AR111303A1 - REPLACED PIRROLIDINONES AND ITS SALTS AND THEIR USE AS HERBICIDE ACTIVE INGREDIENTS - Google Patents
REPLACED PIRROLIDINONES AND ITS SALTS AND THEIR USE AS HERBICIDE ACTIVE INGREDIENTSInfo
- Publication number
- AR111303A1 AR111303A1 ARP180100756A ARP180100756A AR111303A1 AR 111303 A1 AR111303 A1 AR 111303A1 AR P180100756 A ARP180100756 A AR P180100756A AR P180100756 A ARP180100756 A AR P180100756A AR 111303 A1 AR111303 A1 AR 111303A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- alkoxy
- aryl
- alkynyl
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- 239000004480 active ingredient Substances 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 8
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 6
- -1 amino, hydroxy Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 3
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 125000006636 (C3-C8) cycloalkylcarbonyl group Chemical group 0.000 abstract 2
- 241000196324 Embryophyta Species 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 244000038559 crop plants Species 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 150000004040 pyrrolidinones Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000006717 (C3-C10) cycloalkenyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 abstract 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000007983 Tris buffer Substances 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000005141 aryl amino sulfonyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000005135 aryl sulfinyl group Chemical group 0.000 abstract 1
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- RFMQOHXWHFHOJF-UHFFFAOYSA-N cyano thiocyanate Chemical group N#CSC#N RFMQOHXWHFHOJF-UHFFFAOYSA-N 0.000 abstract 1
- 230000012010 growth Effects 0.000 abstract 1
- 125000005224 heteroarylcarbonylamino group Chemical group 0.000 abstract 1
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 150000002540 isothiocyanates Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000005648 plant growth regulator Substances 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Pirrolidinonas sustituidas y sus sales y su uso como ingredientes activos herbicidas, en particular para controlar malezas y/o malas hierbas en cultivos de plantas útiles y/o como reguladores del crecimiento de las plantas para influir en el crecimiento de cultivos de plantas útiles. Reivindicación 1: Pirrolidinonas sustituidas de la fórmula (1) o sus sales, en las que Q es un arilo opcionalmente sustituido, heteroarilo, C₃₋₁₀-cicloalquilo o C₃₋₁₀-cicloalquenilo, donde cada anillo o cada sistema de anillos opcionalmente puede estar sustituido con hasta 5 sustituyentes del grupo R⁶; o es un anillo heterocíclico de 5 - 7 miembros opcionalmente sustituido; o es un sistema de anillos bicíclico de 8 - 10 miembros opcionalmente sustituido, en el que cada