HRP20140471T1 - Spiroheterocikliäśki n-oksipiperidini kao pesticidi - Google Patents
Spiroheterocikliäśki n-oksipiperidini kao pesticidi Download PDFInfo
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- HRP20140471T1 HRP20140471T1 HRP20140471AT HRP20140471T HRP20140471T1 HR P20140471 T1 HRP20140471 T1 HR P20140471T1 HR P20140471A T HRP20140471A T HR P20140471AT HR P20140471 T HRP20140471 T HR P20140471T HR P20140471 T1 HRP20140471 T1 HR P20140471T1
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- HR
- Croatia
- Prior art keywords
- c5alkyl
- halogen
- nitro
- cyano
- c3alkoxy
- Prior art date
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- 239000000575 pesticide Substances 0.000 title claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 43
- 150000002367 halogens Chemical group 0.000 claims 39
- 125000004093 cyano group Chemical group *C#N 0.000 claims 37
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 34
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims 31
- -1 C1-C3alkoxy Chemical group 0.000 claims 27
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 27
- 150000001875 compounds Chemical class 0.000 claims 19
- 125000001072 heteroaryl group Chemical group 0.000 claims 19
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 14
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- 241000607479 Yersinia pestis Species 0.000 claims 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 6
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 6
- 239000003921 oil Substances 0.000 claims 6
- 241001465754 Metazoa Species 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 4
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
- 125000001246 bromo group Chemical group Br* 0.000 claims 4
- 125000005240 diheteroarylamino group Chemical group 0.000 claims 4
- 125000001153 fluoro group Chemical group F* 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 125000005241 heteroarylamino group Chemical group 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 2
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 2
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 claims 2
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 2
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 238000002405 diagnostic procedure Methods 0.000 claims 2
- 238000009472 formulation Methods 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 238000001356 surgical procedure Methods 0.000 claims 2
- 238000011282 treatment Methods 0.000 claims 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 claims 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- 230000000855 fungicidal effect Effects 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- 125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 claims 1
- 239000002480 mineral oil Substances 0.000 claims 1
- 235000010446 mineral oil Nutrition 0.000 claims 1
- 239000003750 molluscacide Substances 0.000 claims 1
- 230000002013 molluscicidal effect Effects 0.000 claims 1
- 239000005645 nematicide Substances 0.000 claims 1
- 125000003566 oxetanyl group Chemical group 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- 150000004714 phosphonium salts Chemical class 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000005648 plant growth regulator Substances 0.000 claims 1
- 230000001681 protective effect Effects 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- 238000007363 ring formation reaction Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 235000013311 vegetables Nutrition 0.000 claims 1
Classifications
-
- 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
- C07D471/10—Spiro-condensed systems
-
- 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
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
- C07D211/94—Oxygen atom, e.g. piperidine N-oxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Claims (20)
1. Spojevi sa formulom I
[image]
naznačeni time da
X , Y i Z međusobno neovisno su C1-4alkil, C3-6cikloalkil, C1-4haloalkil, C14alkoksi, halogen, fenil ili fenil supstituiran s C1-4alkil, C1-4haloalkil, halogen ili cijano;
