JP2016539092A5 - - Google Patents
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- Publication number
- JP2016539092A5 JP2016539092A5 JP2016523965A JP2016523965A JP2016539092A5 JP 2016539092 A5 JP2016539092 A5 JP 2016539092A5 JP 2016523965 A JP2016523965 A JP 2016523965A JP 2016523965 A JP2016523965 A JP 2016523965A JP 2016539092 A5 JP2016539092 A5 JP 2016539092A5
- Authority
- JP
- Japan
- Prior art keywords
- chloro
- pyridin
- give
- pyrazole
- pyrazol
- 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.)
- Pending
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- JRNVHPAWUHSFAL-UHFFFAOYSA-N 3-(3-chloropyrazol-1-yl)pyridine Chemical compound N1=C(Cl)C=CN1C1=CC=CN=C1 JRNVHPAWUHSFAL-UHFFFAOYSA-N 0.000 claims 24
- 238000000034 method Methods 0.000 claims 19
- FGZZEUJHZDWFNY-WEVVVXLNSA-N (2E)-2-(pyridin-3-ylhydrazinylidene)acetic acid Chemical compound OC(=O)\C=N\Nc1cccnc1 FGZZEUJHZDWFNY-WEVVVXLNSA-N 0.000 claims 17
- MXERTNXQEMIYGL-UHFFFAOYSA-N 3-chloro-1-pyridin-3-ylpyrazol-4-amine Chemical compound N1=C(Cl)C(N)=CN1C1=CC=CN=C1 MXERTNXQEMIYGL-UHFFFAOYSA-N 0.000 claims 16
- LQWHCKGJTOYJDZ-UHFFFAOYSA-N 5-chloro-2-pyridin-3-yl-3,4-dihydropyrazole-3-carbonitrile Chemical compound ClC1=NN(C(C1)C#N)c1cccnc1 LQWHCKGJTOYJDZ-UHFFFAOYSA-N 0.000 claims 14
- HTMNAAPFKKFGHH-UHFFFAOYSA-N methyl 5-chloro-2-pyridin-3-yl-3,4-dihydropyrazole-3-carboxylate Chemical compound COC(=O)C1CC(Cl)=NN1c1cccnc1 HTMNAAPFKKFGHH-UHFFFAOYSA-N 0.000 claims 13
- WEIBBYLPUCCXKG-UHFFFAOYSA-N 3-(3-chloro-4-nitropyrazol-1-yl)pyridine Chemical compound N1=C(Cl)C([N+](=O)[O-])=CN1C1=CC=CN=C1 WEIBBYLPUCCXKG-UHFFFAOYSA-N 0.000 claims 12
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims 11
- 239000002585 base Substances 0.000 claims 11
- KRWUJDPGMUODRM-UHFFFAOYSA-N 5-chloro-N-ethyl-2-pyridin-3-yl-1H-pyrazol-5-amine Chemical compound ClC1(NN(C=C1)C=1C=NC=CC1)NCC KRWUJDPGMUODRM-UHFFFAOYSA-N 0.000 claims 9
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims 9
- MKYDFIATDBRNHK-UHFFFAOYSA-N N-(3-chloro-1-pyridin-3-ylpyrazol-4-yl)acetamide Chemical compound CC(=O)Nc1cn(nc1Cl)-c1cccnc1 MKYDFIATDBRNHK-UHFFFAOYSA-N 0.000 claims 9
- 239000000460 chlorine Substances 0.000 claims 9
- OXIRKNVNDYSDCD-UHFFFAOYSA-N 5-chloro-2-pyridin-3-ylpyrazole-3-carboxylic acid Chemical compound OC(=O)C1=CC(Cl)=NN1C1=CC=CN=C1 OXIRKNVNDYSDCD-UHFFFAOYSA-N 0.000 claims 8
- AFEVZFBTBLAWGB-UHFFFAOYSA-N 5-chloro-2-pyridin-3-ylpyrazole-3-carboxylic acid hydrochloride Chemical compound Cl.OC(=O)c1cc(Cl)nn1-c1cccnc1 AFEVZFBTBLAWGB-UHFFFAOYSA-N 0.000 claims 8
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 claims 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 7
- 229910052801 chlorine Inorganic materials 0.000 claims 7
- HBWHYODJXYJXDC-UHFFFAOYSA-N methyl 5-chloro-2-pyridin-3-ylpyrazole-3-carboxylate Chemical compound COC(=O)c1cc(Cl)nn1-c1cccnc1 HBWHYODJXYJXDC-UHFFFAOYSA-N 0.000 claims 7
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 6
- XMPZTFVPEKAKFH-UHFFFAOYSA-P ceric ammonium nitrate Chemical compound [NH4+].[NH4+].[Ce+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O XMPZTFVPEKAKFH-UHFFFAOYSA-P 0.000 claims 6
- -1 3-chloro-1H-pyrazol-1-yl Chemical group 0.000 claims 5
