HRP20120705T1 - Spiroheterociklički derivati pirolidin diona koji su korisni kao pesticidi - Google Patents
Spiroheterociklički derivati pirolidin diona koji su korisni kao pesticidi Download PDFInfo
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- HRP20120705T1 HRP20120705T1 HRP20120705AT HRP20120705T HRP20120705T1 HR P20120705 T1 HRP20120705 T1 HR P20120705T1 HR P20120705A T HRP20120705A T HR P20120705AT HR P20120705 T HRP20120705 T HR P20120705T HR P20120705 T1 HRP20120705 T1 HR P20120705T1
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- c5alkyl
- halogen
- cyano
- nitro
- c3alkyl
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- 239000000575 pesticide Substances 0.000 title claims 5
- QFYXSLAAXZTRLG-UHFFFAOYSA-N pyrrolidine-2,3-dione Chemical class O=C1CCNC1=O QFYXSLAAXZTRLG-UHFFFAOYSA-N 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 claims abstract 38
- 150000002367 halogens Chemical group 0.000 claims abstract 37
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 33
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 33
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims abstract 30
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 26
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 18
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims abstract 16
- 150000001875 compounds Chemical class 0.000 claims abstract 15
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 6
- 239000001257 hydrogen Substances 0.000 claims abstract 6
- 150000002431 hydrogen Chemical class 0.000 claims abstract 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract 4
- -1 C1-C1-6alkyloxy) Chemical group 0.000 claims abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract 2
- 229910021529 ammonia Inorganic materials 0.000 claims abstract 2
- 239000002184 metal Substances 0.000 claims abstract 2
- 229910052751 metal Inorganic materials 0.000 claims abstract 2
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 8
- 241000607479 Yersinia pestis Species 0.000 claims 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 6
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 125000005240 diheteroarylamino group Chemical group 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 2
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000005241 heteroarylamino group Chemical group 0.000 claims 2
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 2
- 230000001629 suppression Effects 0.000 claims 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 claims 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 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
- 239000002671 adjuvant Substances 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 230000000855 fungicidal effect Effects 0.000 claims 1
- 239000000417 fungicide Substances 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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000000203 mixture Substances 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
- 229910052760 oxygen Inorganic materials 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
- 239000005648 plant growth regulator Substances 0.000 claims 1
- 238000007363 ring formation reaction Methods 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
- A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
-
- 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
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- 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
- 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
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Public Health (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Spojevi sa formulom I naznačeni time daX , Y i Z, nezavisno jedan od drugoga su C1-4alkil, C3-6cikloalkil, C1-4haloalkil, C1-4alkoksi, halogen, fenil ili fenil supstituiran sa C1-4alkilom ili halogenom, C1-4haloalkil, halogen ili cijano, m i n, nezavisno jedan od drugoga su 0, 1, 2 ili 3, gdje m+n je 0, 1, 2 ili 3, G je vodik, metal, amonijak, sulfonij ili latentna skupina koja je odabrana iz skupina C1-C8alkil, C2-C8haloalkil, fenilC1-C8alkil (pri čemu fenil proizvoljno mo·e biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), heteroarilC1-C8alkil (pri čemu heteroaril proizvoljno mo·e biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom,
Claims (14)
1. Spojevi sa formulom I
[image]
naznačeni time da
X , Y i Z, nezavisno jedan od drugoga su C1-4alkil, C3-6cikloalkil, C1-4haloalkil, C1-4alkoksi, halogen, fenil ili fenil supstituiran sa C1-4alkilom ili halogenom, C1-4haloalkil, halogen ili cijano,
m i n, nezavisno jedan od drugoga su 0, 1, 2 ili 3, gdje m+n je 0, 1, 2 ili 3,
