AR118673A1 - Procedimiento para la preparación de derivados de oxadiazol microbiocidas - Google Patents
Procedimiento para la preparación de derivados de oxadiazol microbiocidasInfo
- Publication number
- AR118673A1 AR118673A1 ARP200101052A ARP200101052A AR118673A1 AR 118673 A1 AR118673 A1 AR 118673A1 AR P200101052 A ARP200101052 A AR P200101052A AR P200101052 A ARP200101052 A AR P200101052A AR 118673 A1 AR118673 A1 AR 118673A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- heterocyclyl
- heteroaryl
- cycloalkyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 150000004866 oxadiazoles Chemical class 0.000 title abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 22
- 125000001072 heteroaryl group Chemical group 0.000 abstract 12
- 125000000623 heterocyclic group Chemical group 0.000 abstract 12
- 229910052757 nitrogen Inorganic materials 0.000 abstract 10
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 9
- 229910052760 oxygen Inorganic materials 0.000 abstract 9
- 229910052717 sulfur Inorganic materials 0.000 abstract 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 8
- 125000005842 heteroatom Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 7
- 150000001875 compounds Chemical class 0.000 abstract 6
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 abstract 5
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 5
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 4
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 125000002950 monocyclic group Chemical group 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- -1 cyano, hydroxyl Chemical group 0.000 abstract 3
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 3
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 3
- 125000006574 non-aromatic ring group Chemical group 0.000 abstract 3
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 2
- 230000003641 microbiacidal effect Effects 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000005277 alkyl imino group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 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
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
-
- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/10—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 carbon chain containing aromatic 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
- C07D413/02—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
- 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
- C07D417/02—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
- C07D417/10—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 carbon chain containing aromatic rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
La presente se refiere a un procedimiento para la preparación de derivados de oxadiazol microbiocidas adecuados para su uso, por ejemplo, como principios activos, que tienen actividad microbiocida, en particular, actividad fungicida. Reivindicación 1: Un procedimiento para la preparación de un compuesto de fórmula (1) en la que A es un compuesto de fórmula (4) ó (5) en la que cada uno de los compuestos de fórmula (4) y (5) está opcionalmente sustituido con 1 ó 2 sustituyentes independientemente seleccionados de halógeno, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxilo C₁₋₄ y haloalcoxilo C₁₋₄; n es 0, 1 ó 2; R¹ y R² se seleccionan independientemente de hidrógeno, halógeno, ciano, hidroxilo, alquilo