m i n, međusobno neovisno su 0, 1, 2 ili 3 i m+n je 0, 1, 2 ili 3;
G je vodik, metal, amonijak, sulfonij ili latentna skupina, odabrana iz skupine koja sadrži C1-C8alkil, C2-C8haloalkil, fenilC1-C8alkil (pri čemu fenil može proizvoljno biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili s nitro), heteroarilC1-C8alkil (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili s nitro), C3-C8alkenil, C3-C8haloalkenil, C3-C8alkinil, C(Xa)-Ra, C(Xb)-Xc-Rb, C(Xd)-N(Rc)-Rd, -SO2-Re,-P(Xe)(Rf)-R9 ili CH2-Xf-Rh pri čemu Xa, Xb, Xc, Xd, Xe i Xf su međusobno neovisno kisik ili sumpor;
Ra je H, C1-C18alkil, C2-C18alkenil, C2-C18alkinil, C1-C10haloalkil, C1-C10cijanoalkil, C1-C10nitroalkil, C1-C10aminoalkil, C1-C5alkilaminoC1-C5alkil, C2-C8dialkilaminoC1-C5alkil, C3-C7cikloalkilC1-C5alkil, C1-C5alkoksiC1-C5alkil, C3-C5alkeniloksiC1-C5alkil, C3-C5alkinilC1-C5Oksialkil, C1-C5alkiltioC1-C5alkil, C1-C5alkilsulfinilC1-C5alkil, C1-C5alkilsulfonilC1-C5alkil, C2-C8alkilideneaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoC1-C5alkil, N-C1-C5alkilkarbonil-N-C1-C5alkilaminoC1-C5alkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil može proizvoljno biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), heteroarilC1-C5alkil, (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro,
Rb je C1-C18alkil, C3-C18alkenil, C3-C18alkinil, C2-C10haloalkil, C1-C10cijanoalkil, C1-C10nitroalkil, C2-C10aminoalkil, C1-C5alkilaminoC1-C5alkil, C2-C8dialkilaminoC1-C5alkil, C3-C7cikloalkilC1-C5alkil, C1-C5alkoksiC1-C5alkil, C3-C5alkeniloksiC1-C5alkil, C3-C5alkiniloksiC1-C5alkil, C1-C5alkiltioC1-C5alkil, C1-C5alkilsulfinilC1-C5alkil, C1-C5alkilsulfonilC1-C5alkil, C2-C8alkilideneaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoC1-C5alkil, N-C1-C5alkilkarbonil-N-C1-C5alkilaminoC1-C5alkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil može proizvoljno biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), heteroarilC1-C5alkil, (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), C3-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3halo-alkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran s C1-C3 alkilom, C1-3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro,
Rc i Rd su svaki međusobno neovisno vodik, C1-C10alkil, C3-C10alkenil, C3-C10alkinil, C2-C10haloalkil, C1-C10cijanoalkil, C1-C10nitroalkil, C1-C10aminoalkil, C1-C5alkilaminoC1-C5alkil, C2-C8dialkilaminoC1-C5alkil, C3-C7cikloalkilC1-C5alkil, C1-C5alkoksiC1-C5alkil, C3-C5alkeniloksiC1-C5alkil, C3-C5alkiniloksiC1-C5alkil, C1-C5alkiltioC1-C5alkil, C1-C5alkilsulfinilC1-C5alkil, C1-C5alkilsulfonilC1-C5alkil, C2-C8alkilideneaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoC1-C5alkil, N-C1-C5alkilkarbonil-N-C2-C5alkilaminoalkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), heteroarilC1-C5alkil, (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran s C1-C3alkil, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroarilamino ili heteroarilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, diheteroarilamino ili diheteroarilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, fenilamino ili fenilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili s nitro, difenilamino ili difenilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili s nitro ili C3-C7cikloalkilamino, di-C3-C7cikloalkilamino ili C3-C7cikloalkoksi ili Rc i Rd se mogu spojiti tako da tvore 3-7 člani prsten, koji proizvoljno sadrži jedan heteroatom odabran od O ili S,
Re je C1-C10alkil, C2-C10alkenil, C2-C10alkinil, C1-C10haloalkil, C1-C10cijanoalkil, C1-C10nitroalkil, C1-C10aminoalkil, C1-C5alkilaminoC1-C5alkil, C2-C8dialkilaminoC1-C5alkil, C3-C7cikloalkilC1-C5alkil, C1-C5alkoksiC1-C5alkil, C3-C5alkeniloksiC1-C5alkil, C3-C5alkiniloksiC1-C5alkil, C1-C5alkiltioC1-C5alkil, C1-C5alkilsulfinilC1-C5alkil, C1-C5alkilsulfonilC1-C5alkil, C2-C8alkilideneaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoC1-C5alkil, N-C1-C5alkilkarbonil-N-C1-C5alkilaminoC1-C5alkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil može proizvoljno biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), heteroarilC1-C5alkil (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili s nitro, heteroarilamino ili heteroarilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili s nitro, diheteroarilamino ili diheteroarilamino supstituiran s C1-C3alkilom, C1-C3haloalkil, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, fenilamino ili fenilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, difenilamino, ili difenilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, ili C3-C7cikloalkilamino, diC3-C7cikloalkilamino ili C3-C7cikloalkoksi, C1-C10alkoksi, C1-C10haloalkoksi, C1-C5alkilamino ili C2-C8dialkilamino