anillo o cada sistema de anillos está compuesto por átomos de carbono y 1 - 5 heteroátomos, que contienen independientemente hasta 2 átomos de O, hasta 2 átomos de S y hasta 5 átomos de N, donde se pueden seleccionar hasta tres átomos de anillo de carbono independientemente de los grupos C(=O) y C(=S) y los átomos de anillo de azufre además se pueden seleccionar de los grupos S, S(=O), S(=O)₂, S(=NR¹) y S(=NR¹)(=O); donde cada anillo o cada sistema de anillos opcionalmente puede estar sustituido con hasta 5 sustituyentes del grupo R⁶, o Q es C₂₋₁₀-alquenilo, C₂₋₁₀-alquinilo, C₂₋₁₀-haloalquenilo, C₂₋₁₀-haloalquinilo, C₃₋₁₀-halocicloalquenilo, C₁₋₁₀-alquilcarbonilo o C₁₋₁₀-alcoxi-C₁₋₁₀-alquilo, C₁₋₁₀-haloalcoxi-C₁₋₁₀-alquilo; Z representa al grupo de fórmula (2); Y es -C(R⁷)(R⁸)-, oxígeno o NR¹; W¹ y W² son independientemente oxígeno o azufre; R¹ es hidrógeno, amino, hidroxi, ciano, formil, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₁₋₈-cianoalquilo, C₁₋₈-hidroxialquilo, C₁₋₈-alcoxi-C₁₋₈-alquilo, arilo-C₁₋₈-alquilo, heteroarilo-C₁₋₈-alquilo, heterociclilo-C₁₋₈-alquilo, C₃₋₁₀-cicloalquilo, C₃₋₁₀-cicloalquilo-C₁₋₈-alquilo, C₃₋₈-halocicloalquilo, C₃₋₈-halocicloalquilo-C₁₋₈-alquilo, C₁₋₈-alquilcarbonilo, C₁₋₈-alcoxicarbonilo, C₂₋₈-alquenilo, C₂₋₈-alquinilo, tris-[C₁₋₈-alquil]silil-C₂₋₈-alquinilo, tris-[C₁₋₈-alquil]sililo; R² es hidrógeno, halógeno, hidroxi, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₁₋₈-hidroxialquilo, C₁₋₈-alcoxi-C₁₋₈-alquilo; R³ es hidrógeno, halógeno, hidroxi, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₁₋₈-hidroxialquilo, C₁₋₈-alcoxi, C₁₋₈-alcoxi-C₁₋₈-alquilo; R⁴ es C₃₋₁₀-cicloalquilo opcionalmente sustituido, C₃₋₁₀-halocicloalquilo, C₃₋₁₀-cianocicloalquilo, C₁₋₁₀-alquilo-C₃₋₁₀-cicloalquilo, C₁₋₁₀-alcoxi-C₃₋₁₀-cicloalquilo, C₁₋₁₀-haloalcoxi-C₃₋₁₀-cicloalquilo, C₁₋₁₀-alquiltio-C₃₋₁₀-cicloalquilo, arilo-C₃₋₁₀-cicloalquilo, heteroarilo-C₃₋₁₀-cicloalquilo, C₁₋₁₀-alcoxicarbonilo-C₃₋₁₀-cicloalquilo, hidroxicarbonil-C₃₋₁₀-cicloalquilo, C₃₋₁₀-cicloalquilo-C₃₋₁₀-cicloalquilo, C₃₋₁₀-cicloalcanonil, y en donde en el caso de que Q es = fenilo, el radical R⁴ no es ciclopentanilo; R⁵ es hidrógeno, hidroxi, amino, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₂₋₈-alquenilo, C₃₋₈-alquinilo, C₁₋₈-alcoxi-C₁₋₈-alquilo, C₁₋₈-haloalcoxi-C₁₋₈-alquilo, C₁₋₈-alquiltio-C₁₋₈-alquilo, C₁₋₈-alquilsulfinilo-C₁₋₈-alquilo, C₁₋₈-alquilsulfonilo-C₁₋₈-alquilo, C₁₋₈-alquilcarbonilo, C₁₋₈-haloalquilcarbonilo, C₃₋₈-cicloalquilcarbonilo, C₁₋₈-alcoxicarbonilo, C₂₋₈-haloalcoxicarbonilo, C₄₋₈-cicloalcoxicarbonilo, C₂₋₈-alquilaminocarbonilo, C₃₋₁₀-dialquilaminocarbonilo, C₃₋₁₀-cicloalquilaminocarbonilo, C₁₋₈-alcoxi, C₁₋₈-alquiltio, C₁₋₈-haloalquiltio, C₃₋₈-cicloalquiltio, C₁₋₈-alquilsulfinilo, C₁₋₈-haloalquilsulfinilo, C₃₋₈-cicloalquilsulfinilo, C₁₋₈-alquilsulfonilo, C₁₋₈-haloalquilsulfonilo, C₃₋₈-cicloalquilsulfonilo, C₁₋₈-alquilaminosulfonilo, C₂₋₈-dialquilaminosulfonilo