- QJFANABRDIUIEI-UHFFFAOYSA-N pyridin-3-ylhydrazine;dihydrochloride Chemical compound Cl.Cl.NNC1=CC=CN=C1 QJFANABRDIUIEI-UHFFFAOYSA-N 0.000 claims 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 5
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 4
- 150000007529 inorganic bases Chemical class 0.000 claims 4
- 239000003960 organic solvent Substances 0.000 claims 4
- 150000003568 thioethers Chemical class 0.000 claims 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 229910017604 nitric acid Inorganic materials 0.000 claims 3
- 230000003647 oxidation Effects 0.000 claims 3
- 238000007254 oxidation reaction Methods 0.000 claims 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 claims 2
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 claims 2
- 241000607479 Yersinia pestis Species 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical class O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 claims 2
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- 230000008878 coupling Effects 0.000 claims 2
- 238000010168 coupling process Methods 0.000 claims 2
- 238000005859 coupling reaction Methods 0.000 claims 2
- 230000007062 hydrolysis Effects 0.000 claims 2
- 238000006460 hydrolysis reaction Methods 0.000 claims 2
- 239000003999 initiator Substances 0.000 claims 2
- 238000006396 nitration reaction Methods 0.000 claims 2
- 150000003254 radicals Chemical class 0.000 claims 2
- 238000007127 saponification reaction Methods 0.000 claims 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- KOPFEFZSAMLEHK-UHFFFAOYSA-N 1h-pyrazole-5-carboxylic acid Chemical class OC(=O)C=1C=CNN=1 KOPFEFZSAMLEHK-UHFFFAOYSA-N 0.000 claims 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical class CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- SXUMSCJUXIVSFX-UHFFFAOYSA-N 3-chloro-n-ethyl-1-pyridin-3-ylpyrazol-4-amine Chemical compound N1=C(Cl)C(NCC)=CN1C1=CC=CN=C1 SXUMSCJUXIVSFX-UHFFFAOYSA-N 0.000 claims 1
- RTANHMOFHGSZQO-UHFFFAOYSA-N 4-methoxy-2,4-dimethylpentanenitrile Chemical compound COC(C)(C)CC(C)C#N RTANHMOFHGSZQO-UHFFFAOYSA-N 0.000 claims 1
- 239000005751 Copper oxide Substances 0.000 claims 1
- 239000007874 V-70 Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 150000004703 alkoxides Chemical class 0.000 claims 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000012320 chlorinating reagent Substances 0.000 claims 1
- 229910000431 copper oxide Inorganic materials 0.000 claims 1
- 238000006114 decarboxylation reaction Methods 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- KTPZOXXVMXIMJI-UHFFFAOYSA-N ethyl 5-chloro-2-pyridin-3-yl-3,4-dihydropyrazole-3-carboxylate Chemical compound CCOC(=O)C1CC(Cl)=NN1c1cccnc1 KTPZOXXVMXIMJI-UHFFFAOYSA-N 0.000 claims 1
- BWSUFRYEIIZITF-UHFFFAOYSA-N ethyl 5-oxo-2-pyridin-3-ylpyrazolidine-3-carboxylate Chemical compound CCOC(=O)C1CC(=O)NN1c1cccnc1 BWSUFRYEIIZITF-UHFFFAOYSA-N 0.000 claims 1
- FZXISDCEHQFFHQ-UHFFFAOYSA-N n-(3-chloro-1-pyridin-3-ylpyrazol-4-yl)-n-ethylacetamide Chemical compound N1=C(Cl)C(N(C(C)=O)CC)=CN1C1=CC=CN=C1 FZXISDCEHQFFHQ-UHFFFAOYSA-N 0.000 claims 1
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 claims 1
