AR071769A1 - Azoles sustituidos como fungicidas, una composicion fungicida que comprende el compuesto y un metodo para controlar enfermedades de las plantas - Google Patents
Azoles sustituidos como fungicidas, una composicion fungicida que comprende el compuesto y un metodo para controlar enfermedades de las plantasInfo
- Publication number
- AR071769A1 AR071769A1 ARP090101679A ARP090101679A AR071769A1 AR 071769 A1 AR071769 A1 AR 071769A1 AR P090101679 A ARP090101679 A AR P090101679A AR P090101679 A ARP090101679 A AR P090101679A AR 071769 A1 AR071769 A1 AR 071769A1
- Authority
- AR
- Argentina
- Prior art keywords
- ring
- independently selected
- members
- alkyl
- carbon
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000000203 mixture Substances 0.000 title abstract 3
- 201000010099 disease Diseases 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 239000000417 fungicide Substances 0.000 title 2
- 230000000855 fungicidal effect Effects 0.000 title 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 14
- 125000001424 substituent group Chemical group 0.000 abstract 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 10
- 229910052799 carbon Inorganic materials 0.000 abstract 10
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 10
- 125000004122 cyclic group Chemical group 0.000 abstract 9
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 7
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 7
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 125000001188 haloalkyl group Chemical group 0.000 abstract 7
- 229910052717 sulfur Inorganic materials 0.000 abstract 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 6
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 6
- 125000000278 alkyl amino alkyl group Chemical group 0.000 abstract 6
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 6
- 125000005842 heteroatom Chemical group 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 239000011593 sulfur Substances 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 4
- -1 C1- alkyl 6 Chemical group 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 4
- 125000003282 alkyl amino group Chemical group 0.000 abstract 3
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 3
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000006448 cycloalkyl cycloalkyl group Chemical group 0.000 abstract 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 125000005724 cycloalkenylene group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 244000053095 fungal pathogen Species 0.000 abstract 1
- 125000006769 halocycloalkoxy group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000004665 trialkylsilyl group Chemical group 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
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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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
- 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
- A01N43/56—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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with 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
- C07D233/68—Halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with 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
- C07D233/88—Nitrogen atoms, e.g. allantoin
-
- 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
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
-
- 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