o C₃₋₈-trialquilsililo; R⁶ es hidrógeno, nitro, amino, ciano, tiocianato, isotiocianato, halógeno, C₁₋₈-alquilo, C₃₋₈-cicloalquilo, C₂₋₈-alquenilo, C₂₋₈-alquinilo, arilo, arilo-C₁₋₈-alquilo, arilo-C₂₋₈-alquenilo, arilo-C₂₋₈-alquinilo, arilo-C₁₋₈-alcoxi, heteroarilo, C₁₋₈-alcoxi-C₁₋₈-alquilo, C₁₋₈-hidroxialquilo, C₁₋₈-haloalquilo, C₃₋₈-halocicloalquilo, C₁₋₈-alcoxi, C₁₋₈-haloalcoxi, ariloxi, heteroariloxi, C₃₋₈-cicloalquiloxi, hidroxi, C₃₋₈-cicloalquilo-C₁₋₈-alcoxi, C₁₋₈-alcoxicarbonilo, hidroxicarbonilo, aminocarbonilo, C₁₋₈-alquilaminocarbonilo, C₃₋₈-cicloalquilaminocarbonilo, C₁₋₈-cianoalquilaminocarbonilo, C₂₋₈-alquenilaminocarbonilo, C₂₋₈-alquinilaminocarbonilo, C₁₋₈-alquilamino, C₁₋₈-alquiltio, C₁₋₈-haloalquiltio, hidrotio, C₁₋₈-bis-alquilamino, C₃₋₈-cicloalquilamino, C₁₋₈-alquilcarbonilamino, C₃₋₈-cicloalquilcarbonilamino, formilamino, C₁₋₈-haloalquilcarbonilamino, C₁₋₈-alcoxicarbonilamino, C₁₋₈-alquilaminocarbonilamino, C₁₋₈-dialquilaminocarbonilamino, C₁₋₈-alquilsulfonilamino, C₃₋₈-cicloalquilsulfonilamino, arilsulfonilamino, hetarilsulfonilamino, aminosulfonilo, C₁₋₈-aminohaloalquilsulfonilo, C₁₋₈-alquilaminosulfonilo, C₁₋₈-bisalquilaminosulfonilo, C₃₋₈-cicloalquilaminosulfonilo, C₁₋₈-haloalquilaminosulfonilo, arilaminosulfonilo, arilo-C₁₋₈-alquilaminosulfonilo, C₁₋₈-alquilsulfonilo, C₃₋₈-cicloalquilsulfonilo, arilsulfonilo, C₁₋₈-alquilsulfinilo, C₃₋₈-cicloalquilsulfinilo, arilsulfinilo, N,S-C₁₋₈-dialquilsulfonimidoil, S-C₁₋₈-alquilsulfonimidoil, C₁₋₈-alquilsulfonilaminocarbonilo, C₃₋₈-cicloalquilsulfonilaminocarbonilo, C₃₋₈-cicloalquilaminosulfonilo, arilo-C₁₋₈-alquilcarbonilamino, C₃₋₈-cicloalquilo-C₁₋₈-alquilcarbonilamino, heteroarilcarbonilamino, C₁₋₈-alcoxi-C₁₋₈-alquilcarbonilamino, C₁₋₈-hidroxialquilcarbonilamino, C₁₋₈-trialquilsililo; y R⁷ y R⁸ son independientemente hidrógeno, hidroxi, halógeno, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₂₋₈-alquenilo, C₂₋₈-alquinilo, C₁₋₈-alcoxi-C₁₋₈-alquilo, C₁₋₈-haloalcoxi-C₁₋₈-alquilo, C₁₋₈-alquiltio-C₁₋₈-alquilo, C₁₋₈-alquilsulfinilo-C₁₋₈-alquilo, C₁₋₈-alquilsulfonilo-C₁₋₈-alquilo, C₁₋₈-alquilcarbonilo, C₁₋₈-haloalquilcarbonilo, C₃₋₈-cicloalquilcarbonilo, C₁₋₈-alcoxicarbonilo, C₂₋₈-haloalcoxicarbonilo, C₃₋₈-cicloalcoxicarbonilo, C₁₋₈-alquilaminocarbonilo, C₁₋₁₀-dialquilaminocarbonilo, C₃₋₁₀-cicloalquilaminocarbonilo, C₁₋₈-alcoxi, C₁₋₈-alquiltio, C₁₋₈-haloalquiltio, C₃₋₈-cicloalquiltio.Substituted pyrrolidinones and their salts and their use as active herbicidal ingredients, in particular to control weeds and / or weeds in useful plant crops and / or as plant growth regulators to influence the growth of useful plant crops. Claim 1: Substituted pyrrolidinones of the formula (1) or salts thereof, wherein Q is an optionally substituted aryl, heteroaryl, C₃₋₁₀-cycloalkyl or