AR104658A1 - Compuestos de pirazol sustituido que contienen pirimidinilo, la preparación y aplicación de los mismos - Google Patents
Compuestos de pirazol sustituido que contienen pirimidinilo, la preparación y aplicación de los mismosInfo
- Publication number
- AR104658A1 AR104658A1 ARP160101436A ARP160101436A AR104658A1 AR 104658 A1 AR104658 A1 AR 104658A1 AR P160101436 A ARP160101436 A AR P160101436A AR P160101436 A ARP160101436 A AR P160101436A AR 104658 A1 AR104658 A1 AR 104658A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- hetero
- haloalkyl
- alkoxy
- alkoxycarbonyl
- Prior art date
Links
- -1 PYRIMIDINYL Chemical class 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 20
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 18
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 abstract 11
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical class 0.000 abstract 7
- 125000004643 (C1-C12) haloalkoxy group Chemical group 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 4
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 abstract 4
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000005002 aryl methyl group Chemical group 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 2
- 125000004992 haloalkylamino group Chemical group 0.000 abstract 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 2
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- NOIXNOMHHWGUTG-UHFFFAOYSA-N 2-[[4-[4-pyridin-4-yl-1-(2,2,2-trifluoroethyl)pyrazol-3-yl]phenoxy]methyl]quinoline Chemical class C=1C=C(OCC=2N=C3C=CC=CC3=CC=2)C=CC=1C1=NN(CC(F)(F)F)C=C1C1=CC=NC=C1 NOIXNOMHHWGUTG-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract 1
- 125000005108 alkenylthio group Chemical group 0.000 abstract 1
- 125000005085 alkoxycarbonylalkoxy 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
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005170 cycloalkyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000006797 haloalkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000006809 haloalkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004693 haloalkylthiocarbonyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- 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
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—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
Abstract
Reivindicación 1: Una clase de compuestos de pirazol sustituido que contienen pirimidinilo representados por la fórmula general (1) en donde: R¹ se selecciona de H, halógeno, ciano, nitro, carboxilo, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, cicloalquilo C₃₋₁₂, alcoxi C₁₋₁₂, haloalcoxi C₁₋₁₂, alquiltio C₁₋₁₂, haloalquiltio C₁₋₁₂, alquilsulfinilo C₁₋₁₂, alquilsulfonilo C₁₋₁₂, alquenilo C₂₋₁₂, haloalquenilo C₂₋₁₂, alquinilo C₂₋₁₂, haloalquinilo C₂₋₁₂, alquenoxi C₃₋₁₂, haloalquenoxi C₃₋₁₂, alquinoxi C₃₋₁₂, haloalquinoxi C₃₋₁₂, alquilamino C₁₋₁₂, di(alquil C₁₋₁₂)amino, alquilaminocarbonilo C₁₋₁₂, haloalquilaminocarbonilo C₁₋₁₂, alcoxicarbonilo C₁₋₁₂ haloalcoxicarbonilo C₁₋₁₂, alcoxi C₁₋₁₂alquilo C₁₋₁₂ o alquiltio C₁₋₁₂alquilo C₁₋₁₂; R² se selecciona de H, halógeno, ciano, nitro, amino, carboxilo, CHO, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, alcoxi C₁₋₁₂ o haloalcoxi C₁₋₁₂; R¹, R² y su anillo conjunto