AR105544A1 - Compuestos de n-carboxamida cíclica útiles como herbicidas - Google Patents
Compuestos de n-carboxamida cíclica útiles como herbicidasInfo
- Publication number
- AR105544A1 AR105544A1 ARP160102329A ARP160102329A AR105544A1 AR 105544 A1 AR105544 A1 AR 105544A1 AR P160102329 A ARP160102329 A AR P160102329A AR P160102329 A ARP160102329 A AR P160102329A AR 105544 A1 AR105544 A1 AR 105544A1
- Authority
- AR
- Argentina
- Prior art keywords
- ring
- independently
- ring members
- alkyl
- alkoxy
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title 1
- 125000001424 substituent group Chemical group 0.000 abstract 13
- -1 hydroxy, amino Chemical group 0.000 abstract 8
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 6
- 125000004122 cyclic group Chemical group 0.000 abstract 6
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 4
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 4
- 125000004434 sulfur atom Chemical group 0.000 abstract 4
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 3
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 3
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 3
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 2
- 125000006592 (C2-C3) alkenyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl 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
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 2
- 125000000278 alkyl amino alkyl 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
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 2
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 2
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 2
- 125000005149 cycloalkylsulfinyl group Chemical group 0.000 abstract 2
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- QHRXQDWXYFNABK-IRXDYDNUSA-N (4S,5S)-N-(3-chlorophenyl)-2-oxo-4-phenyl-5-propan-2-yl-1,3-oxazolidine-3-carboxamide Chemical compound ClC=1C=C(C=CC=1)NC(=O)N1C(O[C@H]([C@@H]1C1=CC=CC=C1)C(C)C)=O QHRXQDWXYFNABK-IRXDYDNUSA-N 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 1
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 1
- 125000006593 (C2-C3) alkynyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- DTXUBBGVGHOGAP-UHFFFAOYSA-N 2-(5-methyl-1,3,4-oxadiazol-2-yl)-5-oxo-n-[3-(trifluoromethyl)phenyl]pyrrolidine-1-carboxamide Chemical compound O1C(C)=NN=C1C1N(C(=O)NC=2C=C(C=CC=2)C(F)(F)F)C(=O)CC1 DTXUBBGVGHOGAP-UHFFFAOYSA-N 0.000 abstract 1
- NIYTZHOKFDFMCH-UHFFFAOYSA-N 2-(5-methyl-1,3,4-oxadiazol-2-yl)-5-oxo-n-phenylpyrrolidine-1-carboxamide Chemical compound O1C(C)=NN=C1C1N(C(=O)NC=2C=CC=CC=2)C(=O)CC1 NIYTZHOKFDFMCH-UHFFFAOYSA-N 0.000 abstract 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 abstract 1
- KXNBPLSCEXNKGF-UHFFFAOYSA-N 2-oxo-n,6-diphenylpiperidine-1-carboxamide Chemical compound C=1C=CC=CC=1C1CCCC(=O)N1C(=O)NC1=CC=CC=C1 KXNBPLSCEXNKGF-UHFFFAOYSA-N 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 125000004648 C2-C8 alkenyl 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
- 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
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 1
- 125000000392 cycloalkenyl 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
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 abstract 1
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 abstract 1
- 125000005170 cycloalkyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000005203 haloalkylcarbonyloxy 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
- 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
- 125000006782 halocycloalkylcarbonyl group Chemical group 0.000 abstract 1
- DBFKLWKOKYDQIB-UHFFFAOYSA-N n-(3,4-dichlorophenyl)-2-(5-methyl-1,3,4-oxadiazol-2-yl)-5-oxopyrrolidine-1-carboxamide Chemical compound O1C(C)=NN=C1C1N(C(=O)NC=2C=C(Cl)C(Cl)=CC=2)C(=O)CC1 DBFKLWKOKYDQIB-UHFFFAOYSA-N 0.000 abstract 1
