2 (2.87 g, 41.5 mmol) in 35 mL of water at room temperature. After the addition, the mixture was warmed to 40° C. and stirred for another hour. Then, 3.69 ml of hydrochloric acid was added to the mixture and stirring was continued for 18 hours. The mixture was extracted with diethyl ether three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum.
  • Step B ethyl 2-amino-2-cyano-acetate
  • Step C ethyl 4-chloro-1,2,5-thiadiazole-3-carboxylate
  • Disulphur dichloride (4.06 g, 30 mmol) was added to a solution of ethyl 2-amino-2-cyano-acetate (1.28 g, 10 mmol) in 10 ml of DMF at ambient temperature. The mixture was stirred at ambient temperature for 16 h and poured into ice, extracted three times with dichloromethane. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum. The residue was purified by column chromatography on silica gel to give the title compound (1.2 g, y: 63%).
  • 1 H NMR 300 Mz, DMSO-d 6 ): ⁇ 1.35 (t, 3H), 4.39 (q, 2H).
  • Step D ethyl 4-ethylsulfanyl-1,2,5-thiadiazole-3-carboxylate
  • Step E 4-ethylsulfanyl-1,2,5-thiadiazole-3-carboxylic acid
  • Step F 3-ethylsulfanyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-1,2,5-thiadiazole (Compound A1.014-B8.010)
  • Step G 3-ethylsulfonyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-1,2,5-thiadiazole (Compound A1.014-B8.012)
  • Example P12 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl) [1,2,4]triazolo[1,5-c]pyrimidine (Compound V16.03)
  • Step A 4-(trifluoromethyl)pyrimidin-1-ium-1,6-diamine, 2,4,6-trimethylbenzenesulfonate salt (MSH)
  • MSH is explosively unstable as a dry powder and is best handled in dichloromethane solution.
  • a Microwave tube equipped with a magnetic stirrer bar, was charged with 2,2,2-trifluoroacetic acid (4.4 g, 2.54 mmol, 2.9 mL). Then, (tert-butoxycarbonylamino) 2,4,6-trimethylbenzenesulfonate (1 g, 2.54 mmol) was added at 0° C. The reaction mixture was stirred at 0° C. for 2 h, ice-water was added and the precipitate was recovered by filtration. The wet cake was washed with water and dissolved in dichloromethane (5 mL) and dried over sodium sulfate.
  • Step B 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)-[1,2,4]triazolo[1,5-c]pyrimidine (Compound V16.03)
  • nitric acid (2.97 g, 2.14 mL, 30.7 mmol) was added and the reaction was stirred 5 h at 85° C. A further portion of nitric acid (2.97 g, 2.14 mL, 30.7 mmol) was added and the reaction was stirred over night at 85° C. After this time, the mixture was poured into ice water and extracted with 250 mL of Et 2 O. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography, eluting with dichloromethane to give the title compound (18% yield).
  • 1 H NMR 400 MHz, CDCl 3 ): 10.32 (s, 1H), 8.82 (s, 1H), 8.30 (s, 1H) ppm.
  • Step B 4-amino-6-(trifluoromethyl)pyridin-3-ol
  • Step C 2-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)oxazolo[5,4-c]pyridine. (Compound A6.006-B1.014)
  • Step D 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)oxazolo[5,4-c]pyridine (Compound V12.05)
  • Step A 1-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]ethanone
  • the reaction mixture was slowly quenched with NH 4 Cl sat aq (50 ml) and HCl 10% (30 ml) and the resulting mixture vigorously stirred for 15 min at room temperature.
  • the aqueous layer was extracted twice with EtOAc, and the combined organic phases washed successively with 10% HCl aq, water and brine, dried over anhydrous Na 2 SO 4 , filtered and concentrated in vacuo.
  • the crude title product (4.335 g, 91%) was used without purification for the next step.
  • Step B 1-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]ethanone
  • Step C 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine
  • Step A 3-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine
  • Step B 3-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine (Compound V16.01)
  • N-methylpyrazin-2-amine (1 g, 9.2 mmol) in dimethyl sulfoxide (20 ml)/water (0.4 ml) at 10° C. was added portionwise N-Iodosuccinimide (4.1 g, 18.4 mmol). The reaction mixture was then allowed to warm slowly to room temperature and stirred at that temperature overnight. An additional aliquot of N-Iodosuccinimide (4.1 g, 18.4 mmol) was then added at room temperature. After stirring for 7 hr, the reaction mixture was poured onto ice (20 g). The precipitate was collected, washed with cold water (20 ml), and dried to provide the title compound (2.15 g, 65%).
  • Step B 5-iodo-N2-methyl-pyrazine-2,3-diamine
  • Step C 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-5-iodo-1-methyl-imidazo[4,5-b]pyrazine
  • This compound was prepared by methods described in the examples above from 5-iodo-N2-methyl-pyrazine-2,3-diamine and 3-ethylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxylic acid.
  • Step D 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-1-methyl-5-(trifluoromethyl)imidazo[4,5-b]pyrazine (Compound A1.026-B1.022)
  • Example P17 3-methyl-2-[3-(methylsulfonylmethyl)-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)imidazo[4,5-b]pyridine (Compound A.014-B1.106)
  • N2-methyl-5-(trifluoromethyl)pyridine-2,3-diamine (0.24 g, 1.3 mmol, prepared as described in WO 2012092051)
  • EDC.HCl (0.24 g, 1.3 mmol)
  • 3-(methylsulfanylmethyl)-5-(trifluoromethyl)pyridine-2-carboxylic acid (0.29 g, crude sample from above) were dissolved in pyridine (15 ml).
  • the brown suspension was stirred at 120° C. for 2 h.
  • the reaction mixture was diluted with water, and extracted EtOAc.
  • the organic layer was separated and washed with brine, dried over Na2SO4 and evaporated.
  • the crude product was purified by chromatography on an RF 200 machine eluting with EtOAc/Cylohexane gradient, to give 0.35 g of a beige solid, which contained the desired product N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-3-(methylsulfanylmethyl)-5-(trifluoromethyl)pyridine-2-carboxamide.
  • This product was dissolved in 1-methylpyrrolidin-2-one (5 ml) with toluene-4-sulphonic acid (0.072 g, 0.41 mmol) and heated in the microwave at 160° C. for 1 h. After this time, the reaction mixture was diluted with water, and extracted with EtOAc.
  • Step B 2-bromo-5-fluoro-4-nitro-1-oxido-Pyridin-1-ium
  • Step F N-(4-amino-6-bromo-3-pyridyl)-3-ethylsulfonyl-N-methyl-5-(trifluoromethyl)pyridine-2-carboxamide
  • Step G 6-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-3-methyl-imidazo[4,5-c]pyridine (Compound V12.20)
  • Step B 6-chloro-N3-methyl-pyridazine-3,4-diamine
  • Step C N-[6-chloro-3-(methylamino)pyridazin-4-yl]-3-ethylsulfanyl-5-(trifluoromethyl)pyridine-2-carboxamide
  • Step D 3-chloro-6-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]-7-methyl-imidazo[4,5-c]pyridazine (Compound A6.015-B1.014)
  • N-[6-chloro-3-(methylamino)pyridazin-4-yl]-3-ethylsulfanyl-5-(trifluoromethyl)pyridine-2-carboxamide 250 mg, 0.64 mmol was dissolved in DMF (2 mL) and toluene (8 mL). p-toluenesulfonic acid monohydrate (0.123 g, 0.70 mmol) was added. The bombe tube was closed, and heated to 160° C. for 4 hr. This was then cooled to rt and evaporated to dryness. The residue was purified by Flash-Master (Solvent: Cyclohexan/EtOAc 2/1) to give the title compound (172 mg, 72%) as a yellow solid.
  • Step D 3-chloro-6-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-methyl-imidazo[4,5-c]pyridazine (Compound V12.17)
  • Table 1 This table discloses 66 compounds of the formula A1.014-B1 wherein the radicals B1 are the radicals B1.049-B1.084, and B1.091-B1.120 shown in table A, and A1.014 is defined in Table L.
  • Table 2 This table discloses 66 compounds of the formula A1.018-B1 wherein the radicals B1 are the radicals B1.049-B1.084, and B1.091-B1.120 shown in table A, and A1.018 is defined in Table L.
  • Table 3 discloses 66 compounds of the formula A1.022-B1 wherein the radicals B1 are the radicals B1.049-B1.084, and B1.091-B1.120 shown in table A, and A1.022 is defined in Table L.
  • Table 4 This table discloses 36 compounds of the formula A1.014-B2 wherein the radicals B2 are the radicals B2.001-B2.036 shown in table B, and A1.014 is defined in Table L.
  • Table 5 This table discloses 36 compounds of the formula A1.018-B2 wherein the radicals B2 are the radicals B2.001-B2.036 shown in table B, and A1.018 is defined in Table L.
  • Table 6 This table discloses 36 compounds of the formula A1.022-B2 wherein the radicals B2 are the radicals B2.001-B2.036 shown in table B, and A1.022 is defined in Table L.
  • Table 7 This table discloses 24 compounds of the formula A1.014-B3 wherein the radicals B3 are the radicals B3.001-B3.024 shown in table C, and A1.014 is defined in Table L.
  • Table 8 This table discloses 24 compounds of the formula A1.018-B3 wherein the radicals B3 are the radicals B3.001-B3.024 shown in table C, and A1.018 is defined in Table L.
  • Table 9 This table discloses 24 compounds of the formula A1.022-B3 wherein the radicals B3 are the radicals B3.001-B3.024 shown in table C, and A1.022 is defined in Table L.
  • Table 10 This table discloses 8 compounds of the formula A1.014-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A1.014 is defined in Table L.
  • Table 11 This table discloses 8 compounds of the formula A1.018-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A1.018 is defined in Table L.
  • Table 12 This table discloses 8 compounds of the formula A1.022-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A1.022 is defined in Table L.
  • Table 13 This table discloses 24 compounds of the formula A1.014-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A1.014 is defined in Table L.
  • Table 14 This table discloses 24 compounds of the formula A1.018-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A1.018 is defined in Table L.
  • Table 15 This table discloses 24 compounds of the formula A1.022-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A1.022 is defined in Table L.
  • Table 16 This table discloses 16 compounds of the formula A1.014-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A1.014 is defined in Table L.
  • Table 17 This table discloses 16 compounds of the formula A1.018-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A1.018 is defined in Table L.
  • Table 18 This table discloses 16 compounds of the formula A1.022-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A1.022 is defined in Table L.
  • Table 19 discloses 54 compounds of the formula A1.014-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A1.014 is defined in Table L.
  • Table 20 This table discloses 54 compounds of the formula A1.018-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A1.018 is defined in Table L.
  • Table 21 This table discloses 54 compounds of the formula A1.022-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A1.022 is defined in Table L.
  • Table 22 This table discloses 12 compounds of the formula A1.014-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A1.014 is defined in Table L.
  • Table 23 This table discloses 12 compounds of the formula A1.018-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A1.018 is defined in Table L
  • Table 24 This table discloses 12 compounds of the formula A1.022-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A1.022 is defined in Table L
  • Table 25 This table discloses 30 compounds of the formula A1.014-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A1.014 is defined in Table L.
  • Table 26 This table discloses 30 compounds of the formula A1.018-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A1.018 is defined in Table L.
  • Table 27 This table discloses 30 compounds of the formula A1.022-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A1.0122 is defined in Table L.
  • Table 28 This table discloses 12 compounds of the formula A1.014-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A1.014 is defined in Table L.
  • Table 29 This table discloses 12 compounds of the formula A1.018-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A1.018 is defined in Table L.
  • Table 30 This table discloses 12 compounds of the formula A1.022-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A1.022 is defined in Table L.
  • Table 31 This table discloses 64 compounds of the formula A1.014-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A1.014 is defined in Table L.
  • Table 29 discloses 64 compounds of the formula A1.018-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A1.018 is defined in Table L.
  • Table 30 discloses 64 compounds of the formula A1.022-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A1.022 is defined in Table L.
  • Table 31 discloses 132 compounds of the formula A2.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A2.006 is defined in Table M.
  • Table 32 This table discloses 132 compounds of the formula A2.018-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A2.018 is defined in Table M.
  • Table 33 This table discloses 36 compounds of the formula A2.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A2.006 is defined in Table M.
  • Table 34 discloses 36 compounds of the formula A2.018-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A2.018 is defined in Table M.
  • Table 35 This table discloses 24 compounds of the formula A2.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A2.0006 is defined in Table M.
  • Table 36 This table discloses 24 compounds of the formula A2.018-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A2.018 is defined in Table M.
  • Table 37 This table discloses 8 compounds of the formula A2.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A2.006 is defined in Table M.
  • Table 38 discloses 8 compounds of the formula A2.018-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A2.018 is defined in Table M.
  • Table 39 discloses 24 compounds of the formula A2.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A2.006 is defined in Table M.
  • Table 40 This table discloses 24 compounds of the formula A2.018-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A2.018 is defined in Table M.
  • Table 42 This table discloses 16 compounds of the formula A2.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A2.006 is defined in Table M.
  • Table 43 This table discloses 16 compounds of the formula A2.018-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A2.018 is defined in Table M.
  • Table 44 discloses 54 compounds of the formula A2.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A2.0106 is defined in Table M.
  • Table 45 This table discloses 54 compounds of the formula A2.018-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A2.018 is defined in Table M.
  • Table 46 This table discloses 12 compounds of the formula A2.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A2.006 is defined in Table M.
  • Table 47 This table discloses 12 compounds of the formula A2.018-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A2.018 is defined in Table M.
  • Table 48 This table discloses 30 compounds of the formula A2.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A2.006 is defined in Table M.
  • Table 49 discloses 30 compounds of the formula A2.018-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A2.018 is defined in Table M.
  • Table 50 This table discloses 12 compounds of the formula A2.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A2.006 is defined in Table M.
  • Table 51 This table discloses 12 compounds of the formula A2.018-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A2.018 is defined in Table M.
  • Table 52 discloses 64 compounds of the formula A2.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A2.006 is defined in Table M.
  • Table 53 This table discloses 64 compounds of the formula A2.018-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A2.018 is defined in Table M.
  • Table 54 discloses 132 compounds of the formula A3.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A3.006 is defined in Table N.
  • Table 55 discloses 132 compounds of the formula A3.018-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A3.018 is defined in Table N.
  • Table 56 This table discloses 36 compounds of the formula A3.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A3.006 is defined in Table N.
  • Table 57 This table discloses 36 compounds of the formula A3.018-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A3.018 is defined in Table N.
  • Table 58 This table discloses 24 compounds of the formula A3.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A3.006 is defined in Table N.
  • Table 59 This table discloses 24 compounds of the formula A3.018-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A3.018 is defined in Table N.
  • Table 60 This table discloses 8 compounds of the formula A3.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A3.006 is defined in Table N.
  • Table 61 This table discloses 8 compounds of the formula A3.018-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A3.018 is defined in Table N.
  • Table 62 This table discloses 24 compounds of the formula A3.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A3.006 is defined in Table N.
  • Table 63 This table discloses 24 compounds of the formula A3.018-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A3.018 is defined in Table N.
  • Table 64 This table discloses 16 compounds of the formula A3.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A3.006 is defined in Table N.
  • Table 65 This table discloses 16 compounds of the formula A3.018-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A3.018 is defined in Table N.
  • Table 66 discloses 54 compounds of the formula A3.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A3.006 is defined in Table N.
  • Table 67 discloses 54 compounds of the formula A3.018-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A3.018 is defined in Table N.
  • Table 68 This table discloses 12 compounds of the formula A3.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A3.006 is defined in Table N.
  • Table 69 This table discloses 12 compounds of the formula A3.0018-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A3.018 is defined in Table N.
  • Table 70 This table discloses 30 compounds of the formula A3.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A3.006 is defined in Table N.
  • Table 71 This table discloses 30 compounds of the formula A3.018-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A3.018 is defined in Table N.
  • Table 72 This table discloses 12 compounds of the formula A3.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A3.006 is defined in Table N.
  • Table 73 discloses 12 compounds of the formula A3.018-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A3.018 is defined in Table N.
  • Table 74 discloses 64 compounds of the formula A3.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A3.006 is defined in Table N.
  • Table 75 This table discloses 64 compounds of the formula A3.018-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A3.018 is defined in Table N.
  • Table 76 This table discloses 132 compounds of the formula A4.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A4.006 is defined in Table O.
  • Table 77 discloses 132 compounds of the formula A4.008-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A4.008 is defined in Table O.
  • Table 78 This table discloses 36 compounds of the formula A4.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A4.006 is defined in Table O.
  • Table 79 discloses 36 compounds of the formula A4.008-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A4.008 is defined in Table O.
  • Table 80 This table discloses 24 compounds of the formula A4.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A4.006 is defined in Table O.
  • Table 81 This table discloses 24 compounds of the formula A4.008-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A4.008 is defined in Table O.
  • Table 82 This table discloses 8 compounds of the formula A4.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A4.006 is defined in Table O.
  • Table 83 discloses 8 compounds of the formula A4.008-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A4.008 is defined in Table O.
  • Table 84 This table discloses 24 compounds of the formula A4.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A4.006 is defined in Table O.
  • Table 85 This table discloses 24 compounds of the formula A4.008-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A4.008 is defined in Table O.
  • Table 86 This table discloses 16 compounds of the formula A4.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A4.006 is defined in Table O.
  • Table 87 This table discloses 16 compounds of the formula A4.008-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A4.008 is defined in Table O.
  • Table 88 discloses 54 compounds of the formula A4.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A4.006 is defined in Table O.
  • Table 89 discloses 54 compounds of the formula A4.008-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A4.008 is defined in Table O.
  • Table 90 This table discloses 12 compounds of the formula A4.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A4.006 is defined in Table O.
  • Table 91 This table discloses 12 compounds of the formula A4.008-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A4.008 is defined in Table O.
  • Table 92 This table discloses 30 compounds of the formula A4.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A4.006 is defined in Table O.
  • Table 93 This table discloses 30 compounds of the formula A4.008-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A4.008 is defined in Table O.
  • Table 94 discloses 12 compounds of the formula A4.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A4.006 is defined in Table O.
  • Table 95 This table discloses 12 compounds of the formula A4.008-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A4.008 is defined in Table O.
  • Table 96 discloses 64 compounds of the formula A4.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A4.006 is defined in Table O.
  • Table 97 discloses 64 compounds of the formula A4.008-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A3.008 is defined in Table O.
  • Table 98 discloses 132 compounds of the formula A5.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A5.006 is defined in Table P.
  • Table 99 This table discloses 36 compounds of the formula A5.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A5.006 is defined in Table P.
  • Table 100 This table discloses 24 compounds of the formula A5.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A5.006 is defined in Table P.
  • Table 101 This table discloses 8 compounds of the formula A5.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A4.006 is defined in Table P.
  • Table 102 This table discloses 24 compounds of the formula A5.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A5.006 is defined in Table P.
  • Table 103 discloses 16 compounds of the formula A5.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A5.006 is defined in Table P.
  • Table 104 discloses 54 compounds of the formula A5.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A5.006 is defined in Table P.
  • Table 105 This table discloses 12 compounds of the formula A5.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A5.006 is defined in Table P.
  • Table 106 This table discloses 30 compounds of the formula A5.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A5.006 is defined in Table P.
  • Table 107 This table discloses 12 compounds of the formula A5.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A5.006 is defined in Table P.
  • Table 108 discloses 64 compounds of the formula A5.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A5.006 is defined in Table P.
  • Table 109 This table discloses 132 compounds of the formula A6.002-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A6.002 is defined in Table Q.
  • Table 110 discloses 132 compounds of the formula A6.014-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A6.014 is defined in Table Q.
  • Table 111 This table discloses 36 compounds of the formula A6.002-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A6.002 is defined in Table Q.
  • Table 112 This table discloses 36 compounds of the formula A6.014-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A6.014 is defined in Table Q.
  • Table 113 discloses 24 compounds of the formula A6.002-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A6.002 is defined in Table Q.
  • Table 114 This table discloses 24 compounds of the formula A6.014-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A6.014 is defined in Table Q.
  • Table 115 This table discloses 8 compounds of the formula A6.002-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A6.002 is defined in Table Q.
  • Table 116 This table discloses 8 compounds of the formula A6.014-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A6.014 is defined in Table Q.
  • Table 117 This table discloses 24 compounds of the formula A6.002-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A6.002 is defined in Table Q.
  • Table 118 This table discloses 24 compounds of the formula A6.014-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A4.014 is defined in Table Q.
  • Table 119 discloses 16 compounds of the formula A6.002-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A6.002 is defined in Table Q.
  • Table 120 This table discloses 16 compounds of the formula A6.014-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A6.014 is defined in Table Q.
  • Table 121 This table discloses 54 compounds of the formula A6.002-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A6.002 is defined in Table Q.
  • Table 122 This table discloses 54 compounds of the formula A6.014-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A6.014 is defined in Table Q.
  • Table 123 This table discloses 12 compounds of the formula A6.002-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A6.002 is defined in Table Q.
  • Table 124 This table discloses 12 compounds of the formula A6.0014-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A6.014 is defined in Table Q.
  • Table 125 This table discloses 30 compounds of the formula A6.002-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A6.002 is defined in Table Q.
  • Table 126 This table discloses 30 compounds of the formula A6.014-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A6.014 is defined in Table Q.
  • Table 127 This table discloses 12 compounds of the formula A6.002-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A6.002 is defined in Table Q.
  • Table 128 This table discloses 12 compounds of the formula A6.014-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A6.014 is defined in Table Q.
  • Table 129 discloses 64 compounds of the formula A6.002-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A6.002 is defined in Table Q.
  • Table 130 discloses 64 compounds of the formula A6.014-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A6.014 is defined in Table Q.
  • Table 131 This table discloses 132 compounds of the formula A7.002-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A7.002 is defined in Table R
  • Table 132 This table discloses 132 compounds of the formula A7.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A7.006 is defined in Table R.
  • Table 133 This table discloses 132 compounds of the formula A7.010-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A7.010 is defined in Table R.
  • Table 134 discloses 54 compounds of the formula A7.002-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A7.002 is defined in Table R.
  • Table 135 This table discloses 54 compounds of the formula A7.006-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A7.006 is defined in Table R.
  • Table 136 This table discloses 54 compounds of the formula A7.010-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A7.010 is defined in Table R.
  • Table 137 This table discloses 12 compounds of the formula A7.002-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A7.002 is defined in Table R.
  • Table 138 This table discloses 12 compounds of the formula A7.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A7.006 is defined in Table R.
  • Table 139 discloses 12 compounds of the formula A7.010-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A7.010 is defined in Table R.
  • Table 140 This table discloses 30 compounds of the formula A7.002-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A7.002 is defined in Table R.
  • Table 142 This table discloses 30 compounds of the formula A7.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A7.006 is defined in Table R.
  • Table 143 discloses 30 compounds of the formula A7.010-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A7.010 is defined in Table R.
  • Table 144 This table discloses 12 compounds of the formula A7.002-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A7.002 is defined in Table R.
  • Table 145 This table discloses 12 compounds of the formula A7.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A7.006 is defined in Table R.
  • Table 146 discloses 12 compounds of the formula A7.010-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A7.010 is defined in Table R.
  • Table 147 discloses 64 compounds of the formula A7.002-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A7.002 is defined in Table R.
  • Table 148 discloses 64 compounds of the formula A7.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A7.006 is defined in Table R.
  • Table 149 discloses 64 compounds of the formula A7.010-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A7.010 is defined in Table R.
  • Table 150 discloses 132 compounds of the formula A8.002-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A8.002 is defined in Table R
  • Table 151 This table discloses 132 compounds of the formula A8.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A8.006 is defined in Table S.
  • Table 152 This table discloses 132 compounds of the formula A8.010-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A8.010 is defined in Table S.
  • Table 153 discloses 54 compounds of the formula A8.002-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A8.002 is defined in Table S.
  • Table 154 discloses 54 compounds of the formula A8.006-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A8.006 is defined in Table R.
  • Table 155 This table discloses 54 compounds of the formula A8.010-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A8.010 is defined in Table R.
  • Table 156 This table discloses 12 compounds of the formula A8.002-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A8.002 is defined in Table S.
  • Table 157 This table discloses 12 compounds of the formula A8.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A8.006 is defined in Table S.
  • Table 158 discloses 12 compounds of the formula A8.010-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A8.010 is defined in Table S.
  • Table 159 This table discloses 30 compounds of the formula A8.002-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A8.002 is defined in Table S.
  • Table 160 This table discloses 30 compounds of the formula A4.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A8.006 is defined in Table S.
  • Table 161 This table discloses 30 compounds of the formula A8.010-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A8.010 is defined in Table S.
  • Table 162 This table discloses 12 compounds of the formula A8.002-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A8.002 is defined in Table S.
  • Table 164 This table discloses 12 compounds of the formula A8.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A8.006 is defined in Table S.
  • Table 165 This table discloses 12 compounds of the formula A8.010-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A8.010 is defined in Table S.
  • Table 166 discloses 64 compounds of the formula A8.002-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A8.002 is defined in Table S.
  • Table 167 discloses 64 compounds of the formula A8.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A8.006 is defined in Table S.
  • Table 168 discloses 64 compounds of the formula A8.010-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A8.010 is defined in Table S.
  • R 40 is halogen, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkylthio, C 1 -C 4 haloalkylsulfonyl, O(C 1 -C 4 haloalkyl), SF 5 , phenylcarbonylthio, mercapto or C 1 -C 4 alkoxycarbonyl;
  • G 21 is nitrogen, CH, C—C 1 -C 6 alkyl, C—C 1 -C 6 haloalkyl, C-halogen, C—CN, C—O—C 1 -C 4 alkyl, C—S—C 1 -C 4 alkyl, C—SO 2 —C 1 -C 4 alkyl, C—S-phenyl, C—SO 2 -phenyl or C—SO 2 —C 1 -C 4 halolakyl; and G 51 is nitrogen, CH, C—C 1 -C 6 alkyl, C—C 1 -
  • R 41 is C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl-C 1 -C 4 alkyl, C 3 -C 6 halocycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl or C 2 -C 6 alkynyl; and R 42 is C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 3 haloalkoxy, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl-C 1 -C 4 alkyl, C 3 -C 6 halocycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl or C 2 -C 4 -C
  • R 43 is C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl-C 1 -C 4 alkyl, C 3 -C 6 halocycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl or C 2 -C 6 alkynyl; and R 44 is C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 3 haloalkoxy, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl-C 1 -C 4 alkyl, C 3 -C 6 halocycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl or C 2 -C 6 alkynyl; and R 44 is C 1 -C 4 alky

Abstract

Compounds of formula I

A-B  (I),
wherein A is a radical selected from the group consisting of formulae A1 to A8:
Figure US20220104496A1-20220407-C00001
wherein the arrow denotes the point of attachment to the radical B; and
B is a radical selected from the group consisting of formulae B1 to B11:
Figure US20220104496A1-20220407-C00002
Figure US20220104496A1-20220407-C00003
wherein the arrow denotes the point of attachment to the radical A; and wherein the substituents are as defined in claim 1, and the agrochemically acceptable salts and all stereoisomers and tautomeric forms of the compounds of formula I can be used as insecticides and can be prepared in a manner known per se.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a divisional of Ser. No. 17/068,334, filed Oct. 12, 2020, which is a continuation of U.S. application Ser. No. 14/898,597, filed Dec. 15, 2015, which is a 371 National Stage application of International Application No. PCT/EP2014/062946, filed Jun. 19, 2014, which claims priority to EP 13174698.4, filed Jul. 2, 2013, EP 13176263.5, filed Jul. 12, 2013, EP 13197069.1, filed Dec. 13, 2013; and International Patent Application No. PCT/CN2014/076736, filed May 4, 2014, the contents of which applications are herein incorporated by reference.
  • The present invention relates to insecticidally active heterocyclic sulfur containing derivatives, to processes for their preparation, to compositions comprising those compounds, and to their use for controlling animal pests (including arthropods and in particular insects or representatives of the order Acarina).
  • Heterocyclic compounds with pesticidal action are known and described, for example, in WO 2009/131237, WO 2011/043404, WO 2011/040629, WO 2010/125985, WO 2012/086848, WO 2013/018928, WO 2013/191113, WO 2013/180193 and WO 2013/180194.
  • There have now been found novel heterocyclic derivatives with pesticidal properties.
  • The present invention accordingly relates to compounds of formula I,

  • A-B  (I),
  • wherein A is a radical selected from the group consisting of formulae A1 to A8:
  • Figure US20220104496A1-20220407-C00004
  • wherein the arrow denotes the point of attachment to the radical B; and
    B is a radical selected from the group consisting of formulae B1 to B11:
  • Figure US20220104496A1-20220407-C00005
    Figure US20220104496A1-20220407-C00006
  • wherein the arrow denotes the point of attachment to the radical A;
    wherein
    L1 is methylene or a direct bond;
    V0 nitrogen or CR5;
    V1 is nitrogen or CR20; V2 is nitrogen or CR21; V3 is nitrogen or CR22; V4 is nitrogen or CR23;
    V5 is nitrogen or CR24; V6 is nitrogen or CR25; V7 is nitrogen or CR26; V8 is nitrogen or CR27;
    V9 is nitrogen, or CR28V10 is nitrogen or CR29; V11 is nitrogen or CR30;
    G1 is nitrogen or CR31;
    G2 is nitrogen or CR32;
    G3 is —NR35, an oxygen atom or a sulfur atom;
    G4 is nitrogen or CR33;
    G5 is nitrogen or CR34;
    J1, J2, J3 together form together a 5 membered heterocyclic ring, which can be saturated or unsaturated, containing one or two atoms selected from the group consisting of nitrogen, oxygen and sulfur, which ring can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, halogen and or C1-C6haloalkyl, with the proviso that if the ring contains two oxygen atoms, or two sulfur atoms, they are separated by one carbon atom;
    R1 and R2 are the same or different and each represents hydrogen, halogen, C1-C6alkyl or C1-C6haloalkyl;
    R3 is a C1-C6alkyl, C2-C6alkenyl or C2-C6alkynyl group which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulfanyl, C1-C6 alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen, C3-C6 cycloalkyl, said C3-C6cycloalkyl itself can be mono- or polysubstituted by substituents selected from halogen and C1-C3alkyl; and by a 5- or 6-membered heterocyclic group, which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulfanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano and nitro;
    or R3 is —CO2R36, —C(O)R36 or hydrogen;
    or R3 is C3-C6cycloalkyl, which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy and halogen;
    or R3 is a 5- or 6-membered heterocyclic group, which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulfanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano and nitro;
    R35 is hydrogen, C1-C6alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6 alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6alkoxycarbonyl, cyano, hydroxy, halogen and C3-C6cycloalkyl, said C3-C6cycloalkyl itself can be mono- or polysubstituted by substituents selected from halogen and C1-C3alkyl; or an N-oxide thereof;
    R4, R5, R20, R21, R22, R23, R24, R25, R26, R27, R28, R29 and R30 are the same or different and represents cyano, nitro, halogen, hydroxy, C1-C6alkenyloxy, C1-C6haloalkoxy, —C(O)R36—C(O)R36 or hydrogen; or
    C1-C6alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of cyano, halogen, hydroxy, C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy,
    C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulfanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen and C3-C6cycloalkyl, said cycloalkyl itself can be substituted by substituents selected from the group consisting of halogen and C1-C3alkyl, or represents
    a phenyl group which can be mono or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulfanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano, and nitro;
    R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18 and R19 are the same or different and represents C1-C6alkyl, C1-C6haloalkyl or hydrogen, and the group CR13R14 can additionally be a carbonyl group C═O;
    R31, R32, R33, R34 and R40 are the same or different and represents C1-C6 alkyl, C1-C6haloalkyl, —OR7, —S(O)nR36, —NR36R37, —CO2R36, —C(O)R36, cyano, nitro, halogen or hydrogen;
    R36 and R37 are the same or different and represents hydrogen, C1-C6alkyl which can be mono- or polysubstituted by substituents selected from C1-C6alkoxy, C1-C6haloalkoxy, C2-C6 alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6 alkylsulfanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen and C3-C6 cycloalkyl, wherein said C3-C6 cycloalkyl can be mono- or polysubstituted by substituents selected from the group consisting of halogen and C1-C3alkyl; or
    R36 and R37 are the same or different and represents
    a phenyl group which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulfanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano, and nitro;
    each m independently represents 0, 1 or 2, and n represents 0, 1 or 2, with the provisos that:
      • a) in —S(O)nR36, R36 is hydrogen when n is 0;
      • b) if B is B1, then A is different from A2, A3 and A5;
      • c) if A is A1, then B is different from B1, B7, B8, B9 and B10;
      • d) if A is A5, then B is different from B10;
        as well as agrochemically acceptable salts, enantiomers, diastereomers, tautomers, and N-oxides of those compounds.
  • Compounds of formula I which have at least one basic centre can form, for example, acid addition salts, for example with strong inorganic acids such as mineral acids, for example perchloric acid, sulfuric acid, nitric acid, nitrose acid, a phosphorus acid or a hydrohalic acid, with strong organic carboxylic acids, such as C1-C4alkanecarboxylic acids which are unsubstituted or substituted, for example by halogen, for example acetic acid, such as saturated or unsaturated dicarboxylic acids, for example oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid or phthalic acid, such as hydroxycarboxylic acids, for example ascorbic acid, lactic acid, malic acid, tartaric acid or citric acid, or such as benzoic acid, or with organic sulfonic acids, such as C1-C4alkane- or arylsulfonic acids which are unsubstituted or substituted, for example by halogen, for example methane- or p-toluenesulfonic acid. Compounds of formula I which have at least one acidic group can form, for example, salts with bases, for example mineral salts such as alkali metal or alkaline earth metal salts, for example sodium, potassium or magnesium salts, or salts with ammonia or an organic amine, such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower-alkylamine, for example ethyl-, diethyl-, triethyl- or dimethylpropylamine, or a mono-, di- or trihydroxy-lower-alkylamine, for example mono-, di- or triethanolamine.
  • The alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl, hexyl, nonyl, decyl and their branched isomers. Alkoxy, alkenyl and alkynyl radicals are derived from the alkyl radicals mentioned. The alkenyl and alkynyl groups can be mono- or polyunsaturated.
  • Halogen is generally fluorine, chlorine, bromine or iodine. This also applies, correspondingly, to halogen in combination with other meanings, such as haloalkyl or halophenyl.
  • Haloalkyl groups preferably have a chain length of from 1 to 6 carbon atoms. Haloalkyl is, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, pentafluoroethyl, 1,1-difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl and 2,2,2-trichloroethyl; preferably trichloromethyl, difluorochloromethyl, difluoromethyl, trifluoromethyl and dichlorofluoromethyl.
  • Alkoxy groups preferably have a preferred chain length of from 1 to 6 carbon atoms. Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy and also the isomeric pentyloxy and hexyloxy radicals; preferably methoxy and ethoxy.
  • Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferably methoxycarbonyl or ethoxycarbonyl. Haloalkoxy groups preferably have a chain length of from 1 to 6 carbon atoms. Haloalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferably difluoromethoxy, 2-chloroethoxy and trifluoromethoxy.
  • Alkylthio groups preferably have a chain length of from 1 to 6 carbon atoms. Alkylthio is, for example, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio or tert-butylthio, preferably methylthio and ethylthio. Alkylsulfinyl is, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl, tert-butylsulfinyl; preferably methylsulfinyl and ethylsulphinyl.
  • Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl or tert-butylsulfonyl; preferably methylsulfonyl or ethylsulfonyl.
  • Alkylamino is, for example, methylamino, ethylamino, n-propylamino, isopropylamino or the isomeric butylamines. Dialkylamino is, for example, dimethylamino, methylethylamino, diethylamino, n-propylmethylamino, dibutylamino and diisopropylamino. Preference is given to alkylamino groups having a chain length of from 1 to 4 carbon atoms.
  • Alkoxyalkyl groups preferably have a chain length of 1 to 6 carbon atoms.
  • Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl or isopropoxyethyl.
  • The cycloalkyl groups preferably have from 3 to 6 ring carbon atoms, for example cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Phenyl, also as part of a substituent such as phenoxy, benzyl, benzyloxy, benzoyl, phenylthio, phenylalkyl, phenoxyalkyl, may be substituted. In this case, the substituents can be in ortho, meta and/or para position. The preferred substituent positions are the ortho and para positions to the ring attachment point.
  • In the context of this invention “mono- to polysubstituted” in the definition of the substituents, means typically, depending on the chemical structure of the substituents, monosubstituted to seven-times substituted, preferably monosubstituted to five-times substituted, more preferably mono-, double- or triple-substituted.
  • “5-membered heterocyclic” in the present invention means a 5-membered aromatic heterocyclic group or 5-membered non-aromatic heterocyclic group, and the “6-membered heterocyclic” means a 6-membered aromatic heterocyclic group or a. 6-membered non-aromatic heterocyclic group. Accordingly, a “5- or 6-membered heterocyclic group” in the present invention means a 5- or 6-membered aromatic heterocyclic group, or a 5- or 6-membered non-aromatic heterocyclic group.
  • “5- or 6-membered heterocyclic group, which can be substituted” in the present invention means a heterocyclic group, wherein the hydrogen atom(s) bound to the carbon atom(s), nitrogen atom(s) and/or sulfur atom(s) is/are optionally substituted by one or more atoms or groups selected from a pre-defined list, wherein the group has two or more atoms or groups selected from a pre-defined list, these atoms or groups are the same or different from each other. In context of an N atom or S atom, when it's oxidized to form an N oxide or sulfone and sulfoxide respectively, the oxidised analog is not substituted; however, such an analog is within the scope of the invention. Examples of 5- or 6-membered heterocyclic group, which can be substituted include pyrrolidin-1-yl group, a 3,3,4,4-tetrafluoropyrrolidin-1-yl group, a tetrahydrofuran-2-yl group, a piperidyl group, a morpholyl group, a thiomorpholyl group, and the like.
  • Examples of a 5- or 6-membered aromatic heterocyclic groups, which can be substituted, are 2-pyrroly, 2-furyl group, 3-furyl, 5-pyrazolyl, a 4-pyrazolyl, 1-pyrroly, I-methyl-2-pyrroly, 2-methylsulfanyl-1-pyrroly, 2-methylsulfinyl-1-pyrroly, 2-methylsulfonyl-1-pyrroly, a 2-methylamino-1-pyrroly group, a 2-dimethylamino-1-pyrroly group, a 5-bromo-2-furyl, a 5-nitro-2-furyl group, a 5-cyano-2-furyl group, a 5-methoxy-2-furyl group, a 5-acetyl-2-furyl, a 5-methoxycarbonyl-2-furyl group, a 2-methyl-3-furyl group, a 2,5-dimethyl-3-furyl group, a 2,4-dimethyl-3-furyl group, a 5-methyl-2-thienyl group, a 3-methyl-2-thienyl group, a 1-methyl-3-trifluoromethyl-5-pyrazolyl group, a 5-chloro-1,3-dimethyl-4-pyrazolyl group, pyrazol-1-yl group, a 3-chloro-pyrazol-1-yl group, a 3-bromopyrazol-1-yl group, a 4-chloropyrazol-1-yl group, a 4-bromopyrazol-1-yl group, an imidazole-1-yl group, a 1,2,4-triazol-1-yl group, a 3-chloro-1,2,4-triazol-1-yl group, a 1,2,3,4-tetrazol-1-yl group, a 1,2,3,5-tetrazol-1-yl group, a 2-thienyl group, a 3-thienyl group, a 3-trifluoromethyl-1,2,4-triazol-1-yl group, a 4-trifluoromethyl pyrazol-1-yl group, pyrazinyl group, a 4-pyrimidinyl group, a 5-pyrimidinyl group, a 2-pyridyl group, a 3-pyridyl group, a
  • 4-pyridyl group, a 3-fluoro-2-pyridyl group, a 4-fluoro-2-pyridyl group, a 5-fluoro-2-pyridyl group, a 6-fluoro-2-pyridyl group, a 2-pyrimidinyl group, a 3-chloro-5-trifluoromethylpyridin-2-yl group, a 5-trifluoromethylpyridin-2-yl group, and the like.
  • In a preferred embodiment of the invention, R35 is C1-C6alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6 alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulfanyl, C1-C6haloalkylsulfanyl, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, C2-C6alkylcarbonyl, C2-C6alkoxycarbonyl, cyano, hydroxy, halogen and C3-C6cycloalkyl, said C3-C6cycloalkyl itself can be mono- or polysubstituted by substituents selected from halogen and C1-C6alkyl; or an N-oxide thereof.
  • Preferably R4, R5, R20, R21, R22, R23, R24, R25, R26, R27, R28, R29, and R30 are the same or different and represents cyano, nitro, halogen, hydroxy, —C(O)R36 or hydrogen; or
  • C1-C6alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of cyano, halogen, hydroxy, C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6 alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen and C3-C6cycloalkyl, said cycloalkyl itself can be substituted by substituents selected from the group consisting of halogen and C1-C6alkyl; or represents
    a phenyl group which can be mono or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano, and nitro.
  • Compounds of formula (I) are made up of a combination of a radical selected from group A and a radical selected from group B.
  • Accordingly, in an embodiment of the invention, the compound of formula (I) is a radical selected from A and any one radical selected from group B, such as
      • a) radical A1 is combined with one radical selected from the group consisting of the radicals B1 to B1;
      • b) radical A2 is combined with one radical selected from the group consisting of the radicals B1 to B1;
      • c) radical A3 is combined with one radical selected from the group consisting of the radicals B1 to B11;
      • d) radical A4 is combined with one radical selected from the group consisting of the radicals B1 to B11;
      • e) radical A5 is combined with one radical selected from the group consisting of the radicals B1 to B11;
      • f) radical A6 is combined with one radical selected from the group consisting of the radicals B1 to B11;
      • g) radical A7 is combined with one radical selected from the group consisting of the radicals B1 to B11; or
      • h) radical A8 is combined with one radical selected from the group consisting of the radicals B1 to B11.
  • Similarly, in another embodiment, the compound of formula (I) is a radical selected from B and any one radical selected from group A, such as
      • a) radical B1 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • b) radical B2 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • c) radical B3 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • d) radical B4 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • e) radical B5 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • f) radical B6 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • g) radical B7 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • e) radical B8 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • f) radical B9 is combined with one radical selected from the group consisting of the radicals A1 to A8;
      • g) radical B10 is combined with one radical selected from the group consisting of the radicals A1 to A8; or
      • h) radical B11 is combined with one radical selected from the group consisting of the radicals A1 to A8.
  • In a further embodiment, radical A is selected from any one of the following more specific radicals Q1 to Q11 from A1 to A8, wherein R1 is as defined in the first aspect:
  • Figure US20220104496A1-20220407-C00007
    Figure US20220104496A1-20220407-C00008
  • Further embodiments of the first aspect are set-out in Table Z below:
  • TABLE Z
    Combinations of A and B for formula (I)
    Embodiment E A group B group
    E1 A1 B1
    E2 A1 B2
    E3 A1 B3
    E4 A1 B4
    E5 A1 B5
    E6 A1 B6
    E7 A1 B7
    E8 A1 B8
    E9 A1 B9
    E10 A1 B10
    E11 A1 B11
    E12 A2 B1
    E13 A2 B2
    E14 A2 B3
    E15 A2 B4
    E16 A2 B5
    E17 A2 B6
    E18 A2 B7
    E19 A2 B8
    E20 A2 B9
    E21 A2 B10
    E22 A2 B11
    E23 A3 B1
    E24 A3 B2
    E25 A3 B3
    E26 A3 B4
    E27 A3 B5
    E28 A3 B6
    E29 A3 B7
    E30 A3 B8
    E31 A3 B9
    E32 A3 B10
    E33 A3 B11
    E34 A4 B1
    E35 A4 B2
    E36 A4 B3
    E37 A4 B4
    E38 A4 B5
    E39 A4 B6
    E40 A4 B7
    E41 A4 B8
    E42 A4 B9
    E43 A4 B10
    E44 A4 B11
    E45 A5 B1
    E46 A5 B2
    E47 A5 B3
    E48 A5 B4
    E49 A5 B5
    E50 A5 B6
    E51 A5 B7
    E52 A5 B8
    E53 A5 B9
    E54 A5 B10
    E55 A5 B11
    E56 A6 B1
    E57 A6 B2
    E58 A6 B3
    E59 A6 B4
    E60 A6 B5
    E61 A6 B6
    E62 A6 B7
    E63 A6 B8
    E64 A6 B9
    E65 A6 B10
    E66 A6 B11
    E67 A7 B1
    E68 A7 B7
    E69 A7 B8
    E70 A7 B9
    E71 A7 B10
    E72 A7 B11
    E73 A8 B1
    E74 A8 B7
    E75 A8 B8
    E76 A8 B9
    E77 A8 B10
    E78 A8 B11
  • In an embodiment of the present invention, a preferred radical A is A1, A6, or A4; especially preferred is A1 and A6; in particular A1.
  • In another preferred embodiment of the present invention, a preferred radical B is B1, B2, B11, B7, B8, B9, B10, B3 or B6; especially preferred is B1, B2, B11, B7, B8, B9, or B10, in particular B1, B2, B11, B7, B8 or B9; such as B1, B2 or B11.
  • Accordingly, formula (I) preferably consists of the following combinations of radicals A and B:
  • A group B group
    A1 B1
    A1 B2
    A1 B11
    A1 B7
    A1 B8
    A1 B9
    A1 B10
    A1 B3
    A6 B1
    A6 B2
    A6 B11
    A6 B7
    A6 B8
    A6 B9
    A6 B10
    A6 B3
    A4 B1
    A4 B2
    A4 B11
    A4 B7
    A4 B8
    A4 B9
    A4 B10
    A4 B3
  • In an embodiment of the present invention, if V0 in B1 is CR5, A is different from A1. In a preferred embodiment, V0 in B1 is CR5 and A is selected from A2, A3, A4, A5 and A6, especially selected from A4 and A6.
  • In an embodiment of the present invention, L1, in reference to each of B, is a direct bond.
  • In another embodiment of the present invention, R1, in reference to each of A, is the same or different and each represents hydrogen, halogen, C1-C3alkyl or C1-C3 haloalkyl; preferably hydrogen, bromine, chlorine, methyl, difluoromethyl or trifluoromethyl.
  • In another embodiment of the present invention, R2, in reference to each of A, is the same or different and each represents, hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably hydrogen.
  • In another embodiment of the present invention, R3, in reference to each of B, is the same or different and each represents C1-C3alkyl or C1-C3haloalkyl; preferably methyl or ethyl.
  • In another embodiment of the present invention, R4, in reference to each of B, is the same or different and each represents, hydrogen or C1-C3alkyl; preferably hydrogen or methyl.
  • Also preferred are compounds of formula I, represented by a combination of the 4 “another embodiment” groups mentioned above.
  • In another embodiment of the present invention, m, in reference to each of B, is the same or different and each represents 0, 1 or 2; preferably 2.
  • In another embodiment of the present invention, R6 and R7, in reference to each of B, is the same or different and each represents C1-C3alkyl or C1-C3haloalkyl; preferably methyl.
  • In another embodiment of the present invention, R10 and R11, in reference to each of B, is the same or different and each represents, hydrogen, C1-C3alkyl or C1-C3haloalkyl; preferably hydrogen or methyl. In a preferred embodiment, R11 is hydrogen and R10 is methyl.
  • In another embodiment of the present invention, R12, R13, and R14, in reference to each of B, is the same or different and each represents, hydrogen, C1-C3 alkyl or C1-C3 haloalkyl; preferably hydrogen or methyl. In a preferred embodiment, R13, and R14 are each hydrogen and R12 is methyl.
  • In another embodiment of the present invention, R15, R16, R17 and R18, in reference to each of B, is the same or different and each represents, hydrogen, C1-C3 alkyl or C1-C3 haloalkyl; preferably hydrogen or methyl. In a preferred embodiment, R15, R16, R17 and R18 are each hydrogen.
  • In another embodiment of the present invention, R19, in reference to each of B, is the same or different and represents, hydrogen, C1-C4 alkyl or C1-C4 haloalkyl; preferably hydrogen or tert-butyl.
  • In another embodiment of the present invention, V1, in reference to each of B, is the same or different and represents CH or N.
  • In another embodiment of the present invention, V0, in reference to each of B, is the same or different and represents CH or N.
  • In another embodiment of the present invention, V2, in reference to each of B, is the same or different and represents, CR21′, where R21′, in reference to each of B, is the same or different and represents, hydrogen, halogen, C1-C3 alkyl, C1-C3 haloalkyl, or phenyl or 4-trifluoromethylphenyl, preferably hydrogen, chlorine, bromine or trifluoromethyl.
  • In another embodiment of the present invention, V3, in reference to each of B, is the same or different and represents, CR22′, where R22′, in reference to each of B, is the same or different and represents, hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl, preferably hydrogen, chlorine, bromine or trifluoromethyl.
  • In another embodiment of the present invention, V4, in reference to each of B, is the same or different and represents, N or CR23′, where R23′, in reference to each of B, is the same or different and represents, hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably V4 represents N or CH.
  • In another embodiment of the present invention, V5, in reference to each of B, is the same or different and represents, N or CR24′, where R24, in reference to each of B, is the same or different and represents, hydrogen, halogen, C1-C6alkyl or C1-C6haloalkyl; preferably V5 represents CH.
  • In another embodiment of the present invention, V6, in reference to each of B, is the same or different and represents, N or CR25′, where R25, in reference to each of B, is the same or different and represents, hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably V5 represents N or CH.
  • In another embodiment of the present invention, V7, in reference to each of B, is the same or different and represents, N or CR26′, where R26′, in reference to each of B, is the same or different and represents, hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably V7 represents N, CH, C-chlorine, C-bromine or C—CF3.
  • In another embodiment of the present invention, V8, in reference to each of B, is the same or different and represents, N or CR27, where R27′, in reference to each of B, is the same or different and represents hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably V8 represents CH.
  • In another embodiment of the present invention, V9, in reference to each of B, is the same or different and represents, N or CR28, where R28′, in reference to each of B, is the same or different and represents hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably V9 represents N or CH.
  • In another embodiment of the present invention, V10, in reference to each of B, is the same or different and represents, N or CR29′, where R29′, in reference to each of B, is the same or different and represents hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably V9 represents N or CH.
  • In another embodiment of the present invention, V11, in reference to each of B, is the same or different and represents N or CR30, where R30, in reference to each of B, is the same or different and represents hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably V9 represents N or CH.
  • In another embodiment of the present invention, G1, in reference to each of A, is the same or different and represents N or CR31′, where R31′, in reference to each of A, is the same or different and represents hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably G1 represents N or CH.
  • In another embodiment of the present invention, G2, in reference to each of A, is the same or different and represents N or CR32′, where R32′, in reference to each of A, is the same or different and represents hydrogen, halogen, C1-C3alkyl or C1-C3haloalkyl; preferably G2 represents N or CH.
  • In another embodiment of the present invention, G3, in reference to each of A, is the same or different and represents oxygen, sulfur or NR35, where R35 is N-methyl, in reference to each of A, is the same or different and represents C1-C3alkyl or C1-C3haloalkyl; preferably G3 represents oxygen, sulfur, or N—CH3.
  • In another embodiment of the present invention, G4, in reference to each of A, is the same or different and represents N or CR33′, where R33′, in reference to each of A, is the same or different and represents C1-C3alkyl or C1-C3haloalkyl; preferably G4 represents N or N—CH3.
  • In another embodiment of the present invention, G5, in reference to each of A, is the same or different and represents N or CR34′, where R34′, in reference to each of A, is the same or different and represents hydrogen, C1-C3alkyl or C1-C3haloalkyl; preferably G5 represents N or N—CH3.
  • In another embodiment of the present invention, J1, in reference to each of radical A4, is N.
  • In another embodiment of the present invention, J2, in reference to each of radical A4, is CH, C1-C3 alkyl or C1-C3 haloalkyl, such as CH, C—CH3, or C—CF3.
  • In another embodiment of the present invention, J3, in reference to each of radical A4, is oxygen or sulfur.
  • The process according to the invention for preparing compounds of formula (I) is carried out in principle by methods known to those skilled in the art, or described for example in WO 2009/131237, WO 2011/043404, WO 2011/040629, WO 2010/125985, WO 2012/086848, WO 2013/018928, WO 2013/191113, WO 2013/180193 and WO 2013/180194, and involves reaction of a compound of formula II,
  • Figure US20220104496A1-20220407-C00009
  • wherein Q is the radical B1, B2, B3, B4, B5, B6, B7, B8, B9 and B11, wherein R3, R4, R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19, V0, V1, V2, V3, V4, V5, V6, V7, V8 and L1 are as described in formula I, and the arrows in the radicals B1-B9 and B11 show the point of attachment to the carbonyl atom of the carboxyl group In formula II, with a compounds of formula III, IV, or V;
  • Figure US20220104496A1-20220407-C00010
  • wherein R1, R2, G1, G2, and G5 are as described in formula (I) and M1 is oxygen, sulfur, or NR35, in the presence of a dehydrating agent such as polyphosphoric acid at temperature between 150° C. to 200° C., to yield compounds of formula Ia, Ib, and Ic, wherein the substituents are as described for formula (I).
  • Figure US20220104496A1-20220407-C00011
  • Such processes are well known and have been described for example in WO 2011/040629 or WO 2009131237 (M1 is oxygen), WO 2011088990 or Inorg. Chimica Acta, 358(9), 2701-2710; 2005 (M1 is sulfur) and J. Am. Chem. Soc., 132(5), 1545-1557, 2010 or WO 2008128968 (M1 is NR35). The process is summarized in scheme 1 for compounds of formula Ia:
  • Figure US20220104496A1-20220407-C00012
  • As can be seen in scheme 1, the formation of Ia occurs through the intermediacy of a compound of formula VI. It is in many cases advantageous to thus prepare compounds of formula (I) through such intermediates. This is illustrated for compounds of formula Ia in scheme 2.
  • Figure US20220104496A1-20220407-C00013
  • In scheme 2 compounds of formula II wherein Q is as previously described, are activated to compounds of formula IIa by methods known to those skilled in the art and described in for example Tetrahedron, 61 (46), 10827-10852, 2005. For example compounds where X0 is halogen are formed by treatment with for example, oxallyl chloride or thionyl chloride in the presence of catalytic quantities of DMF in inert solvents such as methylene chloride or THF at temperatures between 20° C. to 100° C., preferably 25° C. Treatment of IIa with compounds of formula III, optionally in the presence of a base, e.g. trethylamine or pyridine leads to compounds of formula VI. Alternatively, compounds of formula VI can be prepared by treatment of compounds of formula II with dicyclohexyl carbodiimide (DCC) or 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) to give the activated species IIa, wherein X0 is X01 and X02 respectively, in an inert solvent, e.g. pyridine, or THF optionally in the presence of a base, e.g. triethylamine, at temperatures between 50-180° C. Compounds of Formula VI so obtained can then be converted to compounds of formula Ia by dehydration, eg. by heating the compounds in a microwave, in the presence of an acid catalyst, for example methane sulfonic acid, or para-toluene sulfonic acid, in an inert solvent such as N-methyl pyrollidine at temperatures between 25-180° C., preferably 130-170° C. Such processes have been described previously in WO 2010125985. Alternatively, compounds of formula VI can be converted to compounds of formula Ia (wherein M1 is O) using triphenyl phosphine, di-isopropyl azo dicarboxylate in an inert solvent such as THF at temperatures between 25-50° C. Such Mitsunobu conditions have been previously described for such transformations (see WO2009131237). Application of such methods in the reaction of compounds of formula II respectively IIa with compounds of formula IV and V, leads to compounds Ib and Ic via the intermediates VII and VIII respectively.
