AR081810A1 - Piridinilpirazoles biciclicos - Google Patents
Piridinilpirazoles biciclicosInfo
- Publication number
- AR081810A1 AR081810A1 ARP110101052A ARP110101052A AR081810A1 AR 081810 A1 AR081810 A1 AR 081810A1 AR P110101052 A ARP110101052 A AR P110101052A AR P110101052 A ARP110101052 A AR P110101052A AR 081810 A1 AR081810 A1 AR 081810A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- ring
- 6alkyl
- haloalkyl
- cycloalkyl
- Prior art date
Links
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 23
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 9
- 125000003545 alkoxy group Chemical group 0.000 abstract 9
- 125000001188 haloalkyl group Chemical group 0.000 abstract 9
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical class 0.000 abstract 8
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 7
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 6
- 125000004414 alkyl thio group Chemical group 0.000 abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 6
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 abstract 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- 125000000278 alkyl amino alkyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 5
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 5
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 5
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- -1 cyano, hydroxyl Chemical group 0.000 abstract 4
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 4
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 3
- 125000006713 (C5-C10) cycloalkyl group Chemical group 0.000 abstract 3
- 125000005082 alkoxyalkenyl group Chemical group 0.000 abstract 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 3
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 3
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 3
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 3
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 3
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 3
- 125000004983 dialkoxyalkyl group Chemical group 0.000 abstract 3
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 3
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 3
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl 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
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 1
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 1
- 231100000678 Mycotoxin Toxicity 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 abstract 1
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 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
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000005149 cycloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004992 haloalkylamino group Chemical group 0.000 abstract 1
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 abstract 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006769 halocycloalkoxy group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000002636 mycotoxin Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Su uso para combatir microorganismos no deseados en fitoprotección y protección de materiales, así como para reducir la cantidad de micotoxinas en plantas y partes de plantas, así como procedimientos para la preparación de compuestos