AR076839A1 - Derivados fungicidas de pirazol carboxamidas - Google Patents
Derivados fungicidas de pirazol carboxamidasInfo
- Publication number
- AR076839A1 AR076839A1 ARP100101513A ARP100101513A AR076839A1 AR 076839 A1 AR076839 A1 AR 076839A1 AR P100101513 A ARP100101513 A AR P100101513A AR P100101513 A ARP100101513 A AR P100101513A AR 076839 A1 AR076839 A1 AR 076839A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- unsubstituted
- alkyl
- different
- same
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- 239000000417 fungicide Substances 0.000 title abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 22
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 15
- 125000000217 alkyl group Chemical group 0.000 abstract 14
- 125000003545 alkoxy group Chemical group 0.000 abstract 10
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 6
- -1 formyloxy Chemical group 0.000 abstract 6
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 5
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000001188 haloalkyl group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 3
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 2
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 150000002527 isonitriles Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000676 alkoxyimino group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 1
- 125000005015 aryl alkynyl group Chemical group 0.000 abstract 1
- 125000001769 aryl amino group Chemical group 0.000 abstract 1
- 125000004350 aryl cycloalkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000005163 aryl sulfanyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000002184 metal Chemical class 0.000 abstract 1
- 229910052752 metalloid Inorganic materials 0.000 abstract 1
- 150000002738 metalloids Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000005645 nematicide Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- 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
- C07D231/16—Halogen atoms or nitro radicals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- 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
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Su procedimiento de preparacion, su uso como agentes activos fungicidas y/o antimicotoxinas y/o insecticidas y/o nematicidas, particularmente en forma de composiciones fungicidas, y a métodos para luchar contra hongos fitopatogénicos, particularmente de plantas, usando estos compuestos o composiciones. Reivindicacion 1: Un compuesto de formula (1) en donde Y representa CR5 o N; T representa S o O; X1 y X2, que pueden ser iguales o diferentes, representan un átomo de cloro o de fluor; Z1 representa un ciclopropilo no sustituido o un ciclopropilo sustituido con hasta 2 átomos o grupos que pueden ser iguales o diferentes y que pueden seleccionarse de la lista consistente en átomos de halogeno; ciano; alquilo C1-8; o halogenoalquilo C1-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; Z2 y Z3, que pueden ser iguales o diferentes, representan un átomo de hidrogeno; alquilo C1-8 sustituido o sin sustituir; alquenilo C2-8 sustituido o sin sustituir alquinilo C2-8 sustituido o sin sustituir; ciano; isonitrilo; nitro; un átomo de halogeno; alcoxi C1-8 sustituido o sin sustituir; alqueniloxi C2-8 sustituido o sin sustituir; alquiniloxi C2-8 sustituido o sin sustituir; cicloalquilo C3-7 sustituido o sin sustituir; alquil(C1-8)-sulfanilo sustituido o sin sustituir; alquil(C1-8)-sulfonilo sustituido o sin sustituir; alquil(C1-8)-sulfinilo sustituido o sin sustituir; amino; alquil(C1-8)-amino sustituido o sin sustituir; dialquil(C1-8)-amino sustituido o sin sustituir; alcoxi(C1-8)-carbonilo sustituido o sin