AR044745A1 - Compuestos herbicidas de azolcarboxamida, composicion herbicida y metodo para controlar el crecimiento de vegetacion indeseable - Google Patents
Compuestos herbicidas de azolcarboxamida, composicion herbicida y metodo para controlar el crecimiento de vegetacion indeseableInfo
- Publication number
- AR044745A1 AR044745A1 ARP030103803A AR044745A1 AR 044745 A1 AR044745 A1 AR 044745A1 AR P030103803 A ARP030103803 A AR P030103803A AR 044745 A1 AR044745 A1 AR 044745A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- alkenyl
- alkynyl
- alkoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 230000002363 herbicidal effect Effects 0.000 title abstract 3
- 239000004009 herbicide Substances 0.000 title 2
- RLOQBKJCOAXOLR-UHFFFAOYSA-N 1h-pyrrole-2-carboxamide Chemical compound NC(=O)C1=CC=CN1 RLOQBKJCOAXOLR-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 22
- 125000001188 haloalkyl group Chemical group 0.000 abstract 10
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 9
- 125000003545 alkoxy group Chemical group 0.000 abstract 8
- 125000003709 fluoroalkyl group Chemical group 0.000 abstract 8
- 125000003342 alkenyl group Chemical group 0.000 abstract 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 7
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 7
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 7
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 7
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 5
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 4
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 abstract 4
- 125000004991 fluoroalkenyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 3
- 125000004849 alkoxymethyl group Chemical group 0.000 abstract 3
- 125000004428 fluoroalkoxy group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl 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
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 abstract 2
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 2
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 2
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 125000006431 methyl cyclopropyl group Chemical group 0.000 abstract 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 2
- 125000006592 (C2-C3) alkenyl group Chemical group 0.000 abstract 1
- 125000006593 (C2-C3) alkynyl group Chemical group 0.000 abstract 1
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 abstract 1
- -1 C2-4 fluoroalkynyl Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical group C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- 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
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- 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
- C07D231/14—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 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
-
- 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
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Un compuesto que se selecciona entre la fórmula (1), un N-óxido o una sal adecuada para uso en agricultura del mismo; donde j es un resto de grupo de fórmula (2); T es CR6, o N; U es CR7 o N; Y es CR8 o N; Z es CR9 o N; R1a es H, C1-4 alquilo, C1-4 fluoroalquilo, C2-4 alquenilo, C2-4 fluoroalquenilo, C2-4 alquinilo o C2-4 fluoroalquinilo; R1b es halógeno, C1-4 alquilo, C1-4 fluoroalquilo, C2-4 alquenilo, C2-4 fluoroalquenilo, C2-4 alquinilo o C2-4 fluoroalquenilo; R1c es H; R2a es C1-6 alquilo, C1-6 haloalquilo, C2-6 alcoxialquilo, C2-6 alquiltioalquilo, C2-6 alquenilo, C2-6 haloalquenilo, C2-6 alquinilo, C2-6 haloalquinilo, C3-6 cicloalquilo, C4-6 alquilcicloalquilo, C3-6 halocicloalquilo, C4-6 cicloalquilalquilo, C5-6 