- PIUCINZTTJVJNH-UHFFFAOYSA-N n-(4-chlorophenyl)-2-(5-methyl-1,3,4-oxadiazol-2-yl)-5-oxopyrrolidine-1-carboxamide Chemical compound O1C(C)=NN=C1C1N(C(=O)NC=2C=CC(Cl)=CC=2)C(=O)CC1 PIUCINZTTJVJNH-UHFFFAOYSA-N 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
- 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
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- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
-
- 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
-
- 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
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings 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
- C07D233/30—Oxygen or sulfur atoms
- C07D233/32—One oxygen atom
- C07D233/38—One oxygen atom with acyl radicals or hetero atoms directly attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings 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
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
- C07D263/26—Oxygen atoms attached in position 2 with hetero atoms or acyl radicals directly attached to the ring nitrogen atom
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)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pyrrole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto seleccionado de la fórmula (1), N-óxidos y sales de estos, en donde: Q¹ es un anillo fenilo o un sistema de anillo naftalenilo; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁶; o un anillo heterocíclico de 4 a 7 miembros o un sistema de anillo bicíclico de 8 a 10 miembros, cada anillo o sistema de anillo que contiene miembros de anillo seleccionados de átomos de carbono y de 1 a 4 heteroátomos seleccionados, independientemente, de hasta 2 átomos de O, hasta 2 átomos de S y hasta 4 átomos de N, en donde hasta 3 miembros de anillo que son carbono se seleccionan, independientemente, de C(=O) y C(=S), y los miembros de anillo que son átomos de azufre se seleccionan, independientemente, de S(=O)ᵘ(=NR⁷)ᵛ; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁶ en miembros de anillo que son átomos de carbono y seleccionados de R⁸ en miembros de anillo que son átomos de nitrógeno; Q² es un anillo fenilo o un sistema de anillo naftalenilo; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁹; o un anillo heterocíclico de 4 a 7 miembros o un sistema de anillo bicíclico de 8 a 10 miembros, cada anillo o sistema de anillo que contiene miembros de anillo seleccionados de átomos de carbono y de 1 a 4 heteroátomos seleccionados, independientemente, de hasta 2 átomos de O, hasta 2 átomos de S y hasta 4 átomos de N, en donde hasta 3 miembros de anillo que son carbono se seleccionan, independientemente, de C(=O) y C(=S), y los miembros de anillo que son átomos de azufre se seleccionan, independientemente, de S(=O)ᵘ(=NR⁷)ᵛ; cada anillo o sistema de anillo está sustituido opcionalmente con hasta 5 sustituyentes seleccionados, independientemente, de R⁹ en miembros de anillo que son átomos de carbono y seleccionados de R¹⁰ en miembros de anillo que son átomos de nitrógeno; J es -CR²R³- o -CR²R³-CR²ᵃR³ᵃ- (en donde el enlace que se proyecta a la izquierda se conecta a G); G es -O-, -N(R¹)- o -C(R¹⁸)(R¹⁹)-; Y¹ es O, S o NR¹¹; Y² es O ó S; R¹ es H, hidroxi, amino, ciano, formilo, alquilcarbonilalquilo C₃₋₈, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆, cianoalquilo C₂₋₆, cicloalquilo C₃₋₆, cicloalquilalquilo C₄₋₈, alcoxialquilo C₂₋₈, haloalcoxialquilo C₂₋₈, haloalquenilalquilo C₂₋₈, alquiltioalquilo C₂₋₈, alquilsulfinilalquilo C₂₋₈, alquilsulfonilalquilo C₂₋₈, alquilcarbonilo C₂₋₈, haloalquilcarbonilo C₂₋₈, cicloalquilcarbonilo C₄₋₁₀, cicloalquilcarbonilalquilo C₅₋₁₀, 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 Q³; o -W¹Q³; R² y R³ son, cada uno, independientemente, H, halógeno, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄ o alcoxi C₁₋₄; R²ᵃ y R³ᵃ son, cada uno, independientemente, H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₃₋₆ o alcoxi C₁₋₆; R⁴ es H, halógeno, hidroxi, alcoxi C₁₋₄, haloalquilo C₁₋₄ o alquilo C₁₋₄; R⁵ 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 Q⁴; o -W²Q⁴; cada R⁶ y R⁹ es, independientemente, halógeno, hidroxi, ciano, nitro, amino, alquilo C₁₋₈, cianoalquilo C₁₋₈, cianoalcoxi C₁₋₈, haloalquilo 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, 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, 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 Q⁵; o -W³Q⁵; cada R⁷ es, independientemente, H, ciano, alquilcarbonilo C₂₋₃ o haloalquilcarbonilo C₂₋₃; cada R⁸ y R¹⁰ es, independientemente, ciano, alquilo C₁₋₃, alquenilo C₂₋₃, alquinilo C₂₋₃, cicloalquilo C₃₋₆, alcoxialquilo C₂₋₃, alcoxilo C₁₋₃, alquilcarbonilo C₂₋₃, alcoxicarbonilo C₂₋₃, alquilaminoalquilo C₂₋₃ o dialquilaminoalquilo C₃₋₄; cada R¹¹ es, independientemente, H, ciano, hidroxi, CHO, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄, alquilcarbonilo C₂₋₆, haloalquilcarbonilo C₂₋₆, -(C=O)CH₃ o -(C=O)CF₃; W¹ es -O-, -OS(=O)₂-, -C(=O)-, alcanodiilo C₁₋₃, alquenodiilo C₂₋₃, alquinodiilo C₂₋₃, -C(=O)(alquilo C₁₋₃)-, -C(=O)(alquenilo C₂₋₃)-, -C(=O)(alquinilo C₁₋₄)-; W² es -O-, -OS(=O)₂-, -C(=O)- o alcanodiilo C₁₋₃; W³ es -O-, -OS(=O)₂-, -C(=O)- o alcanodiilo C₁₋₃; cada Q³ es fenilo de -CPh=N-O(alquilo C₁₋₄) sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹²; o un anillo heteroaromático de 5 ó 6 miembros, cada uno sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹² y en miembros de anillo que son nitrógeno con hasta 2 sustituyentes seleccionados, independientemente, de R¹⁵; cada Q⁴ es fenilo sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹³; o un anillo heteroaromático de 5 ó 6 miembros, cada uno sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹³ y en miembros de anillo que son nitrógeno con hasta 2 sustituyentes seleccionados, independientemente, de R¹⁶; cada Q⁵ es fenilo sustituido opcionalmente en miembros de anillo con hasta 5 sustituyentes seleccionados, independientemente, de R¹⁴; o un anillo heteroaromático de 5 ó 6 miembros, cada uno sustituido opcionalmente en miembros de anillo que son carbono con hasta 5 sustituyentes seleccionados, independientemente, de R¹⁴ y en miembros de anillo que son nitrógeno con hasta 2 sustituyentes seleccionados, independientemente, de R¹⁷; cada R¹², R¹³ y R¹⁴ 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, haloalquilcarbonilo C₂₋₈, alcoxicarbonilo C₂₋₈, cicloalcoxicarbonilo C₄₋₁₀, cicloalquilalcoxicarbonilo C₅₋₁₂, alquilaminocarbonilo C₂₋₈, dialquilaminocarbonilo C₃₋₁₀, 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 R¹⁵, R¹⁶ y R¹⁷ es, independientemente, H o alquilo C₁₋₆; cada R¹⁸ y R¹⁹ es, independientemente, H, halógeno, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄ o alcoxi C₁₋₄; y cada u y v es, independientemente, 0, 1 ó 2 en cada instancia de S(=O)ᵘ(=NR⁷)ᵛ, siempre que la suma de u y v sea 0, 1 ó 2; siempre que cuando Q¹ sea un anillo fenilo sustituido por R⁶ en la posición 4, G sea -C(R¹⁸)(R¹⁹)-, Y¹ sea O, Y² sea O, J sea -CR²R³-, R² sea H, R³ sea H, R⁴ sea H, R⁵ sea H, R⁶ sea Cl, R¹⁸ sea H y R¹⁹ sea H, entonces Q² es distinto de 2-fluorofenilo; y siempre que el compuesto de la fórmula (1) sea distinto de trans-N-(3-clorofenil)-5-(1-metiletil)-2-oxo-4-fenil-3-oxazolidinacarboxamida (CA núm. 158323-70-7), 2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-N-fenil-1-pirrolidincarboxamida (CA núm. 182815-19-6), N-(4-clorofenil)-2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-1-pirrolidincarboxamida (CA núm. 182815-21-0), N-(3,4-diclorofenil)-2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-1-pirrolidincarboxamida (CA núm. 182815-22-1), 2-(5-metil-1,3,4-oxadiazol-2-il)-5-oxo-N-[3-(trifluorometil)fenil]-1-pirrolidincarboxamida (CA núm. 182815-23-2) o 2-oxo-N,6-difenil-1-piperidincarboxamida (CA núm. 111422-82-3).