sustituir; alquil(C1-8)-carbamoilo sustituido o sin sustituir; dialquil(C1-8)-carbamoílo sustituido sin sustituir; o N-alquilo-C1-8-alcoxicarbamoilo sustituido o sin sustituir; o Z3 y R1 junto con los átomos consecutivos a los que están unidos forman un carbo- o hetero-ciclo parcialmente saturado, de 5, 6 o 7 miembros, sustituido o sin sustituir que comprende hasta 3 heteroátomos y Z2 es como se describe en la presente memoria; o Z2 y Z3 junto con el átomo de carbono al que están unidos forman un cicloalquilo C3-7 sustituido o no sustituido; R1, R2, R3, R4 y R5, que pueden ser iguales o diferentes, representan un átomo de hidrogeno; un átomo de halogeno; nitro; ciano; isonitrilo ; hidroxilo; sulfanilo; amino; pentafluoro-gamma6-sulfanilo; alquilo C1-8 sustituido o sin sustituir; halogenoalquilo C1-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquil(C1-8)-amino sustituido o sin sustituir; dialquil(C1-8)-amino sustituido o sin sustituir; alcoxi C1-8 sustituido o sin sustituir; halogenoalcoxi C1-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alcoxi C1-8-alquilo C1-8; alquil(C1-8)-sulfanilo sustituido o sin sustituir; halogenoalquil (C1-8)sulfanilo que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquenilo C2-8 sustituido o sin sustituir; halogenoalquenilo C2-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquinilo C2-8 sustituido o sin sustituir; halogenoalquinilo C2-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alqueniloxi C2-8 sustituido o sin sustituir; halogenoalqueniloxi C2-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquiniloxi C2-8 sustituido o sin sustituir; halogenoalquiniloxi C2-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; cicloalquilo C3-7 sustituido o sin sustituir; halogenocicloalquilo C3-7 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; cicloalquilo C3-7-alquilo C1-6 sustituido o sin sustituir; cicloalquilo C3-7-alquenilo C2-8 sustituido o sin sustituir; cicloalquilo C3-7-alquinilo C2-8 sustituido o sin sustituir; cicloalquilo C3-7-cicloalquilo C3-7 sustituido o sin sustituir; alquilo C1-8- cicloalquilo C3-7 sustituido o sin sustituir; formilo; formiloxi; formilamino; carboxi; carbamoílo; N-hidroxicarbamoílo; carbamato; alquil(C1-8)hidroxiimino; alquil(C1-8)-carbonilo sustituido o sin sustituir; halogenoalquil (C1-8)carbonilo que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquil(C1-8)-carbamoílo sustituido o sin sustituir; dialquil(C1-8)-carbamoílo sustituido o sin sustituir; N-(sustituido o sin sustituir alquiloxi(C1-8))carbamoílo; alcoxi(C1-8)-carbamoílo sustituido o sin sustituir; N-(sustituido o sin sustituir alquilo(C1-8))-(sustituido o sin sustituir alcoxi(C1-8))-carbamoilo; alcoxi(C1-8)-carbonilo sustituido o sin sustituir; halogenoalcoxi (C1-8)carbonilo que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquilamino(C1-8)-carbonilo sustituido o sin sustituir; dialquilamino(C1-8)-carbonilo sustituido o sin sustituir; alquil(C1-8)-carboniloxi sustituido o sin sustituir; halogenoalquil (C1-8)carboniloxi que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquil(C1-8)-carbonilamino sustituido o sin sustituir; halogenoalquil (C1-8)carbonilamino que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquil(C1-8)-aminocarboniloxi sustituido o sin sustituir; dialquil(C1-8)-aminocarboniloxi sustituido o sin sustituir; alquiloxi(C1-8)-carboniloxi sustituido o sin sustituir; alquil(C1-8)-sulfinilo sustituido o sin sustituir ; halogenoalquilsulfinilo C1-6 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquil(C1-8)-sulfonilo sustituido o sin sustituir; halogenoalquilsulfonilo C1-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alcoxi(C1-8)-imino sustituido o sin