AR100817A1 - Pirazoles y tetrazoles sustituidos con halógeno - Google Patents
Pirazoles y tetrazoles sustituidos con halógenoInfo
- Publication number
- AR100817A1 AR100817A1 ARP150101868A ARP150101868A AR100817A1 AR 100817 A1 AR100817 A1 AR 100817A1 AR P150101868 A ARP150101868 A AR P150101868A AR P150101868 A ARP150101868 A AR P150101868A AR 100817 A1 AR100817 A1 AR 100817A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- amino
- alkoxy
- radical
- Prior art date
Links
- 229910052736 halogen Inorganic materials 0.000 title abstract 7
- 150000002367 halogens Chemical group 0.000 title abstract 7
- KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 title 1
- 150000003536 tetrazoles Chemical class 0.000 title 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 14
- 229910052757 nitrogen Inorganic materials 0.000 abstract 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- -1 cyano, amino Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000006413 ring segment Chemical group 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- BWOVZCWSJFYBRM-UHFFFAOYSA-N carbononitridic isocyanate Chemical compound O=C=NC#N BWOVZCWSJFYBRM-UHFFFAOYSA-N 0.000 abstract 2
- 125000003636 chemical group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 241000239223 Arachnida Species 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 241000244206 Nematoda Species 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000005521 carbonamide group Chemical group 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 244000078703 ectoparasite Species 0.000 abstract 1
- 125000000524 functional group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 150000002390 heteroarenes Chemical class 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- JUTXUCROFBCUPE-UHFFFAOYSA-N n-(sulfanylidenemethylidene)thiohydroxylamine Chemical compound SN=C=S JUTXUCROFBCUPE-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon 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
- A01N43/48—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
- A01N43/64—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
-
- 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
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Los compuestos son en especial apropiados para controlar insectos, arácnidos y nematodos en agricultura y ectoparásitos en medicina veterinaria. Reivindicación 1: Compuestos de la fórmula (1) en donde R¹ representa hidrógeno, o un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₇, alquil C₁₋₆-carbonilo, alcoxi C₁₋₆-carbonilo, arilalquilo C₁₋₃ y heteroarilalquilo C₁₋₃; los grupos químicos A¹ representa CR² o nitrógeno, A² representa CR³ o nitrógeno, A³ representa CR⁴ o nitrógeno, y A⁴ representa CR⁵ o nitrógeno, en donde no más de tres de los grupos químicos A¹ a A⁴ representan al mismo tiempo nitrógeno; R², R³, R⁴ y R⁵ representan, de modo independiente entre sí, hidrógeno, halógeno, ciano, amino, nitro o un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de alquilo C₁₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₆, N-alcoxi C₁₋₆-imino-alquilo C₁₋₃, alquil C₁₋₆-sulfanilo, alquil C₁₋₆-sulfinilo, alquil C₁₋₆-sulfonilo, N-alquil C₁₋₆-amino y N,N-di-alquil C₁₋₆-amino, cuando ninguno de los grupos A² y A³ representa nitrógeno, R³ y R⁴ pueden formar junto con el átomo de carbono al que están unidos un anillo de 5 ó 6 miembros que contiene 0, 1 ó 2 átomos de nitrógeno y/o 0 ó 1 átomo de oxígeno y/o 0 ó 1 átomo de azufre, o cuando ninguno de los grupos A¹ y A² representa nitrógeno, R² y R³ pueden formar junto con el átomo de carbono al que están unidos un anillo de 6 miembros que contiene 0, 1 ó 2 átomos de nitrógeno; W representa oxígeno o azufre; Q representa hidrógeno, hidroxi o un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de amino, N-alquil C₁₋₆-amino, N-alquil C₁₋₆-carbonilamino, N,N-di-alquil C₁₋₆-amino, alquilo C₁₋₆, alcoxi