G je vodik, metal, amonijak, sulfonij ili latentna skupina koja je odabrana iz skupina C1-C8alkil, C2-C8haloalkil, fenilC1-C8alkil (pri čemu fenil proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), heteroarilC1-C8alkil (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili sa nitro), C3-C8alkenil, C3-C8haloalkenil, C3-C8alkinil, C(Xa)-Ra, C(Xb)-Xc-Rb, C(Xd)-N(Rc)-Rd, -SO2-Re, -P(Xe)(Rf)-Rg ili CH2-Xf-Rh pri čemu Xa, Xb, Xc, Xd, Xe i Xf su nezavisno jedan od drugoga 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-C5alkilsuflonilC1-C5alkil, C2-C8alkilidenaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoCiC5alkil, N-C1-C5alkilkarbonil-N-C1-C5alkilaminoC1-C5alkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), heteroarilC1-C5alkil, (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran sa C1-C3 alkilom, 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-C5alkilsuflonilC1-C5alkil, C2-C8alkilidenaminoksiC1-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 proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), heteroarilC1-C5alkil, (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), C3-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran sa C1-C3 alkilom, C1-3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro,
Rc i Rd nezavisno jedan od drugoga su 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-C5alkilsuflonilC1-C5alkil, C2-C8alkilidenaminoksiC1-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 proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsuflonilom, halogenom, cijano ili sa nitro), heteroarilC1-C5alkil, (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroarilamino ili heteroarilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, diheteroarilamino ili diheteroarilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, fenilamino ili fenilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili sa nitro, difenilamino ili difenilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili sa nitro ili C3-C7cikloalkilamino, di-C3-C7cikloalkilamino ili C3-C7cikloalkoksi ili Rc i Rd mogu se spajati zajedno da se formira 3-7 člani prsten, koji proizvoljno sadrži jedan heteroatom koji je 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-C8alkilidenaminoksiC1-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 proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), heteroarilC1-C5alkil (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran sa C1-C3 alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili sa nitro, heteroarilamino ili heteroarilamino supstituiran sa C1-C3 alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili sa nitro, diheteroarilamino ili diheteroarilamino supstituiran sa C1-C3 alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, fenilamino ili fenilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, difenilamino, ili difenilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, ili C3-C7cikloalkilamino, diC3-C7cikloalkilamino ili C3-C7cikloalkoksi, C1-C10alkoksi, C1-C1ohaloalkoksi, C1-C5alkilamino ili C2-C8dialkilamino
Rf i Rg nezavisno jedan od drugoga su 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-C5alkeniloksiC1-5alkil, C3-C5alkiniloksiC1-C5alkil, C1-C5alkiltioC1-C5alkil, C1-C5alkilsulfinilC1-C5alkil, C1-C5alkilsulfonilC1-C5alkil, C2-C8alkilidenaminoksiC1-C5alkil, C1-C5alkilkarbonilC1-C5alkil, C1-C5alkoksikarbonilC1-C5alkil, aminokarbonilC1-C5alkil, C1-C5alkilaminokarbonilC1-C5alkil, C2-C8dialkilaminokarbonilC1-C5alkil, C1-C5alkilkarbonilaminoC1-C5alkil, N-C1-C5alkilkarbonil-N-C2-Calkilaminoalkil, C3-C6trialkilsililC1-C5alkil, fenilC1-C5alkil (pri čemu fenil proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), heteroarilC1-C5alkil (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), C2-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, heteroaril ili heteroaril supstituiran sa C1-C3 alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili sa nitro, heteroarilamino ili heteroarilamino supstituiran sa C1-C3 alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili sa nitro, diheteroarilamino ili diheteroarilamino supstituiran sa C1-C3 alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, fenilamino ili fenilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili nitro, difenilamino, ili difenilamino supstituiran sa C1-C3alkilom, C1-C3haloalkilom, 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 biti naizmjenično 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-C8alkilidenaminoksiC1-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 proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili sa nitro), heteroarilC1-C5alkil (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), fenoksiC1-C5alkil (pri čemu fenil proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3alkilsulfinilom, C1-C3alkilsulfonilom, halogenom, cijano ili sa nitro), heteroariloksiC1-C5alkil (pri čemu heteroaril proizvoljno može biti supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, C1-C3alkiltio, C1-C3akilsulfinilom, C1-C3 alkilsulfonilom, halogenom, cijano ili sa nitro), C3-C5haloalkenil, C3-C8cikloalkil, fenil ili fenil supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom ili sa nitro, ili heteroaril, ili heteroaril supstituiran sa C1-C3alkilom, C1-C3haloalkilom, C1-C3alkoksi, C1-C3haloalkoksi, halogenom, cijano ili sa 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 skupine odabrana od G, te
R1, R2, R3 i R4, nezavisno jedan od drugoga su vodik ili metil, ili
njihova agrokemijski prihvatljiva sol ili N-oksid.
