AR123502A1 - Nuevos compuestos de picolinamida para combatir hongos fitopatógenos - Google Patents
Nuevos compuestos de picolinamida para combatir hongos fitopatógenosInfo
- Publication number
- AR123502A1 AR123502A1 ARP210102541A ARP210102541A AR123502A1 AR 123502 A1 AR123502 A1 AR 123502A1 AR P210102541 A ARP210102541 A AR P210102541A AR P210102541 A ARP210102541 A AR P210102541A AR 123502 A1 AR123502 A1 AR 123502A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- ring
- group
- cycloalkyl
- Prior art date
Links
- 241000233866 Fungi Species 0.000 title 1
- 230000003032 phytopathogenic effect Effects 0.000 title 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical class NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 23
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 12
- 150000002367 halogens Chemical group 0.000 abstract 12
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 10
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 7
- 125000004122 cyclic group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000005842 heteroatom Chemical group 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 4
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- -1 nitro, hydroxy Chemical group 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 150000003573 thiols Chemical class 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 abstract 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000005844 heterocyclyloxy group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000006413 ring segment Chemical group 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000005110 aryl thio group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 239000002184 metal Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—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
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P3/00—Fungicides
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D417/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mycology (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto de fórmula (1) en donde, R¹ se selecciona entre el grupo que consiste en hidroxi, halógeno, alquilo C₁-C₆, haloalquilo C₁-C₆, cicloalquilo C₃-C₆, alcoxi C₁-C₆, cicloalquiloxi C₃-C₆, alquiltio C₁-C₆, cicloalquiltio C₁-C₆, -NHR⁹ y -N(R⁹)₂; R¹ᵃ se selecciona entre el grupo que consiste en hidroxi, halógeno, alquilo C₁-C₆, cicloalquilo C₃-C₆, haloalquilo C₁-C₆ y alcoxi C₁-C₆; R² se selecciona entre el grupo que consiste en hidrógeno, alquilo C₁-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆-alquilo C₁-C₆, -SOₙ-alquilo C₁-C₆, -C(O)-R⁹, -C(O)-OR⁹, -(CH₂)ₘ-O-C(O)-R⁹, -C(O)-N(R⁹)₂, -(CH₂)ₘ-O-C(O)-N(R⁹)₂; R³ se selecciona entre el grupo que consiste en hidrógeno, alquilo C₁-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, alcoxi C₁-C₆-alquilo C₁-C₆, cicloalquilo C₃-C₆, cicloalquil C₃-C₆-alquilo C₁-C₆, -(CH₂)ₘ-OR⁹, -(CH₂)ₘ-C(O)-R⁹, -(CH₂)ₘ-C(O)-OR⁹, -(CH₂)ₘ-C(O)-N(R⁹)₂, -(CH₂)ₘ-O-C(O)-OR⁹, -(CH₂)ₘ-O-C(O)-N(R⁹)₂ y -(CH₂)ₘ-C(O)-alcoxi C₁-C₆; o R² y R³ junto con los átomos a los que están unidos pueden formar un anillo heterocíclico de seis miembros; y uno o más átomos de C del anillo pueden reemplazarse opcionalmente por C(=O), C(=S), C=NR²ᵃ o CR²ᵃN(R²ᵃ)₂; en donde el anillo heterocíclico puede estar opcionalmente sustituido con uno o más grupos iguales o diferentes de R²ᵃ; o R³ y R⁴ junto con los átomos a los que están unidos pueden formar un anillo heterocíclico no aromático de 5 a 6 miembros; en donde el heteroátomo adicional de dicho anillo se selecciona entre N, O ó S(=O)₀₋₂ y uno o más átomos de C del anillo pueden reemplazarse opcionalmente por