C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆, heterocicloalquilo con 3 a 9 átomos del anillo, cicloalquil C₁₋₆-alquilo C₁₋₆, aril C₆-alquilo C₁₋₆, heteroaril-alquilo C₁₋₆ con 5 a 7 átomos del anillo; o Q representa un carbociclo de 6 miembros insaturado dado el caso mono- a polisustituido con V, o representa un anillo heterocíclico de 5 ó 6 miembros insaturado dado el caso mono- a polisustituido con V, en donde V representa, de modo independiente entre sí, halógeno, ciano, amino, nitro o un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de alquilo C₁₋₆, alquenilo C₂₋₄, alquinilo C₂₋₄, cicloalquilo C₃₋₆, alcoxi C₁₋₆, N-alcoxi C₁₋₆-imino-alquilo C₁₋₃, alquil C₁₋₆-sulfanilo, alquil C₁₋₆-sulfinilo, alquil C₁₋₆-sulfonilo, N-alquil C₁₋₆-amino y N,N-di-alquil C₁₋₆-amino; T representa uno de los compuestos heteroaromáticos T1 - T8 de 5 miembros del grupo de fórmulas (2), en donde la unión con el grupo de cabeza del pirazol [C₃N₂Z¹Z²Z³] se indica con un asterisco *, en donde R⁶ representa, de modo independiente entre sí, halógeno, ciano, nitro o un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de amino, alquilo C₁₋₆, alcoxi C₁₋₆, alquil C₁₋₆-carbonilo, alquil C₁₋₆-sulfanilo, alquil C₁₋₆-sulfinilo, alquil C₁₋₆-sulfonilo, N-alquil C₁₋₆-amino y N,N-di-alquil C₁₋₆-amino; y n representa los valores 0 - 2; Z¹ representa un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de alquilo C₁₋₆, alcoxi C₁₋₄, ciano, hidroxicarbonilo, alcoxi C₁₋₄-carbonilo, alquil C₁₋₄-carbamoilo, cicloalquil C₃₋₆-carbamoilo, fenilo, con preferencia un alquilo C₁₋₆ dado el caso sustituido con al menos un radical M¹; Z² representa hidrógeno, halógeno, ciano, nitro o un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de alquilo C₁₋₆, alquil C₁₋₆-carbonilo, alquil C₁₋₆-sulfanilo, alquil C₁₋₆-sulfinilo y alquil C₁₋₆-sulfonilo; Z³ representa hidrógeno o un grupo, sustituido dado el caso con al menos un radical M¹, seleccionado de alquilo C₁₋₆, cicloalquilo C₃₋₆, alquenilo C₁₋₆, alquinilo C₁₋₆, arilo C₆ y hetarilo con 5 ó 6 átomos del anillo; M¹ representa halógeno, ciano, isociano, azido, hidroxi, nitro, formilo, carboxi o un grupo equivalente al grupo carboxi, o un grupo, dado el caso sustituido con al menos un radical M², seleccionado de amino, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alcoxi C₁₋₄-alcoxi C₁₋₄, alcoxi C₁₋₄-alquilo C₁₋₄, alquil C₁₋₄-sulfanilo, haloalquil C₁₋₄-sulfanilo C₁₋₄, alcoxi C₁₋₄-carbonilo, alquil C₁₋₄-carbonilo, carbamoilo, mono- y N,N-dialquil C₁₋₄-aminocarbonilo, acil C₁₋₄-amino, mono- y N,N-dialquil C₁₋₄-amino, trialquil C₁₋₄-sililo, cicloalquilo C₃₋₆, arilo C₆, heterociclilo con 3 a 6 átomos del anillo, en donde cada uno de los últimos grupos cíclicos mencionados también puede estar unido a través de heteroátomos o un grupo funcional divalente -CH₂- o CH₂H₄-, alquil C₁₋₄-sulfinilo, en donde están comprendidos ambos enantiómeros del grupo alquil C₁₋₄-sulfonilo, alquil C₁₋₄-sulfonilo, alquil C₁₋₄-fosfinilo, alquil C₁₋₄-sulfanil-alquilo C₁₋₄, alcoxi C₁₋₄-alquilo C₁₋₄, mono- y N,N-dialquil C₁₋₄-aminoalquilo C₁₋₄ e hidroxialquilo C₁₋₄; y M² representa amino, hidroxi, halógeno, nitro, ciano, isociano, mercapto, isotiocianato, carboxi y carbonamida.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14172922 | 2014-06-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR100817A1 true AR100817A1 (es) | 2016-11-02 |
Family
ID=50972545
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150101868A AR100817A1 (es) | 2014-06-18 | 2015-06-11 | Pirazoles y tetrazoles sustituidos con halógeno |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20170114021A1 (es) |
| EP (1) | EP3157905A1 (es) |
| JP (1) | JP2017519761A (es) |
| CN (1) | CN106795119A (es) |
| AR (1) | AR100817A1 (es) |
| AU (1) | AU2015276315A1 (es) |
| BR (1) | BR112016029361A2 (es) |
| CA (1) | CA2952525A1 (es) |
| CL (1) | CL2016003248A1 (es) |
| MX (1) | MX2016016837A (es) |
| RU (1) | RU2017101427A (es) |