  • Figure US20220104496A1-20220407-C00014
  • Alternatively, compounds of formula (I) can be prepared by reacting compounds of formula IX, X, XI, XII, and XIII;
  • Figure US20220104496A1-20220407-C00015
  • wherein V0, V1, V2, V3, V4, V5, V6, V7, V8 and R4 are as defined for formula (I) and X04 is halogen, with compounds of formula III, IV and V as described in schemes 2 and 3 to give compounds of formula XIV, XV, XVI, XVII, XVIII, XIX, XX, XXI, XXII, XXIII, XIV, XV, XVI, XVII, and XVIII;
  • Figure US20220104496A1-20220407-C00016
    Figure US20220104496A1-20220407-C00017
  • wherein R1, R2, R4, G1, G2, G5, V0, V1, V2, V3, V4, V5, V6, V7, V3, J1, J2 and J3 are as defined in formula I, M1 is oxygen, sulfur, or NR35, and X04 is halogen. Compounds of formula XIV, XV, XVI, XVII, XVIII, XIX, XX, XXI, XXII, XXIII, XXIV, XXV, XXVI, XXVII, and XXVIII can be reacted with compounds of formula XXIX

  • R3—SH  (XXIX)
  • wherein R3 is as described in formula I, in the presence of a suitable base, such as alkali metal carbonates, for example sodium carbonate and potassium carbonate or alkali metal hydrides such as sodium hydride, in a suitable solvent, at temperatures between 25-120° C. to give compounds of formula Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ip, Iq and Ir:
  • Figure US20220104496A1-20220407-C00018
    Figure US20220104496A1-20220407-C00019
    Figure US20220104496A1-20220407-C00020
  • Examples of the solvent to be used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butylmethyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile. Similar chemistry has been previously described, as for example in WO 2013018928. Alternatively, the reaction can be carried out in the presence of a palladium catalyst, such as tris(dibenzylideneacetone)dipalladium(0), in the presence of a phosphor ligand, such as xanthphos, in an inert solvent, for example, xylene at temperatures between 100-160° C., preferably 140° C., as described by Perrio et al in Tetrahedron, 61, 5253-5259, 2005. Compounds represented by the formula (I) wherein m is 1 or 2 can be produced by oxidizing the compounds of formula Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ip, Iq and Ir. The oxidation reaction is generally conducted in the presence of a solvent. Examples of the solvent to be used in the reaction include aliphatic halogenated hydrocarbons such-as dichloromethane and chloroform; alcohols such as methanol and ethanol; acetic acid; water; and mixtures thereof. Examples of the oxidant to be used in the reaction include sodium periodate and m-chloroperbenzoic acid. The amount of the oxidant to be used in the reaction is generally 1 to 3 moles, preferably 1 to 1.2 moles, relative to 1 mole of the compounds Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ip, Iq and Ir to produce compounds of formula (I) where m=1, and preferably 2 to 2.2 moles of oxidant, preferably metachloroperbenzoic acid, relative to 1 mole of the compounds Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ip, Iq and Ir to produce compounds of formula (I) wherein m=2.
  • Compounds of formula I, wherein B is B10, can be prepared by reacting a compound of formula XXX:

  • Q1-X05   (XXX),
  • wherein Q1 is A1, A2, A3, A4, and A8 and X05 is a halogen or a leaving group OSO2R38, and the arrows in the substituents in A1, A2, A3, A4, and A6 show the point attachment of the radical A to the substituent X04, and wherein R38, is C1-C6alkyl, C1-C6haloalkyl, or phenyl optionally substituted by nitro or C1-C3alkyl, with a compound of formula XXXI;
  • Figure US20220104496A1-20220407-C00021
  • wherein, V9, V10, and V11, are as described in formula I, in the presence of a suitable base, such as sodium hydride or cesium carbonate, in an inert solvent such as dimethyl formamide, N-methylpyrollidine, or acetonitrile, at temperatures between 20-150° C., to yield compounds of formula XXXII:
  • Figure US20220104496A1-20220407-C00022
  • Alternatively compounds of formula XXXII can be obtained by reacting compounds of formula XXX with compounds of formula XXXI in an inert solvent such as dioxane, in the presence of a catalytic amount of copper iodide and catalytic amount of a diamine, for example N,N-dimethylethylenediamine or racemic trans-N,N-dimethylcyclohexanediamine, with a base, for example potassium carbonate or potassium phosphate at temperatures between 50-120° C., preferably 90-110° C. Such reactions are well precedented in the literature and described for example in J. Org. Chem., 68, 2609-2617, 2003, and Org. Letts., 9, 643-646, 2007. Compounds of formula XXXII can be reacted with a halogenating reagent such as phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide, or thionyl chloride, optionally in an inert solvent at temperatures between 25-120° C., to give compounds of formula XXXIII, wherein X0s is halogen:
  • Figure US20220104496A1-20220407-C00023
  • Compounds of formula XXXIIII can subsequently be treated with compounds of formula XXIX;

  • R3—SH  (XXIX)
  • wherein R3 is as described in formula I, in the presence of a suitable base, such as an alkaline earth metal hydride, for example sodium hydride and a polar aprotic solvent, such as dimethyl formamide, at temperatures between 25-120° C. to give compounds of formula Is:
  • Figure US20220104496A1-20220407-C00024
  • Oxidation of compound Is by methods known to those skilled in the art, for example using sodium periodate to prepare compounds of formula It, where m=1, or at least two equivalents of meta-chloroperbenozoic (MCPBA) in an inert solvent such as methylene chloride, leads to compounds of formula It where m=2.
  • Figure US20220104496A1-20220407-C00025
  • The synthesis is summarized in scheme 3.
  • Figure US20220104496A1-20220407-C00026
  • The subgroup of compounds of formula I, wherein A is A2 and G5 is CR34, can be represented by the compounds of formula Iu
  • Figure US20220104496A1-20220407-C00027
  • wherein Q is one of the radicals B1, B2, B3, B4, B5, Be, B7, B8, B9 or B11, and R1, R2, G1, G2 and G4 are as described in formula (I) and R34 is C1-C6alkyl or C1-C6haloalkyl can be prepared by reacting a compound of formula XXXIV
  • Figure US20220104496A1-20220407-C00028
  • wherein R1, R2, G1 and G2 are as described in formula (I) with a compound of formula XXXV
  • Figure US20220104496A1-20220407-C00029
  • wherein X07 is a halogen or a leaving group OSO2R38 and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • A further process to prepare compounds of formula Iu, involves reacting a compound of formula XXXIV with a compound of XXXVa
  • Figure US20220104496A1-20220407-C00030
  • In the presence of a Lewis acid, such as Zinc(II)iodide or Indium(III) triflate, in an inert solvent such as chlorobenzene or 1,2,dichlorobenzene, with a catalytic copper(II) salt, such as Cu(II)acetate, under an oxygen or air atmosphere at temperatures between 100-180° C., preferably 110-140° C., to give compounds of formula Iu wherein R34 is hydrogen. Such reactions have previously been described in the literature (see Adv. Synth. Catal. 2013, 355, 1741-1747, and J. Org. Chem., 2013, 78, 12494-12504). Halogenation of compounds of formula Iu, wherein R34 is hydrogen, with a halogenating agent such as N-chlorosuccinamide, N-bromosuccinamide, or N-iodosuccinamide, in a polar aprotic solvent such as acetonitrile or dimethylformamide, at ambient temperature, leads to compounds of formula Iuc
  • Figure US20220104496A1-20220407-C00031
  • wherein Q, R1, R2, G1, G2 and G4 are as described in formula (I), and X15 is halogen. Compounds of formula Iu, can be reacted with compounds R34-M0, wherein M0 is a boronic acid, in the presence of a palladium catalyst to give compounds of formula Iu. When M0 is a boronic acid, the reaction is usually carried out in the presence of a base, for example potassium carbonate, cesium carbonate, or potassium phosphate, in an inert solvent, such as dioxane, optionally in the presence of water, with a palladium(0) catalyst, for example tetrakis(triphenylphosphine)palladium, at a temperature between 80-120° C. Such Suzuki reactions are well precedented in the literature, see for example Masuda, Naoyuki et al, WO 2012133607. Compounds of formula XXXV and XXXVa can be prepared from compounds of formula II by, for example, the methods shown in scheme 4.
  • Figure US20220104496A1-20220407-C00032
  • In scheme 4, an acyl halide of formula IIa is converted to a Weinreb amide Ib upon reaction with N, O-Dimethylhydroxylamine by methods known to those skilled in the art and described for example in C. Ferri, “Reaktionen der Organischen Synthese”, Georg Thieme Verlag, Stuttgart, 1978, page 223ff. the Weinreb amide of formula Ib is then reacted with a Grignard reagent of formula R35CH2MgHal according to the method of Weinreb (Tetrahedron Letters 1981, 22, 3815-3818) to give compounds of formula XXXVb and XXXVa. Compounds of formula XXXVa and XXXVb can also be prepared by treatment of nitrile compounds of formula IIc, wherein Q is as described in formula I, with a Grignard reagent of formula R35CH2MgHal, followed by acidic hydrolysis (as described in C. Ferri, “Reaktionen der Organischen Synthese”, Georg Thieme Verlag, Stuttgart, 1978, page 223ff.).
  • Compounds of formula XXXVa and XXXVb can be halogenated to compounds of formula XXXV, with for example mixtures of bromine and hydrobromic acid in acetic acid (as described in Phosphorus, Sulfur and Silicon and the Related Elements, 2013, 188(12), 1835-1844) or with, for example, copper(II)bromide in an inert solvent, for example chloroform, ethyl acetate and the like, as described in J. Med. Chem., 2013, 56(1), 84-96. Alternatively compounds of formula XXXV where R35 is hydrogen, can be prepared directly from compounds of formula IIa by treatment with diazomethane or trimethyl silyl diazomethane and subsequent treatment with an halogen acid, for example, hydrobromic acid or hydrochloric acid in an inert solvent such as diethyl ether. Such procedures are well known in the literature, for example see Eu. J. Med. Chem., 1987, 22(5), 457-62 and WO 2009010455.
  • In an analogous manner, compounds of formula Iua
  • Figure US20220104496A1-20220407-C00033
  • wherein R1, G1, G2 are as described in formula (I), and G5 is CR34 can be prepared by reacting compounds of formula (XXXIVa),
  • Figure US20220104496A1-20220407-C00034
  • wherein R1, G1, G2, are as described in formula (I) with a compound of formula XXXV or XXXVa analogously to the preparation of compounds of formula Iu. Those skilled in the art will recognize that compounds of formula Iub
  • Figure US20220104496A1-20220407-C00035
  • can be similarly prepared by reaction of compounds of formula XXXIVb with compounds of formula XXXV or XXXVa, wherein G5 is CR34 as described above.
  • Figure US20220104496A1-20220407-C00036
  • The subgroup of compounds of formula I, wherein A is A2 and G5 is nitrogen, can be represented by the compounds of formula Iv;
  • Figure US20220104496A1-20220407-C00037
  • wherein Q is one of the radicals B1, B2, B3, B4, B5, B6, B7, B8, B9 or B11, and R1, R2, G1, G2 and G4 are as described in formula I, can be prepared by reacting a compound of formula XXXVI;
  • Figure US20220104496A1-20220407-C00038
  • wherein R1, R2, G1 and G2 are as described in formula (I) and in which X00 is a halide ion or an anion of the formula —OSO2R38 with a compound of formula IIa
  • Figure US20220104496A1-20220407-C00039
  • wherein X0 is a halogen and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • Compounds of the formula XXXIV above can be prepared through amino-dehalogenation by reacting a compound of formula XXXVII;
  • Figure US20220104496A1-20220407-C00040
  • wherein R1, R2, G1 and G2 are as described in formula (I) and in which X0s is a halogen or a leaving group OSO2R38, with ammonia (either gaseous or aqueous) as a nucleophile. Ammonia may be used in equimolar amounts or in large excess in an appropriate inert solvent, optionally in a pressurised vessel. The reaction may be performed between 0 and 200° C., optionally with microwave irradiation. Ammonia equivalents such as, for example, ammonium hydroxide NH4OH, ammonium acetate NH4OAc, ammonium carbonate (NH4)2CO3 may also be used as a nitrogen source.
  • Compounds of the formula XXXVII can be prepared by reacting a compound of formula XXXVIII
  • Figure US20220104496A1-20220407-C00041
  • wherein R1, R2, G1 and G2 are as described in formula (I) with reagents such as, for example, phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide in an inert solvent.
  • Compounds of the formula XXXVIII are known in the literature. For example, compounds of the formula XXXVIII where G2 is a nitrogen atom and G1 is CR31, and wherein R1 and R2 are as described in formula I, are known from or can be prepared in analogy to EP1371638.
  • Compounds of the formula XXXVI can be prepared via N-amination by reacting a compound of formula XXXIV above with O-mesitylenesulfonylhydroxylamine (MSH) as amination reagent, as described for example by Y. Tamura et al., J. Heterocyclic Chem. 1975, 12, 107-110. MSH is also known in form of a precursor as its ethyl-acetohydroxamate; a pre-treatment with for example perchloric acid HClO4 in tetrahydrofurane liberates the required amination reagent MSH. O-mesitylenesulfonyl-hydroxylamine and related aminating reagents have been reviewed: Y. Tamura et al., Synthesis, 1-17, 1977.
  • The subgroup of compounds of formula I, wherein A is A3 and G5 is nitrogen, can be represented by the compounds of formula Iw
  • Figure US20220104496A1-20220407-C00042
  • wherein Q is one of the radical B1, B2, B3, B4, B5, B6, B7, B8, B9 or B11, and wherein R1, R2, G1, G2 and G4 are as described in formula I.
  • When G4 is CR33 then compounds of the formula Iw can be prepared by reacting a compound of formula XXXIX
  • Figure US20220104496A1-20220407-C00043
  • wherein R1, R2, G1 and G2 are as described in formula (I) with a compound of formula XL
  • Figure US20220104496A1-20220407-C00044
  • wherein X10 is a halogen or a leaving group OSO2R38 and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • Alternatively, when G4 is a nitrogen, compounds of the formula Iw can be prepared by reacting a compound of formula XLI
  • Figure US20220104496A1-20220407-C00045
  • wherein R1, R2, G1 and G2 are as described in formula (I) and in which X11 − is a halide ion or an anion of the formula −OSO2R38 with a compound of formula IIa
  • Figure US20220104496A1-20220407-C00046
  • wherein X0 is a halogen and Q is as defined above, optionally in the presence of a suitable base in an inert solvent.
  • Compounds of the formula XXXIX above can be prepared through amino-dehalogenation by reacting a compound of formula XLII
  • Figure US20220104496A1-20220407-C00047
  • wherein R1, R2, G1 and G2 are as described in formula (I) and in which X12 is a halogen or a leaving group OSO2R38 with ammonia (either gaseous or aqueous) as a nucleophile. Ammonia may be used in equimolar amounts or in large excess in an appropriate inert solvent, optionally in a pressurized vessel. The reaction may be performed between 0 and 200° C., optionally with microwave irradiation. Ammonia equivalents such as, for example, ammonium hydroxide NH4OH, ammonium acetate NH4OAc, and ammonium carbonate (NH4)2CO3 may also be used as a nitrogen source.
  • Compounds of the formula XLII can be prepared by reacting a compound of formula XLIII
  • Figure US20220104496A1-20220407-C00048
  • wherein R1, R2, G1 and G2 are as described in formula (I) with reagents such as, for example, phosphorus oxychloride, phosphorus trichloride or tribromide, phosphorus pentachloride or pentabromide or thionyl chloride in an inert solvent.
  • Compounds of the formula XL can be prepared, for example, in analogy to EP1371638.
  • Compounds of the formula XLI can be prepared via N-amination by reacting a compound of formula XXXIX above with O-mesitylenesulfonylhydroxylamine (MSH)—or one of its equivalent—as amination reagent, as described previously for the preparation of compounds of the formula XXXVI.
  • The subgroup of compounds of formula I, wherein A is A7 and both G5 and G4 are nitrogen, can be represented by the compounds of formula Ix
  • Figure US20220104496A1-20220407-C00049
  • wherein Q is one of the radical B1, B2, B3, B4, B5, B6, B7, B8, B9 or B11, and wherein R1, R2, G1 and G2 are as described in formula I.
  • Compounds of the formula Ic can be prepared by reacting a compound of formula XLIV
  • Figure US20220104496A1-20220407-C00050
  • wherein R1, R2, G1 and G2 are as described in formula (I) with a compound of formula XLV

  • X13-Q   (XLV),
  • wherein X13 is a halogen or a leaving group OSO2R38 and Q is as defined above, where the arrows in the radicals B1, B2, B3, B4, B5, B6, B7, B8, B9 or B11 show the point of attachment of the substituent X13, optionally in the presence of a suitable base in an inert solvent, for example sodium hydride in dimethylformamide, in analogy to, for example, WO10/038081.
  • Alternatively, compounds of the formula Ix can be prepared by reacting a compound of formula XLIV, with a compound of formula XLV under palladium-catalyzed N-arylation conditions as described, for example, in S. L. Buchwald et al., Angew. Chem. Int. Ed., 50, 8944-8947, 2011. Compounds of the formula XLIV above can be prepared through diazotization by treating a compound of formula XLVI
  • Figure US20220104496A1-20220407-C00051
  • wherein R1, R2, G1 and G2 are as described in formula I, with either sodium nitrite and hydrohalic acid in water or with an alkyl nitrite (such as, for example, tert-butyl nitrite or isoamyl nitrite) under anhydrous conditions, optionally in presence of an acid (such as, for example, acetic acid) in an inert solvent (such as, for example, tetrahydrofurane) at temperatures between 0 and 130° C. A typical example involving isoamyl nitrite and acetic acid in refluxing tetrahydrofurane may be found in I. Torrini et al., J. Heterocyclic Chem., 23, 1459-1463, 1986.
  • Compounds of formula (I) wherein R21 is C1-C6alykenylloxy, —C(O)R36 can be prepared as shown in scheme 5, which is illustrated for radical A1-B1:
  • Figure US20220104496A1-20220407-C00052
  • In scheme 5, compounds of formula XLVII, wherein R1, R2, G1, G2, L1, R3, R4, V1 and V0 are as described for formula (I), and X14 is halogen, preferably bromide, are reacted with compounds of formula XLVIII, wherein R39 is C1-C5alkyl which can be mono- or polysubstituted by substituents selected from C1-C6alkoxy, C1-C6haloalkoxy, C2-C6 alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6 alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen and C3-C6 cycloalkyl, wherein said C3-C6 cycloalkyl can be mono- or polysubstituted by substituents selected from the group consisting of halogen and C1-C6alkyl, or a phenyl group which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano, and nitro, in an inert solvent, such as THF, DMF, dioxane, octane, toluene, and xylene, in the presence of a palladium catalyst, such as tetrakis(triphenylphosphine)palladium(0), or Bis(triphenylphosphine)palladium(II) chloride, in an inert solvent, such as toluene, and xylene, and DMF, or a mixture of these, etc. at temperatures between 25-120° C., preferably 50-90° C. The obtained product XLIX is then treated with a mineral acid, for example aqueous hydrochloric acid, in the presence of an organic co-solvent, for example methanol, acetone, ethanol, THF, etc. to give the product of formula 1y, where the substituents R1, R2, G1, G2, L1, R3, R4, V1, V0 and R39 are as previously described. Such processes are well known and have been described previously in for example, Kosugi, Masanori et al, Bull. Chem. Soc. Japan, 60(2), 767-8, 1987.
  • Analogous chemistry can be used to introduce such a substituent in R4, R5, R20, R22, R23, R24, R25, R26, R27, R28, R29, and R30.
  • Compounds of formula II are in many cases commercially available, known in the literature, or can be produced analogously to methods described in the literature. For example 3-ethylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxylic acid (WO 2013180194), 3-ethylsulfonylpyridine-2-carboxylic acid (WO 2013180194), 3-ethylsulfonylpyrazine-2-carboxylic acid (WO 2013180194), 3-ethylsulfonylthiophene-2-carboxylic acid (Synthesis, 2007, (12), 1827-1832), 3-ethylsulfonyl-5-(trifluoromethyl)thiophene-2-carboxylic acid (WO 2013180193), 2-chloro-6-(trifluoromethyl)pyridine-3-carboxylic acid (WO 2013180194), 5-ethylsulfanylthiazole-4-carboxylic acid (WO 2013180193) 2-ethylsulfanylthiophene-3-carboxylic acid (WO 2013180193), and 4-bromo-2-methyl-1,1-dioxo-2,3-dihydrobenzothiophene-7-carboxylic acid (WO 199909023),
  • In further cases, syntheses for compounds of formula II have been especially developed to prepare compounds of formula I and are shown in the following schemes:
  • Figure US20220104496A1-20220407-C00053
  • Figure US20220104496A1-20220407-C00054
  • Figure US20220104496A1-20220407-C00055
  • Figure US20220104496A1-20220407-C00056
  • Figure US20220104496A1-20220407-C00057
  • Figure US20220104496A1-20220407-C00058
  • Figure US20220104496A1-20220407-C00059
  • Compounds of formula III, IV, and V are commercially available, known in the literature, or can be prepared by analogous methods to those in the literature. For example, N-2-methyl-5-(trifluoromethyl)pyridine-2,3-diamine (WO 2012086848), 6-(trifluoromethyl)pyridine-3,4-diamine (WO 2013/048214), N-3-methyl-6-(trifluoromethyl)pyridine-2,3-diamine (WO 2012/086848), N-5-methyl-2-(trifluoromethyl)pyrimidine-4,5-diamine (CAS [1023817-05-1]), N-1-methyl-4-(trifluoromethyl)benzene-1,2-diamine (WO 2005065680), 3-amino-5-(trifluoromethyl)pyridin-2-ol (WO 2011049222), 3-amino-5-(trifluoromethyl)-2 (1H)-Pyridinethione (WO 2011/043404). In further cases, syntheses for compounds of formula III, IV, and V have been especially developed to prepare compounds of formula I and are shown in the following schemes:
  • Figure US20220104496A1-20220407-C00060
  • Figure US20220104496A1-20220407-C00061
  • Figure US20220104496A1-20220407-C00062
  • Figure US20220104496A1-20220407-C00063
  • Further syntheses to compounds of formula I are illustrated in the following schemes:
  • Figure US20220104496A1-20220407-C00064
    Figure US20220104496A1-20220407-C00065
  • Figure US20220104496A1-20220407-C00066
  • For preparing all further compounds of the formula (I) functionalized according to the definitions of A1-A6 and B1—B11 there are a large number of suitable known standard methods, for example alkylation, halogenation, acylation, amidation, oximation, oxidation and reduction, the choice of the preparation methods which are suitable depending on the properties (reactivity) of the substituents in the intermediates.
  • The reactants can be reacted in the presence of a base. Examples of suitable bases are alkali metal or alkaline earth metal hydroxides, alkali metal or alkaline earth metal hydrides, alkali metal or alkaline earth metal amides, alkali metal or alkaline earth metal alkoxides, alkali metal or alkaline earth metal acetates, alkali metal or alkaline earth metal carbonates, alkali metal or alkaline earth metal dialkylamides or alkali metal or alkaline earth metal alkylsilylamides, alkylamines, alkylenediamines, free or N-alkylated saturated or unsaturated cycloalkylamines, basic heterocycles, ammonium hydroxides and carbocyclic amines. Examples which may be mentioned are sodium hydroxide, sodium hydride, sodium amide, sodium methoxide, sodium acetate, sodium carbonate, potassium tert-butoxide, potassium hydroxide, potassium carbonate, potassium hydride, lithium diisopropylamide, potassium bis(trimethylsilyl)amide, calcium hydride, triethylamine, diisopropylethylamine, triethylenediamine, cyclohexylamine, N-cyclohexyl-N,N-dimethylamine, N,N-diethylaniline, pyridine, 4-(N,N-dimethylamino)pyridine, quinuclidine, N-methylmorpholine, benzyltrimethylammonium hydroxide and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).
  • The reactants can be reacted with each other as such, i.e. without adding a solvent or diluent. In most cases, however, it is advantageous to add an inert solvent or diluent or a mixture of these. If the reaction is carried out in the presence of a base, bases which are employed in excess, such as triethylamine, pyridine, N-methylmorpholine or N,N-diethylaniline, may also act as solvents or diluents.
  • The reaction is advantageously carried out in a temperature range from approximately −80° C. to approximately +140° C., preferably from approximately −30° C. to approximately +100° C., in many cases in the range between ambient temperature and approximately +80° C.
  • A compound of formula I can be converted in a manner known per se into another compound of formula I by replacing one or more substituents of the starting compound of formula I in the customary manner by (an)other substituent(s) according to the invention.
  • Depending on the choice of the reaction conditions and starting materials which are suitable in each case, it is possible, for example, in one reaction step only to replace one substituent by another substituent according to the invention, or a plurality of substituents can be replaced by other substituents according to the invention in the same reaction step.
  • Salts of compounds of formula I can be prepared in a manner known per se. Thus, for example, acid addition salts of compounds of formula I are obtained by treatment with a suitable acid or a suitable ion exchanger reagent and salts with bases are obtained by treatment with a suitable base or with a suitable ion exchanger reagent.
  • Salts of compounds of formula I can be converted in the customary manner into the free compounds I, acid addition salts, for example, by treatment with a suitable basic compound or with a suitable ion exchanger reagent and salts with bases, for example, by treatment with a suitable acid or with a suitable ion exchanger reagent.
  • Salts of compounds of formula I can be converted in a manner known per se into other salts of compounds of formula I, acid addition salts, for example, into other acid addition salts, for example by treatment of a salt of inorganic acid such as hydrochloride with a suitable metal salt such as a sodium, barium or silver salt, of an acid, for example with silver acetate, in a suitable solvent in which an inorganic salt which forms, for example silver chloride, is insoluble and thus precipitates from the reaction mixture.
  • Depending on the procedure or the reaction conditions, the compounds of formula I, which have salt-forming properties, can be obtained in free form or in the form of salts.
  • The compounds of formula I and, where appropriate, the tautomer's thereof, in each case in free form or in salt form, can be present in the form of one of the isomers which are possible or as a mixture of these, for example in the form of pure isomers, such as antipodes and/or diastereomers, or as isomer mixtures, such as enantiomer mixtures, for example racemates, diastereomer mixtures or racemate mixtures, depending on the number, absolute and relative configuration of asymmetric carbon atoms which occur in the molecule and/or depending on the configuration of non-aromatic double bonds which occur in the molecule; the invention relates to the pure isomers and also to all isomer mixtures which are possible and is to be understood in each case in this sense hereinabove and hereinbelow, even when stereochemical details are not mentioned specifically in each case.
  • Diastereomer mixtures or racemate mixtures of compounds of formula I, in free form or in salt form, which can be obtained depending on which starting materials and procedures have been chosen can be separated in a known manner into the pure diasteromers or racemates on the basis of the physicochemical differences of the components, for example by fractional crystallization, distillation and/or chromatography.
  • Enantiomer mixtures, such as racemates, which can be obtained in a similar manner can be resolved into the optical antipodes by known methods, for example by recrystallization from an optically active solvent, by chromatography on chiral adsorbents, for example high-performance liquid chromatography (HPLC) on acetyl cellulose, with the aid of suitable microorganisms, by cleavage with specific, immobilized enzymes, via the formation of inclusion compounds, for example using chiral crown ethers, where only one enantiomer is complexed, or by conversion into diastereomeric salts, for example by reacting a basic end-product racemate with an optically active acid, such as a carboxylic acid, for example camphor, tartaric or malic acid, or sulfonic acid, for example camphorsulfonic acid, and separating the diastereomer mixture which can be obtained in this manner, for example by fractional crystallization based on their differing solubilities, to give the diastereomers, from which the desired enantiomer can be set free by the action of suitable agents, for example basic agents.
  • Pure diastereomers or enantiomers can be obtained according to the invention not only by separating suitable isomer mixtures, but also by generally known methods of diastereoselective or enantioselective synthesis, for example by carrying out the process according to the invention with starting materials of a suitable stereochemistry.
  • N-oxides can be prepared by reacting a compound of the formula I with a suitable oxidizing agent, for example the H2O2/urea adduct in the presence of an acid anhydride, e.g. trifluoroacetic anhydride. Such oxidations are known from the literature, for example from J. Med. Chem. 1989, 32, 2561 or WO 2000/15615.
  • It is advantageous to isolate or synthesize in each case the biologically more effective isomer, for example enantiomer or diastereomer, or isomer mixture, for example enantiomer mixture or diastereomer mixture, if the individual components have a different biological activity.
  • The compounds of formula I and, where appropriate, the tautomers thereof, in each case in free form or in salt form, can, if appropriate, also be obtained in the form of hydrates and/or include other solvents, for example those which may have been used for the crystallization of compounds which are present in solid form.
  • The compounds of formula I according to the invention are preventively and/or curatively valuable active ingredients in the field of pest control, even at low rates of application, which have a very favorable biocidal spectrum and are well tolerated by warm-blooded species, fish and plants. The active ingredients according to the invention act against all or individual developmental stages of normally sensitive, but also resistant, animal pests, such as insects or representatives of the order Acarina. The insecticidal or acaricidal activity of the active ingredients according to the invention can manifest itself directly, i. e. in destruction of the pests, which takes place either immediately or only after some time has elapsed, for example during ecdysis, or indirectly, for example in a reduced oviposition and/or hatching rate, a good activity corresponding to a destruction rate (mortality) of at least 50%.
  • The compounds of formula I can be used to combat and control infestations of insect pests such as Lepidoptera, Diptera, Hemiptera, Thysanoptera, Orthoptera, Dictyoptera, Coleoptera, Siphonaptera, Hymenoptera and Isoptera and also other invertebrate pests, for example, acarine, nematode and mollusc pests. Insects, acarines, nematodes and molluscs are hereinafter collectively referred to as pests. The pests which may be combated and controlled by the use of the invention compounds include those pests associated with agriculture (which term includes the growing of crops for food and fibre products), horticulture and animal husbandry, companion animals, forestry and the storage of products of vegetable origin (such as fruit, grain and timber); those pests associated with the damage of man-made structures and the transmission of diseases of man and animals; and also nuisance pests (such as flies).
  • Examples of pest species which may be controlled by the compounds of formula I include: Myzus persicae (aphid), Aphis gossypii (aphid), Aphis fabae (aphid), Lygus spp. (capsids), Dysdercus spp. (capsids), Nilaparvata lugens (planthopper), Nephotettixc incticeps (leafhopper), Nezara spp. (stinkbugs), Euschistus spp. (stinkbugs), Leptocorisa spp. (stinkbugs), Frankliniella occidentalis (thrip), Thrips spp. (thrips), Leptinotarsa decemlineata (Colorado potato beetle), Anthonomus grandis (boll weevil), Aonidiella spp. (scale insects), Trialeurodes spp. (white flies), Bemisia tabaci (white fly), Ostrinia nubilalis (European corn borer), Spodoptera littoralis (cotton leafworm), Heliothis virescens (tobacco budworm), Helicoverpa armigera (cotton bollworm), Helicoverpa zea (cotton bollworm), Sylepta derogata (cotton leaf roller), Pieris brassicae (white butterfly), Plutella xylostella (diamond back moth), Agrotis spp. (cutworms), Chilo suppressalis (rice stem borer), Locusta migratoria (locust), Chortiocetes terminifera (locust), Diabrotica spp. (rootworms), Panonychus ulmi (European red mite), Panonychus citri (citrus red mite), Tetranychus urticae (two-spotted spider mite), Tetranychus cinnabarinus (carmine spider mite), Phyllocoptruta oleivora (citrus rust mite), Polyphagotarsonemus latus (broad mite), Brevipalpus spp. (flat mites), Boophilus microplus (cattle tick), Dermacentor variabilis (American dog tick), Ctenocephalides felis (cat flea), Liriomyza spp. (leafminer), Musca domestica (housefly), Aedes aegypti (mosquito), Anopheles spp. (mosquitoes), Culex spp. (mosquitoes), Lucillia spp. (blowflies), Blattella germanica (cockroach), Periplaneta americana (cockroach), Blatta orientalis (cockroach), termites of the Mastotermitidae (for example Mastotermes spp.), the Kalotermitidae (for example Neotermes spp.), the Rhinotermitidae (for example Coptotermes formosanus, Reticulitermes flavipes, R. speratu, R. virginicus, R. hesperus, and R. santonensis) and the Termitidae (for example Globitermes sulphureus), Solenopsis geminata (fire ant), Monomorium pharaonis (pharaoh's ant), Damalinia spp. and Linognathus spp. (biting and sucking lice), Meloidogyne spp. (root knot nematodes), Globodera spp. and Heterodera spp. (cyst nematodes), Pratylenchus spp. (lesion nematodes), Rhodopholus spp. (banana burrowing nematodes), Tylenchulus spp. (citrus nematodes), Haemonchus contortus (barber pole worm), Caenorhabditis elegans (vinegar eelworm), Trichostrongylus spp. (gastro intestinal nematodes) and Deroceras reticulatum (slug).
  • Further examples of the above mentioned pests are:
  • from the order Acarina, for example, Acalitus spp, Aculus spp, Acaricalus spp, Aceria spp, Acarus siro, Amblyomma spp., Argas spp., Boophilus spp., Brevipalpus spp., Bryobia spp, Calipitrimerus spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides spp, Eotetranychus spp, Eriophyes spp., Hemitarsonemus spp, Hyalomma spp., Ixodes spp., Olygonychus spp, Ornithodoros spp., Polyphagotarsone latus, Panonychus spp., Phyllocoptruta oleivora, Phytonemus spp, Polyphagotarsonemus spp, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Steneotarsonemus spp, Tarsonemus spp. and Tetranychus spp.;
    from the order Anoplura, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Pemphigus spp. and Phylloxera spp.;
    from the order Coleoptera, for example, Agriotes spp., Amphimallon majale, Anomala orientalis, Anthonomus spp., Aphodius spp, Astylus atromaculatus, Ataenius spp, Atomaria linearis, Chaetocnema tibialis, Cerotoma spp, Conoderus spp, Cosmopolites spp., Cotinis nitida, Curculio spp., Cyclocephala spp, Dermestes spp., Diabrotica spp., Diloboderus abderus, Epilachna spp., Eremnus spp., Heteronychus arator, Hypothenemus hampei, Lagria vilosa, Leptinotarsa decemLineata, Lissorhoptrus spp., Liogenys spp, Maecolaspis spp, Maladera castanea, Megascelis spp, Melighetes aeneus, Melolontha spp., Myochrous armatus, Orycaephilus spp., Otiorhynchus spp., Phyllophaga spp, Phlyctinus spp., Popillia spp., Psylliodes spp., Rhyssomatus aubtilis, Rhizopertha spp., Scarabeidae, Sitophilus spp., Sitotroga spp., Somaticus spp, Sphenophorus spp, Sternechus subsignatus, Tenebrio spp., Tribolium spp. and Trogoderma spp.; from the order Diptera, for example, Aedes spp., Anopheles spp, Antherigona soccata, Bactrocea oleae, Bibio hortulanus, Bradysia spp, Calliphora erythrocephala, Ceratitis spp., Chrysomyia spp., Culex spp., Cuterebra spp., Dacus spp., Delia spp, Drosophila melanogaster, Fannia spp., Gastrophilus spp., Geomyza tripunctata, Glossina spp., Hypoderma spp., Hyppobosca spp., Liriomyza spp., Lucilia spp., Melanagromyza spp., Musca spp., Oestrus spp., Orseolia spp., Oscinella frit, Pegomyia hyoscyami, Phorbia spp., Rhagoletis spp, Rivelia quadrifasciata, Scatella spp, Sciara spp., Stomoxys spp., Tabanus spp., Tannia spp. and Tipula spp.;
    from the order Hemiptera, for example, Acanthocoris scabrator, Acrosternum spp, Adelphocoris lineolatus, Amblypelta nitida, Bathycoelia thalassina, Blissus spp, Cimex spp., Clavigralla tomentosicollis, Creontiades spp, Distantiella theobroma, Dichelops furcatus, Dysdercus spp., Edessa spp, Euchistus spp., Eurydema pulchrum, Eurygaster spp., Halyomorpha halys, Horcias nobilellus, Leptocorisa spp., Lygus spp, Margarodes spp, Murgantia histrionic, Neomegalotomus spp, Nesidiocoris tenuis, Nezara spp., Nysius simulans, Oebalus insularis, Piesma spp., Piezodorus spp, Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinophara spp; Thyanta spp, Triatoma spp., Vatiga illudens; Acyrthosium pisum, Adalges spp, Agalliana ensigera, Agonoscena targionii, Aleurodicus spp, Aleurocanthus spp, Aleurolobus barodensis, Aleurothrixus floccosus, Aleyrodes brassicae, Amarasca biguttula, Amritodus atkinsoni, Aonidiella spp., Aphididae, Aphis spp., Aspidiotus spp., Aulacorthum solani, Bactericera cockerelli, Bemisia spp, Brachycaudus spp, Brevicoryne brassicae, Cacopsylla spp, Cavariella aegopodii Scop., Ceroplaster spp., Chrysomphalus aonidium, Chrysomphalus dictyospermi, Cicadella spp, Cofana spectra, Cryptomyzus spp, Cicadulina spp, Coccus hesperidum, Dalbulus maidis, Dialeurodes spp, Diaphorina citri, Diuraphis noxia, Dysaphis spp, Empoasca spp., Eriosoma larigerum, Erythroneura spp., Gascardia spp., Glycaspis brimblecombei, Hyadaphis pseudobrassicae, Hyalopterus spp, Hyperomyzus pallidus, Idioscopus clypealis, Jacobiasca lybica, Laodelphax spp., Lecanium corni, Lepidosaphes spp., Lopaphis erysimi, Lyogenys maidis, Macrosiphum spp., Mahanarva spp, Metcalfa pruinosa, Metopolophium dirhodum, Myndus crudus, Myzus spp., Neotoxoptera sp, Nephotettix spp., Nilaparvata spp., Nippolachnus piri Mats, Odonaspis ruthae, Oregma lanigera Zehnter, Parabemisia myricae, Paratrioza cockerelli, Parlatoria spp., Pemphigus spp., Peregrinus maidis, Perkinsiella spp, Phorodon humuli, Phylloxera spp, Planococcus spp., Pseudaulacaspis spp., Pseudococcus spp., Pseudatomoscelis seriatus, Psylla spp., Pulvinaria aethiopica, Quadraspidiotus spp., Quesada gigas, Recilia dorsalis, Rhopalosiphum spp., Saissetia spp., Scaphoideus spp., Schizaphis spp., Sitobion spp., Sogatella furcifera, Spissistilus festinus, Tarophagus Proserpina, Toxoptera spp, Trialeurodes spp, Tridiscus sporoboli, Trionymus spp, Trioza erytreae, Unaspis citri, Zygina flammigera, Zyginidia scutellaris;
    from the order Heteroptera, for example, Cimex spp., Distantiella theobroma, Dysdercus spp., Euchistus spp., Eurygaster spp., Leptocorisa spp., Nezara spp., Piesma spp., Rhodnius spp., Sahlbergella singularis, Scotinophara spp. and Triatoma spp.;
    from the order Homoptera, for example, Aleurothrixus floccosus, Aleyrodes brassicae, Aonidiella spp., Aphididae, Aphis spp., Aspidiotus spp., Bemisia tabaci, Ceroplaster spp., Chrysomphalus aonidium, Chrysomphalus dictyospermi, Coccus hesperidum, Empoasca spp., Eriosoma larigerum, Erythroneura spp., Gascardia spp., Laodelphax spp., Lecanium corni, Lepidosaphes spp., Macrosiphus spp., Myzus spp., Nephotettix spp., Nilaparvata spp., Parlatoria spp., Pemphigus spp., Planococcus spp., Pseudaulacaspis spp., Pseudococcus spp., Psylla spp., Pulvinaria aethiopica, Quadraspidiotus spp., Rhopalosiphum spp., Saissetia spp., Scaphoideus spp., Schizaphis spp., Sitobion spp., Trialeurodes vaporariorum, Trioza erytreae and Unaspis citri;
    from the order Hymenoptera, for example, Acromyrmex, Arge spp, Atta spp., Cephus spp., Diprion spp., Diprionidae, Gilpinia polytoma, Hoplocampa spp., Lasius spp., Monomorium pharaonis, Neodiprion spp., Pogonomyrmex spp, Slenopsis invicta, Solenopsis spp. and Vespa spp.;
    from the order Isoptera, for example, Coptotermes spp, Corniternes cumulans, Incisitermes spp, Macrotermes spp, Mastotermes spp, Microtermes spp, Reticulitermes spp.; Solenopsis geminate;
    from the order Lepidoptera, for example, Acleris spp., Adoxophyes spp., Aegeria spp., Agrotis spp., Alabama argillaceae, Amylois spp., Anticarsia gemmatalis, Archips spp., Argyresthia spp, Argyrotaenia spp., Autographa spp., Bucculatrix thurberiella, Busseola fusca, Cadra cautella, Carposina nipponensis, Chilo spp., Choristoneura spp., Chrysoteuchia topiaria, Clysia ambiguella, Cnaphalocrocis spp., Cnephasia spp., Cochylis spp., Coleophora spp., Colias lesbia, Cosmophila flava, Crambus spp, Crocidolomia binotalis, Cryptophlebia leucotreta, Cydalima perspectalis, Cydia spp., Diaphania perspectalis, Diatraea spp., Diparopsis castanea, Earias spp., Eldana saccharina, Ephestia spp., Epinotia spp, Estigmene acrea, Etiella zinckinella, Eucosma spp., Eupoecilia ambiguella, Euproctis spp., Euxoa spp., Feltia jaculiferia, Grapholita spp., Hedya nubiferana, Heliothis spp., Hellula undalis, Herpetogramma spp, Hyphantria cunea, Keiferia lycopersicella, Lasmopalpus lignosellus, Leucoptera scitella, Lithocollethis spp., Lobesia botrana, Loxostege bifidalis, Lymantria spp., Lyonetia spp., Malacosoma spp., Mamestra brassicae, Manduca sexta, Mythimna spp, Noctua spp, Operophtera spp., Orniodes indica, Ostrinia nubilalis, Pammene spp., Pandemis spp., Panolis flammea, Papaipema nebris, Pectinophora gossypiela, Perileucoptera coffeella, Pseudaletia unipuncta, Phthorimaea operculella, Pieris rapae, Pieris spp., Plutella xylostella, Prays spp., Pseudoplusia spp, Rachiplusia nu, Richia albicosta, Scirpophaga spp., Sesamia spp., Sparganothis spp., Spodoptera spp., Sylepta derogate, Synanthedon spp., Thaumetopoea spp., Tortrix spp., Trichoplusia ni, Tuta absoluta, and Yponomeuta spp.;
    from the order Mallophaga, for example,
    • Damalinea spp. and Trichodectes spp.;
  • from the order Orthoptera, for example, Blatta spp., Blattella spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Neocurtilla hexadactyla, Periplaneta spp., Scapteriscus spp, and Schistocerca spp.;
    from the order Psocoptera, for example, Liposcelis spp.;
    from the order Siphonaptera, for example, Ceratophyllus spp., Ctenocephalides spp. and Xenopsylla cheopis;
    from the order Thysanoptera, for example,
    Calliothrips phaseoli, Frankliniella spp., Heliothrips spp, Hercinothrips spp., Parthenothrips spp, Scirtothrips aurantii, Sericothrips variabilis, Taeniothrips spp., Thrips spp; and
    from the order Thysanura, for example, Lepisma saccharina.
  • The active ingredients according to the invention can be used for controlling, i. e. containing or destroying, pests of the abovementioned type which occur in particular on plants, especially on useful plants and ornamentals in agriculture, in horticulture and in forests, or on organs, such as fruits, flowers, foliage, stalks, tubers or roots, of such plants, and in some cases even plant organs which are formed at a later point in time remain protected against these pests.
  • Suitable target crops are, in particular, cereals, such as wheat, barley, rye, oats, rice, maize or sorghum; beet, such as sugar or fodder beet; fruit, for example pomaceous fruit, stone fruit or soft fruit, such as apples, pears, plums, peaches, almonds, cherries or berries, for example strawberries, raspberries or blackberries; leguminous crops, such as beans, lentils, peas or soya; oil crops, such as oilseed rape, mustard, poppies, olives, sunflowers, coconut, castor, cocoa or ground nuts; cucurbits, such as pumpkins, cucumbers or melons; fibre plants, such as cotton, flax, hemp or jute; citrus fruit, such as oranges, lemons, grapefruit or tangerines; vegetables, such as spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes or bell peppers; Lauraceae, such as avocado, Cinnamonium or camphor; and also tobacco, nuts, coffee, eggplants, sugarcane, tea, pepper, grapevines, hops, the plantain family, latex plants and ornamentals.
  • In a further aspect, the invention may also relate to a method of controlling damage to plant and parts thereof by plant parasitic nematodes (Endoparasitic-, Semiendoparasitic- and Ectoparasitic nematodes), especially plant parasitic nematodes such as root knot nematodes, Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, Meloidogyne arenaria and other Meloidogyne species; cyst-forming nematodes, Globodera rostochiensis and other Globodera species; Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii, and other Heterodera species; Seed gall nematodes, Anguina species; Stem and foliar nematodes, Aphelenchoides species; Sting nematodes, Belonolaimus longicaudatus and other Belonolaimus species; Pine nematodes, Bursaphelenchus xylophilus and other Bursaphelenchus species; Ring nematodes, Criconema species, Criconemella species, Criconemoides species, Mesocriconema species; Stem and bulb nematodes, Ditylenchus destructor, Ditylenchus dipsaci and other Ditylenchus species; Awl nematodes, Dolichodorus species; Spiral nematodes, Heliocotylenchus multicinctus and other Helicotylenchus species; Sheath and sheathoid nematodes, Hemicycliophora species and Hemicriconemoides species; Hirshmanniella species; Lance nematodes, Hoploaimus species; false rootknot nematodes, Nacobbus species; Needle nematodes, Longidorus elongatus and other Longidorus species; Pin nematodes, Pratylenchus species; Lesion nematodes, Pratylenchus neglectus, Pratylenchus penetrans, Pratylenchus curvitatus, Pratylenchus goodeyi and other Pratylenchus species; Burrowing nematodes, Radopholus similis and other Radopholus species; Reniform nematodes, Rotylenchus robustus, Rotylenchus reniformis and other Rotylenchus species; Scutellonema species; Stubby root nematodes, Trichodorus primitivus and other Trichodorus species, Paratrichodorus species; Stunt nematodes, Tylenchorhynchus claytoni, Tylenchorhynchus dubius and other Tylenchorhynchus species; Citrus nematodes, Tylenchulus species; Dagger nematodes, Xiphinema species; and other plant parasitic nematode species, such as Subanguina spp., Hypsoperine spp., Macroposthonia spp., Melinius spp., Punctodera spp., and Quinisulcius spp.
  • The compounds of the invention may also have activity against the molluscs. Examples of which include, for example, Ampullariidae; Arion (A. ater, A. circumscriptus, A. hortensis, A. rufus); Bradybaenidae (Bradybaena fruticum); Cepaea (C. hortensis, C. Nemoralis); ochlodina; Deroceras (D. agrestis, D. empiricorum, D. laeve, D. reticulatum); Discus (D. rotundatus); Euomphalia; Galba (G. trunculata); Helicelia (H. itala, H. obvia); Helicidae Helicigona arbustorum); Helicodiscus; Helix (H. aperta); Limax (L. cinereoniger, L. flavus, L. marginatus, L. maximus, L. tenellus); Lymnaea; Milax (M. gagates, M. marginatus, M. sowerbyi); Opeas; Pomacea (P. canaticulata); Vallonia and Zanitoides.
  • The term “crops” is to be understood as including also crops that have been rendered tolerant to herbicides like bromoxynil or classes of herbicides (such as, for example, HPPD inhibitors, ALS inhibitors, for example primisulfuron, prosulfuron and trifloxysulfuron, EPSPS (5-enol-pyrovyl-shikimate-3-phosphate-synthase) inhibitors, GS (glutamine synthetase) inhibitors) as a result of conventional methods of breeding or genetic engineering. An example of a crop that has been rendered tolerant to imidazolinones, e.g. imazamox, by conventional methods of breeding (mutagenesis) is Clearfield® summer rape (Canola). Examples of crops that have been rendered tolerant to herbicides or classes of herbicides by genetic engineering methods include glyphosate- and glufosinate-resistant maize varieties commercially available under the trade names RoundupReady® and LibertyLink®.
  • The term “crops” is also to be understood as including also crop plants which have been so transformed by the use of recombinant DNA techniques that they are capable of synthesising one or more selectively acting toxins, such as are known, for example, from toxin-producing bacteria, especially those of the genus Bacillus.
  • Toxins that can be expressed by such transgenic plants include, for example, insecticidal proteins, for example insecticidal proteins from Bacillus cereus or Bacillus popliae; or insecticidal proteins from Bacillus thuringiensis, such as δ-endotoxins, e.g. CryIA(b), CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c, or vegetative insecticidal proteins (VIP), e.g. VIP1, VIP2, VIP3 or VIP3A; or insecticidal proteins of bacteria colonising nematodes, for example Photorhabdus spp. or Xenorhabdus spp., such as Photorhabdus luminescens, Xenorhabdus nematophilus; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins and other insect-specific neurotoxins; toxins produced by fungi, such as Streptomycetes toxins, plant lectins, such as pea lectins, barley lectins or snowdrop lectins; agglutinins; proteinase inhibitors, such as trypsine inhibitors, serine protease inhibitors, patatin, cystatin, papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroidoxidase, ecdysteroid-UDP-glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors, HMG-COA-reductase, ion channel blockers, such as blockers of sodium or calcium channels, juvenile hormone esterase, diuretic hormone receptors, stilbene synthase, bibenzyl synthase, chitinases and glucanases.
  • In the context of the present invention there are to be understood by δ-endotoxins, for example CryIA(b), CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c, or vegetative insecticidal proteins (VIP), for example VIP1, VIP2, VIP3 or VIP3A, expressly also hybrid toxins, truncated toxins and modified toxins. Hybrid toxins are produced recombinantly by a new combination of different domains of those proteins (see, for example, WO 02/15701). Truncated toxins, for example a truncated CryIA(b), are known. In the case of modified toxins, one or more amino acids of the naturally occurring toxin are replaced. In such amino acid replacements, preferably non-naturally present protease recognition sequences are inserted into the toxin, such as, for example, in the case of CryIIIA055, a cathepsin-D-recognition sequence is inserted into a CryIIIA toxin (see WO 03/018810).
  • Examples of such toxins or transgenic plants capable of synthesising such toxins are disclosed, for example, in EP-A-0 374 753, WO 93/07278, WO 95/34656, EP-A-0 427 529, EP-A-451 878 and WO 03/052073.
  • The processes for the preparation of such transgenic plants are generally known to the person skilled in the art and are described, for example, in the publications mentioned above. CryI-type deoxyribonucleic acids and their preparation are known, for example, from WO 95/34656, EP-A-0 367 474, EP-A-0 401 979 and WO 90/13651.
  • The toxin contained in the transgenic plants imparts to the plants tolerance to harmful insects. Such insects can occur in any taxonomic group of insects, but are especially commonly found in the beetles (Coleoptera), two-winged insects (Diptera) and butterflies (Lepidoptera).
  • Transgenic plants containing one or more genes that code for an insecticidal resistance and express one or more toxins are known and some of them are commercially available. Examples of such plants are: YieldGard® (maize variety that expresses a CryIA(b) toxin); YieldGard Rootworm® (maize variety that expresses a CryIIIB(b1) toxin); YieldGard Plus® (maize variety that expresses a CryIA(b) and a CryIIIB(b1) toxin); Starlink® (maize variety that expresses a Cry9(c) toxin); Herculex I® (maize variety that expresses a CryIF(a2) toxin and the enzyme phosphinothricine N-acetyltransferase (PAT) to achieve tolerance to the herbicide glufosinate ammonium); NuCOTN 33B® (cotton variety that expresses a CryIA(c) toxin); Bollgard I® (cotton variety that expresses a CryIA(c) toxin); Bollgard 1® (cotton variety that expresses a CryIA(c) and a CryIIA(b) toxin); VIPCOT® (cotton variety that expresses a VIP toxin); NewLeaf® (potato variety that expresses a CryIIIA toxin); NatureGard® Agrisure® GT Advantage (GA21 glyphosate-tolerant trait), Agrisure® CB Advantage (Bt11 corn borer (CB) trait) and Protecta®.
  • Further examples of such transgenic crops are:
  • 1. Bt11 Maize from Syngenta Seeds SAS, Chemin de l'Hobit 27, F-31 790 St. Sauveur, France, registration number C/FR/96/05/10. Genetically modified Zea mays which has been rendered resistant to attack by the European corn borer (Ostrinia nubilalis and Sesamia nonagrioides) by transgenic expression of a truncated CryIA(b) toxin. Bt11 maize also transgenically expresses the enzyme PAT to achieve tolerance to the herbicide glufosinate ammonium.
    2. Bt176 Maize from Syngenta Seeds SAS, Chemin de l'Hobit 27, F-31 790 St. Sauveur, France, registration number C/FR/96/05/10. Genetically modified Zea mays which has been rendered resistant to attack by the European corn borer (Ostrinia nubilalis and Sesamia nonagrioides) by transgenic expression of a CryIA(b) toxin. Bt176 maize also transgenically expresses the enzyme PAT to achieve tolerance to the herbicide glufosinate ammonium.
    3. MIR604 Maize from Syngenta Seeds SAS, Chemin de l'Hobit 27, F-31 790 St. Sauveur, France, registration number C/FR/96/05/10. Maize which has been rendered insect-resistant by transgenic expression of a modified CryIIIA toxin. This toxin is Cry3A055 modified by insertion of a cathepsin-D-protease recognition sequence. The preparation of such transgenic maize plants is described in WO 03/018810.
    4. MON 863 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/DE/02/9. MON 863 expresses a CryIIIB(b1) toxin and has resistance to certain Coleoptera insects.
    5. IPC 531 Cotton from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/ES/96/02.
    6. 1507 Maize from Pioneer Overseas Corporation, Avenue Tedesco, 7 B-1160 Brussels, Belgium, registration number C/NL/00/10. Genetically modified maize for the expression of the protein Cry1F for achieving resistance to certain Lepidoptera insects and of the PAT protein for achieving tolerance to the herbicide glufosinate ammonium.
    7. NK603×MON 810 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/GB/02/M3/03. Consists of conventionally bred hybrid maize varieties by crossing the genetically modified varieties NK603 and MON 810. NK603×MON 810 Maize transgenically expresses the protein CP4 EPSPS, obtained from Agrobacterium sp. strain CP4, which imparts tolerance to the herbicide Roundup® (contains glyphosate), and also a CryIA(b) toxin obtained from Bacillus thuringiensis subsp. kurstaki which brings about tolerance to certain Lepidoptera, include the European corn borer.
  • Transgenic crops of insect-resistant plants are also described in BATS (Zentrum für Biosicherheit und Nachhaltigkeit, Zentrum BATS, Clarastrasse 13, 4058 Basel, Switzerland) Report 2003.
