JP2016539095A5 - - Google Patents
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- JP2016539095A5 JP2016539095A5 JP2016524093A JP2016524093A JP2016539095A5 JP 2016539095 A5 JP2016539095 A5 JP 2016539095A5 JP 2016524093 A JP2016524093 A JP 2016524093A JP 2016524093 A JP2016524093 A JP 2016524093A JP 2016539095 A5 JP2016539095 A5 JP 2016539095A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrazol
- chloro
- give
- pyridine
- pyridin
- 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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- 150000003568 thioethers Chemical class 0.000 claims 37
- 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 21
- 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 20
- 238000000034 method Methods 0.000 claims 19
- NZUJZWKCHPWMTF-UHFFFAOYSA-N 1-pyridin-3-ylpyrazol-3-amine Chemical compound N1=C(N)C=CN1C1=CC=CN=C1 NZUJZWKCHPWMTF-UHFFFAOYSA-N 0.000 claims 13
- 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 13
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 9
- ZCGXCYMUXMMGDU-UHFFFAOYSA-N 1-pyridin-3-ylpyrazolidin-3-one Chemical compound O=C1CCN(N1)c1cccnc1 ZCGXCYMUXMMGDU-UHFFFAOYSA-N 0.000 claims 9
- DWIACIPVZHPRPO-UHFFFAOYSA-N 3-chloro-n-(3-chloro-1-pyridin-3-ylpyrazol-4-yl)-n-ethylpropanamide Chemical compound N1=C(Cl)C(N(C(=O)CCCl)CC)=CN1C1=CC=CN=C1 DWIACIPVZHPRPO-UHFFFAOYSA-N 0.000 claims 9
- 238000004519 manufacturing process Methods 0.000 claims 9
- QJFANABRDIUIEI-UHFFFAOYSA-N pyridin-3-ylhydrazine;dihydrochloride Chemical compound Cl.Cl.NNC1=CC=CN=C1 QJFANABRDIUIEI-UHFFFAOYSA-N 0.000 claims 9
- 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 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 8
- 241000607479 Yersinia pestis Species 0.000 claims 8
- 239000003960 organic solvent Substances 0.000 claims 8
- 230000000361 pesticidal effect Effects 0.000 claims 8
- YWJVWGBBDPKKMR-UHFFFAOYSA-N N-(3-oxo-1-pyridin-3-ylpyrazolidin-4-yl)acetamide Chemical compound CC(=O)NC1CN(NC1=O)c1cccnc1 YWJVWGBBDPKKMR-UHFFFAOYSA-N 0.000 claims 7
- -1 pyridine 3- (3-Chloro-1H-pyrazol-1-yl) pyridine Chemical compound 0.000 claims 7
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 6
- 229910052783 alkali metal Inorganic materials 0.000 claims 6
- 150000001340 alkali metals Chemical class 0.000 claims 6
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims 6
- 239000012954 diazonium Substances 0.000 claims 6
- 150000001989 diazonium salts Chemical class 0.000 claims 6
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 claims 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 5
- 150000004703 alkoxides Chemical class 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 239000002585 base Substances 0.000 claims 5
- IZPXUHAPZZILIV-UHFFFAOYSA-N 2-pyridin-3-yl-3,4-dihydropyrazol-5-amine Chemical compound C1CC(N)=NN1C1=CC=CN=C1 IZPXUHAPZZILIV-UHFFFAOYSA-N 0.000 claims 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 4
- 230000002152 alkylating effect Effects 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims 4
- 239000003880 polar aprotic solvent Substances 0.000 claims 4
- KEQTWHPMSVAFDA-UHFFFAOYSA-N 2,3-dihydro-1h-pyrazole Chemical compound C1NNC=C1 KEQTWHPMSVAFDA-UHFFFAOYSA-N 0.000 claims 3
- INUNLMUAPJVRME-UHFFFAOYSA-N 3-chloropropanoyl chloride Chemical compound ClCCC(Cl)=O INUNLMUAPJVRME-UHFFFAOYSA-N 0.000 claims 3
- 150000001735 carboxylic acids Chemical class 0.000 claims 3