C₃₋₁₀-cycloalkenyl, where each ring or each ring system may optionally be substituted with up to 5 substituents of the group R⁶; or is an optionally substituted 5-7 membered heterocyclic ring; or is an optionally substituted 8-10-membered bicyclic ring system, in which each ring or each ring system is composed of carbon atoms and 1-5 heteroatoms, which independently contain up to 2 O atoms, up to 2 atoms of S and up to 5 N atoms, where up to three carbon ring atoms can be selected independently of the C (= O) and C (= S) groups and the sulfur ring atoms can also be selected from the S groups, S (= O), S (= O) ₂, S (= NR¹) and S (= NR¹) (= O); where each ring or each ring system may optionally be substituted with up to 5 substituents of the group R⁶, or Q is C₂₋₁₀-alkenyl, C₂₋₁₀-alkynyl, C₂₋₁₀-haloalkenyl, C₂₋₁₀-haloalkynyl, C₃₋₁₀ -halocycloalkenyl, C₁₋₁₀-alkylcarbonyl or C₁₋₁₀-alkoxy-C₁₋₁₀-alkyl, C₁₋₁₀-haloalkoxy-C₁₋₁₀-alkyl; Z represents the group of formula (2); Y is -C (R⁷) (R⁸) -, oxygen or NR¹; W¹ and W² are independently oxygen or sulfur; R¹ is hydrogen, amino, hydroxy, cyano, formyl, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₁₋₈-cyanoalkyl, C₁₋₈-hydroxyalkyl, C₁₋₈-alkoxy-C₁₋₈-alkyl, aryl- C₁₋₈-alkyl, heteroaryl-C₁₋₈-alkyl, heterocyclyl-C₁₋₈-alkyl, C₃₋₁₀-cycloalkyl, C₃₋₁₀-cycloalkyl-C₁₋₈-alkyl, C₃₋₈-halocycloalkyl, C₃₋₈- halocycloalkyl-C₁₋₈-alkyl, C₁₋₈-alkylcarbonyl, C₁₋₈-alkoxycarbonyl, C₂₋₈-alkenyl, C₂₋₈-alkynyl, tris- [C₁₋₈-alkyl] silyl-C₂₋₈-alkynyl, tris - [C₁₋₈-alkyl] silyl; R² is hydrogen, halogen, hydroxy, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₁₋₈-hydroxyalkyl, C₁₋₈-alkoxy-C₁₋₈-alkyl; R³ is hydrogen, halogen, hydroxy, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₁₋₈-hydroxyalkyl, C₁₋₈-alkoxy, C₁₋₈-alkoxy-C₁₋₈-alkyl; R⁴ is optionally substituted C₃₋₁₀-cycloalkyl, C₃₋₁₀-halocycloalkyl, C₃₋₁₀-cyanocycloalkyl, C₁₋₁₀-alkyl-C alquilo-cycloalkyl, C₁₋₁₀-alkoxy-C₃₋₁₀-cycloalkyl, C₁₋₁₀- haloalkoxy-C₃₋₁₀-cycloalkyl, C₁₋₁₀-alkylthio-C₃₋₁₀-cycloalkyl, aryl-C₃₋₁₀-cycloalkyl, heteroaryl-C₃₋₁₀-cycloalkyl, C₁₋₁₀-alkoxycarbonyl-C₃₋₁₀-cycloalkyl, hydroxycarbonyl- C₃₋₁₀-cycloalkyl, C₃₋₁₀-cycloalkyl-C₃₋₁₀-cycloalkyl, C₃₋₁₀-cycloalcanonyl, and where in the case that Q is = phenyl, the radical R⁴ is not cyclopentanyl; R⁵ is hydrogen, hydroxy, amino, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₂₋₈-alkenyl, C₃₋₈-alkynyl, C₁₋₈-alkoxy-C₁₋₈-alkyl, C₁₋₈-haloalkoxy- C₁₋₈-alkyl, C₁₋₈-alkylthio-C₁₋₈-alkyl, C₁₋₈-alkylsulfinyl-C₁₋₈-alkyl, C₁₋₈-alkylsulfonyl-C₁₋₈-alkyl, C₁₋₈-alkylcarbonyl, C₁₋ ₈-haloalkylcarbonyl, C₃₋₈-cycloalkylcarbonyl, C₁₋₈-alkoxycarbonyl, C₂₋₈-haloalkoxycarbonyl, C₄₋₈-cycloalkoxycarbonyl, C₂₋₈-alkylaminocarbonyl, C₃₋₁₀-dialkylaminocarbonyl, C₃₋₁₀-cycloalkylaminocarbonyl, C₁₋₈- alkoxy, C₁₋₈-alkylthio, C₁₋₈-haloalkylthio, C₃₋₈-cycloalkylthio, C₁₋₈-alkylsulfinyl, C₁₋₈-haloalkylsulfinyl, C₃₋₈-cycloalkylsulfinyl, C₁₋₈-alkylsulfonyl, C₁₋₈-haloalkylsulfonyl, C₃₋₈-cycloalkylsulfonyl, C₁₋₈-alkylaminosulfonyl, C₂₋₈-dialkylaminosulfonyl