AR045097A1 - Compuestos 2-piridiniletilbenzamida y sus usos como funguicidas - Google Patents
Compuestos 2-piridiniletilbenzamida y sus usos como funguicidasInfo
- Publication number
- AR045097A1 AR045097A1 ARP040102628A ARP040102628A AR045097A1 AR 045097 A1 AR045097 A1 AR 045097A1 AR P040102628 A ARP040102628 A AR P040102628A AR P040102628 A ARP040102628 A AR P040102628A AR 045097 A1 AR045097 A1 AR 045097A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halogen
- group
- halogen atoms
- alkoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 55
- 150000002367 halogens Chemical class 0.000 abstract 48
- 229910052736 halogen Inorganic materials 0.000 abstract 38
- -1 formyloxy group Chemical group 0.000 abstract 19
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 13
- 125000003545 alkoxy group Chemical group 0.000 abstract 10
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 10
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 125000005037 alkyl phenyl group Chemical group 0.000 abstract 8
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 7
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 5
- 125000003277 amino group Chemical group 0.000 abstract 5
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000003282 alkyl amino group Chemical group 0.000 abstract 4
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy 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
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 229940124530 sulfonamide Drugs 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 1
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 abstract 1
- 125000005242 carbamoyl alkyl group Chemical group 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide 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
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 abstract 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/61—Halogen atoms or nitro radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Compuestos de 2-piridiniletibenzamida y sus usos como fungicidas. Procedimiento para preparar este compuesto. Composición fungicida que comprende un compuesto de fórmula general (1). Reivindicación 1: Un compuesto de fórmula general (1) en la que -n es 1, 2 o 3; -X es igual o diferente y es un átomo de H, un átomo de halógeno, un grupo nitro, un grupo ciano, un grupo hidroxi, un grupo amino, un grupo sulfanilo, un grupo pentafluoro-l6-sulfanilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carboxi, un grupo carbamoilo, un grupo N-hidroxicarbamoilo, un grupo carbamato, un grupo (hidroxiimino)-alquilo (C1-6), un grupo alquilo (C1-8), un grupo alquenilo (C2-8), un grupo alquinilo (C2-8), un grupo alquil(C1-8)amino, un grupo di-alquil(C1-8)amino, un grupo alcoxi(C1-8), un grupo halógenoalcoxi (C1-8) de 1 a 5 átomos de halógeno, un alquil (C1-8)sulfanilo, un halógenoalquil(C1-8)sulfanilo de 1 a 5 átomos de halógeno, un alquenil(C2-8)oxi, un halógenoalquenil(C2-8)oxi de 1 a 5 átomos de halógeno, un alquinil(C3-8)oxi, un halógenoalquinil(C3-8)oxi de 1 a 5 átomos de halógeno, un cicloalquilo(C3-8), un halógenocicloalquilo(C3-8) de 1 a 5 átomos de halógeno, un alquil(C1-8)carbonilo, un halógenoalquil(C1-8)carbonilo de 1 a 5 átomos de halógeno, un alquil(C1-8)carbamoilo, un di-alquil(C1-8)carbamoilo, un (N-alquil(C1-8))oxicarbamoilo, un alcoxi(C1-8)carbamoilo, un (N-alquil(C1-8))-alcoxi(C1-8)carbamoilo, un alcoxi(C1-8)carbonilo, un halógenoalcoxi(C1-8)carbonilo