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Tambien se divulgan composiciones que contienen los compuestos de la formula (1) y metodos para controlar enfermedades en plantas causadas por un patogeno fungico que comprende aplicar una cantidad efectiva de un compuesto o una composicion de la presente. Reivindicacion 1: Un compuesto caracterizado porque se selecciona entre la formula (1), N-oxidos, y sales de los mismos, donde: J es Q2 o R1; X es N, CR2 o CQ3; Y es N o CR3; Z es N o CR4; Q1 es un anillo fenilo o un sistema de anillos naftalenilo, donde cada anillo o sistema de anillos est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5a; o un anillo heteroc¡clico totalmente insaturado de 5 o 6 miembros o un sistema de anillos bic¡clico heteroarom tico de entre 8 y 10 miembros, donde cada anillo o sistema de anillos contiene miembros del anillo seleccionados entre tomos de carbono y hasta 4 hetero tomos seleccionados en forma independiente entre hasta 2 O, hasta 2 S y hasta 4 N, donde hasta 3 miembros carbono del anillo se seleccionan en forma independiente entre C(=O) y C(=S), y los miembros azufre del anillo se seleccionan en forma independiente entre S(O)p(=NR6)f, donde cada anillo o sistema de anillos est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5a sobre miembros carbono del anillo y seleccionados entre ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, alcoxi C1-6, alcoxialquilo C2-6, alquilcarbonilo C2-6, alcoxicarbonilo C2-6, alquilaminoalquilo C2-6 y dialquilaminoalquilo C3-6 sobre miembros nitrogeno del anillo; o C(R7aR7b)W1; W1 es un anillo fenilo opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5a; o un anillo heteroc¡clico totalmente insaturado de 5 o 6 miembros que contiene miembros del anillo seleccionados entre tomos de carbono y hasta 4 hetero tomos seleccionados en forma independiente entre hasta 2 O, hasta 2 S y hasta 4 N, donde hasta 2 miembros carbono del anillo se seleccionan en forma independiente entre C(=O) y C(=S), y los miembros azufre del anillo se seleccionan en forma independiente entre S(=O)p(=NR6)f, el anillo est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5a sobre miembros carbono del anillo y seleccionados entre ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, alcoxi C1-6, alcoxialquilo C2-6, alquilcarbonilo C2-6, alcoxicarbonilo C2-6, alquilaminoalquilo C2-6 y dialquilaminoalquilo C3-6 sobre miembros nitrogeno del anillo; Q2 es un anillo fenilo o un sistema de anillos naftalenilo, donde cada anillo o sistema de anillos est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5b; o un anillo heteroc¡clico totalmente insaturado de 5 o 6 miembros o un sistema de anillos bic¡clico heteroarom tico de entre 8 y 10 miembros, donde cada anillo o sistema de anillos contiene miembros del anillo seleccionados entre tomos de carbono y hasta 4 hetero tomos seleccionados en forma independiente entre hasta 2 O, hasta 2 S y hasta 4 N, donde hasta 3 miembros carbono del anillo se seleccionan en forma independiente entre C(=O) y C(=S), y los miembros azufre del anillo se seleccionan en forma independiente entre S(=O)p(=NR6)f, donde cada anillo o sistema de anillos est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5b sobre miembros carbono del anillo y seleccionados entre ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, alcoxi C1-6, alcoxialquilo C2-6, alquilcarbonilo C2-6, alcoxicarbonilo C2-6, alquilaminoalquilo C2-6 y dialquilaminoalquilo C3-6 sobre miembros nitrogeno del anillo; o C(R7aR7b)W2; W2 es un anillo fenilo opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5b; o un anillo heteroc¡clico totalmente insaturado de 5 o 6 miembros que contiene miembros del anillo seleccionados entre tomos de carbono y hasta 4 hetero tomos seleccionados en forma independiente entre hasta 2 O, hasta 2 S y hasta 4 N donde hasta 2 miembros carbono del anillo se seleccionan en forma independiente entre C(=O) y C(=S), y los miembros azufre del anillo