AR052672A1 - Derivados de pirazina como fungicidas - Google Patents
Derivados de pirazina como fungicidasInfo
- Publication number
- AR052672A1 AR052672A1 ARP060100533A ARP060100533A AR052672A1 AR 052672 A1 AR052672 A1 AR 052672A1 AR P060100533 A ARP060100533 A AR P060100533A AR P060100533 A ARP060100533 A AR P060100533A AR 052672 A1 AR052672 A1 AR 052672A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- cycloalkyl
- ring
- cyano
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 16
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 15
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 150000002367 halogens Chemical group 0.000 abstract 13
- 125000001424 substituent group Chemical group 0.000 abstract 13
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 11
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 10
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 9
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 8
- 125000000304 alkynyl group Chemical group 0.000 abstract 7
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 6
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 5
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 5
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 5
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000004122 cyclic group Chemical group 0.000 abstract 4
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 3
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 3
- 125000003282 alkyl amino group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 3
- 125000004001 thioalkyl group Chemical group 0.000 abstract 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 2
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 2
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 2
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 2
- -1 nitro, hydroxy Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 1
- 125000004983 dialkoxyalkyl group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 244000053095 fungal pathogen Species 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003216 pyrazines Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/18—Oxygen or sulfur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/20—Nitrogen 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
- 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
- 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
- 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
- C07D403/14—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 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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- 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
-
- 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)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Derivados de pirazina, compuestos, sus N-oxidos y sales aceptables para su uso en agricultura, con utilidad como funguicidas. Composiciones que contienen los compuestos de formula (1) y un método para controlar enfermedades de plantas causadas por patogenos fungicos de plantas que involucra aplicar una cantidad efectiva de un compuesto de formula (1). Reivindicacion 1: Un compuesto caracterizado porque se selecciona entre la formula 1, un N-oxido o una sal aceptable para su uso en agricultura del mismo, donde R1 es NR4R5, N=CR19R21, OR6, G1 o G2, o C1-8 alquilo, C2-8 alquenilo, C3-8 alquinilo, C3-8 cicloalquilo, C3-8 cicloalquenilo, C4-8 cicloalquilalquilo, C4-8 alquilcicloalquilo, C4-8 cicloalquenilalquilo o C4-8 alquilcicloalquenilo, cada uno opcionalmente sustituido con uno o más sustituyentes