AR111967A1 - Amidas herbicidas - Google Patents
Amidas herbicidasInfo
- Publication number
- AR111967A1 AR111967A1 ARP180101416A ARP180101416A AR111967A1 AR 111967 A1 AR111967 A1 AR 111967A1 AR P180101416 A ARP180101416 A AR P180101416A AR P180101416 A ARP180101416 A AR P180101416A AR 111967 A1 AR111967 A1 AR 111967A1
- Authority
- AR
- Argentina
- Prior art keywords
- ring
- alkyl
- independently selected
- cyano
- alkoxy
- Prior art date
Links
- 150000001408 amides Chemical class 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 12
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 10
- -1 cyano, hydroxy Chemical group 0.000 abstract 9
- 125000004122 cyclic group Chemical group 0.000 abstract 9
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical group 0.000 abstract 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 9
- 125000001424 substituent group Chemical group 0.000 abstract 9
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 6
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 5
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 5
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 5
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 abstract 5
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 5
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 5
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 4
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 4
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 4
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 4
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 4
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 4
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 4
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 abstract 4
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 4
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 abstract 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 4
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 3
- 125000005149 cycloalkylsulfinyl group Chemical group 0.000 abstract 3
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 2
- 125000003341 7 membered heterocyclic group Chemical group 0.000 abstract 2
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 150000001721 carbon Chemical group 0.000 abstract 2
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 102200029950 rs35898499 Human genes 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 1
- 125000006592 (C2-C3) alkenyl group Chemical group 0.000 abstract 1
- 125000006593 (C2-C3) alkynyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 abstract 1
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 abstract 1
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000004858 cycloalkoxyalkyl group Chemical group 0.000 abstract 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005356 cycloalkylalkenyl group Chemical group 0.000 abstract 1
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 abstract 1
- 125000005357 cycloalkylalkynyl group Chemical group 0.000 abstract 1
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 abstract 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 abstract 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004664 haloalkylsulfonylamino group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005292 haloalkynyloxy group Chemical group 0.000 abstract 1