de 1 a 5 átomos de halógeno, un alquil(C1-8)carboniloxi, un halógenoalquil(C1-8)carboniloxi de 1 a 5 átomos de halógeno, un alquil(C1-8)carbonilamino, halógenoalquil(C1-8)carbonilamino de 1 a 5 átomos de halógeno, un alquil(C1-8)aminocarboniloxi, un di-alquil(C1-8)aminocarboniloxi, un alquil(C1-8)oxicarboniloxi, un alquil(C1-8)sulfenilo, un halógenoalquil(C1-8)sulfenilo de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfinilo, un halógenoalquil(C1-8)sulfinilo de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfonilo, un halógenoalquil(C1-8)sulfonilo de 1 a 5 átomos de halógeno, un (alcoxi(C1-6)imino)-alquilo(C1-6), un (alquenil(C1-6)oxiimino)-alquilo(C1-6), un (alquinil(C1-6)oxiimino)-alquilo(C1-6), un (benciloxiimino)-alquilo(C1-6), un benciloxi, un bencilsulfanilo, un bencilamino, un fenoxi, un fenilsulfanilo o un fenilamino; R1 es un átomo de H, un átomo de halógeno, un grupo nitro, un grupo ciano, un grupo hidroxi, un grupo amino, un grupo sulfanilo, un grupo pentafluoro-l6-sulfanilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carboxi, un grupo carbamoilo, un grupo N-hidroxicarbamoilo, un grupo carbamato, un grupo (hidroxiimino)-alquilo(C1-6), un alquilo(C1-8), un alquenilo (C2-8), un alquinilo(C2-8), un alquil(C1-8)amino, un di-alquil(C1-8)amino, un alcoxi(C1-8), un halógenoalcoxi(C1-8) de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfanilo, un halógenoalquil(C1-8)sulfanilo de 1 a 5 átomos de halógeno, un alquenil(C2-8)oxi, un halógenoalquenil(C2-8)oxi de 1 a 5 átomos de halógeno, un alquinil(C3-8)oxi, un halógenoalquinil(C3-8)oxi de 1 a 5 átomos de halógeno, un cicloalquilo(C3-8), un halógenocicloalquilo(C3-8) de 1 a 5 átomos de halógeno, un alquil(C1-8)carbonilo, un halógenoalquil(C1-8)carbonilo de 1 a 5 átomos de halógeno, un alquil(C1-8)carbamoilo un di-alquil(C1-8)carbamoilo, un N-alquil(C1-8)oxicarbamoilo, un alcoxi(C1-8)carbamoilo, un N-alquil(C1-8)-alcoxi(C1-8)carbamoilo, un alcoxi(C1-8)carbonilo, un halógenoalcoxi(C1-8)carbonilo de 1 a 5 átomos de halógeno, un alquil(C1-8)carboniloxi, un halógenoalquil(C1-8)carboniloxi de 1 a 5 átomos de halógeno, un alquil(C1-8)carbonilamino, un halógenoalquil(C1-8)carbonilamino de 1 a 5 átomos de halógeno, un alquil(C1-8)aminocarboniloxi, un di-alquil(C1-8)aminocarboniloxi, un alquil(C1-8)oxicarboniloxi, un alquil(C1-8)sulfenilo, un halógenoalquil(C1-8)sulfenilo de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfinilo, un halógenoalquil(C1-8)sulfinilo de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfonilo, un halógenoalquil(C1-8)sulfonilo de 1 a 5 átomos de halógeno, un (alcoxi(C1-6)imino)-alquilo(C1-6), un (alquenil(C1-6)oxiimino)-alquilo(C1-6), un (alquinil(C1-6)oxiimino)-alquilo(C1-6), un (benciloxiimino)-alquilo(C1-6), un benciloxi, un bencilsulfanilo opcionalmente sustituido con 1 a 5 átomos de halógeno, un bencilamino, un fenoxi, un fenilsulfanilo opcionalmente sustituido con 1 a 5 átomos de halógeno o un fenilamino; con la condición que X y R1 no sean ambos un átomo de H; -R2 y R3 son iguales o diferentes y son un átomo de H, un átomo de halógeno, un grupo ciano, un grupo hidroxi, un alquilo(C1-6), un halógenoalquilo(C1-6) de 1 a 5 átomos de halógeno, un alquenilo(C2-6), un alcoxi(C1-6), un alquil(C1-6)sulfanilo, un alquil(C1-6)sulfenilo, un alquil(C1-6)sulfinilo, un alcoxi(C1-6)carbonilo, un alquil(C1-6)carboniloxi o un alquil(C1-6)carbonilamino; o R2 y R3 pueden formar juntos un carbociclo de 3, 4, 5 o 6 