  • The term “crops” is to be understood as including also crop plants which have been so transformed by the use of recombinant DNA techniques that they are capable of synthesising antipathogenic substances having a selective action, such as, for example, the so-called “pathogenesis-related proteins” (PRPs, see e.g. EP-A-0 392 225). Examples of such antipathogenic substances and transgenic plants capable of synthesising such antipathogenic substances are known, for example, from EP-A-0 392 225, WO 95/33818, and EP-A-0 353 191. The methods of producing such transgenic plants are generally known to the person skilled in the art and are described, for example, in the publications mentioned above.
  • Antipathogenic substances which can be expressed by such transgenic plants include, for example, ion channel blockers, such as blockers for sodium and calcium channels, for example the viral KP1, KP4 or KP6 toxins; stilbene synthases; bibenzyl synthases; chitinases; glucanases; the so-called “pathogenesis-related proteins” (PRPs; see e.g. EP-A-0 392 225); antipathogenic substances produced by microorganisms, for example peptide antibiotics or heterocyclic antibiotics (see e.g. WO 95/33818) or protein or polypeptide factors involved in plant pathogen defence (so-called “plant disease resistance genes”, as described in WO 03/000906).
  • Crops may also be modified for enhanced resistance to fungal (for example Fusarium, Anthracnose, or Phytophthora), bacterial (for example Pseudomonas) or viral (for example potato leafroll virus, tomato spotted wilt virus, cucumber mosaic virus) pathogens.
  • Crops also include those that have enhanced resistance to nematodes, such as the soybean cyst nematode.
  • Crops that are tolerance to abiotic stress include those that have enhanced tolerance to drought, high salt, high temperature, chill, frost, or light radiation, for example through expression of NF-YB or other proteins known in the art.
  • Crops that exhibit enhanced yield or quality include those with improved flowering or fruit ripening properties (such as delayed ripening); modified oil, starch, amino acid, fatty acid, vitamin, phenolic or other content (such as Vistive™ soybean variety); enhanced nutrient utilisation (such as improved nitrogen assimilation); and enhanced quality plant product (such as higher quality cotton fibre).
  • Further areas of use of the compounds and compositions according to the invention are the protection of stored goods and storerooms and the protection of raw materials, such as wood, textiles, floor coverings or buildings, and also in the hygiene sector, especially the protection of humans, domestic animals and productive livestock against pests of the mentioned type.
  • The present invention also provides a method for controlling pests (such as mosquitoes and other disease vectors; see also http://www.who.int/malaria/vector_control/irs/en/). In one embodiment, the method for controlling pests comprises applying the compositions of the invention to the target pests, to their locus or to a surface or substrate by brushing, rolling, spraying, spreading or dipping. By way of example, an IRS (indoor residual spraying) application of a surface such as a wall, ceiling or floor surface is contemplated by the method of the invention. In another embodiment, it is contemplated to apply such compositions to a substrate such as non-woven or a fabric material in the form of (or which can be used in the manufacture of) netting, clothing, bedding, curtains and tents.
  • In one embodiment, the method for controlling such pests comprises applying a pesticidally effective amount of the compositions of the invention to the target pests, to their locus, or to a surface or substrate so as to provide effective residual pesticidal activity on the surface or substrate. Such application may be made by brushing, rolling, spraying, spreading or dipping the pesticidal composition of the invention. By way of example, an IRS application of a surface such as a wall, ceiling or floor surface is contemplated by the method of the invention so as to provide effective residual pesticidal activity on the surface. In another embodiment, it is contemplated to apply such compositions for residual control of pests on a substrate such as a fabric material in the form of (or which can be used in the manufacture of) netting, clothing, bedding, curtains and tents.
  • Substrates including non-woven, fabrics or netting to be treated may be made of natural fibres such as cotton, raffia, jute, flax, sisal, hessian, or wool, or synthetic fibres such as polyamide, polyester, polypropylene, polyacrylonitrile or the like. The polyesters are particularly suitable. The methods of textile treatment are known, e.g. WO 2008/151984, WO 2003/034823, U.S. Pat. No. 5,631,072, WO 2005/64072, WO2006/128870, EP 1724392, WO2005113886 or WO 2007/090739.
  • Further areas of use of the compositions according to the invention are the field of tree injection/trunk treatment for all ornamental trees as well all sort of fruit and nut trees.
  • In the field of tree injection/trunk treatment, the compounds according to the present invention are especially suitable against wood-boring insects from the order Lepidoptera as mentioned above and from the order Coleoptera, especially against woodborers listed in the following tables AA and BB:
  • TABLE AA
    Examples of exotic woodborers of economic importance.
    Family Species Host or Crop Infested
    Buprestidae Agrilus planipennis Ash
    Cerambycidae Anoplura glabripennis Hardwoods
    Scolytidae Xylosandrus crassiusculus Hardwoods
    X. mutilatus Hardwoods
    Tomicus piniperda Conifers
  • TABLE BB
    Examples of native woodborers of economic importance.
    Family Species Host or Crop Infested
    Buprestidae Agrilus anxius Birch
    Agrilus politus Willow, Maple
    Agrilus sayi Bayberry, Sweetfern
    Agrilus vittaticolllis Apple, Pear, Cranberry,
    Serviceberry, Hawthorn
    Chrysobothris femorata Apple, Apricot, Beech, Boxelder,
    Cherry, Chestnut, Currant, Elm,
    Hawthorn, Hackberry, Hickory,
    Horsechestnut, Linden, Maple,
    Mountain-ash, Oak, Pecan, Pear,
    Peach, Persimmon, Plum, Poplar,
    Quince, Redbud, Serviceberry,
    Sycamore, Walnut, Willow
    Texania campestris Basswood, Beech, Maple, Oak,
    Sycamore, Willow, Yellow-poplar
    Cerambycidae Goes pulverulentus Beech, Elm, Nuttall, Willow, Black
    oak, Cherrybark oak, Water oak,
    Sycamore
    Goes tigrinus Oak
    Neoclytus acuminatus Ash, Hickory, Oak, Walnut, Birch,
    Beech, Maple, Eastern
    hophornbeam, Dogwood,
    Persimmon, Redbud, Holly,
    Hackberry, Black locust,
    Honeylocust, Yellow-poplar,
    Chestnut, Osage-orange,
    Sassafras, Lilac, Mountain-
    mahogany, Pear, Cherry, Plum,
    Peach, Apple, Elm, Basswood,
    Sweetgum
    Neoptychodes trilineatus Fig, Alder, Mulberry, Willow,
    Netleaf hackberry
    Oberea ocellata Sumac, Apple, Peach, Plum,
    Pear, Currant, Blackberry
    Oberea tripunctata Dogwood, Viburnum, Elm,
    Sourwood, Blueberry,
    Rhododendron, Azalea, Laurel,
    Poplar, Willow, Mulberry
    Oncideres cingulata Hickory, Pecan, Persimmon, Elm,
    Sourwood, Basswood,
    Honeylocust, Dogwood,
    Eucalyptus, Oak, Hackberry,
    Maple, Fruit trees
    Saperda calcarata Poplar
    Strophiona nitens Chestnut, Oak, Hickory, Walnut,
    Beech, Maple
    Scolytidae Corthylus columbianus Maple, Oak, Yellow-poplar,
    Beech, Boxelder, Sycamore,
    Birch, Basswood, Chestnut, Elm
    Dendroctonus frontalis Pine
    Dryocoetes betulae Birch, Sweetgum, Wild cherry,
    Beech, Pear
    Monarthrum fasciatum Oak, Maple, Birch, Chestnut,
    Sweetgum, Blackgum, Poplar,
    Hickory, Mimosa, Apple, Peach,
    Pine
    Phloeotribus liminaris Peach, Cherry, Plum, Black
    cherry, Elm, Mulberry, Mountain-
    ash
    Pseudopityophthorus pruinosus Oak, American beech, Black
    cherry, Chickasaw plum,
    Chestnut, Maple, Hickory,
    Hornbeam, Hophornbeam
    Sesiidae Paranthrene simulans Oak, American chestnut
    Sannina uroceriformis Persimmon
    Synanthedon exitiosa Peach, Plum, Nectarine, Cherry,
    Apricot, Almond, Black cherry
    Synanthedon pictipes Peach, Plum, Cherry, Beach,
    Black Cherry
    Synanthedon rubrofascia Tupelo
    Synanthedon scitula Dogwood, Pecan, Hickory, Oak,
    Chestnut, Beech, Birch, Black
    cherry, Elm, Mountain-ash,
    Viburnum, Willow, Apple, Loquat,
    Ninebark, Bayberry
    Vitacea polistiformis Grape
  • In the hygiene sector, the compounds and compositions according to the invention are active against ectoparasites such as hard ticks, soft ticks, mange mites, harvest mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, bird lice and fleas.
  • Examples of such parasites are:
  • Of the order Anoplurida: Haematopinus spp., Linognathus spp., Pediculus spp. and Phtirus spp., Solenopotes spp.
  • Of the order Mallophagida: Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp. and Felicola spp.
  • Of the order Diptera and the suborders Nematocerina and Brachycerina, for example Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia spp., Sarcophaga spp., Oestrus spp., Hypoderma spp., Gasterophilus spp., Hippobosca spp., Lipoptena spp. and Melophagus spp.
  • Of the order Siphonapterida, for example Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp.
  • Of the order Heteropterida, for example Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp.
  • Of the order Blattarida, for example Blatta orientalis, Periplaneta americana, Blattelagermanica and Supella spp.
  • Of the subclass Acaria (Acarida) and the orders Meta- and Meso-stigmata, for example Argas spp., Ornithodorus spp., Otobius spp., Ixodes spp., Amblyomma spp., Boophilus spp., Dermacentor spp., Haemophysalis spp., Hyalomma spp., Rhipicephalus spp., Dermanyssus spp., Raillietia spp., Pneumonyssus spp., Sternostoma spp. and Varroa spp.
  • Of the orders Actinedida (Prostigmata) and Acaridida (Astigmata), for example Acarapis spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp. and Laminosioptes spp.
  • The compounds and compositions according to the invention are also suitable for protecting against insect infestation in the case of materials such as wood, textiles, plastics, adhesives, glues, paints, paper and card, leather, floor coverings and buildings.
  • The compositions according to the invention can be used, for example, against the following pests: beetles such as Hylotrupes bajulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinuspecticornis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubescens, Trogoxylon aequale, Minthesrugicollis, Xyleborus spec., Tryptodendron spec., Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec. and Dinoderus minutus, and also hymenopterans such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus and Urocerus augur, and termites such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis and Coptotermes formosanus, and bristletails such as Lepisma saccharina.
  • The present invention therefore provides an insecticidal, acaricidal, nematicidal or molluscicidal composition, preferably an insecticidal or acaricidal composition comprising an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a compound of formula I and a suitable carrier or diluent therefor.
  • In a further aspect the invention provides a method of combating and controlling pests which comprises applying an insecticidally, acaricidally, nematicidally or molluscicidally effective amount, preferably an insecticidally and acaricidally effective amount of a compound of formula I or a composition comprising a compound of formula I, to a pest, a locus of pest, or to a plant susceptible to attack by a pest, with the exception of a method for treatment of the human or animal body by surgery or therapy and diagnostic methods practised on the human or animal body.
  • The compounds of formula I are preferably used against insects or acarines.
  • The term “plant” as used herein includes seedlings, bushes and trees.
  • The invention also relates to a pesticidal composition, which, in addition to comprising the compound of formula I, comprises formulation adjuvants.
  • The invention therefore also relates to pesticidal compositions such as emulsifiable concentrates, suspension concentrates, directly sprayable or dilutable solutions, spreadable pastes, dilute emulsions, soluble powders, dispersible powders, wettable powders, dusts, granules or encapsulations in polymeric substances, which comprise—at least—one of the active ingredients according to the invention and which are to be selected to suit the intended aims and the prevailing circumstances.
  • In these compositions, the active ingredient is employed in pure form, a solid active ingredient for example in a specific particle size, or, preferably, together with—at least—one of the auxiliaries conventionally used in the art of formulation, such as extenders, for example solvents or solid carriers, or such as surface-active compounds (surfactants).
  • Examples of suitable solvents are: unhydrogenated or partially hydrogenated aromatic hydrocarbons, preferably the fractions C8 to C12 of alkylbenzenes, such as xylene mixtures, alkylated naphthalenes or tetrahydronaphthalene, aliphatic or cycloaliphatic hydrocarbons, such as paraffins or cyclohexane, alcohols such as ethanol, propanol or butanol, glycols and their ethers and esters such as propylene glycol, dipropylene glycol ether, ethylene glycol or ethylene glycol monomethyl ether or ethylene glycol monoethyl ether, ketones, such as cyclohexanone, isophorone or diacetone alcohol, strongly polar solvents, such as N-methylpyrrolid-2-one, dimethyl sulfoxide or N,N-dimethylformamide, water, unepoxidized or epoxidized vegetable oils, such as unexpodized or epoxidized rapeseed, castor, coconut or soya oil, and silicone oils.
  • Solid carriers which are used for example for dusts and dispersible powders are, as a rule, ground natural minerals such as calcite, talc, kaolin, montmorillonite or attapulgite. To improve the physical properties, it is also possible to add highly disperse silicas or highly disperse absorbtive polymers. Suitable particulate adsorptive carriers for granules are porous types, such as pumice, brick grit, sepiolite or bentonite, and suitable non-sorptive carrier materials are calcite or sand. In addition, a large number of granulated materials of inorganic or organic nature can be used, in particular dolomite or comminuted plant residues.
  • Suitable surface-active compounds are, depending on the type of the active ingredient to be formulated, non-ionic, cationic and/or anionic surfactants or surfactant mixtures which have good emulsifying, dispersing and wetting properties. The surfactants mentioned below are only to be considered as examples; a large number of further surfactants which are conventionally used in the art of formulation and suitable according to the invention are described in the relevant literature.
  • Suitable non-ionic surfactants are, especially, polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, of saturated or unsaturated fatty acids or of alkyl phenols which may contain approximately 3 to approximately 30 glycol ether groups and approximately 8 to approximately 20 carbon atoms in the (cyclo)aliphatic hydrocarbon radical or approximately 6 to approximately 18 carbon atoms in the alkyl moiety of the alkyl phenols. Also suitable are water-soluble polyethylene oxide adducts with polypropylene glycol, ethylenediaminopo¬lypropylene glycol or alkyl polypropylene glycol having 1 to approximately 10 carbon atoms in the alkyl chain and approximately 20 to approximately 250 ethylene glycol ether groups and approximately 10 to approximately 100 propylene glycol ether groups. Normally, the abovementioned compounds contain 1 to approximately 5 ethylene glycol units per propy¬lene glycol unit. Examples which may be mentioned are nonylphenoxypolyethoxyethanol, castor oil polyglycol ether, polypropylene glycol/polyethylene oxide adducts, tributylpheno¬xypolyethoxyethanol, polyethylene glycol or octylphenoxypolyethoxyethanol. Also suitable are fatty acid esters of polyoxyethylene sorbitan, such as polyoxyethylene sorbitan trioleate.
  • The cationic surfactants are, especially, quarternary ammonium salts which generally have at least one alkyl radical of approximately 8 to approximately 22 C atoms as substituents and as further substituents (unhalogenated or halogenated) lower alkyl or hydroxyalkyl or benzyl radicals. The salts are preferably in the form of halides, methylsulfates or ethylsulfates. Examples are stearyltrimethylammonium chloride and benzylbis(2-chloroethyl)ethyl¬ammonium bromide. Examples of suitable anionic surfactants are water-soluble soaps or water-soluble synthetic surface-active compounds. Examples of suitable soaps are the alkali, alkaline earth or (unsubstituted or substituted) ammonium salts of fatty acids having approximately 10 to approximately 22 C atoms, such as the sodium or potassium salts of oleic or stearic acid, or of natural fatty acid mixtures which are obtainable for example from coconut or tall oil; mention must also be made of the fatty acid methyl taurates. However, synthetic surfactants are used more frequently, in particular fatty sulfonates, fatty sulfates, sulfonated benzimidazole derivatives or alkylaryl sulfonates. As a rule, the fatty sulfonates and fatty sulfates are present as alkali, alkaline earth or (substituted or unsubstituted) ammonium salts and they generally have an alkyl radical of approximately 8 to approximately 22 C atoms, alkyl also to be understood as including the alkyl moiety of acyl radicals; examples which may be mentioned are the sodium or calcium salts of lignosulfonic acid, of the dodecylsulfuric ester or of a fatty alcohol sulfate mixture prepared from natural fatty acids. This group also includes the salts of the sulfuric esters and sulfonic acids of fatty alcohol/ethylene oxide adducts. The sulfonated benzimidazole derivatives preferably contain 2 sulfonyl groups and a fatty acid radical of approximately 8 to approximately 22 C atoms. Examples of alkylarylsulfonates are the sodium, calcium or triethanolammonium salts of decylbenzenesulfonic acid, of dibutyl¬naphthalenesulfonic acid or of a naphthalenesulfonic acid/formaldehyde condensate. Also possible are, furthermore, suitable phosphates, such as salts of the phosphoric ester of a p-nonylphenol/(4-14)ethylene oxide adduct, or phospholipids. Further suitable phosphates are tris-esters of phosphoric acid with aliphatic or aromatic alcohols and/or bis-esters of alkyl phosphonic acids with aliphatic or aromatic alcohols, which are a high performance oil-type adjuvant. These tris-esters have been described, for example, in WO 01/47356, WO 00/56146, EP-A-0579052 or EP-A-1018299 or are commercially available under their chemical name. Preferred tris-esters of phosphoric acid for use in the new compositions are tris-(2-ethylhexyl) phosphate, tris-n-octyl phosphate and tris-butoxyethyl phosphate, where tris-(2-ethylhexyl) phosphate is most preferred. Suitable bis-ester of alkyl phosphonic acids are bis-(2-ethylhexyl)-(2-ethylhexyl)-phosphonate, bis-(2-ethylhexyl)-(n-octyl)-phosphonate, dibutyl-butyl phosphonate and bis(2-ethylhexyl)-tripropylene-phosphonate, where bis-(2-ethylhexyl)-(n-octyl)-phosphonate is particularly preferred.
  • The compositions according to the invention can preferably additionally include an additive comprising an oil of vegetable or animal origin, a mineral oil, alkyl esters of such oils or mixtures of such oils and oil derivatives. The amount of oil additive used in the composition according to the invention is generally from 0.01 to 10%, based on the spray mixture. For example, the oil additive can be added to the spray tank in the desired concentration after the spray mixture has been prepared. Preferred oil additives comprise mineral oils or an oil of vegetable origin, for example rapeseed oil such as ADIGOR® and MERO®, olive oil or sunflower oil, emulsified vegetable oil, such as AMIGO® (Rhône-Poulenc Canada Inc.), alkyl esters of oils of vegetable origin, for example the methyl derivatives, or an oil of animal origin, such as fish oil or beef tallow. A preferred additive contains, for example, as active components essentially 80% by weight alkyl esters of fish oils and 15% by weight methylated rapeseed oil, and also 5% by weight of customary emulsifiers and pH modifiers. Especially preferred oil additives comprise alkyl esters of C8-C22 fatty acids, especially the methyl derivatives of C12-C18 fatty acids, for example the methyl esters of lauric acid, palmitic acid and oleic acid, being important. Those esters are known as methyl laurate (CAS-111-82-0), methyl palmitate (CAS-112-39-0) and methyl oleate (CAS-112-62-9). A preferred fatty acid methyl ester derivative is Emery® 2230 and 2231 (Cognis GmbH). Those and other oil derivatives are also known from the Compendium of Herbicide Adjuvants, 5th Edition, Southern Illinois University, 2000. Also, alkoxylated fatty acids can be used as additives in the inventive compositions as well as polymethylsiloxane based additives, which have been described in WO 2008/037373.
  • The application and action of the oil additives can be further improved by combining them with surface-active substances, such as non-ionic, anionic or cationic surfactants. Examples of suitable anionic, non-ionic and cationic surfactants are listed on pages 7 and 8 of WO 97/34485. Preferred surface-active substances are anionic surfactants of the dodecylbenzylsulfonate type, especially the calcium salts thereof, and also non-ionic surfactants of the fatty alcohol ethoxylate type. Special preference is given to ethoxylated C12-C22 fatty alcohols having a degree of ethoxylation of from 5 to 40. Examples of commercially available surfactants are the Genapol types (Clariant AG). Also preferred are silicone surfactants, especially polyalkyl-oxide-modified heptamethyltrisiloxanes, which are commercially available e.g. as Silwet L-77®, and also perfluorinated surfactants. The concentration of surface-active substances in relation to the total additive is generally from 1 to 30% by weight. Examples of oil additives that consist of mixtures of oils or mineral oils or derivatives thereof with surfactants are Edenor ME SU®, Turbocharge® (Syngenta AG, CH) and Actipron® (BP Oil UK Limited, GB).
  • The said surface-active substances may also be used in the formulations alone, that is to say without oil additives.
  • Furthermore, the addition of an organic solvent to the oil additive/surfactant mixture can contribute to a further enhancement of action. Suitable solvents are, for example, Solvesso® (ESSO) and Aromatic Solvent® (Exxon Corporation). The concentration of such solvents can be from 10 to 80% by weight of the total weight. Such oil additives, which may be in admixture with solvents, are described, for example, in U.S. Pat. No. 4,834,908. A commercially available oil additive disclosed therein is known by the name MERGE® (BASF Corporation). A further oil additive that is preferred according to the invention is SCORE® (Syngenta Crop Protection Canada.)
  • In addition to the oil additives listed above, in order to enhance the activity of the compositions according to the invention it is also possible for formulations of alkylpyrrolidones, (e.g. Agrimax®) to be added to the spray mixture. Formulations of synthetic latices, such as, for example, polyacrylamide, polyvinyl compounds or poly-1-p-menthene (e.g. Bond®, Courier® or Emerald®) can also be used. Solutions that contain propionic acid, for example Eurogkem Pen-e-trate®, can also be mixed into the spray mixture as activity-enhancing agents.
  • The term “active ingredient” refers to one of the compounds of formula I, especially the compounds of formula I specifically disclosed in the tables. It also refers to mixtures of the compound of formula I, in particular a compound selected from said Table 1, with other insecticides, fungicides, herbicides, safeners, adjuvants and the like, which mixtures are specifically disclosed below.
  • The compositions can also comprise further solid or liquid auxiliaries, such as stabilizers, for example unepoxidized or epoxidized vegetable oils (for example epoxidized coconut oil, rapeseed oil or soya oil), antifoams, for example silicone oil, preservatives, viscosity regulators, binders and/or tackifiers; fertilizers, in particular nitrogen containing fertilizers such as ammonium nitrates and urea as described in WO 2008/017388, which can enhance the efficacy of the inventive compounds; or other active ingredients for achieving specific effects, for example ammonium or phosphonium salts, in particular halides, (hydrogen)sulphates, nitrates, (hydrogen)carbonates, citrates, tartrates, formiates and acetates, as described in WO 2007/068427 and WO 2007/068428, which also can enhance the efficacy of the inventive compounds and which can be used in combination with penetration enhancers such as alkoxalated fatty acids; bactericides, fungicides, nematocides, plant activators, molluscicides or herbicides.
  • The compositions according to the invention are prepared in a manner known per se, in the absence of auxiliaries for example by grinding, screening and/or compressing a solid active ingredient and in the presence of at least one auxiliary for example by intimately mixing and/or grinding the active ingredient with the auxiliary (auxiliaries).
  • The application methods for the compositions, that is the methods of controlling pests of the abovementioned type, such as spraying, atomizing, dusting, brushing on, dressing, scattering or pouring—which are to be selected to suit the intended aims of the prevailing circumstances—and the use of the compositions for controlling pests of the abovementioned type are other subjects of the invention. Typical rates of concentration are between 0.1 and 1000 ppm, preferably between 0.1 and 500 ppm, of active ingredient.
  • A preferred method of application in the field of crop protection is application to the foliage of the plants (foliar application), it being possible to select frequency and rate of application to match the danger of infestation with the pest in question. Alternatively, the active ingredient can reach the plants via the root system (systemic action), by drenching the locus of the plants with a liquid composition or by incorporating the active ingredient in solid form into the locus of the plants, for example into the soil, for example in the form of granules (soil application). In the case of paddy rice crops, such granules can be metered into the flooded paddy-field.
  • The compositions according to the invention are also suitable for the protection of plant propagation material, for example seeds, such as fruit, tubers or kernels, or nursery plants, against pests of the abovementioned type. The propagation material can be treated with the compositions prior to planting, for example seed can be treated prior to sowing. Alternatively, the compositions can be applied to seed kernels (coating), either by soaking the kernels in a liquid composition or by applying a layer of a solid composition. It is also possible to apply the compositions when the propagation material is planted to the site of application, for example into the seed furrow during drilling. These treatment methods for plant propagation material and the plant propagation material comprising a compound of formula (I) as defined above are further subjects of the invention.
  • Further methods of application of the compositions according to the invention comprise drip application onto the soil, dipping of parts of plants such as roots bulbs or tubers, drenching the soil, as well as soil injection. These methods are known in the art.
  • In order to apply a compound of formula I as an insecticide, acaricide, nematicide or molluscicide to a pest, a locus of pest, or to a plant susceptible to attack by a pest, a compound of formula I is usually formulated into a composition which includes, in addition to the compound of formula I, a suitable inert diluent or carrier and, optionally, a formulation adjuvant in form of a surface active agent (SFA) as described herein or, for example, in EP-B-1062217. SFAs are chemicals which are able to modify the properties of an interface (for example, liquid/solid, liquid/air or liquid/liquid interfaces) by lowering the interfacial tension and thereby leading to changes in other properties (for example dispersion, emulsification and wetting).
  • As a rule, the compositions comprise 0.1 to 99%, especially 0.1 to 95%, of active ingredient of the formula I and 1 to 99.9%, especially 5 to 99.9%, of at least one solid or liquid adjuvant, it being possible as a rule for 0 to 25%, especially 0.1 to 20%, of the composition to be surfactants (% in each case meaning percent by weight). Whereas concentrated compositions tend to be preferred for commercial goods, the end consumer as a rule uses dilute compositions which have substantially lower concentrations of active ingredient.
  • Typical rates of concentration are between 0.1 and 1000 ppm, preferably between 0.1 and 500 ppm, of active ingredient. The rate of application per hectare is generally 1 to 2000 g of active ingredient per hectare, in particular 10 to 1000 g/ha, preferably 10 to 600 g/ha.
  • When used in a seed dressing, a compound of formula I is used at a rate of 0.0001 g to 10 g (for example 0.001 g or 0.05 g), preferably 0.005 g to 10 g, more preferably 0.005 g to 4 g, per kilogram of seed.
  • Preferred seed treatment pre-mix formulations are aqueous suspension concentrates. The formulation can be applied to the seeds using conventional treating techniques and machines, such as fluidized bed techniques, the roller mill method, rotostatic seed treaters, and drum coaters. Other methods, such as spouted beds may also be useful. The seeds may be presized before coating. After coating, the seeds are typically dried and then transferred to a sizing machine for sizing. Such procedures are known in the art.
  • The compositions can be chosen from a number of formulation types, including dustable powders (DP), soluble powders (SP), water soluble granules (SG), water dispersible granules (WG), wettable powders (WP), granules (GR) (slow or fast release), soluble concentrates (SL), oil miscible liquids (OL), ultra low volume liquids (UL), emulsifiable concentrates (EC), dispersible concentrates (DC), emulsions (both oil in water (EW) and water in oil (EO)), micro-emulsions (ME), suspension concentrates (SC), oil-based suspension concentrate (OD), aerosols, fogging/smoke formulations, capsule suspensions (CS) and seed treatment formulations. The formulation type chosen in any instance will depend upon the particular purpose en-visaged and the physical, chemical and biological properties of the compound of formula I.
  • Dustable powders (DP) may be prepared by mixing a compound of formula I with one or more solid diluents (for example natural clays, kaolin, pyrophyllite, bentonite, alumina, montmorillonite, kieselguhr, chalk, diatomaceous earths, calcium phosphates, calcium and magnesium carbonates, sulphur, lime, flours, talc and other organic and inorganic solid carriers) and mechanically grinding the mixture to a fine powder.
  • Soluble powders (SP) may be prepared by mixing a compound of formula I with one or more water-soluble inorganic salts (such as sodium bicarbonate, sodium carbonate or magnesium sulphate) or one or more water-soluble organic solids (such as a polysaccharide) and, optionally, one or more wetting agents, one or more dispersing agents or a mixture of said agents to improve water dispersibility/solubility. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water soluble granules (SG).
  • Wettable powders (WP) may be prepared by mixing a compound of formula I with one or more solid diluents or carriers, one or more wetting agents and, preferably, one or more dispersing agents and, optionally, one or more suspending agents to facilitate the dispersion in liquids. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water dispersible granules (WG).
  • Granules (GR) may be formed either by granulating a mixture of a compound of formula I and one or more powdered solid diluents or carriers, or from pre-formed blank granules by absorbing a compound of formula I (or a solution thereof, in a suitable agent) in a porous granular material (such as pumice, attapulgite clays, fuller's earth, kieselguhr, diatomaceous earths or ground corn cobs) or by adsorbing a compound of formula I (or a solution thereof, in a suitable agent) on to a hard core material (such as sands, silicates, mineral carbonates, sulphates or phosphates) and drying if necessary. Agents which are commonly used to aid absorption or adsorption include solvents (such as aliphatic and aromatic petroleum solvents, alcohols, ethers, ketones and esters) and sticking agents (such as polyvinyl acetates, polyvinyl alcohols, dextrins, sugars and vegetable oils). One or more other additives may also be included in granules (for example an emulsifying agent, wetting agent or dispersing agent).
  • Dispersible Concentrates (DC) may be prepared by dissolving a compound of formula I in water or an organic solvent, such as a ketone, alcohol or glycol ether. These solutions may contain a surface active agent (for example to improve water dilution or prevent crystallisation in a spray tank).
  • Emulsifiable concentrates (EC) or oil-in-water emulsions (EW) may be prepared by dissolving a compound of formula I in an organic solvent (optionally containing one or more wetting agents, one or more emulsifying agents or a mixture of said agents). Suitable organic solvents for use in ECs include aromatic hydrocarbons (such as alkylbenzenes or alkylnaphthalenes, exemplified by SOLVESSO 100, SOLVESSO 150 and SOLVESSO 200; SOLVESSO is a Registered Trade Mark), ketones (such as cyclohexanone or methylcyclohexanone) and alcohols (such as benzyl alcohol, furfuryl alcohol or butanol),
  • N-alkylpyrrolidones (such as N-methylpyrrolidone or N-octylpyrrolidone), dimethyl amides of fatty acids (such as C8-C10 fatty acid dimethylamide) and chlorinated hydrocarbons. An EC product may spontaneously emulsify on addition to water, to produce an emulsion with sufficient stability to allow spray application through appropriate equipment. Preparation of an EW involves obtaining a compound of formula I either as a liquid (if it is not a liquid at room temperature, it may be melted at a reasonable temperature, typically below 70° C.) or in solution (by dissolving it in an appropriate solvent) and then emulsifiying the resultant liquid or solution into water containing one or more SFAs, under high shear, to produce an emulsion. Suitable solvents for use in EWs include vegetable oils, chlorinated hydrocarbons (such as chlorobenzenes), aromatic solvents (such as alkylbenzenes or alkylnaphthalenes) and other appropriate organic solvents which have a low solubility in water.
  • Microemulsions (ME) may be prepared by mixing water with a blend of one or more solvents with one or more SFAs, to produce spontaneously a thermodynamically stable isotropic liquid formulation. A compound of formula I is present initially in either the water or the solvent/SFA blend. Suitable solvents for use in MEs include those hereinbefore described for use in in ECs or in EWs. An ME may be either an oil-in-water or a water-in-oil system (which system is present may be determined by conductivity measurements) and may be suitable for mixing water-soluble and oil-soluble pesticides in the same formulation. An ME is suitable for dilution into water, either remaining as a microemulsion or forming a conventional oil-in-water emulsion.
  • Suspension concentrates (SC) may comprise aqueous or non-aqueous suspensions of finely divided insoluble solid particles of a compound of formula I. SCs may be prepared by ball or bead milling the solid compound of formula I in a suitable medium, optionally with one or more dispersing agents, to produce a fine particle suspension of the compound. One or more wetting agents may be included in the composition and a suspending agent may be included to reduce the rate at which the particles settle. Alternatively, a compound of formula I may be dry milled and added to water, containing agents hereinbefore described, to produce the desired end product.
  • Oil-based suspension concentrate (OD) may be prepared similarly by suspending finely divided insoluble solid particles of a compound of formula I in an organic fluid (for example at least one mineral oil or vegetable oil). ODs may further comprise at least one penetration promoter (for example an alcohol ethoxylate or a related compound), at least one non-ionic surfactants and/or at least one anionic surfactant, and optionally at least one additive from the group of emulsifiers, foam-inhibiting agents, preservatives, anti-oxidants, dyestuffs, and/or inert filler materials. An OD is intended and suitable for dilution with water before use to produce a spray solution with sufficient stability to allow spray application through appropriate equipment.
  • Aerosol formulations comprise a compound of formula I and a suitable propellant (for example n-butane). A compound of formula I may also be dissolved or dispersed in a suitable medium (for example water or a water miscible liquid, such as n-propanol) to provide compositions for use in non-pressurised, hand-actuated spray pumps.
  • A compound of formula I may be mixed in the dry state with a pyrotechnic mixture to form a composition suitable for generating, in an enclosed space, a smoke containing said compound. Capsule suspensions (CS) may be prepared in a manner similar to the preparation of EW formulations but with an additional polymerisation stage such that an aqueous dispersion of oil droplets is obtained, in which each oil droplet is encapsulated by a polymeric shell and contains a compound of formula I and, optionally, a carrier or diluent therefor. The polymeric shell may be produced by either an interfacial polycondensation reaction or by a coacervation procedure. The compositions may provide for controlled release of the compound of formula I and they may be used for seed treatment. A compound of formula I may also be formulated in a biodegradable polymeric matrix to provide a slow, controlled release of the compound.
  • A compound of formula I may also be formulated for use as a seed treatment, for example as a powder composition, including a powder for dry seed treatment (DS), a water soluble powder (SS) or a water dispersible powder for slurry treatment (WS), or as a liquid composition, including a flowable concentrate (FS), a solution (LS) or a capsule suspension (CS). The preparations of DS, SS, WS, FS and LS compositions are very similar to those of, respectively, DP, SP, WP, SC, OD and DC compositions described above. Compositions for treating seed may include an agent for assisting the adhesion of the composition to the seed (for example a mineral oil or a film-forming barrier).
  • A composition of the present invention may include one or more additives to improve the biological performance of the composition (for example by improving wetting, retention or distribution on surfaces; resistance to rain on treated surfaces; or uptake or mobility of a compound of formula I). Such additives include surface active agents (SFAs), spray additives based on oils, for example certain mineral oils, vegetable oils or natural plant oils (such as soy bean and rape seed oil), and blends of these with other bio-enhancing adjuvants (ingredients which may aid or modify the action of a compound of formula I). Increasing the effect of a compound of formula I may for example be achieved by adding ammonium and/or phosphonium salts, and/or optionally at least one penetration promotor such as fatty alcohol alkoxylates (for example rape oil methyl ester) or vegetable oil esters.
  • Wetting agents, dispersing agents and emulsifying agents may be surface active agents (SFAs) of the cationic, anionic, amphoteric or non-ionic type.
  • Suitable SFAs of the cationic type include quaternary ammonium compounds (for example cetyltrimethyl ammonium bromide), imidazolines and amine salts.
  • Suitable anionic SFAs include alkali metals salts of fatty acids, salts of aliphatic monoesters of sulphuric acid (for example sodium lauryl sulphate), salts of sulphonated aromatic compounds (for example sodium dodecylbenzenesulphonate, calcium dodecylbenzenesulphonate, butylnaphthalene sulphonate and mixtures of sodium di-isopropyl- and tri-isopropyl-naphthalene sulphonates), ether sulphates, alcohol ether sulphates (for example sodium laureth-3-sulphate), ether carboxylates (for example sodium laureth-3-carboxylate), phosphate esters (products from the reaction between one or more fatty alcohols and phosphoric acid (predominately mono-esters) or phosphorus pentoxide (predominately di-esters), for example the reaction between lauryl alcohol and tetraphosphoric acid; additionally these products may be ethoxylated), sulphosuccinamates, paraffin or olefine sulphonates, taurates and lignosulphonates.
  • Suitable SFAs of the amphoteric type include betaines, propionates and glycinates.
  • Suitable SFAs of the non-ionic type include condensation products of alkylene oxides, such as ethylene oxide, propylene oxide, butylene oxide or mixtures thereof, with fatty alcohols (such as oleyl alcohol or cetyl alcohol) or with alkylphenols (such as octylphenol, nonylphenol or octylcresol); partial esters derived from long chain fatty acids or hexitol anhydrides; condensation products of said partial esters with ethylene oxide; block polymers (comprising ethylene oxide and propylene oxide); alkanolamides; simple esters (for example fatty acid polyethylene glycol esters); amine oxides (for example lauryl dimethyl amine oxide); and lecithins.
  • Suitable suspending agents include hydrophilic colloids (such as polysaccharides, polyvinylpyrrolidone or sodium carboxymethylcellulose) and swelling clays (such as bentonite or attapulgite).
  • A compound of formula I may be applied by any of the known means of applying pesticidal compounds. For example, it may be applied, formulated or unformulated, to the pests or to a locus of the pests (such as a habitat of the pests, or a growing plant liable to infestation by the pests) or to any part of the plant, including the foliage, stems, branches or roots, to the seed before it is planted or to other media in which plants are growing or are to be planted (such as soil surrounding the roots, the soil generally, paddy water or hydroponic culture systems), directly or it may be sprayed on, dusted on, applied by dipping, applied as a cream or paste formulation, applied as a vapour or applied through distribution or incorporation of a composition (such as a granular composition or a composition packed in a water-soluble bag) in soil or an aqueous environment.
  • A compound of formula I may also be injected into plants or sprayed onto vegetation using electrodynamic spraying techniques or other low volume methods, or applied by land or aerial irrigation systems.
  • Compositions for use as aqueous preparations (aqueous solutions or dispersions) are generally supplied in the form of a concentrate containing a high proportion of the active ingredient, the concentrate being added to water before use. These concentrates, which may include DCs, SCs, ODs, ECs, EWs, MEs SGs, SPs, WPs, WGs and CSs, are often required to withstand storage for prolonged periods and, after such storage, to be capable of addition to water to form aqueous preparations which remain homogeneous for a sufficient time to enable them to be applied by conventional spray equipment. Such aqueous preparations may contain varying amounts of a compound of formula I (for example 0.0001 to 10%, by weight) depending upon the purpose for which they are to be used.
  • A compound of formula I may be used in mixtures with fertilisers (for example nitrogen-, potassium- or phosphorus-containing fertilisers, and more particularly ammonium nitrate and/or urea fertilizers). Suitable formulation types include granules of fertiliser. The mixtures suitably contain up to 25% by weight of the compound of formula I.
  • Preferred compositions are composed in particular as follows (%=percent by weight):
    • Emulsifiable Concentrates:
  • active ingredient: 1 to 95%, preferably 5 to 20%
    surfactant: 1 to 30%, preferably 10 to 20%
    solvent: 5 to 98%, preferably 70 to 85%
    • Dusts:
  • active ingredient: 0.1 to 10%, preferably 0.1 to 1%
    solid carrier: 99.9 to 90%, preferably 99.9 to 99%
    • Suspension Concentrates:
  • active ingredient: 5 to 75%, preferably 10 to 50%
    water: 94 to 24%, preferably 88 to 30%
    surfactant: 1 to 40%, preferably 2 to 30%
    • Wettable Powders:
  • active ingredient: 0.5 to 90%, preferably 1 to 80%
    surfactant: 0.5 to 20%, preferably 1 to 15%
    solid carrier: 5 to 99%, preferably 15 to 98%
    • Granulates:
  • active ingredient: 0.5 to 30%, preferably 3 to 15%
    solid carrier: 99.5 to 70%, preferably 97 to 85%
    • PREPARATORY EXAMPLES
  • “Mpt.” means melting point in ° C. Free radicals represent methyl groups.
    • LCMS Methods: Method (SQD13)
  • Spectra were recorded on a Mass Spectrometer from Waters (SQD Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive or negative ions, Capillary: 3.00 kV, Cone range: 30-60 V, Extractor: 2.00 V, Source Temperature: 150° C., Desolvation Temperature: 350° C., Cone Gas Flow: 0 L/Hr, Desolvation Gas Flow: 650 L/Hr, Mass range: 100 to 900 Da) and an Acquity UPLC from Waters: Binary pump, heated column compartment and diode-array detector. Solvent degasser, binary pump, heated column compartment and diode-array detector. Column: Waters UPLC HSS T3, 1.8 □m, 30×2.1 mm, Temp: 60° C., DAD Wavelength range (nm): 210 to 500, Solvent Gradient: A=water+5% MeOH+0.05% HCOOH, B=Acetonitrile+0.05% HCOOH: gradient: gradient: 0 min 0% B, 100% A; 1.2-1.5 min 100% B; Flow (ml/min) 0.85.
    • Method (ZCQ 13):
  • Spectra were recorded on a Mass Spectrometer from Waters (ZQ Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive or negative ions, Capillary: 3.00 kV, Cone range: 30-60 V, Extractor: 2.00 V, Source Temperature: 150° C., Desolvation Temperature: 350° C., Cone Gas Flow: 0 L/Hr, Desolvation Gas Flow: 650 L/Hr, Mass range: 100 to 900 Da) and an Acquity UPLC from Waters: Binary pump, heated column compartment and diode-array detector. Solvent degasser, binary pump, heated column compartment and diode-array detector. Column: Waters UPLC HSS T3, 1.8 □m, 30×2.1 mm, Temp: 60° C., DAD Wavelength range (nm): 210 to 500, Solvent Gradient: A=water+5% MeOH+0.05% HCOOH, B=Acetonitrile+0.05% HCOOH: gradient: gradient: 0 min 0% B, 100% A; 2.7-3.0 min 100% B; Flow (ml/min) 0.85.
    • Method (ZDQ 13):
  • Spectra were recorded on a Mass Spectrometer from Waters (ZQ Single quadrupole mass spectrometer) equipped with an electrospray source (Polarity: positive or negative ions, Capillary: 3.00 kV, Cone range: 30-60 V, Extractor: 2.00 V, Source Temperature: 150° C., Desolvation Temperature: 350° C., Cone Gas Flow: 0 L/Hr, Desolvation Gas Flow: 650 L/Hr, Mass range: 100 to 900 Da) and an Acquity UPLC from Waters: Binary pump, heated column compartment and diode-array detector. Solvent degasser, binary pump, heated column compartment and diode-array detector. Column: Waters UPLC HSS T3, 1.8 □m, 30×2.1 mm, Temp: 60° C., DAD Wavelength range (nm): 210 to 500, Solvent Gradient: A=water+5% MeOH+0.05% HCOOH, B=Acetonitrile+0.05% HCOOH: gradient: gradient: 0 min 0% B, 100% A; 1.2-1.5 min 100% B; Flow (ml/min) 0.85.
    • Method (ZQ2000):
  • ZQ2000 Mass Spectrometer from Waters (Single quadrupole mass spectrometer)
  • Ionisation method: Electrospray
  • Polarity: positive ions
  • Capillary (kV) 3.5, Cone (V) 60.00, Extractor (V) 3.00, Source Temperature (° C.) 150, Desolvation Temperature (° C.) 350, Cone Gas Flow (L/Hr) 50, Desolvation Gas Flow (L/Hr) 800
  • Mass range: 140 to 800 Da
  • DAD Wavelength range (nm): 210 to 400
  • Method Waters ACQUITY UPLC with the following HPLC gradient conditions (Solvent A: Water/Methanol 9:1, 0.1% formic acid and Solvent B: Acetonitrile, 0.1% formic acid)
  • Time (minutes) A (%) B (%) Flow rate (ml/min)
    0 100 0 0.75
    2.5 0 100 0.75
    2.8 0 100 0.75
    3.0 100 0 0.75
  • Type of column: Waters ACQUITY UPLC HSS T3; Column length: 30 mm; Internal diameter of column: 2.1 mm; Particle Size: 1.8 micron; Temperature: 60° C.
  • 1H and 19F NMR Measurements: Measured on a Brucker 400 MHz or 300 MHz spectrometer, chemical shifts given in ppm relevant to a TMS standard. Spectra measured in solvents indicated.
    • Mass Spectroscopy Method MS
  • LC-20AD Mass Spectrometer from Shimadzu (Single quadrupole mass spectrometer)
    • Instrument Parameters:
  • Ionisation method: Electrospray
    Polarity: positive and negative ions
    • Capillary (kV) 1.50
  • Cone (V) unknown
    • Extractor (V) 5.00 Source Temperature (° C.) 200 Desolvation Temperature (° C.) 250 Cone gas Flow (I/Hr) 90 Desolvation gas Flow (I/Hr) 90
  • Mass range: 50 to 1000 Da
    • Example P1: 2-methyl-7-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-4-(trifluoromethyl)-2,3-dihydrobenzothiophene 1,1-dioxide (Compound A1.014-B2.022)
  • Figure US20220104496A1-20220407-C00067
    • Step A: 2-methyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-1,1-dioxo-4-(trifluoromethyl)-2,3-dihydrobenzothiophene-7-carboxamide
  • Figure US20220104496A1-20220407-C00068
  • A suspension of 2-methyl-1,1-dioxo-4-(trifluoromethyl)-2,3-dihydrobenzothiophene-7-carboxylic acid (308 mg, 1.05 mmol, prepared as described in WO 9909023) and N2-methyl-5-(trifluoromethyl)pyridine-2,3-diamine (200 mg 1.05 mmol, prepared as described in WO 2012/092051) in THF (15 ml) was treated 3-(ethyliminomethyleneamino)-N,N-dimethyl-propan-1-amine (487 mg, 3.14 mmol) and pyridine (100 mg, 1.26 mmol). The reaction mixture was stirred for 18 hours and then diluted with ethyl acetate and 1N HCl. The organic phase was separated and the aqueous phase extracted with ethyl acetate. The combined organic phases were washed with water, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography eluting with ethyl acetate:cyclohexane 1:1, gave the title product (105 mg, 21%) as a white solid. LCMS (method SQD13): 468 (M+H), retention time 0.97 min.
    • Step B: 2-methyl-7-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-4-(trifluoromethyl)-2,3-dihydrobenzothiophene 1,1-dioxide (Compound A1.014-B2.022)
  • Figure US20220104496A1-20220407-C00069
  • A solution of 2-methyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-1,1-dioxo-4-(trifluoromethyl)-2,3-dihydrobenzothiophene-7-carboxamide (71 mg, 0.15 mmol) and toluene-4-sulphonic acid (8 mg, 0.05 mmol) dissolved in 1-methylpyrrolidin-2-one (1 ml) was heated at 160° C. for 100 min in the microwave. After this time, the reaction mixture was is poured into water, extracted with ethyl acetate, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The product obtained was triturated with cyclohexane to give the title compound (45 mg, 66%, as a white solid with mpt. 206° C. LCMS (method SQD13): 450 (M+H), retention time 0.99 min.
  • 1H NMR (400 MHz, CDCl3) d ppm 8.77 (d, J=1.5 Hz, 1H); 8.42 (d, J=1.5 Hz, 1H); 8.05 (d, J=8.1 Hz, 1H); 7.75 (d, J=7.1 Hz, 1H); 3.90 (s, 3H); 3.74 (d, J=16.9, 8.1 Hz, 1H) 3.52-3.68 (m, 1H) 3.19 (dd, J=16.87, 8.1 Hz, 1H); 1.55 ppm (d, J=7.0 Hz, 3H).
    • Example P2: 4-bromo-2-methyl-7-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-2,3-dihydrobenzothiophene 1,1-dioxide (Compound A1.014-B2.023)
  • Figure US20220104496A1-20220407-C00070
    • Step A: 4-bromo-2-methyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-1,1-dioxo-2,3-dihydrobenzothiophene-7-carboxamide
  • Figure US20220104496A1-20220407-C00071
  • A solution of 4-bromo-2-methyl-1,1-dioxo-2,3-dihydrobenzothiophene-7-carboxylic acid (320 mg, 1 mmol, prepared as described in WO 9909023) in dichloromethane (10 ml) was treated with oxallyl chloride (170 mg, 1.3 mmol) and 1-2 drops of DMF at room temperature. After 1 hr, N2-methyl-5-(trifluoromethyl)pyridine-2,3-diamine (200 mg, 1.0 mmol), and triethylamine (100 mg, 1.2 mmol) and were added and the reaction mixture stirred at room temperature until reaction completion. The reaction mixture was diluted with methylene chloride, washed with water, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography eluting with ethyl acetate:cyclohexane 1:1 to give the title compound (240 mg, 48%) as a yellow solid. LCMS (method SQD13): 478/480 (M+H), retention time 0.95 min.
    • Step B: 4-bromo-2-methyl-7-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-2,3-dihydrobenzothiophene 1,1-dioxide (A1.014-B2.023)
  • Figure US20220104496A1-20220407-C00072
  • A solution of 4-bromo-2-methyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-1,1-dioxo-2,3-dihydrobenzothiophene-7-carboxamide (210 mg, 0.44 mmol) and toluene-4-sulphonic acid (23 mg, 0.13 mmol) dissolved in 1-methylpyrrolidin-2-one (3 ml) was heated at 160° C. for 1 hr in the microwave. After this time, the reaction mixture was is poured into water, extracted with ethyl acetate, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography eluting with ethyl acetate:cyclohexane (0/100)->(50/50, gave the title compound as white crystals. LCMS (method SQD13): 460/462 (M+H), retention time 0.97 min.
  • 1H NMR (400 MHz, CDCl3) d ppm 8.76 (d, J=1.10 Hz, 1H); 8.41 (d, J=1.1 Hz, 1H); 8.22 (d, J=7.70 Hz, 1H); 7.73 (d, J=7.70 Hz, 1H); 4.02 (dd, J=17.8, 7.5 Hz, 1H); 3.44-3.60 (m, 1H); 3.35 (dd, J=17.8, 7.5 Hz, 1H); 2.74 (s, 3H) 1.51 ppm (d, J=7.0 Hz, 3H).
    • Example P3: 2-[4-ethylsulfonyl-6-(trifluoromethyl) pyridazin-3-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine (A1.014-B1.058)
  • Figure US20220104496A1-20220407-C00073
    • Step A: 5-ethylsulfanyl-3-(trifluoromethyl)-1H-pyridazin-6-one
  • Figure US20220104496A1-20220407-C00074
  • EtSNa (100 mg, 1.2 mmol) was added to a solution of 5-bromo-3-(trifluoromethyl)-1H-pyridazin-6-one (243 mg, 1 mmol, Prepared as described in WO 2008128995) in 10 ml of DMF. After the addition, the mixture was stirred at room temperature for 2 hours. Then the mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give 5-ethylsulfanyl-3-(trifluoromethyl)-1H-pyridazin-6-one (182 mg, 81%). 1H NMR (300 Mz, DMSO-d6): δ: 1.27 (t, 3H), 3.00 (q, 2H), 7.38 (s, 1H), 13.63 (s, 1H); 19F NMR (400 MHz, DMSO-d6): δ−65.49 (s, 3F); ESI-MS: 223 (M−H)−.
    • Step B: 3-chloro-4-ethylsulfanyl-6-(trifluoromethyl)Pyridazine
  • Figure US20220104496A1-20220407-C00075
  • A mixture of 5-ethylsulfanyl-3-(trifluoromethyl)-1H-pyridazin-6-one (5.8 g, 26 mmol) in 25 ml of POCl3 was refluxed for 16 h. Then, the reaction mixture was cooled to room temperature and POCl3 was distilled off under reduced pressure. The residue was poured into water and adjusted to alkaline with sodium hydroxide. The resulting mixture was extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel to give 3-chloro-4-ethylsulfanyl-6-(trifluoromethyl)pyridazine (4.9 g, 79%). 1H NMR (300 Mz, DMSO-d6): δ 1.31 (t, 3H), 3.23 (q, 2H), 8.00 (s, 1H); 1F NMR (300 Mz, DMSO-d6): δ−65.19 (s, 3F); ESI-MS(+): 243 (M+H)+.
    • Step C: methyl 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylate
  • Figure US20220104496A1-20220407-C00076
  • Carbon monoxide gas was introduced to a mixture of 3-chloro-4-ethylsulfanyl-6-(trifluoromethyl)pyridazine (2.5 g, 10 mmol), Pd(OAc)2 (232 mg, 0.1 mmol), dppf (572 mg, 0.1 mmol) and Et3N (3.1 g, 30 mmol) in 30 ml of MeOH, and the internal pressure was increased to 1.5 MPa. Then, the reaction was stirred at 80° C. for 16 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give methyl 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylate (1.0 g, 37%). 1H NMR (300 Mz, DMSO-d6): δ 1.28 (t, 3H), 3.19 (q, 2H), 3.99 (s, 3H), 8.01 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−65.61 (s, 3F); ESI-MS(+): 267(M+H)+, 289 (M+Na)+.
    • Step D: 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylic acid
  • Figure US20220104496A1-20220407-C00077
  • A mixture of methyl 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylate (532 mg, 2 mmol) and LiOH (96 mg, 4 mmol) in 30 ml of THF and 6 ml of H2O was stirred at room temperature for 30 min. Then the mixture was poured into water and adjusted PH to 3˜4 with diluted hydrochloric acid. The resulting mixture was extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure to afford 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylic acid (398 mg, 79%). 1H NMR (300 Mz, DMSO-d6): δ 1.22 (t, 3H), 3.16 (q, 2H), 8.03 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−65.52 (s, 3F); ESI-MS(−): 267(M−H)−.
    • Step E: 4-ethylsulfanyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-6-(trifluoromethyl)pyridazine-3-carboxamide
  • Figure US20220104496A1-20220407-C00078
  • A mixture 4-ethylsulfanyl-6-(trifluoromethyl)pyridazine-3-carboxylic acid (230 mg, 0.9 mmol), N2-methyl-5-(trifluoromethyl)pyridine-2,3-diamine (209 mg, 1.1 mmol, prepared as described in WO 2012092051), HATU (520 mg, 1.4 mmol), DIPEA (235 mg, 1.8 mmol) in 20 ml of DMF was stirred at room temperature for 16 h. Then the mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give 4-ethylsulfanyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-6-(trifluoromethyl)pyridazine-3-carboxamide (369 mg, 95%). 1H NMR (300 Mz, DMSO-d6): δ 1.30 (t, 3H), 2.87 (d, 3H), 3.12 (q, 2H), 7.03 (s, 1H), 7.77 (s, 1H), 8.07 (s, 1H), 8.33 (s, 1H), 10.54 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ: −65.43 (s, 3F), −58.81 (s, 3F); ESI-MS(+): 426 (M+H)+.
    • Step D: 2-[4-Ethylsulfanyl-6-(Trifluoromethyl)Pyridazin-3-Yl]-3-Methyl-6-(Trifluoromethyl)Imidazo[4,5-b]Pyridine (Compound A1.014-B1.050)
  • Figure US20220104496A1-20220407-C00079
  • 4-ethylsulfanyl-N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-6-(trifluoromethyl)pyridazine-3-carboxamide (369 mg, 0.9 mmol) in 10 ml of AcOH was refluxed for 2 hours. Then the reaction mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel to give 2-[4-ethylsulfanyl-6-(trifluoromethyl)pyridazin-3-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine (compound A1.014-B1.050, 181 mg, 51%). 1H NMR (300 Mz, DMSO-d6): δ 1.27 (t, 3H), 3.20 (q, 2H), 4.07 (s, 1H), 8.12 (s, 1H). 8.75 (s, 1H), 8.93 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−66.44 (s, 3F), −58.33 (s, 3F); ESI-MS(+): 408(M+H)+.)+. Mpt. 149-156° C. LCMS (SQD13) Rt. 1.12 min, 408(M+H).
