Composition and method for controlling pests

US9549559B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9549559-B2
Application numberUS-201414764524-A
CountryUS
Kind codeB2
Filing dateJan 30, 2014
Priority dateJan 31, 2013
Publication dateJan 24, 2017
Grant dateJan 24, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention provides a composition for controlling pests comprising a compound represented by the formula (1): wherein each of symbols are the same as defined in the Description, or N-oxide thereof; and at least one compound selected from the group consisting of neonicotinoid compound, synthetic pyrethroid compound, phenylpyrazole compound, macrolide compound, diamide compound, and insecticidal compound selected from the group consisting of pymetrozine, pyridalyl, pyriproxyfen, spirotetramat, sulfoxaflo and flupyradifurone, which has an excellent control efficacy on pests.

First claim

Opening claim text (preview).

The invention claimed is: 1. A composition for controlling pests comprising a compound represented by the formula (1) or N-oxide thereof and at least one compound selected from the below-mentioned Group (A); the formula (1): wherein A 1 represents —NR 7 —, an oxygen atom, or a sulfur atom; A 2 presents a nitrogen atom or ═CR 8 —; R 1 represents a C1-C6 alkyl group which may be substituted with one or more atoms or group selected from Group X; R 2 , R 3 and R 4 are the same or different to each other and each independently represent a C1-C6 alkyl group which may be substituted with one or more atoms or groups selected from Group X, a —OR 10 group, a —S(O) m R 10 group, a —S(O) 2 NR 10 R 11 group, a —NR 10 R 11 group, a —NR 10 CO 2 R 11 group, a —NR 10 C(O)R 11 group, a —CO 2 R 10 group, a —C(O)R 10 group, a —C(O)NR 10 R 11 group, a —SF 5 group, a cyano group, a nitro group, a halogen atom, or a hydrogen atom; R 5 and R 6 are the same or different to each other and each independently represent a C1-C6 alkyl group which may be substituted with one or more atoms or groups selected from Group X, a —OR 10 group, a —S(O) m R 10 group, a —S(O) 2 NR 10 R 11 group, a —NR 10 R 11 group, a —NR 10 CO 2 R 11 group, a —NR 10 C(O)R 11 group, a —CO 2 R 10 group, a —C(O)R 10 group, a —C(O)NR 10 R 11 group, —OC(O)R 10 , a —SF 5 group, a cyano group, a nitro group, a halogen atom, or a hydrogen atom, wherein R 5 and R 6 do not represent a hydrogen atom at the same time; R 7 represents a C1-C6 alkyl group which may be substituted with one or more atoms or groups selected from Group W, a —CO 2 R 10 group, a —C(O)R 10 group, a —CH 2 CO 2 R 10 group, a C3-C6 cycloalkyl group, or a hydrogen atom; R 8 represents a C1-C6 alkyl group which may be substituted with one or more halogen atoms, a —OR 10 group, a —S(O) m R 10 group, a —NR 10 R 11 group, a —CO 2 R 10 group, a —C(O)R 10 group, a cyano group, a nitro group, a halogen atom, or a hydrogen atom; R 10 and R 11 are the same or different to each other and each independently represent a C1-C6 alkyl group which may be substituted with one or more atoms or groups selected from Group X or a hydrogen atom, except for a —S(O) m R 10 group wherein m is 1 or 2 and R 10 is a hydrogen atom; m independently represents 0, 1 or 2; and n represents 0, 1 or 2; Group X comprising a C1-C6 alkoxy group which may be substituted with one or more halogen atoms, a C3-C6 cycloalkyl group which may be substituted with one or more halogen atoms or one or more C1-C3 alkyl groups, a cyano group, a hydroxy group, and a halogen atom; Group W comprising: a C1-C6 alkoxy group which may be substituted with one or more halogen atoms, a C3-C6 cycloalkyl group which may be substituted with one or more halogen atoms, a hydroxy group, a halogen atom, and a cyano group; at least one compound selected from the below-mentioned Group (A): group consisting of the following Sub-group A-1, A-2, A-3, A-4, A-5 and A-6: Sub-group A-1: neonicotinoid compound selected from the group consisting of imidacloprid, clothianidin thiamethoxam, dinotefuran, acetamiprid, thiacloprid and nitenpyram; Sub-group A-2: synthetic pyrethroid compound selected from the group consisting of acrinathrin, bifenthrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, deltamethrin, etofenprox, fenpropathrin, fenvalerate, esfenvalerate, flucythrinate fluvalinate, tau-fluvalinate, halfenprox, permethrin, silafluofen, tefluthrin, tralomethrin and protrifenbute; Sub-group A-3: phenylpyrazole compound selected from the group consisting of ethiprole, fipronil, acetoprole, vaniliprole, pyriprole and pyrafluprole; Sub-group A-4: macrolide compound selected from the group consisting of abamectin, emamectin, emamectin benzoate, milbemectine, doramectin and lepimectin; Sub-group A-5: diamide compound selected from the group consisting of flubendiamide and the compound represented by formula (2): [wherein, R 1 represents a methyl group or a bromine group, R 2 represents a bromine atom, a chlorine atom or a cyano group, R 3 represents a methyl group, a 1-cyclopropylmethyl group or a methoxycarbonylamino group, and R 4 represents a hydrogen atom or an ethyl group] Sub-group A-6: insecticidal compound selected from the group consisting of pymetrozine, pyridalyl, pyriproxyfen, spirotetramat, sulfoxaflo and flupyradifurone. 