de la fórmula (1).Reivindicación 1: Compuestos de la fórmula (1) en la que los símbolos tienen los significados siguientes: Y forma junto con el átomo de nitrógeno adyacente “1” y ambos átomos de carbono “2” y “3” un anillo heterocíclico no aromático de 5 a 7 miembros, en el que los otros miembros del anillo se seleccionan de entre el grupo C(R2)2, O, S, NR3, C(R2)=C(R2), C(R2)=N, N=N, C(=O), C(=S), C(=NR4), S(=O)p(=NR4)q y SiR5aR5b; R2 representa en cada caso, independientemente uno de otro, H, halógeno, ciano, hidroxilo, -CHO, -NHCHO, -N3, -N=C=O, -N=C=S, -SH, -C(=O)NH2, -C(=O)NHCN, -C(=O)OR6, -C(=O)NHOR6a, alquilo C1-5, alquenilo C2-5, alquinilo C2-5, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalquenilo C3-6, haloalquilo C1-5, alcoxi C1-5, haloalcoxi C1-5, cicloalcoxi C3-6, alqueniloxi C2-5, haloalqueniloxi C3-5, alquiniloxi C2-5, alquilcarbonilo C2-5, alquilcarboniloxi C2-5, haloalquilcarboniloxi C2-5, alcoxicarboniloxi C3-5, alquiltio C1-5, haloalquiltio C1-5, cicloalquiltio C3-6, alquil(tiocarbonilo) C2-5, alquiltio(tiocarbonilo) C2-5, alquilsulfinilo C1-5, haloalquilsulfinilo C1-5, cicloalquilsulfinilo C3-6, alquilsulfonilo C1-5, haloalquilsulfonilo C1-5, cicloalquilsulfonilo C3-6, trialquilsililo C3-5, halotrialquilsililo C3-5, alquilamino C1-5, haloalquilamino C2-5, cicloalquilamino C3-6, dialquilamino C2-5 o halodialquilamino C3-5; R3 representa H, -CN, -C(=O)NH2, -C(=O)NHCN, -CHO, -NHCHO, -C(=O)OR6, C(=O)NHOR6a, hidroxilo, alquilo C1-5, alquenilo C2-5, alquinilo C2-5, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalquenilo C3-6, cicloalquilalquilo C4-10, alquilcicloalquilo C4-7, alquilcicloalquilalquilo C5-7, haloalquilo C2-5, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, cicloalquilcarbonilo C3-7, alcoxicarbonilo C1-6, haloalcoxi-carbonilo C1-4, cicloalcoxicarbonilo C3-6, alcoxialquilcarbonilo C2-6, alcoxialcoxicarbonilo C2-6, (alquiltio)carbonilo C1-6, alcoxi(tiocarbonilo) C1-6, alquil(tiocarbonilo) C1-6, alquiltio(tiocarbonilo) C1-6, alquilaminocarbonilo C1-6, cicloalquilaminocarbonilo C3-6, dialquilaminocarbonilo C2-6, alquilamino(tiocarbonilo) C1-6, dialquilamino(tiocarbonilo) C2-6, alcoxi(alquil)aminocarbonilo C2-6, alcoxi C1-5, haloalcoxi C1-5, alquiltio C1-5, haloalquiltio C1-5, cicloalquiltio C3-6, alquilaminosulfonilo C1-5, trialquilsililo C3-5 o halotrialquilsililo C3-5; R4 representa en cada caso H, ciano, amino, hidroxilo, alquilo C1-6, cicloalquilo C3-6, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4, alcoxi C1-4, fenilo o benzoílo; R5a, R5b representan, independientemente uno de otro, alquilo C1-4, alquenilo C2-5, alquinilo C2-5, cicloalquilo C3-5, halocicloalquilo C3-6, cicloalquilalquilo C4-7, alquilcicloalquilo C4-7, alquilcicloalquilalquilo C5-7, haloalquilo C1-5, alcoxi C1-5 o haloalcoxi C1-5; R6 representa en cada caso H, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, cicloalquilalquilo C4-7, alquilcicloalquilo C4-7 o bencilo; R6a representa en cada caso alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, cicloalquilalquilo C4-7 o alquilcicloalquilo C4-7; A representa un anillo de fenilo, que dado el caso puede estar monosustituido o polisustituido con R7 o representa un anillo de tiofenilo, que dado el caso puede estar monosustituido o polisustituido con R8; R7 