    • Step E: 2-[4-ethylsulfonyl-6-(trifluoromethyl)pyridazin-3-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine (A1.014-B1.058)
  • Figure US20220104496A1-20220407-C00080
  • A mixture of 2-[4-ethylsulfanyl-6-(trifluoromethyl)pyridazin-3-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine (109 mg, 0.3 mmol) and m-CPBA (232 mg, 1.3 mmol) in 20 ml of CH2Cl2 was stirred at room temperature for 2 h. Then the mixture was washed with saturated sodium sulfite, aqueous sodium bicarbonate and dried over sodium sulfate. After filtration, the solvent was concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel to afford the title compound (compound A1.014-B1.058) (113 mg, 96%). 1HNMR (300 Mz, DMSO-d6): δ 1.26 (t, 3H), 3.91 (s, 3H), 3.94 (q, 2H), 8.77 (s, 1H), 8.79 (s, 1H), 8.97 (s, 1H); 19F-NMR (300 Mz, DMSO-d6): δ−65.30 (s, 3F), −58.32 (s, 3F); ESI-MS(+): 440(M+H)+.) Mpt. 172-174° C. LCMS (ZCQ13) Rt. 1.06 min, 440(M+H).
    • Example P4: 5-ethylsulfonyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]thiazole (V13.05)
  • Figure US20220104496A1-20220407-C00081
    • Step A ethyl 5-ethylsulfanylthiazole-4-carboxylate
  • Figure US20220104496A1-20220407-C00082
  • A solution of ethyl isocyanoacetate (5.6 g, 0.05 mol) in 100 ml of THF was added dropwise to a suspension of potassium t-butoxide (6.1 g, 0.055 mol) in 20 ml of THF at −40° C. After the addition, the mixture was cooled to −60° C., carbon disulfide (3.8 g, 0.05 mol) was added dropwise while keeping the temperature below −50° C. Then, the mixture was warmed to 10° C. and ethyl bromide (5.4 g, 0.05 mol) was added. The mixture was stirred for another 2 h and concentrated in vacuo. The residue was purified by column chromatography on silica gel to afford the compound ethyl 5-ethylsulfanylthiazole-4-carboxylate (5.6 g, 52%). 1H NMR (300 MHz, DMSO-d6): δ1.27-1.37 (m, 6H), 3.03 (q, 2H), 4.25 (q, 2H), 8.97 (s, 1H); ESI-MS(+): 218(M+H)+, 240(M+Na)+.
    • Step B: 5-ethylsulfanylthiazole-4-carboxylic acid
  • Figure US20220104496A1-20220407-C00083
  • A mixture of ethyl 5-ethylsulfanylthiazole-4-carboxylate (4.6 g, 0.02 mol) and NaOH (1.68 mg, 0.04 mol) in 25 ml of water and 50 ml of THF was stirred at room temperature overnight. Then, the reaction mixture was poured into diluted hydrochloric acid. Then, the deposited precipitate was filtered, washed with water, dried under reduced pressure to obtain the title compound (3.9 g, 90%).
  • 1H NMR (300 MHz, DMSO-d6): δ 1.32 (t, 3H), 3.00 (q, 2H), 8.94 (s, 1H), 12.94 (br s, 1H); ESI-MS(+): 190(M+H)+, 212(M+Na)+; HPLC: 99.9%.
  • Step C: tert-butyl N-[4-amino-6-(trifluoromethyl)-3-pyridyl]carbamate:
  • Figure US20220104496A1-20220407-C00084
  • To a solution of 6-(trifluoromethyl)pyridine-3,4-diamine (3.14 g, 17.73 mmol, prepared as described in U.S. Pat. No. 7,767,687) in THF (50 ml) was added tert-butoxycarbonyl tert-butyl carbonate (4.64 g, 21.27 mmol) and the mixture was stirred at 50° C. After 8 hours, a further 1.1 g (5.0 mmol) of tert-butoxycarbonyl tert-butyl carbonate was added, and stirring at 50° C. continued for a further 4 hours. The reaction mixture was then concentrated in vacuo, and the brown residue was suspended in dichloromethane, filtered and dried in vacuo to give the title compound as white crystals. LCMS (method SQD13): Ret. Time 0.79 min, 278 (M+H).
    • Step D: tert-butyl N-[4-amino-6-(trifluoromethyl)-3-pyridyl]-N-methyl-carbamate
  • Figure US20220104496A1-20220407-C00085
  • To a stirred suspension of sodium hydride (0.648 g, 14.85 mmol) in 30 ml DMF, tert-butyl N-[4-amino-6-(trifluoromethyl)-3-pyridyl]carbamate (3.92 g, 14.14 mmol) dissolved in 20 ml DMF was added dropwise over a period of 20 min at 20-25° C. After 15 min stirring at RT, iodomethane (2.21 g, 15.55 mmol) was added. After 30 min at ambient temperature the mixture was poured onto 200 ml water, extracted twice with ethyl acetate, and the combined organic fractions washed successively with water and brine, dried over Na2SO4 and concentrated in vacuo. The crude product was recrystallised from Ethyl acetate/Heptane to give the title compound (3.18 g) as white crystals. LCMS (method SQD13): ret. time 0.85 min, 292 (M+H).
    • Step E: N3-methyl-6-(trifluoromethyl)pyridine-3,4-diamine
  • Figure US20220104496A1-20220407-C00086
  • To a clear, colourless solution of tert-butyl N-[4-amino-6-(trifluoromethyl)-3-pyridyl]-N-methyl-carbamate (3.53 g, 12.119 mmol) in dioxan, hydrogen chloride (18 ml of a 2M solution in water, 36.36 mmol) was added and the mixture was heated to reflux. After gas evolution had ceased, the reaction mixture was cooled to room temperature, and treated with solid sodium hydrogen carbonate (3.1 g, 36.9 mmol). The slurry was diluted with water and extracted twice with ethyl acetate. The combined organic layers were washed successively with water and brine, dried over Na2SO4 and concentrated in vacuo to give 2.25 g of the title compound as colourless crystals, Mpt, 138-140° C.; LCMS (method SQD13): ret. Time 0.24 min, 192 (M+H).
  • Alternatively, N3-methyl-6-(trifluoromethyl)pyridine-3,4-diamine can be obtained by the following procedure:
  • To a solution of 6-(trifluoromethyl)pyridine-3,4-diamine (2.0 g, 12.2 mmol) and potassium carbonate (3.2 g, 23.1 mmol) in acetonitrile (10 mL) was added iodomethane (0.8 mL). The reaction mixture was stirred at 30° C. overnight. Potassium carbonate was filtered off; the filtrate was dried in vacuo and purified with chromatography column on silica gel (petroleum:EtOAc=4:3) to afford the title compound as a light yellow solid (0.32 g, yield: 37%): 1H NMR (400 MHz, DMSO-d6): δ (ppm) 7.57 (s, 1H), 6.83 (s, 1H), 5.82 (s, 2H), 5.23 (d, J=4.8 Hz, 1H), 2.80 (d, J=4.8 Hz, 3H). 19F NMR (300 MHz, DMSO-d6): δ (ppm) −60.12 (s, 3F). ESI-MS(+): 192 (M+H).
    • Step F: 5-ethylsulfanyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]thiazole (Compound A6.002-B7.037)
  • Figure US20220104496A1-20220407-C00087
  • A mixture of 5-ethylsulfanylthiazole-4-carboxylic acid (567 mg, 3 mmol), N3-methyl-6-(trifluoromethyl)pyridine-3,4-diamine (483 mg, 3 mmol) and N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC.HCL) (576 mg, 3.6 mmol) in 20 ml of pyridine was refluxed for 16 h. The reaction mixture was concentrated in vacuo and purified by column chromatography on silica gel to give title compound (120 mg), 5-ethylsulfanyl-N-[5-(methylamino)-2-(trifluoromethyl)-4-pyridyl]thiazole-4-carboxamide (51 mg and), and N-[4-amino-6-(trifluoromethyl)-3-pyridyl]-5-ethylsulfanyl-N-methyl-thiazole-4-carboxamide (162 mg). The latter two compounds were dissolved in 10 ml of AcOH and refluxed for 16 h. Then the mixture was concentrated in vacuo and the residue was purified by column chromatography on silica gel to give additional title compound (140 mg). 1H NMR (400 MHz, DMSO-d6): δ 1.34 (t, 3H), 3.08 (q, 2H), 4.23 (s, 3H), 8.20 (s, 1H), 9.17 (s, 1H), 9.27 (s, 1H); 19F-NMR (400 MHz, DMSO-d6): δ−59.68 (s, 3F); ESI-MS: 345(M+H)+, 367(M+Na)+; Mpt. 167-169° C.
    • Step G: 5-ethylsulfonyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]thiazole (V13.05
  • Figure US20220104496A1-20220407-C00088
  • 5-ethylsulfanyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]thiazole (140 mg, 0.4 mmol) and m-CPBA (280 mg, 1.6 mmol) in 10 ml of dichloromethane was stirred at room temperature for 0.5 h. Then the mixture was poured into a saturated solution of Na2CO3 and Na2SO3 in water, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (147 mg, 96%). 1H NMR (400 MHz, DMSO-d6): δ 1.28 (t, 3H), 4.04 (q, 2H), 4.05 (s, 3H), 8.32 (s, 1H), 9.29 (s, 1H), 9.70 (s, 1H); 19F-NMR (400 MHz, DMSO-d6): δ−58.84 (s, 3F); ESI-MS(+): 377(M+H)+, 399(M+Na)+; LCMS (method SQD13) Rt. 0.85 min 377 (M+H). Mpt. 178-179° C.
    • Example P5: 2-[5-(difluoromethoxy)-3-ethylsulfonyl-2-pyridyl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine (Compound V12.19)
  • Figure US20220104496A1-20220407-C00089
    • Step A: 2,3-Dichloro-5-[(4-methoxyphenyl)methoxy]pyridine
  • Figure US20220104496A1-20220407-C00090
  • A mixture 5,6-dichloropyridin-3-ol (8.2 g, 50 mmol), 4-Methoxybenzylchloride (11.8 g, 75 mmol) and K2CO3 (21.0 g, 150 mmol) in CH3CN (250 ml) was refluxed for 6 h. Then, the mixture was cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by column chromatography on silica gel to give the title compound (10.0 g, 70% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 3.72 (s, 3H), 5.09 (s, 2H), 6.92 (d, J=8.8 Hz, 2H), 7.35 (d, J=8.8 Hz, 2H), 7.89 (d, J=2.8 Hz, 1H), 8.15 (d, J=2.8 Hz, 1H); ESI-MS (+): 284(M+H)+; Mpt.: 124˜125° C.
    • Step B: Ethyl 3-chloro-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylate
  • Figure US20220104496A1-20220407-C00091
  • CO gas was introduced to a mixture of 2,3-dichloro-5-[(4-methoxyphenyl)methoxy]pyridine (10.0 g, 35.2 mmol), dppf (975 mg, 1.8 mmol), Pd(OAc)2 (158 mg, 0.7 mmol) and Et3N (10.2 ml, 70.4 mmol) in 110 ml of EtOH, and the internal pressure was increased to 1.6 MPa. The reaction mixture was stirred at 125° C. for about 7 hours. Then, the mixture was cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by column chromatography on silica gel to afford the title compound (6.8 g, 60% yield) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6): δ 1.26 (t, J=6.8 Hz, 3H), 3.72 (s, 3H), 4.28 (q, J=6.8 Hz, 2H), 5.15 (s, 2H), 6.92 (d, J=8.0 Hz, 2H), 7.37 (d, J=8.0 Hz, 2H), 7.76 (d, J=2.0 Hz, 1H), 8.32 (d, J=2.0 Hz, 1H); ESI-MS (+): 322 (M+H)+, 345 (M+Na)+; Mp: 45-46° C.
    • Step C: Ethyl 3-ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylate
  • Figure US20220104496A1-20220407-C00092
  • A mixture of ethyl 3-chloro-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylate (6.4 g, 0.02 mol) and EtSNa (3.35 g, 0.04 mol) in 50 ml of DMF was stirred at 90° C. for 4 h. Then, the mixture was poured into water, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give the title compound (3 g, 43% yield). 1H NMR (400 MHz, DMSO-d6): δ 1.22 (t, 3H), 1.29 (t, 3H), 2.97 (q, 2H), 3.76 (s, 3H), 4.27 (q, 2H), 5.24 (s, 2H), 6.96 (d, 2H), 7.34 (d, 1H), 7.41 (d, 2H), 8.15 (d, 1H); ESI-MS(+): 370(M+Na)+.
    • Step D: 3-Ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylic acid
  • Figure US20220104496A1-20220407-C00093
  • A mixture of ethyl-3-ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylate (3 g, 0.009 mol) and NaOH (692 mg, 0.017 mol) in 10 ml of water and 30 ml of THF was stirred at room temperature overnight. Then, the reaction mixture was poured into diluted hydrochloric acid and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel to provide the title compound (2.3 g, 83% yield). 1H NMR (400 MHz, DMSO-d6): δ 1.23 (t, 3H), 2.94 (q, 2H), 3.76 (s, 3H), 5.24 (s, 2H), 6.96 (d, 2H), 7.32 (d, 1H), 7.41 (d, 2H), 8.13 (d, 1H), 12.69 (br s, 1H); ESI-MS(+): 320(M+H)+, 342(M+Na)+.
    • Step E: 3-Ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]-N-[5-(methylamino)-2-(trifluoromethyl)-4-pyridyl]pyridine-2-carboxamide
  • Figure US20220104496A1-20220407-C00094
  • A mixture of compound 3-ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]pyridine-2-carboxylic acid (284 mg, 0.89 mmol), N3-methyl-6-(trifluoromethyl)pyridine-3,4-diamine (149 mg, 0.89 mmol, prepared as described in step E, example P4) and EDC.HCl (188 mg, 0.98 mmol) in 10 ml of pyridine was refluxed for 16 h. Then, the mixture was concentrated in vacuo, diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over Na2SO4, concentrated under reduced pressure to give crude title product (320 mg), which was directly used for the next step without further purification.
    • Step F: 5-ethylsulfanyl-6-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]pyridin-3-ol
  • Figure US20220104496A1-20220407-C00095
  • 3-Ethylsulfanyl-5-[(4-methoxyphenyl)methoxy]-N-[5-(methylamino)-2-(trifluoromethyl)-4-pyridyl]pyridine-2-carboxamide (320 mg) in 10 ml of AcOH was refluxed for 16 h. Then the mixture was concentrated in vacuo and the residue was purified by column chromatography on silica gel to give the title compound (151 mg). 1H-NMR (400 MHz, DMSO-d6): δ 1.18 (t, 3H), 2.91 (q, 2H), 3.96 (s, 3H), 7.34 (d, 1H), 8.11 (d, 1H), 8.22 (s, 1H), 9.18 (s, 1H), 10.74 (s, 1H); 19F-NMR (400 MHz, DMSO-d6): δ−64.84 (s, 3F); ESI-MS(+): 355(M+H)+.
    • Step G: 2-[5-(difluoromethoxy)-3-ethylsulfanyl-2-pyridyl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine
  • Figure US20220104496A1-20220407-C00096
  • At 50° C., CHCIF2 gas was introduced to a mixture of 5-ethylsulfanyl-6-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]pyridin-3-ol (100 mg, 0.28 mmol) and Cs2CO3 (460 mg, 1.41 mmol) in 10 ml of DMF for 2 hours. Then, the mixture was poured into water, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title product (94 mg, 82%). 1H NMR (400 MHz, DMSO-d6): δ 1.35 (t, 3H), 2.93 (q, 2H), 4.07 (s, 3H), 6.67 (t, 1H), 7.52 (d, 1H), 8.19 (s, 1H), 8.36 (d, 1H), 8.95 (s, 1H); 19F-NMR (400 MHz, DMSO-d6): δ−81.81 (d, 1F), −66.25 (s, 3F); ESI-MS(+): 405(M+H)+, 427(M+Na)+, 459(M+MeOH+Na)+; HPLC: 98.2%
    • Step H: 2-[5-(difluoromethoxy)-3-ethylsulfonyl-2-pyridyl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine (Compound V12.19)
  • Figure US20220104496A1-20220407-C00097
  • 2-[5-(difluoromethoxy)-3-ethylsulfanyl-2-pyridyl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine (80 mg, 0.2 mmol) and m-CPBA (136 mg, 0.8 mmol) in 5 ml of dichloromethane was stirred at room temperature for 0.5 h. Then the mixture was poured into a saturated aqueous solution of Na2CO3 and Na2SO3, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (67 mg, 88%). 1H NMR (400 MHz, DMSO-d6): δ 1.19 (m, 3H), 3.78 (d, 3H), 3.90 (s, 3H), 6.77 (t, 1H), 8.11 (s, 2H), 8.30 (d, 1H), 8.86 (d, 1H), 9.00 (s, 1H); 19F-NMR (400 MHz, DMSO-d6): δ−78.62 (d, 1F), −62.07 (s, 3F); ESI-MS(+): 437(M+H)+. Mpt. 146-148° C.; LCMS (method SQD13): Ret. Time 1.03 mins, 405 (M+H).
    • Example P6: 6-(2-Ethanesulfonyl-6-trifluoromethyl-pyridin-3-yl)-3-methyl-2-trifluoromethyl-3,5-dihydro-diimidazo[4,5-b;4′,5′-e]pyridine (Compound V26.03)
  • Figure US20220104496A1-20220407-C00098
    • Step A: 3-methyl-6-nitro-2-(trifluoromethyl)imidazo[4,5-b]pyridine
  • Figure US20220104496A1-20220407-C00099
  • N2-methyl-5-nitro-pyridine-2,3-diamine (10 g, 59.52 mmol) in TFA (10 mL) was stirred at 70° C. for 16 h. The mixture was purified by chromatography on silica to get the pure title compound (9.81 g, 67%) as yellow solid. 1HNMR (300 MHz, d6-DMSO): δ 9.46 (d, J=2.4 Hz, 1H), 9.22 (d, J=2.4 Hz, 1H), 4.04 (s, 3H).
    • Step B: 3-methyl-6-nitro-4-oxido-2-(trifluoromethyl)imidazo[4,5-b]pyridin-4-ium
  • Figure US20220104496A1-20220407-C00100
  • To a solution of 3-methyl-6-nitro-2-(trifluoromethyl)imidazo[4,5-b]pyridine (5.3 g, 21.54 mmol) in dichloromethanedichloromethane (60 ml) was added urea hydrogen peroxide (UHP, 6.17 g, 65.7 mmol), cooled with ice bath, and dropwise added TFAA (13.6 g, 65.7 mmol). The mixture was stirred at ambient temperature for 18 hours. TCL showed about 50% of starting material consumed. Another batch of UHP (6.08 g, 64.63 mmol) and TFAA (13.8 g, 64.63 mmol) was added at 0° C. The mixture was stirred at ambient temperature for another 24 hours. The reaction mixture was diluted with water, stirred and for 20 min. The organic phase was separated and the aqueous phase was back extracted with dichloromethane (3 times). The combined organic phases were washed with water and brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica to give the title compound as a white solid (1.91 g). 1HNMR (300 MHz, d6-DMSO): δ 9.17 (d, J=1.8 Hz, 1H), 8.83 (d, J=1.8 Hz, 1H), 4.41 (d, J=1.2 Hz, 3H).
    • Step C: 5-chloro-3-methyl-6-nitro-2-(trifluoromethyl)imidazo[4,5-b]pyridine
  • Figure US20220104496A1-20220407-C00101
  • 3-methyl-6-nitro-4-oxido-2-(trifluoromethyl)imidazo[4,5-b]pyridin-4-ium (2.8 g, 10.69 mmol) was dissolved in POCl3 (50 mL), and stirred at reflux for 2 hours. The mixture was poured into ice water, extracted with EtOAc (3 times). The organic phase was washed with NaHCO3 (aq) and water, dried over Na2SO4, evaporated to dryness, to get the crude title compound (3.8 g) which used in the next step without further purification.
    • Step D: N5,3-dimethyl-6-nitro-2-(trifluoromethyl)imidazo[4,5-b]pyridin-5-amine
  • Figure US20220104496A1-20220407-C00102
  • To a solution of compound 5-chloro-3-methyl-6-nitro-2-(trifluoromethyl)imidazo[4,5-b]pyridine (3.8 g) in ethanol (40 mL) was added MeNH2 (aq, 5 mL). The reaction mixture was stirred at ambient temperature for 18 hours. The mixture was filtered, and dried in vacuo to get the pure title compound (2.3 g) as a white solid. 1HNMR (300 MHz, d6-DMSO): δ 8.90 (s, 1H), 8.64-8.62 (m, 1H), 3.79 (d, J=1.2 Hz, 3H), 3.07 (d, J=4.8 Hz, 3H).
    • Step E: N5,3-dimethyl-2-(trifluoromethyl)imidazo[4,5-b]pyridine-5,6-diamine
  • Figure US20220104496A1-20220407-C00103
  • To a solution of compound N5,3-dimethyl-6-nitro-2-(trifluoromethyl)imidazo[4,5-b]pyridin-5-amine (2.3 g, 8.36 mmol) in EtOAc (30 mL) and methanol (30 mL) was added 200 mg of palladium on carbon under N2. The mixture was hydrogenated using a hydrogen balloon at rt for 4 h. The mixture was filtered through celite and the filtrate was evaporated to dryness. The residue was purified by chromatography on silica to give the title compound (1.6 g, 78%) as a purple solid. 1HNMR (300 MHz, d6-DMSO): δ 7.01 (s, 1H), 6.29 (d, J=3.3 Hz, 1H), 4.69 (s, 2H), 3.77 (d, J=1.2 Hz, 3H), 2.92 (d, J=4.5 Hz, 3H).
    • Step F: 3-bromo-2-chloro-6-(trifluoromethyl)pyridine
  • Figure US20220104496A1-20220407-C00104
  • A mixture of compound 2-chloro-6-(trifluoromethyl)pyridin-3-amine (5.88 g, 30 mmol, prepared as described in WO 2009110475), isoamyl nitrite (7.02 g, 60 mmol), p-TsOH (6.19 g, 36 mmol), TBAB (19.32 g, 60 mmol) and CuBr2 (1.40 g, 6 mmol) in 60 ml of MeCN was stirred at room temperature for 4 h. Then, the mixture was concentrated in vacuo and the residue was purified by column chromatography on silica gel to give the title compound (5.85 g, 75%). 1H-NMR (300 Mz, DMSO-d6): δ 7.85 (d, 1H), 8.52 (s, 1H); 19F-NMR (300 Mz, DMSO-d6): δ−65.72 (s, 3F).
    • Step G: 3-bromo-2-ethylsulfanyl-6-(trifluoromethyl)pyridine
  • Figure US20220104496A1-20220407-C00105
  • A mixture of 3-bromo-2-chloro-6-(trifluoromethyl)pyridine (5.98 g, 23 mmol) and EtSNa (1.93 g, 23 mmol) in 50 ml of MeCN was stirred for 2 h. Then, the mixture was poured into dilute hydrochloric acid and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (4.06 g, 58%). 1H-NMR (300 Mz, DMSO-d6): δ 1.26 (t, 3H), 3.08 (q, 2H), 7.50 (d, 1H), 8.20 (d, 1H); 19F-NMR (300 Mz, DMSO-d6): δ−65.45 (s, 3F).
    • Step H: ethyl 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carboxylate
  • Figure US20220104496A1-20220407-C00106
  • Carbon monoxide gas was introduced to a mixture of 3-bromo-2-ethylsulfanyl-6-(trifluoromethyl)pyridine (572 mg, 2 mmol), Pd(OAc)2 (90 mg, 0.4 mmol), dppf (444 mg, 0.8 mmol) and Et3N (1.01 g, 10 mmol) in 10 ml of EtOH and 10 ml of DMF and the internal pressure was raised to 2.7 MPa. The mixture was heated at 90° C. for 6 h and cooled to room temperature. Then, it was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (795 mg, 88%). 1H-NMR (300 Mz, DMSO-d6): δ 1.23 (t, 3H), 1.28 (t, 3H), 3.05 (q, 2H), 4.29 (q, 2H), 7.66 (d, 1H), 8.39 (d, 1H); 19F-NMR (300 Mz, DMSO-d6): δ−62.88 (s, 3F).
    • Step I: 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carboxylic acid
  • Figure US20220104496A1-20220407-C00107
  • A mixture of ethyl 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carboxylate (480 mg, 1.7 mmol) and KOH (482 mg, 8.6 mmol) in 10 ml of water and 10 ml of THF was stirred at room temperature for 16 h. The reaction mixture was poured into diluted hydrochloric acid and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to provide the title compound (430 mg, 90%). 1H-NMR (300 Mz, DMSO-d6): δ 1.23 (t, 3H), 3.02 (q, 2H), 7.64 (d, 1H), 8.37 (d, 1H), 13.85 (br s, 1H); 19F-NMR (300 Mz, DMSO-d6): δ−62.78 (s, 3F); ESI-MS(−): 250 (M−H)−.
    • Step J: 2-ethylsulfanyl-N-[3-methyl-5-(methylamino)-2-(trifluoromethyl)imidazo[4,5-b]pyridin-6-yl]-6-(trifluoromethyl) pyridine-3-carboxamide
  • Figure US20220104496A1-20220407-C00108
  • A mixture of 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carboxylic acid (251 mg, 1 mmol), N5,3-dimethyl-2-(trifluoromethyl)imidazo[4,5-b]pyridine-5,6-diamine (245 mg, 1.0 mmol, product from step E in this example), HATU (570 mg, 1.5 mmol) and DIPEA (258 mg, 2 mmol) in 10 ml of DMF was stirred for 16 h. The mixture was concentrated in vacuo and purified by column chromatography on silica gel to give the title compound (408 mg, 84%). 1H NMR (300 Mz, DMSO-d6): δ 1.26 (t, 3H), 2.91 (d, 3H), 3.07 (q, 2H), 3.83 (s, 3H), 6.69 (q, 1H), 7.76 (d, 1H), 7.80 (s, 1H), 8.44 (d, 1H), 9.97 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−62.50 (s, 3F), −57.02 (s, 3F).
    • Step K: 6-(2-Ethylsulfanyl-6-trifluoromethyl-pyridin-3-yl)-3-methyl-2-trifluoromethyl-3,5-dihydro-diimidazo[4,5-;4′,5′-e]pyridine
  • Figure US20220104496A1-20220407-C00109
  • A mixture of 2-ethylsulfanyl-N-[3-methyl-5-(methylamino)-2-(trifluoromethyl)imidazo[4,5-b]pyridin-6-yl]-6-(trifluoromethyl)pyridine-3-carboxamide (382 mg, 0.8 mmol) in 10 ml of AcOH was refluxed for 2 h, Then the mixture was concentrated in vacuo and the residue was purified by column chromatography on silica gel to give the title compound (231 mg, 63%). 1H-NMR (300 Mz, CDCl3): δ 1.33 (t, 3H), 3.22 (q, 2H), 3.85 (s, 3H), 4.09 (s, 3H), 7.51 (d, 1H), 7.86 (d, 1H), 8.59 (d, 1H); 19F NMR (300 Mz, CDCl3): δ−68.64 (s, 3F), −63.72 (s, 3F); ESI-MS(+): 461(M+H)+, 483 (M+Na)+. Mpt. 154-156° C.; LCMS; Ret. Time 1.13 mins, 461 (M+H)
    • Step L: 6-(2-Ethanesulfonyl-6-trifluoromethyl-pyridin-3-yl)-3-methyl-2-trifluoromethyl-3,5-dihydro-diimidazo[4,5-b;4′,5′-e]pyridine (Compound V26.03)
  • Figure US20220104496A1-20220407-C00110
  • A mixture of 6-(2-ethylsulfanyl-6-trifluoromethyl-pyridin-3-yl)-3-methyl-2-trifluoromethyl-3,5-dihydro-diimidazo[4,5-;4′,5′-e]pyridine (161 mg, 0.35 mmol) and m-CPBA (242 mg, 1.4 mmol) in 10 ml of dichloromethane was stirred at room temperature for 2 h. Then the mixture was poured into a saturated solution of NaHCO3 and Na2SO3 in water, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound as a white solid (163 mg, 94%). 1H NMR (300 Mz, CDCl3): δ 1.30 (t, 3H), 3.53 (q, 2H), 3.85 (s, 3H), 4.09 (s, 3H), 8.08 (d, 1H), 8.30 (d, 1H), 8.54 (s, 1H); 19F NMR (300 Mz, CDCl3): δ−63.78 (s, 3F), −59.57 (s, 3F); ESI-MS: 493 (M+H)+, 515(M+Na)+. Mpt. 197-199° C.; LCMS (method SQD13): Ret. Time 0.95 mins, 493 (M+H).
    • Example P7: 4-Ethylsulfonyl-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole (Compound V14.05)
  • Figure US20220104496A1-20220407-C00111
    • Step A: 4-bromo-2-(trifluoromethyl)thiazole
  • Figure US20220104496A1-20220407-C00112
  • A mixture of 2,4-dibromothiazole (24.3 g, 0.1 mol), FSO2CF2COOCH3 (23.0 g, 0.12 mmol) and CuI (19.0 g, 0.1 mol) in 200 ml of DMF was heated for 4 hours at 100° C. Then, the reaction mixture was poured into water and the title compound (22.9 g, 83%) was distilled off at water pump pressure. The product was used without further purification in the next step.
    • Step B: 4-bromo-2-(trifluoromethyl)thiazole-5-carboxylic acid
  • Figure US20220104496A1-20220407-C00113
  • At 60° C., n-BuLi (2.5M in hexane, 62 mmol) was slowly added to i-Pr2NH (6 g, 59 mmol) in 150 ml of anhydrous THF under a nitrogen atmosphere. After the addition, the mixture was stirred at the same temperature for another 0.5 hours. Then, 4-bromo-2-(trifluoromethyl)thiazole (12 g, 52.0 mmol) was slowly added to the above mixture and stirring was continued for 20 min. The mixture was poured into dry ice and stirred for a further hour. The reaction mixture was allowed to warm to ambient temperature, diluted with ethyl acetate and the organic phase washed successively with water and saturated brine, dried over sodium sulfate, filtered and concentrated under vacuum to give the title product (10.1 g, 71%).
    • Step C: 4-bromo-2-(trifluoromethyl)thiazole-5-carbonyl chloride
  • Figure US20220104496A1-20220407-C00114
  • A mixture of 4-bromo-2-(trifluoromethyl)thiazole-5-carboxylic acid (276 mg, 1 mmol) in 10 ml of SOCl2 was refluxed for 4 hours. The excess SOCl2 was distilled off to give the crude title product (295 mg) which was directly used in the next step without further purification.
    • Step D: 4-bromo-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole
  • Figure US20220104496A1-20220407-C00115
  • A mixture of 4-bromo-2-(trifluoromethyl)thiazole-5-carbonyl chloride (477 mg, 1.7 mmol) and N3-methyl-6-(trifluoromethyl)pyridine-3,4-diamine (330 mg, 1.7 mmol, prepared as described in step E, example P4) in 10 ml of toluene was refluxed for 16 h. The reaction mixture was then concentrated in vacuo and the residue purified by column chromatography on silica gel to give the title compound (358 mg, 44%). 1H NMR (300 Mz, DMSO-d6): δ: 3.98 (s, 3H), 8.30 (s, 1H), 9.28 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−61.58 (s, 3F), −57.88 (s, 3F); ESI-MS: 433 (M+H)+.
    • Step E: 4-Ethylsulfanyl-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole
  • Figure US20220104496A1-20220407-C00116
  • EtSNa (123 mg, 1.5 mmol) was added to a mixture of 4-bromo-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole (315 mg, 0.7 mmol) in 10 ml of DMF. After the addition, the mixture was stirred at room temperature for 2 hours. Then the mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel to give the title compound (176 mg, 58%). 1H NMR (300 Mz, DMSO-d6): δ 1.25 (t, 3H), 3.18 (q, 2H), 4.02 (s, 3H), 8.25 (s, 1H), 9.24 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−59.80 (s, 3F), −55.95 (s, 3F); ESI-MS: 413(M+H)+. LCMS (method SQD13): Rt. 1.12 mins, 413 (M+H) Mpt. 92-94° C.
    • Step F: 4-ethylsulfonyl-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole (Compound V14.05)
  • Figure US20220104496A1-20220407-C00117
  • A mixture of 4-ethylsulfanyl-5-[3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridin-2-yl]-2-(trifluoromethyl)thiazole (109 mg, 0.3 mmol) and m-CPBA (228 mg, 1.3 mmol) in 15 ml of CH2Cl2 was stirred for 2 h at room temperature. The reaction mixture was diluted with saturated sodium sulfite and aqueous sodium bicarbonate, and the organic layer separated, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel to give the title compound (71 mg, 61%). 1H NMR (300 Mz, DMSO-d6): δ 1.16 (t, 3H), 3.51 (q, 2H), 3.89 (s, 3H), 8.28 (s, 1H), 9.27 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−59.81 (s, 3F), −55.74 (s, 3F); ESI-MS: 445(M+H)+, 467 (M+Na)+, 499 (M+MeOH+Na)+.
    • Example P8: 4-ethylsulfonyl-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole (Compound V2.11)
  • Figure US20220104496A1-20220407-C00118
    • Step A: 4-bromo-N-methoxy-N-methyl-2-(trifluoromethyl)thiazole-5-carboxamide
  • Figure US20220104496A1-20220407-C00119
  • A mixture of 4-bromo-2-(trifluoromethyl)thiazole-5-carboxylic acid (5.8 g, 21 mmol, prepared as described as described in Step B, example P7), N,O-dimethylhydroxylamine hydrochloride (2.5 g, 25 mmol), HATU (9.6 g, 25 mmol), and DIPEA (5.4 g, 42 mmol) in 35 ml of DMF was stirred at room temperature for 16 h. The mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (4.7 g, 70%). 1H NMR (300 Mz, DMSO-d6): δ 3.27 (s, 3H), 3.68 (s, 3H); 19F NMR (300 Mz, DMSO-d6): δ−56.33 (s, 3F); ESI-MS: 341(M+Na)+.
    • Step B: 1-[4-bromo-2-(trifluoromethyl)thiazol-5-yl]ethanone
  • Figure US20220104496A1-20220407-C00120
  • MeMgBr (3M in THF, 15 ml, 45 mmol) was added dropwise to a solution of 4-bromo-N-methoxy-N-methyl-2-(trifluoromethyl)thiazole-5-carboxamide (5.7 g, 21 mmol) in 30 ml of dry THF under nitrogen atmosphere at 0° C. After the addition, the mixture was allowed to warm to ambient temperature and stirred for 30 min. The mixture was then poured into diluted hydrochloric acid and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel to give the title product (4.8 g, 86%). 1H NMR (300 Mz, DMSO-d6): δ 2.68 (s, 3H); 19F NMR (300 Mz, DMSO-d6): δ−66.14 (s, 3F).
    • Step C: 4-bromo-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole
  • Figure US20220104496A1-20220407-C00121
  • A mixture of 1-[4-bromo-2-(trifluoromethyl)thiazol-5-yl]ethanone (220 mg, 1 mmol), 2-amino-4-(trifluoromethyl)pyridine (193 mg, 1.2 mmol, prepared as described in WO 2011090122), Cu(OAc)2.H2O (12 mg, 0.1 mmol), 1,10-Phenanthroline (18 mg, 0.1 mmol), Znl2 (32 mg, 0.1 mmol) in 12 ml of dichlorobenzene was stirred at 120° C. for 16 h under an air atmosphere. The mixture was concentrated in vacuo and the residue was purified by column chromatography on silica gel to give the title compound (153 mg, 36%). 1H NMR (300 Mz, DMSO-d6): δ 7.25 (d, 1H), 8.12 (s, 1H), 8.84 (d, 1H), 8.96 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−64.34 (s, 3F), −62.89 (s, 3F); ESI-MS(−): 414(M−H)−; HPLC: 97.7%.
    • Step D: 4-ethylsulfanyl-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole
  • Figure US20220104496A1-20220407-C00122
  • EtSNa (157 mg, 1.9 mmol) was added to a mixture of 4-bromo-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole (389 mg, 0.9 mmol) in 15 ml of DMF. After the addition, the mixture was stirred at ambient temperature for 2 hours. The reaction mixture was then poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (281 mg, 76%). 1H NMR (300 Mz, DMSO-d6): δ 1.28 (t, 3H), 3.23 (q, 2H), 7.24 (d, 1H), 8.11 (s, 1H), 8.75 (s, 1H), 8.86 (d, 1H); 19F NMR (300 Mz, DMSO-d6): δ−66.81 (s, 3F), −65.09 (s, 3F); ESI-MS(+): 398(M+H)+; HPLC: 96.3%.
    • Step E: 4-ethylsulfonyl-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole (Compound V2.11)
  • Figure US20220104496A1-20220407-C00123
  • A mixture of 4-ethylsulfanyl-2-(trifluoromethyl)-5-[7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]thiazole (80 mg, 0.2 mmol) and m-CPBA (105 mg, 0.6 mmol) in 10 ml of CH2Cl2 was stirred at ambient temperature for 2 hours. Then the mixture was washed with saturated sodium sulfite and aqueous sodium bicarbonate. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel to give the title compound (66 mg, 77%). 1H NMR (300 Mz, DMSO-d6): δ 1.22 (t, 3H), 3.57 (q, 2H), 7.27 (d, 1H), 8.16 (s, 1H), 8.94 (d, 2H); 19F NMR (300 Mz, DMSO-d6): δ−48.60 (s, 3F), −50.52 (s, 3F); ESI-MS(+): 430(M+H)+; HPLC: 96.9%. Mpt. 126-128° C.
    • Example P9: 3-methyl-2-[3-methylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)imidazo[4,5-c]pyridine (Compound V12.18)
  • Figure US20220104496A1-20220407-C00124
    • Step A: 3-methylsulfonyl-5-(trifluoromethyl)pyridine-2-carbonyl chloride
  • Figure US20220104496A1-20220407-C00125
  • 3-methylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxylic acid (1.0 g, 3.7 mmol, prepared as described in US 20100234603) was suspended in SOCl2 (5 mL), 1 drop of DMF was added to the mixture. The reaction mixture was heated to reflux, and stirred for 3 h. Then it was evaporated to dryness under reduced pressure to give the title compound as white solid (1.1 g, 100%). The residue was used directly for next step without further purification.
    • Step B: N-[5-(methylamino)-2-(trifluoromethyl)-4-pyridyl]-3-methylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxamide
  • Figure US20220104496A1-20220407-C00126
  • To a solution of 3-methylsulfonyl-5-(trifluoromethyl)pyridine-2-carbonyl chloride (80 mg, 0.3 mmol) in 5 ml of toluene was added compound N3-methyl-6-(trifluoromethyl)pyridine-3,4-diamine (60 mg, 1.1 mmol, prepared as described in Step E, example P4), then the reaction mixture was warmed to 100° C. for 5 hours. After that, it was cooled to room temperature and diluted with 15 ml of water and extracted three times with EtOAc. The combined organic layers were dried over sodium sulphate and purified by column chromatography on silica gel (EtOAc:Petroleum ether=1/4) to give the title compound as a white solid (50 mg, 40% yield).
    • Step C: 3-methyl-2-[3-methylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)imidazo[4,5-c]pyridine (Compound V12.18)
  • Figure US20220104496A1-20220407-C00127
  • 5-methyl-N-[2-methyl-5-(methylamino)-4-pyridyl]-3-methylsulfonyl-pyridine-2-carboxamide (85 mg, 0.2 mmol) was added to 5 ml of acetic acid and the reaction mixture warmed to 100° C. for 12 h. The reaction mixture was cooled to room temperature and diluted with 20 ml of water and extracted three times with EtOAc. The combined organic layers were dried over sodium sulphate and purified by column chromatography on silica gel (EtOAc:Petroleum ether=1/4) to give the title compound as a white solid (40 mg, 50% yield). 1H NMR (300 MHz, CDCl3) δ 3.65 (s, 3H), 3.94 (s, 3H), 8.11 (s, 1H), 8.82 (s, 1H), 9.01 (s, 1H), 9.24 (s, 1H). 19F NMR (300 Mz, CDCl3) δ−67.27 (s, 3H), δ−63.34 (s, 3H). ESI-MS: 425(M+1). Mpt. 234-236° C. LCMS (method SQD 13) Rt. 0.93 min, 425 (M+H).
    • Example P10: 2-[2-ethylsulfonyl-6-(trifluoromethyl)-3-pyridyl]-7-(trifluoromethyl)imidazo[1,2-a]pyridine (Compound V3.05)
  • Figure US20220104496A1-20220407-C00128
    • Step A: 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carbonyl chloride
  • Figure US20220104496A1-20220407-C00129
  • A mixture of 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carboxylic acid (502 mg, 2 mmol, prepared as described in step I, example P6) in 10 ml of SOCl2 was refluxed for 4 hours. Then, the excess SOCl2 was evaporated to give the title compound (538 mg, 100%), which was directly used for the next step without further purification.
    • Step B: 2-ethylsulfanyl-N-methoxy-N-methyl-6-(trifluoromethyl)pyridine-3-carboxamide
  • Figure US20220104496A1-20220407-C00130
  • A mixture of the crude product 2-ethylsulfanyl-6-(trifluoromethyl)pyridine-3-carbonyl chloride (538 mg, 2 mmol), N,O-dimethylhydroxylamine hydrochloride (588 mg, 6 mmol) and K2CO3 (1.66 g, 12 mmol) in 10 ml of THF and 1 ml of water was stirred at room temperature for 10 min. Then, the mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (411 mg, y: 70%). 1H-NMR (300 Mz, DMSO-d6): δ 1.23 (t, 3H), 3.10 (q, 2H), 3.23 (s, 3H), 3.45 (s, 3H), 7.64 (d, 1H), 7.94 (d, 1H); 19F NMR (300 Mz, DMSO-d6): δ−62.44 (s, 3F).
    • Step C: 1-[2-ethylsulfanyl-6-(trifluoromethyl)-3-pyridyl]ethanone
  • Figure US20220104496A1-20220407-C00131
  • To a solution of 2-ethylsulfanyl-N-methoxy-N-methyl-6-(trifluoromethyl)pyridine-3-carboxamide (411 mg, 1.4 mmol) in 10 ml of THF was added 1.4 ml of MeMgBr (3M in THF) at room temperature and the reaction allowed to stir for 30 min. Then, the mixture was poured into water and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (290 mg, y: 83%). 1H-NMR (300 Mz, DMSO-d6): δ 1.22 (t, 3H), 2.60 (s, 3H), 3.02 (q, 2H), 7.71 (d, 1H), 7.52 (d, 1H); 19F-NMR (300 Mz, DMSO-d6): δ−67.93 (s, 3F).
    • Step D: 2-[2-ethylsulfanyl-6-(trifluoromethyl)-3-pyridyl]-7-(trifluoromethyl)imidazo[1,2-a]pyridine
  • Figure US20220104496A1-20220407-C00132
  • A mixture of 1-[2-ethylsulfanyl-6-(trifluoromethyl)-3-pyridyl]ethanone (249 mg, 1 mmol), 4-(trifluoromethyl)pyridin-2-amine (162 mg, 1.2 mmol), Cu(OAc)2.H2O (12 mg, 0.1 mmol), Znl2 (32 mg, 0.1 mmol) and 1,10-phenanthroline (18 mg, 0.1 mmol) in 5 ml of dichlorobenzene was stirred at 130° C. for 48 h. Then the mixture was concentrated under vacuum and the residue was purified by column chromatography on silica gel to give the title compound (120 mg, y: 30%). 1H NMR (300 Mz, CDCl3): δ 1.39 (t, 3H), 3.29 (q, 2H), 7.00 (dd, 1H), 7.46 (d, 1H), 7.94 (s, 1H), 8.27 (d, 1H), 8.42 (s, 1H), 8.47 (d, 1H); 19F NMR (300 Mz, CDCl3): δ−69.33 (s, 3F), −64.83 (s, 3F); ESI-MS(+): 392 (M+H)+.
    • Step E: 2-[2-ethylsulfonyl-6-(trifluoromethyl)-3-pyridyl]-7-(trifluoromethyl)imidazo[1,2-a]pyridine (Compound V3.05)
  • Figure US20220104496A1-20220407-C00133
  • A mixture of compound 2-[2-ethylsulfanyl-6-(trifluoromethyl)-3-pyridyl]-7-(trifluoromethyl)imidazo[1,2-a]pyridine (156 mg, 0.4 mmol) and m-CPBA (277 mg, 1.6 mmol) in 10 ml of Ddichloromethane was stirred at ambient temperature for 2 hours. Then the mixture was poured into a saturated solution of NaHCO3 and Na2SO3 in water, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (115 mg, y: 68%)1H-NMR (300 Mz, CDCl3): δ 1.50 (t, 3H), 3.74 (q, 2H), 7.01 (dd, 1H), 7.95 (s, 1H), 7.96 (d, 1H), 8.27 (d, 1H), 8.77 (s, 1H), 8.92 (d, 1H); 19F NMR (300 Mz, CDCl3): δ−73.07 (s, 3F), −69.08 (s, 3F); ESI-MS(+): 424(M+H)+. Mpt. 188-190° C. LCMS (method SQD 13): Rt. 1.07 mins, 424 (M+H).
    • Example P11: 3-ethylsulfonyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-1,2,5-thiadiazole (Compound A1.014-B8.012)
  • Figure US20220104496A1-20220407-C00134
    • Step A: ethyl (2Z)-2-cyano-2-hydroxyimino-acetate
  • Figure US20220104496A1-20220407-C00135
  • H3PO4 (1.83 mL, 27 mmol) was added to a mixture of ethyl cyanacetate (5 g, 44.2 mmol) and NaNO2 (2.87 g, 41.5 mmol) in 35 mL of water at room temperature. After the addition, the mixture was warmed to 40° C. and stirred for another hour. Then, 3.69 ml of hydrochloric acid was added to the mixture and stirring was continued for 18 hours. The mixture was extracted with diethyl ether three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum. The residue was purified by column chromatography on silica gel to give the title compound (4.3 g, y: 69%) 1H NMR (300 Mz, DMSO-d6): δ 1.28 (t, 3H), 4.32 (q, 2H).
    • Step B: ethyl 2-amino-2-cyano-acetate
  • Figure US20220104496A1-20220407-C00136
  • Na2S2O4 (17 g, 105 mmol) was slowly added to a mixture of ethyl (2Z)-2-cyano-2-hydroxyimino-acetate (5 g, 35 mmol) and NaHCO3 (1.5 g, 17 mmol) in 40 ml of water. Then the mixture was stirred at room temperature for 16 h and extracted with chloroform three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum to give the title compound (3.18 g, y: 71%). 1H NMR (300 Mz, DMSO-d6): δ 1.24 (t, 3H), 3.53 (s, 2H), 4.19 (q, 2H), 4.81 (s, 1H).
    • Step C: ethyl 4-chloro-1,2,5-thiadiazole-3-carboxylate
  • Figure US20220104496A1-20220407-C00137
  • Disulphur dichloride (4.06 g, 30 mmol) was added to a solution of ethyl 2-amino-2-cyano-acetate (1.28 g, 10 mmol) in 10 ml of DMF at ambient temperature. The mixture was stirred at ambient temperature for 16 h and poured into ice, extracted three times with dichloromethane. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum. The residue was purified by column chromatography on silica gel to give the title compound (1.2 g, y: 63%). 1H NMR (300 Mz, DMSO-d6): δ 1.35 (t, 3H), 4.39 (q, 2H).
    • Step D: ethyl 4-ethylsulfanyl-1,2,5-thiadiazole-3-carboxylate
  • Figure US20220104496A1-20220407-C00138
  • Na2S.9H2O (2.4 g, 10 mmol) in 10 ml of water was added to a solution of ethyl 4-chloro-1,2,5-thiadiazole-3-carboxylate (1.92 g, 10 mmol) in 30 mL of ethanol and the mixture was refluxed for 4 h. Then the mixture was concentrated in vacuo and a solution of bromoethane (3.24 g, 30 mmol) in 10 ml of DMF was added. The reaction mixture was stirred at ambient temperature for 16 hours, poured into dilute hydrochloric acid and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum. The residue was purified by column chromatography on silica gel to give the title compound (1.57 g, y: 72%). 1H NMR (300 Mz, DMSO-d6): δ 1.34 (t, 3H), 1.36 (t, 3H), 3.19 (q, 2H), 4.37 (q, 2H); ESI-MS (+): 219 (M+H)+, 241 (M+Na)+.
    • Step E: 4-ethylsulfanyl-1,2,5-thiadiazole-3-carboxylic acid
  • Figure US20220104496A1-20220407-C00139
  • A mixture of ethyl 4-ethylsulfanyl-1,2,5-thiadiazole-3-carboxylate (680 mg, 3.12 mmol) and LiOH (240 mg, 10 mmol) in 5 ml of water and 5 ml of THF was stirred at room temperature for 2 h. Then, the reaction mixture was poured into diluted hydrochloric acid and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to provide product the title compound (550 mg, y: 93%). 1H NMR (300 Mz, DMSO-d6): δ 1.35 (t, 3H), 3.12 (q, 2H).
    • Step F: 3-ethylsulfanyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-1,2,5-thiadiazole (Compound A1.014-B8.010)
  • Figure US20220104496A1-20220407-C00140
  • A mixture of 4-ethylsulfanyl-1,2,5-thiadiazole-3-carboxylic acid (570 mg, 3 mmol), N2-methyl-5-(trifluoromethyl)pyridine-2,3-diamine (669 mg, 3.5 mmol, prepared as described in WO 2012092051) and EDC.HCl (672 mg, 3.5 mmol) in 5 ml of pyridine was refluxed for 16 h. Then, the mixture was concentrated under vacuum and purified by column chromatography on silica gel to give the title compound (621 mg, y: 60%). 1H-NMR (300 Mz, DMSO-d6): δ 1.41 (t, 3H), 3.27 (q, 2H), 4.24 (s, 3H), 8.73 (s, 1H), 8.90 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−53.72 (s, 3F); ESI-MS(+): 346 (M+H)+. LCMS (method SQD13): Rt. 1.21 mins, 346 (M+H) Mpt. 188-189° C.
    • Step G: 3-ethylsulfonyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-1,2,5-thiadiazole (Compound A1.014-B8.012)
  • Figure US20220104496A1-20220407-C00141
  • 3-ethylsulfanyl-4-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-1,2,5-thiadiazole (0.87 mmol, 300 mg) and m-CPBA (519 mg, 3 mmol) in 10 ml of DCM was stirred at room temperature for 4 h. Then the mixture was poured into a saturated solution of NaHCO3 and Na2SO3 in water, and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give the title compound (245 mg, 75%). 1H NMR (300 Mz, DMSO-d6): δ 1.31 (t, 3H), 3.97 (q, 2H), 4.00 (s, 3H), 8.76 (s, 1H), 8.94 (s, 1H); 19F NMR (300 Mz, DMSO-d6): δ−53.85 (s, 3F); ESI-MS(+): 378 (M+H)+, 400 (M+Na)+, 432 (M+Na+MeOH)+. LCMS (method SQD13): Rt. 0.93 mins, 378 (M+H) Mpt. 144-146° C.
    • Example P12: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl) [1,2,4]triazolo[1,5-c]pyrimidine (Compound V16.03)
  • Figure US20220104496A1-20220407-C00142
    • Step A: 4-(trifluoromethyl)pyrimidin-1-ium-1,6-diamine, 2,4,6-trimethylbenzenesulfonate salt (MSH)
  • Figure US20220104496A1-20220407-C00143
  • Caution: MSH is explosively unstable as a dry powder and is best handled in dichloromethane solution.
  • A Microwave tube, equipped with a magnetic stirrer bar, was charged with 2,2,2-trifluoroacetic acid (4.4 g, 2.54 mmol, 2.9 mL). Then, (tert-butoxycarbonylamino) 2,4,6-trimethylbenzenesulfonate (1 g, 2.54 mmol) was added at 0° C. The reaction mixture was stirred at 0° C. for 2 h, ice-water was added and the precipitate was recovered by filtration. The wet cake was washed with water and dissolved in dichloromethane (5 mL) and dried over sodium sulfate. The resulting solution was added dropwise to a stirred solution of 6-(trifluoromethyl)pyrimidin-4-amine (0.3723 g, prepared as in WO2007113558) in dichloromethane (5 mL) at 0° C. After 1 hour at 0° C. and one night at RT (white suspension), the reaction mixture was diluted with diethyl ether (8 mL) and the precipitate was recovered by filtration to afford the title compound (0.791 g, 82%).
    • Step B: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)-[1,2,4]triazolo[1,5-c]pyrimidine (Compound V16.03)
  • Figure US20220104496A1-20220407-C00144
  • 4-(trifluoromethyl)pyrimidin-1-ium-1,6-diamine, 2,4,6-trimethylbenzenesulfonate salt (0.3 g, 0.791 mmol), 3-ethylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxylic acid (0.33593 g, 1.1861 mmol) and 3-(ethyliminomethyleneamino)-N,N-dimethyl-propan-1-amine hydrochloride (0.1819098 g, 0.9489 mmol) was dissolved in pyridine (2 mL) and heated for for 3 h at 120° C. After this time, the reaction mixture was poured on water, the aqueous layer was extracted three times with EtOAc. The combined organic layer were washed successively with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was triturated with diethylether, and filtered to give the product as a white powder (110 mg, 33%).
  • 1H NMR (400 MHz, CDCl3): δ (ppm) 9.31 (d, J=2.2 Hz, 1H), 9.17 (d, J=1.5 Hz, 1H), 8.34-8.53 (m, 1H), 3.23 (q, J=7.5 Hz, 2H), 1.37 (t, J=7.5 Hz, 3H). LCMS (method SQD13): Rt: 0.94 min, 426 (M+H). Mpt.: 190-192° C.
    • Example P13: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)oxazolo[5,4-c]pyridine (Compound V12.05)
  • Figure US20220104496A1-20220407-C00145
    • Step A: 4-nitro-6-(trifluoromethyl)pyridin-3-ol
  • Figure US20220104496A1-20220407-C00146
  • To a solution of 6-(trifluoromethyl)pyridin-3-ol (5.00 g, 30.7 mmol) in sulfuric acid (92.0 mL) at 0° C. was added Ice (25.0 g, 1390 mmol) keeping the temperature below 10° C. To this solution was added nitric acid (2.97 g, 2.14 mL, 30.7 mmol) and the mixture was heated at 85° C. for 4 hours. A second portion of nitric acid (2.97 g, 2.14 mL, 30.7 mmol) was added and the reaction was stirred over night at 85° C. LCMS analysis showed ca. 40% conversion and thus nitric acid (2.97 g, 2.14 mL, 30.7 mmol) was added and the reaction was stirred 5 h at 85° C. A further portion of nitric acid (2.97 g, 2.14 mL, 30.7 mmol) was added and the reaction was stirred over night at 85° C. After this time, the mixture was poured into ice water and extracted with 250 mL of Et2O. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography, eluting with dichloromethane to give the title compound (18% yield). 1H NMR (400 MHz, CDCl3): 10.32 (s, 1H), 8.82 (s, 1H), 8.30 (s, 1H) ppm.