miembros; R4 y R5 son iguales o diferentes y son un átomo de H, un átomo de halógeno, un grupo ciano, un alquilo(C1-6) o un halógenoalquilo(C1-6) de 1 a 5 átomos de halógeno; o R4 y R5 pueden formar juntos un carbociclo de 3, 4, 5 o 6 miembros; R6 es un átomo de H, un grupo ciano, un grupo formilo, un grupo hidroxi, un grupo alquilo(C1-6), un halógenoalquilo(C1-6) de 1 a 5 átomos de halógeno, un alcoxi(C1-6), un halógenoalcoxi(C1-6) de 1 a 5 átomos de halógeno, un cicloalquilo(C3-6), un halógenocicloalquilo(C3-6) de 1 a 5 átomos de halógeno, un alquenilo(C2-6), un alquinilo(C2-6), un alcoxi(C1-6)-alquilo(C1-6), un cianoalquilo(C1-6), un aminoalquilo(C1-6), un alquil(C1-6)amino-alquilo(C1-6), un di-alquil(C1-6)amino-alquilo(C1-6), un alquil(C1-6)carbonilo, un halógenoalquil(C1-6)carbonilo de 1 a 5 átomos de halógeno, un alquil(C1-6)oxicarbonilo, un benciloxicarbonilo, un alcoxi(C1-6)-alquil(C1-6)carbonilo, un alquil(C1-6)sulfonilo o un halógenoalquil(C1-6)sulfonilo de 1 a 5 átomos de halógeno; -p es 1, 2, 3 o 4; Y es igual o diferente y es un átomo de H, un átomo de halógeno, un grupo nitro, un grupo ciano, un grupo hidroxi, un grupo amino, un grupo sulfanilo, un grupo pentafluoro-l6-sulfanilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carboxi, un alquilo(C1-8), un halógenoalquilo(C1-8) de 1 a 5 átomos de halógeno, un alquenilo(C2-8), un alquinilo (C2-8), un alquil(C1-8)amino, un di-alquil(C1-8)amino, un alcoxi(C1-8), un halógenoalcoxi(C1-8) de 1 a 5 átomos de halógeno, un alcoxi(C1-8)-alquenilo(C2-8), un alquil(C1-8)sulfanilo, un halógenoalquil(C1-8)sulfanilo de 1 a 5 átomos de halógeno, un alcoxi(C1-8)carbonilo, un halógenoalcoxi(C1-8)carbonilo de 1 a 5 átomos de halógeno, un alquil(C1-8)carboniloxi, un halógenoalquil(C1-8)carboniloxi de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfenilo, un halógenoalquil(C1-8)sulfenilo de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfinilo, un halógenoalquil(C1-8)sulfinilo de 1 a 5 átomos de halógeno, un alquil(C1-8)-sulfonilo, un halógenoalquil(C1-8)sulfonilo de 1 a 5 átomos de halógeno, o una alquil(C1-8)sulfonamida; y R7 es un átomo de halógeno, un grupo nitro, un grupo ciano, un grupo amino, un grupo sulfanilo, un grupo pentafluoro-l6-sulfanilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carboxi, un alquilo(C1-8), un halógenoalquilo(C1-8) de 1 a 5 átomos de halógeno, un alquenilo(C2-8), un alquinilo(C2-8), un alquil(C1-8)amino, un di-alquil(C1-8)amino, un alcoxi(C1-8), un halógenoalcoxi(C1-8) de 1 a 5 átomos de halógeno, un alcoxi(C1-8)-alquenilo(C2-8), un alquil(C1-8)sulfanilo, un halógenoalquil(C1-8)sulfanilo de 1 a 5 átomos de halógeno, un alcoxi (C1-8)carbonilo, un halógenoalcoxi (C1-8)carbonilo de 1 a 5 átomos de halógeno, un alquil(C1-8)carboniloxi, un halógenoalquil(C1-8)carboniloxi de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfenilo, un halógenoalquil(C1-8)sulfenilo de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfinilo, un halógenoalquil(C1-8)sulfinilo de 1 a 5 átomos de halógeno, un alquil(C1-8)sulfonilo, un halógenoalquil(C1-8)sulfonilo de 1 a 5 átomos de halógeno o una alquil(C1-8)sulfonamida; así como sus sales, N-óxidos, complejos metálicos y metaloides.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03356116A EP1500651A1 (en) | 2003-07-25 | 2003-07-25 | N-[2-(2-Pyridinyl)ethyl]benzamide compounds and their use as fungicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR045097A1 true AR045097A1 (es) | 2005-10-12 |