C(=O), C(=S) o C(=NR⁹); el anillo puede estar opcionalmente sustituido con uno o más grupos iguales o diferentes de R³ᵃ; R²ᵃ se selecciona entre el grupo que consiste en halógeno, alquilo C₁-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, cicloalquilo C₃-C₈ y alcoxi C₁-C₄-alquilo C₁-C₄; R³ᵃ se selecciona entre el grupo que consiste en halógeno, alquilo C₁-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, cicloalquilo C₃-C₈ y alcoxi C₁-C₄-alquilo C₁-C₄; W representa O ó S; R⁴ y R⁵ se seleccionan independientemente entre el grupo que consiste en hidrógeno, halógeno, alquilo C₁-C₆, alquenilo C₂-C₆, alquinilo C₂-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, alcoxi C₁-C₆-alquilo C₁-C₆, cicloalquilo C₃-C₆, cicloalquil C₃-C₆-alquilo C₁-C₆, arilo C₆-C₁₀, aralquil C₇-C₁₄ y heterociclilo C₃-C₁₀; cada grupo de R⁴ y R⁵ puede estar opcionalmente sustituido con uno o más grupos seleccionados entre R⁴ᵃ; o R⁴ y R⁵ junto con los átomos a los que están unidos pueden formar un anillo carbocíclico no aromático o anillo heterocíclico no aromático de 3 a 6 miembros; en donde el heteroátomo de dicho anillo se selecciona entre N, O ó S(=O)₀₋₂ y uno o más átomos de C del anillo pueden reemplazarse opcionalmente por C(=O) o C(=S) o C(=NR⁹); el anillo puede estar opcionalmente sustituido con uno o más grupos iguales o diferentes de R⁴ᵃ; R⁴ᵃ se selecciona entre el grupo que consiste en halógeno, ciano, nitro, hidroxilo, tiol, amino, alquilo C₁-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, haloalcoxi C₁-C₆, alquiltio C₁-C₆, haloalquiltio C₁-C₆, cicloalquilo C₃-C₈ y alcoxi C₁-C₄-alquilo C₁-C₄; el anillo A representa un anillo heterocíclico de cinco o seis miembros; en donde el heteroátomo de dicho anillo se selecciona entre N, O, S(=O)₀₋₂, y uno o más átomos de C del anillo o el sistema de anillo pueden reemplazarse opcionalmente por C(=O), C(=S) o C(=NR⁹); dicho anillo A puede estar opcionalmente sustituido con uno o más grupos iguales o diferentes de RA; RA se selecciona entre el grupo que consiste en halógeno, hidroxi, alquilo C₁-C₆, alcoxi C₁-C₄, haloalquilo C₁-C₆, haloalcoxi C₁-C₄ y arilo C₆-C₁₀; R⁶ se selecciona entre el grupo que consiste en hidrógeno, halógeno, hidroxi, alquilo C₁-C₆, alcoxi C₁-C₄, haloalquilo C₁-C₆, haloalcoxi C₁-C₄ y arilo C₆-C₁₀; R⁷ y R⁸ se seleccionan independientemente entre el grupo que consiste en hidroxi, halógeno, alquilo C₁-C₆, alquenilo C₂-C₆, alquinilo C₂-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, alcoxi C₁-C₆-alquilo C₁-C₆, cicloalquilo C₃-C₆, cicloalquil C₃-C₆-alquilo C₁-C₆, arilo C₆-C₁₀, aralquilo C₇-C₁₄, ariloxi C₆-C₁₀, ariltio C₆-C₁₀, aril C₆-C₁₀-alcoxi C₁-C₆, heterociclilo C₃-C₁₀ y heterocicliloxi C₃-C₁₀; cada grupo de R⁷ y R⁸ puede estar opcionalmente sustituido con uno o más grupos seleccionados entre R⁷ᵃ; o R⁷ᵃ se selecciona entre el grupo que consiste en ciano, halógeno, nitro, hidroxilo, tiol, amino, alquilo C₁-C₆, alquenilo C₂-C₆, alquinilo C₂-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, alcoxi C₁-C₆-alquilo C₁-C₆, cicloalquilo C₃-C₆, cicloalquil C₃-C₆-alquilo C₁-C₆, fenilo, bencilo, feniltio, fenil-alcoxi C₁-C₆, heterociclilo C₃-C₁₀ y heterocicliloxi C₃-C₁₀; R⁷ y R⁸ junto con los átomos a los que están unidos pueden formar un anillo o sistema de anillo carbocíclico aromático o no aromático o anillo o sistema de anillo heterocíclico aromático o no aromático de 3 a 14 miembros; en donde el heteroátomo del anillo heterocíclico aromático se selecciona entre N, O y S; en donde el heteroátomo de dicho anillo o sistema de anillo se selecciona entre N, O ó S(=O)₀₋₂ y uno o más átomos de C del anillo o el sistema de anillo