C₁₋₄, alcoxilo C₁₋₄ y haloalquilo C₁₋₄; o R¹ y R², junto con el átomo de carbono al que están unidos, forman un anillo de ciclopropilo; Z es Z¹ o Z²; Z¹ es hidrógeno, halógeno, ciano, -OH o -SH; Z² es alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxilo C₁₋₄, haloalcoxilo C₁₋₄, C₁₋₄, -COOH, -C(=W)-X, -NR³R⁴, -NR³-C(=W)-X, -S(=O)₂-R⁵ o -NR³-S(=O)₂-R⁵; o Z² es cicloalquilo C₃₋₈, cicloalquil C₃₋₈-alquilo C₁₋₂, heterociclilo, heterociclil-alquilo C₁₋₂, fenilo, fenilalquilo C₁₋₂, heteroarilo, heteroaril-alquilo C₁₋₂ o heterodiarilo, en el que el resto heterociclilo es un anillo no aromático de 4 a 7 miembros que comprende 1, 2 ó 3 heteroátomos o grupos seleccionados individualmente de O, S, N, NR⁶, C(=O) y S(=O)₂, y el resto heteroarilo es un anillo aromático monocíclico de 5 ó 6 miembros que comprende 1, 2, 3 ó 4 heteroátomos seleccionados individualmente de N, O y S; en el que cualquiera de dicho cicloalquilo, heterociclilo, fenilo, heteroarilo o heterodiarilo está opcionalmente sustituido con 1 ó 2 sustituyentes, que pueden ser iguales o diferentes, seleccionados de R⁷; W es O ó S; X es halógeno, -NR³R⁴, R⁵, -NR³-[CR⁸R⁹]ₘ-CR¹⁰(=NR⁵), -C(=O)-NR³R⁴, -C(=O)-R⁵, -C(=N-alcoxi C₁₋₄)-R⁵ o -OR¹¹; R³ y R⁴ se seleccionan independientemente de hidrógeno, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxilo C₁₋₄, hidroxialquilo C₁₋₄, alcoxi C₁₋₄-alquilo C₁₋₄, haloalcoxilo C₁₋₄, haloalcoxi C₁₋₂-alquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₂₋₆, alqueniloxi C₃₋₄, alquiniloxilo C₃₋₄, alquilcarboniloxilo C₁₋₄, N-alquilamino C₁₋₄ y N,N-di(alquil C₁₋₄)amino; o R³ y R⁴ se seleccionan independientemente de cicloalquilo C₃₋₈, cicloalquil C₁₋₄;-alquilo C₁₋₂, heterociclilo, heterociclilalquilo C₁₋₂, fenilo, fenilalquilo C₁₋₂, heteroarilo y heteroarilalquilo C₁₋₂, en el que el resto heterociclilo es un anillo no aromático de 4 a 6 miembros que comprende 1, 2 ó 3 heteroátomos o grupos seleccionados individualmente de O, S, N, NR⁶, C(=O) y S(=O)₂, y el resto heteroarilo es un anillo aromático monocíclico de 5 ó 6 miembros que comprende 1, 2, 3 ó 4 heteroátomos seleccionados individualmente de N, O y S; en el que cualquiera de dicho cicloalquilo, heterociclilo, fenilo o heteroarilo está opcionalmente sustituido con 1 ó 2 sustituyentes, que pueden ser iguales o diferentes, seleccionados de R⁷; o R³ y X, junto con el átomo de nitrógeno al que está unido R³, y junto con el grupo -C(=W), forman un heterociclilo, heterociclilalquilo C₁₋₆, heteroarilo, heteroarilalquilo C₁₋₂ o heterodiarilo, en el que el resto heterociclilo es un anillo no aromático de 4 a 7 miembros que comprende 1, 2 ó 3 heteroátomos o grupos seleccionados individualmente de O, S, N, NR⁶, C(=O) y S(=O)₂, y el resto heteroarilo es un anillo aromático monocíclico de 5 ó 6 miembros que comprende 1, 2, 3 ó 4 heteroátomos seleccionados individualmente de N, O y S; en el que cualquiera de dicho heterociclilo, heteroarilo o heterodiarilo está opcionalmente sustituido con 1 ó 2 sustituyentes, que pueden ser iguales o diferentes, seleccionados de R⁷; R⁵ es alquilo C₁₋₄, haloalquilo C₁₋₄, hidroxialquilo C₁₋₄, cianoalquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₂₋₆, alcoxilo C₁₋₄, haloalcoxilo C₁₋₄, o alcoxi C₁₋₄-alquilo C₁₋₄, o haloalcoxi C₁₋₂-alquilo C₁₋₄; o R⁵ es cicloalquilo C₃₋₈, cicloalquil C₃₋₈-alquilo C₁₋₂, heterociclilo, heterociclilalquilo C₁₋₆, fenilo, fenilalquilo