de pirimidina pueden formar un anillo de cinco miembros, un anillo de seis miembros, un anillo de siete miembros o un anillo de ocho miembros que contiene un átomo de carbono, un átomo de nitrógeno, un átomo de oxigeno o un átomo de azufre; X se selecciona de NR³, O ó S; Y se selecciona de NR³, O ó S; R³ se selecciona de H, OH, CHO, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, alcoxi C₁₋₁₂, haloalcoxi C₁₋₁₂, cicloalquilo C₃₋₁₂, alquiltio C₁₋₁₂, alqueniltio C₂₋₁₂, alquenilo C₂₋₁₂, alquinilo C₂₋₁₂, haloalquenilo C₂₋₁₂, haloalquinilo C₂₋₁₂, alcoxi C₁₋₁₂alquilo C₁₋₁₂, haloalcoxi C₁₋₁₂alquilo C₁₋₁₂, alquiltio C₁₋₁₂alquilo C₁₋₁₂, haloalquiltio C₁₋₁₂alquilo C₁₋₁₂, alquilsulfinilo C₁₋₁₂, haloalquilsulfinilo C₁₋₁₂, alquilsulfonilo C₁₋₁₂, haloalquilsulfonilo C₁₋₁₂, alquilaminosulfonilo C₁₋₁₂, di(alquil C₁₋₁₂)aminosulfonilo, alquilsulfonilaminocarbonilo C₁₋₁₂, alquilcarbonilaminosulfonilo C₁₋₁₂, cicloalquiloxicarbonilo C₃₋₁₂, alquilcarbonilo C₁₋₁₂, haloalquilcarbonilo C₁₋₁₂, alcoxicarbonilo C₁₋₁₂, haloalcoxicarbonilo C₁₋₁₂, alquilcarbonil C₁₋₁₂alquilo C₁₋₁₂, alcoxicarbonil C₁₋₁₂alquilo C₁₋₁₂, alquilaminocarbonilo C₁₋₁₂, di(alquil C₁₋₁₂)aminocarbonilo, alquenoxicarbonilo C₂₋₁₂, alquinoxicarbonilo C₂₋₁₂, alcoxi C₁₋₁₂alcoxicarbonilo C₁₋₁₂, alquilaminotio C₁₋₁₂, di(alquil C₁₋₁₂)aminotio, (hetero)arilcarbonilalquilo C₁₋₆, (hetero)arilcarbonilo, (hetero)ariloxicarbonilo, (hetero)arilalquiloxicarbonilo C₁₋₆ o (hetero)arilalquilo C₁₋₆ no sustituidos o también sustituidos por 1 a 5 de los siguientes grupos: halo, nitro, ciano, alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆ o haloalcoxi C₁₋₆; R⁴, R⁵ pueden ser iguales o diferentes y se seleccionan respectivamente de H, halógeno, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, alcoxi C₁₋₁₂ o haloalcoxi C₁₋₁₂; o R⁴, R⁵ y sus carbonos conjuntos también pueden formar un ciclo C₃₋₈; R⁶, R⁷ pueden ser iguales o diferentes y se seleccionan respectivamente de H, halógeno, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, alcoxi C₁₋₁₂ o haloalcoxi C₁₋₁₂; o R⁶, R⁷ y su carbono conjunto también pueden formar un ciclo C₃₋₈; el número entero m se selecciona de 1 a 5; R⁸ se selecciona de H, ciano, halógeno, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, alcoxicarbonilo C₁₋₁₂, haloalcoxicarbonilo C₁₋₁₂, hetero(arilo), (hetero)arilmetilo, (hetero)arilcarbonilo, (hetero)arilmetilcarbonilo o (hetero)ariloxicarbonilo no sustituidos o también sustituidos por 1 a 5 R¹¹; R⁹ se selecciona de H, ciano, halógeno, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, alcoxicarbonilo C₁₋₁₂, haloalquilcarbonilo C₁₋₁₂, (hetero)arilo, (hetero)arilmetilo, (hetero)arilcarbonilo, (hetero)arilmetilcarbonilo o (hetero)ariloxicarbonilo no sustituidos o también sustituidos por 1 a 5 R¹¹; R¹⁰ se selecciona de alquilo C₁₋₁₂, cicloalquilo C₃₋₈, haloalquilo C₁₋₁₂, alquilcarbonilo C₁₋₁₂, haloalquilcarbonilo C₁₋₁₂, alquilsulfonilo C₁₋₁₂ haloalquilsulfonilo C₁₋₁₂, alcoxicarbonilo C₁₋₁₂, alcoxi C₁₋₁₂alquilo C₁₋₁₂, alcoxicarbonil C₁₋₁₂alquilo C₁₋₁₂, (hetero)arilo, (hetero)arilmetilo, (hetero)arilcarbonilo, (hetero)arilmetilcarbonilo o (hetero)ariloxicarbonilo no sustituidos o también sustituidos por 1 a 5 R¹¹; R¹¹ se selecciona de halógeno, OH, amino, ciano, nitro, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, alcoxi