Herbicidal compositions

US2022386605A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2022386605-A1
Application numberUS-202017624108-A
CountryUS
Kind codeA1
Filing dateJun 26, 2020
Priority dateJul 4, 2019
Publication dateDec 8, 2022
Grant date

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 compositions comprising herbicidally active compounds (A) and (B), wherein (A) represents one or more compounds of the general formula (I) or agrochemically acceptable salts thereof [component (A)],and (B) represents one or more herbicides [component (B)]. The application further relates to a method and to the use of the herbicidal composition of the invention for controlling harmful plants or for regulating growth.

First claim

Opening claim text (preview).

1 . A composition comprising one or more herbicidally active compounds (A) and (B), wherein (A) represents one or more compounds of formula (I) or one or more agrochemically acceptable salts thereof [herbicides (A)], in which G denotes a group of the formula OR 4 or NR 11 R 12 ; R 1 and R 2 are each independently hydrogen, halogen or cyano, or are (C 1 -C 4 )-alkyl or (C 1 -C 4 )-alkoxy, each substituted by m radicals from the group consisting of halogen and cyano; R 3 is cyano or fluorine, or is (C 1 -C 5 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 2 -C 5 )-alkenyl, (C 2 -C 5 )-alkynyl or (C 1 -C 5 )-alkoxy, each substituted by m radicals from the group consisting of halogen, cyano, (C 1 -C 5 )-alkoxy and hydroxy; R 4 is hydrogen, or is (C 1 -C 12 )-alkyl, (C 3 -C 7 )-cycloalkyl, (C 3 -C 7 )-cycloalkyl-(C 1 -C 8 )-alkyl, (C 2 -C 8 )-alkenyl, (C 5 -C 6 )-cycloalkenyl or (C 2 -C 8 )-alkynyl, each substituted by m radicals from the group consisting of halogen, cyano, (C 1 -C 6 )-alkoxy, hydroxy and aryl; Y is oxygen or sulfur; W is oxygen or sulfur; Z represents a monounsaturated cyclopentane ring substituted by k radicals from the group of R 10 , where the arrow in each case represents a bond to the group C═W of the formula (I); R 10 is halogen, cyano or CO 2 R 7 , or is (C 1 -C 2 )-alkyl or (C 1 -C 2 )-alkoxy, each substituted by m radicals from the group consisting of fluorine and chlorine; R 11 , R 12 are each independently hydrogen, cyano, OR 7 , S(O) n RS, SO 2 NR 6 R 7 , CO 2 R, CONR 6 R 8 , COR 6 , NR 6 R 8 , NR 6 COR 8 , NR 6 CONR 8 R 8 , NR 6 CO 2 R 8 , NR 6 SO 2 R 8 , NR 6 SO 2 NR 6 R 8 , C(R 6 )═NOR 8 , optionally substituted aryl, optionally substituted heteroaryl or optionally substituted heterocyclyl, or are (C 1 -C 12 )-alkyl, (C 3 -C 8 )-cycloalkyl, (C 3 -C 7 )-cycloalkyl-(C 1 -C 7 )-alkyl, (C 2 -C 12 )-alkenyl, (C 5 -C 7 )-cycloalkenyl or (C 2 -C 12 )-alkynyl, each substituted by m radicals from the group consisting of halogen, cyano, nitro, OR 7 , S(O) n R 5 , SO 2 NR 6 R 7 , CO 2 R, CONR 6 R 8 , COR 6 , NR 6 R 8 , NR 6 COR 8 , NR 6 CONR 8 R 8 , NR 6 CO 2 R 8 , NR 6 SO 2 R 8 , NR 6 SO 2 NR 6 R 8 , C(R 6 )═NOR 8 , optionally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl, or R 11 and R 12 together with the nitrogen atom to which they are bonded form a saturated or partly or fully unsaturated five-, six- or seven-membered ring which is optionally mono- to hexasubstituted by radicals from the group consisting of halogen, cyano, nitro, (C 1 -C 6 )-alkyl, halo-(C 1 -C 6 )-alkyl, oxo, OR 7 , S(O) n R 5 , SO 2 NR 6 R 7 , CO 2 R, CONR 6 R 8 , COR 6 , NR 6 R 8 , NR 6 COR 8 , NR 6 CONR 8 R 8 , NR 6 CO 2 R 8 , NR 6 SO 2 R 8 , NR 6 SO 2 NR 6 R 8 and C(R 6 )═NOR 8 and which, in addition to that nitrogen atom, contains r carbon atoms, o oxygen atoms, p sulfur atoms and q elements from the group consisting of NR 7 and NCOR 7 as ring atoms; X 2 , X 4 and X 6 are each independently hydrogen, halogen or cyano, or are (C 1 -C 2 )-alkyl, in each case substituted by m radicals from the group consisting of fluorine, chlorine, bromine and (C 1 -C 2 )-alkoxy; X 3 and X 5 are each independently hydrogen, fluorine, chlorine, bromine, iodine, hydroxy, cyano, nitro, S(O) n R 6 or CO 2 R 7 , or are (C 1 -C 3 )-alkyl, (C 1 -C 3 )-alkoxy, (C 3 -C 4 )-cycloalkyl, (C 2 -C 3 )-alkenyl or (C 2 -C 3 )-alkynyl, each substituted by m radicals from the group consisting of fluorine, chlorine and bromine; R 5 is (C 1 -C 8 )-alkyl, (C 3 -C 6 )-cycloalkyl or aryl, each substituted by m radicals from the group consisting of halogen, cyano and hydroxy; R 6 is hydrogen or R 5 ; R 7 is hydrogen, or is (C 