- 238000005660 chlorination reaction Methods 0.000 claims 3
- SMWNFFKPVLVOQQ-UHFFFAOYSA-N methyl 2-acetamidoprop-2-enoate Chemical compound COC(=O)C(=C)NC(C)=O SMWNFFKPVLVOQQ-UHFFFAOYSA-N 0.000 claims 3
- 239000007800 oxidant agent Substances 0.000 claims 3
- 230000001590 oxidative effect Effects 0.000 claims 3
- 235000010288 sodium nitrite Nutrition 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical compound NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 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
- NYPYPOZNGOXYSU-UHFFFAOYSA-N 3-bromopyridine Chemical compound BrC1=CC=CN=C1 NYPYPOZNGOXYSU-UHFFFAOYSA-N 0.000 claims 2
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 230000003197 catalytic effect Effects 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
- 230000000694 effects Effects 0.000 claims 2
- 230000008030 elimination Effects 0.000 claims 2
- 238000003379 elimination reaction Methods 0.000 claims 2
- 239000003999 initiator Substances 0.000 claims 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims 2
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 claims 2
- 150000003254 radicals Chemical class 0.000 claims 2
- HUPVIAINOSTNBJ-HWKANZROSA-N (e)-3-ethoxyprop-2-enenitrile Chemical compound CCO\C=C\C#N HUPVIAINOSTNBJ-HWKANZROSA-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
- FCYVWWWTHPPJII-UHFFFAOYSA-N 2-methylidenepropanedinitrile Chemical compound N#CC(=C)C#N FCYVWWWTHPPJII-UHFFFAOYSA-N 0.000 claims 1
- QEQXVMAGRPVXEK-UHFFFAOYSA-N 3-(5-chloro-3,4-dihydropyrazol-2-yl)pyridine Chemical compound ClC1=NN(CC1)c1cccnc1 QEQXVMAGRPVXEK-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
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims 1
- 239000007874 V-70 Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 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
- 229910000336 copper(I) sulfate Inorganic materials 0.000 claims 1
- WIVXEZIMDUGYRW-UHFFFAOYSA-L copper(i) sulfate Chemical compound [Cu+].[Cu+].[O-]S([O-])(=O)=O WIVXEZIMDUGYRW-UHFFFAOYSA-L 0.000 claims 1
- 150000002148 esters Chemical class 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
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- FNNIAKKPBXJGNJ-UHFFFAOYSA-N pyrazolidine-1-carboxylic acid Chemical compound OC(=O)N1CCCN1 FNNIAKKPBXJGNJ-UHFFFAOYSA-N 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-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 (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361892129P | 2013-10-17 | 2013-10-17 | |
| US61/892,129 | 2013-10-17 | ||
| US201462042554P | 2014-08-27 | 2014-08-27 | |
| US62/042,554 | 2014-08-27 | ||
| PCT/US2014/061010 WO2015058021A1 (en) | 2013-10-17 | 2014-10-17 | Processes for the preparation of pesticidal compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016539095A JP2016539095A (ja) | 2016-12-15 |
| JP2016539095A5 true JP2016539095A5 (OSRAM) | 2017-12-28 |
Family
ID=52826741
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016524093A Pending JP2016539095A (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 (5) | US9108946B2 (OSRAM) |
| EP (1) | EP3057429A4 (OSRAM) |
| JP (1) | JP2016539095A (OSRAM) |
| KR (1) | KR20160072155A (OSRAM) |
| CN (1) | CN105636440A (OSRAM) |
| CA (1) | CA2925873A1 (OSRAM) |
| IL (1) | IL245065A0 (OSRAM) |
| MX (1) | MX2016004943A (OSRAM) |
| WO (1) | WO2015058021A1 (OSRAM) |
