AR032779A1 - Derivados de ciclohexenona de benzazolonas, acidos benzazolonacarboxilicos, agentes que contienen por lo menos un derivado de ciclohexenona, procedimiento para combatir el crecimiento indeseado de plantas y uso de dichos derivados como herbicidas - Google Patents
Derivados de ciclohexenona de benzazolonas, acidos benzazolonacarboxilicos, agentes que contienen por lo menos un derivado de ciclohexenona, procedimiento para combatir el crecimiento indeseado de plantas y uso de dichos derivados como herbicidasInfo
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- AR032779A1 AR032779A1 ARP010105671A ARP010105671A AR032779A1 AR 032779 A1 AR032779 A1 AR 032779A1 AR P010105671 A ARP010105671 A AR P010105671A AR P010105671 A ARP010105671 A AR P010105671A AR 032779 A1 AR032779 A1 AR 032779A1
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- Prior art keywords
- alkyl
- alkoxy
- halogenoalkoxy
- halogenoalkyl
- alkynyl
- Prior art date
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- 239000002253 acid Substances 0.000 title abstract 2
- 150000007513 acids Chemical class 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 239000003795 chemical substances by application Substances 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 29
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 21
- 125000001188 haloalkyl group Chemical group 0.000 abstract 17
- -1 Benzazolone cyclohexenone derivatives Chemical class 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 12
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 12
- 125000000217 alkyl group Chemical group 0.000 abstract 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract 11
- 239000001257 hydrogen Substances 0.000 abstract 11
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 10
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 9
- 125000000304 alkynyl group Chemical group 0.000 abstract 9
- 125000000623 heterocyclic group Chemical group 0.000 abstract 9
- 150000002431 hydrogen Chemical group 0.000 abstract 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 8
- 150000002367 halogens Chemical group 0.000 abstract 8
- 125000003342 alkenyl group Chemical group 0.000 abstract 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006529 (C3-C6) alkyl group Chemical group 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 230000009418 agronomic effect Effects 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy 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
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical group O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000006678 phenoxycarbonyl group Chemical group 0.000 abstract 1
- 230000008635 plant growth Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
Derivados de ciclohexenona de benzazolonas de la formula general (1), en donde A, R1, R2, R3 y Hex tienen los significados indicados a continuacion: AO, S, SO, SO2 o NR6; R1 es halogeno, alquilo C1-4, halogenoalquilo C1-4, hidroxialquilo C1-4, alcoxi C1-4-alquilo C1-4, halogenoalcoxi C1-4-alquilo C1-4, halogenoalquiltio C1-4-alquilo C1-4, alquiltio C1-4-alquilo C1-4, alquilsulfonilo C1-4-alquilo C1-4, halogeno-alquilsulfonilo C1-4-alquilo C1-4, alcoxi C1-4, hidroxialcoxi C1-4, halogenoalcoxi C1-4, alcoxi C1-4-alcoxi C1-4, halogenoalcoxi C1-4-alcoxi C1-4, alquiltio C1-4, halogenoalquiltio C1-4, alquilsulfonilo C1-4, halogenoalquilsulfonilo C1-4; R2 es hidrogeno, hidroxi, nitro, amino, alquilamino