- 125000006769 halocycloalkoxy group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004971 nitroalkyl group Chemical group 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 125000006513 pyridinyl methyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000565 sulfonamide group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
Classifications
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
-
- 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
- C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
- C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Reivindicación 1: Un compuesto de la fórmula (1), los N-óxidos, sales y estereoisómeros del mismo, en donde W es -NRARB o -ORC; RA es H, ciano, CHO, alquilcarbonilo C₂₋₄, alquilo C₁₋₄; o fenilo sustituido o no sustituido con halógeno o alquilo C₁₋₄; RB es H, ciano, hidroxi, CHO, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆, alcoxialquilo C₂₋₈, haloalcoxialquilo C₂₋₈, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, alcoxicarbonilo C₂₋₈, haloalcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, cicloalquilaminocarbonilo C₄₋₁₀, alcoxi C₁₋₆, alquiltio C₁₋₆, haloalquiltio C₁₋₆, cicloalquiltio C₃₋₈, alquilsulfinilo C₁₋₆, haloalquilsulfinilo C₁₋₆, cicloalquilsulfinilo C₃₋₈, alquilsulfonilo C₁₋₆, haloalquilsulfonilo C₁₋₆, cicloalquilsulfonilo C₃₋₈, alquilaminosulfonilo C₁₋₆, dialquilaminosulfonilo C₂₋₈ o trialquilsililo C₃₋₁₀; o un anillo de fenilo o un sistema de anillo de naftalenilo, cada uno de los anillos o sistemas de anillo sustituido o no sustituido con hasta 5 sustituyentes independientemente seleccionados de R¹⁶; o un anillo heterocíclico de 4 a 7 miembros sustituido o no sustituido con hasta 5 sustituyentes independientemente seleccionados de R¹⁶; o RA y RB se toman junto con el átomo de nitrógeno al cual ambos están enlazados y forman un anillo de 4, 5 ó 6 miembros que contiene miembros del anillo seleccionados de carbono, oxígeno, nitrógeno y -C(=O)-; o se toman juntos como un sistema de anillo tricíclico de 8 a 13 miembros, cada uno de los anillos o sistema de anillo contiene miembros del anillo seleccionados de carbono, nitrógeno y -C(=O)- y sustituido o no sustituido con halógeno, ciano o alquilo C₁₋₄; RC es haloalquilo C₁₋₄, haloalquilcarbonilo C₂₋₄, cicloalquilo C₃₋₆; o fenilo sustituido o no sustituido con halógeno, ciano o alquilo C₁₋₄; o un anillo aromático de 6 miembros que contiene nitrógeno sustituido o no sustituido con halógeno, ciano o alquilo C₁₋₄; J es -CR²R³-, -CR²R³-CR⁴R⁵-, -NR⁶- o -O-; Y es O, S o NR¹⁵; R¹ es H, hidroxi, amino, ciano, CHO, alquilcarbonilalquilo C₃₋₈, -C(alquilo C₁₋₄)=N-O(alquilo C₁₋₄), -C(O)NH₂, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆, cianoalquilo C₂₋₆, cicloalquilo C₃₋₆, cicloalquenilo C₃₋₈, cicloalquilalquilo C₄₋₈, alcoxialquilo C₂₋₈, alcoxialcoxialquilo C₃₋₈, haloalcoxialquilo C₂₋₈, haloalquenilalquilo C₂₋₈, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquisulfonilalquilo C₂₋₈, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, cicloalquilcarbonilalquilo C₅₋₁₀, alcoxicarbonilo C₂₋₈, haloalcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, cicloalquilaminocarbonilo C₄₋₁₀, alcoxi C₁₋₆, alquiltio C₁₋₆, haloalquiltio C₁₋₆, cicloalquiltio C₃₋₈, alquilsulfinilo C₁₋₆, haloalquilsulfinilo