or C₃₋₈-tri alkylsilyl; R⁶ is hydrogen, nitro, amino, cyano, thiocyanate, isothiocyanate, halogen, C₁₋₈-alkyl, C₃₋₈-cycloalkyl, C₂₋₈-alkenyl, C₂₋₈-alkynyl, aryl, aryl-C₁₋₈-alkyl, aryl-C₂₋₈-alkenyl, aryl-C₂₋₈-alkynyl, aryl-C₁₋₈-alkoxy, heteroaryl, C₁₋₈-alkoxy-C₁₋₈-alkyl, C₁₋₈-hydroxyalkyl, C₁₋₈-haloalkyl, C₃₋₈-halocycloalkyl, C₁₋₈-alkoxy, C₁₋₈-haloalkoxy, aryloxy, heteroaryloxy, C₃₋₈-cycloalkyloxy, hydroxy, C₃₋₈-cycloalkyl-C₁₋₈-alkoxy, C₁₋₈-alkoxycarbonyl, hydroxycarbonyl, aminocarbonyl, C₁₋₈-alkylaminocarbonyl, C₃₋₈-cycloalkylaminocarbonyl, C₁₋₈-cyanoalkylaminocarbonyl, C₂₋₈-alkenylaminocarbonyl, C₂₋₈-alkylaminocarbonyl, C₁₋₈-alkylamino, C₁₋₈-alkylthio, C₁₋₈-haloalkylthio, hydrotium, C₁₋₈-bis-alkylamino, C₃₋₈-cycloalkylamino, C₁₋₈-alkylcarbonylamino, C₃₋₈-cycloalkylcarbonyl amino, formylamino, C₁₋₈-haloalkylcarbonylamino, C₁₋₈-alkoxycarbonylamino, C₁₋₈-alkylaminocarbonylamino, C₁₋₈-dialkylaminocarbonylamino, C₁₋₈-alkylsulfonylamino, C₃₋₈-cycloalkylsulfonylamino, arylsulfonylamino, hetarylsulfonylamino, aminosulfonyl, C₁₋₈- aminohaloalkylsulfonyl, C₁₋₈-alkylaminosulfonyl, C₁₋₈-bisalkylaminosulfonyl, C₃₋₈-cycloalkylaminosulfonyl, C₁₋₈-haloalkylaminosulfonyl, arylaminosulfonyl, aryl-C₁₋₈-alkylaminosulfonyl, C₁₋₈-alkylsulfonyl, C₃₋₈-cycloalkylsulfonyl, arylsulfonyl, arylsulfonyl, arylsulfonyl C₁₋₈-alkylsulfinyl, C₃₋₈-cycloalkylsulfinyl, arylsulfinyl, N, S-C₁₋₈-dialkylsulfonymidoyl, S-C₁₋₈-alkylsulfonimidoyl, C₁₋₈-alkylsulfonylaminocarbonyl, C₃₋₈-cycloalkylsulfonylaminocarbonyl, C₃₋₈-cycloalkylaminosulfonyl, aryl-C₁₋₈-alkylcarbonylamino, C₃₋₈-cycloalkyl-C₁₋₈-alkylcarbonylamino, heteroarylcarbonylamino, C ₋₈-alkoxy-C₁₋₈-alkylcarbonylamino, C₁₋₈-hidroxialquilcarbonilamino, C₁₋₈-trialkylsilyl; and R⁷ and R⁸ are independently hydrogen, hydroxy, halogen, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₂₋₈-alkenyl, C₂₋₈-alkynyl, C₁₋₈-alkoxy-C₁₋₈-alkyl, C₁₋ ₈-haloalkoxy-C₁₋₈-alkyl, C₁₋₈-alkylthio-C₁₋₈-alkyl, C₁₋₈-alkylsulfinyl-C₁₋₈-alkyl, C₁₋₈-alkylsulfonyl-C₁₋₈-alkyl, C₁₋₈- alkylcarbonyl, C₁₋₈-haloalkylcarbonyl, C₃₋₈-cycloalkylcarbonyl, C₁₋₈-alkoxycarbonyl, C₂₋₈-haloalkoxycarbonyl, C₃₋₈-cycloalkoxycarbonyl, C₁₋₈-alkylaminocarbonyl, C₁₋₁₀-dialkylaminocarbonyl, C₃₋₁₀-cycloalkylaminocarbonyl, C₁₋₈-alkoxy, C₁₋₈-alkylthio, C₁₋₈-haloalkylthio, C₃₋₈-cycloalkylthio.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17163796 | 2017-03-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR111303A1 true AR111303A1 (en) | 2019-06-26 |
Family
ID=58461156
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP180100756A AR111303A1 (en) | 2017-03-30 | 2018-03-28 | REPLACED PIRROLIDINONES AND ITS SALTS AND THEIR USE AS HERBICIDE ACTIVE INGREDIENTS |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR111303A1 (en) |
