CA3013960A1 - Substituted imidazolyl-carboxamides as pest control agents - Google Patents
Substituted imidazolyl-carboxamides as pest control agents Download PDFInfo
- Publication number
- CA3013960A1 CA3013960A1 CA3013960A CA3013960A CA3013960A1 CA 3013960 A1 CA3013960 A1 CA 3013960A1 CA 3013960 A CA3013960 A CA 3013960A CA 3013960 A CA3013960 A CA 3013960A CA 3013960 A1 CA3013960 A1 CA 3013960A1
- Authority
- CA
- Canada
- Prior art keywords
- alkyl
- spp
- cyano
- alkoxy
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 241000607479 Yersinia pestis Species 0.000 title claims abstract description 39
- NMIZONYLXCOHEF-UHFFFAOYSA-N 1h-imidazole-2-carboxamide Chemical class NC(=O)C1=NC=CN1 NMIZONYLXCOHEF-UHFFFAOYSA-N 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 210
- 241001465754 Metazoa Species 0.000 claims abstract description 55
- -1 nitro, cyano, amino Chemical group 0.000 claims description 129
- 239000000203 mixture Substances 0.000 claims description 98
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 88
- 229910052736 halogen Inorganic materials 0.000 claims description 88
- 150000002367 halogens Chemical class 0.000 claims description 88
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 87
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 71
- 238000009472 formulation Methods 0.000 claims description 71
- 239000001257 hydrogen Substances 0.000 claims description 67
- 229910052739 hydrogen Inorganic materials 0.000 claims description 67
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 47
- 238000000034 method Methods 0.000 claims description 45
- 229910052731 fluorine Inorganic materials 0.000 claims description 43
- 239000011737 fluorine Substances 0.000 claims description 43
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 42
- 239000000460 chlorine Substances 0.000 claims description 42
- 229910052801 chlorine Inorganic materials 0.000 claims description 42
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 41
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 35
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 34
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 34
- 229910052794 bromium Inorganic materials 0.000 claims description 34
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 32
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 32
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 31
- 125000001072 heteroaryl group Chemical group 0.000 claims description 31
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 25
- 150000003839 salts Chemical class 0.000 claims description 25
- 125000003118 aryl group Chemical group 0.000 claims description 23
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 20
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 125000003342 alkenyl group Chemical group 0.000 claims description 18
- 125000000304 alkynyl group Chemical group 0.000 claims description 16
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 15
- 125000000623 heterocyclic group Chemical group 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 14
- 125000005842 heteroatom Chemical group 0.000 claims description 13
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 13
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 11
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 11
- 125000001153 fluoro group Chemical group F* 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 11
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 10
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 10
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 10
- 229920006395 saturated elastomer Polymers 0.000 claims description 10
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- 239000005864 Sulphur Substances 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 9
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 9
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 239000000543 intermediate Substances 0.000 claims description 8
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 7
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 241000282414 Homo sapiens Species 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- 239000003905 agrochemical Substances 0.000 claims description 5
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 230000001225 therapeutic effect Effects 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000003107 substituted aryl group Chemical group 0.000 claims description 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 3
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 3
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 3
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 3
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 3
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 claims description 3
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 3
- UQZPGHOJMQTOHB-UHFFFAOYSA-N 2-chloro-n-(2-chloroethyl)-n-ethylethanamine Chemical compound ClCCN(CC)CCCl UQZPGHOJMQTOHB-UHFFFAOYSA-N 0.000 claims description 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 2
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims description 2
- 125000006413 ring segment Chemical group 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 31
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 1
- 229910052721 tungsten Inorganic materials 0.000 abstract description 13
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- 241000196324 Embryophyta Species 0.000 description 90
- 150000003254 radicals Chemical class 0.000 description 70
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 36
- 239000002904 solvent Substances 0.000 description 35
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 33
- 238000005160 1H NMR spectroscopy Methods 0.000 description 30
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- 239000004480 active ingredient Substances 0.000 description 25
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
- 238000002156 mixing Methods 0.000 description 20
- 238000012360 testing method Methods 0.000 description 19
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