se seleccionan en forma independiente entre S(=O)p(NR6)f, el anillo est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5b sobre miembros carbono del anillo y seleccionados entre ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, alcoxi C1-6, alcoxialquilo C2-6, alquilcarbonilo C2-6, alcoxicarbonilo C2-6, alquilaminoalquilo C2-6 y dialquilaminoalquilo C3-6 sobre miembros nitrogeno del anillo; Q3 es un anillo fenilo o un sistema de anillos naftalenilo, donde cada anillo o sistema de anillos est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5c; o un anillo heteroc¡clico totalmente insaturado de 5 o 6 miembros o un sistema de anillos bic¡clico heteroarom tico de entre 8 y 10 miembros, donde cada anillo o sistema de anillos contiene miembros del anillo seleccionados entre tomos de carbono y hasta 4 hetero tomos seleccionados en forma independiente entre hasta 2 O, hasta 2 S y hasta 4 N, donde hasta 3 miembros carbono del anillo se seleccionan en forma independiente entre C(=O) y C(=S), y los miembros azufre del anillo se seleccionan en forma independiente entre S(=O)p(NR6)f, donde cada anillo o sistema de anillos est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5c sobre miembros carbono del anillo y seleccionados entre ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, alcoxi C1-6, alcoxialquilo C2-6, alquilcarbonilo C2-6, alcoxicarbonilo C2-6, alquilaminoalquilo C2-6 y dialquilaminoalquilo C3-6 sobre miembros nitrogeno del anillo; o C(R7aR7b)W3; W3 es un anillo fenilo opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5c; o un anillo heteroc¡clico totalmente insaturado de 5 o 6 miembros que contiene miembros del anillo seleccionados entre tomos de carbono y hasta 4 hetero tomos seleccionados en forma independiente entre hasta 2 O, hasta 2 S y hasta 4 N, donde hasta 2 miembros carbono del anillo se seleccionan en forma independiente entre C(=O) y C(=S), y los miembros azufre del anillo se seleccionan en forma independiente entre S(=O)p(=NR6)f, el anillo est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre R5c sobre miembros carbono del anillo y seleccionados entre ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, alcoxi C1-6, alcoxialquilo C2-6, alquilcarbonilo C2-6, alcoxicarbonilo C2-6, alquilaminoalquilo C2-6 y dialquilaminoalquilo C3-6 sobre miembros nitrogeno del anillo; R1 es alquilo C1-7, alquenilo C2-7, alquinilo C2-7, haloalquilo C1-7, haloalquenilo C2-7, cicloalquilo C3-7, halocicloalquilo C3-7, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, cicloalquilcicloalquilo C6-14, alcoxi C1-7, haloalcoxi C1-7, alcoxialquilo C2-7, alquiltio C1-7, haloalquiltio C1-7, alquiltioalquilo C2-7, alquilsulfinilo C1-7, alquilsulfonilo C1-7, haloalquilsulfinilo C1-7, haloalquilsulfonilo C1-7, alquilamino C1-7, dialquilamino C2-7, alquilcarbonilamino C2-7 o hidroxialquilo C1-7; cada R2, R3 y R4 es en forma independiente H, halogeno, ciano, amino, nitro, -CHO, alquenilo C2-7, alquinilo C2-7, haloalquenilo C2-7, cicloalquilo C3-7, halocicloalquilo C3-7, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, cicloalquilcicloalquilo C6-14, alcoxi C1-7, haloalcoxi C1-7, alcoxialquilo C2-7, alquiltio C1-7, haloalquiltio C1-7, alquiltioalquilo C2-7, alquilsulfinilo C1-7, alquilsulfonilo C1-7, haloalquilsulfinilo C1-7, haloalquilsulfonilo C1-7, alquilamino C1-7, dialquilamino C2-7, hidroxialquilo C1-7, -SCN o CH=NOR11; o alquilo C1-7 o haloalquilo C1-7, donde cada uno est opcionalmente sustituido con hasta 3 sustituyentes seleccionados en forma independiente entre hidroxi, ciano, C(=O)OR8, C(=O)NR9aR9b, C(=O)R10 y CH=NOR11; cada R5a, R5b y R5c es en forma independiente halogeno, ciano, hidroxi, nitro, alquilo C1-7, alquenilo C2-7, alquinilo