seleccionados entre el grupo que consiste en halogeno, ciano, nitro, hidroxi, C1-4 alcoxi, C1-4 haloalcoxi, C1-4 alquiltio, C1-4 alquilamino, C1-4 alquilsulfinilo, C1-4 alquilsulfonilo, C2-6 alcoxicarbonilo, C2-6 alquilcarbonilo, C3-6 trialquilsililo, G1 y G2; A es O, S o NR7; R7 es H, C1-4 alquilo, C1-4 haloalquilo, C2-6 alquilcarbonilo o C2-6 alcoxicarbonilo; R2 es ciano, NR8-N=CR9R10, O-N=CR9R10, NR8- NR11R12, O-NR11R12, CR13=NOR14, CR13=NNR11R12, C(W) NR22R23, NC(=O)R30, NC(=O)NR31 o NC(=O)OR32; o R2 es un anillo heteroaromático de 5 o 6 miembros o un sistema de anillos bicíclico heteroaromático de 8, 9 o 10 miembros, donde cada anillo o sistema de anillos está opcionalmente sustituido con hasta 5 sustituyentes seleccionados entre R24; o anillo heterocíclico saturado o parcialmente de 5 o 6 miembros, incluyendo opcionalmente entre 1 y 3 miembros del anillo seleccionados entre el grupo que consiste en C(=O), C(=S), S(O), o S(O)2, opcionalmente sustituido con hasta 5 sustituyentes seleccionados entre R24; W es O, S o =NR25; R3 es H, halogeno, ciano, C1-6 alquilo, C1-4 haloalquilo, C3-6 cicloalquilo, C3-6 halocicloalquilo, C2-6 alquenilo, C3-6 alquinilo, C1-4 alcoxi, C1-4 haloalcoxi, C1-4 alquiltio, C1-4 haloalquiltio, C2-5 alcoxicarbonilo, hidroxicarbonilo, -SCN o -CHO; cada uno de R4 y R5 es en forma independiente H, o C1-8 alquilo, C3-8 alquenilo, C3-8 alquinilo, C3-8 cicloalquilo, C3-8 cicloalquenilo, C4-8 cicloalquilalquilo o C4-8 cicloalquenilalquilo, cada uno opcionalmente sustituido con entre 1 y 4 sustituyentes seleccionados entre halogeno, ciano, C1-6 alcoxi, C1-6 tioalquilo, C2-6 alquilcarbonilo, C2-6 alcoxicarbonilo, C2-6 dialquilamino, -SCN y C3-6 trialquilsililo; o R4 y R5 se toman juntos como -(CH2)3-, -(CH2)4-, -(CH2)5-, -(CH2)6-, -CH2CH2OCH2CH2- o CH2CH(CH3)OCH(CH3)CH2-; R6 es H, o C1-8 alquilo, C3-8 alquenilo, C3-8 alquinilo, C3-8 cicloalquilo, C3-8 cicloalquenilo, C4-8 cicloalquilalquilo o C4-8 cicloalquenilalquilo, cada uno opcionalmente sustituido con 1 y 4 sustituyentes seleccionados entre halogeno, ciano, C1-6 alcoxi, C1-6 tioalquilo, C2-6 alquilcarbonilo, C2-6 alcoxicarbonilo, C2-6 dialquilamino, -SCN y C3-6 trialquilsililo; R8 es H, C1-4 alquilo o C1-4 haloalquilo; R9 es C1-4 alquilo o C1-4 haloalquilo; R10 es H, C1-4 alquilo o C1-4 haloalquilo; o R9 y R10 se toman juntos como -(CH2)3-, -(CH2)4-, -(CH2)5- o -(CH2)6-; R11 es H, C1-4 alquilo o C1-4 haloalquilo; R12 es H, C1-4 alquilo o C1-4 haloalquilo, C2-3 alquilcarbonilo o C2-3 alcoxicarbonilo; o R11 y R12 se toman juntos como -(CH2)4-, -(CH2)5-, -CH2CH2OCH2CH2- o CH2CH(CH3) OCH(CH3)CH2-; R13 es H, NH2, C1-4 alquilo o C1-4 haloalquilo; R14 es H, C1-4 alquilo o C1-4 haloalquilo; J es C1-8 alquilo, C2-8 alquenilo, C3-8 alquinilo, C3-8 cicloalquilo, C3-8 cicloalquenilo, C4-8 cicloalquilalquilo, C4-8 alquilcicloalquilo, C4-8 cicloalquenilalquilo o C4-8 alquilcicloalquenilo, cada uno opcionalmente sustituido con uno o más sustituyentes seleccionados entre el grupo que consiste en halogeno, ciano, nitro, hidroxi, C1-4 alcoxi, C1-4 haloalcoxi, C1-4 alquiltio, C1-4 alquilsulfinilo, C1-4 alquilsulfonilo, C2-6 alcoxicarbonilo, C2-6 alquilcarbonilo, C3-6 trialquilsililo y C1-4 alquilamino; o J es un anillo heteroaromático de 5 o 6 miembros o un sistema de anillos bicíclico heteroaromático de 8, 9 o 10 miembros fenilo, bencilo, naftaleno, donde cada anillo o sistema de anillos está opcionalmente sustituido con hasta 5 sustituyentes seleccionados entre halogeno, C1-6 alquilo, C2-6 alquenilo, C2-6 alquinilo, C3-6 cicloalquilo, C1-6 haloalquilo, C2-6 haloalquenilo, ciano, nitro, C1-6 