2. The composition for controlling pests according to claim 1 , wherein in the compound represented by the formula (1) or N-oxide thereof, R 1 is a C1-C6 alkyl group which may be substituted with one or more atoms or groups selected from Group Y; R 2 and R 4 are hydrogen atoms; R 3 is a C1-C3 alkyl group which may be substituted with one or more halogen atoms, a —C(OR 10 ) 3 group, a halogen atom, or a hydrogen atom; R 5 is a C1-C3 alkyl group which may be substituted with one or more halogen atoms, a —OR 10 group, a —S(O) m R 10 group, a —CO 2 R 10 group, a —SF 5 group, or a halogen atom; R 6 is a —OR 10 group, a —NR 10 R 11 group, a —CO 2 R 10 group, a —C(O)NR 10 R 11 group, —OC(O)R 10 , a cyano group, a halogen atom, or a hydrogen atom; R 7 is a C1-C6 alkyl group which may be substituted with one or more halogen atoms, a —CH 2 CO 2 R 10 group, a C3-C6 cycloalkyl group, or a hydrogen atom, R 8 is a C1-C3 alkyl group which may be substituted with one or more halogen atoms, a —OR 10 group, a —S(O) m R 10 group, a cyano group, a halogen atom, or a hydrogen atom; R 10 and R 11 are the same or different to each other and each independently represent a C1-C3 alkyl group which may be substituted with one or more halogen atoms or a hydrogen atom, except for a —S(O) m R 10 group wherein m is 1 or 2 and R 10 is a hydrogen atom; and Group Y comprising: a C3-C6 cycloalkyl group which may be substituted with one or more halogen atoms and a halogen atom. 3. The composition for controlling pests according to claim 1 , wherein in the compound represented by the formula (1) or N-oxide thereof, R 1 is a C1-C3 alkyl group which may be substituted with one or more halogen atoms; R 2 and R 4 are hydrogen atoms; R 3 is a C1-C3 alkyl group which may be substituted with one or more halogen atoms, a —C(OR 10 ) 3 group, a halogen atom, or a hydrogen atom; R 5 is a C1-C3 alkyl group which may be substituted with one or more halogen atoms, a —OR 10 group, a —S(O) m R 10 group, or a halogen atom; R 6 is a cyano group, a —NR 10 R 11 group, a halogen atom, or a hydrogen atom; R 7 is a C1-C6 alkyl group which may be substituted with one or more halogen atoms; R 8 is a —S(O) m R 10 group, a cyano group, a halogen atom, or a hydrogen atom; and R 10 and R 11 are the same or different to each other and each independently represent a C1-C3 alkyl group which may be substituted with one or more halogen atoms. 4. The composition for controlling pests according to claim 1 , wherein in the compound represented by the formula (1) or N-oxide thereof: R 1 is an ethyl group; R 2 and R 4 are hydrogen atoms; R 3 is a C1-C3 alkyl group which may be substituted with one or more halogen atoms, a —C(OR 10 ) 3 group, a halogen atom, or a hydrogen atom; R 5 is a C1-C3 haloalkyl group, a —OR 20 group, a —S(O) m R 20 group, or a halogen atom; R 6 is a cyano group, a —NR 10 R 11 group, a halogen atom, or a h

Assignees

Inventors

Classifications

  • 1,2,3- or 1,2,4-triazines; Hydrogenated 1,2,3- or 1,2,4-triazines · CPC title

  • Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring · CPC title

  • six-membered rings · CPC title

  • A01N43/90Primary

    having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system · CPC title

  • the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9549559B2 cover?
The present invention provides a composition for controlling pests comprising a compound represented by the formula (1): wherein each of symbols are the same as defined in the Description, or N-oxide thereof; and at least one compound selected from the group consisting of neonicotinoid compound, synthetic pyrethroid compound, phenylpyrazole compound, macrolide compo…
Who is the assignee on this patent?
Sumitomo Chemical Co
What technology area does this patent fall under?
Primary CPC classification A01N43/90. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jan 24 2017 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 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).