    • Step B: 4-amino-6-(trifluoromethyl)pyridin-3-ol
  • Figure US20220104496A1-20220407-C00147
  • To a solution of 4-nitro-6-(trifluoromethyl)pyridin-3-ol (1.15 g, 5.53 mmol) in ethanol (50 mL) and tetrahydrofuran (10 mL) was added Palladium on carbon (0.12 g) under argon. A hydrogen atmosphere was applied (balloon) and the mixture was stirred over night at room temperature. After complete reduction, the mixture was filtered over celite and the cake washed with ethanol. The solvent was removed in vacuo and the residue was purified by flash chromatography (cyclohexane/ethyl acetate) to give the title compound (0.98 g, quantitative) as a red gum. 1H NMR (400 MHz, CDCl3): 7.92 (s, 1H), 6.92 (s, 1H), 4.75 (s, 2H) ppm.
    • Step C: 2-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)oxazolo[5,4-c]pyridine. (Compound A6.006-B1.014)
  • Figure US20220104496A1-20220407-C00148
  • To a solution of 4-amino-6-(trifluoromethyl)pyridin-3-ol (100 mg, 0.56 mmol) and 3-ethylsulfanyl-5-(trifluoromethyl)pyridine-2-carboxylic acid (155 mg, 0.62 mmol, prepared as described in WO 2013018928) in polyphosphoric acid (2 mL) were stirred at 185° C. for 24 hours. The reaction mixture was then poured into water (50 mL) under vigorous stirring, and the pH was adjusted to 8 with NaOH (2N). The aqueous phase was extracted with dichloromethane (×2), and the combined organic phases and dried over sodium sulphate. The solvent was evaporated in vacuo and the residue was purified by flash chromatography (cyclohexane/ethyl acetate) to give the title compound (75 mg, 34%).
  • 1H NMR (400 MHz, CDCl3): 9.20 (s, 1H), 8.82 (s, 1H), 8.32 (s, 1H), 7.98 (s, 1H), 3.14 (q, 2H), 1.54 (t, 3H) ppm. LCMS (method SQD13): Rt: 1.15 min, 394 (M+H).
    • Step D: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)oxazolo[5,4-c]pyridine (Compound V12.05)
  • Figure US20220104496A1-20220407-C00149
  • To a solution of 2-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)oxazolo[5,4-c]pyridine (60 mg, 0.153 mmol) in dichloromethane (10 mL) was added m-CPBA (83 mg, 0.34 mmol). The resulting yellow solution was stirred for 1 hour at room temperature and then a further 60 mg of m-CPBA were added. The reaction mixture was stirred for a further 2 h at room temperature and then poured into a saturated solution of potassium carbonate. The aqueous phase was extracted 2 times with dichloromethane and the combined organic phases dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (cyclohexane/ethyl acetate) to give the title compound (49 mg, 75%) as a white powder (75%).
  • 1H NMR (400 MHz, CDCl3): 9.28 (s, 1H), 9.22 (s, 1H), 8.84 (s, 1H), 8.24 (s, 1H), 3.98 (q, 2H), 1.48 (t, 3H) ppm. LCMS (method SQD13): Rt. 1.02 min, 426 (M+H+).
    • Example P14: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine (Compound V16.02)
  • Figure US20220104496A1-20220407-C00150
    • Step A: 1-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]ethanone
  • Figure US20220104496A1-20220407-C00151
  • A solution of bromo(methyl)magnesium (1.4 M in THF:Toluen 1:3, 14 MI, 18.95 mmol) toluene dry (90 mL) was cooled to 0° C. and treated dropwise with a solution of 3-ethylsulfanyl-5-(trifluoromethyl)pyridine-2-carbonitrile (4.00 g, 17.23 mmol, prepared as described in WO 2013018928) dissolved in 30 ml of toluene. The reaction was allowed to stir for 30 min. at 0° C. LCMS analysis after this time showed reaction completion. The reaction mixture was slowly quenched with NH4Cl sat aq (50 ml) and HCl 10% (30 ml) and the resulting mixture vigorously stirred for 15 min at room temperature. The aqueous layer was extracted twice with EtOAc, and the combined organic phases washed successively with 10% HCl aq, water and brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The crude title product (4.335 g, 91%) was used without purification for the next step.
  • 1H NMR (400 MHz, CDCl3): δ (ppm) 8.62 (s, 1H), 7.85 (d, J=1.1 Hz, 1H), 2.96 (q, J=7.3 Hz, 2H), 2.74 (s, 3H), 1.43 (t, J=7.5 Hz, 3H). LCMS (method SQD13): Ret. Time 1.05 min, 250 (M+H).
    • Step B: 1-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]ethanone
  • Figure US20220104496A1-20220407-C00152
  • At 0° C. m-CPBA (24.29 g, 98.53 mmol) was added portionwise to a solution of 1-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]ethanone (11.98 g, 48.06 mmol) in chloroform (400 mL) at 0° C. The resulting mixture was allowed to warm up to RT and stirred for 20 h. The reaction mixture was then quenched with 200 mL NaHCO3 aq. and 50 mL saturated sodium thiosulfate aqueous solution and extracted with three times with EtOAc. The combined organic phases were washed successively with aqueous NaHCO3 and brine, dried over Na2SO4 and concentrated in vacuo. Purification on a 220 g column on the torrent machine eluting with EtOAc/heptane gave the title compound (8.5 g, 63%) as a white solid.
  • 1H NMR (400 MHz, CDCl3): δ (ppm) 9.07 (d, J=1.1 Hz, 1H), 8.59 (d, J=1.5 Hz, 1H), 3.58 (q, J=7.3 Hz, 2H), 2.74 (s, 3H), 1.38 (t, J=7.5 Hz, 3H). LCMS (method SQD13): Ret. Time 0.87 min, 282 (M+H).
    • Step C: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine
  • Figure US20220104496A1-20220407-C00153
  • A mixture of 6-(trifluoromethyl)pyrimidin-4-amine (232 mg, 1.0607 mmol, prepared as described in WO2007113558), 1-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]ethanone (200 mg, 0.71 mmol), copper(I)iodide (7.0 mg, 0.036 mmol), In(III)triflate (4.0 mg, 0.0071 mmol) and 1-methyl-2-pyrrolidone (4 mL) were stirred for 19 hr at 120° C. LC-MS: desired product and starting material, and thus the reaction was stirred for a further 27 hr at 120° C. Reaction mixture was cooled to ambient temperature and water and ethylacetate were added. Aqueous layer was extracted 2 times with ethylacetate and the combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The product was purified by combiflash chromatography with column of 12 g and a gradient of cyclohexane+0-80% ethylacetate, to give the title compound (96 mg, 31%) as a white solid. 1H NMR (400 MHz, CDCl3): δ (ppm) 9.20 (s, 1H), 9.14 (s, 1H), 8.80 (d, J=1.5 Hz, 1H), 8.44 (s, 1H), 7.99 (s, 1H), 4.10 (q, J=7.5 Hz, 2H), 1.43 (t, J=7.5 Hz, 3H). LCMS (method SQD13): Rt: 0.98 min, 425 (M+H). Mpt. 180-181° C.
    • Example P15: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-3-methyl-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine (Compound V16.01)
  • Figure US20220104496A1-20220407-C00154
    • Step A: 3-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine
  • Figure US20220104496A1-20220407-C00155
  • 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine (52 mg, 0.123 mmol) was dissolved in acetonitrile (1 mL) and treated with N-bromosuccinimide (24.5 mg, 0.135 mmol) at ambient temperature. Reaction mixture was stirred over night at room temperature. The reaction mixture was concentrated in vacuo and purified by combiflash chromatography with a column of 4 g and a gradient cyclohexane+0-50% ethylacetate. The title product was obtained as a white solid.
  • 1H NMR (400 MHz, CDCl3): δ (ppm) 9.22 (d, J=0.7 Hz, 1H), 9.20 (s, 1H), 8.77 (d, J=1.5 Hz, 1H), 7.94 (s, 1H), 4.00 (q, J=7.6 Hz, 2H), 1.40-1.47 (t, J=7.6 Hz, 3H). LCMS (method SQD13): Rt: 1.04 min, 503/505 (M+H).
    • Step B: 3-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine (Compound V16.01)
  • Figure US20220104496A1-20220407-C00156
  • A suspension of 3-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-(trifluoromethyl)imidazo[1,2-c]pyrimidine (100 mg, 0.199 mmol) and potassium carbonate (84 mg, 0.60 mmol) in 1,4-dioxane (3 mL) was purged with argon for 10 min and then treated with 2,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinane (30.0 mg, 0.24 mmol, 0.0332 mL) and Pd(Ph3)4 (23 mg, 0.02 mmol). The reaction mixture was heated at 95° C. for 12 hr. LCMS analysis showed the desired product and starting material, and thus the mixture was cooled and purged with argon for 10 min and treated with 2,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinane (30.0 mg, 0.24 mmol, 0.0332 mL) and Pd(Ph3)4 (23 mg, 0.02 mmol). The reaction mixture was heated for a further 5 hr 95° C. until reaction completion. The reaction mixture was diluted with NH4Cl sat sol, and water, and then extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The product was purified by Combiflash chromatography with a column of 12 g and a gradient cyclohexane 0-50% ethylacetate. This gave the title product (51 mg, 59%) as a white solid. 1H NMR (400 MHz, CDCl3): δ (ppm) 9.17 (d, J=1.5 Hz, 1H), 9.01 (s, 1H), 8.77 (d, J=1.5 Hz, 1H), 4.10 (q, J=7.6 Hz, 2H), 2.78 (s, 3H), 1.40-1.47 (t, 7.6 Hz, 3H). LCMS (method SQD13): Rt: 1.01 min, 439 (M+H). Mpt. 240-242° C.
    • Example P16: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-1-methyl-5-(trifluoromethyl)imidazo[4,5-b]pyrazine (Compound A1.026-B1.022)
  • Figure US20220104496A1-20220407-C00157
    • Step A: 3,5-diiodo-N-methyl-pyrazin-2-amine
  • Figure US20220104496A1-20220407-C00158
  • To a stirred solution of N-methylpyrazin-2-amine (1 g, 9.2 mmol) in dimethyl sulfoxide (20 ml)/water (0.4 ml) at 10° C. was added portionwise N-Iodosuccinimide (4.1 g, 18.4 mmol). The reaction mixture was then allowed to warm slowly to room temperature and stirred at that temperature overnight. An additional aliquot of N-Iodosuccinimide (4.1 g, 18.4 mmol) was then added at room temperature. After stirring for 7 hr, the reaction mixture was poured onto ice (20 g). The precipitate was collected, washed with cold water (20 ml), and dried to provide the title compound (2.15 g, 65%). 1H NMR (300 MHz, DMSO-d6) δ (ppm): 8.14 (s, 1H), 6.69 (br, 1H), 2.77 (d, 3H, J=4.5 Hz); ESI-MS(−): 360.
    • Step B: 5-iodo-N2-methyl-pyrazine-2,3-diamine
  • Figure US20220104496A1-20220407-C00159
  • NH3(g) in EtOH (15 ml) was added to 3,5-diiodo-N-methyl-pyrazin-2-amine (2.15 g, 6 mmol) and the mixture was heated to 150° C. in a sealed tube for 18 h. After the solution was cooled, dichloromethane and water (1:1, 200 ml) were added. The aqueous phase was extracted with methylene chloride (50 ml) and the combined organic layers were dried over Na2SO4 and concentrated to give the title compound as a white solid. (1.19 g, 80%). 1H NMR (300 MHz, DMSO-d6) δ (ppm): 7.41 (s, 1H) 6.35 (br, 3H), 2.78 (s, 3H); ESI-MS (−): 249, ESI-MS (+): 251.
    • Step C: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-5-iodo-1-methyl-imidazo[4,5-b]pyrazine
  • Figure US20220104496A1-20220407-C00160
  • This compound was prepared by methods described in the examples above from 5-iodo-N2-methyl-pyrazine-2,3-diamine and 3-ethylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxylic acid.
    • Step D: 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-1-methyl-5-(trifluoromethyl)imidazo[4,5-b]pyrazine (Compound A1.026-B1.022)
  • Figure US20220104496A1-20220407-C00161
  • A mixture of compound 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-5-iodo-1-methyl-imidazo[4,5-b]pyrazine (497 mg, 1 mmol), FSO2CF2COOMe (384 mg, 2 m mol) and CuI (191 mg, 1 mmol) in 5 ml of DMF was stirred at 120° C. under an nitrogen atmosphere for 24 h. Then the mixture was poured into dilute hydrochloric acid and extracted with ethyl acetate three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum. The crude product was purified by column chromatography on silica gel to give the title compound (197.5 mg, Y: 45%). 1H NMR (300 MHz, CDCl3) δ (ppm): 9.26 (s, 1H), 8.88 (s, 1H), 8.75 (s, 1H), 3.98 (m, 5H), 1.42 (t, J=6.9 Hz, 3H). 19F NMR (300 Mz, CDCl3) δ (ppm): −62.15; −65.18. ESI-MS: 440(M+H), 462(M+Na+). Mpt. 162-165° C. LCMS (method SQD13): Rt. 1.04 mins, 440 (M+H).
    • Example P17: 3-methyl-2-[3-(methylsulfonylmethyl)-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)imidazo[4,5-b]pyridine (Compound A.014-B1.106)
  • Figure US20220104496A1-20220407-C00162
  • Ethyl 3-methyl-5-(trifluoromethyl)pyridine-2-carboxylate (1.0 g 4.29 mmol, prepared as described in J. Amer. Chem. Soc., 2013, 135, 12122-12134) was dissolved in acetonitrile (40 ml) and treated with N-bromsuccinamide (1.21 g, 6.43 mmol) and benzoyl peroxide (0.150 g, 0.600 mmol). A sunlamp was used to irradiate the reaction mixture which was heated at reflux (75° C. bath temp.) After 10 hr, the mixture was cooled, filtered, and concentrated in vacuo. The crude product (1.27 g), which contained mainly ethyl 3-(bromomethyl)-5-(trifluoromethyl)pyridine-2-carboxylate, was used in the next step without further purification.
  • Ethyl 3-(bromomethyl)-5-(trifluoromethyl)pyridine-2-carboxylate (0.5 g, 1.6 mmol, prepared as above) was dissolved in DMF, cooled to 0° C., and treated with sodium methanethiolate (0.22 g, 3.2 mmol) The mixture was allowed to warm up to RT and was stirred over night. The reaction mixture was diluted NH4Cl aq., and extracted with TBME (2×). The remaining aqueous layer was acidified with 6N HCl aq and extracted 3× with dichloromethane. The combined dichloromethane layers were dried over Na2SO4, filtered and evaporated to give 0.31 g of a beige solid, which contains the desired 3-(methylsulfanylmethyl)-5-(trifluoromethyl)pyridine-2-carboxylic acid. This was used in the next step without further purification.
  • N2-methyl-5-(trifluoromethyl)pyridine-2,3-diamine (0.24 g, 1.3 mmol, prepared as described in WO 2012092051), EDC.HCl (0.24 g, 1.3 mmol) and 3-(methylsulfanylmethyl)-5-(trifluoromethyl)pyridine-2-carboxylic acid (0.29 g, crude sample from above) were dissolved in pyridine (15 ml). The brown suspension was stirred at 120° C. for 2 h. The reaction mixture was diluted with water, and extracted EtOAc. The organic layer was separated and washed with brine, dried over Na2SO4 and evaporated. The crude product was purified by chromatography on an RF 200 machine eluting with EtOAc/Cylohexane gradient, to give 0.35 g of a beige solid, which contained the desired product N-[2-(methylamino)-5-(trifluoromethyl)-3-pyridyl]-3-(methylsulfanylmethyl)-5-(trifluoromethyl)pyridine-2-carboxamide. This product was dissolved in 1-methylpyrrolidin-2-one (5 ml) with toluene-4-sulphonic acid (0.072 g, 0.41 mmol) and heated in the microwave at 160° C. for 1 h. After this time, the reaction mixture was diluted with water, and extracted with EtOAc. The organic layer was washed with water and brine, dried over sodium sulfate and concentrated in vacuo. Purification over a silica gel cartridge (Rf200), eluting with Cyclohexane/EtOAc gave 3-methyl-2-[3-(methylsulfanylmethyl)-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)imidazo[4,5-b]pyridine (140 mg) as a white solid. LCMS (method SQD13): Rt. 1.17 mins, 407 (M+H).
  • A solution of 3-methyl-2-[3-(methylsulfanylmethyl)-5-(trifluoromethyl)-2-pyridyl]-6-(trifluoromethyl)imidazo[4,5-b]pyridine (100 mg, 0.25 mmol) in dichloromethane was cooled to 0° C. and MCPBA (61 mg, 0.25 mmol) was added at 0° C. LC/MS after 1 h showed sulphoxide and sulphone and thus a further 61 mg of MCPBA was added. Upon reaction completion, the mixture was quenched 2M Na2CO3 and dichloromethane. The organic layer was separated, washed once with water, dried over Na2SO4, filtered and concentrated in vacuo. Purification over a silica gel cartridge (Rf200), eluting with Cyclohexane/EtOAc gave the title compound (80 mg, 70%) as a white solid. LCMS (method SQD13): Rt. 1.02 mins, 439 (M+H). 1H NMR (400 MHz, CDCl3): δ (ppm) 9.08 (d, J=1.5 Hz, 1H), 8.79 (d, J=1.5 Hz, 1H), 8.34-8.36 (m, 1H), 8.33 (d, J=1.8 Hz, 1H), 5.25 (s., 2H), 4.13 (s, 3H), 2.93 (s, 3H).
    • Example P18: 6-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-3-methyl-imidazo[4,5-c]pyridine (Compound V12.20)
  • Figure US20220104496A1-20220407-C00163
    • Step A: 2-bromo-5-fluoro-1-oxido-pyridin-1-ium
  • Figure US20220104496A1-20220407-C00164
  • To a stirred solution of 2-bromo-5-fluoropyridine (5.0 g, 28.4 mmol) in TFA (10.0 mL) was added H2O2 (30%, 15 mL) dropwise at 0° C., the mixture was stirred under reflux overnight. After cooling, the reaction system was poured onto ice-water, extracted with dichloromethane/methanol (10:1, 50 mL×3), the organic layer was washed with saturated sodium bicarbonate solution and brine, and dried over anhydrous sodium sulfate. After filtration and concentration in vacuo, the crude product (off white solid, 4.6 g, y: 84%) was used for the next step without further purification.
    • Step B: 2-bromo-5-fluoro-4-nitro-1-oxido-Pyridin-1-ium
  • Figure US20220104496A1-20220407-C00165
  • To a solution of 2-bromo-5-fluoro-1-oxido-pyridin-1-ium (4.6 g, 23.9 mmol) in sulphuric acid (conc.) (20 mL) was added fuming nitric acid (10 mL) slowly at 0° C. After the addition the reaction temperature was raised to 120° C., and stirring continued at this temperature for 4 h. After cooling to room temperature, the reaction solution was poured onto ice-water. The pH value was adjusted to 1 with NH4OH. The precipitate was filtered and oven dried to afford the title compound (2.3 g, 40%) as light yellow solid.
    • Step C: 6-bromo-N-methyl-4-nitro-1-oxido-pyridin-1-ium-3-amine
  • Figure US20220104496A1-20220407-C00166
  • To a solution of 2-bromo-5-fluoro-4-nitro-1-oxido-pyridin-1-ium (1.1 g, 4.6 mmol) in ethanol (10 mL) was added MeNH2/ethanol (4 mL). The reaction mixture was stirred at room temperature for 4 h. The mixture was concentrated in vacuo to give the title compound as a solid which was used for the next step without further purification.
    • Step D: 6-bromo-N-methyl-4-nitro-pyridin-3-amine
  • Figure US20220104496A1-20220407-C00167
  • To a solution of 6-bromo-N-methyl-4-nitro-1-oxido-pyridin-1-ium-3-amine (crude from above, 4.6 mmol) in dichloromethane (10 mL) was added PBr3 (1.0 mL). The reaction mixture was stirred at ambient temperature for 1 hour. The mixture was dried under vacuum to give the title compound as a jacinth solid and used for the next step without further purification.
    • Step E: 6-bromo-N3-methyl-pyridine-3,4-diamine
  • Figure US20220104496A1-20220407-C00168
  • To a solution of 6-bromo-N-methyl-4-nitro-pyridin-3-amine (crude, 4.6 mmol) in methanol (10 mL) was added Raney Ni (20% wt), and hydrazine hydrate (1.0 mL) was added dropwise at 0° C. The reaction mixture was stirred at room temperature for a few minutes. Raney Ni was filtered off through celite; the filtrate was dried in vacuo and purified with chromatography column on silica gel (dichloromethane:methanol, 10:1) to afford the title compound as a light purple solid (0.6 g, three-step yield, 63%). 1H NMR (400 MHz, DMSO-d6): δ (ppm) 7.20 (s, 1H), 6.65 (s, 1H), 6.54 (brs, 2H), 3.34 (s, 1H), 2.69 (d, J=6.4 Hz, 3H). ESI-MS(+): 203 (M+H).
    • Step F: N-(4-amino-6-bromo-3-pyridyl)-3-ethylsulfonyl-N-methyl-5-(trifluoromethyl)pyridine-2-carboxamide
  • Figure US20220104496A1-20220407-C00169
  • To a stirred solution of 6-bromo-N3-methyl-pyridine-3,4-diamine (0.60 g, 2.96 mmol), 3-ethylsulfonyl-5-(trifluoromethyl)pyridine-2-carboxylic acid (0.92 g, 3.26 mmol, prepared as in WO 2013180194) and HATU (1.4 g, 3.68 mmol) in DMF (5.0 mL) was added DIPEA (1.2 ml, 7.26 mmol). The system was stirred at room temperature overnight. The reaction was diluted with EtOAc and H2O, the organic layer was washed with brine and water, dried over anhydrous sodium sulfate. After filtration and concentration in vacuo, the crude title product was used for the next step without further purification.
    • Step G: 6-bromo-2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-3-methyl-imidazo[4,5-c]pyridine (Compound V12.20)
  • Figure US20220104496A1-20220407-C00170
  • A solution of N-(4-amino-6-bromo-3-pyridyl)-3-ethylsulfonyl-N-methyl-5-(trifluoromethyl)pyridine-2-carboxamide (crude, 2.96 mmol) in acetic acid (5.0 mL) was stirred at 120° C. overnight. The mixture was evaporated to dryness. The residue was purified by chromatography on silica gel (Petroleum ether:EtOAc=4:1) to afford the title compound as white solid (0.65 g, two-step yield: 48%). 1H NMR (400 MHz, DMSO-d6): δ (ppm) 9.53 (s, 1H), 8.94 (s, 1H), 8.74 (s, 1H), 8.01 (s, 1H), 3.83 (q, J=7.6 Hz, 2H), 3.79 (s, 3H), 1.19 (t, J=7.2 Hz, 3H). 19F NMR (300 MHz, DMSO-d6): δ (ppm) −60.42 (s, 3F). ESI-MS(+): 449 (M+H), 472(M+Na); ESI-MS(−): 447 (M−H). Mpt. 188-190° C. LCMS (method SQD13): Rt. 0.95 min, 449/451 (M+H).
    • Example P19: 3-chloro-6-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-methyl-imidazo[4,5-c]pyridazine (Compound V12.17)
  • Figure US20220104496A1-20220407-C00171
    • Step A: 3,6-dichloropyridazin-4-amine
  • Figure US20220104496A1-20220407-C00172
  • 4-Bromo-3,6-dichloro-pyridazine (15.0 g, 65.8 mmol, prepared as described in WO 2008116815) was dissolved in EtOH (73.1 mL) and introduced into an autoclave. At rt, gaseous NH3 (4.48 g, 263 mmol) was introduced, and the reaction mixture was then stirred over night at reflux. The solution was concentrated in vacuo and the residue was triturated with EtOAc, the insoluble part was filtrated off, and the mother liquor evaporated to give the crude product. This was purified by Flash-Chromatography, eluting with cyclohexan/EtOAc 1/1+2.5% Et3N, to give the title compound as a pale brown solid (5.82 g, 53%). LCMS (method ZCQ13): Rt. 0.3 min, 164/166/168 (M+H).
    • Step B: 6-chloro-N3-methyl-pyridazine-3,4-diamine
  • Figure US20220104496A1-20220407-C00173
  • In an autoclave, 3,6-dichloropyridazin-4-amine (2.35 g, 14.3 mmol) was treated with Methylamine dissolved in EtOH (20.2 g, 215 mmol, 26.7 mL) and heated to 100° C. After 48 h at 100° C. LCMS showed no more starting material. The reaction mixture was evaporated to dryness. The crude product was diluted in dichloromethane and 4 ml Et3N was added. The mixture was stirred 5′ at rt and evaporated. The residue was diluted with 5 ml water and the insoluble material was filtrated and dried to give the title product 1.35 g, 57%) as a pale brown solid. LCMS (Method ZCQ13): Rt. 0.17 min, 157/159 (M−H).
    • Step C: N-[6-chloro-3-(methylamino)pyridazin-4-yl]-3-ethylsulfanyl-5-(trifluoromethyl)pyridine-2-carboxamide
  • Figure US20220104496A1-20220407-C00174
  • 6-Chloro-N3-methyl-pyridazine-3,4-diamine (0.3 g, 1.89 mmol) dissolved in Pyridine (14.6 mL), was treated with 3-Ethylsulfanyl-5-(trifluoromethyl)pyridine-2-carboxylic acid (0.499 g, 1.99 mmol, prepared as described in WO 2013018928) and EDCI.HCl (0.4352 g, 2.27 mmol). The reaction mixtures was stirred 4 h at rt, and then treated with a further portion of EDCI.HCl (0.4352 g, 2.27 mmol). The mixture was stirred over night at rt. The reaction mixture was then concentrated in vacuo and the residue taken up in EtOAc and water. The phases were separated and the organic phase washed with brine, dried over Na2SO4, and concentrated in vacuo. The crude product was purified by Flash-Master (Solvent: Cyclohexan/EtOAc 3/1 to give the title compound as a white solid (250 mg, 33%). LCMS (method ZCQ13) Ret. Time 1.01 min, 392/394(M+H).
    • Step D: 3-chloro-6-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]-7-methyl-imidazo[4,5-c]pyridazine (Compound A6.015-B1.014)
  • Figure US20220104496A1-20220407-C00175
  • N-[6-chloro-3-(methylamino)pyridazin-4-yl]-3-ethylsulfanyl-5-(trifluoromethyl)pyridine-2-carboxamide (250 mg, 0.64 mmol) was dissolved in DMF (2 mL) and toluene (8 mL). p-toluenesulfonic acid monohydrate (0.123 g, 0.70 mmol) was added. The bombe tube was closed, and heated to 160° C. for 4 hr. This was then cooled to rt and evaporated to dryness. The residue was purified by Flash-Master (Solvent: Cyclohexan/EtOAc 2/1) to give the title compound (172 mg, 72%) as a yellow solid.
  • 1H NMR (400 MHz, CDCl3): δ (ppm) 8.65-8.88 (m, 1H), 7.86-8.05 (m, 2H), 4.13-4.27 (m, 3H), 3.04 (q, J=7.5 Hz, 2H), 1.41 (t, J=7.5 Hz, 3H). LCMS (method ZCQ13): Ret. Time 1.01 min, 374/376(M+H). Mpt.: 156°-158° C.
    • Step D: 3-chloro-6-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-7-methyl-imidazo[4,5-c]pyridazine (Compound V12.17)
  • Figure US20220104496A1-20220407-C00176
  • 3-chloro-6-[3-ethylsulfanyl-5-(trifluoromethyl)-2-pyridyl]-7-methyl-imidazo[4,5-c]pyridazine (0.14 g, 0.3745 mmol) was dissolved in dichloromethane (8 mL). At 0° C. MCPBA (0.1747 g, 0.7491 mmol) was added, and the mixture was stirred 1 h at 0° C., then 3 h at rt. The reaction was quenched with sat sodium thiosulphate solution. The separated organic phase was washed with aq NaHCO3 and brine, dried over Na2SO4, filtrated and concentrated in vacuo. The crude product was purified by Flash-Master (Solvent: Cyclohexan/EtOAc 1/1) to give the title compound (164 mg, 96%) as a white solid. 1H NMR (400 MHz, CDCl3): δ (ppm) 9.28 (d, J=1.5 Hz, 1H), 8.78 (d, J=1.8 Hz, 1H), 7.71-8.03 (m, 1H), 4.02 (s, 3H), 3.84 (q, J=7.6 Hz, 2H), 1.40 (t, J=7.5 Hz, 3H). LCMS (method ZCQ13): Ret. Time 0.91 min, 406/408 (M+H). Mpt. 228-229° C.
  • Specific examples of compounds of formula (I) are illustrated in the Tables 1 to 130 below, wherein Tables A to K depict the groups B and Tables L to Q depict groups A:

  • A-B  (I)
  • TABLE A
    Radicals of formula B1 (DB denotes a direct bond, i.e. the sulphur is attached directly to
    the aromatic ring)
    B1
    Figure US20220104496A1-20220407-C00177
    Radical R3 R4 V0 V1 V2 m L1
    B1.001 CH3 H C—H N C—H 0 DB
    B1.002 CH3 H C—H N C—CF3 0 DB
    B1.003 CH3 H C—H N C—Br 0 DB
    B1.004 CH3 H C—H N C—Cl 0 DB
    B1.005 CH3 H C—H N C—H 1 DB
    B1.006 CH3 H C—H N C—CF3 1 DB
    B1.007 CH3 H C—H N C—Br 1 DB
    B1.008 CH3 H C—H N C—Cl 1 DB
    B1.009 CH3 H C—H N C—H 2 DB
    B1.010 CH3 H C—H N C—CF3 2 DB
    B1.011 CH3 H C—H N C—Br 2 DB
    B1.012 CH3 H C—H N C—Cl 2 DB
    B1.013 CH2CH3 H C—H N C—H 0 DB
    B1.014 CH2CH3 H C—H N C—CF3 0 DB
    B1.015 CH2CH3 H C—H N C—Br 0 DB
    B1.016 CH2CH3 H C—H N C—Cl 0 DB
    B1.017 CH2CH3 H C—H N C—H 1 DB
    B1.018 CH2CH3 H C—H N C—CF3 1 DB
    B1.019 CH2CH3 H C—H N C—Br 1 DB
    B1.020 CH2CH3 H C—H N C—Cl 1 DB
    B1.021 CH2CH3 H C—H N C—H 2 DB
    B1.022 CH2CH3 H C—H N C—CF3 2 DB
    B1.023 CH2CH3 H C—H N C—Br 2 DB
    B1.024 CH2CH3 H C—H N C—Cl 2 DB
    B1.025 CH3 H C—H CH C—H 0 DB
    B1.026 CH3 H C—H CH C—CF3 0 DB
    B1.027 CH3 H C—H CH C—Br 0 DB
    B1.028 CH3 H C—H CH C—Cl 0 DB
    B1.029 CH3 H C—H CH C—H 1 DB
    B1.030 CH3 H C—H CH C—CF3 1 DB
    B1.031 CH3 H C—H CH C—Br 1 DB
    B1.032 CH3 H C—H CH C—Cl 1 DB
    B1.033 CH3 H C—H CH C—H 2 DB
    B1.034 CH3 H C—H CH C—CF3 2 DB
    B1.035 CH3 H C—H CH C—Br 2 DB
    B1.036 CH3 H C—H CH C—Cl 2 DB
    B1.037 CH2CH3 H C—H CH C—H 0 DB
    B1.038 CH2CH3 H C—H CH C—CF3 0 DB
    B1.039 CH2CH3 H C—H CH C—Br 0 DB
    B1.040 CH2CH3 H C—H CH C—Cl 0 DB
    B1.041 CH2CH3 H C—H CH C—H 1 DB
    B1.042 CH2CH3 H C—H CH C—CF3 1 DB
    B1.043 CH2CH3 H C—H CH C—Br 1 DB
    B1.044 CH2CH3 H C—H CH C—Cl 1 DB
    B1.045 CH2CH3 H C—H CH C—H 2 DB
    B1.046 CH2CH3 H C—H CH C—CF3 2 DB
    B1.047 CH2CH3 H C—H CH C—Br 2 DB
    B1.048 CH2CH3 H C—H CH C—Cl 2 DB
    B1.049 CH2CH3 H N N C—H 0 DB
    B1.050 CH2CH3 H N N C—CF3 0 DB
    B1.051 CH2CH3 H N N C—Br 0 DB
    B1.052 CH2CH3 H N N C—Cl 0 DB
    B1.053 CH2CH3 H N N C—H 1 DB
    B1.054 CH2CH3 H N N C—CF3 1 DB
    B1.055 CH2CH3 H N N C—Br 1 DB
    B1.056 CH2CH3 H N N C—Cl 1 DB
    B1.057 CH2CH3 H N N C—H 2 DB
    B1.058 CH2CH3 H N N C—CF3 2 DB
    B1.059 CH2CH3 H N N C—Br 2 DB
    B1.060 CH2CH3 H N N C—Cl 2 DB
    B1.061 CH3 H N C—H C—H 0 DB
    B1.062 CH3 H N C—H C—CF3 0 DB
    B1.063 CH3 H N C—H C—Br 0 DB
    B1.064 CH3 H N C—H C—Cl 0 DB
    B1.065 CH3 H N C—H C—H 1 DB
    B1.066 CH3 H N C—H C—CF3 1 DB
    B1.067 CH3 H N C—H C—Br 1 DB
    B1.068 CH3 H N C—H C—Cl 1 DB
    B1.069 CH3 H N C—H C—H 2 DB
    B1.070 CH3 H N C—H C—CF3 2 DB
    B1.071 CH3 H N C—H C—Br 2 DB
    B1.072 CH3 H N C—H C—Cl 2 DB
    B1.073 CH2CH3 H N C—H C—H 0 DB
    B1.074 CH2CH3 H N C—H C—CF3 0 DB
    B1.075 CH2CH3 H N C—H C—Br 0 DB
    B1.076 CH2CH3 H N C—H C—Cl 0 DB
    B1.077 CH2CH3 H N C—H C—H 1 DB
    B1.078 CH2CH3 H N C—H C—CF3 1 DB
    B1.079 CH2CH3 H N C—H C—Br 1 DB
    B1.080 CH2CH3 H N C—H C—Cl 1 DB
    B1.081 CH2CH3 H N C—H C—H 2 DB
    B1.082 CH2CH3 H N C—H C—CF3 2 DB
    B1.083 CH2CH3 H N C—H C—Br 2 DB
    B1.084 CH2CH3 H N C—H C—Cl 2 DB
    B1.085 CH3 H C—H C—H N 0 DB
    B1.086 CH3 H C—H C—H N 1 DB
    B1.087 CH3 H C—H C—H N 2 DB
    B1.088 CH2CH3 H C—H C—H N 0 DB
    B1.089 CH2CH3 H C—H C—H N 1 DB
    B1.090 CH2CH3 H C—H C—H N 2 DB
    B1.091 CH3 H C—H N N 0 DB
    B1.092 CH3 H C—H N N 1 DB
    B1.093 CH3 H C—H N N 2 DB
    B1.094 CH2CH3 H C—H N N 0 DB
    B1.095 CH2CH3 H C—H N N 1 DB
    B1.096 CH2CH3 H C—H N N 2 DB
    B1.097 CH3 H C—H N C—H 0 CH2
    B1.098 CH3 H C—H N C—CF3 0 CH2
    B1.099 CH3 H C—H N C—Br 0 CH2
    B1.100 CH3 H C—H N C—Cl 0 CH2
    B1.101 CH3 H C—H N C—H 1 CH2
    B1.102 CH3 H C—H N C—CF3 1 CH2
    B1.103 CH3 H C—H N C—Br 1 CH2
    B1.104 CH3 H C—H N C—Cl 1 CH2
    B1.105 CH3 H C—H N C—H 2 CH2
    B1.106 CH3 H C—H N C—CF3 2 CH2
    B1.107 CH3 H C—H N C—Br 2 CH2
    B1.108 CH3 H C—H N C—Cl 2 CH2
    B1.109 CH2CH3 H C—H C—H C—H 0 CH2
    B1.110 CH2CH3 H C—H C—H C—CF3 0 CH2
    B1.111 CH2CH3 H C—H C—H C—Br 0 CH2
    B1.112 CH2CH3 H C—H C—H C—Cl 0 CH2
    B1.113 CH2CH3 H C—H C—H C—H 1 CH2
    B1.114 CH2CH3 H C—H C—H C—CF3 1 CH2
    B1.115 CH2CH3 H C—H C—H C—Br 1 CH2
    B1.116 CH2CH3 H C—H C—H C—Cl 1 CH2
    B1.117 CH2CH3 H C—H C—H C—H 2 CH2
    B1.118 CH2CH3 H C—H C—H C—CF3 2 CH2
    B1.119 CH2CH3 H C—H C—H C—Br 2 CH2
    B1.120 CH2CH3 H C—H C—H C—Cl 2 CH2
    B1.121 CH2CH3 CH3 C—H N C—H 0 DB
    B1.122 CH2CH3 CH3 C—H N C—CF3 0 DB
    B1.123 CH2CH3 CH3 C—H N C—Br 0 DB
    B1.124 CH2CH3 CH3 C—H N C—Cl 0 DB
    B1.125 CH2CH3 CH3 C—H N C—H 1 DB
    B1.126 CH2CH3 CH3 C—H N C—CF3 1 DB
    B1.127 CH2CH3 CH3 C—H N C—Br 1 DB
    B1.128 CH2CH3 CH3 C—H N C—Cl 1 DB
    B1.129 CH2CH3 CH3 C—H N C—H 2 DB
    B1.130 CH2CH3 CH3 C—H N C—CF3 2 DB
    B1.131 CH2CH3 CH3 C—H N C—Br 2 DB
    B1.132 CH2CH3 CH3 C—H N C—Cl 2 DB
  • TABLE B
    Radicals of Formula B2
    B2
    Figure US20220104496A1-20220407-C00178
    Radical R6 R7 V1 V2 m
    B2.001 CH3 H N C—H 0
    B2.002 CH3 H N C—CF3 0
    B2.003 CH3 H N C—Br 0
    B2.004 CH3 H N C—Cl 0
    B2.005 CH3 H N C—H 1
    B2.006 CH3 H N C—CF3 1
    B2.007 CH3 H N C—Br 1
    B2.008 CH3 H N C—Cl 1
    B2.009 CH3 H N C—H 2
    B2.010 CH3 H N C—CF3 2
    B2.011 CH3 H N C—Br 2
    B2.012 CH3 H N C—Cl 2
    B2.013 CH3 H C—H C—H 0
    B2.014 CH3 H C—H C—CF3 0
    B2.015 CH3 H C—H C—Br 0
    B2.016 CH3 H C—H C—Cl 0
    B2.017 CH3 H C—H C—H 1
    B2.018 CH3 H C—H C—CF3 1
    B2.019 CH3 H C—H C—Br 1
    B2.020 CH3 H C—H C—Cl 1
    B2.021 CH3 H C—H C—H 2
    B2.022 CH3 H C—H C—CF3 2
    B2.023 CH3 H C—H C—Br 2
    B2.024 CH3 H C—H C—Cl 2
    B2.025 CH3 CH3 C—H C—H 0
    B2.026 CH3 CH3 C—H C—CF3 0
    B2.027 CH3 CH3 C—H C—Br 0
    B2.028 CH3 CH3 C—H C—Cl 0
    B2.029 CH3 CH3 C—H C—H 1
    B2.030 CH3 CH3 C—H C—CF3 1
    B2.031 CH3 CH3 C—H C—Br 1
    B2.032 CH3 CH3 C—H C—Cl 1
    B2.033 CH3 CH3 C—H C—H 2
    B2.034 CH3 CH3 C—H C—CF3 2
    B2.035 CH3 CH3 C—H C—Br 2
    B2.036 CH3 CH3 C—H C—Cl 2
  • TABLE C
    Radicals of Formula B3
    B3
    Figure US20220104496A1-20220407-C00179
    Radical R10 V1 V2 m
    B3.001 CH3 N C—H 0
    B3.002 CH3 N C—CF3 0
    B3.003 CH3 N C—Br 0
    B3.004 CH3 N C—Cl 0
    B3.005 CH3 N C—H 2
    B3.006 CH3 N C—CF3 2
    B3.007 CH3 N C—Br 2
    B3.008 CH3 N C—Cl 2
    B3.009 CH3 C—H C—H 0
    B3.010 CH3 C—H C—CF3 0
    B3.011 CH3 C—H C—Br 0
    B3.012 CH3 C—H C—Cl 0
    B3.013 CH3 C—H C—H 2
    B3.014 CH3 C—H C—CF3 2
    B3.015 CH3 C—H C—Br 2
    B3.016 CH3 C—H C—Cl 2
    B3.017 CH3 C—H C—H 0
    B3.018 CH3 C—H C—CF3 0
    B3.019 CH3 C—H C—Br 0
    B3.020 CH3 C—H C—Cl 0
    B3.021 CH3 C—H C—H 2
    B3.022 CH3 C—H C—CF3 2
    B3.023 CH3 C—H C—Br 2
    B3.024 CH3 C—H C—Cl 2
  • TABLE D
    Radicals of formula B4
    B4
    Figure US20220104496A1-20220407-C00180
    Radical R12 V1 V2
    B4.001 CH3 N C—H
    B4.002 CH3 N C—CF3
    B4.003 CH3 N C—Br
    B4.004 CH3 N C—Cl
    B4.005 CH3 C—H C—H
    B4.006 CH3 C—H C—CF3
    B4.007 CH3 C—H C—Br
    B4.008 CH3 C—H C—Cl
  • TABLE E
    Radicals of formula B5
    B5
    Figure US20220104496A1-20220407-C00181
    Radical V1 V2 m
    B5.001 N C—H 0
    B5.002 N C—CF3 0
    B5.003 N C—Br 0
    B5.004 N C—Cl 0
    B5.005 N C—H 1
    B5.006 N C—CF3 1
    B5.007 N C—Br 1
    B5.008 N C—Cl 1
    B5.009 N C—H 2
    B5.010 N C—CF3 2
    B5.011 N C—Br 2
    B5.012 N C—-Cl 2
    B5.013 C—H C—H 0
    B5.014 C—H C—CF3 0
    B5.015 C—H C—Br 0
    B5.016 C—H C—Cl 0
    B5.017 C—H C—H 1
    B5.018 C—H C—CF3 1
    B5.019 C—H C—Br 1
    B5.020 C—H C—Cl 1
    B5.021 C—H C—H 2
    B5.022 C—H C—CF3 2
    B5.023 C—H C—Br 2
    B5.024 C—H C—Cl 2
  • TABLE F
    Radicals of formula B6
    Figure US20220104496A1-20220407-C00182
    Radical R19 V1 V2
    B6.001 C(CH3)3 N C—H
    B6.002 C(CH3)3 N C—CF3
    B6.003 C(CH3)3 N C—Br
    B6.004 C(CH3)3 N C—Cl
    B6.005 C(CH3)3 C—H C—H
    B6.006 C(CH3)3 C—H C—CF3
    B6.007 C(CH3)3 C—H C—Br
    B6.008 C(CH3)3 C—H C—Cl
    B6.009 H N C—H
    B6.010 H N C—CF3
    B6.011 H N C—Br
    B6.012 H N C—Cl
    B6.013 H C—H C—H
    B6.014 H C—H C—CF3
    B6.015 H C—H C-Br
    B6.016 H C—H C—Cl
  • TABLE G
    Radicals of formula B7
    B7
    Figure US20220104496A1-20220407-C00183
    Radical R3 V4 V3 m
    B7.001 CH3 C—H C—H 0
    B7.002 CH3 C—H C—CF3 0
    B7.003 CH3 C—H C—Br 0
    B7.004 CH3 C—H C—Cl 0
    B7.005 CH3 C—H C—H 1
    B7.006 CH3 C—H C—CF3 1
    B7.007 CH3 C—H C—Br 1
    B7.008 CH3 C—H C—Cl 1
    B7.009 CH3 C—H C—H 2
    B7.010 CH3 C—H C—CF3 2
    B7.011 CH3 C—H C—Br 2
    B7.012 CH3 C−H C—Cl 2
    B7.013 CH2CH3 C—H C—H 0
    B7.014 CH2CH3 C—H C—CF3 0
    B7.015 CH2CH3 C—H C—Br 0
    B7.016 CH2CH3 C—H C—Cl 0
    B7.017 CH2CH3 C—H C—H 1
    B7.018 CH2CH3 C—H C—CF3 1
    B7.019 CH2CH3 C—H C—Br 1
    B7.020 CH2CH3 C—H C—Cl 1
    B7.021 CH2CH3 C—H C—H 2
    B7.022 CH2CH3 C—H C—CF3 2
    B7.023 CH2CH3 C—H C—Br 2
    B7.024 CH2CH3 C—H C—Cl 2
    B7.025 CH3 N C—H 0
    B7.026 CH3 N C—CF3 0
    B7.027 CH3 N C—Br 0
    B7.028 CH3 N C—Cl 0
    B7.029 CH3 N C—H 1
    B7.030 CH3 N C—CF3 1
    B7.031 CH3 N C—Br 1
    B7.032 CH3 N C—Cl 1
    B7.033 CH3 N C—H 2
    B7.034 CH3 N C—CF3 2
    B7.035 CH3 N C—Br 2
    B7.036 CH3 N C—Cl 2
    B7.037 CH2CH3 N C—H 0
    B7.038 CH2CH3 N C—CF3 0
    B7.039 CH2CH3 N C—Br 0
    B7.040 CH2CH3 N C—Cl 0
    B7.041 CH2CH3 N C—H 1
    B7.042 CH2CH3 N C−CF3 1
    B7.043 CH2CH3 N C—Br 1
    B7.044 CH2CH3 N C—Cl 1
    B7.045 CH2CH3 N C—H 2
    B7.046 CH2CH3 N C—CF3 2
    B7.047 CH2CH3 N C—Br 2
    B7.048 CH2CH3 N C—Cl 2
    B7.049 CH3 N N 0
    B7.050 CH3 N N 1
    B7.051 CH3 N N 2
    B7.052 CH2CH3 N N 0
    B7.053 CH2CH3 N N 1
    B7.054 CH2CH3 N N 2
  • TABLE H
    Radicals of formula B8
    B8
    Figure US20220104496A1-20220407-C00184
    Radical R3 V5 V6 m
    B8.001 CH3 C—H C—H 0
    B8.002 CH3 C—H C—H 1
    B8.003 CH3 C—H C—H 2
    B8.004 CH2CH3 C—H C—H 0
    B8.005 CH2CH3 C—H C—H 1
    B8.006 CH2CH3 C—H C—H 2
    B8.007 CH3 C—H N 0
    B8.008 CH3 C—H N 1
    B8.009 CH3 C—H N 2
    B8.010 CH2CH3 C—H N 0
    B8.011 CH2CH3 C—H N 1
    B8.012 CH2CH3 C—H N 2
  • TABLE I
    Radicals of formula B9
    B9
    Figure US20220104496A1-20220407-C00185
    Radical R3 V8 V7 m
    B9.001 CH3 C—H C—H 0
    B9.002 CH3 C—H C—CF3 0
    B9.003 CH3 C—H C—Br 0
    B9.004 CH3 C—H C—Cl 0
    B9.005 CH3 C—H C—H 1
    B9.006 CH3 C—H C—CF3 1
    B9.007 CH3 C—H C—Br 1
    B9.008 CH3 C—H C—Cl 1
    B9.009 CH3 C—H C—H 2
    B9.010 CH3 C—H C—CF3 2
    B9.011 CH3 C—H C—Br 2
    B9.012 CH3 C—H C—Cl 2
    B9.013 CH2CH3 C—H C—H 0
    B9.014 CH2CH3 C—H C—CF3 0
    B9.015 CH2CH3 C—H C—Br 0
    B9.016 CH2CH3 C—H C—Cl 0
    B9.017 CH2CH3 C—H C—H 1
    B9.018 CH2CH3 C—H C—CF3 1
    B9.019 CH2CH3 C—H C—Br 1
    B9.020 CH2CH3 C—H C—Cl 1
    B9.021 CH2CH3 C—H C—H 2
    B9.022 CH2CH3 C—H C—CF3 2
    B9.023 CH2CH3 C—H C—Br 2
    B9.024 CH2CH3 C—H C—Cl 2
    B9.025 CH3 C—H N 0
    B9.026 CH3 C—H N 1
    B9.027 CH3 C—H N 2
    B9.028 CH2CH3 C—H N 0
    B9.029 CH2CH3 C—H N 1
    B9.030 CH2CH3 C—H N 2
  • TABLE J
    Radicals of formula B10
    B10
    Figure US20220104496A1-20220407-C00186
    Radical R3 V9 V10 V11 m
    B10.001 CH2CH3 C—H C—H C—H 0
    B10.002 CH2CH3 C—H C—H C—H 1
    B10.003 CH2CH3 C—H C—H C—H 2
    B10.004 CH2CH3 N C—H C—H 0
    B10.005 CH2CH3 N C—H C—H 1
    B10.006 CH2CH3 N C—H C—H 2
    B10.007 CH2CH3 N C—H N 0
    B10.008 CH2CH3 N C—H N 1
    B10.009 CH2CH3 N C—H N 2
    B10.010 CH2CH3 N N N 0
    B10.011 CH2CH3 N N N 1
    B10.012 CH2CH3 N N N 2
  • TABLE K
    Radicals of formula B11
    B11
    Figure US20220104496A1-20220407-C00187
    Radical R3 V1 V0 V2 m
    B11.001 CH3 C—H C—H C—H 0
    B11.002 CH3 C—H C—H C—CF3 0
    B11.003 CH3 C—H C—H C—Br 0
    B11.004 CH3 C—H C—H C—Cl 0
    B11.005 CH3 C—H C—H C—H 1
    B11.006 CH3 C—H C—H C—CF3 1
    B11.007 CH3 C—H C—H C—Br 1
    B11.008 CH3 C—H C—H C—Cl 1
    B11.009 CH3 C—H C—H C—H 2
    B11.010 CH3 C—H C—H C—CF3 2
    B11.011 CH3 C—H C—H C—Br 2
    B11.012 CH3 C—H C—H C—Cl 2
    B11.013 CH3 N C—H C—H 0
    B11.014 CH3 N C—H C—CF3 0
    B11.015 CH3 N C—H C—Br 0
    B11.016 CH3 N C—H C—Cl 0
    B11.017 CH3 N C—H C—H 1
    B11.018 CH3 N C—H C—CF3 1
    B11.019 CH3 N C—H C—Br 1
    B11.020 CH3 N C—H C—Cl 1
    B11.021 CH3 N C—H C—H 2
    B11.022 CH3 N C—H C—CF3 2
    B11.023 CH3 N C—H C—Br 2
    B11.024 CH3 N C—H C—Cl 2
    B11.025 CH2CH3 C—H C—H C—H 0
    B11.026 CH2CH3 C—H C—H C—CF3 0
    B11.027 CH2CH3 C—H C—H C—Br 0
    B11.028 CH2CH3 C—H C—H C—Cl 0
    B11.029 CH2CH3 C—H C—H C—H 1
    B11.030 CH2CH3 C—H C—H C—CF3 1
    B11.031 CH2CH3 C—H C—H C—Br 1
    B11.032 CH2CH3 C—H C—H C—Cl 1
    B11.033 CH2CH3 C—H C—H C—H 2
    B11.034 CH2CH3 C—H C—H C—CF3 2
    B11.035 CH2CH3 C—H C—H C—Br 2
    B11.036 CH2CH3 C—H C—H C—Cl 2
    B11.037 CH2CH3 N C—H C—H 0
    B11.038 CH2CH3 N C—H C—CF3 0
    B11.039 CH2CH3 N C—H C—Br 0
    B11.040 CH2CH3 N C—H C—Cl 0
    B11.041 CH2CH3 N C—H C—H 1
    B11.042 CH2CH3 N C—H C—CF3 1
    B11.043 CH2CH3 N C—H C—Br 1
    B11.044 CH2CH3 N C—H C—Cl 1
    B11.045 CH2CH3 N C—H C—H 2
    B11.046 CH2CH3 N C—H C—CF3 2
    B11.047 CH2CH3 N C—H C—Br 2
    B11.048 CH2CH3 N C—H C—Cl 2
    B11.049 CH2CH3 C—H C—H N 0
    B11.051 CH2CH3 C—H C—H N 1
    B11.052 CH2CH3 C—H C—H N 2
    B11.053 CH2CH3 C—H N C—H 0
    B11.054 CH2CH3 C—H N C—CF3 0
    B11.055 CH2CH3 C—H N C—Br 0
    B11.056 CH2CH3 C—H N C—Cl 0
    B11.057 CH2CH3 C—H N C—H 1
    B11.058 CH2CH3 C—H N C—CF3 1
    B11.059 CH2CH3 C—H N C—Br 1
    B11.060 CH2CH3 C—H N C—Cl 1
    B11.061 CH2CH3 C—H N C—H 2
    B11.062 CH2CH3 C—H N C—CF3 2
    B11.063 CH2CH3 C—H N C—Br 2
    B11.064 CH2CH3 C—H N C—Cl 2
  • TABLE L
    Radicals of formula A1
    A1
    Figure US20220104496A1-20220407-C00188
    Radical R1 R2 G1 G2 G3
    A1.001 CH3 H C—H C—H N—CH3
    A1.002 CF3 H C—H C—H N—CH3
    A1.003 Cl H C—H C—H N—CH3
    A1.004 Br H C—H C—H N—CH3
    A1.005 CH3 H C—H C—H O
    A1.006 CF3 H C—H C—H O
    A1.007 Cl H C—H C—H O
    A1.008 Br H C—H C—H O
    A1.009 CH3 H C—H C—H S
    A1.010 CF3 H C—H C—H S
    A1.011 Cl H C—H C—H S
    A1.012 Br H C—H C—H S
    A1.013 CH3 H C—H N N—CH3
    A1.014 CF3 H C—H N N—CH3
    A1.015 Cl H C—H N N—CH3
    A1.016 Br H C—H N N—CH3
    A1.017 CH3 H C—H N O
    A1.018 CF3 H C—H N O
    A1.019 Cl H C—H N O
    A1.020 Br H C—H N O
    A1.021 CH3 H C—H N S
    A1.022 CF3 H C—H N S
    A1.023 Cl H C—H N S
    A1.024 Br H C—H N S
    A1.025 CH3 H N N N—CH3
    A1.026 CF3 H N N N—CH3
    A1.027 Cl H N N N—CH3
    A1.028 Br H N N N—CH3
    A1.029 CH3 H N N O
    A1.030 CF3 H N N O
    A1.031 Cl H N N O
    A1.032 Br H N N O
    A1.033 CH3 H N N S
    A1.034 CF3 H N N S
    A1.035 Cl H N N S
    A1.036 Br H N N S
  • TABLE M
    Radicals of formula A2
    A2
    Figure US20220104496A1-20220407-C00189
    Radical R1 R2 G1 G2 G5
    A2.001 CH3 H C—H C—H N
    A2.002 CF3 H C—H C—H N
    A2.003 Cl H C—H C—H N
    A2.004 Br H C—H C—H N
    A2.005 CH3 H C—H N N
    A2.006 CF3 H C—H N N
    A2.007 Cl H C—H N N
    A2.008 Br H C—H N N
    A2.009 CH3 H N N N
    A2.010 CF3 H N N N
    A2.011 Cl H N N N
    A2.012 Br H N N N
    A2.013 CH3 H C—H C—H C—CH3
    A2.014 CF3 H C—H C—H C—CH3
    A2.015 Cl H C—H C—H C—CH3
    A2.016 Br H C—H C—H C—CH3
    A2.017 CH3 H C—H N C—CH3
    A2.018 CF3 H C—H N C—CH3
    A2.019 Cl H C—H N C—CH3
    A2.020 Br H C—H N C—CH3
    A2.021 CH3 H N N C—CH3
    A2.022 CF3 H N N C—CH3
    A2.023 Cl H N N C—CH3
    A2.024 Br H N N C—CH3
  • TABLE N
    Radicals of formula A3
    A3
    Figure US20220104496A1-20220407-C00190
    Radical R1 R2 G1 G2 G4
    A3.001 CH3 H C—H C—H N
    A3.002 CF3 H C—H C—H N
    A3.003 Cl H C—H C—H N
    A3.004 Br H C—H C—H N
    A3.005 CH3 H C—H N N
    A3.006 CF3 H C—H N N
    A3.007 Cl H C—H N N
    A3.008 Br H C—H N N
    A3.009 CH3 H N N N
    A3.010 CF3 H N N N
    A3.011 Cl H N N N
    A3.012 Br H N N N
    A3.013 CH3 H C—H C—H C—CH3
    A3.014 CF3 H C—H C—H C—CH3
    A3.015 Cl H C—H C—H C—CH3
    A3.016 Br H C—H C—H C—CH3
    A3.017 CH3 H C—H N C—CH3
    A3.018 CF3 H C—H N C—CH3
    A3.019 Cl H C—H N C—CH3
    A3.020 Br H C—H N C—CH3
    A3.021 CH3 H N N C—CH3
    A3.022 CF3 H N N C—CH3
    A3.023 Cl H N N C—CH3
    A3.024 Br H N N C—CH3
  • TABLE O
    Radicals of formula A4
    A4
    Figure US20220104496A1-20220407-C00191
    Radical J2 J3 G1 G2 G3
    A4.001 C—H O C—H C—H N—CH3
    A4.002 C—CF3 O C—H C—H N—CH3
    A4.003 C—H S C—H C—H N—CH3
    A4.004 C—CF3 S C—H C—H N—CH3
    A4.005 C—H O C—H N N—CH3
    A4.006 C—CF3 O C—H N N—CH3
    A4.007 C—H S C—H N N—CH3
    A4.008 C—CF3 S C—H N N—CH3
  • TABLE P
    Radicals of formula A4
    A5
    Figure US20220104496A1-20220407-C00192
    Radical R1 R2 G1 G2 G5 G4
    A5.001 CH3 H C—H C—H N N
    A5.002 CF3 H C—H C—H N N
    A5.003 Cl H C—H C—H N N
    A5.004 Br H C—H C—H N N
    A5.005 CH3 H C—H N N N
    A5.006 CF3 H C—H N N N
    A5.007 Cl H C—H N N N
    A5.008 Br H C—H N N N
    A5.009 CH3 H C—H C—H C—CH3 N
    A5.010 CF3 H C—H C—H C—CH3 N
    A5.011 Cl H C—H C—H C—CH3 N
    A5.012 Br H C—H C—H C—CH3 N
    A5.013 CH3 H C—H N C—CH3 N
    A5.014 CF3 H C—H N C—CH3 N
    A5.015 Cl H C—H N C—CH3 N
    A5.016 Br H C—H N C—CH3 N
  • TABLE Q
    Radicals of formula A6
    A6
    Figure US20220104496A1-20220407-C00193
    Radical R1 G1 G2 G3
    A6.001 CH3 C—H C—H N—CH3
    A6.002 CF3 C—H C—H N—CH3
    A6.003 Cl C—H C—H N—CH3
    A6.004 Br C—H C—H N—CH3
    A6.005 CH3 C—H C—H O
    A6.006 CF3 C—H C—H O
    A6.007 Cl C—H C—H O
    A6.008 Br C—H C—H O
    A6.009 CH3 C—H C—H S
    A6.010 CF3 C—H C—H S
    A6.011 Cl C—H C—H S
    A6.012 Br C—H C—H S
    A3.013 CH3 C—H N N—CH3
    A6.014 CF3 C—H N N—CH3
    A6.015 Cl C—H N N—CH3
    A6.016 Br C—H N N—CH3
    A6.017 CH3 C—H N O
    A6.018 CF3 C—H N O
    A6.019 Cl C—H N O
    A6.020 Br C—H N O
    A6.021 CH3 C—H N S
    A6.022 CF3 C—H N S
    A6.023 Cl C—H N S
    A6.024 Br C—H N S
  • TABLE R
    Radicals of formula A7a
    A7a
    Figure US20220104496A1-20220407-C00194
    Radical R1 G1 G2 G3
    A7.001 CH3 C—H C—H C—CH3
    A7.002 CF3 C—H C—H C—CH3
    A7.003 Cl C—H C—H C—CH3
    A7.004 Br C—H C—H C—CH3
    A7.005 CH3 C—H C—H C—H
    A7.006 CF3 C—H C—H C—H
    A7.007 Cl C—H C—H C—H
    A7.008 Br C—H C—H C—H
    A7.009 CH3 C—H C—H N
    A7.010 CF3 C—H C—H N
    A7.011 Cl C—H C—H N
    A7.012 Br C—H C—H N
  • TABLE S
    Radicals of formula A8a
    A8a
    Figure US20220104496A1-20220407-C00195
    Radical R1 G1 G2 G4
    A8.001 CH3 C—H C—H C—H
    A8.002 CF3 C—H C—H C—H
    A8.003 Cl C—H C—H C—H
    A8.004 Br C—H C—H C—H
    A8.005 CH3 C—H C—H C—CH3
    A8.006 CF3 C—H C—H C—CH3
    A8.007 Cl C—H C—H C—CH3
    A8.008 Br C—H C—H C—CH3
    A8.009 CH3 C—H C—H N
    A8.010 CF3 C—H C—H N
    A8.011 Cl C—H C—H N
    A8.012 Br C—H C—H N
  • Table 1: This table discloses 66 compounds of the formula A1.014-B1 wherein the radicals B1 are the radicals B1.049-B1.084, and B1.091-B1.120 shown in table A, and A1.014 is defined in Table L.