sustituir; (alcoxi (C1-8)-imino)-alquilo (C1-8); (alqueniloxi(C1-8)-imino)-alquilo(C1-8) sustituido o sin sustituir; (alquinil C1-8-oxiimino)-alquilo(C1-8); un (benciloxiimino)-alquilo(C1-8); tri(alquil(C1-8) sustituido o sin sustituir)sililo; tri(alquil C1-8 sustituido o sin sustituir)silil-alquilo C1-8; benciloxi que puede estar sustituido por hasta 5 grupos Q; bencilsulfanilo que puede estar sustituido por hasta 5 grupos Q; bencilamino que puede estar sustituido por hasta 5 grupos Q; arilo que puede estar sustituido por hasta 7 grupos Q; ariloxi que puede estar sustituido por hasta 7 grupos Q; arilamino que puede estar sustituido por hasta 7 grupos Q; arilsulfanilo que puede estar sustituido por hasta 7 grupos Q; aril-alquilo C1-8 que puede estar sustituido con hasta 7 grupos Q; aril-alquenilo C2-8 que puede estar sustituido con hasta 7 grupos Q; aril-alquinilo C2-8 que puede estar sustituido con hasta 7 grupos Q; piridinilo que puede estar sustituido con hasta 4 grupos Q; piridiniloxi que puede estar sustituido con hasta 4 grupos Q; aril-cicloalquilo C3-7 que puede estar sustituido con hasta 7 grupos Q; o dos sustituyentes vecinos R junto con los átomos de carbono consecutivos a los que están unidos forman un carbo- o hetero-ciclo saturado de 5 o 6 miembros sustituido o in sustituir que comprende hasta 3 heteroátomos y los otros sustituyentes R son como se describen en la presente memoria; o R1 y Z3 junto con los átomos consecutivos a los que están unidos forman un carbo- o hetero-ciclo parcialmente saturado, de 5, 6 o 7 miembros, sustituido o sin sustituir que comprende hasta 3 heteroátomos y R2 a R5 son como se describen en la presente memoria; Q, que puede ser igual o diferente, representa un átomo de halogeno, ciano; nitro; alquilo C1-8; alcoxi C1-8; alquil (C1-8)sulfanilo; halogenoalquilo C1-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; halogenoalcoxi C1-8 que comprende hasta 9 átomos de halogeno que pueden ser iguales o diferentes; alquil tri(C1-8)sililo o alquil tri(C1-8) alquilo (C1-8)sililo; con la condicion que cuando Y representa N, y T representa O, y Z1 representa un grupo ciclopropilo, y R1 representa un átomo de cloro y R3 representa un grupo trifluorometilo, y R2 y R4 representa un átomo de hidrogeno, entonces al menos uno de los sustituyentes Z2 o Z3 no es un átomo de hidrogeno, así como sales, N-oxidos, complejos metálicos, complejos metaloídicos e isomeros geométricos u opticamente activos de los mismos.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09356035A EP2251331A1 (en) | 2009-05-15 | 2009-05-15 | Fungicide pyrazole carboxamides derivatives |
| EP09356058 | 2009-11-19 | ||
| US28617609P | 2009-12-14 | 2009-12-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR076839A1 true AR076839A1 (es) | 2011-07-13 |
Family
ID=42325337
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100101513A AR076839A1 (es) | 2009-05-15 | 2010-05-04 | Derivados fungicidas de pirazol carboxamidas |
Country Status (25)
| Country | Link |
|---|---|
| US (3) | US8772266B2 (es) |
| EP (2) | EP2430000B1 (es) |
| JP (2) | JP5824449B2 (es) |
| KR (1) | KR101726461B1 (es) |
| CN (2) | CN102421757B (es) |
| AR (1) | AR076839A1 (es) |
| AU (1) | AU2010247385B2 (es) |
| BR (2) | BRPI1007645B1 (es) |
| CA (1) | CA2761269C (es) |
| CL (1) | CL2011002840A1 (es) |
| CO (1) | CO6460782A2 (es) |
| DK (1) | DK2430000T3 (es) |
| EA (1) | EA023111B1 (es) |
| ES (1) | ES2561215T3 (es) |
| HR (1) | HRP20160062T1 (es) |
| HU (1) | HUE027401T2 (es) |
| MX (1) | MX2011012012A (es) |
| NZ (2) | NZ595589A (es) |
| PH (1) | PH12015501026B1 (es) |
| PL (1) | PL2430000T3 (es) |
| PT (1) | PT2430000E (es) |
| TW (2) | TWI514967B (es) |
| UA (1) | UA117454C2 (es) |