Family
ID=33484064
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040102628A AR045097A1 (es) | 2003-07-25 | 2004-07-23 | Compuestos 2-piridiniletilbenzamida y sus usos como funguicidas |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US7723364B2 (es) |
| EP (2) | EP1500651A1 (es) |
| JP (1) | JP4857108B2 (es) |
| KR (1) | KR101130600B1 (es) |
| CN (1) | CN1826320B (es) |
| AR (1) | AR045097A1 (es) |
| AU (1) | AU2004262580B9 (es) |
| BR (1) | BRPI0411501B1 (es) |
| CA (1) | CA2532176C (es) |
| CO (1) | CO5660288A2 (es) |
| CR (1) | CR8197A (es) |
| EC (1) | ECSP056220A (es) |
| ES (1) | ES2529569T3 (es) |
| IL (1) | IL172230A (es) |
| MX (1) | MXPA06000889A (es) |
| PL (3) | PL1651604T3 (es) |
| PT (1) | PT1651604E (es) |
| RU (1) | RU2352562C2 (es) |
| TW (1) | TWI361185B (es) |
| UA (1) | UA86594C2 (es) |
| WO (1) | WO2005014545A2 (es) |
| ZA (1) | ZA200600691B (es) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI368482B (en) * | 2003-12-19 | 2012-07-21 | Bayer Sas | New 2-pyridinylethylbenzamide derivatives |
| EP1674455A1 (en) * | 2004-12-21 | 2006-06-28 | Bayer CropScience S.A. | Process for the preparation of a 2-ethylaminopyridine derivative |
| ES2383903T3 (es) * | 2004-12-21 | 2012-06-27 | Bayer Cropscience Ag | Procedimiento para la preparación de un derivado de 2-piridiletilcarboxamida |
| DE602006003756D1 (de) * | 2005-05-03 | 2009-01-02 | Bayer Cropscience Sa | Neue heterocyclylethylbenzamid-derivate |
| PT1885712E (pt) | 2005-05-18 | 2011-04-29 | Bayer Cropscience Ag | Novos derivados de 2-piridinilcicloalquilcrboxamida como fungicidas |
| TWI435863B (zh) * | 2006-03-20 | 2014-05-01 | Nihon Nohyaku Co Ltd | N-2-(雜)芳基乙基甲醯胺衍生物及含該衍生物之蟲害防治劑 |
| MX2008016538A (es) | 2006-07-06 | 2009-01-19 | Bayer Cropscience Ag | Composicion pesticida que comprende un derivado de piridiletilbenzamida y un compuesto insecticida. |
| JP2009542601A (ja) * | 2006-07-06 | 2009-12-03 | バイエル・クロツプサイエンス・エス・アー | N−(4−ピリジン−2−イルブチル)ベンズアミド誘導体及び殺真菌剤としてのその使用 |
| EP2081900A2 (en) * | 2006-10-18 | 2009-07-29 | Bayer CropScience SA | New n-(3-pyridin-2-ylpropyl)benzamide derivatives |
| WO2008061866A1 (en) * | 2006-11-20 | 2008-05-29 | Bayer Cropscience Sa | New benzamide derivatives |
| EP2606728A1 (en) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | Compounds with nematicidal activity |
| PH12014500977A1 (en) | 2011-11-02 | 2014-06-09 | Bayer Ip Gmbh | Compounds with nematicidal activity |
| EP2589294A1 (en) | 2011-11-02 | 2013-05-08 | Bayer CropScience AG | Compounds with nematicidal activity |
| MX2014004849A (es) | 2011-11-02 | 2014-08-27 | Bayer Ip Gmbh | Compuesto con actividad nematicida. |
| EP2589292A1 (en) | 2011-11-02 | 2013-05-08 | Bayer CropScience AG | Compounds with nematicidal activity |
| EP2606727A1 (en) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | Compounds with nematicidal activity |
| PL2782565T3 (pl) | 2011-11-25 | 2020-08-24 | Bayer Intellectual Property Gmbh | Zastosowanie arylo- i heteroarylokarboksyamidów jako środki endopasożytobójcze |
| TW201427947A (zh) | 2012-10-12 | 2014-07-16 | Lundbeck & Co As H | 環狀胺 |
| EP2730570A1 (de) | 2012-11-13 | 2014-05-14 | Bayer CropScience AG | Pyridyloxyalkylcarboxamide und deren Verwendung als Endoparasitizide und Nematizide |
| CN105121411B (zh) | 2013-04-15 | 2017-10-10 | 杜邦公司 | 杀真菌酰胺 |
| UY35772A (es) | 2013-10-14 | 2015-05-29 | Bayer Cropscience Ag | Nuevos compuestos plaguicidas |