  • Table 2: This table discloses 66 compounds of the formula A1.018-B1 wherein the radicals B1 are the radicals B1.049-B1.084, and B1.091-B1.120 shown in table A, and A1.018 is defined in Table L.
  • Table 3: This table discloses 66 compounds of the formula A1.022-B1 wherein the radicals B1 are the radicals B1.049-B1.084, and B1.091-B1.120 shown in table A, and A1.022 is defined in Table L.
  • Table 4: This table discloses 36 compounds of the formula A1.014-B2 wherein the radicals B2 are the radicals B2.001-B2.036 shown in table B, and A1.014 is defined in Table L.
  • Table 5: This table discloses 36 compounds of the formula A1.018-B2 wherein the radicals B2 are the radicals B2.001-B2.036 shown in table B, and A1.018 is defined in Table L.
  • Table 6: This table discloses 36 compounds of the formula A1.022-B2 wherein the radicals B2 are the radicals B2.001-B2.036 shown in table B, and A1.022 is defined in Table L.
  • Table 7: This table discloses 24 compounds of the formula A1.014-B3 wherein the radicals B3 are the radicals B3.001-B3.024 shown in table C, and A1.014 is defined in Table L.
  • Table 8: This table discloses 24 compounds of the formula A1.018-B3 wherein the radicals B3 are the radicals B3.001-B3.024 shown in table C, and A1.018 is defined in Table L.
  • Table 9: This table discloses 24 compounds of the formula A1.022-B3 wherein the radicals B3 are the radicals B3.001-B3.024 shown in table C, and A1.022 is defined in Table L.
  • Table 10: This table discloses 8 compounds of the formula A1.014-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A1.014 is defined in Table L.
  • Table 11: This table discloses 8 compounds of the formula A1.018-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A1.018 is defined in Table L.
  • Table 12: This table discloses 8 compounds of the formula A1.022-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A1.022 is defined in Table L.
  • Table 13: This table discloses 24 compounds of the formula A1.014-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A1.014 is defined in Table L.
  • Table 14: This table discloses 24 compounds of the formula A1.018-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A1.018 is defined in Table L.
  • Table 15: This table discloses 24 compounds of the formula A1.022-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A1.022 is defined in Table L.
  • Table 16: This table discloses 16 compounds of the formula A1.014-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A1.014 is defined in Table L.
  • Table 17: This table discloses 16 compounds of the formula A1.018-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A1.018 is defined in Table L.
  • Table 18: This table discloses 16 compounds of the formula A1.022-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A1.022 is defined in Table L.
  • Table 19: This table discloses 54 compounds of the formula A1.014-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A1.014 is defined in Table L.
  • Table 20: This table discloses 54 compounds of the formula A1.018-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A1.018 is defined in Table L.
  • Table 21: This table discloses 54 compounds of the formula A1.022-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A1.022 is defined in Table L.
  • Table 22: This table discloses 12 compounds of the formula A1.014-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A1.014 is defined in Table L.
  • Table 23: This table discloses 12 compounds of the formula A1.018-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A1.018 is defined in Table L
  • Table 24: This table discloses 12 compounds of the formula A1.022-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A1.022 is defined in Table L
  • Table 25: This table discloses 30 compounds of the formula A1.014-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A1.014 is defined in Table L.
  • Table 26: This table discloses 30 compounds of the formula A1.018-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A1.018 is defined in Table L.
  • Table 27: This table discloses 30 compounds of the formula A1.022-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A1.0122 is defined in Table L.
  • Table 28: This table discloses 12 compounds of the formula A1.014-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A1.014 is defined in Table L.
  • Table 29: This table discloses 12 compounds of the formula A1.018-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A1.018 is defined in Table L.
  • Table 30: This table discloses 12 compounds of the formula A1.022-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A1.022 is defined in Table L.
  • Table 31: This table discloses 64 compounds of the formula A1.014-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A1.014 is defined in Table L.
  • Table 29: This table discloses 64 compounds of the formula A1.018-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A1.018 is defined in Table L.
  • Table 30: This table discloses 64 compounds of the formula A1.022-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A1.022 is defined in Table L.
  • Table 31: This table discloses 132 compounds of the formula A2.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A2.006 is defined in Table M.
  • Table 32: This table discloses 132 compounds of the formula A2.018-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A2.018 is defined in Table M.
  • Table 33: This table discloses 36 compounds of the formula A2.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A2.006 is defined in Table M.
  • Table 34: This table discloses 36 compounds of the formula A2.018-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A2.018 is defined in Table M.
  • Table 35: This table discloses 24 compounds of the formula A2.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A2.0006 is defined in Table M.
  • Table 36: This table discloses 24 compounds of the formula A2.018-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A2.018 is defined in Table M.
  • Table 37: This table discloses 8 compounds of the formula A2.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A2.006 is defined in Table M.
  • Table 38: This table discloses 8 compounds of the formula A2.018-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A2.018 is defined in Table M.
  • Table 39: This table discloses 24 compounds of the formula A2.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A2.006 is defined in Table M.
  • Table 40: This table discloses 24 compounds of the formula A2.018-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A2.018 is defined in Table M.
  • Table 42: This table discloses 16 compounds of the formula A2.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A2.006 is defined in Table M.
  • Table 43: This table discloses 16 compounds of the formula A2.018-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A2.018 is defined in Table M.
  • Table 44: This table discloses 54 compounds of the formula A2.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A2.0106 is defined in Table M.
  • Table 45: This table discloses 54 compounds of the formula A2.018-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A2.018 is defined in Table M.
  • Table 46: This table discloses 12 compounds of the formula A2.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A2.006 is defined in Table M.
  • Table 47: This table discloses 12 compounds of the formula A2.018-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A2.018 is defined in Table M.
  • Table 48: This table discloses 30 compounds of the formula A2.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A2.006 is defined in Table M.
  • Table 49: This table discloses 30 compounds of the formula A2.018-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A2.018 is defined in Table M.
  • Table 50: This table discloses 12 compounds of the formula A2.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A2.006 is defined in Table M.
  • Table 51: This table discloses 12 compounds of the formula A2.018-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A2.018 is defined in Table M.
  • Table 52: This table discloses 64 compounds of the formula A2.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A2.006 is defined in Table M.
  • Table 53: This table discloses 64 compounds of the formula A2.018-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A2.018 is defined in Table M.
  • Table 54: This table discloses 132 compounds of the formula A3.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A3.006 is defined in Table N.
  • Table 55: This table discloses 132 compounds of the formula A3.018-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A3.018 is defined in Table N.
  • Table 56: This table discloses 36 compounds of the formula A3.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A3.006 is defined in Table N.
  • Table 57: This table discloses 36 compounds of the formula A3.018-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A3.018 is defined in Table N.
  • Table 58: This table discloses 24 compounds of the formula A3.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A3.006 is defined in Table N.
  • Table 59: This table discloses 24 compounds of the formula A3.018-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A3.018 is defined in Table N.
  • Table 60: This table discloses 8 compounds of the formula A3.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A3.006 is defined in Table N.
  • Table 61: This table discloses 8 compounds of the formula A3.018-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A3.018 is defined in Table N.
  • Table 62: This table discloses 24 compounds of the formula A3.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A3.006 is defined in Table N.
  • Table 63: This table discloses 24 compounds of the formula A3.018-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A3.018 is defined in Table N.
  • Table 64: This table discloses 16 compounds of the formula A3.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A3.006 is defined in Table N.
  • Table 65: This table discloses 16 compounds of the formula A3.018-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A3.018 is defined in Table N.
  • Table 66: This table discloses 54 compounds of the formula A3.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A3.006 is defined in Table N.
  • Table 67: This table discloses 54 compounds of the formula A3.018-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A3.018 is defined in Table N.
  • Table 68: This table discloses 12 compounds of the formula A3.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A3.006 is defined in Table N.
  • Table 69: This table discloses 12 compounds of the formula A3.0018-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A3.018 is defined in Table N.
  • Table 70: This table discloses 30 compounds of the formula A3.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A3.006 is defined in Table N.
  • Table 71: This table discloses 30 compounds of the formula A3.018-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A3.018 is defined in Table N.
  • Table 72: This table discloses 12 compounds of the formula A3.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A3.006 is defined in Table N.
  • Table 73: This table discloses 12 compounds of the formula A3.018-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A3.018 is defined in Table N.
  • Table 74: This table discloses 64 compounds of the formula A3.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A3.006 is defined in Table N.
  • Table 75: This table discloses 64 compounds of the formula A3.018-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A3.018 is defined in Table N.
  • Table 76: This table discloses 132 compounds of the formula A4.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A4.006 is defined in Table O.
  • Table 77: This table discloses 132 compounds of the formula A4.008-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A4.008 is defined in Table O.
  • Table 78: This table discloses 36 compounds of the formula A4.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A4.006 is defined in Table O.
  • Table 79: This table discloses 36 compounds of the formula A4.008-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A4.008 is defined in Table O.
  • Table 80: This table discloses 24 compounds of the formula A4.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A4.006 is defined in Table O.
  • Table 81: This table discloses 24 compounds of the formula A4.008-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A4.008 is defined in Table O.
  • Table 82: This table discloses 8 compounds of the formula A4.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A4.006 is defined in Table O.
  • Table 83: This table discloses 8 compounds of the formula A4.008-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A4.008 is defined in Table O.
  • Table 84: This table discloses 24 compounds of the formula A4.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A4.006 is defined in Table O.
  • Table 85: This table discloses 24 compounds of the formula A4.008-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A4.008 is defined in Table O.
  • Table 86: This table discloses 16 compounds of the formula A4.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A4.006 is defined in Table O.
  • Table 87: This table discloses 16 compounds of the formula A4.008-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A4.008 is defined in Table O.
  • Table 88: This table discloses 54 compounds of the formula A4.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A4.006 is defined in Table O.
  • Table 89: This table discloses 54 compounds of the formula A4.008-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A4.008 is defined in Table O.
  • Table 90: This table discloses 12 compounds of the formula A4.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A4.006 is defined in Table O.
  • Table 91: This table discloses 12 compounds of the formula A4.008-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A4.008 is defined in Table O.
  • Table 92: This table discloses 30 compounds of the formula A4.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A4.006 is defined in Table O.
  • Table 93: This table discloses 30 compounds of the formula A4.008-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A4.008 is defined in Table O.
  • Table 94: This table discloses 12 compounds of the formula A4.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A4.006 is defined in Table O.
  • Table 95: This table discloses 12 compounds of the formula A4.008-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A4.008 is defined in Table O.
  • Table 96: This table discloses 64 compounds of the formula A4.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A4.006 is defined in Table O.
  • Table 97: This table discloses 64 compounds of the formula A4.008-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A3.008 is defined in Table O.
  • Table 98: This table discloses 132 compounds of the formula A5.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A5.006 is defined in Table P.
  • Table 99: This table discloses 36 compounds of the formula A5.006-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A5.006 is defined in Table P.
  • Table 100: This table discloses 24 compounds of the formula A5.006-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A5.006 is defined in Table P.
  • Table 101: This table discloses 8 compounds of the formula A5.006-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A4.006 is defined in Table P.
  • Table 102: This table discloses 24 compounds of the formula A5.006-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A5.006 is defined in Table P.
  • Table 103: This table discloses 16 compounds of the formula A5.006-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A5.006 is defined in Table P.
  • Table 104: This table discloses 54 compounds of the formula A5.006-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A5.006 is defined in Table P.
  • Table 105: This table discloses 12 compounds of the formula A5.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A5.006 is defined in Table P.
  • Table 106: This table discloses 30 compounds of the formula A5.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A5.006 is defined in Table P.
  • Table 107: This table discloses 12 compounds of the formula A5.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A5.006 is defined in Table P.
  • Table 108: This table discloses 64 compounds of the formula A5.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A5.006 is defined in Table P.
  • Table 109: This table discloses 132 compounds of the formula A6.002-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A6.002 is defined in Table Q.
  • Table 110: This table discloses 132 compounds of the formula A6.014-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A6.014 is defined in Table Q.
  • Table 111: This table discloses 36 compounds of the formula A6.002-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A6.002 is defined in Table Q.
  • Table 112: This table discloses 36 compounds of the formula A6.014-B2 wherein the radicals B2 are the radicals B2.001-B2.0036 shown in table B, and A6.014 is defined in Table Q.
  • Table 113: This table discloses 24 compounds of the formula A6.002-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A6.002 is defined in Table Q.
  • Table 114: This table discloses 24 compounds of the formula A6.014-B3 wherein the radicals B3 are the radicals B3.001-B3.0024 shown in table C, and A6.014 is defined in Table Q.
  • Table 115: This table discloses 8 compounds of the formula A6.002-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A6.002 is defined in Table Q.
  • Table 116: This table discloses 8 compounds of the formula A6.014-B4 wherein the radicals B4 are the radicals B4.001-B4.008 shown in table D, and A6.014 is defined in Table Q.
  • Table 117: This table discloses 24 compounds of the formula A6.002-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A6.002 is defined in Table Q.
  • Table 118: This table discloses 24 compounds of the formula A6.014-B5 wherein the radicals B5 are the radicals B5.001-B5.024 shown in table E, and A4.014 is defined in Table Q.
  • Table 119: This table discloses 16 compounds of the formula A6.002-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A6.002 is defined in Table Q.
  • Table 120: This table discloses 16 compounds of the formula A6.014-B6 wherein the radicals B6 are the radicals B6.001-B6.016 shown in table F, and A6.014 is defined in Table Q.
  • Table 121: This table discloses 54 compounds of the formula A6.002-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A6.002 is defined in Table Q.
  • Table 122: This table discloses 54 compounds of the formula A6.014-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A6.014 is defined in Table Q.
  • Table 123: This table discloses 12 compounds of the formula A6.002-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A6.002 is defined in Table Q.
  • Table 124: This table discloses 12 compounds of the formula A6.0014-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A6.014 is defined in Table Q.
  • Table 125: This table discloses 30 compounds of the formula A6.002-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A6.002 is defined in Table Q.
  • Table 126: This table discloses 30 compounds of the formula A6.014-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A6.014 is defined in Table Q.
  • Table 127: This table discloses 12 compounds of the formula A6.002-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A6.002 is defined in Table Q.
  • Table 128: This table discloses 12 compounds of the formula A6.014-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A6.014 is defined in Table Q.
  • Table 129: This table discloses 64 compounds of the formula A6.002-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A6.002 is defined in Table Q.
  • Table 130: This table discloses 64 compounds of the formula A6.014-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A6.014 is defined in Table Q.
  • Table 131: This table discloses 132 compounds of the formula A7.002-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A7.002 is defined in Table R Table 132: This table discloses 132 compounds of the formula A7.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A7.006 is defined in Table R.
  • Table 133: This table discloses 132 compounds of the formula A7.010-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A7.010 is defined in Table R.
  • Table 134: This table discloses 54 compounds of the formula A7.002-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A7.002 is defined in Table R.
  • Table 135: This table discloses 54 compounds of the formula A7.006-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A7.006 is defined in Table R.
  • Table 136: This table discloses 54 compounds of the formula A7.010-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A7.010 is defined in Table R.
  • Table 137: This table discloses 12 compounds of the formula A7.002-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A7.002 is defined in Table R.
  • Table 138: This table discloses 12 compounds of the formula A7.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A7.006 is defined in Table R.
  • Table 139: This table discloses 12 compounds of the formula A7.010-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A7.010 is defined in Table R.
  • Table 140: This table discloses 30 compounds of the formula A7.002-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A7.002 is defined in Table R.
  • Table 142: This table discloses 30 compounds of the formula A7.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A7.006 is defined in Table R.
  • Table 143: This table discloses 30 compounds of the formula A7.010-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A7.010 is defined in Table R.
  • Table 144: This table discloses 12 compounds of the formula A7.002-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A7.002 is defined in Table R.
  • Table 145: This table discloses 12 compounds of the formula A7.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A7.006 is defined in Table R.
  • Table 146: This table discloses 12 compounds of the formula A7.010-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A7.010 is defined in Table R.
  • Table 147: This table discloses 64 compounds of the formula A7.002-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A7.002 is defined in Table R.
  • Table 148: This table discloses 64 compounds of the formula A7.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A7.006 is defined in Table R.
  • Table 149: This table discloses 64 compounds of the formula A7.010-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A7.010 is defined in Table R.
  • Table 150: This table discloses 132 compounds of the formula A8.002-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A8.002 is defined in Table R
  • Table 151: This table discloses 132 compounds of the formula A8.006-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A8.006 is defined in Table S.
  • Table 152: This table discloses 132 compounds of the formula A8.010-B1 wherein the radicals B1 are the radicals B1.001-B1.132 shown in table A, and A8.010 is defined in Table S.
  • Table 153: This table discloses 54 compounds of the formula A8.002-B7 wherein the radicals B7 are the radicals B7.001-B7.054 shown in table G, and A8.002 is defined in Table S.
  • Table 154: This table discloses 54 compounds of the formula A8.006-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A8.006 is defined in Table R.
  • Table 155: This table discloses 54 compounds of the formula A8.010-B7 wherein the B7 are the radicals B7.001-B7.054 shown in table G, and A8.010 is defined in Table R.
  • Table 156: This table discloses 12 compounds of the formula A8.002-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A8.002 is defined in Table S.
  • Table 157: This table discloses 12 compounds of the formula A8.006-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A8.006 is defined in Table S.
  • Table 158: This table discloses 12 compounds of the formula A8.010-B8 wherein the radicals B8 are the radicals B8.001-B8.012 shown in table H, and A8.010 is defined in Table S.
  • Table 159: This table discloses 30 compounds of the formula A8.002-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A8.002 is defined in Table S.
  • Table 160: This table discloses 30 compounds of the formula A4.006-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A8.006 is defined in Table S.
  • Table 161: This table discloses 30 compounds of the formula A8.010-B9 wherein the radicals B9 are the radicals B9.001-B9.030 shown in table I, and A8.010 is defined in Table S.
  • Table 162: This table discloses 12 compounds of the formula A8.002-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A8.002 is defined in Table S.
  • Table 164: This table discloses 12 compounds of the formula A8.006-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A8.006 is defined in Table S.
  • Table 165: This table discloses 12 compounds of the formula A8.010-B10 wherein the radicals B10 are the radicals B10.001-B10.012 shown in table J, and A8.010 is defined in Table S.
  • Table 166: This table discloses 64 compounds of the formula A8.002-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A8.002 is defined in Table S.
  • Table 167: This table discloses 64 compounds of the formula A8.006-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A8.006 is defined in Table S.
  • Table 168: This table discloses 64 compounds of the formula A8.010-B11 wherein the radicals B11 are the radicals B11.001-B11.064 shown in table K, and A8.010 is defined in Table S.
  • TABLE T
    Physical-chemical data for compounds of formula I:
    Ret.
    Entry Time (M + H) Mpt.
    No. Compound (min) Measured Method ° C.
    T.1 A1.014-B2.023 199-200
    T.2 A1.014-B3.012 1.2 384/386 SQD13 169-170
    T.3 A1.014-B2.036 150-160
    T.4 A2.014-B1.022 194-195
    T.5 A1.014-B3.016 197-198
    T.6 A1.028-B1.022 140-141
    T.7 A1.028-B1.013 122-123
    T.8 A1.014-B1.098 1.13 369 ZCQ13
    T.9 A1.014-B1.106  101-103.5
    T.10 A2.018-B1.045 185-185
    T.11 A2.022-B1.022 167-168
    T.12 A1.014-B7.038 161-163
    T.13 A1.026-B1.022 190-192
    T.14 A1.014-B7.014 79-80
    T.15 A1.014-B7.022 139-141
    T.16 A1.026-B1.014 1.51 370 ZCQ13
    T.17 A1.014-B11.014 143-145
    T.18 A1.014-B11.022 181-183
    T.19 A1.028-B1.014 1.11 418/420 ZQD13 159-162
    T.20 A1.014-B7.038 1.27 413 ZQD13 206-209
    T.21 A1.014-B7.046 1.14 445 ZQD13 107-109
    T.22 A1.026-B1.022 1.04 440 SQD13 162-165
    T.23 A6.02-B1.014 1.08 406 SQD13 137-140
    T.24 A1.014-B7.014 1.21 412 ZQD13 135-137
    T.25 A1.014-B7.022 1.08 444 ZQD13 152-154
    T.26 A1.026-B1.014 1.13 408 ZQD13 172-175
    T.27 A1.014-B8.10 188-189
    T.28 A1.014-B8.012 144-146
    T.29 A6.02-B1.038 136-138
    T.30 A6.02-B9.014 82-84
    T.31 A6.02-B7.037 167-169
    T.32 A1.014-B11.014 122-124
    T.33 A6.015-B1.014 1.01 374/376 ZCQ13   156°-158° C.
    T.34 A1.014-B1.050 1.12 408 SQD13 149-150
    T.35 A1.014-B1.058 1.06 440 ZCQ13 172-174
  • TABLE U
    Physical-chemical data of especially preferred
    compounds of formula I and its intermediates:
    Entry COMPOUND RT [M + H]
    No. (IUPAC name) (min) (measured) Method Mpt. ° C.
    U.1 2-(3-ethylsulfonyl-2-pyridyl)-7- 208-209
    (trifluoromethyl)imidazo[1,2-
    b]pyridazine
    U.2 2-(3-ethylsulfonyl-2-pyridyl)-5- 0.82 357 SQD13
    (trifluoromethyl)-1H-imidazo[4,5-
    b]pyridine
    U.3 2-(3-Ethylsulfanyl-5-trifluoro-methyl- 1.15 461 SQD13 191-193
    pyridin-2-yl)-3,5-dimethyl-6-
    trifluoromethyl-3,5-dihydro-
    diimidazo[4,5-b;4′,5′-e]pyridine
    U.4 2-(3-Ethylsulfanyl-pyridin-2-yl)-3, 0.97 393 SQD13 129-131
    5-dimethyl-6-trifluoromethyl-3,5-
    dihydro-diimidazo[4,5-b;4′,5′-e]pyridine
    U.5 2-[3-ethylsulfanyl-5-(trifluoromethyl)-2- 1.09 393 SQD13 222-224
    pyridyl]-6-(trifluoromethyl)-3H-
    imidazo[4,5-c]pyridine
    U.6 2-[3-ethylsulfanyl-5-(trifluoromethyl)-2- 1.08 407 SQD13 119-121
    pyridyl]-1-methyl-6-
    (trifluoromethyl)imidazo[4,5-c]pyridine
    U.7 4-ethylsulfanyl-5-[3-methyl-6- 1.22 413 SQD13 100-102
    (trifluoromethyl)imidazo[4,5-b]pyridin-2-
    yl]-2-(trifluoromethyl)thiazole
    U.8 4-ethylsulfonyl-5-[3-methyl-6- 1.02 445 SQD13 172-174
    (trifluoromethyl)imidazo[4,5-b]pyridin-2-
    yl]-2-(trifluoromethyl)thiazole
    U.9 6-(3-ethylsulfonyl-2-pyridyl)-3- 199-201
    (trifluoromethyl)imidazo[1,2-
    b][1,2,4]triazine
    U.10 3-methyl-2-[3-(oxiran-2- 1.03 467 ZQD13
    ylmethylsulfonyl)-5-(trifluoromethyl)-2-
    pyridyl]-6-(trifluoromethyl)imidazo[4,5-
    b]pyridine
    U.11 3-methyl-2-[3-(oxetan-3- 1.01 481 ZQD13
    ylmethylsulfonyl)-5-(trifluoromethyl)-2-
    pyridyl]-6-(trifluoromethyl)imidazo[4,5-
    b]pyridine
    U.12 3-methyl-2-[3-(tetrahydrofuran-3- 1.05 495 ZQD13
    ylmethylsulfonyl)-5-(trifluoromethyl)-2-
    pyridyl]-6-(trifluoromethyl)imidazo[4,5-
    b]pyridine
    U.13 3-methyl-2-[3-(tetrahydrofuran-2- 1.11 495 ZQD13
    ylmethylsulfonyl)-5-(trifluoromethyl)-2-
    pyridyl]-6-(trifluoromethyl)imidazo[4,5-
    b]pyridine
    U.14 2-[6-chloro-3-ethylsulfonyl-5- 1.14 473/475 ZQD13
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.15 5-ethylsulfonyl-6-[3-methyl-6- 0.91 455 ZQD13
    (trifluoromethyl)imidazo[4,5-b]pyridin-2-
    yl]-3-(trifluoromethyl)pyridin-2-ol
    U.16 2-(3-ethylsulfanyl-5-methyl-2-pyridyl)-3- 1.17 407 ZQD13 141-143
    methyl-5-(trifluoromethyl)imidazo[4,5-
    b]pyridine
    U.17 2-[3-cyclobutylsulfonyl-5- 1.12 465 SQD13 149-150
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.18 3-methyl-2-[3-pyrimidin-2-ylsulfonyl-5- 1.64   489.00 ZQ2000
    (trifluoromethyl)-2-pyridyl]-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.19 3-methyl-2-[3-(4-pyridylsulfonyl)-5- 1.50 488 ZQ2000
    (trifluoromethyl)-2-pyridyl]-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.20 2-[3-cyclohexylsulfonyl-5- 2.02 493 ZQ2000
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.21 2-[3-cyclopentylsulfonyl-5- 1.91 479 ZQ2000
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.22 2-[[2-[3-methyl-6- 1.66 495 ZQ2000
    (trifluoromethyl)imidazo[4,5-b]pyridin-2-
    yl]-5-(trifluoromethyl)-3-pyridyl]sulfonyl]-
    1,3,4-thiadiazole
    U.23 3-methyl-2-[3-(2-thienylsulfonyl)-5- 1.76 493 ZQ2000
    (trifluoromethyl)-2-pyridyl]-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.24 3-methyl-2-[3-(2-thienylsulfinyl)-5- 1.94 477 ZQ2000
    (trifluoromethyl)-2-pyridyl]-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.25 2-[3-(cyclobutylmethylsulfonyl)-5- 1.18 479 ZQD13 110-111
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.26 2-[3-[2-(1,3-dioxan-2-yl)ethylsulfanyl]-5- 1.16 493 ZQD13 100-101
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.27 2-[3-[2-(1,3-dioxolan-2-yl)ethylsulfanyl]- 1.1 465 ZQD13 104-105
    5-(trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.28 2-[3-[2-(1,3-dioxan-2-yl)ethylsulfonyl]-5- 144-145
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.29 2-[3-[2-(1,3-dioxolan-2-yl)ethylsulfonyl]- 140-141
    5-(trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.30 2-[3-(1,3-dioxolan-2-ylmethylsulfonyl)-5- 149-150
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.31 2-[3-ethylsulfanyl-5-(trifluoromethyl)-2- 124-126
    pyridyl]-6-(trifluoromethyl)pyrazolo[1,5-
    a]pyrimidine
    U.32 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2- 189-191
    pyridyl]-6-(trifluoromethyl)pyrazolo[1,5-
    a]pyrimidine
    U.33 4-bromo-5-[3-methyl-6- 1.03 431/433 ZQD13
    (trifluoromethyl)imidazo[4,5-c]pyridin-2-
    yl]-2-(trifluoromethyl)thiazole
    U.34 4-ethylsulfanyl-5-[3-methyl-6- 92-94
    (trifluoromethyl)imidazo[4,5-c]pyridin-2-
    yl]-2-(trifluoromethyl)thiazole
    U.35 2-[3-ethylsulfanyl-6- 206-208
    (trifluoromethyl)pyrazin-2-yl]-3-methyl-
    6-(trifluoromethyl)imidazo[4,5-b]pyridine
    U.36 2-[3-ethylsulfonyl-6- 214-216
    (trifluoromethyl)pyrazin-2-yl]-3-methyl-
    6-(trifluoromethyl)imidazo[4,5-b]pyridine
    U.37 2-[5-(difluoromethoxy)-3-ethylsulfanyl- 82-83
    2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.38 2-[5-(difluoromethoxy)-3-ethylsulfonyl- 115-117
    2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.39 2-[2-ethylsulfanyl-4- 120-122
    (trifluoromethyl)phenyl]-1-methyl-6-
    (trifluoromethyl)imidazo[4,5-c]pyridine
    U.40 2-[2-ethylsulfonyl-4- 237-239
    (trifluoromethyl)phenyl]-1-methyl-6-
    (trifluoromethyl)imidazo[4,5-c]pyridine
    U.41 5-bromo-2-[3-ethylsulfonyl-5- 94-97
    (trifluoromethyl)-2-pyridyl]-1-methyl-
    imidazo[4,5-b]pyridine
    U.42 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2- 202-204
    pyridyl]-1-methyl-5-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.43 5-bromo-2-(3-ethylsulfonyl-2-pyridyl)-1- 183-186
    methyl-imidazo[4,5-b]pyridine
    U.44 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2- 191-192
    pyridyl]-7-(trifluoromethyl)imidazo[1,2-
    a]pyridine
    U.45 3-chloro-2-[3-ethylsulfonyl-5- 195-197
    (trifluoromethyl)-2-pyridyl]-7-
    (trifluoromethyl)imidazo[1,2-a]pyridine
    U.46 3-bromo-2-[3-ethylsulfonyl-5- 202-204
    (trifluoromethyl)-2-pyridyl]-7-
    (trifluoromethyl)imidazo[1,2-a]pyridine
    U.47 3-bromo-2-[3-ethylsulfonyl-5- 180-182
    (trifluoromethyl)-2-pyridyl]-7-
    (trifluoromethyl)imidazo[1,2-
    c]pyrimidine
    U.48 2-[3-(1,3-dioxan-2-ylmethylsulfonyl)-5- 1.09 511 SQD13
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.49 3-bromo-2-(3-ethylsulfonyl-2-pyridyl)-7- 174-175
    (trifluoromethyl)imidazo[1,2-
    c]pyrimidine
    U.50 2-[3-(4-methoxyphenyl)sulfinyl-5- 156-158
    (trifluoromethyl)-2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-b]pyridine
    U.51 3-bromo-2-[3-ethylsulfonyl-5- 223-224
    (trifluoromethyl)-2-pyridyl]-6-
    (trifluoromethyl)imidazo[1,2-a]pyrazine
    U.52 6-bromo-2-[3-ethylsulfonyl-5- 221-223
    (trifluoromethyl)-2-pyridyl]imidazo[1,2-
    a]pyrazine
    U.53 3-bromo-2-(3-ethylsulfonyl-2-pyridyl)-6- 200-212
    (trifluoromethyl)imidazo[1,2-a]pyrazine
    U.54 6-bromo-2-(3-ethylsulfonyl-2- 219-220
    pyridyl)imidazo[1,2-a]pyrazine
    U.55 2-(3-Ethylsulfanyl-5-trifluoromethyl- 164-166
    thiophen-2-yl)-3,5-dimethyl-6-
    trifluoromethyl-3,5-dihydro-
    diimidazo[4,5-b;4′,5′-e]pyridine
    U.56 2-(5-Ethylsulfanyl-thiazol-4-yl)-3, 200-202
    5-dimethyl-6-trifluoromethyl-3,5-dihydro-
    diimidazo[4,5-b;4′,5′-e]pyridine
    U.57 2-[2-ethylsulfanyl-6-(trifluoromethyl)-3- 115-117
    pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-c]pyridine
    U.58 2-[2-ethylsulfanyl-6-(trifluoromethyl)-3- 117-119
    pyridyl]-7-(trifluoromethyl)imidazo[1,2-
    a]pyridine
    U.59 2-[5-(difluoromethoxy)-3-ethylsulfanyl- 146-148
    2-pyridyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-c]pyridine
    U.60 3-ethylsulfanyl-4-[3-methyl-6- 163-165
    (trifluoromethyl)imidazo[4,5-b]pyridin-2-
    yl]isothiazole
    U.61 2-[3-ethylsulfanyl-5-(trifluoromethyl)-2-  98-100
    thienyl]-7-(trifluoromethyl)imidazo[1,2-
    a]pyridine
    U.62 4-bromo-2-(trifluoromethyl)-5-[7- 152-154
    (trifluoromethyl)imidazo[1,2-a]pyridin-2-
    yl]thiazole
    U.63 2-(4-Ethylsulfanyl-2-trifluoromethyl- 196-198
    thiazol-5-yl)-3,5-dimethyl-6-
    trifluoromethyl-3,5-dihydro-
    diimidazo[4,5-b;4′,5′-e]pyridine
    U.64 2-(2-Ethylsulfanyl-6-trifluoromethyl- 154-156
    pyridin-3-yl)-3,5-dimethyl-6-
    trifluoromethyl-3,5-dihydro-
    diimidazo[4,5-b;4′,5′-e]pyridine
    U.65 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2- 1.56 439 ZCQ13
    pyridyl]-3-methyl-7-
    (trifluoromethyl)imidazo[1,2-
    a]pyrimidine
    U.66 4-ethylsulfanyl-2-(trifluoromethyl)-5- 1.25 398 SQD13 115-117
    [7-(trifluoromethyl)imidazo[1,2-
    a]pyridin-2-yl]thiazole
    U.67 3-bromo-2-[3-ethylsulfonyl-5- 1.13 507/509 SQD13 176-178
    (trifluoromethyl)-2-thienyl]-7-
    (trifluoromethyl)imidazo[1,2-
    a]pyridine
    U.68 2-[3-ethylsulfanyl-5-(trifluoromethyl)- 1.22 398 SQD13 94-96
    2-thienyl]-7-(trifluoromethyl)-
    [1,2,4]triazolo[1,5-a]pyridine
    U.69 4-bromo-2-(trifluoromethyl)-5-[7- 1.15 417/419 SQD13 90-91
    (trifluoromethyl)-[1,2,4]triazolo[1,5-
    a]pyridin-2-yl]thiazole
    U.70 4-ethylsulfanyl-2-(trifluoromethyl)-5- 1.24 399 SQD13 102-103
    [7-(trifluoromethyl)-
    [1,2,4]triazolo[1,5-a]pyridin-2-
    yl]thiazole
    U.71 2-[3-ethylsulfanyl-5-(trifluoromethyl)- 1.22 398 SQD13 121-123
    2-thienyl]-6-(trifluoromethyl)-
    [1,2,4]triazolo[1,5-a]pyridine
    U.72 2-(2-Ethylsulfanyl-5-trifluoromethyl- 1.18 466 SQD13 121-123
    thiophen-3-yl)-3,5-dimethyl-6-
    trifluoromethyl-3,5-dihydro-
    diimidazo[4,5-b;4′,5′-e]pyridine
    U.73 2-(2-Ethylsulfanyl-4-trifluoromethyl- 1.13 460 SQD13 201-203
    phenyl)-3,5-dimethyl-6-trifluoromethyl-
    3,5-dihydro-diimidazo[4,5-
    b;4′,5′-e]pyridine
    U.74 2-[2-ethylsulfanyl-5-(trifluoromethyl)- 1.12 412 SQD13 148-150
    3-thienyl]-3-methyl-6-
    (trifluoromethyl)imidazo[4,5-
    c]pyridine
  • Preference is given to a group of compounds of formula I defined as embodiments (1) to (7) which are illustrated below:
  • An especially preferred group of compounds of formula I according to the invention is defined as embodiment (1) and comprises combinations of
  • (1): Radical A2 with radicals B selected from B7, B9 and E11;
    wherein A2 is preferably represented by the radical A2.1
  • Figure US20220104496A1-20220407-C00196
  • wherein R40 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl; G21 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C6haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and G51 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C6haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and the radicals B7, B9 and E11 are preferably represented by the radicals selected from B7.1, B9.1 and B11.1
  • Figure US20220104496A1-20220407-C00197
  • wherein m is 0, 1 or 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00198
  • wherein m is 0, 1 or 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
  • Figure US20220104496A1-20220407-C00199
  • wherein m is 0, 1 or 2;
    R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
  • Especially preferred compounds according to embodiment (1) are represented by embodiment (1.1), wherein
  • (1.1) in the radical A2.1
  • Figure US20220104496A1-20220407-C00200
  • R40 is C1-C4haloalkyl, in particular trifluoromethyl;
    G21 is nitrogen or CH; and
    G51 is nitrogen or C—C1-C5 alkyl, in particular nitrogen or C-methyl;
    and in the radicals B7.1, B9.1 and B11.1
  • Figure US20220104496A1-20220407-C00201
  • m is 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, preferably ethyl; and
    R42 is C1-C4haloalkyl, preferably trifluoromethyl;
  • Figure US20220104496A1-20220407-C00202
  • m is 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, preferably ethyl; and
    R44 is C1-C4haloalkyl, preferably trifluoromethyl;
  • Figure US20220104496A1-20220407-C00203
  • m is 2;
    R45 is C1-C4alkyl, preferably ethyl; and
    R46 is C1-C4haloalkyl, preferably trifluoromethyl.
  • A further especially preferred group of compounds of formula I according to the invention is defined as embodiment (2) and comprises combinations of
  • (2): Radical A3 with radicals B selected from B7, B9 and B11;
    wherein A3 is preferably represented by the radical A3.1
  • Figure US20220104496A1-20220407-C00204
  • wherein R47 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
    G41 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C6haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and
    G22 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C6haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and the radicals B7, B9 and B11 are preferably represented by the radicals selected from B7.1, B9.1 and B11.1
  • Figure US20220104496A1-20220407-C00205
  • wherein m is 0, 1 or 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00206
  • wherein m is 0, 1 or 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
  • Figure US20220104496A1-20220407-C00207
  • wherein m is 0, 1 or 2;
    R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
  • Especially preferred compounds according to embodiment (2) are represented by embodiment (2.1), wherein
  • (2.1) in the radical A3.1
  • Figure US20220104496A1-20220407-C00208
  • R47 is C1-C4haloalkyl, in particular trifluoromethyl;
    G22 is nitrogen or CH; and
    G41 is nitrogen, or C—C1-C5 alkyl, in particular nitrogen or C-methyl;
    and in the radicals B7.1, B9.1 and B11.1
  • Figure US20220104496A1-20220407-C00209
  • m is 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, preferably ethyl; and
    R42 is C1-C4haloalkyl, preferably trifluoromethyl;
  • Figure US20220104496A1-20220407-C00210
  • m is 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, preferably ethyl; and
    R44 is C1-C4haloalkyl, preferably trifluoromethyl;
  • Figure US20220104496A1-20220407-C00211
  • m is 2;
    R45 is C1-C4alkyl, preferably ethyl; and
    R46 is C1-C4haloalkyl, preferably trifluoromethyl.
  • A further especially preferred group of compounds of formula I according to the invention is defined as embodiment (3) and comprises combinations of
  • (3): Radical A4 with radical B1,
    wherein A4 is preferably represented by the radical A4.1
  • Figure US20220104496A1-20220407-C00212
  • wherein R48 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl; J3 is sulfur oxygen or N-methyl; and
    R49 is hydrogen, C1-C6 alkyl, C1-C6haloalkyl, halogen, CN, O—C1-C4alkyl, S—C1-C4alkyl, SO2—C1-C4alkyl, S-phenyl, SO2-phenyl or SO2—C1-C4halolakyl;
    and the radical 1 is
  • Figure US20220104496A1-20220407-C00213
  • wherein m is 0, 1 or 2;
    R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Preferred compounds according to embodiment (3) are also represented by embodiment (3.1), wherein
  • (3.1) in the radical A4.1
  • Figure US20220104496A1-20220407-C00214
  • R48 is C1-C4haloalkyl, in particular trifluoromethyl;
    J3 is oxygen, sulphur or N-methyl; and
    R49 is hydrogen or C1-C6 alkyl, in particular hydrogen or methyl;
    and the radicals B1, B7, B9 and B11 are preferably represented by the radicals selected from B1.1, B7.1, B9.1 and B11.1
  • Figure US20220104496A1-20220407-C00215
  • wherein m is 0, 1 or 2;
    R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00216
  • wherein m is 0, 1 or 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00217
  • wherein m is 0, 1 or 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
  • Figure US20220104496A1-20220407-C00218
  • wherein m is 0, 1 or 2;
    R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
  • Further especially preferred compounds according to embodiment (3) are represented by embodiment (3.2), wherein (3.2) in the radical A4.1
  • Figure US20220104496A1-20220407-C00219
  • R48 is C1-C4haloalkyl, in particular trifluoromethyl;
    J3 is oxygen, sulphur or N-methyl; and
    R49 is hydrogen or C1-C6 alkyl, in particular hydrogen or methyl;
    and in the radical B1.1
  • Figure US20220104496A1-20220407-C00220
  • m is 2;
    V11 is nitrogen or methine;
    R51 is C1-C4alkyl, preferably ethyl; and
    R50 is hydrogen or C1-C4haloalkyl, preferably hydrogen or trifluoromethyl.
  • A further especially preferred group of compounds of formula I according to the invention is defined as embodiment (4) and comprises combinations of
  • (4): Radical A5 with radicals B selected from 1, B7, B9 and E11;
    wherein A5 is preferably represented by the radical A5.1
  • Figure US20220104496A1-20220407-C00221
  • wherein
    G55 is nitrogen or C—R53;
    R53 is C1-C4alkyl;
    G25 is nitrogen or methine; and
    R52 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
    and the radicals B1, B7, B9 and B11 are preferably represented by the radicals selected from B1.1, B7.1, B9.1 and E11.1
  • Figure US20220104496A1-20220407-C00222
  • wherein m is 0, 1 or 2;
    R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00223
  • wherein m is 0, 1 or 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00224
  • wherein m is 0, 1 or 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
  • Figure US20220104496A1-20220407-C00225
  • wherein m is 0, 1 or 2;
    R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
  • Especially preferred compounds according to embodiment (4) are represented by embodiment (4.1), wherein
  • (4.1) in the radical A5.1
  • Figure US20220104496A1-20220407-C00226
  • R52 is C1-C4haloalkyl, in particular trifluoromethyl;
    G55 is nitrogen or C—C1-C4alkyl, preferably nitrogen or methyl; and
    G25 is nitrogen or methine;
    and in the radical B1.1
  • Figure US20220104496A1-20220407-C00227
  • m is 2;
    V11 is nitrogen or methine;
    R51 is C1-C4alkyl, preferably ethyl; and
    R50 is hydrogen or C1-C4haloalkyl, preferably hydrogen or trifluoromethyl; in the radical B7.1
  • Figure US20220104496A1-20220407-C00228
  • m is 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, preferably ethyl; and
    R42 is C1-C4haloalkyl, preferably trifluoromethyl;
    in the radical B9.1
  • Figure US20220104496A1-20220407-C00229
  • m is 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, preferably ethyl; and
    R44 is C1-C4haloalkyl, preferably trifluoromethyl;
    and in the radical B11.1
  • Figure US20220104496A1-20220407-C00230
  • m is 2;
    R45 is C1-C4alkyl, preferably ethyl; and
    R46 is C1-C4haloalkyl, preferably trifluoromethyl.
  • A further especially preferred group of compounds of formula I according to the invention is defined as embodiment (5) and comprises combinations of
  • (5): Radical A6 with radicals B selected from 1, B7, B9 and B11;
    wherein A6 is preferably represented by the radical A6.1
  • Figure US20220104496A1-20220407-C00231
  • wherein
    G36 is N—R55, oxygen or sulfur;
    R55 is C1-C4alkyl;
    G26 is nitrogen or methine; and
    R54 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
    and the radicals B1, B7, B9 and B11 are preferably represented by the radicals selected from B1.1, B7.1, B9.1 and B11.1
  • Figure US20220104496A1-20220407-C00232
  • wherein m is 0, 1 or 2;
    R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00233
  • wherein m is 0, 1 or 2;
    is nitrogen or methine;
    R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00234
  • wherein m is 0, 1 or 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
  • Figure US20220104496A1-20220407-C00235
  • wherein m is 0, 1 or 2;
    R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
  • Especially preferred compounds according to embodiment (5) are represented by embodiment (5.1), wherein
  • (5.1) in the radical A6.1
  • Figure US20220104496A1-20220407-C00236
  • R54 is C1-C4haloalkyl, in particular trifluoromethyl;
    G36 is N—C1-C4alkyl, oxygen or sulfur; preferably N—CH3, oxygen or sulfur; and
    G26 is nitrogen or methine;
    and in the radical B1.1
  • Figure US20220104496A1-20220407-C00237
  • m is 2;
    V11 is nitrogen or methine;
    R51 is C1-C4alkyl, preferably ethyl; and
    R50 is hydrogen or C1-C4haloalkyl, preferably hydrogen or trifluoromethyl; in the radical B7.1
  • Figure US20220104496A1-20220407-C00238
  • m is 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, preferably ethyl; and
    R42 is C1-C4haloalkyl, preferably trifluoromethyl;
    in the radical B9.1
  • Figure US20220104496A1-20220407-C00239
  • m is 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, preferably ethyl; and
    R44 is C1-C4haloalkyl, preferably trifluoromethyl;
    and in the radical B11.1
  • Figure US20220104496A1-20220407-C00240
  • m is 2;
    R45 is C1-C4alkyl, preferably ethyl; and
    R46 is C1-C4haloalkyl, preferably trifluoromethyl.
  • A further especially preferred group of compounds of formula I according to the invention is defined as embodiment (6) and comprises combinations of
  • (6): Radical A7 with radicals B selected from 1, B7, B9 and E11;
    wherein A7 is preferably represented by the radical A7.1
  • Figure US20220104496A1-20220407-C00241
  • wherein
    G57 is nitrogen or C—R57;
    R57 is hydrogen or C1-C4alkyl; and
    R56 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
    and the radicals B1, B7, B9 and B11 are preferably represented by the radicals selected from B1.1, B7.1, B9.1 and B11.1
  • Figure US20220104496A1-20220407-C00242
  • wherein m is 0, 1 or 2;
    R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00243
  • wherein m is 0, 1 or 2;
    V82 is nitrogen methine;
    R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00244
  • wherein m is 0, 1 or 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
  • Figure US20220104496A1-20220407-C00245
  • wherein m is 0, 1 or 2;
    R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
  • Especially preferred compounds according to embodiment (6) are represented by embodiment (6.1), wherein
  • (6.1) in the radical A7.1
  • Figure US20220104496A1-20220407-C00246
  • R56 is C1-C4haloalkyl, in particular trifluoromethyl; and
    G57 is nitrogen, C—H or C—C1-C4alkyl; preferably nitrogen, C—H or C—CH3;
    and in the radical B1.1
  • Figure US20220104496A1-20220407-C00247
  • m is 2;
    V11 is nitrogen or methine;
    R51 is C1-C4alkyl, preferably ethyl; and
    R50 is hydrogen or C1-C4haloalkyl, preferably hydrogen or trifluoromethyl; in the radical B7.1
  • Figure US20220104496A1-20220407-C00248
  • m is 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, preferably ethyl; and
    R42 is C1-C4haloalkyl, preferably trifluoromethyl;
    in the radical B9.1
  • Figure US20220104496A1-20220407-C00249
  • m is 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, preferably ethyl; and
    R44 is C1-C4haloalkyl, preferably trifluoromethyl;
    and in the radical B11.1
  • Figure US20220104496A1-20220407-C00250
  • m is 2;
    R45 is C1-C4alkyl, preferably ethyl; and
    R46 is C1-C4haloalkyl, preferably trifluoromethyl.
  • A further especially preferred group of compounds of formula I according to the invention is defined as embodiment (7) and comprises combinations of
  • (7): Radical A8 with radicals B selected from 1, B7, B9 and E11;
    wherein A8 is preferably represented by the radical A8.1
  • Figure US20220104496A1-20220407-C00251
  • wherein
    G48 is nitrogen or C—R59;
    R59 is hydrogen or C1-C4alkyl; and
    R58 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
    and the radicals B1, B7, B9 and B11 are preferably represented by the radicals selected from B1.1, B7.1, B9.1 and E11.1
  • Figure US20220104496A1-20220407-C00252
  • wherein m is 0, 1 or 2;
    R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00253
  • wherein m is 0, 1 or 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
  • Figure US20220104496A1-20220407-C00254
  • wherein m is 0, 1 or 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
  • Figure US20220104496A1-20220407-C00255
  • wherein m is 0, 1 or 2;
    R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
    R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
  • Especially preferred compounds according to embodiment (7) are represented by embodiment (7.1), wherein
  • (7.1) in the radical A8.1
  • Figure US20220104496A1-20220407-C00256
  • R58 is C1-C4haloalkyl, in particular trifluoromethyl; and
    G48 is nitrogen, C—H or C—C1-C4alkyl; preferably nitrogen, C—H or C—CH3;
    and in the radical B1.1
  • Figure US20220104496A1-20220407-C00257
  • m is 2;
    V11 is nitrogen or methine;
    R51 is C1-C4alkyl, preferably ethyl; and
    R50 is hydrogen or C1-C4haloalkyl, preferably hydrogen or trifluoromethyl; in the radical B7.1
  • Figure US20220104496A1-20220407-C00258
  • m is 2;
    V82 is nitrogen or methine;
    R41 is C1-C4alkyl, preferably ethyl; and
    R42 is C1-C4haloalkyl, preferably trifluoromethyl;
    in the radical B9.1
  • Figure US20220104496A1-20220407-C00259
  • m is 2;
    V81 is nitrogen or methine,
    R43 is C1-C4alkyl, preferably ethyl; and
    R44 is C1-C4haloalkyl, preferably trifluoromethyl;
    and in the radical B11.1
  • Figure US20220104496A1-20220407-C00260
  • m is 2;
    R45 is C1-C4alkyl, preferably ethyl; and
    R46 is C1-C4haloalkyl, preferably trifluoromethyl.