C₁₋₆, cicloalquilsulfinilo C₃₋₈, alquilsulfonilo C₁₋₆, haloalquilsulfonilo C₁₋₆, cicloalquilsulfonilo C₃₋₈, alquilaminosulfonilo C₁₋₆, dialquilaminosulfonilo C₂₋₈, trialquilsililo C₃₋₁₀; o -CPh=N-O(alquilo C₁₋₄) donde el fenilo está sustituido o no sustituido con hasta 5 sustituyentes independientemente seleccionados de R¹³; o G¹; Q¹ es un anillo de fenilo o un sistema de anillo de naftalenilo, cada uno de los anillos o sistemas de anillos sustituidos o no sustituidos con hasta 5 sustituyentes independientemente seleccionados de R¹⁰; o un anillo heterocíclico de 4 a 7 miembros; o un sistema de anillo bicíclico de 8 a 10 miembros, cada uno de los anillos o sistemas de anillos contiene miembros del anillo seleccionados de átomos de carbono y de 1 a 5 heteroátomos independientemente seleccionados de hasta 2 O, hasta 2 S y hasta 5 átomos de N, en donde hasta 3 miembros de carbono del anillo se seleccionan independientemente C(=O) y C(=S) y los miembros de átomos de azufre del anillo se seleccionan independientemente de S(=O)ᵘ(=NR¹⁴)ᵛ, cada uno de los anillos sistemas de anillos sustituidos o no sustituidos con hasta 5 sustituyentes independientemente seleccionados de R¹⁰ sobre los miembros de átomos de carbono del anillo y seleccionados de R¹² sobre miembros de átomos de nitrógeno del anillo; Q² es un anillo de fenilo o un sistema de anillo de naftalenilo, cada uno de los anillos o sistemas de anillos sustituido o no sustituido con hasta 5 sustituyentes independientemente seleccionados de R¹¹; o un anillo heterocíclico de 4 a, 7 miembros; o un sistema de anillo bicíclico de 8 a 10 miembros, cada uno de los anillos o sistemas de anillos contiene miembros del anillo seleccionados de átomos de carbono y de 1 a 4 heteroátomos independientemente seleccionados de hasta 2 O, hasta 2 S y hasta 5 átomos de N, en donde hasta 3 miembros de carbono del anillo se seleccionan independientemente C(=O) y C(=S) y los miembros de átomos de azufre del anillo se seleccionan independientemente de S(=O)ᵘ(=NR¹⁴)ᵛ, cada uno de los anillos o sistemas de anillos sustituido o no sustituido con hasta 5 sustituyentes independientemente seleccionados de R¹¹ sobre los miembros de átomos de carbono del anillo y seleccionados de R¹³ sobre los miembros de átomos de nitrógeno del anillo; cada uno de R² y R³ es independientemente H, halógeno, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄ o alcoxi C₁₋₄; o R² y R³ se toman junto con el átomo de carbono al cual ambos están enlazados y forman un anillo de cicloalquilo C₃₋₇; cada uno de R⁴ y R⁵ es independientemente H, halógeno, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄ o alcoxi C₁₋₄; R⁶ es alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆ o alcoxi C₁₋₆; o R¹ y R⁶ se toman juntos como un alquileno C₃₋₆ o -CH₂OCH₂-; cada uno de R⁷ y R⁸ es independientemente H, halógeno, hidroxi, alcoxi C₁₋₄, haloalquilo C₁₋₄ o alquilo C₁₋₄; R⁹ es H, hidroxi, amino, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆, alcoxialquilo C₂₋₈, haloalcoxialquilo C₂₋₈, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, alcoxicarbonilo C₂₋₈, haloalcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, cicloalquilaminocarbonilo C₄₋₁₀, alcoxi C₁₋₆, alquiltio C₁₋₆, haloalquiltio C₁₋₆, cicloalquiltio C₃₋₈, alquilsulfinilo C₁₋₆, haloalquilsulfinilo C₁₋₆, cicloalquilsulfinilo C₃₋₈, alquilsulfonilo