AR066613A1 - Derivados fungicidas de fenil-pirimidinil-amino - Google Patents
Derivados fungicidas de fenil-pirimidinil-aminoInfo
- Publication number
- AR066613A1 AR066613A1 ARP080102095A ARP080102095A AR066613A1 AR 066613 A1 AR066613 A1 AR 066613A1 AR P080102095 A ARP080102095 A AR P080102095A AR P080102095 A ARP080102095 A AR P080102095A AR 066613 A1 AR066613 A1 AR 066613A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- unsubstituted
- alkyl
- halogen atoms
- group
- 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 49
- -1 phenyl-pyrimidinyl-amino Chemical class 0.000 abstract 21
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 17
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000001188 haloalkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 4
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 4
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 3
- 125000003277 amino group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000005115 alkyl carbamoyl 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
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 238000000034 method Methods 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
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 abstract 1
- 125000005353 silylalkyl group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 1
- 125000004963 sulfonylalkyl group Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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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
- 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
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-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
- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D417/14—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 three or more hetero rings
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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Se refiere a procedimiento de preparacion, a la preparacion de compuestos intermedios, a su utilizacion como agentes fungicidas activos, específicamente en forma de composiciones fungicidas, y a los métodos para el control de hongos fitopatogenos,especialmente de plantas, utilizando estos compuestos o composiciones. Reivindicacion 1: Un derivado de fenil-pirimidinil-amino de formula (1) en donde Q1 independientemente representa un átomo de halogeno, un grupo nitro, un grupo hidroxi, ungrupo ciano, un grupo amino, un grupo sulfanilo, un grupo pentafluoro-?6-sulfanilo , un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carbamoilo, un grupo N-hidroxicarbamoílo, un grupo carbamato, un grupo (hidroxiimino)-alquil C1-6, un alquilo C1-8, un tri(alquil C1-8)silil-alquil C1-8 sustituido o no sustituido, un cicloalquilo C1-8 sustituido o no sustituido, tri(alquil C1-6)silil-cicloalquil C1-8 sustituido o no sustituido, un halogenoalquil C1-8 que tiene 1 a 5 átomos dehalogeno, un haIogenocicloalquilo C1-8 que tiene 1 a 5 átomos de halogeno, un alquenilo C2-8, un alquinilo C2-8, un alquenil C2-8-oxi, un alquinil C2-8-oxi, un alquil C1-8-amino, un di-alquil C1-8-amino, un alcoxi C1-8, un halogenoalcoxi C1-8 quetiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfanilo, un halogenoalquil C1-8-sulfanilo que tiene 1 a 5 tomos de halogeno, un alquenil C2-8-oxi, un halogenoalquenil C2-8-oxi que tiene 1a 5 átomos de halogeno, un alquinil C3-8-oxi, unhalogenoalquinil C3-8-oxi que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carbonilo, un halogenoalquil C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carbamoilo, un di-alquil C1-8-carbamoilo un alquil N-C1-8-oxicarbamoílo, unalcoxi C1-8-carbamoílo, un N-alquil C1-8-alcoxi C1-8-carbamoílo, un alcoxi C1-8-carbonilo, un halogenoalcoxi C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carboniloxi, un haIogenoalquil C1-8-carboniloxi que tiene 1 a 5 átomos dehalogeno, un alquil C1-8-carbonilamino, un halogenoalquil C1-8-carbonilamino que tiene 1 a 5 átomos de halogeno, un alquil C1-8-aminocarboniloxi, un di-alquil C1-8-aminocarboniloxi, un alquil