2. Postupak za dobivanje spojeva sa formulom I prema zahtjevu 1, naznačen time da G je vodik, koji se sastoji od ciklizacije spoja formule IV
[image]
pri čemu X, Y, Z, m, n, R, R1, R2, R3, i R4 imaju značenja dodijeljena u zahtjevu 1, i R14 je C1-4alkil, kod baznih uvjeta.
3. Pesticidni pripravak naznačen time da sadrži pesticidno učinkovitu količinu barem jednog spoja sa formulom I prema zahtjevu 1.
4. Pesticidni pripravak prema zahtjevu 3, naznačen time da pored toga što sadrži spoj sa formulom I, sadrži formulaciju adjuvanata.
5. Pesticidni pripravak prema zahtjevu 3, naznačen time da pored toga što sadrži spoj sa formulom I, sadrži barem jedan dodatni insekticid, akaricid, nematicid ili moluskicid.
6. Pesticidni pripravak prema zahtjevu 3, naznačen time da pored toga što sadrži spoj sa formulom I, sadrži barem jedan dodatni fungicid, herbicid ili regulator rasta biljke.
7. Postupak za suzbijanje i kontrolu štetnika naznačen time da se sastoji od primjene pesticidno učinkovite količine spoja sa formulom I na štetočine, na lokus štetočina, ili na biljku osjetljivu na napade štetočina.
8. Postupak za suzbijanje i kontrolu štetnika naznačen time da se sastoji od primjene pesticidnog pripravka prema zahtjevu 3n a štetočine, na lokus štetočina ili na biljku osjetljivu na napade štetočina.
9. Spojevi sa formulom IV
[image]
naznačeni time da X, Y, Z, m, n, R, R1, R2, R3 i R4 imaju značenja dodijeljena u zahtjevu 1, i R14 je C1-4alkil.
10. Spojevi sa formulom V
[image]
ili njihove soli,
naznačeni time da R, R1, R2, R3 i R4 imaju značenja dodijeljena u zahtjevu 1, i R14 je C1-4alkil.
11. Spojevi sa formulom VII
[image]
ili njihove soli,
naznačeni time da R1, R2, R3 i R4 imaju značenja dodijeljena u zahtjevu 1 i R je C1-C6alkil, C2-C6alkenil, C3-C6alkinil ili benzil.
12. Spojevi sa formulom XI
[image]
naznačeni time da X, Y, Z, m, n, R, R1, R2, R3, i R4 imaju značenja dodijeljena u zahtjevu 1.
13. Spojevi sa formulom VIII
[image]
ili njihove soli,
naznačeni time da R, R1, R2, R3 i R4 imaju značenja dodijeljena u zahtjevu 1.
14. Spojevi sa formulom IX
[image]
naznačeni time da R1, R2, R3 i R4 imaju značenja dodijeljena u zahtjevu 1 i R je C1-C6alkil, C2-C6alkenil, C3-C6alkinil ili benzil.
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FR1526656A (fr) * | 1966-06-15 | 1968-05-24 | Sankyo Co | Nouveaux composés 2, 2-diméthyl-4, 4, 6, 6-tétrasubstitué-pipéridine-1-oxydes et procédé pour leur préparation |
GB1145943A (en) * | 1966-09-19 | 1969-03-19 | Sankyo Co | Stabilization of polymers |
FR1501917A (fr) * | 1966-09-28 | 1967-11-18 | Commissariat Energie Atomique | Acide aminé radicalaire et ses complexes métalliques |
JPS4920973B1 (hr) * | 1970-05-28 | 1974-05-29 | ||
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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 |
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