C1-6, di(alquilo C1-6)amino, ciano, CHO, alcoxi C1-6, alquilo C1-6, hidroxialquilo C1-6, halogenoalquilo C1-6, alcoxi C1-6-alquilo C1-6, halogenoalcoxi C1-6-alquilo C1-6, alquenilo C2-6, halogenoalquenilo C2-6, halogenoalcoxi C1-6-alquenilo C2-6, alcoxi C1-6-alquenilo C2-6, alquinilo C2-6, halogenoalquinilo C2-6, halogenoalcoxi C1-6-alquinilo C2-6, alcoxi C1-6-alquinilo C2-6, alquilsulfonilo C1-6, halogenoalquilsulfonilo C1-6, (alquilo C1-6)carbonilo, halogenoalquilcarbonilo C1-6, hidroxicarbonilo-alquilo C1-4, alcoxicarbonilo C1-6-alquilo C1-6, un resto de la formula C(O)OR4, CON(R5)2 o C(=NOR4a)R4b, arilo, arilo-alquilo C1-4, arilsulfonilo, arilcarbonilo, cicloalquilo C3-6, cicloalquenilo C3-6, heterociclilo de 3, 4, 5, 6 o 7 miembros, heterocicliclo de 3, 4, 5, 6 o 7 miembros alquilo C1-6, en donde cada resto arilo, cicloalquilo, cicloalquenilo y cada resto heterociclilo pueden ser no sustituidos o llevar uno, dos, tres o cuatro sustituyentes, elegidos en cada caso entre halogeno, halogenoalquilo C1-4, alcoxi C1-4 y halogenoalcoxi C1-4; R3 es hidrogeno, alquilo C1-4, halogenoalquilo C1-4, alcoxi C1-4-alquilo C1-4, halogenoalcoxi C1-4-alquilo C1-4 o halogeno; en donde: R4 significa alquilo C1-6, halogenoalquilo C1-6, alcoxi C1-6-alquilo C1-6, halogenoalcoxi C1-6-alquilo C1-6, alquenilo C2-6, halogenoalquenilo C2-6, halogenoalcoxi C1-6-alquenilo C2-6, alcoxi C1-6-alquenilo C2-6, alquinilo C2-6, halogenoalquinilo C2-6, halogenoalcoxi C1-6-alquinilo C2-6, alcoxi C1-6-alquinilo C2-6; R4a, R4b pueden presentar independientemente uno de otro los significados mencionados para R4 y R4b puede representar hidrogeno; R5 independientemente uno de otro representan hidrogeno, alquilo C1-6, halogenoalquilo C1-6, alcoxi C1-6-alquilo C1-6, (halogenoalcoxi C1-6)-alquilo, alquenilo C1-6, halogenoalquenilo C2-6, halogenoalquilo C1-6-alquenilo C2-6, halogenoalcoxi C1-6-alquenilo C2-6, alcoxi C1-6-alquenilo C2-6, alquinilo C2-6, halogenoalquinilo C2-6, halogenoalquilo C1-6-alquinilo C2-6, halogenoalcoxi C1-6-alquinilo C2-6, alcoxi C1-6-alquinilo C2-6, o juntos forman un heterociclo de 3 a 7 miembros, el cual puede estar opcionalmente parcial o completamente halogenado y/o puede llevar uno, dos o tres sustituyentes, seleccionados entre alquilo C1-6, halogenoalquilo C1-6, alcoxi C1-6, halogenoalcoxi C1-6; R6 significa hidrogeno, alquilo C1-4, halogenoalquilo C1-4, haloalcoxi C1-4-alquilo C1-4, alcoxi C1-4-alquilo C1-4; y Hex significa (3-oxo-1-ciclohexen-2-il)carbonilo sustituido de la formula (2) o (1,3-dioxo-2-ciclohexil)metilideno sustituido de la formula (3), en donde las variables R7 a R13 tienen el siguiente significado: R7 es hidroxi, mercapto, halogeno, OR14, SR14, SOR15, SO2R15, OSO2R15, P(O)R16R17, OP(O)R16R17, P(S)R16R17, OP(S)R16R17, NR18R19, ONR18R19 o heterociclilo ligado a N, que puede estar halogenado parcial o completamente y/o puede llevar uno a tres de los siguientes restos: nitro, ciano, alquilo C1-4, halogenoalquilo C1-4, alcoxi C1-4 o halogenoalcoxi C1-4; R8, R12 independientemente uno del otro, hidrogeno, alquilo C1-4 o alcoxicarbonilo C1-4; R9, R11, R13 independientemente uno de otro, hidrogeno o alquilo C1-4; R10 es hidrogeno , halogeno, hidroxi, alquilo C1-6, halogenoalquilo C1-6, di-(alcoxi C1-6)-metilo, (alcoxi C1-6)-(alquiltio C1-6)-metilo, di-(alquiltio C1-6)metilo, alcoxi C1-6, halogenoalcoxi C1-6, alquiltio C1-6, halogenoalquiltio C1-6, alquilsulfinilo