AR100743A1 - Compuestos de [1,2,4]triazol sustituido - Google Patents
Compuestos de [1,2,4]triazol sustituidoInfo
- Publication number
- AR100743A1 AR100743A1 ARP150101786A ARP150101786A AR100743A1 AR 100743 A1 AR100743 A1 AR 100743A1 AR P150101786 A ARP150101786 A AR P150101786A AR P150101786 A ARP150101786 A AR P150101786A AR 100743 A1 AR100743 A1 AR 100743A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- alkoxy
- halogen
- independently selected
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- QWENRTYMTSOGBR-UHFFFAOYSA-N 1H-1,2,3-Triazole Chemical class C=1C=NNN=1 QWENRTYMTSOGBR-UHFFFAOYSA-N 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 13
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 12
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 11
- 229910052736 halogen Inorganic materials 0.000 abstract 11
- 150000002367 halogens Chemical class 0.000 abstract 11
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 9
- 125000001188 haloalkyl group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 150000002431 hydrogen Chemical group 0.000 abstract 5
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 3
- 125000006650 (C2-C4) alkynyl 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
- 125000001931 aliphatic group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004104 aryloxy group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- -1 C2−4 halogenoalkenyl Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- AUQDITHEDVOTCU-UHFFFAOYSA-N cyclopropyl cyanide Chemical compound N#CC1CC1 AUQDITHEDVOTCU-UHFFFAOYSA-N 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C1/00—Apparatus, or methods of use thereof, for testing or treating seed, roots, or the like, prior to sowing or planting
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C1/00—Apparatus, or methods of use thereof, for testing or treating seed, roots, or the like, prior to sowing or planting
- A01C1/06—Coating or dressing seed
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/08—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing boron
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Environmental Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Soil Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Toxicology (AREA)
Abstract
Reivindicación 1: Compuestos caracterizados por la fórmula (1) en donde R¹ es C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo o C₃₋₆ cicloalquilo; en donde las porciones alifáticas de R¹ son no sustituidas o tienen 1, 2, 3 o hasta la mayor cantidad posible de grupos R¹ᵃ idénticos o diferentes: R¹ᵃ se selecciona, independientemente entre sí, de halógeno, OH, CN, C₁₋₄ alcoxi, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo y C₁₋₄ halógenoalcoxi; en donde las porciones cicloalquilo de R¹ son no sustituidas o tienen 1, 2, 3, 4, 5 o hasta la mayor cantidad de grupos R¹ᵇ idénticos o diferentes: R¹ᵇ se selecciona, independientemente entre sí, de halógeno, OH, CN, C₁₋₄ alquilo, C₁₋₄ alcoxi, C₁₋₄ halógenoalquilo, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo y C₁₋₄ halógenoalcoxi; R² es hidrógeno, C₁₋₄ alquilo, C₂₋₄ alquenilo o C₂₋₄ alquinilo; en donde las porciones alifáticas de R² son no sustituidas o tienen 1, 2, 3 o hasta la mayor cantidad posible de grupos R²ᵃ idénticos o diferentes: R²ᵃ se selecciona, independientemente entre sí, de halógeno, OH, CN, C₁₋₄ alcoxi, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo y C₁₋₄ halógenoalcoxi; R³ se selecciona de hidrógeno, halógeno, CN, C₁₋₄ alquilo, C₁₋₄ alcoxi, C₂₋₄ alquenilo, C₂₋₄ alquinilo, C₃₋₆ cicloalquilo y S(O)ₚ(C₁₋₄ alquilo), en donde p es 0, 1 ó 2, y en donde cada R³ es no sustituido o se sustituye adicionalmente con 1, 2, 3 ó 4 R³ᵃ: R³ᵃ se selecciona, independientemente entre sí, de halógeno, CN, OH, C₁₋₄ alquilo, C₁₋₄ halógenoalquilo, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo, C₁₋₄ alcoxi y C₁₋₄ halógenoalcoxi; R⁴, R⁵ y R⁶ se seleccionan, independientemente entre sí, de hidrógeno, halógeno, C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₁₋₄ alcoxi, C₃₋₆ cicloalquilo, C₃₋₆ cicloalquenilo, C₃₋₆ cicloalquil-C₁₋₄ alquilo, -N(RA)₂, C₃₋₆ halógenocicloalquilo, arilo y ariloxi; R⁴ y R⁵ son juntos =O, y R⁶ es como se definió anteriormente; R⁴ y R⁵ son juntos =C(Rᵃ)₂, y R⁶ es como se definió anteriormente, y Rᵃ es como se define a continuación; o R⁴ y R⁵ forman juntos un carbociclo o heterociclo, y R⁶ es como se definió anteriormente; en donde las porciones alifáticas de R⁴, R⁵ y R⁶ son no sustituidas o se sustituyen adicionalmente con 1, 2, 3 ó 4 de grupos Rᵃ idénticos o diferentes: Rᵃ se selecciona, independientemente entre sí, de halógeno, OH, CN, C₁₋₄ alquilo, C₁₋₄ halógenoalquilo, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo, C₁₋₄ alcoxi, C₁₋₄ halógenoalcoxi y Si(Rˢ)₃, en donde Rˢ es C₁₋₄ alquilo; en donde las porciones cicloalquilo de R⁴, R⁵ y R⁶ son no sustituidas o tienen 1, 2, 3, 4, 5 o hasta la mayor cantidad de grupos Rᵇ idénticos o diferentes: Rᵇ se selecciona, independientemente entre sí, de halógeno, OH, CN, C₁₋₄ alquilo, C₁₋₄ alcoxi, C₁₋₄ halógenoalquilo, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo y C₁₋₄ halógenoalcoxi; en donde las porciones arilo y ariloxi de R⁴, R⁵ y R⁶ son no sustituidas o se sustituyen adicionalmente con 1, 2, 3 ó 4 grupos Rᶜ idénticos o diferentes: Rᶜ se selecciona, independientemente entre sí, de halógeno, OH, CN, C₁₋₄ alquilo, C₁₋₄ halógenoalquilo, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo, C₁₋₄ alcoxi y C₁₋₄ halógenoalcoxi; en donde el carbociclo o heterociclo juntos formados por R⁴ y R⁵ es no sustituido o tiene 1, 2, 3 ó 4 grupos Rᵈ idénticos o diferentes: Rᵈ se selecciona, independientemente entre sí, de halógeno, CN, NO₂, C₁₋₄ alquilo, C₁₋₄ halógenoalquilo, C₁₋₄ alcoxi, C₁₋₄ halógenoalcoxi, C₂₋₄ alquenilo, C₂₋₄ halógenoalquenilo, C₂₋₄ alquinilo, C₂₋₄ halógenoalquinilo y -C(O)O-C₁₋₄ alquilo; y en donde RA se selecciona, independientemente entre sí, de C₁₋₄ alquilo, C₁₋₄ halógenoalquilo y -C(O)O-C₁₋₄ alquilo; X es O, S(O)ₙ, en donde n es 0, 1 ó 2, o NRN; RN se selecciona de hidrógeno, C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₁₋₆ alcoxi, -C(O)C₁₋₆ alquilo, C₃₋₆ cicloalquilo, C₃₋₆ cicloalquil-C₁₋₄ alquilo, -S(O)₂-C₁₋₆ alquilo y -S(O)₂-arilo, en donde RN es no sustituido o se sustituye adicionalmente con 1, 2, 3 ó 4 de grupos RNᵃ idénticos o diferentes: RNᵃ se selecciona, independientemente entre sí, de halógeno, CN, OH, C₁₋₄ alquilo, C₁₋₄ halógenoalquilo, C₃₋₆ cicloalquilo, C₃₋₆ halógenocicloalquilo, C₁₋₄ alcoxi y C₁₋₄ halógenoalcoxi; siempre que al menos uno de R⁴, R⁵ y R⁶ no sea hidrógeno; siempre que cuando R² y R³ sean hidrógeno, y R⁴⁻⁶ sean F, entonces R¹ no sea C(CH₃)₃, CH(OH)CH₃, CHCH₃CH=CH₂ o ciclopropan-2-carbonitrilo; y siempre que cuando R² y R³ sean hidrógeno, -CR⁴R⁵R⁶ sea CF₂CHFCI, entonces R¹ no sea CH₃; y los N-óxidos y las sales de estos aceptables en la agricultura.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14171468 | 2014-06-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR100743A1 true AR100743A1 (es) | 2016-10-26 |
Family
ID=50884296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150101786A AR100743A1 (es) | 2014-06-06 | 2015-06-04 | Compuestos de [1,2,4]triazol sustituido |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US10450279B2 (es) |
| EP (1) | EP3152196B1 (es) |
| JP (1) | JP6529521B2 (es) |
| KR (1) | KR20170013995A (es) |
| CN (1) | CN106536530A (es) |
| AR (1) | AR100743A1 (es) |
| AU (1) | AU2015270428B2 (es) |
| BR (1) | BR112016028476B1 (es) |
| CA (1) | CA2950812C (es) |
| CL (1) | CL2016003145A1 (es) |
| CO (1) | CO2017000064A2 (es) |
| CR (1) | CR20160602A (es) |
| EA (1) | EA035041B1 (es) |
| IL (1) | IL249367B (es) |
| MX (1) | MX2016016143A (es) |
| PL (1) | PL3152196T3 (es) |
| UA (1) | UA122392C2 (es) |
| WO (1) | WO2015185708A1 (es) |
| ZA (1) | ZA201700019B (es) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112016013263B1 (pt) | 2013-12-12 | 2020-08-25 | Basf Se | compostos, composição, uso de um composto e método para o combate dos fungos fitopatogênicos |