- 239000007800 oxidant agent Substances 0.000 claims 1
- 239000003880 polar aprotic solvent Substances 0.000 claims 1
- FNNIAKKPBXJGNJ-UHFFFAOYSA-N pyrazolidine-1-carboxylic acid Chemical compound OC(=O)N1CCCN1 FNNIAKKPBXJGNJ-UHFFFAOYSA-N 0.000 claims 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361892132P | 2013-10-17 | 2013-10-17 | |
| US61/892,132 | 2013-10-17 | ||
| US201462001928P | 2014-05-22 | 2014-05-22 | |
| US62/001,928 | 2014-05-22 | ||
| US201462042559P | 2014-08-27 | 2014-08-27 | |
| US62/042,559 | 2014-08-27 | ||
| PCT/US2014/061027 WO2015058028A1 (en) | 2013-10-17 | 2014-10-17 | Processes for the preparation of pesticidal compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016539092A JP2016539092A (ja) | 2016-12-15 |
| JP2016539092A5 true JP2016539092A5 (enExample) | 2017-12-28 |
Family
ID=52826740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016523965A Pending JP2016539092A (ja) | 2013-10-17 | 2014-10-17 | 有害生物防除性化合物の製造方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (6) | US9102654B2 (enExample) |
| EP (1) | EP3057430A4 (enExample) |
| JP (1) | JP2016539092A (enExample) |
| KR (1) | KR20160072154A (enExample) |
| CN (1) | CN105636441B (enExample) |
| CA (1) | CA2925595A1 (enExample) |
| IL (1) | IL244885A0 (enExample) |
| MX (1) | MX2016004942A (enExample) |
| WO (1) | WO2015058028A1 (enExample) |
Families Citing this family (223)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016536295A (ja) | 2013-10-17 | 2016-11-24 | ダウ アグロサイエンシィズ エルエルシー | 有害生物防除性化合物の製造方法 |
| CA2926095A1 (en) * | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| MX2016004942A (es) | 2013-10-17 | 2016-06-28 | Dow Agrosciences Llc | Procesos para la preparacion de compuestos plaguicidas. |
| CN105636440A (zh) | 2013-10-17 | 2016-06-01 | 美国陶氏益农公司 | 制备杀虫化合物的方法 |
| EP3057431A4 (en) | 2013-10-17 | 2017-04-05 | Dow AgroSciences LLC | Processes for the preparation of pesticidal compounds |
| CN105636446B (zh) | 2013-10-17 | 2018-07-13 | 美国陶氏益农公司 | 制备杀虫化合物的方法 |
| JP6487426B2 (ja) | 2013-10-17 | 2019-03-20 | ダウ アグロサイエンシィズ エルエルシー | 有害生物防除化合物の調製法 |
| CA2954345A1 (en) | 2014-07-31 | 2016-02-04 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| EP3186230A4 (en) | 2014-07-31 | 2018-01-10 | Dow AgroSciences, LLC | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| BR112017000418A2 (pt) | 2014-07-31 | 2017-11-07 | Dow Agrosciences Llc | processo para a preparação de 3-(3-cloro-1h-pirazol-1-il)piridina |
| EP3183238A4 (en) | 2014-08-19 | 2018-01-10 | Dow AgroSciences LLC | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| BR112017004613A2 (pt) | 2014-09-12 | 2017-12-05 | Dow Agrosciences Llc | processo para a preparação de 3-(3-cloro-1h-pirazol-1-il)piridina |
| RU2018119344A (ru) | 2015-10-26 | 2019-11-28 | Байер Кропсайенс Акциенгезельшафт | Конденсированные бициклические гетероциклические производные в качестве средства для борьбы с вредителями |
| WO2017093180A1 (de) | 2015-12-01 | 2017-06-08 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| MX2018006749A (es) | 2015-12-03 | 2018-08-15 | Bayer Cropscience Ag | Derivados de 3-(acetil)-1-[(1,3-tiazol-5-il)metil]-1h-imidazo[1,2- a]piridin-4-io-2-olato halogenados mesoionicos y compuestos relacionados como insecticidas. |