alcoxi, C1-6 haloalcoxi, C1-6 alquiltio, C1-6 alquilsulfinilo, C1-6 alquilsulfonilo, C1-6 haloalquiltio, C1-6 haloalquilsulfinilo, C1-6 haloalquilsulfonilo, C1-6 alquilamino, C2-6 dialquilamino, C2-6 alquilcarbonilo, C2-6 alcoxicarbonilo, C2-6 alquilaminocarbonilo, C3-6 dialquilaminocarbonilo y C3-6 trialquilsililo; G1 es un anillo carbocíclico o heterocíclico no aromático de entre 3 y 7 miembros, que incluye opcionalmente 1 o 2 miembros del anillo seleccionados entre el grupo que consiste en C(=O), C(=S), S(O) y S(O)2 y opcionalmente sustituido con entre 1 y 4 sustituyentes seleccionados entre R17; G2 es un anillo fenilo, anillo heteroaromático de 5 o 6 miembros, donde cada anillo o sistema de anillos está opcionalmente sustituido con entre 1 y 4 sustituyentes seleccionados en forma independiente entre R18; cada R17 es en forma independiente C1-2 alquilo, C1-2 haloalquilo, halogeno, ciano, nitro o C1-2 alcoxi; cada R18 es en forma independiente C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C3-6 cicloalquilo, C1-4 haloalquilo, C2-4 haloalquenilo, C2-4 haloalquinilo, C3-6 halocicloalquilo, halogeno, ciano, nitro, C1-4 alcoxi, C1-4 haloalcoxi, C1-4 alquiltio, C1-4 alquilsulfinilo, C1-4 alquilsulfonilo, C1-4 alquilamino, C2-8 dialquilamino, C3-6 cicloalquilamino, (C1-4 alquil)(C3-6 cicloalquil)amino, C2-4 alquilcarbonilo, C2-6 alcoxicarbonilo, C2-6 alquilaminocarbonilo, C3-8 dialquilaminocarbonilo o C3-8 trialquilsililo; cada R19 y R21 es en forma independiente H, C1-4 alquilo, C1-4 haloalquilo o C3-8 cicloalquilo; o R19 y R21 se toman juntos como -(CH2)4-, -(CH2)5-, -CH2CH2OCH2CH2- o CH2CH(CH3)OCH(CH3)CH2-; cada R22 y R23 es en forma independiente H, C1-4 alquilo, C3-8 cicloalquilo, C4-8 cicloalquilalquilo cada uno opcionalmente sustituido con entre 1 y 4 sustituyentes seleccionados entre halogeno, ciano, alcoxi C1-6, C1-6 tioalquilo, C2-6 alquilcarbonilo, C2-6 alcoxicarbonilo, C2-6 dialquilamino, -SCN y C3-6 trialquilsililo; o R22 y R23 se toman juntos como -(CH2)4-, -(CH2)5-, -CH2CH2OCH2CH2- o CH2CH(CH3)OCH(CH3)CH2-;cada R24 es en forma independiente halogeno, C1-6 alquilo, C2-6 alquenilo, C2-6 alquinilo, C3-6 cicloalquilo, C1-6 haloalquilo, C2-6 alcoxialquilo, C3-6 dialcoxialquilo, C2-6 haloalquenilo, ciano, nitro, C1-6 alcoxi, C1-6 haloalcoxi, C1-6 alquiltio, C1-6 alquilsulfinilo, C1-6 alquilsulfonilo, C1-6 haloalquiltio, C1-6 haloalquilsulfinilo, C1-6 haloalquilsulfonilo, C1-6 alquilamino, C2-6 dialquilamino, C2-6 alquilcarbonilo, C2-6 alcoxicarbonilo, C2-6 alquilaminocarbonilo, C3-6 dialquilaminocarbonilo o C3-6 trialquilsililo; y R25 es H, C1-4 alquilo o C1-4 haloalquilo; R30 es H, C1-6 alquilo, C1-4 haloalquilo, C3-6 cicloalquilo, C3-6 halocicloalquilo, C2-6 alquenilo o C3-6 alquinilo; o anillo fenilo, anillo heteroaromático de 5 o 6 miembros, donde cada anillo o sistema de anillos está opcionalmente sustituido con entre 1 y 4 sustituyentes seleccionados en forma independiente entre C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C3-6 cicloalquilo, C1-4 haloalquilo, C2-4 haloalquenilo, C2-4 haloalquinilo, C3-6 halocicloalquilo, halogeno, ciano, nitro, C1-4 alcoxi y C1-4 haloalcoxi, y cada R31 y R32 es en forma independiente C1-6 alquilo, C1-4 haloalquilo, C3-6 cicloalquilo, C3-6 halocicloalquilo, C2-6 alquenilo o C3-6 alquinilo; o anillo fenilo, opcionalmente sustituido con entre 1 y 4 sustituyentes seleccionados en forma independiente entre C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C3-6 cicloalquilo, C1-4 haloalquilo, C2-4 halogeno, ciano, nitro, C1-4 alcoxi y C1-4 haloalcoxi, con la condicion de que cuando R2 es NR8-N= CR9R10, O-N=CR9R10, NR8-NR11R12, O-NR11R12, CR13=NOR14 o CR13=NNR11R12, entonces J es fenilo sustituido con al menos un sustituyente seleccionado entre halogeno y metilo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US65319005P | 2005-02-15 | 2005-02-15 |