representa, independientemente uno de otro, halógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquilcicloalquilo C4-7, haloalquilo C1-6, haloalquenilo C2-6, ciano, nitro, 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 C1-6, dialquilamino C2-6, alquilcarbonilo C1-6, alcoxicarbonilo C1-6, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C2-6 o trialquilsililo C3-6; R8 representa independientemente uno de otro halógeno, ciano, alquilo C1-3, alcoxi C1-3, haloalquilo C1-3, haloalcoxi C1-3; R1 representa H, halógeno, ciano, hidroxilo, alquilo C1-4, CONR9aR9b, COOH, COOR12, -NR9aR9b, -N(R9b)COR9a, -N(R9b)CSR9a, -N(R9b)COOR12, -N(R9b)SO2R12, -NR10-NR11aR11b, -S(O)mR12, -OR12, -N=CR13aR13b o -NR10N=CR14aR14b; R9a y R11a representan en cada caso, independientemente uno de otro, H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, alcoxialquilo C2-6, alcoxialcoxialquilo C3-6, alcoxialquenilo C3-6, alcoxialquinilo C3-6, dialcoxialquilo C3-6, trialcoxialquilo C4-10, haloalcoxialquilo C2-6, alcoxihaloalquilo C2-6, haloalcoxihaloalquilo C2-6, hidroxialquilo C1-6, cianoalquilo C1-10, alquiltioalquilo C2-6, alquilsulfinilalquilo C2-6, alquilaminoalquilo C3-6, haloalquilaminoalquilo C3-6, cicloalquilaminoalquilo C5-10, dialquilaminoalquilo C4-10, halodialquilaminoalquilo C4-10, cicloalquil(alquil)aminoalquilo C5-10 o -(CR15aR15b)mR16; R9b y R11b representan en cada caso, independientemente uno de otro, H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, alcoxialquilo C2-6, alcoxialcoxialquilo C3-6, alcoxialquenilo C3-6, alcoxialquinilo C3-6, dialcoxialquilo C3-6, trialcoxialquilo C4-10, haloalcoxialquilo C2-6, alcoxihaloalquilo C2-6, haloalcoxihaloalquilo C2-6, hidroxialquilo C1-6, cianoalquilo C1-10, alquiltioalquilo C2-6, alquilsulfinilalquilo C2-6, alquilaminoalquilo C3-6, haloalquilaminoalquilo C3-6, cicloalquilaminoalquilo C5-10, dialquilaminoalquilo C4-10, halodialquila6minoalquilo C4-10, cicloalquil(alquil)aminoalquilo C5-10 o -(CR15aR15b)mR16; o R9a y R9b, o R11a y R11b forman en cada caso, con el átomo de nitrógeno o la unidad (NCO) o la unidad (NCS), al/a la que están unidos, un anillo de 3 a 6 miembros, que dado el caso puede contener adicionalmente miembros del anillo seleccionados de entre el grupo O, NR3, C(=O), C(=S), C(=NR4), SiR5aR5b y S(=O)p(=NR4)q y que dado el caso puede estar sustituido en los átomos de carbono del anillo con 1 a 4 sustituyentes seleccionados del grupo constituido por halógeno, -CN, alquilo C1-2 y alcoxi C1-2; R12 representa en cada caso alquilo C1-10, alquenilo C2-10, alquinilo C2-10, haloalquilo C1-10, haloalquenilo C2-10, haloalquinilo C2-10, alcoxialquilo C2-10, alcoxialcoxialquilo C3-10, alcoxialquenilo C3-10, alcoxialquinilo C3-10, dialcoxialquilo C3-10, trialcoxialquilo C4-10, haloalcoxialquilo C2-10, alcoxihaloalquilo C2-10, haloalcoxihaloalquilo C2-10, hidroxialquilo C2-10, cianoalquilo C2-10, alquiltioalquilo C2-10, alquilsulfinilalquilo C2-10, alquilaminoalquilo C3-10, haloalquilaminoalquilo C3-10, cicloalquilaminoalquilo C5-10, dialquilaminoalquilo C4-10, halodialquilaminoalquilo C4-10, cicloalquil(alquil)aminoalquilo C6-10 o -(CR15aR15b)mR16; R15a, R15b representan independientemente uno de otro H, halógeno, alquilo C1-5, haloalquilo C1-5 o alcoxi C1-5; o un par geminal de R15a