C₁₋₁₂, haloalcoxi C₁₋₁₂, cicloalquilo C₃₋₁₂, alquilamino C₁₋₁₂, haloalquilamino C₁₋₁₂, di(alquil C₁₋₁₂)amino, halodi(alquil C₁₋₁₂), C(=O)NR¹²R¹³, alquiltio C₁₋₁₂, haloalquiltio C₁₋₁₂, alquenilo C₂₋₁₂, alquinilo C₂₋₁₂, alquenoxi C₂₋₁₂, haloalquenoxi C₂₋₁₂, alquinoxi C₂₋₁₂, haloalquinoxi C₂₋₁₂, alquilsulfonilo C₁₋₁₂, haloalquilsulfonilo C₁₋₁₂, alquilcarbonilo C₁₋₁₂, haloalquilcarbonilo C₁₋₁₂, alcoxicarbonilo C₁₋₁₂, haloalcoxicarbonilo C₁₋₁₂, alcoxi C₁₋₁₂alquilo C₁₋₁₂, haloalcoxi C₁₋₁₂alquilo C₁₋₁₂, alquiltio C₁₋₁₂alquilo C₁₋₁₂, haloalquiltio C₁₋₁₂alquilo C₁₋₁₂, alcoxicarbonil C₁₋₁₂alquilo C₁₋₁₂, haloalcoxicarbonil C₁₋₁₂alquilo C₁₋₁₂, alquiltiocarbonil C₁₋₁₂alquilo C₁₋₁₂, haloalquiltiocarbonil C₁₋₁₂alquilo C₁₋₁₂, alquilcarboniloxi C₁₋₁₂, haloalquilcarboniloxi C₁₋₁₂, alcoxicarboniloxi C₁₋₁₂, haloalcoxicarboniloxi C₁₋₁₂, alquilsulfoniloxi C₁₋₁₂, haloalquilsulfoniloxi C₁₋₁₂, alcoxi C₁₋₁₂alcoxi C₁₋₁₂ o haloalcoxi C₁₋₁₂alcoxi C₁₋₁₂; R¹², R¹³ pueden ser iguales o diferentes y se seleccionan respectivamente de H, alquilo C₁₋₁₂ o haloalquilo C₁₋₁₂; W se selecciona de H, halógeno, alquilo C₁₋₁₂, haloalquilo C₁₋₁₂, cicloalquilo C₃₋₈, alcoxi C₁₋₁₂, alquiltio C₁₋₁₂; o alquilsulfonilo C₁₋₁₂; la posición de Y unido al anillo de pirazol es desde la posición 3, la posición 4 o la posición 5; cuando Y está unido a la posición 3 del pirazol, R⁸ está en la posición 4, R⁹ está en la posición 5; cuando Y está unido a la posición 4 de pirazol, R⁸ está en la posición 3, R⁹ está en la posición 5; cuando Y está unido a la posición 5 de pirazol, R⁸ está en la posición 3, R⁹ está en la posición 4; o las sales formadas a partir de los compuestos representados por la fórmula general (1).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510252832 | 2015-05-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR104658A1 true AR104658A1 (es) | 2017-08-02 |
Family
ID=57319458
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP160101436A AR104658A1 (es) | 2015-05-18 | 2016-05-17 | Compuestos de pirazol sustituido que contienen pirimidinilo, la preparación y aplicación de los mismos |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US11008339B2 (es) |
| EP (2) | EP3702355B1 (es) |
| CN (1) | CN106167484B (es) |
| AR (1) | AR104658A1 (es) |
| AU (1) | AU2016264519B2 (es) |
| BR (2) | BR112017024665B1 (es) |
| CA (1) | CA2982206C (es) |
| ES (1) | ES2824119T3 (es) |
| RU (1) | RU2687089C2 (es) |
| UA (2) | UA124524C2 (es) |
| WO (1) | WO2016184378A1 (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10743535B2 (en) | 2017-08-18 | 2020-08-18 | H&K Solutions Llc | Insecticide for flight-capable pests |
| CN109776427B (zh) * | 2017-11-13 | 2022-08-23 | 沈阳中化农药化工研发有限公司 | 嘧啶双胺类化合物及其用途 |
| EP3719015A4 (en) * | 2017-11-29 | 2021-04-21 | Shenyang Sinochem Agrochemicals R & D Co., Ltd. | SUBSTITUTED PYRIMIDINE COMPOUND AND MANUFACTURING METHOD FOR ITS AND USES THEREOF |
| CN109836417A (zh) * | 2017-11-29 | 2019-06-04 | 沈阳中化农药化工研发有限公司 | 取代嘧啶类化合物及其制备方法和作为杀菌剂的用途 |
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| RU2017135214A (ru) | 2019-04-10 |
| CA2982206A1 (en) | 2016-11-24 |
| US20180141961A1 (en) | 2018-05-24 |
| CN106167484B (zh) | 2020-03-17 |
| AU2016264519B2 (en) | 2018-06-28 |
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