Publications (1)
Publication Number | Publication Date |
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AR052672A1 true AR052672A1 (es) | 2007-03-28 |
Family
ID=36572198
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060100533A AR052672A1 (es) | 2005-02-15 | 2006-02-15 | Derivados de pirazina como fungicidas |
Country Status (8)
Country | Link |
---|---|
US (1) | US20080194585A1 (es) |
EP (1) | EP1848711A1 (es) |
JP (1) | JP2008530231A (es) |
AR (1) | AR052672A1 (es) |
CA (1) | CA2598897A1 (es) |
GT (1) | GT200600061A (es) |
TW (1) | TW200640881A (es) |
WO (1) | WO2006089060A1 (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2008015648A (es) * | 2006-06-21 | 2009-01-09 | Du Pont | Pirazinonas como inhibidores de proliferacion celular. |
WO2008107398A2 (en) * | 2007-03-02 | 2008-09-12 | Basf Se | Pyrazine compounds |
PT2268624E (pt) * | 2008-04-29 | 2013-11-07 | Merck Patent Gmbh | Derivados de arilpirazinona estimuladores da secreção de insulina, métodos para a sua obtenção e seu uso para o tratamento da diabetes |
EA031063B1 (ru) * | 2009-05-06 | 2018-11-30 | Байер Кропсайенс Лп | Способ повышения жизнеспособности и/или урожайности сельскохозяйственных растений при практически несуществующем давлении патогенов |
TW201247631A (en) | 2011-04-28 | 2012-12-01 | Du Pont | Herbicidal pyrazinones |
WO2018225816A1 (ja) * | 2017-06-07 | 2018-12-13 | 三井化学アグロ株式会社 | 含窒素複素環化合物ならびにそれを有効成分とする農園芸用殺菌剤 |
Family Cites Families (7)
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CN1202159A (zh) * | 1995-09-22 | 1998-12-16 | 住友化学工业株式会社 | 吡嗪-2-酮衍生物,它们的应用及用于制备它们的中间体 |
US6271238B1 (en) * | 1996-09-06 | 2001-08-07 | Nippon Kayaku Kabushiki Kaisha | Acetamide derivatives and protease inhibitors |
US6117876A (en) * | 1997-04-14 | 2000-09-12 | American Cyanamid Company | Fungicidal trifluorophenyl-triazolopyrimidines |
US6664255B1 (en) * | 1999-05-19 | 2003-12-16 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrazinones useful for selective inhibition of the coagulation cascade |
EP1392309B1 (en) * | 2001-05-14 | 2007-01-17 | Bristol-Myers Squibb Company | Substituted pyrazinones, pyridines and pyrimidines as corticotropin releasing factor ligands |
PL371059A1 (en) * | 2001-11-19 | 2005-06-13 | Basf Aktiengesellschaft | 5-phenylpyrimidines, agents comprising the same, method for production and use thereof |
TW200500341A (en) * | 2002-11-12 | 2005-01-01 | Astrazeneca Ab | Novel compounds |
-
2006
- 2006-01-24 TW TW095102632A patent/TW200640881A/zh unknown
- 2006-02-13 GT GT200600061A patent/GT200600061A/es unknown
- 2006-02-14 JP JP2007556300A patent/JP2008530231A/ja not_active Abandoned
- 2006-02-14 US US11/883,659 patent/US20080194585A1/en not_active Abandoned
- 2006-02-14 CA CA002598897A patent/CA2598897A1/en not_active Abandoned
- 2006-02-14 WO PCT/US2006/005528 patent/WO2006089060A1/en active Application Filing
- 2006-02-14 EP EP06735278A patent/EP1848711A1/en not_active Withdrawn
- 2006-02-15 AR ARP060100533A patent/AR052672A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
US20080194585A1 (en) | 2008-08-14 |
JP2008530231A (ja) | 2008-08-07 |
GT200600061A (es) | 2006-10-18 |
CA2598897A1 (en) | 2006-08-24 |
WO2006089060A1 (en) | 2006-08-24 |
TW200640881A (en) | 2006-12-01 |
EP1848711A1 (en) | 2007-10-31 |
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