y R15b forma junto con el átomo de carbono al que están unidos C(=O) o un anillo de cicloalquilo C3-6 o un anillo de halocicloalquilo C3-6; R16 representa fenilo, cicloalquilo C3-8, cicloalquenilo C3-8, un anillo heteroaromático de 5 ó 6 miembros o naftalenilo o un sistema de anillo bicíclico heteroaromático de 8, 9 ó 10 miembros o un anillo heterocíclico no aromático de 5 ó 6 miembros, que dado el caso contiene miembros de anillo seleccionados entre el grupo C(=O), C(=S), C(=NR4), SiR5aR5b y S(=O)p(=NR4)q; cada anillo o cada sistema de anillo puede estar, dado el caso, sustituido en los átomos de carbono del anillo con hasta 5 sustituyentes seleccionados independientemente unos de otros de R17; R17 representa en cada caso, independientemente uno de otro, halógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, alquilcicloalquilo C4-10, halocicloalquilo C3-6, haloalquilo C1-6, haloalquenilo C2-6, ciano, nitro, alcoxi C1-6, cicloalcoxi C3-8, halocicloalcoxi C3-8, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, haloalquilsulfinilo C1-6, haloalquilsulfonilo C1-6, alquilamino C1-6, dialquilamino C1-6, alquilcarbonilo C1-6, alcoxicarbonilo C1-6, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C3-6, trialquilsililo C3-6, fenilo, naftalenilo o un anillo heteroaromático de 5 ó 6 miembros; m representa 0, 1 ó 2; R10 representa en cada caso H, alquilo C1-5, alquenilo C2-5, alquinilo C2-5, cicloalquilo C3-6, halocicloalquilo C3-6, haloalquilo C1-5, haloalquenilo C2-5, haloalquinilo C2-5, alcoxialquilo C2-5, alquilcarbonilo C2-5 o alcoxi C1-5; R13a, R13b representan independientemente uno de otro H, -CN, -C(=O)OR18, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, cicloalquenilo C3-8, cicloalquilalquilo C4-10, alquilcicloalquilo C4-10, alquilcicloalquilalquilo C5-10, alquilamino C1-6, dialquilamino C2-6, alquilaminoalquilo C2-6, haloalquilaminoalquilo C2-6, cicloalquilaminoalquilo C4-6, dialquilaminoalquilo C3-6, halodialquilaminoalquilo C3-6, cicloalquil(alquil)aminoalquilo C5-10, alcoxi C1-6, haloalcoxi C1-6, cicloalcoxi C3-10, alquiltio C1-10, haloalquiltio C1-10, cicloalquiltio C3-10, trialquilsililo C3-10 o halotrialquilsililo C3-10 o fenilo o un anillo heteroaromático de 5 ó 6 miembros o un sistema de anillo bicíclico heteroaromático de 8, 9 ó 10 miembros o un anillo heterocíclico no aromático de 5 ó 6 miembros, que dado el caso contiene miembros de anillo seleccionados entre el grupo NR3, C(=O), C(=S), C(=NR4), SiR5aR5b y S(=O)p(NR4)q; cada anillo o cada sistema de anillo puede estar, dado el caso, sustituido en los átomos de carbono del anillo con 1 a 5 sustituyentes seleccionados del grupo constituido por alquilo C1-3, halógeno, -CN y alcoxi C1-3; o R13a y R13b forman conjuntamente con el átomo de carbono al que están unidos un anillo de 3 a 6 miembros, pud
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| Publication number | Priority date | Publication date | Assignee | Title |
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| EP2763993B1 (en) * | 2011-10-06 | 2017-04-19 | Bayer Intellectual Property GmbH | Heterocyclylpyri(mi)dinylpyrazole |
| LT3313838T (lt) * | 2015-06-29 | 2019-06-10 | Astrazeneca Ab | Policikliniai amido dariniai, kaip cdk9 slopikliai |