| UY (1) | UY37654A (en) |
| WO (1) | WO2018177836A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201901559D0 (en) | 2019-02-05 | 2019-03-27 | Syngenta Crop Protection Ag | Herbicidal compositions |
| GB202012143D0 (en) * | 2020-08-05 | 2020-09-16 | Syngenta Crop Protection Ag | Herbicidal compounds |
| CN117800945B (en) * | 2023-12-22 | 2025-12-19 | 贵州大学 | Pyrrolidone-containing 2-phenylpyridine derivative, synthesis method, application and herbicide thereof |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MA19709A1 (en) | 1982-02-17 | 1983-10-01 | Ciba Geigy Ag | APPLICATION OF QUINOLEIN DERIVATIVES TO THE PROTECTION OF CULTIVATED PLANTS. |
| DE3382743D1 (en) | 1982-05-07 | 1994-05-11 | Ciba Geigy | Use of quinoline derivatives to protect crops. |
| DE3334799A1 (en) | 1983-09-26 | 1985-04-04 | Bayer Ag, 5090 Leverkusen | 1,3-DIARYL-5-METHYLENE PERHYDROPYRIMIDINE-2-ONE |
| DE3525205A1 (en) | 1984-09-11 | 1986-03-20 | Hoechst Ag, 6230 Frankfurt | PLANT PROTECTIVE AGENTS BASED ON 1,2,4-TRIAZOLE DERIVATIVES AND NEW DERIVATIVES OF 1,2,4-TRIAZOLE |
| EP0191736B1 (en) | 1985-02-14 | 1991-07-17 | Ciba-Geigy Ag | Use of quinoline derivatives for the protection of crop plants |
| DE3633840A1 (en) | 1986-10-04 | 1988-04-14 | Hoechst Ag | PHENYLPYRAZOLIC CARBONIC ACID DERIVATIVES, THEIR PRODUCTION AND USE AS PLANT GROWTH REGULATORS AND SAFENERS |
| DE3775527D1 (en) | 1986-10-22 | 1992-02-06 | Ciba Geigy Ag | 1,5-DIPHENYLPYRAZOLE-3-CARBONIC ACID DERIVATIVES FOR THE PROTECTION OF CROPS. |
| DE3808896A1 (en) | 1988-03-17 | 1989-09-28 | Hoechst Ag | PLANT PROTECTION AGENTS BASED ON PYRAZOL CARBON SEA DERIVATIVES |
| DE3817192A1 (en) | 1988-05-20 | 1989-11-30 | Hoechst Ag | PLANT-PROTECTIVE AGENTS CONTAINING 1,2,4-TRIAZOLE DERIVATIVES AND NEW DERIVATIVES OF 1,2,4-TRIAZOLE |
| DE58903221D1 (en) | 1988-10-20 | 1993-02-18 | Ciba Geigy Ag | Sulfamoylphenylharnstoffe. |
| US4874422A (en) | 1988-12-27 | 1989-10-17 | Ici Americas Inc. | 1-Phenyl-3-carboxyamidopyrrolidones and their use as herbicides |
| DE3939010A1 (en) | 1989-11-25 | 1991-05-29 | Hoechst Ag | ISOXAZOLINE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PLANT PROTECTIVE AGENT |
| DE3939503A1 (en) | 1989-11-30 | 1991-06-06 | Hoechst Ag | NEW PYRAZOLINE FOR THE PROTECTION OF CULTURAL PLANTS AGAINST HERBICIDES |
| DE59108636D1 (en) | 1990-12-21 | 1997-04-30 | Hoechst Schering Agrevo Gmbh | New 5-chloroquinoline-8-oxyalkanecarboxylic acid derivatives, process for their preparation and their use as antidots of herbicides |
| TW259690B (en) | 1992-08-01 | 1995-10-11 | Hoechst Ag | |
| DE4331448A1 (en) | 1993-09-16 | 1995-03-23 | Hoechst Schering Agrevo Gmbh | Substituted isoxazolines, processes for their preparation, compositions containing them and their use as safeners |