Rf i Rg su svaki međusobno neovisno C1-C10alkil, C2-C10alkenil, C2-C10alkinil, C1-C10alkoksi, C1-C10haloalkil, C1-C10cijanoalkil, C1-C10nitroalkil, C1-C10aminoalkil, C1-C5alkilaminoC1-C5alkil, C2-C8dialkilaminoC1-C5alkil, C3-C7cikloalkilC1-C5alkil, C1-C5alkoksiC1-C5alkil, C3-C5alkeniloksiC1-C5alkil, C3-C5alkiniloksiC1-C5alkil, C1-C5alkiltioC1-C5alkil, C1-C5alkilsulfinilC1-C5alkil, C1-C5alkilsulfonilC1-C5alkil, C2-C8alkilideneaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoC1-C5alkil, N-C1-C5alkilkarbonil-N-C2-C5alkilaminoalkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), heteroarilC1-C5alkil (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano, ili s nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogen, cijano ili nitro, heteroaril ili heteroaril supstituiran s C1-C3 alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili s nitro, heteroarilamino ili heteroarilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili s nitro, diheteroarilamino ili diheteroarilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, fenilamino ili fenilamino supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, difenilamino, ili difenilamino supstituiran s C1-C3alkilom, C1-3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, ili C3-C7cikloalkilamino, diC3-C7cikloalkilamino ili C3-C7cikloalkoksi, C1-C10haloalkoksi, C1-C5alkilamino ili C2-C8dialkilamino, benziloksi ili fenoksi, pri čemu benzil i fenil skupine mogu zauzvrat biti supstituirane sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, i
Rh je C1-C10alkil, C3-C10alkenil, C3-C10alkinil, C1-C10haloalkil, C1-C10cijanoalkil, C1-C10nitroalkil, C2-C10aminoalkil, C1-C5alkilaminoC1-C5alkil, C2-C8dialkilaminoC1-C5alkil, C3-C7cikloalkilC1-C5alkil, C1-C5alkoksiC1-C5alkil, C3-C5alkeniloksiC1-C5alkil, C3-C5alkiniloksiC1-C5alkil, C1-C5alkiltioC1-C5alkil, C1-C5alkilsulfinilC1-C5alkil, C1-C5alkilsulfonilC1-C5alkil, C2-C8alkilideneaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoC1-C5alkil, N-C1-C5alkilkarbonil-N-C1-C5alkilaminoC1-C5alkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili s nitro), heteroarilC1-C5alkil (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili s nitro), fenoksiC1-C5alkil (pri čemu fenil može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili s nitro), heteroariloksiC1-C5alkil (pri čemu heteroaril može proizvoljno biti supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3akilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili s nitro), C3-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom ili s nitro, ili heteroaril, ili heteroaril supstituiran s C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili s nitro;
R je vodik, C1-6alkil, C1-6haloalkil, C1-6cijanoalkil, benzil, C1-4alkoksi(C1-4)alkil, C1-4alkoksi(C1-4)alkoksi(C1-4)alkil ili skupina odabrana od G; i
A je C1-6alkil, C1-6haloalkil, C3-6cikloalkil, C3-6cikloalkil(C1-4)alkil, ili C3-6cikloalkil(C1-4)alkil gdje je u cikloalkilnom dijelu metilenska skupina zamijenjena sa O,S ili NR0, gdje R0 je C16alkil ili C1-6alkoksi, ili A je C2-6alkenil, C2-6haloalkenil, C3-6alkinil, C1-6cijanoalkil, benzil, C14alkoksi(C1-4)alkil, C1-4alkoksi(C1-4)alkoksi(C1-4)alkil, oksetanil, tetrahidrofuranil, tetrahidropiranil, C1-6alkilkarbonil, C1-6alkoksikarbonil, C3-6cikloalkil karbonil, N-di(C16alkil)karbamoil, benzoil, C1-6alkilsulfonil, fenilsulfonil, C1-4alkiltio(C1-4)alkil, C14alkilsulfinil(C1-4)alkil ili C1-4alkilsulfonil(C1-4)alkil;
ili njihova agrokemijski prihvatljiva sol ili N-oksid.