C1-6, halogenoalquilsulfinilo C1-6, alquilsulfonilo C1-6, halogenoalquilsulfonilo C1-6, alcoxicarbonilo C1-6, 1,3-dioxolan-2-ilo, 1,3-dioxan-2-ilo,1,3-oxatiolan-2-ilo, 1,3-oxatian-2-ilo, 1,3-ditiolan-2-ilo o 1,3-ditian-2-ilo, en donde los seis restos mencionados en ultimo término pueden estar sustituidos por uno a tres restos alquilo C1-4; o R9 y R11 o R11 y R13 forman juntos una union pi o una cadena alquileno C1-5, que puede llevar uno, dos o tres restos del siguiente grupo: halogeno, ciano, alquilo C1-4, halogenoalquilo C1-4, o alcoxicarbonilo C1-4; o R9 y R13 forman juntos una cadena alquilo C1-4, que puede llevar uno o tres restos del siguientes grupo: halogeno, ciano, alquilo C1-4, halogenoalquilo C1-4, o alcoxicarbonilo C1-4; o R10 y R11 forman juntos una cadena ûO-(CH2)p-O-, -O-(CH2)p-S-, -S-(CH2)p-S-, -O-(CH2)q- o -S-(CH2)q-, en donde p representa 2, 3, 4 o 5 y q representa 2, 3, 4, 5 o 6, y la cual puede estar sustituida por uno, dos o tres restos del siguiente grupo: halogeno, ciano, alquilo C1-4, halogenoalquilo C1-4 o alcoxicarbonilo C1-4; o R10 y R11 forman junto con el carbono, al cual están unidos, un grupo carbonilo; en donde: R14 significa alquilo C1-6, alquenilo C3-6, halogeno-alquilo C3-6,alquinilo C3-6, halogenoalquinilo C3-6, cicloalquilo C3-6, alquilcarbonilo C1-6, alquenilcarbonilo C2-6, alquinilcarbonilo C2-6, cicloalquilcarbonilo C3-6, alcoxicarbonilo C1-6, alqueniloxicarbonilo C3-6, alquiniloxicarboniloC3-6, alquiltiocarbonilo C1-6, alquilaminocarbonilo C1-6, alquenilaminocarbonilo C3-6, alquinilamino-carbonilo C3-6, N,N-di(alquilo C1-6)amino-carbonilo, N-(alquenilo C3-6)-N-(alquilo C1-6)-aminocarbonilo, N-(alquinilo C3-6)-N-(alquilo C1-6)-aminocarbonilo, N-(alcoxi C1-6)-(alquilo C1-6)-aminocarbonilo, N-(alquenilo C3-6)-N-(alcoxi C1-6)-aminocarbonilo, N-(alquinilo C3-6)-N-(alcoxi C1-6)-aminocarbonilo, di-(alquilo C1-6)-aminotiocarbonilo, alcoxiimino C1-6-alquilo C1-6, en donde los restos alquilo, cicloalquilo o alcoxi mencionados pueden estar parcial o completamente halogenados y/o pueden llevar uno, dos o tres de los siguientes grupos: ciano, alcoxi C1-4, alquiltio C1-4, di-(alquilo C1-4)amino, alquilcarbonilo C1-4, alcoxicarbonilo C1-4, alcoxi C1-4-alcoxicarbonilo C1-4, hidroxicarbonilo, alquilaminocarbonilo C1-4, di-(alquilo C1-4) amino-carbonilo, aminocarbonilo, alquilcarboniloxi C1-4, o cicloalquilo C3-6; fenilo, fenilo-alquilo C1-6, fenilcarbonilo-alquilo C1-6, fenilcarbonilo, fenoxicarbonilo, fenoxitiocarbonilo, fenilaminocarbonilo, N-(alquilo C1-6)-N-fenilaminocarbonilo, fenilo-alquenilcarbonil C2-6, heterociclilo, heterociclilo-alquilo C1-6, heterociclilcarbonilo-alquilo C1-6, heterociclil-carbonilo, hetero-cicliloxicarbonilo, heterocicliloxitiocarbonilo, heterociclilaminocarbonilo, N-(alquilo C1-6)-N-heterociclilaminocarbonilo o heterociclilo-alquenilcarbonilo C1-6, en donde el resto fenilo o heterociclilo de los ultimos 18 sustituyentes puede estar halogenado parcial o completamente y/o llevar uno a tres de los siguientes restos: nitro, ciano, alquilo C1-4, halogenoalquilo C1-4, alcoxi C1-4 o halogenoalcoxi C1-4; R15 significa alquilo C1-6, alquenilo C3-6, alquinilo C3-6 o cicloalquilo C3-6, en donde los cuatro restos mencionados pueden estar halogenados parcial o completamente y/o llevar uno, dos o tres de los siguientes grupos: ciano, alcoxi C1-4, halogeno-alcoxi C1-4, alquiltio C1-4, halogenoalquiltio C1-4, alquilcarbonilo C1-4, alcoxicarbonilo