C2-7, haloalquilo C1-7, haloalquenilo C2-7, cicloalquilo C3-7, halocicloalquilo C3-7, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, cicloalquilcicloalquilo C6-14, cicloalcoxi C3-7, halocicloalcoxi C3-7, alcoxi C1-7, haloalcoxi C1-7, alquiltio C1-6, haloalquiltio C1-7, alquilsulfinilo C1-7, alquilsulfonilo C1-7, haloalquilsulfinilo C1-7, haloalquilsulfonilo C1-7, alquilamino C1-7, dialquilamino C2-7, alquilcarbonilo C2-7, alcoxicarbonilo C2-7, alquilcarbonilamino C2-7, trialquilsililo C3-10, SF5, -SCN, C(=S)NH2 o -U-V-T; cada U es en forma independiente O, S(=O)n, NR12 o un enlace directo; cada V es en forma independiente alquileno C1-6, alquenileno C2-6, alquinileno C3-6, cicloalquileno C3-6 o cicloalquenileno C3-6, donde hasta 3 tomos de carbono se seleccionan en forma independiente entre C(=O), donde cada uno est opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre halogeno, ciano, nitro, hidroxi, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6 y haloalcoxi C1-6; cada T es en forma independiente NR13aR13b, OR14 o S(=O)nR14; cada R7a es en forma independiente H, ciano o alquilo C1-4; cada R7b es en forma independiente H o alquilo C1-4; o un par de R7a y R7b unidos al mismo tomo de carbono se toman junto con el tomo de carbono para formar un anillo carboc¡clico saturado de entre 3 y 6 miembros; cada R6 es en forma independiente H, ciano, alquilo C1-3 o haloalquilo C1-3; cada R8, R9a, R9b, R10 y R11 es en forma independiente H, alquilo C1-7, alquenilo C2-7, alquinilo C2-7, haloalquilo C1-7, haloalquenilo C2-7, cicloalquilo C3-7 o halocicloalquilo C3-7; cada R12 es en forma independiente H, alquilo C1-6, haloalquilo C1-6, alquilcarbonilo C2-6, alc
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12699008P | 2008-05-08 | 2008-05-08 |
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| ARP090101679A AR071769A1 (es) | 2008-05-08 | 2009-05-08 | Azoles sustituidos como fungicidas, una composicion fungicida que comprende el compuesto y un metodo para controlar enfermedades de las plantas |
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| EP (1) | EP2274284A2 (es) |
| AR (1) | AR071769A1 (es) |
| CL (1) | CL2009001094A1 (es) |
| PE (1) | PE20091953A1 (es) |
| TW (1) | TW200950698A (es) |
| UY (1) | UY31811A (es) |
| WO (2) | WO2009137538A2 (es) |
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| AR075713A1 (es) | 2009-03-03 | 2011-04-20 | Du Pont | Pirazoles fungicidas |
| IN2012DN01693A (es) * | 2009-08-26 | 2015-06-05 | Novartis Ag | |
| TW201117722A (en) * | 2009-11-04 | 2011-06-01 | Du Pont | Fungicidal mixtures |
| AR079545A1 (es) * | 2009-12-21 | 2012-02-01 | Bayer Cropscience Ag | Tienilpiri(mi)dinilazol |
| WO2012023143A1 (en) | 2010-08-19 | 2012-02-23 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
| TWI504350B (zh) | 2010-09-01 | 2015-10-21 | Du Pont | 殺真菌吡唑及其混合物 |
| TW201245155A (en) * | 2010-09-01 | 2012-11-16 | Du Pont | Fungicidal pyrazoles |
| AU2011307289A1 (en) * | 2010-09-29 | 2013-02-21 | E. I. Du Pont De Nemours And Company | Fungicidal imidazoles |
| 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 |
| WO2014009425A1 (en) | 2012-07-12 | 2014-01-16 | Chiesi Farmaceutici S.P.A. | Inhibition of enzymes |
| EP3010908A1 (en) | 2013-02-20 | 2016-04-27 | E. I. du Pont de Nemours and Company | Fungicidal pyrazoles |
| CN105683164A (zh) | 2013-08-20 | 2016-06-15 | 杜邦公司 | 杀真菌吡唑类 |
| US20170037014A1 (en) | 2014-05-06 | 2017-02-09 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
| US10246420B2 (en) | 2014-07-24 | 2019-04-02 | Bayer Cropscience Aktiengesellschaft | Pyrazole derivatives |
| BR112017018140A2 (pt) | 2015-03-19 | 2018-04-10 | Du Pont | ?composto, composição fungicida e método de controle de doenças de plantas? |