2. Spoj prema zahtjevu 1 naznačen time da G je skupina odabrana od -C(Xa)-Ra ili -C(Xb)-Xc-Rb, i značenja za Xa, Ra, Xb, Xc i Rb su kako je definirano u zahtjevu 1.
3. Spoj prema zahtjevu 1 naznačen time da R je vodik, metil, etil, trifluorometil, alil, propargil, benzil, metoksimetil, etoksimetil ili metoksietil, X je metil, etil, ciklopropil, metoksi, fluoro, bromo ili kloro, Y i Z, međusobno neovisno su metil, etil, ciklopropil, metoksi, fluoro, kloro, bromo, fenil ili fenil supstituiran s halogen ili C1-C2alkil, G je vodik i A je kako je definirano u zahtjevu 1.
4. Spoj prema bilo kojem zahtjevu 1 ili zahtjevu 3 naznačen time da R je metil, etil, alil, propargil, metoksimetil, X je metil, etil, ciklopropil, metoksi, fluoro, bromo ili kloro, Y i Z, međusobno neovisno su metil, etil, ciklopropil, metoksi, fluoro, kloro, bromo, fenil ili fenil supstituiran s halogen ili C1-C2alkil, G je vodik i A je kako je definirano u zahtjevu 1.
5. Spoj prema bilo kojem zahtjevu od 1, 3 i 4 naznačen time da R je metil, etil, metoksimetil, X je metil, etil, ciklopropil, metoksi, fluoro, bromo ili kloro, Y i Z, međusobno neovisno su metil, etil, ciklopropil, metoksi, fluoro, kloro, bromo, fenil ili fenil supstituiran s halogenom ili C1-C2alkilom, G je vodik i A je metil, etil, izopropil, trifluorometil, 2,2,2-trifluoroetil, 2,2-difluoroetil, 2-fluoroetil, ciklopropil, ciklobutil, ciklopentil, cikloheksil, ciklopropilmetil, ciklobutilmetil, ciklopentilmetil, cikloheksilmetil, oksetan-3-ilmetil, tetrahidrofuran-2-ilmetil, tetrahidropiran-2-ilmetil, tetrahidrofuran-3-ilmetil, tetrahidropiran-3-ilmetil, tetrahidropiran-4-ilmetil, alil, propargil, benzil, metoksimetil, etoksimetil, metoksietil, metoksipropil, metoksietoksimetil, metoksimetoksietil, oksetanil-3-il, tetrahidropiran-4-il ili metiltioetil.
6. Spoj prema bilo kojem zahtjevu od 1 i 3 do 5 naznačen time da R je metil, etil, metoksimetil, X je metil, etil, ciklopropil, metoksi, fluoro, bromo ili kloro, Y i Z, međusobno neovisno su metil, etil, ciklopropil, metoksi, fluoro, kloro, bromo, fenil ili fenil supstituiran s halogenom ili C1-C2alkilom, G je vodik i A je metil, etil, izopropil, trifluorometil, 2,2,2-trifluoroetil, 2,2-difluoroetil, 2-fluoroetil, ciklopropil, cikloheksil, ciklopropilmetil, alil, propargil, benzil, metoksimetil, etoksimetil, metoksietil, metoksietoksimetil, metoksimetoksietil, oksetanilil.
7. Postupak za pripravu spojeva sa formulom I prema bilo kojem zahtjevu od 1 do 6, naznačen time da G je vodik, koji se sastoji od ciklizacije spoja sa formulom IV
[image]
pri čemu X, Y, Z, m, n, R i A imaju značenja koja su im dodijeljena u bilo kojem od patentnih zahtjeva 1 do 6, i R14 je C1-6alkil, pod bazičnim uvjetima.
8. Pesticidni pripravak naznačen time da sadrži pesticidno učinkovitu količinu barem jednog spoja sa formulom I prema bilo kojem zahtjevu od 1 do 6.
9. Pesticidni pripravak prema zahtjevu 8, naznačen time da pored toga što sadrži spoj sa formulom I, sadrži pomoćna sredstva za formulaciju.