  • Especially preferred compounds of formula I of the invention are listed in the following tables V1 to V26. The tables V1 to V26 represent further embodiments of the invention: In these tables Et is CH2CH3, Me is CH3, NMe is N—CH3, CMe is C-Me etc.
  • TABLE V1
    Compounds of the formula A2.1-B7.1:
    (A2.1-B7.1)
    Figure US20220104496A1-20220407-C00261
    Ret. Time
    No. R40 R41 R42 m G21 G51 V82 Mpt. ° C. (mins) (M + H) Method
    V1.01 CF3 Et CF3 2 CH N CH 160-161
    V1.02 CF3 Et CF3 2 N N CH 156-159
    V1.03 CF3 Et CF3 2 CH CMe CH
    V1.04 CF3 Et CF3 2 N CMe CH
    V1.05 CF3 Et CF3 2 CH CH CH
    V1.06 CF3 Et CF3 2 N CH CH 187-190
    V1.07 CF3 Et CF3 2 CH CH N
    V1.08 CF3 Et H 2 CH CH N
  • TABLE V2
    Compounds of the formula A2.1-B9.1:
    (A2.1-B9.1)
    Figure US20220104496A1-20220407-C00262
    Ret. time
    No. R40 R43 R44 V81 m G21 G51 Mpt. ° C. (mins) (M + H) Method
    V2.01 CF3 Et CF3 CH 2 CH N 136-138 1.08 430 SQD13
    V2.02 CF3 Et CF3 CH 2 N N 109-111
    V2.03 CF3 Et CF3 CH 2 CH CMe 190-192 1.08 443 SQD13
    V2.04 CF3 Et CF3 CH 2 N CMe 92-94 1.11 444 SQD13
    V2.05 CF3 Et CF3 CH 2 CH CH 174-176 1.13 429 SQD13
    V2.06 CF3 Et CF3 CH 2 N CH 209-211 1.11 430 SQD13
    V2.07 CF3 Et CF3 N 2 CH N 129-130 1.10 431 SQD13
    V2.08 CF3 Et CF3 N 2 N N 119-120
    V2.09 CF3 Et CF3 N 2 CH CMe
    V2.10 CF3 Et CF3 N 2 N CMe
    V2.11 CF3 Et CF3 N 2 CH CH 126-128
    V2.12 CF3 Et CF3 N 2 N CH 192-194
  • TABLE V3
    Compounds of the formula A2.1-B11.1:
    (A2.1-B11.1)
    Figure US20220104496A1-20220407-C00263
    Ret. time
    No. R40 R45 R46 m G21 G51 Mpt. ° C. (mins) (M + H) Method
    V3.01 CF3 Et CF3 2 CH N 133-134 0.95 425 SQD13
    V3.02 CF3 Et CF3 2 N N 158-159 0.93 426 SQD13
    V3.03 CF3 Et CF3 2 CH CMe
    V3.04 CF3 Et CF3 2 N CMe 106-108 1.01 439 SQD13
    V3.05 CF3 Et CF3 2 CH CH 188-190 1.07 424 SQD13
    V3.06 CF3 Et CF3 2 N CH 135-137 1.03 425 SQD13
  • TABLE V4
    Compounds of the formula A3.1-B7.1:
    (A3.1-B7.1)
    Figure US20220104496A1-20220407-C00264
    Ret. time
    No. R47 R41 R42 m G22 G41 V82 Mpt. ° C. (mins) (M + H) Method
    V4.01 CF3 Et CF3 2 CH N CH 198-199
    V4.02 CF3 Et CF3 2 N N CH 195-197
    V4.03 CF3 Et CF3 2 CH CMe CH
    V4.04 CF3 Et CF3 2 N CMe CH
    V4.05 CF3 Et CF3 2 CH CH CH
    V4.06 CF3 Et CF3 2 N CH CH
  • TABLE V5
    Compounds of the formula A3.1-B9.1:
    (A3.1-B9.1)
    Figure US20220104496A1-20220407-C00265
    Ret. time
    No. R47 R43 R44 m G22 G41 V81 Mpt. ° C. (mins) (M + H) Method
    V5.01  CF3 Et CF3 2 CH N CH 147-149 1.08 430 SQD13
    V5.02  CF3 Et CF3 2 N N CH 156-158
    V5.03  CF3 Et CF3 2 CH CMe CH
    V5.04  CF3 Et CF3 2 N CMe CH
    V5.05  CF3 Et CF3 2 CH CH CH
    V5.06  CF3 Et CF3 2 N CH CH
    V5.07  CF3 Et CF3 2 CH N N 127-128 1.0 431 SQD13
    V5.08  CF3 Et CF3 2 N N N 130-131
    V5.09  CF3 Et CF3 2 CH CMe N
    V5.010 CF3 Et CF3 2 N CMe N
    V5.011 CF3 Et CF3 2 CH CH N
    V5.012 CF3 Et CF3 2 N CH N
  • TABLE V6
    Compounds of the formula A3.1-B11.1:
    (A3.1-B11.1)
    Figure US20220104496A1-20220407-C00266
    Ret. time
    No. R47 R45 R46 m G22 G41 Mpt. ° C. (mins) (M + H) Method
    V6.01 CF3 Et CF3 2 CH N 155-156 0.95 425 SQD13
    V6.02 CF3 Et CF3 2 N N 201-203 0.89 426 SQD13
    V6.03 CF3 Et CF3 2 CH CMe
    V6.04 CF3 Et CF3 2 N CMe
    V6.05 CF3 Et CF3 2 CH CH
    V6.06 CF3 Et CF3 2 N CH
  • TABLE V7
    Compounds of the formula A4.1-B1.1:
    (A4.1-B1.1)
    Figure US20220104496A1-20220407-C00267
    Ret. time
    No. R48 R51 R50 m J3 R49 V11 Mpt. ° C. (mins) (M + H) Method
    V7.01 CF3 Et CF3 2 O Me N
    V7.02 CF3 Et CF3 2 S Me N
    V7.03 CF3 Et CF3 2 O Me CH
    V7.04 CF3 Et CF3 2 S Me CH
    V7.05 CF3 Et H 2 O Me N
    V7.06 CF3 Et H 2 S Me N
    V7.07 CF3 Et H 2 O Me CH
    V7.08 CF3 Et H 2 S Me CH
    V7.09 CF3 Et CF3 2 NMe Me N 206-208 1.04 493 SQD13
    V7.10 CF3 Et CF3 2 NMe Me CH 210-212 1.02 492 SDQ13
    V7.11 CF3 Et H 2 NMe Me N 152-154 0.87 425 ZQD13
    V7.12 CF3 Et H 2 NMe Me CH 234-236 0.90 424 SQD13
  • TABLE V8
    Compounds of the formula A5.1-B1.1:
    (A5.1-B1.1)
    Figure US20220104496A1-20220407-C00268
    Ret. time
    No. R52 R51 R50 m G25 G55 V11 Mpt. (mins) (M + H) Method
    V8.01 CF3 Et CF3 2 CH N N
    V8.02 CF3 Et CF3 2 CH N CH
    V8.03 CF3 Et H 2 CH N N
    V8.04 CF3 Et H 2 CH N CH
    V8.05 CF3 Et CF3 2 N N N
    V8.06 CF3 Et CF3 2 N N CH
    V8.07 CF3 Et H 2 N N N
    V8.08 CF3 Et H 2 N N CH
    V8.09 CF3 Et CF3 2 CH CMe N
    V8.10 CF3 Et CF3 2 CH CMe CH
    V8.11 CF3 Et H 2 CH CMe N
    V8.12 CF3 Et H 2 CH CMe CH
  • TABLE V9
    Compounds of the formula A5.1-B7.1:
    (A5.1-B7.1)
    Figure US20220104496A1-20220407-C00269
    Ret. time
    No. R52 R41 R42 m G25 G55 V82 Mpt. ° C. (mins) (M + H) Method
    V9.01 CF3 Et CF3 2 CH N CH
    V9.02 CF3 Et CF3 2 N N CH
    V9.03 CF3 Et CF3 2 N CMe CH
  • TABLE V10
    Compounds of the formula A5.1-B9.1:
    (A5.1-B9.1)
    Figure US20220104496A1-20220407-C00270
    Ret. time
    No. R52 R43 R44 m G25 G55 V81 Mpt. ° C. (mins) (M + H) Method
    V10.01 CF3 Et CF3 2 CH N CH
    V10.02 CF3 Et CF3 2 N N CH
    V10.03 CF3 Et CF3 2 N CMe CH
    V10.04 CF3 Et CF3 2 CH N N
    V10.05 CF3 Et CF3 2 N N N
    V10.06 CF3 Et CF3 2 N CMe N
  • TABLE VII
    Compounds of the formula A5.1-B11.1:
    (A5.1-B11.1)
    Figure US20220104496A1-20220407-C00271
    Ret. time
    No. R52 R45 R46 m G25 G55 Mpt. ° C. (mins) (M + H) Method
    V11.01 CF3 Et CF3 2 CH N
    V11.02 CF3 Et CF3 2 N N
    V11.03 CF3 Et CF3 2 N CMe
  • TABLE V12
    Compounds of the formula A6.1-B1.1:
    (A6.1-B1.1)
    Figure US20220104496A1-20220407-C00272
    No. R54 R51 R50 m G26 G36 V11 Mpt. ° C. Ret. time (mins) (M + H) Method
    V12.01 CF3 Et CF3 2 CH NMe N 214-216 0.99 439 ZQD13
    V12.02 CF3 Et CF3 2 CH NMe CH 168-170 0.98 438 ZQD13
    V12.03 CF3 Et H 2 CH NMe N 211-213 0.81 371 ZQD13
    V12.04 CF3 Et H 2 CH NMe CH 192-195
    V12.05 CF3 Et CF3 2 CH O N 1.02 426 SQD13
    V12.06 CF3 Et CF3 2 CH O CH 1.04 423 SQD13
    V12.07 CF3 Et H 2 CH O N 0.87 358 SQD13
    V12.08 CF3 Et H 2 CH O CH
    V12.09 CF3 Et CF3 2 CH S N
    V12.10 CF3 Et CF3 2 CH S CH
    V12.11 CF3 Et H 2 CH S N
    V12.12 CF3 Et H 2 CH S CH
    V12.13 CF3 Et CF3 2 N NMe N
    V12.14 CF3 Et CF3 2 N NMe CH
    V12.15 CF3 Et H 2 N NMe N
    V12.16 CF3 Et H 2 N NMe CH
    V12.17 Cl Et CF3 2 N NMe N 228-229 0.91 406/408 ZCQ13
    V12.18 CF3 Me CF3 2 CH NMe N 234-236 0.93 425 SQD13
    V12.19 CF3 Et OCHF2 2 CH NMe N 146-148 1.03 405 SQD13
    V12.20 Br Et CF3 2 CH NMe N 188-190 0.95 449/451 SQD13
  • TABLE V13
    Compounds of the formula A6.1-B7.1:
    (A6.1-B7.1)
    Figure US20220104496A1-20220407-C00273
    No. R54 R41 R42 m G26 G36 V82 Mpt. ° C. Ret. time (mins) (M + H) Method
    V13.01 CF3 Et CF3 2 CH NMe CH 188-191
    V13.02 CF3 Et CF3 2 CH O CH
    V13.03 CF3 Et CF3 2 N NMe CH
    V13.04 CF3 Et CF3 2 CH S CH
    V13.05 CF3 Et H 2 CH NMe N 178-179 0.85 377 SQD13
  • TABLE V14
    Compounds of the formula A6.1-B9.1:
    (A6.1-B9.1)
    Figure US20220104496A1-20220407-C00274
    No. R54 R43 R44 m G26 G36 V81 Mpt. ° C. Ret. time (mins) (M + H) Method
    V14.01 CF3 Et CF3 2 CH NMe CH 115-117 1.09 407 SQD13
    V14.02 CF3 Et CF3 2 CH O CH
    V14.03 CF3 Et CF3 2 N NMe CH
    V14.04 CF3 Et CF3 2 CH S CH
    V14.05 CF3 Et CF3 2 CH NMe N 168-170 0.95 445 SQD13
    V14.06 CF3 Et CF3 2 CH O N
    V14.07 CF3 Et CF3 2 N NMe N
    V14.08 CF3 Et CF3 2 CH S N
  • TABLE V15
    Compounds of the formula A6.1-B11.1:
    (A6.1-B11.1)
    Figure US20220104496A1-20220407-C00275
    No. R54 R45 R46 m G26 G36 Mpt. ° C. Ret. time (mins) (M + H) Method
    V15.01 CF3 Et CF3 2 CH NMe 209-211 1.09 407 SQD13
    V15.02 CF3 Et CF3 2 CH O
    V15.03 CF3 Et CF3 2 N NMe
    V15.04 CF3 Et CF3 2 CH S
  • TABLE V16
    Compounds of the formula A7.1-B1.1:
    (A7.1-B1.1)
    Figure US20220104496A1-20220407-C00276
    No. R56 R51 R50 m G57 V11 Mpt. ° C. Ret. time (mins) (M + H) Method
    V16.01 CF3 Et CF3 2 CMe N  240-242° 1.01 439 SQD13
    V16.02 CF3 Et CF3 2 CH N 180-181 0.98 425 SQD13
    V16.03 CF3 Et CF3 2 N N 190-192 0.94 426 SQD13
    V16.04 CF3 Et CF3 2 CMe CH
    V16.05 CF3 Et CF3 2 CH CH 1.02 424 SQD13
    V16.06 CF3 Et CF3 2 N CH 148-150 0.87 357 SQD13
    V16.07 CF3 Et H 2 CMe N 0.81 371 SQD13
    V16.08 CF3 Et H 2 CH N 216-217 0.79 357 SQD13
    V16.09 CF3 Et H 2 N N 0.76 358 SQD13
    V16.10 CF3 Et H 2 CMe CH
    V16.11 CF3 Et H 2 CH CH 166-167 0.88 356 SQD13
    V16.12 CF3 Et H 2 N CH 193-195 1.01 425 SQD13
  • TABLE V17
    Compounds of the formula A7.1-B7.1:
    (A7.1-B7.1)
    Figure US20220104496A1-20220407-C00277
    No. R56 R41 R42 m G57 V82 Mpt. ° C. Ret. time (mins) (M + H) Method
    V17.01 CF3 Et CF3 2 CMe CH
    V17.02 CF3 Et CF3 2 H CH
    V17.03 CF3 Et CF3 2 N CH
    V17.04 CF3 Et H 2 H N
  • TABLE V18
    Compounds of the formula A7.1-B9.1:
    (A7.1-B9.1)
    Figure US20220104496A1-20220407-C00278
    No. R56 R43 R44 m G57 V81 Mpt. ° C. Ret. time (mins) (M + H) Method
    V18.01 CF3 Et CF3 2 CMe CH
    V18.02 CF3 Et CF3 2 H CH 201-202° C. 1.08 430 SQD13
    V18.03 CF3 Et CF3 2 N CH 161-162 1.04 431 SQD13
    V18.04 CF3 Et CF3 2 CMe N
    V18.05 CF3 Et CF3 2 H N 163-165 1.06 431 SQD13
    V18.06 CF3 Et CF3 2 N N 157-158 0.97 432 SQD13
  • TABLE V19
    Compounds of the formula A7.1-B11.1:
    (A7.1-B11.1)
    Figure US20220104496A1-20220407-C00279
    No. R56 R45 R46 m G57 Mpt. °. Ret. time (mins) (M + H) Method
    V19.01 CF3 Et CF3 2 CMe
    V19.02 CF3 Et CF3 2 CH 0.99 425 SQD13
    V19.03 CF3 Et CF3 2 N 0.94 426 SQD13
  • TABLE V20
    Compounds of the formula A8.1-B1.1:
    (A8.1-B1.1)
    Figure US20220104496A1-20220407-C00280
    No. R58 R51 R50 m G48 V11 Mpt. ° C. Ret. time (mins) (M + H) Method
    V20.01 CF3 Et CF3 2 CMe N 245-246 1.00 439 SQD13
    V20.02 CF3 Et CF3 2 CH N 197-203 0.97 425 SQD13
    V20.03 CF3 Et CF3 2 N N
    V20.04 CF3 Et CF3 2 CMe CH
    V20.05 CF3 Et CF3 2 CH CH 1.00 424 SQD13
    V20.06 CF3 Et CF3 2 N CH
    V20.07 CF3 Et H 2 CMe N 272-273 0.80 371 SQD13
    V20.08 CF3 Et H 2 CH N 208-218 0.77 357 ZCQ13
    V20.09 CF3 Et H 2 N N
    V20.10 CF3 Et H 2 CMe CH
    V20.11 CF3 Et H 2 CH CH
    V20.12 CF3 Et H 2 N CH
  • TABLE V21
    Compounds of the formula A8.1-B7.1:
    (A8.1-B7.1)
    Figure US20220104496A1-20220407-C00281
    No. R58 R41 R42 m G48 V82 Mpt. ° C. Ret. time (mins) (M + H) Method
    V21.01 CF3 Et CF3 2 CMe CH
    V21.02 CF3 Et CF3 2 CH CH
    V21.03 CF3 Et CF3 2 N CH
  • TABLE V22
    Compounds of the formula A8.1-B9.1:
    (A8.1-B9.1)
    Figure US20220104496A1-20220407-C00282
    No. R58 R43 R44 m G48 V81 Mpt. ° C. Ret. time (mins) (M + H) Method
    V22.01 CF3 Et CF3 2 C—Me CH
    V22.02 CF3 Et CF3 2 CH CH 204-205 1.07 430 SQD13
    V22.03 CF3 Et CF3 2 N CH
    V22.04 CF3 Et CF3 2 CMe N
    V22.05 CF3 Et CF3 2 CH N
    V22.06 CF3 Et CF3 2 N N
  • TABLE V23
    Compounds of the formula A8.1-B11.1:
    (A8.1-B11.1)
    Figure US20220104496A1-20220407-C00283
    No. R58 R45 R46 m G48 Mpt. ° C. Ret. time (mins) (M + H) Method
    V23.01 CF3 Et CF3 2 CMe
    V23.02 CF3 Et CF3 2 CH 0.98 425 SQD13
    V23.03 CF3 Et CF3 2 N
  • TABLE V24
    Compounds of the formula A4.1-B7.1:
    (A4.1-B7.1)
    Figure US20220104496A1-20220407-C00284
    No. R48 R41 m J3 R49 R42 V82 Mpt. ° C. Ret. time (mins) (M + H) Method
    V24.01 CF3 Et 2 O Me CF3 CH
    V24.02 CF3 Et 2 S Me CF3 CH
    V24.03 CF3 Et 2 NMe Me CF3 CH
    V24.04 CF3 Et 2 NMe Me CF3 CH 185-187 1.06 498 SQD13
    V24.05 CF3 Et 2 Me Me H N 214-216 0.90 431 SQD13
  • TABLE V25
    Compounds of the formula A4.1-B9.1:
    (A4.1-B9.1)
    Figure US20220104496A1-20220407-C00285
    No. R48 R43 R44 m J3 R49 V81 Mpt. ° C. Ret. time (mins) (M + H) Method
    V25.01 CF3 Et CF3 2 O Me CH
    V25.02 CF3 Et CF3 2 S Me CH
    V25.03 CF3 Et CF3 2 NMe Me CH 158-160 1.03 498 SQD13
    V25.04 CF3 Et CF3 2 O Me N
    V25.05 CF3 Et CF3 2 S Me N
    V25.06 CF3 Et CF3 2 NMe N 170-172 0.99 499 SQ13
  • TABLE V26
    Compounds of the formula A4.1-B11.1:
    (A4.1-B11.1)
    Figure US20220104496A1-20220407-C00286
    No. R48 R45 R46 m J3 R49 Mpt. ° C. Ret. time (mins) (M + H) Method
    V26.01 CF3 Et CF3 2 O Me
    V26.02 CF3 Et CF3 2 S Me
    V26.03 CF3 Et CF3 2 NMe Me 197-199 0.95 493 SQD13
    • Formulation Examples (%=Percent by Weight)
  • Example F1: Emulsion concentrates a) b) c)
    Active ingredient 25% 40% 50%
    Calcium dodecylbenzenesulfonate  5%  8%  6%
    Castor oil polyethylene  5% — —
    glycol ether (36 mol of EO)
    Tributylphenoxypolyethylene glycol — 12%  4%
    ether (30 mol of EO)
    Cyclohexanone — 15% 20%
    Xylene mixture 65% 25% 20%
  • Emulsions of any desired concentration can be prepared from such concentrates by dilution with water.
  • Example F2: Solutions a) b) c) d)
    Active ingredient 80% 10% 5% 95%
    Ethylene glycol monomethyl 20% — — —
    ether
    Polyethylene glycol — 70% — —
    MW 400
    N-Methylpyrrolid-2-one — 20% — —
    Epoxidized coconut oil — — 1%  5%
    Petroleum ether — — 94%  —
    (boiling range: 160-190°)
  • The solutions are suitable for use in the form of microdrops.
  • Example F3: Granules a) b) c) d)
    Active ingredient 5% 10%  8% 21%
    Kaolin 94%  — 79% 54%
    Highly disperse silica 1% — 13%  7%
    Attapulgite — 90% — 18%
  • The active ingredient is dissolved in dichloromethane, the solution is sprayed onto the carrier(s), and the solvent is subsequently evaporated in vacuo.
  • Example F4: Dusts a) b)
    Active ingredient 2% 5%
    Highly disperse silica 1% 5%
    Talc 97%  —
    Kaolin — 90% 
  • Ready-to-use dusts are obtained by intimately mixing the carriers and the active ingredient.
  • Example F5: Wettable powders a) b) c)
    Active ingredient 25%  50% 75%
    Sodium lignosulfonate 5%  5% —
    Sodium lauryl sulfate 3% —  5%
    Sodium diisobutyl- —  6% 10%
    naphthalenesulfonate
    Octylphenoxypolyethylene glycol —  2% —
    ether (7-8 mol of EO)
    Highly disperse silica 5% 10% 10%
    Kaolin 62%  27% —
  • The active ingredient is mixed with the additives and the mixture is ground thoroughly in a suitable mill. This gives wettable powders, which can be diluted with water to give suspensions of any desired concentration.
    • Example F6: Extruder Granules
  • Active ingredient 10%
    Sodium lignosulfonate  2%
    Carboxymethylcellulose  1%
    Kaolin 87%
  • The active ingredient is mixed with the additives, and the mixture is ground, moistened with water, extruded, granulated and dried in a stream of air.
    • Example F7: Coated Granules
  • Active ingredient 3%
    Polyethylene glycol (MW 200) 3%
    Kaolin 94% 
  • In a mixer, the finely ground active ingredient is applied uniformly to the kaolin, which has been moistened with the polyethylene glycol. This gives dust-free coated granules.
    • Example F8: Suspension Concentrate
  • Active ingredient 40%
    Ethylene glycol 10%
    Nonylphenoxypolyethylene glycol ether (15 mol of EO)  6%
    Sodium lignosulfonate 10%
    Carboxymethylcellulose  1%
    37% aqueous formaldehyde solution 0.2% 
    Silicone oil (75% aqueous emulsion) 0.8% 
    Water 32%
  • The finely ground active ingredient is mixed intimately with the additives. Suspensions of any desired concentration can be prepared from the thus resulting suspension concentrate by dilution with water.
  • Example F9: Powders for dry seed treatment a) b) c)
    active ingredient 25% 50% 75%
    light mineral oil  5%  5%  5%
    highly dispersed silicic acid  5%  5% —
    Kaolin 65% 40% —
    Talcum — — 20%
  • The combination is thoroughly mixed with the adjuvants and the mixture is thoroughly ground in a suitable mill, affording powders that can be used directly for seed treatment.
    • Example F10: Emulsifiable Concentrate
  • active ingredient 10%
    octylphenol polyethylene glycol ether (4-5 mol of ethylene  3%
    oxide)
    calcium dodecylbenzenesulfonate  3%
    castor oil polyglycol ether (35 mol of ethylene oxide)  4%
    Cyclohexanone 30%
    xylene mixture 50%
  • Emulsions of any required dilution, which can be used in plant protection, can be obtained from this concentrate by dilution with water.
    • Example F11: Flowable Concentrate for Seed Treatment
  • active ingredients 40% 
    propylene glycol 5%
    copolymer butanol PO/EO 2%
    Tristyrenephenole with 10-20 moles EO 2%
    1,2-benzisothiazolin-3-one (in the form of a 20% solution in 0.5% 
    water)
    monoazo-pigment calcium salt 5%
    Silicone oil (in the form of a 75% emulsion in water) 0.2% 
    Water 45.3%  
  • The finely ground combination is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired dilution can be obtained by dilution with water. Using such dilutions, living plants as well as plant propagation material can be treated and protected against infestation by microorganisms, by spraying, pouring or immersion.
  • The activity of the compositions according to the invention can be broadened considerably, and adapted to prevailing circumstances, by adding other insecticidally, acaricidally and/or fungicidally active ingredients. The mixtures of the compounds of formula I with other insecticidally, acaricidally and/or fungicidally active ingredients may also have further surprising advantages which can also be described, in a wider sense, as synergistic activity. For example, better tolerance by plants, reduced phytotoxicity, insects can be controlled in their different development stages or better behaviour during their production, for example during grinding or mixing, during their storage or during their use.
  • Suitable additions to active ingredients here are, for example, representatives of the following classes of active ingredients: organophosphorus compounds, nitrophenol derivatives, thioureas, juvenile hormones, formamidines, benzophenone derivatives, ureas, pyrrole derivatives, carbamates, pyrethroids, chlorinated hydrocarbons, acylureas, pyridylmethyleneamino derivatives, macrolides, neonicotinoids and Bacillus thuringiensis preparations.
  • The following mixtures of the compounds of formula I with active ingredients are preferred (the abbreviation “TX” means “one compound selected from the group consisting of the compounds described in Tables 1 to 168 and V1 to V26 of the present invention”):
  • an adjuvant selected from the group of substances consisting of petroleum oils (alternative name) (628)+TX,
    an acaricide selected from the group of substances consisting of acequinocyl ([57960-19-7] [CCN])+TX, fenpyroxymate [134098-61-6][CCN]+TX, flucythrinate [70124-77-5][CCN]+TX, 1,1-bis(4-chlorophenyl)-2-ethoxyethanol (IUPAC name) (910)+TX, hexythiazox [78587-05-0][CCN]+TX, 2,4-dichlorophenyl benzenesulfonate (IUPAC/Chemical Abstracts name) (1059)+TX, 2-fluoro-N-methyl-N-1-naphthylacetamide (IUPAC name) (1295)+TX, 4-chlorophenyl phenyl sulfone (IUPAC name) (981)+TX, abamectin (1)+TX, acequinocyl (3)+TX, acetoprole [CCN]+TX, acrinathrin (9)+TX, aldicarb (16)+TX, aldoxycarb (863)+TX, alpha-cypermethrin (202)+TX, amidithion (870)+TX, amidoflumet [CCN]+TX, amidothioate (872)+TX, amiton (875)+TX, amiton hydrogen oxalate (875)+TX, amitraz (24)+TX, aramite (881)+TX, arsenous oxide (882)+TX, AVI 382 (compound code)+TX, AZ 60541 (compound code)+TX, azinphos-ethyl (44)+TX, azinphos-methyl (45)+TX, azobenzene (IUPAC name) (888)+TX, azocyclotin (46)+TX, azothoate (889)+TX, benomyl (62)+TX, benoxafos (alternative name) [CCN]+TX, benzoximate (71)+TX, benzyl benzoate (IUPAC name) [CCN]+TX, bifenazate (74)+TX, bifenthrin (76)+TX, binapacryl (907)+TX, brofenvalerate (alternative name)+TX, bromo-cyclen (918)+TX, bromophos (920)+TX, bromophos-ethyl (921)+TX, bromopropylate (94)+TX, buprofezin (99)+TX, butocarboxim (103)+TX, butoxycarboxim (104)+TX, butylpyridaben (alternative name)+TX, calcium polysulfide (IUPAC name) (111)+TX, camphechlor (941)+TX, carbanolate (943)+TX, carbaryl (115)+TX, carbofuran (118)+TX, carbophenothion (947)+TX, CGA 50′439 (development code) (125)+TX, chinomethionat (126)+TX, chlorbenside (959)+TX, chlordimeform (964)+TX, chlordimeform hydrochloride (964)+TX, chlorfenapyr (130)+TX, chlorfenethol (968)+TX, chlorfenson (970)+TX, chlorfensulfide (971)+TX, chlorfenvinphos (131)+TX, chlorobenzilate (975)+TX, chloromebuform (977)+TX, chloromethiuron (978)+TX, chloropropylate (983)+TX, chlorpyrifos (145)+TX, chlorpyrifos-methyl (146)+TX, chlorthiophos (994)+TX, cinerin I (696)+TX, cinerin II (696)+TX, cinerins (696)+TX, clofentezine (158)+TX, closantel (alternative name) [CCN]+TX, coumaphos (174)+TX, crotamiton (alternative name) [CCN]+TX, crotoxyphos (1010)+TX, cufraneb (1013)+TX, cyanthoate (1020)+TX, cyflumetofen [400882-07-7]+TX, cyhalothrin (196)+TX, cyhexatin (199)+TX, cypermethrin (201)+TX, DCPM (1032)+TX, DDT (219)+TX, demephion (1037)+TX, demephion-O (1037)+TX, demephion-S (1037)+TX, demeton (1038)+TX, demeton-methyl (224)+TX, demeton-O (1038)+TX, demeton-O-methyl (224)+TX, demeton-S (1038)+TX, demeton-S-methyl (224)+TX, demeton-S-methylsulfon (1039)+TX, diafenthiuron (226)+TX, dialifos (1042)+TX, diazinon (227)+TX, dichlofluanid (230)+TX, dichlorvos (236)+TX, dicliphos (alternative name)+TX, dicofol (242)+TX, dicrotophos (243)+TX, dienochlor (1071)+TX, dimefox (1081)+TX, dimethoate (262)+TX, dinactin (alternative name) (653)+TX, dinex (1089)+TX, dinex-diclexine (1089)+TX, dinobuton (269)+TX, dinocap (270)+TX, dinocap-4 [CCN]+TX, dinocap-6 [CCN]+TX, dinocton (1090)+TX, dinopenton (1092)+TX, dinosulfon (1097)+TX, dinoterbon (1098)+TX, dioxathion (1102)+TX, diphenyl sulfone (IUPAC name) (1103)+TX, disulfiram (alternative name) [CCN]+TX, disulfoton (278)+TX, DNOC (282)+TX, dofenapyn (1113)+TX, doramectin (alternative name) [CCN]+TX, endosulfan (294)+TX, endothion (1121)+TX, EPN (297)+TX, eprinomectin (alternative name) [CCN]+TX, ethion (309)+TX, ethoate-methyl (1134)+TX, etoxazole (320)+TX, etrimfos (1142)+TX, fenazaflor (1147)+TX, fenazaquin (328)+TX, fenbutatin oxide (330)+TX, fenothiocarb (337)+TX, fenpropathrin (342)+TX, fenpyrad (alternative name)+TX, fenpyroximate (345)+TX, fenson (1157)+TX, fentrifanil (1161)+TX, fenvalerate (349)+TX, fipronil (354)+TX, fluacrypyrim (360)+TX, fluazuron (1166)+TX, flubenzimine (1167)+TX, flucycloxuron (366)+TX, flucythrinate (367)+TX, fluenetil (1169)+TX, flufenoxuron (370)+TX, flumethrin (372)+TX, fluorbenside (1174)+TX, fluvalinate (1184)+TX, FMC 1137 (development code) (1185)+TX, formetanate (405)+TX, formetanate hydrochloride (405)+TX, formothion (1192)+TX, formparanate (1193)+TX, gamma-HCH (430)+TX, glyodin (1205)+TX, halfenprox (424)+TX, heptenophos (432)+TX, hexadecyl cyclopropanecarboxylate (IUPAC/Chemical Abstracts name) (1216)+TX, hexythiazox (441)+TX, iodomethane (IUPAC name) (542)+TX, isocarbophos (alternative name) (473)+TX, isopropyl O-(methoxyaminothiophosphoryl)salicylate (IUPAC name) (473)+TX, ivermectin (alternative name) [CCN]+TX, jasmolin I (696)+TX, jasmolin II (696)+TX, jodfenphos (1248)+TX, lindane (430)+TX, lufenuron (490)+TX, malathion (492)+TX, malonoben (1254)+TX, mecarbam (502)+TX, mephosfolan (1261)+TX, mesulfen (alternative name) [CCN]+TX, methacrifos (1266)+TX, methamidophos (527)+TX, methidathion (529)+TX, methiocarb (530)+TX, methomyl (531)+TX, methyl bromide (537)+TX, metolcarb (550)+TX, mevinphos (556)+TX, mexacarbate (1290)+TX, milbemectin (557)+TX, milbemycin oxime (alternative name) [CCN]+TX, mipafox (1293)+TX, monocrotophos (561)+TX, morphothion (1300)+TX, moxidectin (alternative name) [CCN]+TX, naled (567)+TX, NC-184 (compound code)+TX, NC-512 (compound code)+TX, nifluridide (1309)+TX, nikkomycins (alternative name) [CCN]+TX, nitrilacarb (1313)+TX, nitrilacarb 1:1 zinc chloride complex (1313)+TX, NNI-0101 (compound code)+TX, NNI-0250 (compound code)+TX, omethoate (594)+TX, oxamyl (602)+TX, oxydeprofos (1324)+TX, oxydisulfoton (1325)+TX, pp′-DDT (219)+TX, parathion (615)+TX, permethrin (626)+TX, petroleum oils (alternative name) (628)+TX, phenkapton (1330)+TX, phenthoate (631)+TX, phorate (636)+TX, phosalone (637)+TX, phosfolan (1338)+TX, phosmet (638)+TX, phosphamidon (639)+TX, phoxim (642)+TX, pirimiphos-methyl (652)+TX, polychloroterpenes (traditional name) (1347)+TX, polynactins (alternative name) (653)+TX, proclonol (1350)+TX, profenofos (662)+TX, promacyl (1354)+TX, propargite (671)+TX, propetamphos (673)+TX, propoxur (678)+TX, prothidathion (1360)+TX, prothoate (1362)+TX, pyrethrin I (696)+TX, pyrethrin II (696)+TX, pyrethrins (696)+TX, pyridaben (699)+TX, pyridaphenthion (701)+TX, pyrimidifen (706)+TX, pyrimitate (1370)+TX, quinalphos (711)+TX, quintiofos (1381)+TX, R-1492 (development code) (1382)+TX, RA-17 (development code) (1383)+TX, rotenone (722)+TX, schradan (1389)+TX, sebufos (alternative name)+TX, selamectin (alternative name) [CCN]+TX, SI-0009 (compound code)+TX, sophamide (1402)+TX, spirodiclofen (738)+TX, spiromesifen (739)+TX, SSI-121 (development code) (1404)+TX, sulfiram (alternative name) [CCN]+TX, sulfluramid (750)+TX, sulfotep (753)+TX, sulfur (754)+TX, SZI-121 (development code) (757)+TX, tau-fluvalinate (398)+TX, tebufenpyrad (763)+TX, TEPP (1417)+TX, terbam (alternative name)+TX, tetrachlorvinphos (777)+TX, tetradifon (786)+TX, tetranactin (alternative name) (653)+TX, tetrasul (1425)+TX, thiafenox (alternative name)+TX, thiocarboxime (1431)+TX, thiofanox (800)+TX, thiometon (801)+TX, thioquinox (1436)+TX, thuringiensin (alternative name) [CCN]+TX, triamiphos (1441)+TX, triarathene (1443)+TX, triazophos (820)+TX, triazuron (alternative name)+TX, trichlorfon (824)+TX, trifenofos (1455)+TX, trinactin (alternative name) (653)+TX, vamidothion (847)+TX, vaniliprole [CCN] and YI-5302 (compound code)+TX,
    an algicide selected from the group of substances consisting of bethoxazin [CCN]+TX, copper dioctanoate (IUPAC name) (170)+TX, copper sulfate (172)+TX, cybutryne [CCN]+TX, dichlone (1052)+TX, dichlorophen (232)+TX, endothal (295)+TX, fentin (347)+TX, hydrated lime [CCN]+TX, nabam (566)+TX, quinoclamine (714)+TX, quinonamid (1379)+TX, simazine (730)+TX, triphenyltin acetate (IUPAC name) (347) and triphenyltin hydroxide (IUPAC name) (347)+TX,
    an anthelmintic selected from the group of substances consisting of abamectin (1)+TX, crufomate (1011)+TX, doramectin (alternative name) [CCN]+TX, emamectin (291)+TX, emamectin benzoate (291)+TX, eprinomectin (alternative name) [CCN]+TX, ivermectin (alternative name) [CCN]+TX, milbemycin oxime (alternative name) [CCN]+TX, moxidectin (alternative name) [CCN]+TX, piperazine [CCN]+TX, selamectin (alternative name) [CCN]+TX, spinosad (737) and thiophanate (1435)+TX,
    an avicide selected from the group of substances consisting of chloralose (127)+TX, endrin (1122)+TX, fenthion (346)+TX, pyridin-4-amine (IUPAC name) (23) and strychnine (745)+TX, a bactericide selected from the group of substances consisting of 1-hydroxy-1H-pyridine-2-thione (IUPAC name) (1222)+TX, 4-(quinoxalin-2-ylamino)benzenesulfonamide (IUPAC name) (748)+TX, 8-hydroxyquinoline sulfate (446)+TX, bronopol (97)+TX, copper dioctanoate (IUPAC name) (170)+TX, copper hydroxide (IUPAC name) (169)+TX, cresol [CCN]+TX, dichlorophen (232)+TX, dipyrithione (1105)+TX, dodicin (1112)+TX, fenaminosulf (1144)+TX, formaldehyde (404)+TX, hydrargaphen (alternative name) [CCN]+TX, kasugamycin (483)+TX, kasugamycin hydrochloride hydrate (483)+TX, nickel bis(dimethyldithiocarbamate) (IUPAC name) (1308)+TX, nitrapyrin (580)+TX, octhilinone (590)+TX, oxolinic acid (606)+TX, oxytetracycline (611)+TX, potassium hydroxyquinoline sulfate (446)+TX, probenazole (658)+TX, streptomycin (744)+TX, streptomycin sesquisulfate (744)+TX, tecloftalam (766)+TX, and thiomersal (alternative name) [CCN]+TX,
    a biological agent selected from the group of substances consisting of Adoxophyes orana GV (alternative name) (12)+TX, Agrobacterium radiobacter (alternative name) (13)+TX, Amblyseius spp. (alternative name) (19)+TX, Anagrapha falcifera NPV (alternative name) (28)+TX, Anagrus atomus (alternative name) (29)+TX, Aphelinus abdominalis (alternative name) (33)+TX, Aphidius colemani (alternative name) (34)+TX, Aphidoletes aphidimyza (alternative name) (35)+TX, Autographa californica NPV (alternative name) (38)+TX, Bacillus firmus (alternative name) (48)+TX, Bacillus sphaericus Neide (scientific name) (49)+TX, Bacillus thuringiensis Berliner (scientific name) (51)+TX, Bacillus thuringiensis subsp. aizawai (scientific name) (51)+TX, Bacillus thuringiensis subsp. israelensis (scientific name) (51)+TX, Bacillus thuringiensis subsp. japonensis (scientific name) (51)+TX, Bacillus thuringiensis subsp. kurstaki (scientific name) (51)+TX, Bacillus thuringiensis subsp. tenebrionis (scientific name) (51)+TX, Beauveria bassiana (alternative name) (53)+TX, Beauveria brongniartii (alternative name) (54)+TX, Chrysoperla carnea (alternative name) (151)+TX, Cryptolaemus montrouzieri (alternative name) (178)+TX, Cydia pomonella GV (alternative name) (191)+TX, Dacnusa sibirica (alternative name) (212)+TX, Diglyphus isaea (alternative name) (254)+TX, Encarsia formosa (scientific name) (293)+TX, Eretmocerus eremicus (alternative name) (300)+TX, Helicoverpa zea NPV (alternative name) (431)+TX, Heterorhabditis bacteriophora and H. megidis (alternative name) (433)+TX, Hippodamia convergens (alternative name) (442)+TX, Leptomastix dactylopii (alternative name) (488)+TX, Macrolophus caliginosus (alternative name) (491)+TX, Mamestra brassicae NPV (alternative name) (494)+TX, Metaphycus helvolus (alternative name) (522)+TX, Metarhizium anisopliae var. acridum (scientific name) (523)+TX, Metarhizium anisopliae var. anisopliae (scientific name) (523)+TX, Neodiprion sertifer NPV and N. lecontei NPV (alternative name) (575)+TX, Orius spp. (alternative name) (596)+TX, Paecilomyces fumosoroseus (alternative name) (613)+TX, Phytoseiulus persimilis (alternative name) (644)+TX, Spodoptera exigua multicapsid nuclear polyhedrosis virus (scientific name) (741)+TX, Steinernema bibionis (alternative name) (742)+TX, Steinernema carpocapsae (alternative name) (742)+TX, Steinernema feltiae (alternative name) (742)+TX, Steinernema glaseri (alternative name) (742)+TX, Steinernema riobrave (alternative name) (742)+TX, Steinernema riobravis (alternative name) (742)+TX, Steinernema scapterisci (alternative name) (742)+TX, Steinernema spp. (alternative name) (742)+TX, Trichogramma spp. (alternative name) (826)+TX, Typhlodromus occidentalis (alternative name) (844) and Verticillium lecanii (alternative name) (848)+TX,
    a soil sterilant selected from the group of substances consisting of iodomethane (IUPAC name) (542) and methyl bromide (537)+TX,
    a chemosterilant selected from the group of substances consisting of apholate [CCN]+TX, bisazir (alternative name) [CCN]+TX, busulfan (alternative name) [CCN]+TX, diflubenzuron (250)+TX, dimatif (alternative name) [CCN]+TX, hemel [CCN]+TX, hempa [CCN]+TX, metepa [CCN]+TX, methiotepa [CCN]+TX, methyl apholate [CCN]+TX, morzid [CCN]+TX, penfluron (alternative name) [CCN]+TX, tepa [CCN]+TX, thiohempa (alternative name) [CCN]+TX, thiotepa (alternative name) [CCN]+TX, tretamine (alternative name) [CCN] and uredepa (alternative name) [CCN]+TX,
    an insect pheromone selected from the group of substances consisting of (E)-dec-5-en-1-yl acetate with (E)-dec-5-en-1-ol (IUPAC name) (222)+TX, (E)-tridec-4-en-1-yl acetate (IUPAC name) (829)+TX, (E)-6-methylhept-2-en-4-ol (IUPAC name) (541)+TX, (E,Z)-tetradeca-4,10-dien-1-yl acetate (IUPAC name) (779)+TX, (Z)-dodec-7-en-1-yl acetate (IUPAC name) (285)+TX, (Z)-hexadec-11-enal (IUPAC name) (436)+TX, (Z)-hexadec-11-en-1-yl acetate (IUPAC name) (437)+TX, (Z)-hexadec-13-en-11-yn-1-yl acetate (IUPAC name) (438)+TX, (Z)-icos-13-en-10-one (IUPAC name) (448)+TX, (Z)-tetradec-7-en-1-al (IUPAC name) (782)+TX, (Z)-tetradec-9-en-1-ol (IUPAC name) (783)+TX, (Z)-tetradec-9-en-1-yl acetate (IUPAC name) (784)+TX, (7E,9Z)-dodeca-7,9-dien-1-yl acetate (IUPAC name) (283)+TX, (9Z,11E)-tetradeca-9,11-dien-1-yl acetate (IUPAC name) (780)+TX, (9Z,12E)-tetradeca-9,12-dien-1-yl acetate (IUPAC name) (781)+TX, 14-methyloctadec-1-ene (IUPAC name) (545)+TX, 4-methylnonan-5-ol with 4-methylnonan-5-one (IUPAC name) (544)+TX, alpha-multistriatin (alternative name) [CCN]+TX, brevicomin (alternative name) [CCN]+TX, codlelure (alternative name) [CCN]+TX, codlemone (alternative name) (167)+TX, cuelure (alternative name) (179)+TX, disparlure (277)+TX, dodec-8-en-1-yl acetate (IUPAC name) (286)+TX, dodec-9-en-1-yl acetate (IUPAC name) (287)+TX, dodeca-8+TX, 10-dien-1-yl acetate (IUPAC name) (284)+TX, dominicalure (alternative name) [CCN]+TX, ethyl 4-methyloctanoate (IUPAC name) (317)+TX, eugenol (alternative name) [CCN]+TX, frontalin (alternative name) [CCN]+TX, gossyplure (alternative name) (420)+TX, grandlure (421)+TX, grandlure I (alternative name) (421)+TX, grandlure II (alternative name) (421)+TX, grandlure Ill (alternative name) (421)+TX, grandlure IV (alternative name) (421)+TX, hexalure [CCN]+TX, ipsdienol (alternative name) [CCN]+TX, ipsenol (alternative name) [CCN]+TX, japonilure (alternative name) (481)+TX, lineatin (alternative name) [CCN]+TX, litlure (alternative name) [CCN]+TX, looplure (alternative name) [CCN]+TX, medlure [CCN]+TX, megatomoic acid (alternative name) [CCN]+TX, methyl eugenol (alternative name) (540)+TX, muscalure (563)+TX, octadeca-2,13-dien-1-yl acetate (IUPAC name) (588)+TX, octadeca-3,13-dien-1-yl acetate (IUPAC name) (589)+TX, orfralure (alternative name) [CCN]+TX, oryctalure (alternative name) (317)+TX, ostramone (alternative name) [CCN]+TX, siglure [CCN]+TX, sordidin (alternative name) (736)+TX, sulcatol (alternative name) [CCN]+TX, tetradec-11-en-1-yl acetate (IUPAC name) (785)+TX, trimedlure (839)+TX, trimedlure A (alternative name) (839)+TX, trimedlure B1 (alternative name) (839)+TX, trimedlure B2 (alternative name) (839)+TX, trimedlure C (alternative name) (839) and trunc-call (alternative name) [CCN]+TX,
    an insect repellent selected from the group of substances consisting of 2-(octylthio)ethanol (IUPAC name) (591)+TX, butopyronoxyl (933)+TX, butoxy(polypropylene glycol) (936)+TX, dibutyl adipate (IUPAC name) (1046)+TX, dibutyl phthalate (1047)+TX, dibutyl succinate (IUPAC name) (1048)+TX, diethyltoluamide [CCN]+TX, dimethyl carbate [CCN]+TX, dimethyl phthalate [CCN]+TX, ethyl hexanediol (1137)+TX, hexamide [CCN]+TX, methoquin-butyl (1276)+TX, methylneodecanamide [CCN]+TX, oxamate [CCN] and picaridin [CCN]+TX, an insecticide selected from the group of substances consisting of momfluorothrin [609346-29-4]+TX, pyrafluprole [315208-17-4]+TX, flometoquin [875775-74-9]+TX, flupyradifuron [951659-40-8]+TX, 1-dichloro-1-nitroethane (IUPAC/Chemical Abstracts name) (1058)+TX, 1,1-dichloro-2,2-bis(4-ethylphenyl)ethane (IUPAC name) (1056), +TX, 1,2-dichloropropane (IUPAC/Chemical Abstracts name) (1062)+TX, 1,2-dichloropropane with 1,3-dichloropropene (IUPAC name) (1063)+TX, 1-bromo-2-chloroethane (IUPAC/Chemical Abstracts name) (916)+TX, 2,2,2-trichloro-1-(3,4-dichlorophenyl)ethyl acetate (IUPAC name) (1451)+TX, 2,2-dichlorovinyl 2-ethylsulfinylethyl methyl phosphate (IUPAC name) (1066)+TX, 2-(1,3-dithiolan-2-yl)phenyl dimethylcarbamate (IUPAC/Chemical Abstracts name) (1109)+TX, 2-(2-butoxyethoxy)ethyl thiocyanate (IUPAC/Chemical Abstracts name) (935)+TX, 2-(4,5-dimethyl-1,3-dioxolan-2-yl)phenyl methylcarbamate (IUPAC/Chemical Abstracts name) (1084)+TX, 2-(4-chloro-3,5-xylyloxy)ethanol (IUPAC name) (986)+TX, 2-chlorovinyl diethyl phosphate (IUPAC name) (984)+TX, 2-imidazolidone (IUPAC name) (1225)+TX, 2-isovalerylindan-1,3-dione (IUPAC name) (1246)+TX, 2-methyl(prop-2-ynyl)aminophenyl methylcarbamate (IUPAC name) (1284)+TX, 2-thiocyanatoethyl laurate (IUPAC name) (1433)+TX, 3-bromo-1-chloroprop-1-ene (IUPAC name) (917)+TX, 3-methyl-1-phenylpyrazol-5-yl dimethylcarbamate (IUPAC name) (1283)+TX, 4-methyl(prop-2-ynyl)amino-3,5-xylyl methylcarbamate (IUPAC name) (1285)+TX, 5,5-dimethyl-3-oxocyclohex-1-enyl dimethylcarbamate (IUPAC name) (1085)+TX, abamectin (1)+TX, acephate (2)+TX, acetamiprid (4)+TX, acethion (alternative name) [CCN]+TX, acetoprole [CCN]+TX, acrinathrin (9)+TX, acrylonitrile (IUPAC name) (861)+TX, alanycarb (15)+TX, aldicarb (16)+TX, aldoxycarb (863)+TX, aldrin (864)+TX, allethrin (17)+TX, allosamidin (alternative name) [CCN]+TX, allyxycarb (866)+TX, alpha-cypermethrin (202)+TX, alpha-ecdysone (alternative name) [CCN]+TX, aluminium phosphide (640)+TX, amidithion (870)+TX, amidothioate (872)+TX, aminocarb (873)+TX, amiton (875)+TX, amiton hydrogen oxalate (875)+TX, amitraz (24)+TX, anabasine (877)+TX, athidathion (883)+TX, AVI 382 (compound code)+TX, AZ 60541 (compound code)+TX, azadirachtin (alternative name) (41)+TX, azamethiphos (42)+TX, azinphos-ethyl (44)+TX, azinphos-methyl (45)+TX, azothoate (889)+TX, Bacillus thuringiensis delta endotoxins (alternative name) (52)+TX, barium hexafluorosilicate (alternative name) [CCN]+TX, barium polysulfide (IUPAC/Chemical Abstracts name) (892)+TX, barthrin [CCN]+TX, Bayer 22/190 (development code) (893)+TX, Bayer 22408 (development code) (894)+TX, bendiocarb (58)+TX, benfuracarb (60)+TX, bensultap (66)+TX, beta-cyfluthrin (194)+TX, beta-cypermethrin (203)+TX, bifenthrin (76)+TX, bioallethrin (78)+TX, bioallethrin S-cyclopentenyl isomer (alternative name) (79)+TX, bioethanomethrin [CCN]+TX, biopermethrin (908)+TX, bioresmethrin (80)+TX, bis(2-chloroethyl) ether (IUPAC name) (909)+TX, bistrifluron (83)+TX, borax (86)+TX, brofenvalerate (alternative name)+TX, bromfenvinfos (914)+TX, bromocyclen (918)+TX, bromo-DDT (alternative name) [CCN]+TX, bromophos (920)+TX, bromophos-ethyl (921)+TX, bufencarb (924)+TX, buprofezin (99)+TX, butacarb (926)+TX, butathiofos (927)+TX, butocarboxim (103)+TX, butonate (932)+TX, butoxycarboxim (104)+TX, butylpyridaben (alternative name)+TX, cadusafos (109)+TX, calcium arsenate [CCN]+TX, calcium cyanide (444)+TX, calcium polysulfide (IUPAC name) (111)+TX, camphechlor (941)+TX, carbanolate (943)+TX, carbaryl (115)+TX, carbofuran (118)+TX, carbon disulfide (IUPAC/Chemical Abstracts name) (945)+TX, carbon tetrachloride (IUPAC name) (946)+TX, carbophenothion (947)+TX, carbosulfan (119)+TX, cartap (123)+TX, cartap hydrochloride (123)+TX, cevadine (alternative name) (725)+TX, chlorbicyclen (960)+TX, chlordane (128)+TX, chlordecone (963)+TX, chlordimeform (964)+TX, chlordimeform hydrochloride (964)+TX, chlorethoxyfos (129)+TX, chlorfenapyr (130)+TX, chlorfenvinphos (131)+TX, chlorfluazuron (132)+TX, chlormephos (136)+TX, chloroform [CCN]+TX, chloropicrin (141)+TX, chlorphoxim (989)+TX, chlorprazophos (990)+TX, chlorpyrifos (145)+TX, chlorpyrifos-methyl (146)+TX, chlorthiophos (994)+TX, chromafenozide (150)+TX, cinerin I (696)+TX, cinerin II (696)+TX, cinerins (696)+TX, cis-resmethrin (alternative name)+TX, cismethrin (80)+TX, clocythrin (alternative name)+TX, cloethocarb (999)+TX, closantel (alternative name) [CCN]+TX, clothianidin (165)+TX, copper acetoarsenite [CCN]+TX, copper arsenate [CCN]+TX, copper oleate [CCN]+TX, coumaphos (174)+TX, coumithoate (1006)+TX, crotamiton (alternative name) [CCN]+TX, crotoxyphos (1010)+TX, crufomate (1011)+TX, cryolite (alternative name) (177)+TX, CS 708 (development code) (1012)+TX, cyanofenphos (1019)+TX, cyanophos (184)+TX, cyanthoate (1020)+TX, cyclethrin [CCN]+TX, cycloprothrin (188)+TX, cyfluthrin (193)+TX, cyhalothrin (196)+TX, cypermethrin (201)+TX, cyphenothrin (206)+TX, cyromazine (209)+TX, cythioate (alternative name) [CCN]+TX, d-limonene (alternative name) [CCN]+TX, d-tetramethrin (alternative name) (788)+TX, DAEP (1031)+TX, dazomet (216)+TX, DDT (219)+TX, decarbofuran (1034)+TX, deltamethrin (223)+TX, demephion (1037)+TX, demephion-O (1037)+TX, demephion-S (1037)+TX, demeton (1038)+TX, demeton-methyl (224)+TX, demeton-O (1038)+TX, demeton-O-methyl (224)+TX, demeton-S (1038)+TX, demeton-S-methyl (224)+TX, demeton-S-methylsulphon (1039)+TX, diafenthiuron (226)+TX, dialifos (1042)+TX, diamidafos (1044)+TX, diazinon (227)+TX, dicapthon (1050)+TX, dichlofenthion (1051)+TX, dichlorvos (236)+TX, dicliphos (alternative name)+TX, dicresyl (alternative name) [CCN]+TX, dicrotophos (243)+TX, dicyclanil (244)+TX, dieldrin (1070)+TX, diethyl 5-methylpyrazol-3-yl phosphate (IUPAC name) (1076)+TX, diflubenzuron (250)+TX, dilor (alternative name) [CCN]+TX, dimefluthrin [CCN]+TX, dimefox (1081)+TX, dimetan (1085)+TX, dimethoate (262)+TX, dimethrin (1083)+TX, dimethylvinphos (265)+TX, dimetilan (1086)+TX, dinex (1089)+TX, dinex-diclexine (1089)+TX, dinoprop (1093)+TX, dinosam (1094)+TX, dinoseb (1095)+TX, dinotefuran (271)+TX, diofenolan (1099)+TX, dioxabenzofos (1100)+TX, dioxacarb (1101)+TX, dioxathion (1102)+TX, disulfoton (278)+TX, dithicrofos (1108)+TX, DNOC (282)+TX, doramectin (alternative name) [CCN]+TX, DSP (1115)+TX, ecdysterone (alternative name) [CCN]+TX, E1 1642 (development code) (1118)+TX, emamectin (291)+TX, emamectin benzoate (291)+TX, EMPC (1120)+TX, empenthrin (292)+TX, endosulfan (294)+TX, endothion (1121)+TX, endrin (1122)+TX, EPBP (1123)+TX, EPN (297)+TX, epofenonane (1124)+TX, eprinomectin (alternative name) [CCN]+TX, esfenvalerate (302)+TX, etaphos (alternative name) [CCN]+TX, ethiofencarb (308)+TX, ethion (309)+TX, ethiprole (310)+TX, ethoate-methyl (1134)+TX, ethoprophos (312)+TX, ethyl formate (IUPAC name) [CCN]+TX, ethyl-DDD (alternative name) (1056)+TX, ethylene dibromide (316)+TX, ethylene dichloride (chemical name) (1136)+TX, ethylene oxide [CCN]+TX, etofenprox (319)+TX, etrimfos (1142)+TX, EXD (1143)+TX, famphur (323)+TX, fenamiphos (326)+TX, fenazaflor (1147)+TX, fenchlorphos (1148)+TX, fenethacarb (1149)+TX, fenfluthrin (1150)+TX, fenitrothion (335)+TX, fenobucarb (336)+TX, fenoxacrim (1153)+TX, fenoxycarb (340)+TX, fenpirithrin (1155)+TX, fenpropathrin (342)+TX, fenpyrad (alternative name)+TX, fensulfothion (1158)+TX, fenthion (346)+TX, fenthion-ethyl [CCN]+TX, fenvalerate (349)+TX, fipronil (354)+TX, flonicamid (358)+TX, flubendiamide (CAS. Reg. No.: 272451-65-7)+TX, flucofuron (1168)+TX, flucycloxuron (366)+TX, flucythrinate (367)+TX, fluenetil (1169)+TX, flufenerim [CCN]+TX, flufenoxuron (370)+TX, flufenprox (1171)+TX, flumethrin (372)+TX, fluvalinate (1184)+TX, FMC 1137 (development code) (1185)+TX, fonofos (1191)+TX, formetanate (405)+TX, formetanate hydrochloride (405)+TX, formothion (1192)+TX, formparanate (1193)+TX, fosmethilan (1194)+TX, fospirate (1195)+TX, fosthiazate (408)+TX, fosthietan (1196)+TX, furathiocarb (412)+TX, furethrin (1200)+TX, gamma-cyhalothrin (197)+TX, gamma-HCH (430)+TX, guazatine (422)+TX, guazatine acetates (422)+TX, GY-81 (development code) (423)+TX, halfenprox (424)+TX, halofenozide (425)+TX, HCH (430)+TX, HEOD (1070)+TX, heptachlor (1211)+TX, heptenophos (432)+TX, heterophos [CCN]+TX, hexaflumuron (439)+TX, HHDN (864)+TX, hydramethylnon (443)+TX, hydrogen cyanide (444)+TX, hydroprene (445)+TX, hyquincarb (1223)+TX, imidacloprid (458)+TX, imiprothrin (460)+TX, indoxacarb (465)+TX, iodomethane (IUPAC name) (542)+TX, IPSP (1229)+TX, isazofos (1231)+TX, isobenzan (1232)+TX, isocarbophos (alternative name) (473)+TX, isodrin (1235)+TX, isofenphos (1236)+TX, isolane (1237)+TX, isoprocarb (472)+TX, isopropyl O-(methoxyaminothiophosphoryl)salicylate (IUPAC name) (473)+TX, isoprothiolane (474)+TX, isothioate (1244)+TX, isoxathion (480)+TX, ivermectin (alternative name) [CCN]+TX, jasmolin I (696)+TX, jasmolin II (696)+TX, jodfenphos (1248)+TX, juvenile hormone I (alternative name) [CCN]+TX, juvenile hormone II (alternative name) [CCN]+TX, juvenile hormone Ill (alternative name) [CCN]+TX, kelevan (1249)+TX, kinoprene (484)+TX, lambda-cyhalothrin (198)+TX, lead arsenate [CCN]+TX, lepimectin (CCN)+TX, leptophos (1250)+TX, lindane (430)+TX, lirimfos (1251)+TX, lufenuron (490)+TX, lythidathion (1253)+TX, m-cumenyl methylcarbamate (IUPAC name) (1014)+TX, magnesium phosphide (IUPAC name) (640)+TX, malathion (492)+TX, malonoben (1254)+TX, mazidox (1255)+TX, mecarbam (502)+TX, mecarphon (1258)+TX, menazon (1260)+TX, mephosfolan (1261)+TX, mercurous chloride (513)+TX, mesulfenfos (1263)+TX, metaflumizone (CCN)+TX, metam (519)+TX, metam-potassium (alternative name) (519)+TX, metam-sodium (519)+TX, methacrifos (1266)+TX, methamidophos (527)+TX, methanesulfonyl fluoride (IUPAC/Chemical Abstracts name) (1268)+TX, methidathion (529)+TX, methiocarb (530)+TX, methocrotophos (1273)+TX, methomyl (531)+TX, methoprene (532)+TX, methoquin-butyl (1276)+TX, methothrin (alternative name) (533)+TX, methoxychlor (534)+TX, methoxyfenozide (535)+TX, methyl bromide (537)+TX, methyl isothiocyanate (543)+TX, methylchloroform (alternative name) [CCN]+TX, methylene chloride [CCN]+TX, metofluthrin [CCN]+TX, metolcarb (550)+TX, metoxadiazone (1288)+TX, mevinphos (556)+TX, mexacarbate (1290)+TX, milbemectin (557)+TX, milbemycin oxime (alternative name) [CCN]+TX, mipafox (1293)+TX, mirex (1294)+TX, monocrotophos (561)+TX, morphothion (1300)+TX, moxidectin (alternative name) [CCN]+TX, naftalofos (alternative name) [CCN]+TX, naled (567)+TX, naphthalene (IUPAC/Chemical Abstracts name) (1303)+TX, NC-170 (development code) (1306)+TX, NC-184 (compound code)+TX, nicotine (578)+TX, nicotine sulfate (578)+TX, nifluridide (1309)+TX, nitenpyram (579)+TX, nithiazine (1311)+TX, nitrilacarb (1313)+TX, nitrilacarb 1:1 zinc chloride complex (1313)+TX, NNI-0101 (compound code)+TX, NNI-0250 (compound code)+TX, nornicotine (traditional name) (1319)+TX, novaluron (585)+TX, noviflumuron (586)+TX, O-5-dichloro-4-iodophenyl O-ethyl ethylphosphonothioate (IUPAC name) (1057)+TX, O,O-diethyl O-4-methyl-2-oxo-2H-chromen-7-yl phosphorothioate (IUPAC name) (1074)+TX, O,O-diethyl O-6-methyl-2-propylpyrimidin-4-yl phosphorothioate (IUPAC name) (1075)+TX, O,O,O′,O′-tetrapropyl dithiopyrophosphate (IUPAC name) (1424)+TX, oleic acid (IUPAC name) (593)+TX, omethoate (594)+TX, oxamyl (602)+TX, oxydemeton-methyl (609)+TX, oxydeprofos (1324)+TX, oxydisulfoton (1325)+TX, pp′-DDT (219)+TX, para-dichlorobenzene [CCN]+TX, parathion (615)+TX, parathion-methyl (616)+TX, penfluron (alternative name) [CCN]+TX, pentachlorophenol (623)+TX, pentachlorophenyl laurate (IUPAC name) (623)+TX, permethrin (626)+TX, petroleum oils (alternative name) (628)+TX, PH 60-38 (development code) (1328)+TX, phenkapton (1330)+TX, phenothrin (630)+TX, phenthoate (631)+TX, phorate (636)+TX, phosalone (637)+TX, phosfolan (1338)+TX, phosmet (638)+TX, phosnichlor (1339)+TX, phosphamidon (639)+TX, phosphine (IUPAC name) (640)+TX, phoxim (642)+TX, phoxim-methyl (1340)+TX, pirimetaphos (1344)+TX, pirimicarb (651)+TX, pirimiphos-ethyl (1345)+TX, pirimiphos-methyl (652)+TX, polychlorodicyclopentadiene isomers (IUPAC name) (1346)+TX, polychloroterpenes (traditional name) (1347)+TX, potassium arsenite [CCN]+TX, potassium thiocyanate [CCN]+TX, prallethrin (655)+TX, precocene I (alternative name) [CCN]+TX, precocene II (alternative name) [CCN]+TX, precocene Ill (alternative name) [CCN]+TX, primidophos (1349)+TX, profenofos (662)+TX, profluthrin [CCN]+TX, promacyl (1354)+TX, promecarb (1355)+TX, propaphos (1356)+TX, propetamphos (673)+TX, propoxur (678)+TX, prothidathion (1360)+TX, prothiofos (686)+TX, prothoate (1362)+TX, protrifenbute [CCN]+TX, pymetrozine (688)+TX, pyraclofos (689)+TX, pyrazophos (693)+TX, pyresmethrin (1367)+TX, pyrethrin 1 (696)+TX, pyrethrin II (696)+TX, pyrethrins (696)+TX, pyridaben (699)+TX, pyridalyl (700)+TX, pyridaphenthion (701)+TX, pyrimidifen (706)+TX, pyrimitate (1370)+TX, pyriproxyfen (708)+TX, quassia (alternative name) [CCN]+TX, quinalphos (711)+TX, quinalphos-methyl (1376)+TX, quinothion (1380)+TX, quintiofos (1381)+TX, R-1492 (development code) (1382)+TX, rafoxanide (alternative name) [CCN]+TX, resmethrin (719)+TX, rotenone (722)+TX, RU 15525 (development code) (723)+TX, RU 25475 (development code) (1386)+TX, ryania (alternative name) (1387)+TX, ryanodine (traditional name) (1387)+TX, sabadilla (alternative name) (725)+TX, schradan (1389)+TX, sebufos (alternative name)+TX, selamectin (alternative name) [CCN]+TX, SI-0009 (compound code)+TX, SI-0205 (compound code)+TX, SI-0404 (compound code)+TX, SI-0405 (compound code)+TX, silafluofen (728)+TX, SN 72129 (development code) (1397)+TX, sodium arsenite [CCN]+TX, sodium cyanide (444)+TX, sodium fluoride (IUPAC/Chemical Abstracts name) (1399)+TX, sodium hexafluorosilicate (1400)+TX, sodium pentachlorophenoxide (623)+TX, sodium selenate (IUPAC name) (1401)+TX, sodium thiocyanate [CCN]+TX, sophamide (1402)+TX, spinosad (737)+TX, spiromesifen (739)+TX, spirotetrmat (CCN)+TX, sulcofuron (746)+TX, sulcofuron-sodium (746)+TX, sulfluramid (750)+TX, sulfotep (753)+TX, sulfuryl fluoride (756)+TX, sulprofos (1408)+TX, tar oils (alternative name) (758)+TX, tau-fluvalinate (398)+TX, tazimcarb (1412)+TX, TDE (1414)+TX, tebufenozide (762)+TX, tebufenpyrad (763)+TX, tebupirimfos (764)+TX, teflubenzuron (768)+TX, tefluthrin (769)+TX, temephos (770)+TX, TEPP (1417)+TX, terallethrin (1418)+TX, terbam (alternative name)+TX, terbufos (773)+TX, tetrachloroethane [CCN]+TX, tetrachlorvinphos (777)+TX, tetramethrin (787)+TX, theta-cypermethrin (204)+TX, thiacloprid (791)+TX, thiafenox (alternative name)+TX, thiamethoxam (792)+TX, thicrofos (1428)+TX, thiocarboxime (1431)+TX, thiocyclam (798)+TX, thiocyclam hydrogen oxalate (798)+TX, thiodicarb (799)+TX, thiofanox (800)+TX, thiometon (801)+TX, thionazin (1434)+TX, thiosultap (803)+TX, thiosultap-sodium (803)+TX, thuringiensin (alternative name) [CCN]+TX, tolfenpyrad (809)+TX, tralomethrin (812)+TX, transfluthrin (813)+TX, transpermethrin (1440)+TX, triamiphos (1441)+TX, triazamate (818)+TX, triazophos (820)+TX, triazuron (alternative name)+TX, trichlorfon (824)+TX, trichlormetaphos-3 (alternative name) [CCN]+TX, trichloronat (1452)+TX, trifenofos (1455)+TX, triflumuron (835)+TX, trimethacarb (840)+TX, triprene (1459)+TX, vamidothion (847)+TX, vaniliprole [CCN]+TX, veratridine (alternative name) (725)+TX, veratrine (alternative name) (725)+TX, XMC (853)+TX, xylylcarb (854)+TX, YI-5302 (compound code)+TX, zeta-cypermethrin (205)+TX, zetamethrin (alternative name)+TX, zinc phosphide (640)+TX, zolaprofos (1469) and ZXI 8901 (development code) (858)+TX, cyantraniliprole [736994-63-19]+TX, chlorantraniliprole [500008-45-7]+TX, cyenopyrafen [560121-52-0]+TX, cyflumetofen [400882-07-7]+TX, pyrifluquinazon [337458-27-2]+TX, spinetoram [187166-40-1+187166-15-0]+TX, spirotetramat [203313-25-1]+TX, sulfoxaflor [946578-00-3]+TX, flufiprole [704886-18-0]+TX, meperfluthrin [915288-13-0]+TX, tetramethylfluthrin [84937-88-2]+TX and a compound of the formula B1E