C₁₋₆, haloalquilsulfonilo C₁₋₆, cicloalquilsulfonilo C₃₋₈, alquilaminosulfonilo C₁₋₆, dialquilaminosulfonilo C₂₋₈ o trialquilsililo C₃₋₁₀; o G¹; cada uno de R¹⁰ y R¹¹ es independientemente halógeno, hidroxi, ciano, nitro, amino, alquilo C₁₋₈, cianoalquilo C₁₋₈, cianoalcoxi C₁₋₈, haloalquilo C₁₋₈, hidroxialquilo C₁₋₈, nitroalquilo C₁₋₈, alquenilo C₂₋₈, haloalquenilo C₂₋₈, nitroalquenilo C₂₋₈, alquinilo C₂₋₈, haloalquinilo C₂₋₈, alcoxialquilo C₂₋₈, alcoxialcoxialquilo C₃₋₈, haloalcoxialquilo C₂₋₈, haloalcoxihaloalcoxi C₂₋₈, cicloalquilo C₃₋₆, ciclopropilmetilo, 1-metilciclopropilo, 2-metilciclopropilo, cicloalquilalquilo C₄₋₁₀, halocicloalquilalquilo C₄₋₁₀, alquilcicloalquilalquilo C₅₋₁₂, cicloalquilalquenilo C₅₋₁₂, cicloalquilalquinilo C₅₋₁₂, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈, alquilcicloalquilo C₄₋₁₀, cicloalquilcicloalquilo C₆₋₁₂, cicloalquenilo C₃₋₈, halocicloalquenilo C₃₋₈, haloalcoxialcoxi C₂₋₈, alcoxialcoxi C₂₋₈, cicloalcoxialquilo C₄₋₁₀, alcoxialcoxialquilo C₃₋₁₀, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alquilamino C₂₋₈, dialquilamino C₂₋₈, halodialquilamino C₂₋₈, alquilaminoalquilo C₂₋₈, haloalquilaminoalquilo C₂₋₈, cicloalquilaminoalquilo C₄₋₁₀, dialquilaminoalquilo C₃₋₁₀, -CHO, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, -C(=O)OH, alcoxicarbonilo C₂₋₈, haloalcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, cicloalquilalcoxicarbonilo C₅₋₁₂, -C(=O)NH₂, alquilaminocarbonilo C₂₋₈, cicloalquilaminocarbonilo C₄₋₁₀, dialquilaminocarbonilo C₃₋₁₀, alcoxi C₁₋₈, haloalcoxi C₁₋₈, alcoxialcoxi C₂₋₈, alqueniloxi C₂₋₈, haloalqueniloxi C₂₋₈, alquiniloxi C₃₋₈, haloalquiniloxi C₃₋₈, cicloalcoxi C₃₋₈, halocicloalcoxi C₃₋₈, cicloalquilalcoxi C₄₋₁₀, alquilcarbonilalcoxi C₃₋₁₀, alquilcarboniloxi C₂₋₈, haloalquilcarboniloxi C₂₋₈, cicloalquilcarboniloxi C₄₋₁₀, alquilsulfoniloxi C₁₋₈, haloalquilsulfoniloxi C₁₋₈, alquiltio C₁₋₈, haloalquiltio C₁₋₈, cicloalquiltio C₃₋₈, alquilsulfinilo C₁₋₈, haloalquilsulfinilo C₁₋₈, alquilsulfonilo C₁₋₈, haloalquilsulfonilo C₁₋₈, cicloalquilsulfonilo C₃₋₈, formilamino, alquilcarbonilamino C₂₋₈, haloalquilcarbonilamino C₂₋₈, cicloalquilamino C₃₋₈, alcoxicarbonilamino C₂₋₈, alquilsulfonilamino C₁₋₆, haloalquilsulfonilamino C₁₋₆, -SF₅, -SCN, SO₂NH₂, trialquilsililo C₃₋₁₂, trialquilsililalquilo C₄₋₁₂ o trialquilsililalcoxi C₄₋₁₂; o G²; o R²⁰S(=O)=N-, R²⁰S(=O)₂NR¹⁹-C(=O)- o R²⁰(R¹⁹N=)qS(=O)ₚ-, en donde el enlace que se proyecta hacia la derecha indica el punto de conexión con Q¹; cada uno de R¹² y R¹³ es independientemente ciano, alquilo C₁₋₃, hidroxialquilo C₁₋₈, alquenilo C₂₋₃, alquinilo C₂₋₃, cicloalquilo C₃₋₆, alcoxialquilo C₂₋₃, alcoxi C₁₋₃, alquilcarbonilo C₂₋₃, alcoxicarbonilo C₂₋₃, alquilaminoalquilo C₂₋₃ o dialquilaminoalquilo C₃₋₄; cada uno de R¹⁴ es independientemente H, ciano, alquilcarbonilo C₂₋₃ o haloalquilcarbonilo C₂₋₃; R¹⁵ es H, ciano, hidroxi, CHO, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄, alquilcarbonilo C₂₋₆ o haloalquilcarbonilo C₂₋₆; cada uno G¹ es independientemente de fenilo; o un anillo heterocíclico de 5 sustituyentes independientemente seleccionados de R¹⁷; cada uno de G² es independientemente fenilo, fenilmetilo, piridinilmetilo, fenilcarbonilo, fenoxi, feniletinilo, fenilsulfonilo o un anillo heterocíclico de 5 ó 6 miembros, cada uno sustituido con, hasta. 