WO2000064895A1 - Dithiazoldioxydes substitues par hetaryle utilises comme agents phytosanitaires - Google Patents

Dithiazoldioxydes substitues par hetaryle utilises comme agents phytosanitaires Download PDF

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Publication number
WO2000064895A1
WO2000064895A1 PCT/EP2000/003157 EP0003157W WO0064895A1 WO 2000064895 A1 WO2000064895 A1 WO 2000064895A1 EP 0003157 W EP0003157 W EP 0003157W WO 0064895 A1 WO0064895 A1 WO 0064895A1
Authority
WO
WIPO (PCT)
Prior art keywords
butyl
different
stands
butoxy
fluorine
Prior art date
Application number
PCT/EP2000/003157
Other languages
German (de)
English (en)
Inventor
Christiane Boie
Ulrich Heinemann
Bernd-Wieland Krüger
Hermann Uhr
Martin Vaupel
Martin Kugler
Ulrike Wachendorff-Neumann
Klaus Stenzel
Karl-Heinz Kuck
Peter Lösel
Shin-Ichi Narabu
Original Assignee
Bayer Aktiengesellschaft
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Aktiengesellschaft filed Critical Bayer Aktiengesellschaft
Priority to AU49128/00A priority Critical patent/AU4912800A/en
Publication of WO2000064895A1 publication Critical patent/WO2000064895A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
    • 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
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • R 5 , R 6 and R 7 are identical or different and independently of one another represent hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, pyridyl, nitro, cyano or halogen,
  • the reaction temperatures can be varied over a wide temperature range in this process. In general, one works between -30 ° C and + 100 ° C, preferably between -10 ° C and + 60 ° C. If appropriate, the reactions are carried out in the presence of bases; all customary bases can be used here. These preferably include tertiary amines, such as triethylamine, diisopropylethylamine or pyridine; Alkali hydroxides such as sodium and potassium hydroxide and alkali carbonates and hydrogen carbonates such as potassium carbonate and sodium hydrogen carbonate.
  • bases all customary bases can be used here. These preferably include tertiary amines, such as triethylamine, diisopropylethylamine or pyridine; Alkali hydroxides such as sodium and potassium hydroxide and alkali carbonates and hydrogen carbonates such as potassium carbonate and sodium hydrogen carbonate.
  • Possible diluents which can be used are both water and all organic solvents. These preferably include hydrocarbons such as toluene, xylene or hexane, chlorinated hydrocarbons such as chlorobenzene and chloroform, ketones such as acetone, ethers such as tetrahydrofuran, diethyl ether, methyl tert-butyl ether and dioxane, nitriles such as acetonitrile and
  • Xanthomonas species such as, for example, Xanthomonas campestris pv. Oryzae;
  • Pyricularia species such as, for example, Pyricularia oryzae; Fusarium species, such as, for example, Fusarium culmorum; Botrytis species, such as, for example, Botrytis cinerea; Septoria species, such as, for example, Septoria nodorum; Leptosphaeria species, such as, for example, Leptosphaeria nodorum; Cercospora species, such as, for example, Cercospora canescens;
  • the treatment of the plants and parts of plants according to the invention with the active compounds is carried out directly or by acting on their surroundings, living space or storage space using the customary treatment methods, for example by dipping, spraying, Evaporation, nebulization, scattering, spreading and, in the case of propagation material, in particular in the case of seeds, furthermore by means of single or multi-layer coating.
  • Trichoderma like Trichoderma viride
  • the active ingredients can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine encapsulations in polymeric substances and in coating compositions for seeds, and ULV -Cold and warm mist formulations.
  • Famoxadone Fenapanil, Fenarimol, Fenbuconazol, Fenfuram, Fenitropan, Fenpiclonil, Fenpropidin, Fenpropimo ⁇ h, Fentinacetat, Fentinhydroxyd, Ferbam, Ferimzon, Fluazinam, Flumetover, Fluoromid, Fluquinconazol, Flusrimidol, Flusrimidol, Flusrimidol, Folus Fosetyl-aluminum, fosetyl sodium, fthalide, fuberidazole, furalaxyl, furametpyr, furcarbonil, furconazole, furconazole-cis, furmecyclox, guazatin,
  • Eflusilanate, Emamectin, Empenthrin, Endosulfan, Entomopfthora spp. Esfenvalate, Ethiofencarb, Ethion, Ethoprophos, Etofenprox, Etoxazole, Etrimfos, Fenamiphos, Fenazaquin, Fenbutatin oxide, Fenitrothion, Fenothimocarb, Fenacroth
  • a specified amount of active compound preparation of the desired concentration is pipetted onto a standardized amount of synthetic feed. After the methanol has evaporated, a film can lid with about 100 plutella eggs is placed on each cavity. The newly hatched larvae migrate to the treated synthetic food.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

L'invention concerne de nouveaux dithiazoldioxydes substitués par hétaryle, des procédés permettant de les préparer et leur utilisation dans le domaine phytosanitaire et dans celui de la protection des matériaux.
PCT/EP2000/003157 1999-04-22 2000-04-10 Dithiazoldioxydes substitues par hetaryle utilises comme agents phytosanitaires WO2000064895A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU49128/00A AU4912800A (en) 1999-04-22 2000-04-10 Hetaryl-substituted dithiazole dioxides used as plant protection agents

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19918297.3 1999-04-22
DE1999118297 DE19918297A1 (de) 1999-04-22 1999-04-22 Hetarylsubstituierte Dithiazoldioxide

Publications (1)

Publication Number Publication Date
WO2000064895A1 true WO2000064895A1 (fr) 2000-11-02

Family

ID=7905506

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2000/003157 WO2000064895A1 (fr) 1999-04-22 2000-04-10 Dithiazoldioxydes substitues par hetaryle utilises comme agents phytosanitaires

Country Status (3)

Country Link
AU (1) AU4912800A (fr)
DE (1) DE19918297A1 (fr)
WO (1) WO2000064895A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10681909B2 (en) 2014-08-29 2020-06-16 Fmc Corporation Herbicidal triazoles

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3345374A (en) * 1962-09-04 1967-10-03 Bayer Ag Certain oxathiazole and dithiazole derivatives
DE2608488A1 (de) * 1975-03-05 1976-09-16 Ciba Geigy Ag Iso(thio)harnstoffe
DE19545635A1 (de) * 1995-12-07 1997-06-12 Bayer Ag Dithiazoldioxide
WO1998029400A1 (fr) * 1997-01-03 1998-07-09 Bayer Aktiengesellschaft Arylthio-dithiazindioxydes et leur utilisation comme pesticides
DE19721627A1 (de) * 1997-05-23 1998-11-26 Bayer Ag S-Pyridyl-dithiazoldioxide

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3345374A (en) * 1962-09-04 1967-10-03 Bayer Ag Certain oxathiazole and dithiazole derivatives
DE2608488A1 (de) * 1975-03-05 1976-09-16 Ciba Geigy Ag Iso(thio)harnstoffe
DE19545635A1 (de) * 1995-12-07 1997-06-12 Bayer Ag Dithiazoldioxide
WO1998029400A1 (fr) * 1997-01-03 1998-07-09 Bayer Aktiengesellschaft Arylthio-dithiazindioxydes et leur utilisation comme pesticides
DE19721627A1 (de) * 1997-05-23 1998-11-26 Bayer Ag S-Pyridyl-dithiazoldioxide
WO1998052945A1 (fr) * 1997-05-23 1998-11-26 Bayer Aktiengesellschaft Derives de pyridylthio-dithiazoldioxyde et leur utilisation comme agents de lutte contre les parasites

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10681909B2 (en) 2014-08-29 2020-06-16 Fmc Corporation Herbicidal triazoles

Also Published As

Publication number Publication date
DE19918297A1 (de) 2000-10-26
AU4912800A (en) 2000-11-10

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