| TW (1) | TW201625547A (es) |
| WO (1) | WO2015193218A1 (es) |
| ZA (1) | ZA201700302B (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR101816A1 (es) * | 2014-04-02 | 2017-01-18 | Bayer Cropscience Ag | Derivados de 3-[(pirazol-5-il)-heteroaril]-benzamidas como agentes pesticidas |
| EP3416959B1 (en) | 2016-02-18 | 2021-05-12 | Syngenta Participations AG | Pesticidally active pyrazole derivatives |
| WO2018177993A1 (de) | 2017-03-31 | 2018-10-04 | Bayer Cropscience Aktiengesellschaft | Pyrazole zur bekämpfung von arthropoden |
| KR20190134623A (ko) | 2017-03-31 | 2019-12-04 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 절지동물을 방제하기 위한 트리시클릭 카르복스아미드 |
| EP3606919A1 (en) | 2017-04-05 | 2020-02-12 | Syngenta Participations AG | Pesticidally active pyrazole derivatives |
| EP3606917A1 (en) | 2017-04-05 | 2020-02-12 | Syngenta Participations AG | Pesticidally active pyrazole derivatives |
| US11472797B2 (en) | 2017-04-05 | 2022-10-18 | Syngenta Participations Ag | Pesticidally active pyrazole derivatives |
| EP3665166A1 (en) | 2017-08-11 | 2020-06-17 | Syngenta Participations AG | Pesticidally active pyrazole derivatives |
| AR112672A1 (es) | 2017-08-11 | 2019-11-27 | Syngenta Participations Ag | Derivados de tiofeno activos como plaguicidas |
| AR112673A1 (es) | 2017-08-11 | 2019-11-27 | Syngenta Participations Ag | Derivados de pirazol activos como plaguicidas |
| US20200288713A1 (en) | 2017-08-11 | 2020-09-17 | Syngenta Participations Ag | Pesticidally active pyrazole derivatives |
| US11459318B2 (en) | 2017-10-06 | 2022-10-04 | Syngenta Participations Ag | Pesticidally active pyrrole derivatives |
| WO2019068820A1 (en) | 2017-10-06 | 2019-04-11 | Syngenta Participations Ag | PYRROLE DERIVATIVES ACTIVE ON THE PESTICIDE PLAN |
| WO2020164994A1 (en) | 2019-02-13 | 2020-08-20 | Syngenta Crop Protection Ag | Pesticidally active pyrazole derivatives |
| WO2020164993A1 (en) | 2019-02-13 | 2020-08-20 | Syngenta Crop Protection Ag | Pesticidally active pyrazole derivatives |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG175925A1 (en) * | 2009-05-15 | 2011-12-29 | Novartis Ag | Aryl pyridine as aldosterone synthase inhibitors |
| AR083875A1 (es) * | 2010-11-15 | 2013-03-27 | Bayer Cropscience Ag | N-aril pirazol(tio)carboxamidas |
| CN103354811A (zh) * | 2011-02-09 | 2013-10-16 | 先正达参股股份有限公司 | 杀虫化合物 |
-
2015
- 2015-06-11 AR ARP150101868A patent/AR100817A1/es unknown
- 2015-06-15 RU RU2017101427A patent/RU2017101427A/ru unknown
- 2015-06-15 CN CN201580044033.9A patent/CN106795119A/zh active Pending
- 2015-06-15 MX MX2016016837A patent/MX2016016837A/es unknown
- 2015-06-15 CA CA2952525A patent/CA2952525A1/en not_active Abandoned
- 2015-06-15 BR BR112016029361A patent/BR112016029361A2/pt not_active Application Discontinuation
- 2015-06-15 US US15/318,930 patent/US20170114021A1/en not_active Abandoned
- 2015-06-15 WO PCT/EP2015/063277 patent/WO2015193218A1/de not_active Ceased
- 2015-06-15 EP EP15728550.3A patent/EP3157905A1/de not_active Withdrawn
- 2015-06-15 JP JP2016573546A patent/JP2017519761A/ja active Pending
- 2015-06-15 AU AU2015276315A patent/AU2015276315A1/en not_active Abandoned
- 2015-06-16 TW TW104119338A patent/TW201625547A/zh unknown
-
2016
- 2016-12-16 CL CL2016003248A patent/CL2016003248A1/es unknown
-
2017
- 2017-01-13 ZA ZA2017/00302A patent/ZA201700302B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CL2016003248A1 (es) | 2017-08-04 |
| RU2017101427A (ru) | 2018-07-18 |
| JP2017519761A (ja) | 2017-07-20 |
| US20170114021A1 (en) | 2017-04-27 |
| CA2952525A1 (en) | 2015-12-23 |
| TW201625547A (zh) | 2016-07-16 |
| EP3157905A1 (de) | 2017-04-26 |
| BR112016029361A2 (pt) | 2017-10-31 |
| AU2015276315A1 (en) | 2017-01-12 |
| MX2016016837A (es) | 2017-10-12 |
| ZA201700302B (en) | 2019-06-26 |
| WO2015193218A1 (de) | 2015-12-23 |
| CN106795119A (zh) | 2017-05-31 |
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