pueden reemplazarse opcionalmente por C(=O), C(=S) o C(=NR⁹); el anillo o sistema de anillo puede estar opcionalmente sustituido con uno o más grupos iguales o diferentes de R⁸ᵃ; con la condición de que cuando R⁷ y R⁸ forman un anillo aromático, entonces R⁶ está ausente; R⁸ᵃ se selecciona entre el grupo que consiste en halógeno, ciano, nitro, hidroxilo, tiol, amino, alquilo C₁-C₆, haloalquilo C₁-C₆, alcoxi C₁-C₆, alcoxi C₁-C₄-alquilo C₁-C₄, haloalcoxi C₁-C₆, alquiltio C₁-C₆, haloalquiltio C₁-C₆, cicloalquilo C₃-C₈, fenilo, bencilo, y heterociclilo C₃-C₁₀; R⁹ se selecciona entre el grupo que consiste en hidrógeno, formilo, alquilo C₁-C₄, alquenilo C₂-C₄, alquinilo C₂-C₄, haloalquilo C₁-C₄, cicloalquilo C₃-C₅, cicloalquil C₃-C₅-alquilo C₁-C₃, arilo C₆-C₁₀, aralquil C₇-C₁₄ y heterociclilo C₃-C₁₀; cada grupo de R¹ a R⁹; R¹ᵃ, R²ᵃ, RA, R⁴ᵃ, R⁷ᵃ y R⁸ᵃ puede estar opcionalmente sustituido con uno o más grupos seleccionados entre el grupo que consiste en halógeno, ciano, nitro, R, OR, SR, N(R)₂, COR y CON(R)₂; R se seleccionan independientemente entre el grupo que consiste en hidrógeno, alquilo C₁-C₄, alquenilo C₂-C₄, alquinilo C₂-C₄, haloalquilo C₁-C₄, haloalquenilo C₂-C₄, haloalquinilo C₂-C₄, alcoxi C₁-C₄, haloalcoxi C₁-C₄, cicloalquilo C₃-C₆, halocicloalquilo C₃-C₆, arilo C₆-C₁₀, aril C₆-C₁₀-alcoxi C₁-C₄, aralquil C₇-C₁₄ y heterociclilo C₃-C₁₀; n es un número entero seleccionado de 0 a 2 y m es un número entero seleccionado de 0 a 3; y/o N-óxidos, complejos metálicos, isómeros, polimorfos y sales agrícolamente aceptables del mismo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN202011039959 | 2020-09-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR123502A1 true AR123502A1 (es) | 2022-12-07 |
Family
ID=78333038
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP210102541A AR123502A1 (es) | 2020-09-15 | 2021-09-14 | Nuevos compuestos de picolinamida para combatir hongos fitopatógenos |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP4214203A1 (es) |
| AR (1) | AR123502A1 (es) |
| TW (1) | TW202227423A (es) |
| UY (1) | UY39424A (es) |
| WO (1) | WO2022058878A1 (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116874441B (zh) * | 2023-06-21 | 2025-07-22 | 贵州大学 | 一种含1,2,4-噁二唑的柔性芳基甲酰胺类衍生物及其制备方法和用途 |
| CN119504592B (zh) * | 2024-11-19 | 2025-07-29 | 深圳智微通科技有限公司 | 3-氨基-5-(4-苯氧基苯基)-4-氰基-1h-吡唑的合成方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| FR1339175A (fr) * | 1962-11-13 | 1963-10-04 | Geigy Ag J R | Nouveaux dérivés de l'oxazine et leur préparation |
| CH419162A (de) * | 1962-10-24 | 1966-08-31 | Geigy Ag J R | Verfahren zur Herstellung von neuen Oxazinderivaten |
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| CA2005658A1 (en) | 1988-12-19 | 1990-06-19 | Eliahu Zlotkin | Insecticidal toxins, genes encoding these toxins, antibodies binding to them and transgenic plant cells and plants expressing these toxins |
| EP0392225B1 (en) | 1989-03-24 | 2003-05-28 | Syngenta Participations AG | Disease-resistant transgenic plants |
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-
2021
- 2021-09-14 AR ARP210102541A patent/AR123502A1/es not_active Application Discontinuation
- 2021-09-14 UY UY0001039424A patent/UY39424A/es unknown
- 2021-09-14 EP EP21798096.0A patent/EP4214203A1/en not_active Withdrawn
- 2021-09-14 WO PCT/IB2021/058347 patent/WO2022058878A1/en not_active Ceased
- 2021-09-15 TW TW110134501A patent/TW202227423A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW202227423A (zh) | 2022-07-16 |
| EP4214203A1 (en) | 2023-07-26 |
| UY39424A (es) | 2022-03-31 |
| WO2022058878A1 (en) | 2022-03-24 |
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