| WO2018052838A1 (en) | 2016-09-16 | 2018-03-22 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
| WO2018139560A1 (ja) | 2017-01-26 | 2018-08-02 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| WO2018190350A1 (ja) | 2017-04-10 | 2018-10-18 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| CA3059702A1 (en) | 2017-04-10 | 2018-10-18 | Mitsui Chemicals Agro, Inc. | Pyridone compounds and agricultural and horticultural fungicides containing the same as active ingredients |
| MY190386A (en) | 2017-04-11 | 2022-04-20 | Mitsui Chemicals Agro Inc | Pyridone compounds and agricultural and horticultural fungicides containing the same as active ingredients |
| EP3634417B1 (en) | 2017-05-17 | 2023-07-12 | Arcus Biosciences, Inc. | Quinazoline-pyrazole derivatives for the treatment of cancer-related disorders |
| JP7157738B2 (ja) | 2017-06-08 | 2022-10-20 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| EP3778583B1 (en) * | 2018-03-30 | 2025-06-18 | Sumitomo Chemical Company, Limited | Heterocyclic compound and arthropod pest control composition containing same |
| WO2020022360A1 (ja) * | 2018-07-24 | 2020-01-30 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| US12114658B2 (en) | 2018-07-25 | 2024-10-15 | Mitsui Chemicals Crop & Life Solutions, Inc. | Compounds having a nitrogen-containing unsaturated six-membered ring and agricultural and horticultural fungicides containing the same as active ingredients |
| CA3121202A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN111819947B (zh) * | 2020-07-17 | 2022-03-04 | 新疆农业大学 | 一种利于天山花楸种子破除休眠的催芽方法 |
| MX2023003035A (es) * | 2020-09-14 | 2023-06-06 | Genzyme Corp | Compuestos como moduladores de bis-fosfoglicerato mutasa para el tratamiento de la anemia de celulas falciforme. |
| BR112023015584A2 (pt) | 2021-02-02 | 2023-10-24 | Liminal Biosciences Ltd | Antagonistas de gpr84 e usos dos mesmos |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| FR2707295A1 (fr) * | 1993-06-07 | 1995-01-13 | Rhone Poulenc Agrochimie | Fongicides pyrazoles substitués en position 3 par un hétérocycle. |
| TW467902B (en) * | 1996-07-31 | 2001-12-11 | Bristol Myers Squibb Co | Diphenyl heterocycles as potassium channel modulators |
| GB9709317D0 (en) * | 1997-05-09 | 1997-06-25 | Agrevo Uk Ltd | Fungicides |
| NL2000397C2 (nl) * | 2006-01-05 | 2007-10-30 | Pfizer Prod Inc | Bicyclische heteroarylverbindingen als PDE10 inhibitoren. |
| EP2053044A1 (en) * | 2007-10-26 | 2009-04-29 | Syngenta Participations AG | Novel imidazole derivatives |
| EP2053045A1 (en) * | 2007-10-26 | 2009-04-29 | Syngenta Participations AG | Novel imidazole derivatives |
| EP2053046A1 (en) * | 2007-10-26 | 2009-04-29 | Syngeta Participations AG | Novel imidazole derivatives |
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- 2009-05-06 WO PCT/US2009/042922 patent/WO2009137538A2/en not_active Ceased
- 2009-05-06 TW TW098115009A patent/TW200950698A/zh unknown
- 2009-05-07 EP EP09743637A patent/EP2274284A2/en not_active Withdrawn
- 2009-05-07 CL CL2009001094A patent/CL2009001094A1/es unknown
- 2009-05-07 WO PCT/US2009/043096 patent/WO2009137651A2/en not_active Ceased
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Also Published As
| Publication number | Publication date |
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| WO2009137538A3 (en) | 2012-04-19 |
| WO2009137538A2 (en) | 2009-11-12 |
| PE20091953A1 (es) | 2010-01-09 |
| EP2274284A2 (en) | 2011-01-19 |
| WO2009137651A3 (en) | 2012-04-26 |
| UY31811A (es) | 2010-01-05 |
| WO2009137651A8 (en) | 2010-03-18 |
| TW200950698A (en) | 2009-12-16 |
| CL2009001094A1 (es) | 2010-10-08 |
| WO2009137651A2 (en) | 2009-11-12 |
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