| WO (1) | WO2010130767A2 (es) |
| ZA (1) | ZA201109214B (es) |
Families Citing this family (113)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2185548A1 (en) * | 2007-07-31 | 2010-05-19 | Bayer CropScience SA | Fungicide 2-pyridyl-methylene-thio carboxamide or 2-pyridyl-methylene-n-substituted carboximidamide derivatives |
| US8338441B2 (en) | 2009-05-15 | 2012-12-25 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
| AR076839A1 (es) * | 2009-05-15 | 2011-07-13 | Bayer Cropscience Ag | Derivados fungicidas de pirazol carboxamidas |
| EP2560961B1 (de) * | 2010-04-23 | 2016-11-16 | Bayer Intellectual Property GmbH | Verfahren zum herstellen von 5-fluor-1-alkyl-3-fluoralkyl-1h-pyrazol-4-carbonsäurechloriden und -fluoriden |
| PL2576517T3 (pl) * | 2010-06-03 | 2015-06-30 | Bayer Ip Gmbh | N-[(het)aryloalkilo)]pirazolo(tio)karboksyamidy i ich analogi heteropodstawione |
| MX2013004278A (es) * | 2010-10-21 | 2013-06-05 | Bayer Ip Gmbh | N-bencil carboxamidas heterociclicas. |
| WO2012059497A1 (en) | 2010-11-02 | 2012-05-10 | Bayer Cropscience Ag | N-hetarylmethyl pyrazolylcarboxamides |
| BR112013017060A2 (pt) | 2011-01-05 | 2016-09-20 | Syngenta Participations Ag | derivados de pirasol-4-il carboxamida como microbiocidas |
| ES2532715T3 (es) | 2011-02-21 | 2015-03-31 | Syngenta Participations Ag | Nuevos microbicidas de carboxamida |
| DK2699092T3 (en) * | 2011-04-22 | 2016-01-11 | Bayer Ip Gmbh | ACTIVE COMPOSITIONS CONTAINING A FUNGICID CARBOXAMIDE DERIVATIVE AND AN INSECTICID OR ACARICID OR NEMATICID COMPOUND |
| EA023712B1 (ru) * | 2011-04-22 | 2016-07-29 | Байер Интеллекчуал Проперти Гмбх | Комбинации активных соединений, содержащие производное соединение (тио)карбоксамида и фунгицидное соединение |
| TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
| EP2831049B1 (en) | 2012-03-26 | 2016-04-27 | Bayer Intellectual Property GmbH | N-cycloalkyl-n-[(cycloalkenylphenyl)methylene]-(thio)carboxamide derivatives |
| CN104428294B (zh) * | 2012-04-20 | 2017-07-14 | 拜尔农科股份公司 | N‑环烷基‑n‑[(杂环基苯基)亚甲基]‑(硫代)羧酰胺衍生物 |
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| CL2008002241A1 (es) | 2007-07-31 | 2009-12-28 | Bayer Cropscience Sa | Compuestos derivados de (hetero)aril-metilen-n-cicloalquil carboxamida condensados de 6 elementos con n-sustituido; composicion funguicida que comprende uno de dichos compuestos; y metodo para el control hongos fitopatogenos de cultivos agricolas. |
| KR101316247B1 (ko) | 2007-07-31 | 2013-10-08 | 엘지전자 주식회사 | 로터리 식 2단 압축기 |
| ES2359877T3 (es) | 2007-07-31 | 2011-05-27 | Bayer Cropscience Ag | Derivados fungicidas de n-cicloalquil-bencil-tiocarboxamidas o n-cicloalquil-bencil-amidina-n'-sustituida. |
| EP2185548A1 (en) * | 2007-07-31 | 2010-05-19 | Bayer CropScience SA | Fungicide 2-pyridyl-methylene-thio carboxamide or 2-pyridyl-methylene-n-substituted carboximidamide derivatives |
| CL2008002242A1 (es) * | 2007-07-31 | 2009-08-21 | Bayer Cropscience Ag | Compuestos derivados de n-cicloalquil-n-carboxamida, tiocarboxamida, biciclicas o derivados de carboximidamida n-sustituida; composicion fungicida; y metodo para controlar los hongos fitopatogenos de los cultivos. |
| AR076839A1 (es) * | 2009-05-15 | 2011-07-13 | Bayer Cropscience Ag | Derivados fungicidas de pirazol carboxamidas |
| EP2325173A1 (de) * | 2009-11-19 | 2011-05-25 | Bayer CropScience AG | Verfahren zum Herstellen von 5-Fluor-1-alkyl-3-fluoralkyl-1H-pyrazol-4-carbonsäurechloriden |
| EP2560961B1 (de) * | 2010-04-23 | 2016-11-16 | Bayer Intellectual Property GmbH | Verfahren zum herstellen von 5-fluor-1-alkyl-3-fluoralkyl-1h-pyrazol-4-carbonsäurechloriden und -fluoriden |
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