C₁₋₂, heteroarilo, heteroarilalquilo C₁₋₂ o heterodiarilo, en el que el resto heterociclilo es un anillo no aromático de 4 a 6 miembros que comprende 1, 2 ó 3 heteroátomos o grupos seleccionados individualmente de O, S, N, NR⁶, C(=O) y S(=O)₂, y el resto heteroarilo es un anillo aromático monocíclico de 5 ó 6 miembros que comprende 1, 2, 3 ó 4 heteroátomos seleccionados individualmente de N, O y S; en el que cualquiera de dicho cicloalquilo, heterociclilo, fenilo, heteroarilo o heterodiarilo está opcionalmente sustituido con 1 ó 2 sustituyentes, que pueden ser iguales o diferentes, seleccionados de R⁷; R⁶ es hidrógeno, alquilo C₁₋₄, alcoxilo C₁₋₄, formilo, (alquil C₁₋₄)carbonilo, (alcoxilo C₁₋₄)carbonilo, N-(alquil C₁₋₄)aminocarbonilo, N,N-di(alquil C₁₋₄)aminocarbonilo, (alquil C₁₋₄)sulfonilo, N-(alquil C₁₋₄)aminosulfonilo o N,N-di(alquil C₁₋₄)aminosulfonilo; R⁷ es hidrógeno, ciano, hidroxilo, alquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₂₋₆, haloalquilo C₁₋₄, haloalquenilo C₂₋₄, alcoxilo C₁₋₄, haloalcoxilo C₁₋₄, alqueniloxilo C₃₋₄, alquiniloxilo C₃₋₄, N-alquilamino C₁₋₄, N,N-di(alquil C₁₋₄)amino, alquilcarbonilo C₁₋₄, alcoxicarbonilo C₁₋₄, aminocarbonilo, (alquil C₁₋₄)carbonilamino-alquilo C₁₋₄, N-alquilaminocarbonilo C₁₋₄, N,N-dialquilaminocarbonilo C₁₋₄, alcoxicarbonilamino C₁₋₄, N-alcoxi C₁₋₄aminocarbonilo, N-alquil C₁₋₄-N-alcoxi C₁₋₄aminocarbonilo, cicloalquilaminocarbonilo C₃₋₈, N-cicloalquil C₃₋₈-alquilaminocarbonilo C₁₋₂, N-alcoxi C₁₋₄-alquilaminocarbonilo C₁₋₄, N-alcoxi C₁₋₄-alquilimino C₁₋₄, alquilsulfinilo C₁₋₄ o alquilsulfanilo C₁₋₄; m es 0, 1 ó 2; R⁸ y R⁹ se seleccionan independientemente de hidrógeno, halógeno, ciano, alquilo C₁₋₄ y haloalquilo C₁₋₄; o R⁸ y R⁹, junto con el átomo de carbono al que están unidos, forman un anillo de ciclopropilo; R¹⁰ es hidrógeno, alquilo C₁₋₆, alquenilo C₂₋₄, alquinilo C₂₋₆, haloalquilo C₁₋₄, cicloalquilo C₃₋₈ o fenilo; R¹¹ es alquilo C₁₋₈, haloalquilo C₁₋₄, hidroxialquilo C₁₋₆, alcoxi C₁₋₄-alquilo C₁₋₆, haloalcoxi C₁₋₂-alquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₂₋₆ o alquilcarboniloxi C₁₋₄-alquilo C₁₋₄; comprendiendo dicho procedimiento la etapa de hacer reaccionar un compuesto de fórmula (2) en la que A, n, R¹, R² y Z son tal como se definieron para el compuesto de fórmula (1), con un compuesto de fórmula (3) en la que R¹² es alquilo C₁₋₄.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN201911015611 | 2019-04-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR118673A1 true AR118673A1 (es) | 2021-10-20 |
Family
ID=70292983
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP200101052A AR118673A1 (es) | 2019-04-18 | 2020-04-15 | Procedimiento para la preparación de derivados de oxadiazol microbiocidas |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US12264138B2 (es) |
| EP (1) | EP3956318A1 (es) |
| JP (1) | JP7658912B2 (es) |
| CN (1) | CN113748105B (es) |
| AR (1) | AR118673A1 (es) |
| BR (1) | BR112021020673A2 (es) |
| CL (1) | CL2021002713A1 (es) |
| CO (1) | CO2021013497A2 (es) |
| IL (1) | IL286566A (es) |
| MX (1) | MX2021012542A (es) |
| UY (1) | UY38667A (es) |
| WO (1) | WO2020212513A1 (es) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7735311B2 (ja) | 2020-04-28 | 2025-09-08 | ビーエーエスエフ ソシエタス・ヨーロピア | ミトコンドリアチトクロムｂタンパク質中にＱｏ阻害剤ＩＩに対して耐性を付与するアミノ酸置換Ｆ１２９Ｌを含む植物病原性菌類を駆除するためのストロビルリン型化合物の使用 |