Families Citing this family (225)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20160075565A (ko) | 2013-10-17 | 2016-06-29 | 다우 아그로사이언시즈 엘엘씨 | 살충성 화합물의 제조 방법 |
| JP2016536296A (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 |
| EP3057431A4 (en) | 2013-10-17 | 2017-04-05 | Dow AgroSciences LLC | Processes for the preparation of pesticidal compounds |
| WO2015058024A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| MX2016004946A (es) | 2013-10-17 | 2016-06-28 | Dow Agrosciences Llc | Procesos para la preparacion de compuestos plaguicidas. |
| CA2925873A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| WO2015058028A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| US9029555B1 (en) | 2014-07-31 | 2015-05-12 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine |
| CN106470976A (zh) | 2014-07-31 | 2017-03-01 | 美国陶氏益农公司 | 制备3‑(3‑氯‑1h‑吡唑‑1‑基)吡啶的方法 |
| AR098110A1 (es) * | 2014-07-31 | 2016-05-04 | Dow Agrosciences Llc | Proceso para la preparación de 3-(3-cloro-1h-pirazol-1-il)piridina |
| BR112017002735A2 (pt) | 2014-08-19 | 2017-12-19 | Dow Agrosciences Llc | processo para a preparação de 3-(3-cloro-1h-pirazol-1-il)piridina |
| KR20170058388A (ko) | 2014-09-12 | 2017-05-26 | 다우 아그로사이언시즈 엘엘씨 | 3-(3-클로로-1h-피라졸-1-일)피리딘의 제조 방법 |
| WO2017072039A1 (de) | 2015-10-26 | 2017-05-04 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| WO2017093180A1 (de) | 2015-12-01 | 2017-06-08 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| AU2016363632A1 (en) | 2015-12-03 | 2018-06-07 | Bayer Cropscience Aktiengesellschaft | Mesoionic halogenated 3-(acetyl)-1-((1,3-thiazol-5-yl)methyl)-1h-imidazo(1,2-a)pyridin-4-ium-2-olate derivatives and related compounds as insecticides |
| CA3013962A1 (en) | 2016-02-11 | 2017-08-17 | Bayer Cropscience Aktiengesellschaft | Substituted 2-(het)aryl-imidazolyl-carboxyamides as pest control agents |
| MX2018009809A (es) | 2016-02-11 | 2018-09-10 | Bayer Cropscience Ag | 2-oximidazolilcarboxamidas sustituidas como plaguicidas. |
| WO2017144341A1 (de) | 2016-02-23 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| JP2019510020A (ja) | 2016-03-15 | 2019-04-11 | 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 | 害虫を防除するための置換スルホニルアミド類 |
| BR112018068681A2 (pt) | 2016-03-16 | 2019-01-15 | Bayer Cropscience Ag | derivados de n-(cianobenzil)-6-(ciclopropil-carbonilamino)-4-(fenil)-piridina-2-carboxamida e compostos relacionados como pesticidas e agentes de proteção de plantas |
| WO2017174414A1 (de) | 2016-04-05 | 2017-10-12 | Bayer Cropscience Aktiengesellschaft | Naphthalin-derivate als schädlingsbekämpfungsmittel |
| SG11201808214TA (en) | 2016-04-15 | 2018-10-30 | Bayer Animal Health Gmbh | Pyrazolopyrimidine derivatives |
| KR20180135956A (ko) | 2016-04-25 | 2018-12-21 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 치환된 2-알킬이미다졸릴-카르복스아미드 |
| 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 |
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| WO2017198452A1 (en) | 2016-05-16 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in soybean |
| WO2017198453A1 (en) | 2016-05-16 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in potato, tomato or alfalfa |
| WO2017198454A1 (en) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in cotton |
| WO2017198451A1 (en) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in small grain cereals such as wheat and rice |
| WO2017198455A2 (en) | 2016-05-17 | 2017-11-23 | Bayer Cropscience Nv | Method for increasing yield in beta spp. plants |