| WO2018017633A1 (en) | 2016-07-21 | 2018-01-25 | Bristol-Myers Squibb Company | TGF Beta RECEPTOR ANTAGONISTS |
| AU2021342792A1 (en) * | 2020-09-17 | 2023-06-01 | Janssen Pharmaceutica Nv | Casein kinase 1 delta modulators |
Family Cites Families (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1037399B (de) | 1955-03-23 | 1958-08-28 | Erich Sulzmann | Waschanlage zum Waschen und Spuelen von textilen Flaechengebilden |
| US4272417A (en) | 1979-05-22 | 1981-06-09 | Cargill, Incorporated | Stable protective seed coating |
| US4245432A (en) | 1979-07-25 | 1981-01-20 | Eastman Kodak Company | Seed coatings |
| US4808430A (en) | 1987-02-27 | 1989-02-28 | Yazaki Corporation | Method of applying gel coating to plant seeds |
| GB8810120D0 (en) | 1988-04-28 | 1988-06-02 | Plant Genetic Systems Nv | Transgenic nuclear male sterile plants |
| US5559137A (en) | 1994-05-16 | 1996-09-24 | Smithkline Beecham Corp. | Compounds |
| AU5575896A (en) | 1995-04-20 | 1996-11-07 | American Cyanamid Company | Structure-based designed herbicide resistant products |
| US5876739A (en) | 1996-06-13 | 1999-03-02 | Novartis Ag | Insecticidal seed coating |
| US6087496A (en) | 1998-05-22 | 2000-07-11 | G. D. Searle & Co. | Substituted pyrazoles suitable as p38 kinase inhibitors |
| EP1000055A1 (en) | 1997-05-22 | 2000-05-17 | G.D. Searle & Co. | SUBSTITUTED PYRAZOLES AS p38 KINASE INHIBITORS |
| US6979686B1 (en) | 2001-12-07 | 2005-12-27 | Pharmacia Corporation | Substituted pyrazoles as p38 kinase inhibitors |
| US6514977B1 (en) | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
| AR037061A1 (es) | 1997-05-22 | 2004-10-20 | Searle & Co | Compuesto derivado de pirazol sustituido, procesos para preparar dicho compuesto, composicion farmaceutica que lo contiene y su uso en la preparacion de medicamentos |
| US6503904B2 (en) | 1998-11-16 | 2003-01-07 | Syngenta Crop Protection, Inc. | Pesticidal composition for seed treatment |
| EP1142890B1 (en) | 1998-12-25 | 2005-08-03 | Teikoku Hormone Mfg. Co., Ltd. | Aminopyrazole derivatives |
| CN1281604C (zh) | 1999-06-03 | 2006-10-25 | 帝国脏器制药株式会社 | 取代吡唑化合物 |
| EP1212714B1 (en) | 1999-06-30 | 2008-08-13 | Silverbrook Research Pty. Limited | Method and system for user registration on terminal |
| WO2001030154A2 (de) * | 1999-10-25 | 2001-05-03 | Basf Aktiengesellschaft | Pyrazole enthaltende agrochemische zusammensetzungen und ihre verwendung als fungizide flanzenschutzmittel |
| US6660690B2 (en) | 2000-10-06 | 2003-12-09 | Monsanto Technology, L.L.C. | Seed treatment with combinations of insecticides |
| WO2002057265A1 (en) | 2001-01-22 | 2002-07-25 | Sankyo Company, Limited | Compounds substituted with bicyclic amino groups |
| US20020134012A1 (en) | 2001-03-21 | 2002-09-26 | Monsanto Technology, L.L.C. | Method of controlling the release of agricultural active ingredients from treated plant seeds |
| EP1372642A1 (en) * | 2001-03-30 | 2004-01-02 | SmithKline Beecham Corporation | Use of pyrazolopyridines as therapeutic compounds |
| US6962914B2 (en) | 2001-04-27 | 2005-11-08 | Smithkline Beecham Corporation | Pyrazolopyridinyl pyridine and pyrimidine therapeutic compounds |
| SK287857B6 (sk) * | 2001-05-24 | 2012-01-04 | Eli Lilly And Company | Novel pyrrole derivatives as pharmaceutical agents |
| GB0129476D0 (en) | 2001-12-10 | 2002-01-30 | Syngenta Participations Ag | Organic compounds |