C1-8-oxicarboniloxi, un alquil C1-8-sulfenilo, unhalogenoalquil C1-8-sulfenilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfinilo, un halogenoalquil C1-8-sulfinilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfonilo, un halogenoalquil C1-8-sulfonilo que tiene 1 a 5 átomos dehalogeno, un alquil C1-8-aminosulfamoilo, un dialquil C1-8-aminosulfamoilo, un (alcoxi C1-6-imino)- alquil C1-6, un alquenil (C1-6-oxiimino)-alquil C1-6, un alquinil (C1-6-oxiimino)-aIquil C1-6, un 2-oxopirrolidin-1-ilo, (benciloxiimino)-alquil C1-6sustituido o no sustituido, alcoxialquil C1-8 sustituido o no sustituido, halogenoalcoxialquilo C1-8 sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, benciloxi sustituido o no sustituido, bencilsulfanilo sustituido o no sustituido,bencilamino sustituido o no sustituido, fenoxi sustituido o no sustituido, fenilsulfanilo sustituido o no sustituido o fenilamino sustituido o no sustituido; p representa 0,1, 2, 3, 4 o 5; Ra representa un átomo de hidrogeno, un grupo ciano, ungrupo formilo, un grupo formiloxi, un alcoxi C1-8-carbonilo, un halogenoalcoxi C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carbonilo, un halogenoalquil C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfonilo, un halogenoalquil C1-8-sulfonilo que tiene 1 a 5 átomos de halogeno, un alquilo C1-8, un cicloalquilo C1-8, un halogenoalquilo C1-8 que tiene 1 a 5 átomos de halogeno, un halogenocicloalquilo C1-8 que tiene 1 a 5 átomos de halogeno, unalquenilo C2-8, un alquinilo C2-8, un alcoxialquilo C1-6, un halogenoalcoxialquilo C1-8 que tiene 1 a 5 átomos de halogeno, Rb y Rc independientemente representan un átomo de hidrogeno, un átomo de halogeno, un ciano, un alquilo C1-8, uncicloalquilo C1-8, un halogenoalquilo C1-8 que tiene 1 a 5 átomos de halogeno, un halogenocicloalquilo C1-8 que tiene 1 a 5 átomos de halogeno; L1 representa un resto piridilo sustituido o no sustituido; Y representa O, S, NRd, CReRf; L2 representaun enlace directo, O, S, NR9, CRhRi; Q2 representa un átomo de hidrogeno, un átomo de halogeno, un grupo nitro, un grupo hidroxi, un grupo ciano, un grupo amino, un grupo sulfanilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, ungrupo carbamoílo, un grupo N-hidroxicarbamoílo, un grupo carbamato, un grupo (hidroxiimino)-alquilo C1-6 sustituido o no sustituido, alquilo C1-8 sustituido o no sustituido, tri(alquil C1-8)sililo-alquilo C1-8 sustituido o no sustituido,cicloalquilo C1-8 sustituido o no sustituido, tri(alquil C1-8)sililo-cicloalquilo C1-8 sustituido o no sustituido, halogenoalquilo C1-8 sustituido o no sustituido que tiene de 1 a 5 átomos de halogeno, halogenocicloalquilo C1-8 sustituido o nosustituido que tiene 1 a 5 átomos de halogeno, un alquenilo C2-8, alquinilo C2-8 sustituido o no sustituido, alquil C1-8 amino sustituido o no sustituido, di-alquil C1-8 amino sustituido o no sustituido, alcoxi C1-6 sustituido o no sustituido,halogenoalcoxi C1-8 sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquenil C2-8 oxi sustituido o no sustituido, alquinil C2-8 oxi sustituido o no sustituido, alquil C1-8-sulfanilo sustituido o no sustituido, halogenoalquil C1-8-sulfanilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquenil C2-8-oxi sustituido o no sustituido, halogenoalquenil C2-8 oxi sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquinil C3-8-oxi sustituido o nosustituido, halogenoalquinil C3-8-oxi sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-carbonilo sustituido o no sustituido, halogenoalquil C1-8 carbonilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno,alquil C1-8-carbamoilo sustituido o no sustituido, di-alquil C1-8-carbamoilo sustituido o no sustituido, alquil N-C1-8-oxicarbamoilo sustituido o no sustituido, alcoxi C1-8-carbamoilo sustituido o no sustituido, N-alquil C1-8-alcoxi C1-8-carbamoilosustituido o no sustituido, alcoxi C1-8-carbonilo sustituido o no sustituido, halogenoalcoxi C1-8-carbonilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-carboniloxi sustituido o no sustituido, halogenoalquil C1-8-carboniloxi sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-carbonilamino sustituido o no sustituido, halogenoalquil C1-8-carbonilamino sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-aminocarboniloxi sustituido o no sustituido, dialquil C1-8-aminocarboniloxi sustituido o no sustituido, alquil C1-8-oxicarboniloxi sustituido o no sustituido, alquil C1-8-sulfenilo sustituido o no sustituido, halogenoalquil C1-8-sulfenilo sustituidoo no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-sulfinilo sustituido o no sustituido, halogenoalquil C1-8-sulfinilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-sulfonilo sustituido o no sustituido,halogenoalquil C1-8-sulfonilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-aminosulfamoilo sustituido o no sustituido, dialquil C1-8-aminosulfamoilo sustituido o no sustituido, (alcoxi C1-6-imino)-alquil C1-6 sustituidoo no sustituido, alquenil (C1-6-oxiimino)-alquil C1-6 sustituido o no sustituido, (alquinil C1-6-oxiimino)-alquilo C1-6 sustituido o no sustituido, (2-oxopirrolidin-1-il) alquilo C1-8, (2-oxopirrolidin-1-il) halogenoalquil C1-8 que tiene 1 a 5átomos de halogeno, (2-oxopiperidin-1-il) alquil C1-8, (2-oxopiperidin-1-il) halogenoalquil C1-8 que tiene 1 a 5 átomos de halogeno, (2-oxoazepan-1-il) alquil C1-8, (2-oxoazepan-1-il) halogenoalquil C1-8 que tiene 1 a 5 átomos de halogeno,(benciloxiimino)-alquil C1-6 sustituido o no sustituido, alcoxialquil C1-8 sustituido o no sustituido, halogenoalcoxi C1-8 alquil sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, benciloxi sustituido o no sustituido, bencilsulfanilosustituido o no sustituido, bencilamino sustituido o no sustituido, fenoxi sustituido o no sustituido, fenilsulfanilo sustituido o no sustituido, fenilamino sustituido o no sustituido, un heterociclo sustituido o no sustituido de 4, 5, 6 o 7elementos que comprende hasta 4 heteroátomos seleccionados en la lista consistente en N, O, S; L2 y Q2 puede formar conjuntamente un heterociclo de 4, 5, 6 o 7 elementos sustituido o no sustituido, que comprende hasta 4 heteroátomos seleccionados enla lista consistente en N, O, S; Rd, Re, Rf, Rg, Rh y Ri representan independientemente un átomo de hidrogeno, un átomo de halogeno, un grupo nitro, un grupo ciano, un grupo hidroxi, un grupo amino, un grupo sulfanilo, un grupo formilo, un grupoformiloxi, un grupo formilamino, un grupo carbamoilo, un grupo N-hidroxicarbamoílo, un grupo carbamato, un grupo (hidroxiimino)-alquilo C1-6 sustituido o no sustituido, alquilo C1-8 sustituido o no sustituido, tri(alquil C1-8)sililo, tri( alquil C1-8)sililo-alquilo C1-8 sustituido o no sustituido, cicloalquilo C1-8 sustituido o no sustituido, tri(alquil C1-8)silil-cicloalquilo C1-8 sustituido o no sustituido, halogenoalquilo C18 sustituido o no sustituido que tiene de 1 a 5 átomos de halogeno,halogenocicloalquilo C1-8 sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, un alquenilo C2-8, alquinilo C2-8 sustituido o no sustituido, alquil C1-8 amino sustituido o no sustituido, di-alquil C1-8 amino sustituido o no sustituido,alcoxi C1-8 sustituido o no sustituido, halogenoalcoxi C1-8 sustituido o no sustituido que tiene 1 a 5 tomos de halogeno, alquenil C2-8-oxi sustituido o no sustituido, alquinil C2-8-oxi sustituido o no sustituido, alquil C1-8-sulfanilo sustituido ono sustituido, halogenoalquil C1-8-sulfanilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquenil C2-8-oxi sustituido o no sustituido, halogenoalquenil C2-8-oxi sustituido o no sustituido que tiene 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07356067 | 2007-05-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR066613A1 true AR066613A1 (es) | 2009-09-02 |
Family
ID=38694918
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080102095A AR066613A1 (es) | 2007-05-16 | 2008-05-16 | Derivados fungicidas de fenil-pirimidinil-amino |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20100137309A1 (es) |
| EP (1) | EP2155713A1 (es) |
| JP (1) | JP2010526856A (es) |
| KR (1) | KR20100017181A (es) |
| CN (1) | CN101687839A (es) |
| AR (1) | AR066613A1 (es) |
| AU (1) | AU2008249959A1 (es) |