  • Figure US20220104496A1-20220407-C00287
  • with the common name triflumezopyrim (disclosed in WO 2012/092115)+TX; a molluscicide selected from the group of substances consisting of bis(tributyltin) oxide (IUPAC name) (913)+TX, bromoacetamide [CCN]+TX, calcium arsenate [CCN]+TX, cloethocarb (999)+TX, copper acetoarsenite [CCN]+TX, copper sulfate (172)+TX, fentin (347)+TX, ferric phosphate (IUPAC name) (352)+TX, metaldehyde (518)+TX, methiocarb (530)+TX, niclosamide (576)+TX, niclosamide-olamine (576)+TX, pentachlorophenol (623)+TX, sodium pentachlorophenoxide (623)+TX, tazimcarb (1412)+TX, thiodicarb (799)+TX, tributyltin oxide (913)+TX, trifenmorph (1454)+TX, trimethacarb (840)+TX, triphenyltin acetate (IUPAC name) (347) and triphenyltin hydroxide (IUPAC name) (347)+TX, pyriprole [394730-71-3]+TX,
    a nematicide selected from the group of substances consisting of AKD-3088 (compound code)+TX, 1,2-dibromo-3-chloropropane (IUPAC/Chemical Abstracts name) (1045)+TX, 1,2-dichloropropane (IUPAC/Chemical Abstracts name) (1062)+TX, 1,2-dichloropropane with 1,3-dichloropropene (IUPAC name) (1063)+TX, 1,3-dichloropropene (233)+TX, 3,4-dichlorotetrahydrothiophene 1,1-dioxide (IUPAC/Chemical Abstracts name) (1065)+TX, 3-(4-chlorophenyl)-5-methylrhodanine (IUPAC name) (980)+TX, 5-methyl-6-thioxo-1,3,5-thiadiazinan-3-ylacetic acid (IUPAC name) (1286)+TX, 6-isopentenylaminopurine (alternative name) (210)+TX, abamectin (1)+TX, acetoprole [CCN]+TX, alanycarb (15)+TX, aldicarb (16)+TX, aldoxycarb (863)+TX, AZ 60541 (compound code)+TX, benclothiaz [CCN]+TX, benomyl (62)+TX, butylpyridaben (alternative name)+TX, cadusafos (109)+TX, carbofuran (118)+TX, carbon disulfide (945)+TX, carbosulfan (119)+TX, chloropicrin (141)+TX, chlorpyrifos (145)+TX, cloethocarb (999)+TX, cytokinins (alternative name) (210)+TX, dazomet (216)+TX, DBCP (1045)+TX, DCIP (218)+TX, diamidafos (1044)+TX, dichlofenthion (1051)+TX, dicliphos (alternative name)+TX, dimethoate (262)+TX, doramectin (alternative name) [CCN]+TX, emamectin (291)+TX, emamectin benzoate (291)+TX, eprinomectin (alternative name) [CCN]+TX, ethoprophos (312)+TX, ethylene dibromide (316)+TX, fenamiphos (326)+TX, fenpyrad (alternative name)+TX, fensulfothion (1158)+TX, fosthiazate (408)+TX, fosthietan (1196)+TX, furfural (alternative name) [CCN]+TX, GY-81 (development code) (423)+TX, heterophos [CCN]+TX, iodomethane (IUPAC name) (542)+TX, isamidofos (1230)+TX, isazofos (1231)+TX, ivermectin (alternative name) [CCN]+TX, kinetin (alternative name) (210)+TX, mecarphon (1258)+TX, metam (519)+TX, metam-potassium (alternative name) (519)+TX, metam-sodium (519)+TX, methyl bromide (537)+TX, methyl isothiocyanate (543)+TX, milbemycin oxime (alternative name) [CCN]+TX, moxidectin (alternative name) [CCN]+TX, Myrothecium verrucaria composition (alternative name) (565)+TX, NC-184 (compound code)+TX, oxamyl (602)+TX, phorate (636)+TX, phosphamidon (639)+TX, phosphocarb [CCN]+TX, sebufos (alternative name)+TX, selamectin (alternative name) [CCN]+TX, spinosad (737)+TX, terbam (alternative name)+TX, terbufos (773)+TX, tetrachlorothiophene (IUPAC/Chemical Abstracts name) (1422)+TX, thiafenox (alternative name)+TX, thionazin (1434)+TX, triazophos (820)+TX, triazuron (alternative name)+TX, xylenols [CCN]+TX, YI-5302 (compound code) and zeatin (alternative name) (210)+TX, fluensulfone [318290-98-1]+TX, a nitrification inhibitor selected from the group of substances consisting of potassium ethylxanthate [CCN] and nitrapyrin (580)+TX,
    a plant activator selected from the group of substances consisting of acibenzolar (6)+TX, acibenzolar-S-methyl (6)+TX, probenazole (658) and Reynoutria sachalinensis extract (alternative name) (720)+TX,
    a rodenticide selected from the group of substances consisting of 2-isovalerylindan-1,3-dione (IUPAC name) (1246)+TX, 4-(quinoxalin-2-ylamino)benzenesulfonamide (IUPAC name) (748)+TX, alpha-chlorohydrin [CCN]+TX, aluminium phosphide (640)+TX, antu (880)+TX, arsenous oxide (882)+TX, barium carbonate (891)+TX, bisthiosemi (912)+TX, brodifacoum (89)+TX, bromadiolone (91)+TX, bromethalin (92)+TX, calcium cyanide (444)+TX, chloralose (127)+TX, chlorophacinone (140)+TX, cholecalciferol (alternative name) (850)+TX, coumachlor (1004)+TX, coumafuryl (1005)+TX, coumatetralyl (175)+TX, crimidine (1009)+TX, difenacoum (246)+TX, difethialone (249)+TX, diphacinone (273)+TX, ergocalciferol (301)+TX, flocoumafen (357)+TX, fluoroacetamide (379)+TX, flupropadine (1183)+TX, flupropadine hydrochloride (1183)+TX, gamma-HCH (430)+TX, HCH (430)+TX, hydrogen cyanide (444)+TX, iodomethane (IUPAC name) (542)+TX, lindane (430)+TX, magnesium phosphide (IUPAC name) (640)+TX, methyl bromide (537)+TX, norbormide (1318)+TX, phosacetim (1336)+TX, phosphine (IUPAC name) (640)+TX, phosphorus [CCN]+TX, pindone (1341)+TX, potassium arsenite [CCN]+TX, pyrinuron (1371)+TX, scilliroside (1390)+TX, sodium arsenite [CCN]+TX, sodium cyanide (444)+TX, sodium fluoroacetate (735)+TX, strychnine (745)+TX, thallium sulfate [CCN]+TX, warfarin (851) and zinc phosphide (640)+TX,
    a synergist selected from the group of substances consisting of 2-(2-butoxyethoxy)ethyl piperonylate (IUPAC name) (934)+TX, 5-(1,3-benzodioxol-5-yl)-3-hexylcyclohex-2-enone (IUPAC name) (903)+TX, farnesol with nerolidol (alternative name) (324)+TX, MB-599 (development code) (498)+TX, MGK 264 (development code) (296)+TX, piperonyl butoxide (649)+TX, piprotal (1343)+TX, propyl isomer (1358)+TX, S421 (development code) (724)+TX, sesamex (1393)+TX, sesasmolin (1394) and sulfoxide (1406)+TX,
    an animal repellent selected from the group of substances consisting of anthraquinone (32)+TX, chloralose (127)+TX, copper naphthenate [CCN]+TX, copper oxychloride (171)+TX, diazinon (227)+TX, dicyclopentadiene (chemical name) (1069)+TX, guazatine (422)+TX, guazatine acetates (422)+TX, methiocarb (530)+TX, pyridin-4-amine (IUPAC name) (23)+TX, thiram (804)+TX, trimethacarb (840)+TX, zinc naphthenate [CCN] and ziram (856)+TX, a virucide selected from the group of substances consisting of imanin (alternative name) [CCN] and ribavirin (alternative name) [CCN]+TX,
    a wound protectant selected from the group of substances consisting of mercuric oxide (512)+TX, octhilinone (590) and thiophanate-methyl (802)+TX,
    and biologically active compounds selected from the group consisting of azaconazole (60207-31-0]+TX, bitertanol [70585-36-3]+TX, bromuconazole [116255-48-2]+TX, cyproconazole [94361-06-5]+TX, difenoconazole [119446-68-3]+TX, diniconazole [83657-24-3]+TX, epoxiconazole [106325-08-0]+TX, fenbuconazole [114369-43-6]+TX, fluquinconazole [136426-54-5]+TX, flusilazole [85509-19-9]+TX, flutriafol [76674-21-0]+TX, hexaconazole [79983-71-4]+TX, imazalil [35554-44-0]+TX, imibenconazole [86598-92-7]+TX, ipconazole [125225-28-7]+TX, metconazole [125116-23-6]+TX, myclobutanil [88671-89-0]+TX, pefurazoate [101903-30-4]+TX, penconazole [66246-88-6]+TX, prothioconazole [178928-70-6]+TX, pyrifenox [88283-41-4]+TX, prochloraz [67747-09-5]+TX, propiconazole [60207-90-1]+TX, simeconazole [149508-90-7]+TX, tebuconazole [107534-96-3]+TX, tetraconazole [112281-77-3]+TX, triadimefon [43121-43-3]+TX, triadimenol [55219-65-3]+TX, triflumizole [99387-89-0]+TX, triticonazole [131983-72-7]+TX, ancymidol [12771-68-5]+TX, fenarimol [60168-88-9]+TX, nuarimol [63284-71-9]+TX, bupirimate [41483-43-6]+TX, dimethirimol [5221-53-4]+TX, ethirimol [23947-60-6]+TX, dodemorph [1593-77-7]+TX, fenpropidine [67306-00-7]+TX, fenpropimorph [67564-91-4]+TX, spiroxamine [118134-30-8]+TX, tridemorph [81412-43-3]+TX, cyprodinil [121552-61-2]+TX, mepanipyrim [110235-47-7]+TX, pyrimethanil [53112-28-0]+TX, fenpiclonil [74738-17-3]+TX, fludioxonil [131341-86-1]+TX, benalaxyl [71626-11-4]+TX, furalaxyl [57646-30-7]+TX, metalaxyl [57837-19-1]+TX, R-metalaxyl [70630-17-0]+TX, ofurace [58810-48-3]+TX, oxadixyl [77732-09-3]+TX, benomyl [17804-35-2]+TX, carbendazim [10605-21-7]+TX, debacarb [62732-91-6]+TX, fuberidazole [3878-19-1]+TX, thiabendazole [148-79-8]+TX, chlozolinate [84332-86-5]+TX, dichlozoline [24201-58-9]+TX, iprodione [36734-19-7]+TX, myclozoline [54864-61-8]+TX, procymidone [32809-16-8]+TX, vinclozoline [50471-44-8]+TX, boscalid [188425-85-6]+TX, carboxin [5234-68-4]+TX, fenfuram [24691-80-3]+TX, flutolanil [66332-96-5]+TX, mepronil [55814-41-0]+TX, oxycarboxin [5259-88-1]+TX, penthiopyrad [183675-82-3]+TX, thifluzamide [130000-40-7]+TX, guazatine [108173-90-6]+TX, dodine [2439-10-3] [112-65-2] (free base)+TX, iminoctadine [13516-27-3]+TX, azoxystrobin [131860-33-8]+TX, mandestrobin [173662-97-0]+TX, dimoxystrobin [149961-52-4]+TX, enestroburin {Proc. BCPC, Int. Congr., Glasgow, 2003, 1, 93}+TX, fluoxastrobin [361377-29-9]+TX, kresoxim-methyl [143390-89-0]+TX, metomi-nostrobin [133408-50-1]+TX, trifloxystrobin [141517-21-7]+TX, orysastrobin [248593-16-0]+TX, picoxystrobin [117428-22-5]+TX, pyraclostrobin [175013-18-0]+TX, ferbam [14484-64-1]+TX, 3-[5-(4-chlorophenyl)-2,3-dimethyl-3-isoxazolidinyl]pyridine (SYP-Z048), mancozeb [8018-01-7]+TX, maneb [12427-38-2]+TX, metiram [9006-42-2]+TX, propineb [12071-83-9]+TX, thiram [137-26-8]+TX, zineb [12122-67-7]+TX, ziram [137-30-4]+TX, captafol [2425-06-1]+TX, captan [133-06-2]+TX, dichlofluanid [1085-98-9]+TX, fluoroimide [41205-21-4]+TX, folpet [133-07-3]+TX, tolylfluanid [731-27-1]+TX, bordeaux mixture [8011-63-0]+TX, copperhydroxid [20427-59-2]+TX, copperoxychlorid [1332-40-7]+TX, coppersulfat [7758-98-7]+TX, copperoxid [1317-39-1]+TX, mancopper [53988-93-5]+TX, oxine-copper [10380-28-6]+TX, dinocap [131-72-6]+TX, nitrothal-isopropyl [10552-74-6]+TX, edifenphos [17109-49-8]+TX, iprobenphos [26087-47-8]+TX, isoprothiolane [50512-35-1]+TX, phosdiphen [36519-00-3]+TX, pyrazophos [13457-18-6]+TX, tolclofos-methyl [57018-04-9]+TX, acibenzolar-S-methyl [135158-54-2]+TX, anilazine [101-05-3]+TX, benthiavalicarb [413615-35-7]+TX, blasticidin-S [2079-00-7]+TX, chinomethionat [2439-01-2]+TX, chloroneb [2675-77-6]+TX, chlorothalonil [1897-45-6]+TX, cyflufenamid [180409-60-3]+TX, cymoxanil [57966-95-7]+TX, dichlone [117-80-6]+TX, diclocymet [139920-32-4]+TX, diclomezine [62865-36-5]+TX, dicloran [99-30-9]+TX, diethofencarb [87130-20-9]+TX, dimethomorph [110488-70-5]+TX, SYP-L190 (Flumorph) [211867-47-9]+TX, dithianon [3347-22-6]+TX, ethaboxam [162650-77-3]+TX, etridiazole [2593-15-9]+TX, famoxadone [131807-57-3]+TX, fenamidone [161326-34-7]+TX, fenoxanil [115852-48-7]+TX, fentin [668-34-8]+TX, ferimzone [89269-64-7]+TX, fluazinam [79622-59-6]+TX, fluopicolide [239110-15-7]+TX, flusulfamide [106917-52-6]+TX, fenhexamid [126833-17-8]+TX, fosetyl-aluminium [39148-24-8]+TX, hymexazol [10004-44-1]+TX, iprovalicarb [140923-17-7]+TX, IKF-916 (Cyazofamid) [120116-88-3]+TX, kasugamycin [6980-18-3]+TX, methasulfocarb [66952-49-6]+TX, metrafenone [220899-03-6]+TX, pencycuron [66063-05-6]+TX, phthalide [27355-22-2]+TX, polyoxins [11113-80-7]+TX, probenazole [27605-76-1]+TX, propamocarb [25606-41-1]+TX, proquinazid [189278-12-4]+TX, pyroquilon [57369-32-1]+TX, quinoxyfen [124495-18-7]+TX, quintozene [82-68-8]+TX, sulfur [7704-34-9]+TX, tiadinil [223580-51-6]+TX, triazoxide [72459-58-6]+TX, tricyclazole [41814-78-2]+TX, triforine [26644-46-2]+TX, validamycin [37248-47-8]+TX, zoxamide (RH7281) [156052-68-5]+TX, mandipropamid [374726-62-2]+TX, and SDHI inhibitors selected from the group consisting of penflufen ([494793-67-8], U.S. Pat. No. 7,538,073 (N-[2-(1,3-dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide)+TX, furametpyr ([123572-88-3] (5-chloro-N-(1,3-dihydro-1,1,3-trimethyl-4-isobenzofuranyl)-1,3-dimethyl-1H-pyrazole-4-carboxamide)+TX, penthiopyrad (U.S. Pat. No. 5,747,518, [183675-82-3], (N-[2-(1,3-dimethylbutyl)-3-thienyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide)+TX, bixafen (U.S. Pat. No. 7,329,633, [581809-46-3], (N-(3′,4′-dichloro-5-fluoro[1,1′-biphenyl]-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide)+TX, isopyrazam (U.S. Pat. No. 7,598,395, [881685-58-1] (mixture of 2 syn-isomers 3-(difluoromethyl)-1-methyl-N-[(1RS,4SR,9RS)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]pyrazole-4-carboxamide and 2 anti-isomers 3-(difluoromethyl)-1-methyl-N-[(1RS,4SR,9SR)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]pyrazole-4-carboxamide)+TX, sedaxane (EP 1480955B1, [874967-67-6](mixture of 2 cis-isomers 2′-[(1RS,2RS)-1,1′-bicycloprop-2-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxanilide and 2 trans-isomers 2′-[(1RS,2SR)-1,1′-bicycloprop-2-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxanilide)+TX, fluxapyroxad (U.S. Pat. No. 8,008,232, [907204-31-3] (3-(difluoromethyl)-1-methyl-N-(3′,4′,5′-trifluoro[1,1′-biphenyl]-2-yl)-1H-pyrazole-4-carboxamide)+TX, solatenol (WO 2007/048556 (3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid (9-dichloromethylene-1,2,3,4-tetrahydro-1,4-methano-naphthalen-5-yl)-amide)+TX, the compound 3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]pyrazole-4-carboxamide (described in WO 2010/063700)+TX, thifluzamide (U.S. Pat. No. 5,045,554, [130000-40-7] (N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)-5-thiazolecarboxamide)+TX, boscalid (U.S. Pat. No. 5,589,493, [188425-85-6 (2-chloro-N-(4′-chloro[1,1′-biphenyl]-2-yl)-3-pyridinecarboxamide)+TX, oxycarboxin ([5259-88-1] (5,6-dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide 4,4-dioxide)+TX, carboxin ([5234-68-4] (5,6-dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide)+TX, fluopyram (U.S. Pat. No. 7,572,818, [658066-35-4], (N-[2-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethyl]-2-(trifluoromethyl)benzamide)+TX, flutolanil ([24691-80-3], (2-methyl-N-phenyl-3-furancarboxamide, fenfuram), U.S. Pat. No. 4,093,743, CA Reg. No. 66332-96-5 (N-[3-(1-methylethoxy)phenyl]-2-(trifluoromethyl)benzamide)+TX, mepronil ([55814-41-0], (2-methyl-N-[3-(1-methylethoxy)phenyl]benzamide)+TX and benodanil ([15310-01-7], (2-iodo-N-phenylbenzamide)+TX;
    and the compounds [(3S,4R,4aR,6S,6aS,12R,12aS,12bS)-3-[(cyclopropylcarbonyl)oxy]-1,3,4,4a,5,6,6a,12,12a,12b-decahydro-6,12-dihydroxy-4,6a,12b-trimethyl-11-oxo-9-(3-pyridinyl)-2H,11H naphtho[2,1-b]pyrano[3,4-e]pyran-4-yl]methyl-cyclopropanecarboxylate [915972-17-7]+TX, 1,3,5-trimethyl-N-(2-methyl-1-oxopropyl)-N-[3-(2-methylpropyl)-4-[2,2,2-trifluoro-1-methoxy-1-(trifluoromethyl)ethyl]phenyl]-1H-pyrazole-4-carboxamide [926914-55-8]+TX and 4-oxo-4-[(2-phenylethyl)amino]-butyric acid (disclosed in WO 2010/137677)+TX.
  • The references in brackets behind the active ingredients, e.g. [3878-19-1] refer to the Chemical Abstracts Registry number. The above described mixing partners are known. Where the active ingredients are included in “The Pesticide Manual” [The Pesticide Manual—A World Compendium; Thirteenth Edition; Editor: C. D. S. TomLin; The British Crop Protection Council], they are described therein under the entry number given in round brackets hereinabove for the particular compound; for example, the compound “abamectin” is described under entry number (1). Where “[CCN]” is added hereinabove to the particular compound, the compound in question is included in the “Compendium of Pesticide Common Names”, which is accessible on the internet [A. Wood; Compendium of Pesticide Common Names, Copyright © 1995-2013]; for example, the compound “acetoprole” is described under the internet address http://www.alanwood.net/pesticides/acetoprole.html.
  • Most of the active ingredients described above are referred to hereinabove by a so-called “common name”, the relevant “ISO common name” or another “common name” being used in individual cases. If the designation is not a “common name”, the nature of the designation used instead is given in round brackets for the particular compound; in that case, the IUPAC name, the IUPAC/Chemical Abstracts name, a “chemical name”, a “traditional name”, a “compound name” or a “development code” is used or, if neither one of those designations nor a “common name” is used, an “alternative name” is employed.
  • The active ingredient mixture of the compounds of formula I selected from Tables 1 to 168 and V1 to V26 with active ingredients described above comprises a compound selected from Tables 1 to 130 and an active ingredient as described above preferably in a mixing ratio of from 100:1 to 1:6000, especially from 50:1 to 1:50, more especially in a ratio of from 20:1 to 1:20, even more especially from 10:1 to 1:10, very especially from 5:1 and 1:5, special preference being given to a ratio of from 2:1 to 1:2, and a ratio of from 4:1 to 2:1 being likewise preferred, above all in a ratio of 1:1, or 5:1, or 5:2, or 5:3, or 5:4, or 4:1, or 4:2, or 4:3, or 3:1, or 3:2, or 2:1, or 1:5, or 2:5, or 3:5, or 4:5, or 1:4, or 2:4, or 3:4, or 1:3, or 2:3, or 1:2, or 1:600, or 1:300, or 1:150, or 1:35, or 2:35, or 4:35, or 1:75, or 2:75, or 4:75, or 1:6000, or 1:3000, or 1:1500, or 1:350, or 2:350, or 4:350, or 1:750, or 2:750, or 4:750. Those mixing ratios are ratios by weight.
  • The mixtures as described above can be used in a method for controlling pests, which comprises applying a composition comprising a mixture as described above to the pests or their environment, with the exception of a method for treatment of the human or animal body by surgery or therapy and diagnostic methods practised on the human or animal body.
  • The mixtures comprising a compound of formula I selected from Tables 1 to 168 and V1 to V26 and one or more active ingredients as described above can be applied, for example, in a single “ready-mix” form, in a combined spray mixture composed from separate formulations of the single active ingredient components, such as a “tank-mix”, and in a combined use of the single active ingredients when applied in a sequential manner, i.e. one after the other with a reasonably short period, such as a few hours or days. The order of applying the compounds of formula I selected from Tables 1 to 168 and V1 to V26 and the active ingredients as described above is not essential for working the present invention.
    • BIOLOGICAL EXAMPLES Example B1: Spodoptera littoralis (Egyptian Cotton Leaf Worm)
  • Test compounds were applied by pipette from 10′000 ppm DMSO stock solutions into 24-well plates and mixed with agar. Lettuce seeds were placed on the agar and the multi well plate was closed by another plate which contains also agar. After 7 days the roots have absorbed the compound and the lettuce has grown into the lid plate. The lettuce leafs were now cut off into the lid plate. Spodoptera eggs were pipetted through a plastic stencil on a humid gel blotting paper and the plate closed with it. The samples were assessed for mortality, anti-feedant effect and growth inhibition in comparison to untreated samples 6 days after infestation.
  • The following compounds gave an effect of at least 80% in at least one of the three categories (mortality, anti-feedancy, or growth inhibition) at a test rate of 12.5 ppm:
  • V20.02, V20.01, V16.02, V12.02, V16.01, V12.01, and V12.03
    • Example B2: Spodoptera littoralis (Egyptian Cotton Leaf Worm)
  • Cotton leaf discs were placed on agar in 24-well microtiter plates and sprayed with aqueous test solutions prepared from 10′000 ppm DMSO stock solutions. After drying the leaf discs were infested with five L1 larvae. The samples were assessed for mortality 3 days after infestation. The following compounds resulted in at least 80% mortality at an application rate of 200 ppm: The following compounds resulted in at least 80% control at an application rate of 200 ppm:
  • V14.01, V12.18, V16.08, V20.02, V16.02, V12.20, V12.02, V16.01, V12.01, V7.11, V12.03, V25.03 and V7.09
    • Example B3: Plutella xylostella (Diamond Back Moth)
  • 24-well microtiter plates with artificial diet were treated with aqueous test solutions prepared from 10′000 ppm DMSO stock solutions by pipetting. After drying, the plates were infested with L2 larvae (10 to 15 per well). The samples were assessed for mortality 5 days after infestation.
  • The following compounds resulted in at least 80% mortality at an application rate of 200 ppm:
  • V14.01, V16.08, V20.08, V20.02, V16.09, V16.03, V16.07, V16.02, V12.02, V16.01, V12.01, V7.11, V12.03, V13.05, V25.03 and V7.09
    • Example B4: Diabrotica balteata (Corn Root Worm)
  • 24-well microtiter plates with artificial diet were treated with aqueous test solutions prepared from 10′000 ppm DMSO stock solutions by pipetting. After drying, the plates were infested with L2 larvae (6 to 10 per well). The samples were assessed for mortality and growth inhibition in comparison to untreated samples 5 days after infestation.
  • The following compounds gave an effect of at least 80% in at least one of the two categories (mortality or growth inhibition) at an application rate of 200 ppm:
  • V14.01, V12.18, V16.08, V20.02, V16.09, V16.03, V16.07, V16.02, V12.20, V12.02, V12.01, V7.11, V12.03, V13.05, V25.03 and V7.09.
    • Example B5: Myzus persicae (Green Peach Aphid)
  • Sunflower leaf discs were placed on agar in a 24-well microtiter plate and sprayed with aqueous test solutions prepared from 10′000 ppm DMSO stock solutions. After drying, the leaf discs were infested with an aphid population of mixed ages. The samples were assessed for mortality 6 days after infestation.
  • The following compounds resulted in at least 80% mortality at an application rate of 200 ppm:
  • V14.01, V16.08, V20.08, V16.09, V16.03, V16.07, V16.02, V12.20, V12.02, V14.05, V16.01, V12.17, V12.01, V7.11, V12.03, V25.03 and V7.09.
    • Example B6: Myzus persicae (Green Peach Aphid)
  • Roots of pea seedlings infested with an aphid population of mixed ages were placed directly in the aqueous test solutions prepared from 10,000 DMSO stock solutions. The samples were assessed for mortality 6 days after placing seedlings in test solutions.
  • The following compounds resulted in at least 80% mortality at a test rate of 24 ppm:
  • V16.08, V20.08, V16.09, V16.03, V16.07, V12.20, V12.02, V14.05, V12.17, V12.01, and V12.03.
    • Example B7: Myzus persicae (Green Peach Aphid)
  • Test compounds from 10′000 ppm DMSO stock solutions were applied by pipette into 24-well microtiter plates and mixed with sucrose solution. The plates were closed with a stretched Parafilm. A plastic stencil with 24 holes was placed onto the plate and infested pea seedlings were placed directly on the Parafilm. The infested plate was closed with a gel blotting paper and another plastic stencil and then turned upside down. The samples were assessed for mortality 5 days after infestation.
  • The following compounds resulted in at least 80% mortality at a test rate of 12 ppm:
  • V12.20, V12.02, V14.05, V16.01, V12.17, V12.01, V7.11, V12.03, and V7.09
    • Example B8: Thrips tabaci (Onion Thrips)
  • Sunflower leaf discs were placed on agar in 24-well microtiter plates and sprayed with aqueous test solutions prepared from 10′000 ppm DMSO stock solutions. After drying the leaf discs were infested with a thrips population of mixed ages. The samples were assessed for mortality 6 days after infestation.
  • The following compounds resulted in at least 80% mortality at an application rate of 200 ppm:
  • V12.01, V12.03, and V7.09
    • Example B9: Frankliniella occidentalis (Western Flower Thrips)
  • Sunflower leaf discs were placed on agar in 24-well microtiter plates and sprayed with aqueous test solutions prepared from 10′000 DMSO stock solutions. After drying the leaf discs were infested with a Frankliniella population of mixed ages. The samples were assessed for mortality 7 days after infestation.
  • The following compounds resulted in at least 80% mortality at an application rate of 200 ppm:
  • V12.02
    • Example B10: Bemisia tabaci (Cotton White Fly)
  • Cotton leaf discs were placed on agar in 24-well microtiter plates and sprayed with aqueous test solutions prepared from 10′000 ppm DMSO stock solutions. After drying the leaf discs were infested with adult white flies. The samples were checked for mortality 6 days after incubation.
  • The following compounds resulted in at least 80% mortality at an application rate of 200 ppm:
  • V12.20, V12.02, V12.01, V13.05, V25.03 and V7.09.
    • Example B11: Tetranychus urticae (Two-Spotted Spider Mite)
  • Bean leaf discs on agar in 24-well microtiter plates were sprayed with aqueous test solutions prepared from 10,000 ppm DMSO stock solutions. After drying the leaf discs were infested with a mite population of mixed ages. The samples were assessed for mortality on mixed population (mobile stages) 8 days after infestation.
  • The following compounds resulted in at least 80% mortality at an application rate of 200 ppm:
  • V14.01, V12.18, V20.08, and V16.02.
    • Example B12: Aedes aegypti (Yellow Fever Mosquito)
  • larvicide, contact/feeding activity, curative
  • 10 to 15 Aedes larvae (L2) together with a nutrition mixture were placed in 96-well microtiter plates.
  • Test compounds were pipetted into the wells. After an incubation period of 2 days insects were assessed for mortality and growth inhibition.
  • The following compounds gave an effect of at least 80% in at least one of the two categories (mortality or growth inhibition) at a test rate of 5 ppm:
  • V12.01

Claims (17)

What is claimed is:
1. A compound of formula I,

A-B  (I),
wherein A is a radical selected from the group consisting of formulae A1 to A8:
Figure US20220104496A1-20220407-C00288
wherein the arrow denotes the point of attachment to the radical B; and
B is a radical selected from the group consisting of formulae B1 to B11:
Figure US20220104496A1-20220407-C00289
Figure US20220104496A1-20220407-C00290
wherein the arrow denotes the point of attachment to the radical A;
wherein
L1 is methylene or a direct bond;
V0 nitrogen or CR5;
V1 is nitrogen or CR20;
V2 is nitrogen or CR21;
V3 is nitrogen or CR22;
V4 is nitrogen or CR23;
V5 is nitrogen or CR24;
V5 is nitrogen or CR25;
V7 is nitrogen or CR26;
V8 is nitrogen or CR27;
V9 is nitrogen, or CR28;
V10 is nitrogen or CR29;
V11 is nitrogen or CR30;
G1 is nitrogen or CR31;
G2 is nitrogen or CR32;
G3 is —NR35, an oxygen atom or a sulphur atom;
G4 is nitrogen or CR33;
G5 is nitrogen or CR34;
J1, J2, J3 together form together a 5 membered heterocyclic ring, which can be saturated or unsaturated, containing one or two atoms selected from the group consisting of nitrogen, oxygen and sulphur, which ring can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, halogen and or C1-C6haloalkyl, with the proviso that if the ring contains two oxygen atoms, or two sulphur atoms, they are separated by one carbon atom;
R1 and R2 are the same or different and each represents, hydrogen, halogen, C1-C6alkyl or C1-C6haloalkyl;
R3 is a C1-C6alkyl, C2-C6 alkenyl or C2-C6 alkynyl group which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen, C3-C6cycloalkyl, said C3-C6cycloalkyl itself can be mono- or polysubstituted by substituents selected from halogen and C1-C3alkyl; and by a 5- or 6-membered heterocyclic group, which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano and nitro;
or R3 is C3-C6cycloalkyl, which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy and halogen;
or R3 is a 5- or 6-membered heterocyclic group, which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano and nitro;
or R3 is —CO2R36, —C(O)R36 or hydrogen;
R35 is hydrogen, C1-C6alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6 alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6alkoxycarbonyl, cyano, hydroxy, halogen and C3-C6cycloalkyl, said C3-C6cycloalkyl itself can be mono- or polysubstituted by substituents selected from halogen and C1-C3alkyl; or an N-oxide thereof;
R4, R5, R20, R21, R22, R23, R24, R25, R26, R27, R28, R29, and R30 are the same or different and represents cyano, nitro, halogen, hydroxy, C1-C6alkenyloxy, C1-C5-haloalkoxy, C3-C6cycloalkyl, —C(O)R36 or hydrogen; or
C1-C6alkyl which can be mono- or polysubstituted by substituents selected from the group consisting of cyano, halogen, hydroxy, C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6 alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen and C3-C6cycloalkyl, said cycloalkyl itself can be substituted by substituents selected from the group consisting of halogen and C1-C3alkyl; or represents
a phenyl group which can be mono or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano, and nitro;
R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18 and R19 are the same or different and represents C1-C6 alkyl, C1-C6 haloalkyl, or hydrogen, and the group CR13R14 can additionally be a carbonyl group C═O;
R31, R32, R33 and R34 are the same or different and represents C1-C6alkyl, C1-C6haloalkyl, —OR7, —S(O)nR36, —NR36R37, —CO2R36,—C(O)R36, cyano, nitro, halogen or hydrogen;
R36 and R37 are the same or different and represents hydrogen, C1-C6alkyl which can be mono- or polysubstituted by substituents selected from C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyloxy, C2-C6haloalkenyloxy, C2-C6alkynyloxy, C2-C6haloalkynyloxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, cyano, hydroxy, halogen and C3-C6 cycloalkyl, wherein said C3-C6 cycloalkyl can be mono- or polysubstituted by substituents selected from the group consisting of halogen and C1-C3alkyl; or
R36 and R37 are the same or different and represents
a phenyl group which can be mono- or polysubstituted by substituents selected from the group consisting of C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylsulphanyl, C1-C6haloalkylsulphanyl, C1-C6alkylsulphinyl, C1-C6haloalkylsulphinyl, C1-C6alkylsulphonyl, C1-C6haloalkylsulphonyl, C2-C6alkylcarbonyl, C2-C6haloalkylcarbonyl, C2-C6alkoxycarbonyl, C2-C6haloalkoxycarbonyl, C1-C6alkylamino, C1-C6haloalkylamino, C2-C8dialkylamino, C2-C8halodialkylamino, halogen, cyano, and nitro;
each m independently represents 0, 1 or 2, and n represents 0, 1 or 2, with the proviso that:
a) in —S(O)nR36, R36 is hydrogen when n is 0;
b) if B is 1, then A is different from A2, A3 and A5;
c) if A is A1, then B is different from 1, B7, B8, B9 and B10;
d) if A is A5, then B is different from B10;
or an agrochemically acceptable salt, enantiomer, diastereomer, tautomer, or N-oxide thereof.
2. A compound of formula I according to claim 1, represented by the combinations of Radical A2 with radicals B selected from B7, B9 and B11;
wherein A2 is represented by the radical A2.1
Figure US20220104496A1-20220407-C00291
wherein R40 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
G21 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C6haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and
G51 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C06haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and the radicals B7, B9 and B11 are represented by the radicals selected from B7.1, B9.1 and B11.1
Figure US20220104496A1-20220407-C00292
wherein m is 0, 1 or 2;
V82 is nitrogen or methine;
R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00293
wherein m is 0, 1 or 2;
V81 is nitrogen or methine,
R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
Figure US20220104496A1-20220407-C00294
wherein m is 0, 1 or 2;
R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
3. A compound of formula I according to claim 1, represented by the combinations of Radical A3 with radicals B selected from B7, B9 and B11;
wherein A3 is represented by the radical A3.1
Figure US20220104496A1-20220407-C00295
wherein R47 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
G41 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C6haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and
G22 is nitrogen, CH, C—C1-C6 alkyl, C—C1-C6haloalkyl, C-halogen, C—CN, C—O—C1-C4alkyl, C—S—C1-C4alkyl, C—SO2—C1-C4alkyl, C—S-phenyl, C—SO2-phenyl or C—SO2—C1-C4halolakyl; and the radicals B7, B9 and B11 are represented by the radicals selected from B7.1, B9.1 and B11.1
Figure US20220104496A1-20220407-C00296
wherein m is 0, 1 or 2;
V82 is nitrogen or methine;
R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00297
wherein m is 0, 1 or 2;
V81 is nitrogen or methine,
R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
Figure US20220104496A1-20220407-C00298
wherein m is 0, 1 or 2;
R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
4. A compound of formula I according to claim 1, represented by the combinations of Radical A4 with radical B1;
wherein A4 is represented by the radical A4.1
Figure US20220104496A1-20220407-C00299
wherein R48 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
J3 is sulphur, oxygen or N-methyl; and
R49 is hydrogen, C1-C6 alkyl, C1-C6haloalkyl, halogen, CN, O—C1-C4alkyl, S—C1-C4alkyl, SO2—C1-C4alkyl, S-phenyl, SO2-phenyl or SO2—C1-C4halolakyl;
and the radical 1 is
Figure US20220104496A1-20220407-C00300
wherein m is 0, 1 or 2;
R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
5. A compound of formula I according to claim 1, represented by the combinations of Radical A5 with radicals B selected from 1, B7, B9 and B11;
wherein A5 is represented by the radical A5.1
Figure US20220104496A1-20220407-C00301
wherein
G55 is nitrogen or C—R53;
R53 is C1-C4alkyl;
G25 is nitrogen or methine; and
R52 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
and the radicals B1, B7, B9 and B11 are represented by the radicals selected from B1.1, B7.1, B9.1 and B11.1
Figure US20220104496A1-20220407-C00302
wherein m is 0, 1 or 2;
R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00303
wherein m is 0, 1 or 2;
V82 is nitrogen or methine;
R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00304
wherein m is 0, 1 or 2;
V81 is nitrogen or methine;
R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
Figure US20220104496A1-20220407-C00305
wherein m is 0, 1 or 2;
R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
6. A compound of formula I according to claim 1, represented by the combinations of Radical A6 with radicals B selected from 1, B7, B9 and B11;
wherein A6 is represented by the radical A6.1
Figure US20220104496A1-20220407-C00306
wherein
G36 is N—R55, oxygen or sulfur;
R55 is C1-C4alkyl;
G26 is nitrogen or methine; and
R54 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
and the radicals B1, B7, B9 and B11 are represented by the radicals selected from B1.1, B7.1, B9.1 and B11.1
Figure US20220104496A1-20220407-C00307
wherein m is 0, 1 or 2;
R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00308
wherein m is 0, 1 or 2;
V82 is nitrogen or methine;
R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00309
wherein m is 0, 1 or 2;
V81 is nitrogen or methine,
R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
Figure US20220104496A1-20220407-C00310
wherein m is 0, 1 or 2;
R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
7. A compound of formula I according to claim 1, represented by the combinations of radical A7 with radicals B selected from 1, B7, B9 and B11;
wherein A7 is represented by the radical A7.1
Figure US20220104496A1-20220407-C00311
wherein
G57 is nitrogen or C—R57;
R57 is hydrogen or C1-C4alkyl; and
R56 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
and the radicals B1, B7, B9 and B11 are represented by the radicals selected from B1.1, B7.1, B9.1 and B11.1
Figure US20220104496A1-20220407-C00312
wherein m is 0, 1 or 2;
R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00313
wherein m is 0, 1 or 2;
V82 is nitrogen or methine;
R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00314
wherein m is 0, 1 or 2;
V81 is nitrogen or methine;
R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
Figure US20220104496A1-20220407-C00315
wherein m is 0, 1 or 2;
R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
8. A compound of formula I according to claim 1, represented by the combinations of Radical A8 with radicals B selected from 1, B7, B9 and B11;
wherein A8 is preferably represented by the radical A8.1
Figure US20220104496A1-20220407-C00316
wherein
G48 is nitrogen or C—R59;
R59 is hydrogen or C1-C4alkyl; and
R58 is halogen, C1-C4haloalkyl, C1-C4haloalkylthio, C1-C4haloalkylsulfonyl, O(C1-C4haloalkyl), SF5, phenylcarbonylthio, mercapto or C1-C4alkoxycarbonyl;
and the radicals B1, B7, B9 and B11 are preferably represented by the radicals selected from B1.1, B7.1, B9.1 and B11.1
Figure US20220104496A1-20220407-C00317
wherein m is 0, 1 or 2;
R51 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R50 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00318
wherein m is 0, 1 or 2;
V82 is nitrogen or methine;
R41 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R42 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl;
Figure US20220104496A1-20220407-C00319
wherein m is 0, 1 or 2;
V81 is nitrogen or methine;
R43 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R44 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
Figure US20220104496A1-20220407-C00320
wherein m is 0, 1 or 2;
R45 is C1-C4alkyl, C1-C4haloalkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl; and
R46 is C1-C4alkyl, C1-C4haloalkyl, C1-C3haloalkoxy, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C4alkyl, C3-C6halocycloalkyl, C2-C6alkenyl, C2-C6haloalkenyl or C2-C6alkynyl.
9. A compound of formula I according to 1, wherein L1, in reference to each of B, is a direct bond.
10. A compound of formula I according to 1, wherein R1, in reference to each of A, is the same or different and each represents hydrogen, halogen, C1-C3 alkyl or C1-C3 haloalkyl.
11. A compound of formula I according to 10, wherein R2, in reference to each of A, is the same or different and each represents hydrogen, halogen, C1-C3 alkyl or C1-C3haloalkyl.
12. A compound of formula I according to 10, wherein R3, in reference to each of B, is the same or different and each represents C1-C3 alkyl or C1-C3 haloalkyl.
13. A compound of formula I according to 10, wherein R4, in reference to each of B, is the same or different and each represents hydrogen or C1-C3 alkyl.
14. An insecticidal, acaricidal, nematicidal or molluscicidal composition, comprising an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a compound of formula I according to claim 1 and a suitable carrier or diluent therefor.
15. A method of combating and controlling pests which comprises applying an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a compound of formula I according to claim 1 or a composition comprising a compound of formula I, to a pest, a locus of pest, or to a plant susceptible to attack by a pest, with the exception of a method for treatment of the human or animal body by surgery or therapy and diagnostic methods practised on the human or animal body.
16. A method for the protection of plant propagation material from the attack by pests, which comprises treating the propagation material or the site, where the propagation material is planted, with a composition according to claim 14.
17. Plant propagation material treated in accordance with the method described in claim 16.
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