| UA129922C2 (uk) | 2020-04-28 | 2025-09-10 | Басф Се | ЗАСТОСУВАННЯ СПОЛУК СТРОБІЛУРИНОВОГО ТИПУ ДЛЯ БОРОТЬБИ З ФІТОПАТОГЕННИМИ ГРИБАМИ, ЯКІ МІСТЯТЬ АМІНОКИСЛОТНУ ЗАМІНУ F129L В МІТОХОНДРІАЛЬНОМУ БІЛКУ ЦИТОХРОМІ b, ЩО НАДАЄ СТІЙКОСТІ ДО Qо ІНГІБІТОРІВ IІІ |
| UA129899C2 (uk) | 2020-04-28 | 2025-09-03 | Басф Се | ЗАСТОСУВАННЯ СПОЛУК СТРОБІЛУРИНОВОГО ТИПУ ДЛЯ БОРОТЬБИ З ФІТОПАТОГЕННИМИ ГРИБАМИ, ЯКІ МІСТЯТЬ АМІНОКИСЛОТНУ ЗАМІНУ F129L В МІТОХОНДРІАЛЬНОМУ БІЛКУ ЦИТОХРОМІ b, ЩО НАДАЄ СТІЙКОСТІ ДО Qo ІНГІБІТОРІВ IV |
| KR20230005260A (ko) | 2020-04-28 | 2023-01-09 | 바스프 에스이 | Qo 억제제 I 에 대한 내성을 부여하는 미토콘드리아 시토크롬 b 단백질 내에 아미노산 치환 F129L 을 함유하는 식물병원성 진균의 퇴치를 위한 스트로빌루린 유형 화합물의 용도 |
| US20230255200A1 (en) | 2020-07-08 | 2023-08-17 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors vi |
| EP3939961A1 (en) | 2020-07-16 | 2022-01-19 | Basf Se | Strobilurin type compounds and their use for combating phytopathogenic fungi |
| EP4195928B1 (en) | 2020-08-11 | 2025-06-18 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors viii |
| WO2022106304A1 (en) | 2020-11-23 | 2022-05-27 | BASF Agro B.V. | Compositions comprising mefentrifluconazole |
| WO2022117373A1 (en) | 2020-12-01 | 2022-06-09 | Basf Se | Mixtures containing metarylpicoxamid |
| WO2022128554A1 (en) | 2020-12-15 | 2022-06-23 | Basf Se | Mixtures containing n-methoxy-n-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]cyclopropanecarboxamide |
| AR124367A1 (es) * | 2020-12-17 | 2023-03-22 | Fmc Corp | Oxadiazoles fungicidas y sus mezclas |
| US20240389594A1 (en) | 2020-12-23 | 2024-11-28 | Basf Se | Pesticidal mixtures |
| EP4018830A1 (en) | 2020-12-23 | 2022-06-29 | Basf Se | Pesticidal mixtures |
| EP4341257A1 (en) | 2021-05-18 | 2024-03-27 | Basf Se | New substituted quinolines as fungicides |
| IL308529A (en) | 2021-05-18 | 2024-01-01 | Basf Se | New converted pyridines as fungicides |
| KR20240008857A (ko) | 2021-05-18 | 2024-01-19 | 바스프 에스이 | 살진균제로서의 신규한 치환된 피리딘 |
| MX2024000380A (es) | 2021-07-08 | 2024-01-29 | Basf Se | Preparacion de amidoximas sustituidas. |
| MX2024000710A (es) * | 2021-07-14 | 2024-02-08 | Basf Se | Un proceso para producir trifluoroacetatos de alquilo. |
| EP4380926A1 (en) | 2021-08-02 | 2024-06-12 | Basf Se | (3-quinolyl)-quinazoline |
| EP4380927A1 (en) | 2021-08-02 | 2024-06-12 | Basf Se | (3-pirydyl)-quinazoline |
| WO2023072671A1 (en) | 2021-10-28 | 2023-05-04 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ix |
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| CA2462601A1 (en) | 2001-10-03 | 2003-04-10 | Pharmacia Corporation | Prodrugs of substituted polycyclic compounds useful for selective inhibition of the coagulation cascade |
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| BR112019020134B1 (pt) * | 2017-03-31 | 2023-05-09 | Syngenta Participations Ag | Composições fungicidas |
| CN113979962A (zh) | 2017-03-31 | 2022-01-28 | 先正达参股股份有限公司 | 杀真菌组合物 |
| WO2018184985A1 (en) * | 2017-04-05 | 2018-10-11 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2018219773A1 (en) * | 2017-06-02 | 2018-12-06 | Syngenta Participations Ag | Fungicidal compositions |
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| CL2021002713A1 (es) | 2022-05-27 |
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| JP7658912B2 (ja) | 2025-04-08 |
| EP3956318A1 (en) | 2022-02-23 |
| BR112021020673A2 (pt) | 2021-12-07 |
| IL286566A (en) | 2021-10-31 |
| UY38667A (es) | 2020-11-30 |
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