alquilcicloalquilalquilo, -CR20(OR21)(OR22) o SiR23R24R25; R2b es C1-6 alquilo, C1-6 haloalquilo, C2-6 alcoxialquilo, C2-6 alquiltioalquilo, C2-6 alquenilo, C2-6 haloalquenilo, C2-6 alquinilo, C2-6 haloalquinilo, C3-6 cicloalquilo, C4-6 alquilcicloalquilo, C3-6 halocicloalquilo, C4-6 cicloalquilalquilo o C5-6 alquilcicloalquilalquilo; R3 es H, F o C1-2 alquilo; o R2a o R2b se toman junto con R3 como -C(R26a)(R26b)-(Y1)s-(CH2)t-(Y2)u o -C(R26a)(R26b)-(Y1)v-CH=CH-(Y2)w, donde el extremo izquierdo del radical está conectado como R2a o R2b, y el extremo derecho del radical está conectado como R3; R4 es H, C1-2 alquilo, C2-6 alquilcarbonilo, C2-6 alcoxicarbonilo, C2-6 alcoxialquilo o C2-6 alquiltioalquilo; R5 es C(W1)NR10R11, C(O)OR12, COR13, C(NOR14)R15, -CN, OR16, S(O)mR17, S(O)2NR18R19, OS(O)2R27, o P(O)R28aR28b; R6 es H, F, C1-2 alquilo, C1-2 fluoroalquilo, C1-2 alcoxi, C1-2 fluoroalcoxi, C1-2 alquiltio o C1-2 fluoroalquilo; o R5 y R6 se toman juntos como un radical seleccionado entre -C(W1)N(R11)(CH2)n- y -C(NOR14)CH2(CH2)u donde el extremo derecho del radical está conectado al anillo por T; R7 es H, F, C1-2 alquilo, C1-2 fluoroalquilo, C1-2 alcoxi, C1-2 fluoroalcoxi, C1-2 alquiltio o C1-2 fluoroalquiltio; R8 y R9 se seleccionan en forma independiente entre H, F, C1-2 alquilo, C1-2 fluoroalquilo, C1-2 alcoxi, C1-2 fluoroalcoxi, C1-2 alquiltio y C1-2 fluoroalquiltio; R10 es H, C1-4 alquilo, C1-4 haloalquilo, C3-4 alquenilo, C2-4 alcoximetilo o C2-4 alquiltiometilo; R11 es H, C1-5 alquilo, C1-5 haloalquilo, C2-5 alquenilo, C3-5 haloalquenilo, C3-5 alquinilo, C3-5 cicloalquilo, C4-5 cicloalquilalquilo, C1-3 alcoxi, C2-5 alcoxialquilo o C2-5 alquiltioalquilo; o R10 y R11 se toman juntos como -(CH2)4-, -(CH2)5-, -CH2CH=CHCH2- o -(CH2)2O(CH2)2-, cada uno opcionalmente sustituido con 1-2 C1-2 alquilo; cada R12 es en forma independiente C1-5 alquilo, C1-5 haloalquilo, C2-4 alcoxialquilo, C2-4 alquiltioalquilo, C2-5 alquenilo, C3-5 haloalquenilo, C3-5 alquinilo, C3-5 cicloalquilo o C4-5 cicloalquilalquilo; R13 es C1-3 alquilo, C1-3 haloalquilo o ciclopropilo; R14 es H, C1-4 alquilo, C1-4 haloalquilo, C3-4 alquenilo, C2-6 alquilcarbonilo o C2-6 alcoxicarbonilo; R15 es C1-3 alquilo, C1-3 haloalquilo o ciclopropilo; R16 es C1-4 alquilo, C1-4 haloalquilo, C2-3 alcoxialquilo, C2-3 alquiltioalquilo, C2-4 alquenilo, C3-4 haloalquenilo, C3-4 alquinilo, C3-5 cicloalquilo o ciclopropilmetilo; R17 es C1-4 alquilo, C1-4 haloalquilo, C2-4 alquenilo, C3-4 haloalquenilo, C3-4 alquinilo, C3-4 cicloalquilo o ciclopropilmetilo; cada R18 es en forma independiente H, C1-4 alquilo, C1-4 haloalquilo, C3-4 alquenilo, C2-4 alcoximetilo o C2-4 alquiltiometilo; cada R19 es en forma independiente H, C1-5 alquilo, C1-5 haloalquilo, C2-5 alquenilo, C3-5 haloalquenilo, C3-5 alquinilo, C3-5 cicloalquilo, C4-5 cicloalquilalquilo, C1-3 alcoxi, C2-5 alcoxialquilo o C2-5 alquiltioalquilo; R20 es C1-4 alquilo, ciclopropilo, ciclopropilmetilo o metilciclopropilo; R21 es C1-3 alquilo; R22 es C1-3 alquilo; o R21 y R22 se toman juntos como -CH2CH2- o -CH2CH2CH2-, cada uno opcionalmente sustituido con 1-2 metilo; R23 es C1-2 alquilo o C1-2 haloalquilo; R24 es C1-2 alquilo o C1-2 haloalquilo; R25 es C1-2 alquilo o C1-2 haloalquilo; R26a y R26b son en forma independiente H o C1-2 alquilo; R27 es C1-3 alquilo, C1-3 haloalquilo o ciclopropilo; R28a y R28b son en forma independiente C1-2 alquilo o C1-2 alcoxi; W es O o S; W1 es O o S; Y1 y Y2 son en forma independiente CH2, O, S, NH o NCH3; m es 0, 1 ó 2; n es 1 ó 2; s es 0 ó 1; t es 1 ó 2; y u es 0 ó 1; siempre que la suma de s, t y u es 2 ó 3; y v es 0 ó 1; w es 0 ó 1; siempre que la suma de v y w sea 0 ó 1; con la condición de que a) cuando