| DE19621522A1 (en) | 1996-05-29 | 1997-12-04 | Hoechst Schering Agrevo Gmbh | New N-acylsulfonamides, new mixtures of herbicides and antidots and their use |
| EP0929543B1 (en) | 1996-09-26 | 2001-10-31 | Syngenta Participations AG | Herbicidal composition |
| DE19652961A1 (en) | 1996-12-19 | 1998-06-25 | Hoechst Schering Agrevo Gmbh | New 2-fluoroacrylic acid derivatives, new mixtures of herbicides and antidots and their use |
| US6071856A (en) | 1997-03-04 | 2000-06-06 | Zeneca Limited | Herbicidal compositions for acetochlor in rice |
| DE19727410A1 (en) | 1997-06-27 | 1999-01-07 | Hoechst Schering Agrevo Gmbh | 3- (5-tetrazolylcarbonyl) -2-quinolones and crop protection agents containing them |
| DE19742951A1 (en) | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoic acid amides, crop protection agents containing them and process for their preparation |
| AR031027A1 (en) | 2000-10-23 | 2003-09-03 | Syngenta Participations Ag | AGROCHEMICAL COMPOSITIONS |
| US7355053B2 (en) | 2002-10-18 | 2008-04-08 | Basf Aktiengesellschaft | 1-phenylpyrrolidine-2-one-3-carboxamides |
| AU2004224813B2 (en) | 2003-03-26 | 2010-11-25 | Bayer Cropscience Ag | Use of aromatic hydroxy compounds as safeners |
| DE10335726A1 (en) | 2003-08-05 | 2005-03-03 | Bayer Cropscience Gmbh | Use of hydroxyaromatics as safener |
| DE10335725A1 (en) | 2003-08-05 | 2005-03-03 | Bayer Cropscience Gmbh | Safener based on aromatic-aliphatic carboxylic acid derivatives |
| DE102004023332A1 (en) | 2004-05-12 | 2006-01-19 | Bayer Cropscience Gmbh | Quinoxaline-2-one derivatives, crop protection agents containing them, and processes for their preparation and their use |
| WO2007023719A1 (en) | 2005-08-22 | 2007-03-01 | Kumiai Chemical Industry Co., Ltd. | Agent for reducing chemical injury and herbicide composition with reduced chemical injury |
| WO2007023764A1 (en) | 2005-08-26 | 2007-03-01 | Kumiai Chemical Industry Co., Ltd. | Agent for reduction of harmful effect of herbicide and herbicide composition having reduced harmful effect |
| EP1987717A1 (en) | 2007-04-30 | 2008-11-05 | Bayer CropScience AG | Pyridon carboxamides, agents containing these but not impacting useful plants and method for their manufacture and application |
| EP1987718A1 (en) | 2007-04-30 | 2008-11-05 | Bayer CropScience AG | Utilisation of pyridine-2-oxy-3-carbon amides as safener |
| KR101667063B1 (en) | 2008-09-02 | 2016-10-17 | 닛산 가가쿠 고교 가부시키 가이샤 | Ortho-substituted haloalkylsulfonanilide derivative and herbicide |
| CN101838227A (en) | 2010-04-30 | 2010-09-22 | 孙德群 | Safener of benzamide herbicide |
| KR102395827B1 (en) | 2013-12-03 | 2022-05-10 | 에프엠씨 코포레이션 | Pyrrolidinones as herbicides |
| US9944602B2 (en) | 2014-07-02 | 2018-04-17 | E. I. Du Pont De Nemours And Company | Piperidinone herbicides |
| KR102542215B1 (en) | 2014-12-08 | 2023-06-12 | 에프엠씨 코포레이션 | 3-oxo-3-(arylamino)propanoates, a process for their preparation, and their use in preparing pyrrolidinones |