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| WO2014065413A1 (ja) | 2012-10-26 | 2014-05-01 | 日本たばこ産業株式会社 | トリアゾール・イソオキサゾール化合物およびその医薬用途 |
| EP3077374B1 (en) * | 2013-12-03 | 2020-02-05 | FMC Corporation | Pyrrolidinones as herbicides |
| GB201321743D0 (en) | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic agents |
| RU2555370C1 (ru) | 2014-02-12 | 2015-07-10 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Самарский государственный технический университет" | Способ энантиоселективного синтеза диэтил[3-метил-(1s)-(нитрометил)бутил]малоната формулы i |
| UA125012C2 (uk) | 2014-07-02 | 2021-12-29 | ЕфЕмСі КОРПОРЕЙШН | Піперидинонові гербіциди |
| KR102542215B1 (ko) | 2014-12-08 | 2023-06-12 | 에프엠씨 코포레이션 | 3-옥소-3-(아릴아미노)프로파노에이트, 이의 제조방법 및 피롤리디논 제조에 있어서 이의 용도 |
| EP3280709B1 (en) | 2015-04-10 | 2021-05-26 | FMC Corporation | Substituted cyclic amides as herbicides |
| RU2734932C2 (ru) | 2015-04-27 | 2020-10-26 | ЭфЭмСи Корпорейшн | Бутиролактоны в качестве гербицидов |
| CA2980643C (en) | 2015-05-12 | 2023-10-17 | E I Du Pont De Nemours And Company | 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 |
| CA3047724A1 (en) | 2016-12-21 | 2018-06-28 | Fmc Corporation | Nitrone herbicides |
| UA126576C2 (uk) | 2017-03-21 | 2022-11-02 | ЕфЕмСі КОРПОРЕЙШН | Гербіцидна суміш, композиція та спосіб |
| KR102620213B1 (ko) | 2017-03-21 | 2024-01-03 | 에프엠씨 코포레이션 | 피롤리디논 및 이의 제조 방법 |
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- 2016-07-15 RU RU2018103198A patent/RU2720994C2/ru active
- 2016-07-15 WO PCT/US2016/042448 patent/WO2017023515A1/en not_active Ceased
- 2016-07-15 JP JP2018504837A patent/JP6937290B2/ja not_active Expired - Fee Related
- 2016-07-15 EP EP16741810.2A patent/EP3328836B1/en not_active Not-in-force
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| AU2016303209B2 (en) | 2021-04-01 |
| AU2016303209A1 (en) | 2018-02-01 |
| JP6937290B2 (ja) | 2021-09-22 |
| JP2018525373A (ja) | 2018-09-06 |
| BR112018001964B1 (pt) | 2022-05-10 |
| RU2018103198A3 (es) | 2019-11-19 |
| BR112018001964A2 (pt) | 2019-05-07 |
| CN108137512B (zh) | 2022-05-31 |
| US11178873B2 (en) | 2021-11-23 |
| RU2018103198A (ru) | 2019-08-28 |
| RU2720994C2 (ru) | 2020-05-15 |
| EP3328836B1 (en) | 2021-03-24 |
| WO2017023515A1 (en) | 2017-02-09 |
| CN108137512A (zh) | 2018-06-08 |
| CA2993000A1 (en) | 2017-02-09 |
| US20180213788A1 (en) | 2018-08-02 |
| CA2993000C (en) | 2024-01-23 |
| EP3328836A1 (en) | 2018-06-06 |
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