j es ciclopropilo, ciclopropilmetilo o metilciclopropilo; R21 es C1-3 alquilo; R22 es C1-3 alquilo; o R21 y R22 se toman juntos como -CH2CH2- o -CH2CH2CH2-, cada uno opcionalmente sustituido con 1-2 metilo; R23 es C1-2 alquilo o C1-2 haloalquilo; R24 es C1-2 alquilo o C1-2 haloalquilo; R25 es C1-2 alquilo o C1-2 haloalquilo; R26a y R26b son en forma independiente H o C1-2 alquilo; R27 es C1-3 alquilo, C1-3 haloalquilo o ciclopropilo; R28a y R28b son en forma independiente C1-2 alquilo o C1-2 alcoxi; W es O o S; W1 es O o S; Y1 y Y2 son en forma independiente CH2, O, S, NH o NCH3; m es 0, 1 ó 2; n es 1 ó 2; s es 0 ó 1; t es 1 ó 2; y u es 0 ó 1; siempre que la suma de s, t y u es 2 ó 3; y v es 0 ó 1; w es 0 ó 1; siempre que la suma de v y w sea 0 ó 1; con la condición de que a) cuando j es J-1, R1a es CH3 y R5 es C(W1)NR10R11, C(O)OR12, COR13, OR16 o S(O)mR17, al menos uno de T, U, Y y Z sea N o C-F; b) cuando J es J-1, R1a es CH3, R5 es C(W1)NR10R11, C(O)OR12, COR13, OR16 o S(O)mR17 y T es N, al menos uno de U, Y y Z sea N o C-F; c) cuando R5 es C(W1)NR10R11 o C(NOR14)R15; R9 sea distinto de alcoxi o alquiltio; d) cuando R5 es C(W1)NR10R11, R6 sea distinto de alquilo o alcoxi; e) cuando R5 es COR13, R1a o R1b se seleccione entre los radicales del grupo que comprende C1-3 alquilo, C1-3 fluoroalquilo, C2-3 alquenilo; C2-3 fluoroalquenilo, C2-3 alquinilo o C2-3 fluoroalquinilo, donde cada radical es no ramificado y está conectado a través de un átomo de carbono terminal al anillo azol; f) cuando R5 y R6 se toman juntos como -C(W1)N(R10)(CH2)n- y n es 1, R10 sea C1-4 alquilo, C1-4 haloalquilo, C3-4 alquenilo, C2-4 alcoximetilo o C2-4 alquiltiometilo; g) cuando al menos uno de R10 y R11 es haloalquilo, R1a o R1b sea CH2CH3 o CH2CF3 y R2a o R2b sea tert-butilo, isopropilo o ciclopropilo; h) cuando J es J-2 o J-6, R7 y R9 sean H; i) cuando J es J-2 o J-6, y R2b es C1-2 alquilo, R1b sea halógeno, C2-4 alquilo, C1-4 fluoroalquilo, C2-4 alquenilo, C2-4 fluoroalquinilo, C2-4 alquinilo o C2-4 fluoroalquinilo; j) cuando R1a es CH3 y R5 es C(NOR14)R15, R7 sea distinto de alquilo; k) cuando T es N, Z sea CR9, l) cuando T es N, R7 es alcoxi, R11 sea H; m) cuando R7 y R9 son F, y uno de R10 y R11 es H, el otro entre R10 y R11 sea distinto de H; n) cuando Z es N y uno de R10 y R11 es H, el otro entre R10 y R11 sea distinto de trifluorometilo; o) cuando J es J-8 y R2b es C5-6 cicloalquilo, R5 sea C(O)NR10R11; y p) cuando J es J-8 y R7 es distinto de H, R2b sea tert-butilo y R5 sea C(O)NR10R11. También se describe la composición herbicida que comprende dichos compuestos y el método para controlar el crecimiento de vegetación indeseable, usando los mismos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41969602P | 2002-10-18 | 2002-10-18 | |
| US47386603P | 2003-05-27 | 2003-05-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR044745A1 true AR044745A1 (es) | 2005-10-05 |
Family
ID=32110262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030103803 AR044745A1 (es) | 2002-10-18 | 2003-10-17 | Compuestos herbicidas de azolcarboxamida, composicion herbicida y metodo para controlar el crecimiento de vegetacion indeseable |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR044745A1 (es) |
| AU (1) | AU2003301443A1 (es) |
| WO (1) | WO2004035545A2 (es) |
Families Citing this family (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE482200T1 (de) | 2003-05-01 | 2010-10-15 | Bristol Myers Squibb Co | Als kinaseinhibitoren geeignete arylsubstituierte pyrazolamidverbindungen |
| BR122015015718B1 (pt) | 2004-01-28 | 2016-05-10 | Mitsui Chemicals Inc | derivados de amida |
| US7297700B2 (en) * | 2005-03-24 | 2007-11-20 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
