AR097935A1 - DERIVATIVES OF PIRIDAZINONES USEFUL AS HERBICIDES - Google Patents
DERIVATIVES OF PIRIDAZINONES USEFUL AS HERBICIDESInfo
- Publication number
- AR097935A1 AR097935A1 ARP140103716A ARP140103716A AR097935A1 AR 097935 A1 AR097935 A1 AR 097935A1 AR P140103716 A ARP140103716 A AR P140103716A AR P140103716 A ARP140103716 A AR P140103716A AR 097935 A1 AR097935 A1 AR 097935A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- group
- haloalkyl
- alkynyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
Abstract
Reivindicación 1: Un compuesto de fórmula (1) o una sal o N-óxido del mismo, en donde, R¹ se selecciona del grupo que consiste en alquilo C₁₋₄, alcoxi C₁₋₂-alquilo C₁₋₂, alquenilo C₂₋₄, haloalquilo C₁₋₄, haloalquenilo C₁₋₄, alquinilo C₂₋₄ y haloalquinilo C₂₋₄; R² se selecciona del grupo que consiste en hidrógeno, halógeno, ciano, alquilo C₁₋₆, haloalquilo C₁₋₆, haloalcoxi C₁₋₆, haloalcoxi C₁₋₃-alquilo C₁₋₃, alcoxi C₁₋₆ alcoxi C₁₋₃-alquilo C₁₋₃, alcoxi C₁₋₃-alcoxi C₁₋₃-alquilo C₁₋₃-, cicloalquilo C₃₋₆, alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquinilo C₂₋₆, hidroxialquilo C₁₋₆, alquil C₁₋₆carbonilo, -S(O)ₚ-alquilo C₁₋₆, amino, alquil C₁₋₆amino, dialquil C₁₋₆amino, -C(alquil C₁₋₃)=N-O-alquilo C₁₋₃ y haloalquinilo C₂₋₆; cada R³ se selecciona independientemente del grupo que consiste en hidrógeno, halógeno, nitro, ciano, amino, alquilo C₁₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₆, alcoxi C₁₋₆carbonilo y -S(O)ₚ-alquilo C₁₋₆; R⁴ se selecciona del grupo que consiste en alquenilo C₂₋₆, alquinilo C₂₋₆ haloalquenilo C₂₋₆, haloalquinilo C₂₋₆, alcoxi C₁₋₃-alquilo C₁₋₃, alquil C₁₋₃-S-(R¹⁰), alquil C₁₋₆sulfonilo, -S-(R¹⁰), fenilo opcionalmente sustituido, heteroarilo opcionalmente sustituido y cianoalquilo C₁₋₆-; R⁵ se selecciona del grupo que consiste en hidrógeno, hidroxilo, halógeno, alquilo C₁₋₃, haloalquilo C₁₋₃ cicloalquilo C₃₋₆, alcoxi C₁₋₃; G es hidrógeno o -C(O)-R⁶; R⁶ se selecciona del grupo que consiste en alquilo C₁₋₆, alquenilo C₁₋₆, alquinilo C₁₋₆, alquil C₁₋₆-S-, alcoxi C₁₋₆, -NR⁷R⁸ y fenilo opcionalmente sustituido por uno o más R⁹; R⁷ y R⁸ se seleccionan independientemente del grupo que consiste en alquilo C₁₋₆, alcoxi C₁₋₆-; o R⁷ y R⁸ juntos pueden formar un anillo morfolinilo; R⁹ se selecciona del grupo que consiste en halógeno, ciano, nitro, alquilo C₁₋₃, haloalquilo C₁₋₃, alcoxi C₁₋₃ y haloalcoxi C₁₋₃; R¹⁰ es alquilo C₁₋₆; n = 0, 1, 2, 3 ó 4; y p = 0, 1 ó 2.Claim 1: A compound of formula (1) or a salt or N-oxide thereof, wherein, R¹ is selected from the group consisting of C₁₋₄ alkyl, C₁₋₂ alkoxy-C₁₋₂ alkyl, C₂₋₄ alkenyl , C₁₋₄ haloalkyl, C₁₋₄ haloalkenyl, C₂₋₄ alkynyl and C₂₋₄ haloalkynyl; R² is selected from the group consisting of hydrogen, halogen, cyano, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ haloalkoxy, C₁₋₃ haloalkoxy-C₁₋₃ alkyl, C₁₋₆ alkoxy C₁₋₃ alkoxy-C alquilo alkyl ₋₃, C₁₋₃ alkoxy-C₁₋₃-alkoxy-C alquilo-alkyl, C₃₋₆ cycloalkyl, C₂₋₆ alkenyl, C₂₋₆ haloalkenyl, C₂₋₆ alkynyl, C₁₋₆ hydroxyalkyl, C₁₋₆carbonyl alkyl, - S (O) ₚ-C₁₋₆ alkyl, amino, C₁₋₆amino alkyl, Cquilamino dialkyl, -C (C₁₋₃ alkyl) = NO-C₁₋₃ alkyl and C₂₋₆ haloalkynyl; each R³ is independently selected from the group