| CA3031139A1 (en) | 2016-07-19 | 2018-01-25 | Bayer Cropscience Aktiengesellschaft | Condensed bicyclic heterocycle derivatives as pest control agents |
| EP3490363A1 (en) | 2016-07-29 | 2019-06-05 | Bayer CropScience Aktiengesellschaft | Formulation comprising a beneficial p. bilaii strain and talc for use in seed treatment |
| KR20190037305A (ko) | 2016-08-10 | 2019-04-05 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 치환된 2-헤테로시클릴 이미다졸릴-카르복스아미드 |
| JP2019526547A (ja) | 2016-08-11 | 2019-09-19 | 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 | 置換されているピラゾリニル誘導体、それらを製造する方法、並びに、除草剤及び／又は植物成長調節剤としてのそれらの使用 |
| KR102419244B1 (ko) | 2016-08-15 | 2022-07-08 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 축합 바이시클릭 헤테로사이클 유도체 |
| MX2019003136A (es) | 2016-09-19 | 2019-07-18 | Bayer Cropscience Ag | Derivados de pirazolo [1,5-a]piridina y su uso como pesticidas. |
| AU2017340690B2 (en) | 2016-10-06 | 2021-05-20 | Bayer Cropscience Aktiengesellschaft | 2-(Het)aryl-substituted condensed bicyclic heterocycle derivatives as pest control agents |
| 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 |
| PL3538512T3 (pl) | 2016-11-11 | 2021-11-22 | Bayer Animal Health Gmbh | Nowe pochodne chinolino-3-karboksyamidu o działaniu przeciw robakom pasożytniczym |
| WO2018095953A1 (de) | 2016-11-23 | 2018-05-31 | Bayer Cropscience Aktiengesellschaft | 2-[3-(alkylsulfonyl)-2h-indazol-2-yl]-3h-imidazo[4,5-b]pyridin-derivate und ähnliche verbindungen als schädlingsbekämpfungsmittel |
| JP2020502168A (ja) | 2016-12-16 | 2020-01-23 | 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 | 殺有害生物剤としてのチアジアゾール誘導体 |
| BR112019012262A2 (pt) | 2016-12-16 | 2019-12-03 | Bayer Ag | imidazopiridinas mesoiônicas para uso como inseticidas |
| WO2018125817A1 (en) | 2016-12-29 | 2018-07-05 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| CN110139853B (zh) | 2016-12-29 | 2023-06-16 | 美国陶氏益农公司 | 用于制备杀有害生物化合物的方法 |
| US20180186753A1 (en) * | 2016-12-29 | 2018-07-05 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| US11058115B2 (en) | 2017-01-10 | 2021-07-13 | Bayer Aktiengesellschaft | Heterocycle derivatives as pesticides |
| EP3568395A1 (de) | 2017-01-10 | 2019-11-20 | Bayer Aktiengesellschaft | Heterocyclen-derivate als schädlingsbekämpfungsmittel |
| 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 |
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-
2014
- 2014-10-17 CA CA2925873A patent/CA2925873A1/en not_active Abandoned
- 2014-10-17 EP EP14853997.6A patent/EP3057429A4/en not_active Withdrawn
- 2014-10-17 US US14/517,591 patent/US9108946B2/en not_active Expired - Fee Related
- 2014-10-17 WO PCT/US2014/061010 patent/WO2015058021A1/en not_active Ceased
- 2014-10-17 CN CN201480056339.1A patent/CN105636440A/zh active Pending
- 2014-10-17 KR KR1020167012457A patent/KR20160072155A/ko not_active Withdrawn
- 2014-10-17 JP JP2016524093A patent/JP2016539095A/ja active Pending
- 2014-10-17 MX MX2016004943A patent/MX2016004943A/es unknown
-
2015
- 2015-05-19 US US14/715,956 patent/US9414594B2/en not_active Expired - Fee Related
-
2016
- 2016-04-12 IL IL245065A patent/IL245065A0/en unknown
- 2016-05-27 US US15/166,784 patent/US9580405B2/en not_active Expired - Fee Related
- 2016-12-23 US US15/389,530 patent/US20170101392A1/en not_active Abandoned
-
2017
- 2017-10-24 US US15/791,746 patent/US20180044319A1/en not_active Abandoned
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