| EP1911751A4 (en) * | 2005-06-21 | 2010-10-20 | Mitsui Chemicals Agro Inc | AMID DERIVATIVE AND PESTICIDE CONTAINING SUCH A COMPOUND |
| MX2008000584A (es) * | 2005-07-18 | 2008-03-14 | Syngenta Participations Ag | Derivados de pirazol-4-carboxamida como microbicidas. |
| KR101430949B1 (ko) | 2005-12-01 | 2014-08-18 | 바스프 에스이 | 술폰아미드의 제조 방법 |
| US7714014B2 (en) * | 2005-12-09 | 2010-05-11 | The Regents Of The University Of California | Targeting GLI proteins in human cancer by small molecules |
| CA2645556C (en) * | 2006-03-16 | 2016-05-24 | Renovis, Inc. | Bicycloheteroaryl compounds as p2x7 modulators and uses thereof |
| TWI464148B (zh) | 2006-03-16 | 2014-12-11 | Evotec Us Inc | 作為ｐ２ｘ7調節劑之雙環雜芳基化合物與其用途 |
| US20090298825A1 (en) * | 2006-03-16 | 2009-12-03 | Kelly Michael G | Bicycloheteroaryl Compounds as P2x7 Modulators and Uses Thereof |
| GB0617575D0 (en) * | 2006-09-06 | 2006-10-18 | Syngenta Ltd | Herbicidal compounds and compositions |
| UA103006C2 (ru) | 2007-08-27 | 2013-09-10 | Басф Се | Пиразольные соединения для борьбы с бесхребетными вредителями |
| CN101821233B (zh) | 2007-10-12 | 2016-06-29 | 巴斯夫欧洲公司 | 生产磺酸二酰胺的方法 |
| US8097712B2 (en) | 2007-11-07 | 2012-01-17 | Beelogics Inc. | Compositions for conferring tolerance to viral disease in social insects, and the use thereof |
| UA103633C2 (ru) * | 2008-09-24 | 2013-11-11 | Басф Се | Пиразольные соединения для борьбы с бесхребетными вредителями |
| ES2710701T3 (es) | 2008-09-24 | 2019-04-26 | Basf Se | Compuestos de pirazol para el control de plagas de invertebrados |
| EP2184273A1 (de) | 2008-11-05 | 2010-05-12 | Bayer CropScience AG | Halogen-substituierte Verbindungen als Pestizide |
| BRPI1008770B8 (pt) | 2009-02-27 | 2018-07-31 | Dow Agrosciences Llc | n-alcóxiamidas de 6-(fenila substituída)-4-aminopicolinatos e 2-(fenila substituída)-6-amino-4 pirimidinacarboxilatos, seus processos de produção, composição herbicida, bem como métodos de controle de vegetação indesejável |
| EP2253617A1 (de) | 2009-05-20 | 2010-11-24 | Bayer CropScience AG | Halogen-substituierte Verbindungen als Pestizide |
| ES2472918T3 (es) | 2009-07-06 | 2014-07-03 | Basf Se | Compuestos de piridazina para controlar plagas de invertebrados |
| BR112012000149B8 (pt) | 2009-07-06 | 2021-01-12 | Basf Se | compostos de piridazina, método para controlar pragas invertebradas e método para proteger material de propagação de planta e/ou as plantas |
| CN102469785A (zh) | 2009-07-24 | 2012-05-23 | 巴斯夫欧洲公司 | 防治无脊椎动物害虫的吡啶衍生物 |
| EP2308866A1 (de) | 2009-10-09 | 2011-04-13 | Bayer CropScience AG | Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide |
| US8962584B2 (en) | 2009-10-14 | 2015-02-24 | Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. | Compositions for controlling Varroa mites in bees |
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| CN109156471B (zh) * | 2018-08-29 | 2020-12-15 | 浙江工业大学 | 一种1,3-二甲基-1h-吡唑-4-酰胺衍生物在制备除草剂中的应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0253775A (ja) * | 1988-08-18 | 1990-02-22 | Nissan Chem Ind Ltd | ピラゾールカルボキサミド誘導体及び除草剤 |
| JPH02129171A (ja) * | 1988-11-08 | 1990-05-17 | Nissan Chem Ind Ltd | ピラゾールカルボキサニリド誘導体及び有害生物防除剤 |
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- 2003-10-15 WO PCT/US2003/032965 patent/WO2004035545A2/en not_active Ceased
- 2003-10-15 AU AU2003301443A patent/AU2003301443A1/en not_active Abandoned
- 2003-10-17 AR ARP030103803 patent/AR044745A1/es unknown
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| AU2003301443A1 (en) | 2004-05-04 |
| AU2003301443A8 (en) | 2004-05-04 |
| WO2004035545A3 (en) | 2004-08-05 |
| WO2004035545A2 (en) | 2004-04-29 |
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