consisting of hydrogen, halogen, nitro, cyano, amino, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₃₋₆ cycloalkyl, C alco alkoxy, C₁₋₆carbonyl alkoxy and -S (O) ₚ-C₁₋₆ alkyl; R⁴ is selected from the group consisting of C₂₋₆ alkenyl, C₂₋₆ alkynyl C₂₋₆ haloalkenyl, C₂₋₆ haloalkynyl, C₁₋₃ alkoxy-C₁₋₃ alkyl, C₁₋₃-S- (R¹⁰) alkyl, C₁ alkyl Ulfsulfonyl, -S- (R¹⁰), optionally substituted phenyl, optionally substituted heteroaryl and C₁₋₆- cyanoalkyl; R⁵ is selected from the group consisting of hydrogen, hydroxyl, halogen, C₁₋₃ alkyl, C₁₋₃ haloalkyl C₃₋₆ cycloalkyl, C₁₋₃ alkoxy; G is hydrogen or -C (O) -R⁶; R⁶ is selected from the group consisting of C₁₋₆ alkyl, C₁₋₆ alkenyl, C₁₋₆ alkynyl, C₁₋₆-S- alkyl, C₁₋₆ alkoxy, -NR⁷R⁸ and phenyl optionally substituted by one or more R⁹; R⁷ and R⁸ are independently selected from the group consisting of C₁₋₆ alkyl, C₁₋₆- alkoxy; or R⁷ and R⁸ together can form a morpholinyl ring; R⁹ is selected from the group consisting of halogen, cyano, nitro, C₁₋₃ alkyl, C₁₋₃ haloalkyl, C₁₋₃ alkoxy and C₁₋₃ haloalkoxy; R¹⁰ is C₁₋₆ alkyl; n = 0, 1, 2, 3 or 4; and p = 0, 1 or 2.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1317791.0A GB201317791D0 (en) | 2013-10-08 | 2013-10-08 | Herbicidal compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
AR097935A1 true AR097935A1 (en) | 2016-04-20 |
Family
ID=49630371
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP140103716A AR097935A1 (en) | 2013-10-08 | 2014-10-06 | DERIVATIVES OF PIRIDAZINONES USEFUL AS HERBICIDES |
Country Status (3)
Country | Link |
---|---|
AR (1) | AR097935A1 (en) |
GB (1) | GB201317791D0 (en) |
WO (1) | WO2015052095A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3368523B1 (en) | 2015-10-28 | 2021-07-14 | FMC Corporation | Novel pyridazinone herbicides |
US10913719B2 (en) | 2015-10-28 | 2021-02-09 | Fmc Corporation | Intermediates to prepare pyridazinone herbicides, and a process to prepare them |
TWI785022B (en) * | 2017-03-28 | 2022-12-01 | 美商富曼西公司 | Novel pyridazinone herbicides |
PE20211219A1 (en) | 2018-09-27 | 2021-07-05 | Fmc Corp | PYRIDAZINONE HERBICIDES AND PYRIDAZINONE INTERMEDIATES USED TO PREPARE A HERBICIDE |
JP2024517155A (en) | 2021-04-27 | 2024-04-19 | バイエル・アクチエンゲゼルシヤフト | Substituted pyridazinones, their salts or N-oxides and their use as herbicidal active substances - Patents.com |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CL2008003785A1 (en) * | 2007-12-21 | 2009-10-09 | Du Pont | Pyridazine derived compounds; herbicidal compositions comprising said compounds; and method of controlling the growth of unwanted vegetation. |
WO2011045271A1 (en) * | 2009-10-15 | 2011-04-21 | Bayer Cropscience Ag | Herbicidally active, heterocyclyl-substituted pyridazinones |
GB201206598D0 (en) * | 2012-04-13 | 2012-05-30 | Syngenta Ltd | Herbicidal compounds |
-
2013
- 2013-10-08 GB GBGB1317791.0A patent/GB201317791D0/en not_active Ceased
-
2014
- 2014-10-03 WO PCT/EP2014/071264 patent/WO2015052095A1/en active Application Filing
- 2014-10-06 AR ARP140103716A patent/AR097935A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2015052095A1 (en) | 2015-04-16 |
GB201317791D0 (en) | 2013-11-20 |
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