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 3 -C 4 )-alkenyl or (C 3 -C 4 )-alkynyl, each substituted by m radicals from the group consisting of halogen, cyano and (C1-C 2 )-alkoxy; R 8 is hydrogen, or is (C 1 -C 8 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 3 -C 8 )-alkenyl or (C 3 -C 8 )-alkynyl, each substituted by m radicals from the group consisting of halogen, cyano and (C1-C 2 )-alkoxy; the index k is 0, 1 or 2; where, when k>1, R 10 may independently be the same or different; the index m is 0, 1, 2, 3, 4 or 5; the index n is 0, 1 or 2; the index o is 0, 1 or 2; the index p is 0 or 1; the index q is 0 or 1; and the index r is 3, 4, 5 or 6; and (B) represents one or more herbicides [component (B)] from the group of the active herbicidal ingredients (B1) to (B111), in which (B1) represents active herbicidal ingredients from the group of the 1,3-diketo compounds selected from (B1.1) alloxydim, (B11.2) bicyclopyrone, (B11.3) butroxydim, (B11.4) clethodim, (B11.5) cycloxydim, (B11.6) fenquinotrione, (B11.7) mesotrione, (B11.8) pinoxaden, (B11.9) profoxydim, (B1.10) sethoxydim, (B11.11) sulcotrione, (B1.12) SYP-9121 (B1.13) tefuryltrione, (B11.14) tembotrione, (B1.15) tepraloxydim, (B1.16) tralkoxydim, (B1.17) Y13161, (B1.18) Y13287; (B2) represents active herbicidal ingredients from the group of the (sulfon)amides selected from (B2.1) acetochlor, (B2.2) alachlor, (B2.3) amidosulfuron, (B2.4) asulam, (B2.5) azimsulfuron, (B2.6) beflubutamid, (B2.7) bensulfuron, (B2.8) butachlor, (B2.9) carbetamide, (B2.10) chlorimuron, (B2.11) chlorpropham, (B2.12) chlorsulfuron, (B2.13) cinosulfuron, (B2.14) cloransulam, (B2.15) cyclosulfamuron, (B2.16) desmedipham, (B2.17) diclosulam, (B2.18) diflufenican, (B2.19) dimethachlor, (B2.20) dimethenamid, (B2.21) esprocarb, (B2.22) ethametsulfuron, (B2.23) ethoxysulfuron, (B2.24) flazasulfuron, (B2.25) florasulam, (B2.26) flucarbazone, (B2.27) flucetosulfuron, (B2.28) flufenacet, (B2.29) flumetsulam, (B2.30) flupyrsulfuron, (B2.31) foramsulfuron, (B2.32) halosulfuron, (B2.33) imazosulfuron, (B2.34) iodosulfuron, (B2.35) ipfencarbazone, (B2.36) mefenacet, (B2.37) mesosulfuron, (B2.38) metazachlor, (B2.39) metazosulfuron, (B2.40) metolachlor, (B2.41) metosulam, (B2.42) metsulfuron, (B2.43) nicosulfuron, (B2.44) orthosulfamuron, (B2.45) oxasulfuron, (B2.46) penoxsulam, (B2.47) pethoxamide, (B2.48) phenmedipham, (B2.49) picolinafen, (B2.50) pretilachlor, (B2.51) primisulfuron, (B2.52) propachlor, (B2.53) propanil, (B2.54) propham; (B2.55) propisochlor, (B2.56) propoxycarbazone, (B2.57) propyrisulfuron, (B2.58) propyzamide, (B2.59) prosulfocarb, (B2.60) prosulfuron, (B2.61) pyrazosulfuron, (B2.62) pyroxsulam, (B2.63) rimsulfuron, (B2.64) S-metolachlor, (B2.65) sulfometuron, (B2.66) sulfosulfuron, (B2.67) thenylchlor, (B2.68) thiencarbazone, (B2.69) thifensulfuron, (B2.70) tri-allate, (B2.71) triasulfuron, (B2.72) tribenuron, (B2.73) trifloxysulfuron, (B2.74) triflusulfuron, (B2.75) tritosulfuron, (B2.76) esprocarb, (B2.77) profluazol, (B2.78) tri-allate; (B3) represents active herbicidal ingredients from the group of the aryl nitriles selected from (B3.1) bromoxynil, (B3.2) chlorthiamid, (B3.3) dichlobenil, (B3.4) ioxynil, (B3.5) pyraclonil; (B4) represents active herbicidal ingredients from the group of the azoles selected from (B4.1) amicarbazone, (B4.2) amitrole, (B4.3) azafenidin, (B4.4) benzofenap, (B4.5) benzuofucaotong, (B4.6) biscarfentrazone, (B4.7) cafenstrole, (B4.8) carfentrazone,

Assignees

Inventors

Classifications

  • Herbicides; Algicides · CPC title

  • A01N43/26Primary

    five-membered rings · CPC title

  • selective · CPC title

  • A01N43/80Primary

    five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2 · 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 US2022386605A1 cover?
The present invention provides compositions comprising herbicidally active compounds (A) and (B), wherein (A) represents one or more compounds of the general formula (I) or agrochemically acceptable salts thereof [component (A)],and (B) represents one or more herbicides [component (B)]. The application further relates to a method and to the use of the herbicidal composition of the invention for…
Who is the assignee on this patent?
Bayer Ag
What technology area does this patent fall under?
Primary CPC classification A01N43/26. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Dec 08 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).