10. Pesticidni pripravak prema zahtjevu 9, naznačen time da pomoćno sredstvo za formulaciju je ulje biljnog ili životinjskog podrijetla, mineralno ulje, alkil esteri takvih ulja ili smjese takvih ulja i derivati ulja, ili je gnojivo ili amonijeva ili fosfonijeva sol, proizvoljno u smjesi s gore navedenim uljima i derivatima ulja.
11. Pesticidni pripravak prema zahtjevu 8, naznačen time da pored toga što sadrži spoj sa formulom I, sadrži barem jedan dodatni insekticid, akaricid, nematicid ili moluskicid.
12. Pesticidni pripravak prema zahtjevu 8, naznačen time da pored toga što sadrži spoj sa formulom I, sadrži barem jedan dodatni fungicid, herbicid, zaštitnu tvar ili regulator rasta biljke.
13. Postupak suzbijanja i kontrole štetočina, koji obuhvaća primjenu na štetočine, na lokus štetočina, ili na biljku osjetljivu na napad štetočina pesticidno učinkovite količine spoja sa formulom I kako je definirano u bilo kojem zahtjevu od 1 do 6, s izuzetkom postupka liječenja ljudskog ili životinjskog tijela kirurškim zahvatom ili liječenja i dijagnostičkih postupaka koji se primjenjuju na ljudskom ili životinjskom tijelu.
14. Postupak suzbijanja i kontrole štetočina, koji obuhvaća primjenu na štetočine, na lokus štetočina, ili na biljku osjetljivu na napad štetočina pesticidnog pripravka prema zahtjevu 8, s izuzetkom postupka liječenja ljudskog ili životinjskog tijela kirurškim zahvatom ili liječenja i dijagnostičkih postupaka koji se primjenjuju na ljudskom ili životinjskom tijelu.
15. Spojevi sa formulom IV
[image]
ili njihove soli, naznačeni time da X, Y, Z, m, n, R i A imaju značenja koja su im dodijeljena u bilo kojem od patentnih zahtjeva 1 do 6, i R14 je C1-6alkil.
16. Spojevi sa formulom V
[image]
ili njihove soli, naznačeni time da R i A imaju značenja koja su im dodijeljena u bilo kojem od patentnih zahtjeva 1 do 6, i R14 je C1-6alkil.
17. Spojevi sa formulom VIII
[image]
ili njihove soli, naznačeni time da R i A imaju značenja koja su im dodijeljena u bilo kojem od patentnih zahtjeva 1 do 6.
18. Spojevi sa formulom XI
[image]
ili njihove soli, naznačeni time da X, Y, Z, m, n, R i A imaju značenja koja su im dodijeljena u bilo kojem od patentnih zahtjeva 1 do 6.
19. Spojevi sa formulom VII
[image]
ili njihove soli, naznačeni time da R i A imaju značenja koja su im dodijeljena u bilo kojem od patentnih zahtjeva 1 do 6.
20. Spojevi sa formulom XIV
[image]
ili njihove soli, naznačeni time da X, Y, Z, m, n, R i A imaju značenja koja su im dodijeljena u bilo kojem od patentnih zahtjeva 1 do 6, i T je vodik, C1-4alkoksi, di(C1-4alkoksi), nitro ili kloro.
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AU7186494A (en) | 1993-07-02 | 1995-01-24 | Bayer Aktiengesellschaft | Substituted spiroheterocyclic 1h-3-arylpyrrolidine-2,4-dione derivatives, methods of preparing them and their use as pest-control agents |
DE19813354A1 (de) * | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
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GB0213715D0 (en) * | 2002-06-14 | 2002-07-24 | Syngenta Ltd | Chemical compounds |
GB0328908D0 (en) * | 2003-12-12 | 2004-01-14 | Syngenta Participations Ag | Chemical compounds |
GB0328907D0 (en) * | 2003-12-12 | 2004-01-14 | Syngenta Participations Ag | Chemical compounds |
EP1692939A1 (en) * | 2005-02-19 | 2006-08-23 | Bayer CropScience S.A. | Pesticidal substituted piperidines |
GB0720126D0 (en) | 2007-10-15 | 2007-11-28 | Syngenta Participations Ag | Chemical compounds |
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MX2011005307A (es) | 2008-12-02 | 2011-06-01 | Syngenta Participations Ag | N-oxiamidas espiroheterociclicas como pesticidas. |
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