| CR20160579A (es) | 2014-05-13 | 2017-05-09 | Basf Se | Compuestos de [1,2,4] Triazol e Imidazol sustituidos como fungicidas |
| AR100743A1 (es) | 2014-06-06 | 2016-10-26 | Basf Se | Compuestos de [1,2,4]triazol sustituido |
| EP3230259B1 (en) | 2014-12-08 | 2024-04-03 | The Research Foundation for The State University of New York | Anti-fungals targeting the synthesis of fungal shingolipids |
| EP3370524A1 (en) | 2015-11-05 | 2018-09-12 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
| EA201891146A1 (ru) | 2015-11-19 | 2018-12-28 | Басф Се | Замещенные оксадиазолы для борьбы с фитопатогенными грибами |
| CN108347937A (zh) | 2015-11-19 | 2018-07-31 | 巴斯夫欧洲公司 | 用于防除植物病原性真菌的取代噁二唑 |
| CN105693638B (zh) * | 2016-01-05 | 2018-12-04 | 浙江博仕达作物科技有限公司 | 一种杀菌化合物、杀菌剂组合物和制剂及其应用 |
| CN105669576B (zh) * | 2016-02-22 | 2018-12-04 | 浙江博仕达作物科技有限公司 | 一种杀菌化合物、杀菌剂组合物和制剂及其应用 |
| CA3020532A1 (en) | 2016-04-11 | 2017-10-19 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
| EP3468958B1 (en) | 2016-06-09 | 2020-12-16 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
| WO2018232298A1 (en) | 2017-06-16 | 2018-12-20 | The Research Foundation For The State University Of New York | Anti-fungals compounds targeting the synthesis of fungal sphingolipids |
| CA3071569C (en) | 2017-11-13 | 2020-12-29 | Kureha Corporation | Azole derivative, intermediate compound, method for producing azole derivative, agricultural or horticultural chemical agent, and protective agent for industrial material |
| US10916575B2 (en) | 2018-04-04 | 2021-02-09 | Samsung Electronics Co., Ltd. | Image sensor and method of manufacturing image sensor |
| EP3670501A1 (en) | 2018-12-17 | 2020-06-24 | Basf Se | Substituted [1,2,4]triazole compounds as fungicides |
| KR102404296B1 (ko) | 2019-04-19 | 2022-05-31 | 가부시끼가이샤 구레하 | 농원예용 살균제, 식물 병해 방제 방법 및 식물 병해 방제용 제품 |
| CN113135863B (zh) * | 2020-01-18 | 2024-01-16 | 东莞市东阳光农药研发有限公司 | 一种新型三唑类化合物及其在农业中的应用 |
| WO2021249800A1 (en) | 2020-06-10 | 2021-12-16 | Basf Se | Substituted [1,2,4]triazole compounds as fungicides |
| CN116171273B (zh) | 2020-08-06 | 2024-05-14 | 株式会社吴羽 | 化合物的制造方法 |
| CN113788798B (zh) * | 2021-10-27 | 2023-08-04 | 襄阳道农道生物科技有限公司 | 氘代的杀菌化合物及其制法和用途 |
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- 2015-06-05 CR CR20160602A patent/CR20160602A/es unknown
- 2015-06-05 US US15/316,418 patent/US10450279B2/en active Active
- 2015-06-05 EP EP15725391.5A patent/EP3152196B1/en active Active
- 2015-06-05 CN CN201580041856.6A patent/CN106536530A/zh active Pending
- 2015-06-05 KR KR1020177000357A patent/KR20170013995A/ko not_active Ceased
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- 2015-06-05 AU AU2015270428A patent/AU2015270428B2/en active Active
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- 2015-06-05 EA EA201692526A patent/EA035041B1/ru not_active IP Right Cessation
- 2015-06-05 UA UAA201700046A patent/UA122392C2/uk unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| CA2950812A1 (en) | 2015-12-10 |
| US20170158646A1 (en) | 2017-06-08 |
| WO2015185708A1 (en) | 2015-12-10 |
| CN106536530A (zh) | 2017-03-22 |
| MX2016016143A (es) | 2017-03-28 |
| EP3152196B1 (en) | 2020-03-18 |
| IL249367B (en) | 2019-11-28 |
| CA2950812C (en) | 2023-10-24 |
| AU2015270428B2 (en) | 2019-02-28 |
| EP3152196A1 (en) | 2017-04-12 |
| IL249367A0 (en) | 2017-02-28 |
| CR20160602A (es) | 2017-06-13 |
| EA201692526A1 (ru) | 2017-05-31 |
| JP2017519747A (ja) | 2017-07-20 |
| ZA201700019B (en) | 2018-11-28 |
| BR112016028476A8 (pt) | 2021-03-23 |
| KR20170013995A (ko) | 2017-02-07 |
| US10450279B2 (en) | 2019-10-22 |
| CO2017000064A2 (es) | 2017-06-20 |
| UA122392C2 (uk) | 2020-11-10 |
| PL3152196T3 (pl) | 2020-10-19 |
| BR112016028476B1 (pt) | 2021-06-22 |
| AU2015270428A1 (en) | 2016-12-22 |
| EA035041B1 (ru) | 2020-04-21 |
| BR112016028476A2 (pt) | 2017-08-22 |
| JP6529521B2 (ja) | 2019-06-12 |
| CL2016003145A1 (es) | 2017-08-18 |
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