| JP2005525382A (ja) | 2002-03-07 | 2005-08-25 | スミスクライン ビーチャム コーポレーション | ピラゾロピリミジンおよびピラゾロトリアジン誘導体ならびにそれを含む医薬組成物 |
| ATE365740T1 (de) | 2002-05-10 | 2007-07-15 | Smithkline Beecham Corp | Substituierte pyrazolopyrimidine |
| GB0217786D0 (en) | 2002-07-31 | 2002-09-11 | Glaxo Group Ltd | Compounds |
| WO2004013135A1 (en) | 2002-07-31 | 2004-02-12 | Smithkline Beecham Corporation | 2-phenylpyridin-4-yl derivatives as alk5 inhibitors |
| JPWO2004029043A1 (ja) | 2002-09-25 | 2006-01-26 | 宇部興産株式会社 | ピラゾール化合物 |
| BRPI0415896A (pt) | 2003-10-28 | 2007-01-09 | Pharmacia Corp | combinações compreendendo um inibidor de hsp90 e um inibidor de fosfodiesterase para tratamento ou prevenção de neoplasia |
| WO2005044194A2 (en) | 2003-10-28 | 2005-05-19 | Pharmacia Corporation | TREATMENT OR PREVENTION OF NEOPLASIA BY USE OF AN Hsp90 INHIBITOR |
| EP1910370B1 (en) | 2005-07-22 | 2015-04-22 | Eli Lilly And Company | A pyridin quinolin substituted pyrrolo [1,2-b] pyrazole monohydrate as tgf-beta inhibitor |
| TW200740435A (en) | 2005-08-10 | 2007-11-01 | Takeda Pharmaceuticals Co | Therapeutic agent for diabetes |
| US20080234130A1 (en) | 2005-08-24 | 2008-09-25 | Pioneer Hi-Bred International, Inc. | Compositions providing tolerance to multiple herbicides and methods of use thereof |
| CA2771677A1 (en) | 2005-08-31 | 2007-03-08 | Monsanto Technology Llc | Nucleotide sequences encoding insecticidal proteins |
| NL2000397C2 (nl) | 2006-01-05 | 2007-10-30 | Pfizer Prod Inc | Bicyclische heteroarylverbindingen als PDE10 inhibitoren. |
| JP2009525350A (ja) | 2006-02-01 | 2009-07-09 | スミスクライン ビーチャム コーポレーション | Rafキナーゼ阻害薬として有用なピロロ[2,3,b]ピリジン誘導体 |
| JP2009530261A (ja) | 2006-03-16 | 2009-08-27 | ファイザー・プロダクツ・インク | ピラゾール化合物 |
| US20090192164A1 (en) | 2006-06-28 | 2009-07-30 | Aska Pharmaceutical Co., Ltd. | Treating agent of inflammatory bowel disease |
| DE102006037399A1 (de) | 2006-08-10 | 2008-02-14 | Archimica Gmbh | Verfahren zur Herstellung von Arylaminen |
| WO2008024978A2 (en) * | 2006-08-24 | 2008-02-28 | Serenex, Inc. | Tetrahydroindolone and tetrahydroindazolone derivatives |
| GB0708141D0 (en) | 2007-04-26 | 2007-06-06 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| EP2217600B1 (en) * | 2007-12-12 | 2012-12-05 | E. I. du Pont de Nemours and Company | Fungicidal bicyclic pyrazoles |
| HRP20120577T1 (hr) | 2008-07-24 | 2012-08-31 | Nerviano Medical Sciences S.R.L. | 3,4-diarilpirazoli kao inhibitori proteinskih kinaza |
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Also Published As
| Publication number | Publication date |
|---|---|
| CA2795523A1 (en) | 2011-10-13 |
| CN102947303A (zh) | 2013-02-27 |
| EA201291007A1 (ru) | 2013-05-30 |
| JP5738978B2 (ja) | 2015-06-24 |
| EP2556073A1 (de) | 2013-02-13 |
| CO6630131A2 (es) | 2013-03-01 |
| EA201591127A1 (ru) | 2015-09-30 |
| KR101797066B1 (ko) | 2017-11-13 |
| CA2795523C (en) | 2018-06-19 |
| EA023272B1 (ru) | 2016-05-31 |
| MX2012011637A (es) | 2012-11-23 |
| EP2556073B1 (de) | 2014-07-23 |
| WO2011124539A1 (de) | 2011-10-13 |
| JP2013523794A (ja) | 2013-06-17 |
| KR20130040843A (ko) | 2013-04-24 |
| US8507472B2 (en) | 2013-08-13 |
| BR112012025718A2 (pt) | 2023-12-05 |
| US20110251178A1 (en) | 2011-10-13 |
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