| BR112018016360A2 (pt) | 2016-02-11 | 2018-12-18 | Bayer Cropscience Aktiengesellschaft | 2-(het)arilimidazolilcarboxiamidas substituídas como pesticidas |
| CN108699045B (zh) | 2016-02-11 | 2021-02-12 | 拜耳作物科学股份公司 | 作为害虫防治剂的取代2-氧代咪唑基羧酰胺 |
| WO2017144341A1 (de) | 2016-02-23 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| WO2017157735A1 (de) | 2016-03-15 | 2017-09-21 | Bayer Cropscience Aktiengesellschaft | Substituierte sulfonylamide zur bekämpfung tierischer schädlinge |
| TW201808906A (zh) | 2016-03-16 | 2018-03-16 | 拜耳作物科學股份有限公司 | 作為殺蟲劑之經取代吡啶化合物 |
| WO2017174414A1 (de) | 2016-04-05 | 2017-10-12 | Bayer Cropscience Aktiengesellschaft | Naphthalin-derivate als schädlingsbekämpfungsmittel |
| CA3020793C (en) | 2016-04-15 | 2024-05-21 | Bayer Animal Health Gmbh | Pyrazolopyrimidine derivatives |
| JP2019514893A (ja) | 2016-04-25 | 2019-06-06 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 有害生物防除剤としての置換２−アルキルイミダゾリル−カルボキサミド類 |
| EP3241830A1 (de) | 2016-05-04 | 2017-11-08 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| WO2017198449A1 (en) | 2016-05-15 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in brassicaceae |
| EP3245865A1 (en) | 2016-05-17 | 2017-11-22 | Bayer CropScience Aktiengesellschaft | Method for increasing yield in brassicaceae |
| WO2017198450A1 (en) | 2016-05-15 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in maize |
| WO2017198453A1 (en) | 2016-05-16 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in potato, tomato or alfalfa |
| WO2017198452A1 (en) | 2016-05-16 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in soybean |
| WO2017198455A2 (en) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in beta spp. plants |
| WO2017198451A1 (en) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in small grain cereals such as wheat and rice |
| WO2017198454A1 (en) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in cotton |
| CN109311823B (zh) * | 2016-07-15 | 2023-01-24 | 泸州东方农化有限公司 | 一种1,2,4-三唑-3-硫酮化合物的合成方法及其中间体 |
| BR112019001135B1 (pt) | 2016-07-19 | 2022-11-01 | Bayer Cropscience Aktiengesellschaft | Derivados de heterociclo bicíclico fundido como pesticidas, seu uso, formulação agroquímica, e método para controlar pragas animais |
| WO2018019937A1 (en) | 2016-07-29 | 2018-02-01 | Bayer Cropscience Aktiengesellschaft | Formulation comprising a beneficial p. bilaii strain and talc for use in seed treatment |
| US10660333B2 (en) | 2016-08-10 | 2020-05-26 | Bayer Cropscience Aktiengesellschaft | Substituted 2-heterocyclylimidazolylcarboxamides as pesticides |
| MA45918A (fr) | 2016-08-15 | 2019-06-19 | Bayer Ag | Dérivés hétérocycliques bicycliques condensés utilisés comme pesticides |
| CN109963860A (zh) | 2016-09-19 | 2019-07-02 | 拜耳作物科学股份公司 | 吡唑并[1,5-a]吡啶衍生物及其作为农药的用途 |
| EP3523299B1 (de) | 2016-10-06 | 2021-04-14 | Bayer CropScience Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlings-bekämpfungsmittel |
| WO2018065288A1 (de) | 2016-10-07 | 2018-04-12 | Bayer Cropscience Aktiengesellschaft | 2-[2-phenyl-1-(sulfonylmethyl)vinyl]-imidazo[4,5-b]pyridin-derivate und verwandte verbindungen als schädlingsbekämpfungsmittel im pflanzenschutz |