C1-4 o halogenoalcoxicarbonilo C1-4, fenilo, fenilo-alquilo C1-4, heterociclilo o heterociclilo-alquilo C1-4, en donde el resto fenilo o heterociclilo de los cuatro sustituyentes mencionados en ultimo término puede estar halogenado parcial o completamente y/o puede llevar uno, dos o tres de los siguientes restos: nitro, ciano, alquilo C1-4, halogenoalquilo C1-4, alcoxi C1-4, halogenoalcoxi C1-4 o alcoxicarbonilo C1-4; R16 y R17 independientemente uno de otro significan hidrogeno, hidroxi, alquilo C1-6, alcoxi C1-6, alquiltio C1-6, fenilo, fenilo-alquilo C1-4 o fenoxi, en donde los tres sustituyentes mencionados en ultimo término pueden estar halogenados parcial o completamente y/o llevar uno, dos o tres de los siguientes restos: nitro, ciano, alquilo C1-4, halogenoalquilo C1-4, alcoxi C1-4, halogenoalcoxi C1-4 o alcoxicarbonilo C1-4; R18 significa hidrogeno, alquilo C1-6, alquenilo C3-6, halogenoalquenilo C3-6, alquinilo C3-6, halogenoalquinilo C3-6, cicloalquilo C3-6, alquilcarbonilo C1-6, hidroxi, alcoxi C1-6, alqueniloxi C3-6, alquiniloxi C3-6, amino, alquilamino C1-6, di-(alquilo C1-6)amino o alquilcarbonilamino C1-6, en donde los restos alquilo cicloalquilo o alcoxi mencionados pueden estar halogenados parcial o completamente y/o pueden llevar uno, dos o tres de los siguientes restos: ciano, alcoxicarbonilo C1-4, alquilaminocarbonil C1-4, di-(alquilo C1-4)-aminocarbonilo o cicloalquilo C3-6, fenilo, fenilo-alquilo C1-4, fenilcarbonilo, heterociclilo, heterociclilo-alquilo C1-4 o heterociclilcarbonilo, en donde el resto fenilo o heterociclilo de los seis sustituyentes mencionados en ultimo término pueden estar parcial o completamente halogenados y/o pueden llevar uno a tres de los siguientes restos: nitro, ciano, alquilo C1-4, halogenoalquilo C1-4, alcoxi C1-4 o halogenoalcoxi C1-4; R19 significa hidrogeno, alquilo C1-6, alquenilo C3-6 o alquinilo C3-6; así como también sus sales utiles en agricultura. Acidos benzazolonacarboxílicos de la formula general (5), en donde A, R1, R2 y R3 tienen el significado indicado anteriormente, utiles como intermediarios de síntesis de los compuestos de formula (1). Composiciones agronomicas que contienen por lo menos un derivado ciclohexenona de la formula (1) o una sal de (1) util en agricultura y sustancias auxiliares usuales. Procedimiento para combatir el crecimiento indeseado de plantas, mediante el cual se deja actuar una cantidad acti
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10061551 | 2000-12-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR032779A1 true AR032779A1 (es) | 2003-11-26 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010105671A AR032779A1 (es) | 2000-12-11 | 2001-12-06 | Derivados de ciclohexenona de benzazolonas, acidos benzazolonacarboxilicos, agentes que contienen por lo menos un derivado de ciclohexenona, procedimiento para combatir el crecimiento indeseado de plantas y uso de dichos derivados como herbicidas |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6908884B2 (es) |
| EP (1) | EP1341776A1 (es) |
| JP (1) | JP2004526679A (es) |
| AR (1) | AR032779A1 (es) |
| AU (1) | AU2002234560A1 (es) |
| CA (1) | CA2431267A1 (es) |
| WO (1) | WO2002048121A1 (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6480510B1 (en) * | 1998-07-28 | 2002-11-12 | Serconet Ltd. | Local area network of serial intelligent cells |
