AR111303A1 - Pirrolidinonas sustituidas y sus sales y su uso como ingredientes activos herbicidas - Google Patents
Pirrolidinonas sustituidas y sus sales y su uso como ingredientes activos herbicidasInfo
- 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.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17163796 | 2017-03-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR111303A1 true AR111303A1 (es) | 2019-06-26 |
Family
ID=58461156
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP180100756A AR111303A1 (es) | 2017-03-30 | 2018-03-28 | Pirrolidinonas sustituidas y sus sales y su uso como ingredientes activos herbicidas |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR111303A1 (es) |
| UY (1) | UY37654A (es) |
| WO (1) | WO2018177836A1 (es) |
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 (zh) * | 2023-12-22 | 2025-12-19 | 贵州大学 | 一种含吡咯烷酮的2-苯基吡啶衍生物及其合成方法、应用和除草剂 |
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| KR102542215B1 (ko) | 2014-12-08 | 2023-06-12 | 에프엠씨 코포레이션 | 3-옥소-3-(아릴아미노)프로파노에이트, 이의 제조방법 및 피롤리디논 제조에 있어서 이의 용도 |
| 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 (pt) | 2015-05-29 | 2022-02-22 | Fmc Corporation | Composto, composições herbicidas, mistura de herbicidas e método para controlar o crescimento de vegetação indesejada |
| CN107709310B (zh) | 2015-06-02 | 2021-09-24 | Fmc公司 | 取代的环酰胺及其作为除草剂的用途 |
-
2018
- 2018-03-21 WO PCT/EP2018/057154 patent/WO2018177836A1/de not_active Ceased
- 2018-03-28 AR ARP180100756A patent/AR111303A1/es unknown
- 2018-04-02 UY UY0001037654A patent/UY37654A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2018177836A1 (de) | 2018-10-04 |
| UY37654A (es) | 2018-10-31 |
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