| TW201822637A (zh) | 2016-11-07 | 2018-07-01 | 德商拜耳廠股份有限公司 | 用於控制動物害蟲的經取代磺醯胺類 |
| DK3538512T3 (da) | 2016-11-11 | 2021-07-05 | Bayer Animal Health Gmbh | Nye anthelmintiske quinolin-3-carboxamid-derivater |
| KR20190084310A (ko) | 2016-11-23 | 2019-07-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 살충제로서의 2-[3-(알킬술포닐)-2H-인다졸-2-일]-3H-이미다조[4,5-b]피리딘 유도체 및 유사한 화합물 |
| WO2018108730A1 (de) | 2016-12-16 | 2018-06-21 | Bayer Aktiengesellschaft | Mesoionische imidazopyridine als insektizide |
| CN110382493A (zh) | 2016-12-16 | 2019-10-25 | 拜耳农作物科学股份公司 | 作为农药的噻二唑衍生物 |
| ES2914788T3 (es) * | 2016-12-29 | 2022-06-16 | Corteva Agriscience Llc | Procesos para la preparación de compuestos pesticidas |
| US10100033B2 (en) | 2016-12-29 | 2018-10-16 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| WO2018125817A1 (en) | 2016-12-29 | 2018-07-05 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| UY37556A (es) | 2017-01-10 | 2018-07-31 | Bayer Ag | Derivados heterocíclicos como pesticidas |
| TW201837026A (zh) | 2017-01-10 | 2018-10-16 | 德商拜耳廠股份有限公司 | 作為除害劑之雜環衍生物（二） |
| WO2018138050A1 (de) | 2017-01-26 | 2018-08-02 | Bayer Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| TW201833107A (zh) | 2017-02-06 | 2018-09-16 | 德商拜耳廠股份有限公司 | 作為殺蟲劑之經２－（雜）芳基取代的稠合雜環衍生物 |
| EP3369320A1 (de) | 2017-03-02 | 2018-09-05 | Bayer CropScience Aktiengesellschaft | Wirkstoff zur bekämpfung von wanzen |
| EP3609887A1 (de) | 2017-04-12 | 2020-02-19 | Bayer Aktiengesellschaft | Mesoionische imidazopyridine als insektizide |
| JP2020517624A (ja) | 2017-04-21 | 2020-06-18 | バイエル・アクチエンゲゼルシヤフト | 殺虫剤としてのメソイオン性イミダゾピリジン類 |
| CN110582503B (zh) | 2017-04-24 | 2022-05-31 | 拜耳公司 | 作为有害物防治剂的稠合双环杂环化合物衍生物 |
| TWI782983B (zh) | 2017-04-27 | 2022-11-11 | 德商拜耳廠股份有限公司 | 雜芳基苯基胺基喹啉及類似物 |
| EP3585791B1 (en) | 2017-04-27 | 2024-10-16 | Elanco Animal Health GmbH | New bicyclic pyrazole derivatives |
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-
2014
- 2014-10-17 MX MX2016004942A patent/MX2016004942A/es unknown
- 2014-10-17 KR KR1020167012456A patent/KR20160072154A/ko not_active Withdrawn
- 2014-10-17 CN CN201480056340.4A patent/CN105636441B/zh not_active Expired - Fee Related
- 2014-10-17 CA CA2925595A patent/CA2925595A1/en not_active Abandoned
- 2014-10-17 US US14/517,587 patent/US9102654B2/en not_active Expired - Fee Related
- 2014-10-17 EP EP14854656.7A patent/EP3057430A4/en not_active Withdrawn
- 2014-10-17 WO PCT/US2014/061027 patent/WO2015058028A1/en not_active Ceased
- 2014-10-17 JP JP2016523965A patent/JP2016539092A/ja active Pending
-
2015
- 2015-05-21 US US14/718,627 patent/US9255083B2/en not_active Expired - Fee Related
-
2016
- 2016-01-06 US US14/988,786 patent/US9434712B2/en not_active Expired - Fee Related
- 2016-04-04 IL IL244885A patent/IL244885A0/en unknown
- 2016-07-29 US US15/223,142 patent/US9670178B2/en not_active Expired - Fee Related
-
2017
- 2017-04-27 US US15/498,691 patent/US9862702B2/en not_active Expired - Fee Related
- 2017-12-08 US US15/835,795 patent/US20180099945A1/en not_active Abandoned
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