| BR (1) | BRPI0809755A2 (es) |
| CA (1) | CA2683074A1 (es) |
| CL (1) | CL2008001460A1 (es) |
| CO (1) | CO6251205A2 (es) |
| IL (1) | IL201319A0 (es) |
| MX (1) | MX2009012217A (es) |
| RU (1) | RU2459819C2 (es) |
| TW (1) | TW200901880A (es) |
| WO (1) | WO2008138992A1 (es) |
| ZA (1) | ZA200907389B (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010055077A1 (en) * | 2008-11-13 | 2010-05-20 | Bayer Cropscience Sa | Substituted (pyridyl)-azinylamine derivatives as fungicides |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0310550B1 (de) * | 1987-09-28 | 1993-05-26 | Ciba-Geigy Ag | Schädlingsbekämpfungsmittel |
| ES2167377T3 (es) * | 1993-10-01 | 2002-05-16 | Novartis Ag | Derivados de piridina farmacologicamente activos y procedimientos para la preparacion de los mismos. |
| DE69434721T2 (de) * | 1993-10-01 | 2006-11-09 | Novartis Ag | Pharmacologisch wirksame pyrimidinderivate und verfahren zu deren herstellung |
| CA2148931A1 (en) * | 1993-10-01 | 1995-04-13 | Jurg Zimmermann | Pyrimidineamine derivatives and processes for the preparation thereof |
| GB0014022D0 (en) * | 2000-06-08 | 2000-08-02 | Novartis Ag | Organic compounds |
| WO2002024681A2 (en) * | 2000-09-20 | 2002-03-28 | Ortho-Mcneil Pharmaceutical, Inc. | Pyrazine derivatives as modulators of tyrosine kinases |
| GB0100102D0 (en) * | 2001-01-03 | 2001-02-14 | Syngenta Participations Ag | Organic compounds |
| GB0123589D0 (en) * | 2001-10-01 | 2001-11-21 | Syngenta Participations Ag | Organic compounds |
| WO2003037891A1 (en) * | 2001-11-01 | 2003-05-08 | Janssen Pharmaceutica N.V. | Heteroaryl amines as glycogen synthase kinase 3beta inhibitors (gsk3 inhibitors) |
| GB0129476D0 (en) * | 2001-12-10 | 2002-01-30 | Syngenta Participations Ag | Organic compounds |
| GB0307268D0 (en) * | 2003-03-28 | 2003-05-07 | Syngenta Ltd | Organic compounds |
| WO2010055077A1 (en) * | 2008-11-13 | 2010-05-20 | Bayer Cropscience Sa | Substituted (pyridyl)-azinylamine derivatives as fungicides |
-
2008
- 2008-05-16 MX MX2009012217A patent/MX2009012217A/es not_active Application Discontinuation
- 2008-05-16 AR ARP080102095A patent/AR066613A1/es not_active Application Discontinuation
- 2008-05-16 KR KR1020097024205A patent/KR20100017181A/ko not_active Withdrawn
- 2008-05-16 US US12/451,440 patent/US20100137309A1/en not_active Abandoned
- 2008-05-16 CN CN200880016299A patent/CN101687839A/zh active Pending
- 2008-05-16 AU AU2008249959A patent/AU2008249959A1/en not_active Abandoned
- 2008-05-16 RU RU2009146565/04A patent/RU2459819C2/ru not_active IP Right Cessation
- 2008-05-16 CL CL2008001460A patent/CL2008001460A1/es unknown
- 2008-05-16 EP EP08759704A patent/EP2155713A1/en not_active Withdrawn
- 2008-05-16 TW TW097118186A patent/TW200901880A/zh unknown
- 2008-05-16 JP JP2010507936A patent/JP2010526856A/ja not_active Withdrawn
- 2008-05-16 BR BRPI0809755-0A patent/BRPI0809755A2/pt not_active Application Discontinuation
- 2008-05-16 WO PCT/EP2008/056072 patent/WO2008138992A1/en not_active Ceased
- 2008-05-16 CA CA002683074A patent/CA2683074A1/en not_active Abandoned
-
2009
- 2009-10-01 IL IL201319A patent/IL201319A0/en unknown
- 2009-10-21 ZA ZA200907389A patent/ZA200907389B/xx unknown
- 2009-12-14 CO CO09142656A patent/CO6251205A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0809755A2 (pt) | 2014-09-23 |
| CL2008001460A1 (es) | 2008-11-21 |
| KR20100017181A (ko) | 2010-02-16 |
| TW200901880A (en) | 2009-01-16 |
| MX2009012217A (es) | 2009-12-01 |
| US20100137309A1 (en) | 2010-06-03 |
| WO2008138992A1 (en) | 2008-11-20 |
| ZA200907389B (en) | 2010-07-28 |
| RU2009146565A (ru) | 2011-06-27 |
| RU2459819C2 (ru) | 2012-08-27 |
| CN101687839A (zh) | 2010-03-31 |
| CO6251205A2 (es) | 2011-02-21 |
| CA2683074A1 (en) | 2008-11-20 |
| IL201319A0 (en) | 2010-05-31 |
| JP2010526856A (ja) | 2010-08-05 |
| EP2155713A1 (en) | 2010-02-24 |
| AU2008249959A1 (en) | 2008-11-20 |
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Legal Events
| Date | Code | Title | Description |
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| FA | Abandonment or withdrawal |