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Classifications
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- 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
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-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
- A01N43/48—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
- 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
- A01N43/84—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- 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
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Catching Or Destruction (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EPEP16155136.1 | 2016-02-11 | ||
| EP16155136 | 2016-02-11 | ||
| PCT/EP2017/052497 WO2017137337A1 (de) | 2016-02-11 | 2017-02-06 | Substituierte imidazolyl-carboxamide als schädlingsbekämpfungsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA3013960A1 true CA3013960A1 (en) | 2017-08-17 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA3013960A Abandoned CA3013960A1 (en) | 2016-02-11 | 2017-02-06 | Substituted imidazolyl-carboxamides as pest control agents |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US10501441B2 (OSRAM) |
| JP (1) | JP6892452B2 (OSRAM) |
| KR (1) | KR20180107141A (OSRAM) |
| CN (1) | CN109071507A (OSRAM) |
| AR (1) | AR107588A1 (OSRAM) |
| AU (1) | AU2017217580A1 (OSRAM) |
| BR (1) | BR112018016362A2 (OSRAM) |
| CA (1) | CA3013960A1 (OSRAM) |
| CL (1) | CL2018002295A1 (OSRAM) |
| CO (1) | CO2018008397A2 (OSRAM) |
| IL (1) | IL260829B (OSRAM) |
| MX (1) | MX2018009805A (OSRAM) |
| PH (1) | PH12018501705A1 (OSRAM) |
| RU (1) | RU2018132164A (OSRAM) |
| TW (1) | TW201741299A (OSRAM) |
| UY (1) | UY37119A (OSRAM) |
| WO (1) | WO2017137337A1 (OSRAM) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3414236A1 (de) * | 2016-02-11 | 2018-12-19 | Bayer CropScience Aktiengesellschaft | Substituierte 2-(het)aryl-imidazolyl-carboxyamide als schädlingsbekämpfungsmittel |
| RU2018132198A (ru) * | 2016-02-11 | 2020-03-12 | Байер Кропсайенс Акциенгезельшафт | Замещенные имидазолил-карбоксамиды в качестве средств для борьбы с вредителями |
| RU2018132172A (ru) * | 2016-02-11 | 2020-03-11 | Байер Кропсайенс Акциенгезельшафт | Замещенные 2-оксиимидазолил-карбоксамиды в качестве средств для борьбы с вредителями |
| RU2019106494A (ru) * | 2016-08-10 | 2020-09-14 | Байер Кропсайенс Акциенгезельшафт | Замещенные 2-гетероциклил-имидазолил-карбоксамиды в качестве средств для борьбы с вредителями |
| WO2019137995A1 (en) | 2018-01-11 | 2019-07-18 | Basf Se | Novel pyridazine compounds for controlling invertebrate pests |
| CN111116483B (zh) * | 2019-11-25 | 2022-12-20 | 浙江师范大学 | 一种2-咪唑基咪唑类化合物及其制备方法 |
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|---|---|---|---|---|
| ZA200305582B (en) | 2001-03-05 | 2004-07-19 | Du Pont | Heterocyclic diamide invertebrate pest control agents. |
| FR2827286A1 (fr) * | 2001-07-11 | 2003-01-17 | Aventis Cropscience Sa | Nouveaux composes fongicides |
| JPWO2005051949A1 (ja) * | 2003-11-26 | 2007-06-21 | 住友製薬株式会社 | 新規縮合イミダゾール誘導体 |
| EP2236505A1 (de) * | 2009-04-03 | 2010-10-06 | Bayer CropScience AG | Acylierte Aminopyridine und - pyridazine als Insektizide |
| AU2010259002B2 (en) * | 2009-06-08 | 2014-03-20 | Nantbio, Inc. | Triazine derivatives and their therapeutical applications |
| JP2013500246A (ja) * | 2009-07-24 | 2013-01-07 | ビーエーエスエフ ソシエタス・ヨーロピア | 無脊椎動物系害虫防除用ピリジン誘導体化合物 |
| TWI702212B (zh) * | 2015-02-09 | 2020-08-21 | 德商拜耳作物科學股份有限公司 | 作為除害劑之經取代的２－硫基咪唑基羧醯胺類 |
| EP3414236A1 (de) * | 2016-02-11 | 2018-12-19 | Bayer CropScience Aktiengesellschaft | Substituierte 2-(het)aryl-imidazolyl-carboxyamide als schädlingsbekämpfungsmittel |
| RU2018132172A (ru) * | 2016-02-11 | 2020-03-11 | Байер Кропсайенс Акциенгезельшафт | Замещенные 2-оксиимидазолил-карбоксамиды в качестве средств для борьбы с вредителями |
-
2017
- 2017-02-06 WO PCT/EP2017/052497 patent/WO2017137337A1/de not_active Ceased
- 2017-02-06 MX MX2018009805A patent/MX2018009805A/es unknown
- 2017-02-06 AU AU2017217580A patent/AU2017217580A1/en not_active Abandoned
- 2017-02-06 BR BR112018016362-7A patent/BR112018016362A2/pt not_active Application Discontinuation
- 2017-02-06 CN CN201780022855.6A patent/CN109071507A/zh active Pending
- 2017-02-06 CA CA3013960A patent/CA3013960A1/en not_active Abandoned
- 2017-02-06 KR KR1020187022834A patent/KR20180107141A/ko not_active Withdrawn
- 2017-02-06 JP JP2018541607A patent/JP6892452B2/ja not_active Expired - Fee Related
- 2017-02-06 US US16/076,797 patent/US10501441B2/en not_active Expired - Fee Related
- 2017-02-06 RU RU2018132164A patent/RU2018132164A/ru not_active Application Discontinuation
- 2017-02-09 TW TW106104209A patent/TW201741299A/zh unknown
- 2017-02-10 UY UY0001037119A patent/UY37119A/es not_active Application Discontinuation
- 2017-02-10 AR ARP170100332A patent/AR107588A1/es unknown
-
2018
- 2018-07-29 IL IL260829A patent/IL260829B/en active IP Right Grant
- 2018-08-10 CO CONC2018/0008397A patent/CO2018008397A2/es unknown
- 2018-08-10 PH PH12018501705A patent/PH12018501705A1/en unknown
- 2018-08-10 CL CL2018002295A patent/CL2018002295A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW201741299A (zh) | 2017-12-01 |
| MX2018009805A (es) | 2018-09-10 |
| UY37119A (es) | 2017-09-29 |
| IL260829B (en) | 2021-05-31 |
| CN109071507A (zh) | 2018-12-21 |
| WO2017137337A1 (de) | 2017-08-17 |
| KR20180107141A (ko) | 2018-10-01 |
| PH12018501705A1 (en) | 2019-06-10 |
| AU2017217580A1 (en) | 2018-08-16 |
| BR112018016362A2 (pt) | 2018-12-18 |
| CL2018002295A1 (es) | 2018-11-30 |
| AR107588A1 (es) | 2018-05-16 |
| RU2018132164A (ru) | 2020-03-12 |
| US10501441B2 (en) | 2019-12-10 |
| US20190047987A1 (en) | 2019-02-14 |
| CO2018008397A2 (es) | 2018-08-21 |
| JP6892452B2 (ja) | 2021-06-23 |
| JP2019507745A (ja) | 2019-03-22 |
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Legal Events
| Date | Code | Title | Description |
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| FZDE | Discontinued |
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| FZDE | Discontinued |
Effective date: 20210831 |