| AU2016246410B2 (en) | 2015-04-10 | 2020-11-05 | Fmc Corporation | Substituted cyclic amides as herbicides |
| EP3288928B1 (en) | 2015-04-27 | 2021-10-13 | FMC Corporation | Butyrolactones as herbicides |
| EP3294743B1 (en) | 2015-05-12 | 2019-08-21 | FMC Corporation | Aryl substituted bicyclic compounds as herbicides |
| BR112017022743B1 (en) | 2015-05-29 | 2022-02-22 | Fmc Corporation | Compost, herbicide compositions, herbicide mixture and method for controlling the growth of unwanted vegetation |
| CN107709310B (en) | 2015-06-02 | 2021-09-24 | Fmc公司 | Substituted cyclic amides and their use as herbicides |
-
2018
- 2018-03-21 WO PCT/EP2018/057154 patent/WO2018177836A1/en not_active Ceased
- 2018-03-28 AR ARP180100756A patent/AR111303A1/en unknown
- 2018-04-02 UY UY0001037654A patent/UY37654A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2018177836A1 (en) | 2018-10-04 |
| UY37654A (en) | 2018-10-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR105456A1 (en) | PIRIDINE COMPOUNDS WITH FUNGICIDE ACTION | |
| AR108557A1 (en) | HERBICIDE URACILPIRIDINS | |
| AR104487A1 (en) | QUINOLINE COMPOUNDS | |
| AR106763A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
| AR106762A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
| AR100171A1 (en) | DIAMINOTRIAZINE COMPOUNDS AND ITS USE AS A HERBICIDE | |
| AR113842A1 (en) | THIAZOL DERIVATIVES MICROBIOCIDES | |
| AR103561A1 (en) | HERBICIDE Phenylpyridines | |
| PE20180603A1 (en) | TRIAZOLE DERIVATIVES, ITS INTERMEDIARIES AND THEIR USE AS FUNGICIDES | |
| AR109152A1 (en) | HERBICIDE PIRIMIDINE COMPOUNDS | |
| AR114807A1 (en) | PLANTS THAT HAVE A HIGHER TOLERANCE TO HERBICIDES | |
| AR088097A1 (en) | HERBICIDE COMPOUNDS | |
| AR110386A1 (en) | HERBICIDE PHENILTRIAZOLINONES | |
| AR106258A1 (en) | PIRIDINE COMPOUNDS | |
| AR120868A1 (en) | SUBSTITUTED THIOPHENE-2-CARBOXAMIDES AND SUBSTITUTED THIOPHENE-2-CARBOXYLIC ACIDS AND THEIR DERIVATIVES | |
| AR108680A1 (en) | BENZOXABOROL COMPOUNDS | |
| AR090376A1 (en) | HERBICIDE COMPOUNDS | |
| AR107955A1 (en) | DERIVATIVES OF PIRIDINO- / PIRIMIDINO-PIRIDINA, WITH HERBICITY ACTIVITY | |
| AR103266A1 (en) | REPLACED CYCLIC COMPOUNDS WITH A CONDENSED RING SYSTEM TO COMBAT INVERTEBRATE PESTS | |
| AR111303A1 (en) | REPLACED PIRROLIDINONES AND ITS SALTS AND THEIR USE AS HERBICIDE ACTIVE INGREDIENTS | |
| AR109076A1 (en) | DERIVATIVES OF BICYCLIC HETEROCICLES CONDENSED AS PESTICIDES | |
| AR118051A1 (en) | HETEROCYCLIC COMPOUNDS FOR THE CONTROL OF INVERTEBRATE PESTS | |
| AR095059A1 (en) | HERBICIDE COMPOUNDS | |
| AR105460A1 (en) | SUBSTITUTED DERIVATIVES OF 2-PYRIMIDINE FURANO / TIENOCICLOALQUILAMINO AND ITS USE FOR THE CONTROL OF GROWTH OF NON-DESIRABLE PLANTS | |
| AR119000A1 (en) | ARYL AMIDINES FUNGICIDES |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |