Heterocyclic compounds as pesticides

US11548854B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11548854-B2
Application numberUS-202017093130-A
CountryUS
Kind codeB2
Filing dateNov 9, 2020
Priority dateOct 2, 2012
Publication dateJan 10, 2023
Grant dateJan 10, 2023

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present application relates to the use of heterocyclic compounds for controlling animal pests including arthropods, insects and nematodes, to novel heterocyclic compounds, to processes for their preparation and to intermediates for preparing the heterocyclic compounds.

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound of formula (I) in which A represents in which the broken line represents the bond to Q and in which A furthermore carries m substituents R2, Q represents in which the nitrogen is attached to ring A and the arrow represents the bond to D and D represents the radical of the formula in which the nitrogen is attached to Q and the arrow represents the bond to B, B represents a radical from the group consisting of in which the broken line represents the bond to D and in which B furthermore carries n substituents R7, Z represents oxygen or sulphur, R2 represents a radical selected from the group consisting of halogen, cyano, nitro, amino, hydroxy, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -alkoxy, C 3 -C 6 -alkenyloxy, C 3 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 6 -alkylcarbonyloxy, C 2 -C 6 -alkenylcarbonyloxy, C 2 -C 6 -alkynylcarbonyloxy, C 3 -C 6 -cycloalkylcarbonyloxy, C 1 -C 6 -alkoxycarbonyloxy, C 1 -C 6 -alkylsulphonyloxy, C 1 -C 6 -alkylamino, di-(C 1 -C 6 -alkyl)-amino, C 3 -C 6 -alkenylamino, C 3 -C 6 -alkynylamino, C 3 -C 6 -cycloalkylamino, C 1 -C 6 -alkylcarbonylamino, C 2 -C 6 -alkenylcarbonylamino, C 2 -C 6 -alkynylcarbonylamino, C 3 -C 6 -cycloalkylcarbonylamino, C 1 -C 6 -alkoxycarbonylamino, C 1 -C 6 -alkylsulphonylamino, C 1 -C 6 -alkylthio, C 3 -C 6 -alkenylthio, C 3 -C 6 -alkynylthio, C 3 -C 6 -cycloalkylthio, C 1 -C 6 -alkylsulphinyl, C 1 -C 6 -alkylsulphonyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkoxyimino-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxycarbonyl, aminocarbonyl, C 1 -C 6 -alkylaminocarbonyl, di-(C 1 -C 6 -alkyl)-aminocarbonyl, aminothiocarbonyl, C 1 -C 6 -alkylaminosulphonyl, C 1 -C 6 -alkylsulphonylamino, C 1 -C 6 -alkylcarbonylamino, C 1 -C 6 -alkylthiocarbonylamino, C 4 -C 12 -bicycloalkyl, aryl, aryloxy, arylamino, arylthio, heteroaryl, heteroaryloxy, heteroarylamino and heteroarylthio, each of which is optionally substituted by one or more identical or different substituents, where the substituents independently of one another are selected from the group consisting of halogen, cyano, nitro, hydroxy, amino, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 3 -C 6 -cycloalkyl, C 1 -C 6 -haloalkoxy, and C 1 -C 6 -alkylthio, aryl, aryloxy, arylthio, heteroaryl, heteroaryloxy and heteroarylthio, R3 represents a radical selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkyl and C 1 -C 6 -haloalkoxy, R4 represents a radical selected from the group consisting of hydrogen, halogen, amino, hydroxy, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkyl and C 1 -C 6 -haloalkoxy, R5 represents a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl, C 3 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl-C 1 -C 6 -alkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkylcarbonyl, C 2 -C 6 -alkenylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 2 -C 6 -haloalkenylcarbonyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -alkylsulphonyl and C 1 -C 6 -haloalkylsulphonyl or represents C(═O)—B, R6 represents a radical selected from the group consisting of hydrogen (only in the radicals B-33 and B-36), halogen, cyano, nitro, amino, hydroxy, carboxyl, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -alkoxy, C 3 -C 6 -alkenyloxy, C 3 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 6 -alkylcarbonyloxy, C 2 -C 6 -alkenylcarbonyloxy, C 2 -C 6 -alkynylcarbonyloxy, C 3 -C 6 -cycloalkylcarbonyloxy, C 1 -C 6 -alkoxycarbonyloxy, C 1 -C 6 -alkylsulphonyloxy, C 3 -C 6 -alkenylamino, C 3 -C 6 -alkynylamino, C 3 -C 6 -cycloalkylamino, C 1 -C 6 -alkylcarbonylamino, C 2 -C 6 -alkenylcarbonylamino, C 2 -C 6 -alkynylcarbonylamino, C 3 -C 6 -cycloalkylcarbonylamino, C 1 -C 6 -alkoxycarbonylamino, C 1 -C 6 -alkylsulphonylamino, C 1 -C 6 -alkylthio, C 3 -C 6 -alkenylthio, C 3 -C 6 -alkynylthio, C 3 -C 6 -cycloalkylthio, C 1 -C 6 -alkylsulphinyl, C 1 -C 6 -alkylsulphonyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkoxyimino-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxycarbonyl, aminocarbonyl, C 1 -C 6 -alkylaminocarbonyl, di-(C 1 -C 6 -alkyl)-aminocarbonyl, aminothiocarbonyl, C 1 -C 6 -alkylaminosulphonyl, C 1 -C 6 -alkylsulphonylamino, C 1 -C 6 -alkylcarbonyl amino, C 1 -C 6 -haloalkylcarbonylamino, C 1 -C 6 -alkylthiocarbonylamino, C 4 -C 12 -bicycloalkyl, aryl, aryloxy, heteroaryl, and heteroaryloxy, each of which is optionally substituted by one or more identical or different substituents, where the substituents independently of one another are selected from the group consisting of halogen, cyano, nitro, hydroxy, amino, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 3 -C 6 -cycloalkyl, C 1 -C 6 -haloalkoxy and C 1 -C 6 -alkylthio, R7 represents a radical selected from the group consisting of halogen, nitro, cyano, amino, hydroxy, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -alkoxy, C 3 -C 6 -alkenyloxy, C 3 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 6 -alkylcarbonyloxy, C 2 -C 6 -alkenylcarbonyloxy, C 2 -C 6 -alkynylcarbonyloxy, C 3 -C 6 -cycloalkylcarbonyloxy, C 1 -C 6 -alkoxycarbonyloxy, C 1 -C 6 -alkylsulphonyloxy, C 1 -C 6 -alkylcarbonylamino, C 2 -C 6 -alkenylcarbonylamino, C 2 -C 6 -alkynylcarbonylamino, C 3 -C 6 -cycloalkylcarbonylamino, C 1 -C 6 -alkoxycarbonylamino, C 1 -C 6 -alkylsulphonylamino, C 3 -C 6 -alkenylamino, C 3 -C 6 -alkynylamino, C 1 -C 6 -alkylthio, C 3 -C 6 -alkenylthio, C 3 -C 6 -alkynylthio, C 3 -C 6 -cycloalkylthio, C 1 -C 6 -alkylsulphinyl, C 1 -C 6 -alkylsulphonyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkoxyimino-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxycarbonyl, aminocarbonyl, C 1 -C 6 -alkylaminocarbonyl, di-(C 1 -C 6 -alkyl)-aminocarbonyl, aminothiocarbonyl, C 1 -C 6 -alkylaminosulphonyl, C 1 -C 6 -alkylthiocarbonylamino, aryl, aryloxy, heteroaryl, heteroaryloxy, C 4 -C 12 -bicycloalkyl, each of which is optionally substituted by one or more identical or different substituents, where the substituents independently of one another are selected from the group consisting of halogen, cyano, nitro, hydroxy, amino, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 3 -C 6 -cycloalkyl, C 1 -C 6 -haloalkoxy and C 1 -C 6 -alkylthio, R9 represents a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, haloalkyl, C 3 -C 6 -alkenyl, C 3 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl-C 1 -C 6 -alkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkylcarbonyl, C 2 -C 6 -alkenylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 2 -C 6 -haloalkenylcarbonyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -alkylsulphonyl and C 1 -C 6 -haloalkylsulphonyl, m represents a number selected from the group consisting of 0, 1, 2 and 3, where for m>1 the radicals R2 may be identical or different and n represents a number selected from the group consisting of 0, 1, 2 and 3, where for n>1 the radicals

Assignees

Inventors

Classifications

  • 1,4-Diazines; Hydrogenated 1,4-diazines · CPC title

  • 1,2-Diazines; Hydrogenated 1,2-diazines · CPC title

  • Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis · CPC title

  • 1,2-Diazoles; Hydrogenated 1,2-diazoles · CPC title

  • having one double bond between ring members or between a ring member and a non-ring member · CPC title

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Frequently asked questions

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What does patent US11548854B2 cover?
The present application relates to the use of heterocyclic compounds for controlling animal pests including arthropods, insects and nematodes, to novel heterocyclic compounds, to processes for their preparation and to intermediates for preparing the heterocyclic compounds.
Who is the assignee on this patent?
Bayer Cropscience Ag
What technology area does this patent fall under?
Primary CPC classification C07D231/40. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 10 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).