| AR032779A1 (es) * | 2000-12-11 | 2003-11-26 | Basf Ag | Derivados de ciclohexenona de benzazolonas, acidos benzazolonacarboxilicos, agentes que contienen por lo menos un derivado de ciclohexenona, procedimiento para combatir el crecimiento indeseado de plantas y uso de dichos derivados como herbicidas |
| CN104053656A (zh) | 2011-11-16 | 2014-09-17 | 巴斯夫欧洲公司 | 取代的1,2,5-噁二唑化合物及其作为除草剂的用途ii |
| IN2014MN02331A (es) | 2012-04-27 | 2015-08-14 | Basf Se | |
| WO2014184019A1 (en) | 2013-05-15 | 2014-11-20 | Basf Se | N-(1,2,5-oxadiazol-3-yl)carboxamide compounds and their use as herbicides |
| CN115960086B (zh) * | 2021-10-09 | 2024-05-28 | 山东先达农化股份有限公司 | 一种吡唑-苯并咪唑酮类化合物及其制备方法和应用、一种杀草剂 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1340284C (en) | 1987-03-19 | 1998-12-22 | Zeneca Inc. | Herbicidal substituted cyclic diones |
| DE4403670A1 (de) * | 1994-02-07 | 1995-09-07 | Basf Ag | 2-Aroylcyclohexandione, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Herbizide oder das Pflanzenwachstum regulierende Mittel |
| DE4427995A1 (de) * | 1994-08-08 | 1996-02-15 | Basf Ag | Saccharinderivate |
| CA2213124C (en) * | 1995-02-24 | 2005-04-26 | Basf Aktiengesellschaft | Benzoyl derivatives |
| DE19532311A1 (de) * | 1995-09-01 | 1997-03-06 | Basf Ag | Benzoylderivate |
| DE19638484A1 (de) * | 1996-09-20 | 1998-03-26 | Basf Ag | Hetaroylderivate |
| US6165944A (en) * | 1997-01-17 | 2000-12-26 | Basf Aktiengesellschaft | 4-(3-heterocyclyl-1-benzoyl) pyrazoles and their use as herbicides |
| US6140272A (en) * | 1997-05-07 | 2000-10-31 | Basf Aktiengesellschaft | Substituted 4-benzoyl-pyrazoles |
| AU760018B2 (en) | 1998-10-06 | 2003-05-08 | Idemitsu Kosan Co. Ltd | Triketone derivative and herbicide |
| CN1332739A (zh) * | 1998-12-04 | 2002-01-23 | 巴斯福股份公司 | 3-(杂环基)苯甲酰基吡唑衍生物 |
| US6500750B1 (en) * | 1999-04-05 | 2002-12-31 | Motorola, Inc. | Semiconductor device and method of formation |
| WO2000068210A1 (de) * | 1999-05-07 | 2000-11-16 | Basf Aktiengesellschaft | Benzohetero cyclylcyclo hexenone und ihre verwendung als herbizide |
| AU2001262282A1 (en) * | 2000-05-18 | 2001-11-26 | Basf Aktiengesellschaft | 3-(4,5-dihydroisoxazole-5-yl)benzoylcyclohexenones and the use thereof as herbicides |
| AR032779A1 (es) * | 2000-12-11 | 2003-11-26 | Basf Ag | Derivados de ciclohexenona de benzazolonas, acidos benzazolonacarboxilicos, agentes que contienen por lo menos un derivado de ciclohexenona, procedimiento para combatir el crecimiento indeseado de plantas y uso de dichos derivados como herbicidas |
-
2001
- 2001-12-06 AR ARP010105671A patent/AR032779A1/es not_active Application Discontinuation
- 2001-12-10 CA CA002431267A patent/CA2431267A1/en not_active Abandoned
- 2001-12-10 AU AU2002234560A patent/AU2002234560A1/en not_active Abandoned
- 2001-12-10 WO PCT/EP2001/014475 patent/WO2002048121A1/de not_active Ceased
- 2001-12-10 EP EP01985385A patent/EP1341776A1/de not_active Withdrawn
- 2001-12-10 US US10/433,013 patent/US6908884B2/en not_active Expired - Fee Related
- 2001-12-10 JP JP2002549652A patent/JP2004526679A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2004526679A (ja) | 2004-09-02 |
| EP1341776A1 (de) | 2003-09-10 |
| WO2002048121A1 (de) | 2002-06-20 |
| US20040063584A1 (en) | 2004-04-01 |
| CA2431267A1 (en) | 2002-06-20 |
| AU2002234560A1 (en) | 2002-06-24 |
| US6908884B2 (en) | 2005-06-21 |
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| Date | Code | Title | Description |
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| FA | Abandonment or withdrawal |