5 sustituyentes independientemente seleccionados de R¹⁸; cada uno R¹⁶, R¹⁷ y R¹⁸ es independientemente halógeno, ciano, hidroxi, amino, nitro, -CHO, -C(=O)OH, -C(=O)NH₂, -SO₂NH₂, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, alquilcarbonilo C₂₋₈, hidroxialquilo C₁₋₈, haloalquilcarbonilo C₂₋₈, alcoxialquilo C₂₋₆, alquilaminoalquilo C₂₋₆, alcoxicarbonilo C₂₋₈, cicloalquilo C₃₋₈, cicloalcoxicarbonilo C₄₋₁₀, cicloalquilalcoxicarbonilo C₅₋₁₂, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, dialquilaminoalquilo C₃₋₈, alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquilcarboniloxi C₂₋₈, alquiltio C₁₋₆, haloalquiltio C₁₋₆, alquilsulfinilo C₁₋₆, haloalquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, haloalquilsulfonilo C₁₋₆, alquilaminosulfonilo C₁₋₆, dialquilaminosulfonilo C₂₋₈, trialquilsililo C₃₋₁₀, alquilamino C₁₋₆, dialquilamino C₂₋₈, alquilcarbonilamino C₂₋₈, alquilsulfonilamino C₁₋₆, fenilo, piridinilo o tienilo; cada uno de R¹⁹ es independientemente H, ciano, alquilcarbonilo C₂₋₃ o haloalquilcarbonilo C₂₋₃; cada uno de R²⁰ es independientemente H, alquilo C₁₋₆, cicloalquilo C₃₋₈, cicloalquilalquilo C₄₋₈, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆, alcoxialquilo C₂₋₈, haloalcoxialquilo C₂₋₈, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alcoxi C₁₋₆, trialquilsililo C₃₋₁₀ o G¹; cada uno de u y v es independientemente 0, 1 ó 2, siempre que la suma de u y v sea 0, 1 ó 2; y cada uno de p y q es independientemente 0, 1 ó 2, siempre que la suma de u y v sea 0, 1 ó 2 y cuando p es 0, q no es 1 ó 2.
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| JP7325328B2 (ja) | 2016-12-21 | 2023-08-14 | エフ エム シー コーポレーション | ニトロン除草剤 |
| CN110691516B (zh) | 2017-03-21 | 2022-10-28 | Fmc公司 | 吡咯烷酮及其制备方法 |
| UA126576C2 (uk) | 2017-03-21 | 2022-11-02 | ЕфЕмСі КОРПОРЕЙШН | Гербіцидна суміш, композиція та спосіб |
| AR111839A1 (es) | 2017-05-30 | 2019-08-21 | Fmc Corp | Lactamas 3-sustituidas herbicidas |
-
2018
- 2018-05-29 AR ARP180101416A patent/AR111967A1/es not_active Application Discontinuation
- 2018-05-30 JP JP2019566131A patent/JP7184813B2/ja active Active
- 2018-05-30 US US16/614,870 patent/US11357230B2/en active Active
- 2018-05-30 RU RU2019143102A patent/RU2019143102A/ru unknown
- 2018-05-30 BR BR112019024988-5A patent/BR112019024988B1/pt not_active IP Right Cessation
- 2018-05-30 AU AU2018277537A patent/AU2018277537B2/en not_active Ceased
- 2018-05-30 EP EP18732560.0A patent/EP3630721B1/en not_active Not-in-force
- 2018-05-30 CN CN201880049311.3A patent/CN110944977A/zh active Pending
- 2018-05-30 CA CA3064578A patent/CA3064578A1/en active Pending
- 2018-05-30 WO PCT/US2018/035015 patent/WO2018222646A1/en not_active Ceased
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|---|---|
| AU2018277537B2 (en) | 2022-04-14 |
| BR112019024988A2 (pt) | 2020-06-16 |
| JP2020522493A (ja) | 2020-07-30 |
| RU2019143102A (ru) | 2021-06-30 |
| CA3064578A1 (en) | 2018-12-06 |
| EP3630721A1 (en) | 2020-04-08 |
| WO2018222646A1 (en) | 2018-12-06 |
| US11357230B2 (en) | 2022-06-14 |
| RU2019143102A3 (es) | 2021-10-01 |
| JP7184813B2 (ja) | 2022-12-06 |
| BR112019024988B1 (pt) | 2023-12-26 |
| EP3630721B1 (en) | 2022-01-05 |
| US20200154709A1 (en) | 2020-05-21 |
| CN110944977A (zh) | 2020-03-31 |
| AU2018277537A1 (en) | 2019-11-28 |
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