| US10029986B2 (en) | 2014-02-18 | 2018-07-24 | Nissan Chemical Industries, Ltd. | Alkynyl pyridine-substituted amide compound and pesticide |
| KR102610959B1 (ko) * | 2016-12-21 | 2023-12-06 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 니트릴의 촉매적 수소화 |
| CN109293565B (zh) * | 2018-10-26 | 2021-08-06 | 江苏七洲绿色化工股份有限公司 | 一种氟吡菌酰胺的制备方法 |
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| US3900481A (en) * | 1974-04-01 | 1975-08-19 | Riker Laboratories Inc | Derivatives of pyrrolidine and piperidine |
| DE2417763A1 (de) * | 1974-04-11 | 1975-10-30 | Bayer Ag | Carbonsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| DE2428673A1 (de) * | 1974-06-14 | 1976-01-02 | Bayer Ag | Carbonsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| IL84944A (en) * | 1987-01-19 | 1992-02-16 | Ici Plc | Pharmaceutical compositions containing 1,2-dihydro-3h-indazolone derivatives,some new such compounds and their preparation |
| TW575562B (en) * | 1998-02-19 | 2004-02-11 | Agrevo Uk Ltd | Fungicides |
| EP1204323B1 (en) * | 1999-08-18 | 2004-07-14 | Aventis CropScience GmbH | Fungicides |
| MXPA03002338A (es) * | 2000-09-18 | 2003-09-10 | Du Pont | Piridinilamidas y piridinilimidas para uso como fungicidas. |
| WO2004016088A2 (en) * | 2002-08-12 | 2004-02-26 | Bayer Cropscience S.A. | Novel 2-pyridylethylbenzamide derivative |
| EP1389614A1 (fr) * | 2002-08-12 | 2004-02-18 | Bayer CropScience S.A. | Nouveaux dérivés de N-[2-(2-pyridyl)éthyl]benzamide comme fongicides |
-
2003
- 2003-07-25 EP EP03356116A patent/EP1500651A1/en not_active Withdrawn
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2004
- 2004-06-24 TW TW093118326A patent/TWI361185B/zh not_active IP Right Cessation
- 2004-07-19 UA UAA200602052A patent/UA86594C2/uk unknown
- 2004-07-19 ES ES04764137.8T patent/ES2529569T3/es not_active Expired - Lifetime
- 2004-07-19 KR KR1020057023687A patent/KR101130600B1/ko not_active Expired - Fee Related
- 2004-07-19 MX MXPA06000889A patent/MXPA06000889A/es active IP Right Grant
- 2004-07-19 EP EP04764137.8A patent/EP1651604B1/en not_active Expired - Lifetime
- 2004-07-19 WO PCT/EP2004/009145 patent/WO2005014545A2/en not_active Ceased
- 2004-07-19 CA CA2532176A patent/CA2532176C/en not_active Expired - Fee Related
- 2004-07-19 US US10/566,051 patent/US7723364B2/en not_active Expired - Fee Related
- 2004-07-19 PL PL04764137T patent/PL1651604T3/pl unknown
- 2004-07-19 AU AU2004262580A patent/AU2004262580B9/en not_active Ceased
- 2004-07-19 CN CN2004800191713A patent/CN1826320B/zh not_active Expired - Fee Related
- 2004-07-19 PL PL407615A patent/PL407615A1/pl unknown
- 2004-07-19 PT PT47641378T patent/PT1651604E/pt unknown
- 2004-07-19 BR BRPI0411501-5A patent/BRPI0411501B1/pt not_active IP Right Cessation
- 2004-07-19 RU RU2006105492/04A patent/RU2352562C2/ru not_active IP Right Cessation
- 2004-07-19 PL PL379385A patent/PL379385A1/pl unknown
- 2004-07-19 JP JP2006520820A patent/JP4857108B2/ja not_active Expired - Fee Related
- 2004-07-23 AR ARP040102628A patent/AR045097A1/es not_active Application Discontinuation
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- 2005-11-28 IL IL172230A patent/IL172230A/en active IP Right Grant
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2006
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- 2006-01-24 ZA ZA200600691A patent/ZA200600691B/en unknown
- 2006-01-30 CO CO06008282A patent/CO5660288A2/es not_active Application Discontinuation
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