JP2019510020A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2019510020A5 JP2019510020A5 JP2018548442A JP2018548442A JP2019510020A5 JP 2019510020 A5 JP2019510020 A5 JP 2019510020A5 JP 2018548442 A JP2018548442 A JP 2018548442A JP 2018548442 A JP2018548442 A JP 2018548442A JP 2019510020 A5 JP2019510020 A5 JP 2019510020A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- radical
- alkylsulfonyl
- 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
Links
- -1 cycloheteroalkyl Chemical group 0.000 claims 128
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 108
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 73
- 150000003254 radicals Chemical class 0.000 claims 52
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 51
- 229910052736 halogen Inorganic materials 0.000 claims 47
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 39
- 150000002367 halogens Chemical class 0.000 claims 36
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 35
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 33
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 28
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 26
- 125000001424 substituent group Chemical group 0.000 claims 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 22
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 21
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 19
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 18
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 18
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 18
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 18
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 18
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 17
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 17
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 claims 16
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 16
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 16
- 125000005843 halogen group Chemical group 0.000 claims 16
- 125000001072 heteroaryl group Chemical group 0.000 claims 16
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 15
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 15
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 15
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims 14
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 14
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims 14
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims 14
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims 14
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000004076 pyridyl group Chemical group 0.000 claims 13
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical group C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims 12
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 12
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 12
- 125000003118 aryl group Chemical group 0.000 claims 12
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 11
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 10
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 9
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 9
- 125000005842 heteroatom Chemical group 0.000 claims 9
- 229910052760 oxygen Inorganic materials 0.000 claims 9
- 239000001301 oxygen Substances 0.000 claims 9
- 239000011593 sulfur Chemical group 0.000 claims 9
- 229910052717 sulfur Inorganic materials 0.000 claims 9
- 229930192474 thiophene Chemical group 0.000 claims 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 8
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 8
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical group C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims 8
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 8
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 claims 7
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 7
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims 6
- 125000005059 halophenyl group Chemical group 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 6
- 125000001624 naphthyl group Chemical group 0.000 claims 6
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 claims 5
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 5
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 5
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 5
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 5
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 5
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 5
- 150000003852 triazoles Chemical class 0.000 claims 5
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical group C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 claims 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 4
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 4
- 125000004404 heteroalkyl group Chemical group 0.000 claims 4
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- 229920006395 saturated elastomer Polymers 0.000 claims 4
- 238000006467 substitution reaction Methods 0.000 claims 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 238000009472 formulation Methods 0.000 claims 3
- 125000004254 isoquinolin-1-yl group Chemical group [H]C1=C([H])C2=C([H])C([H])=C([H])C([H])=C2C(*)=N1 0.000 claims 3
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 150000002831 nitrogen free-radicals Chemical class 0.000 claims 3
- 125000004553 quinoxalin-5-yl group Chemical group N1=CC=NC2=C(C=CC=C12)* 0.000 claims 3
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 2
- 239000004606 Fillers/Extenders Substances 0.000 claims 2
- 239000003905 agrochemical Substances 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000004188 dichlorophenyl group Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 2
- 230000000361 pesticidal effect Effects 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims 1
- 150000002829 nitrogen Chemical class 0.000 claims 1
- 210000000056 organ Anatomy 0.000 claims 1
- 230000001850 reproductive effect Effects 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 238000011282 treatment Methods 0.000 claims 1
- FOAVHYBFDIDICF-UHFFFAOYSA-N CC1=CCCC#CC1c1nc(C(O)O)n[n]1C Chemical compound CC1=CCCC#CC1c1nc(C(O)O)n[n]1C FOAVHYBFDIDICF-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16160293.3 | 2016-03-15 | ||
| EP16160293 | 2016-03-15 | ||
| PCT/EP2017/055405 WO2017157735A1 (de) | 2016-03-15 | 2017-03-08 | Substituierte sulfonylamide zur bekämpfung tierischer schädlinge |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2019510020A JP2019510020A (ja) | 2019-04-11 |
| JP2019510020A5 true JP2019510020A5 (https=) | 2020-04-16 |
Family
ID=55532175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018548442A Pending JP2019510020A (ja) | 2016-03-15 | 2017-03-08 | 害虫を防除するための置換スルホニルアミド類 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US20200288710A1 (https=) |
| EP (1) | EP3429355B1 (https=) |
| JP (1) | JP2019510020A (https=) |
| KR (1) | KR20180125960A (https=) |
| CN (1) | CN109152368A (https=) |
| AR (1) | AR107877A1 (https=) |
| AU (1) | AU2017233739A1 (https=) |
| BR (1) | BR112018068638A2 (https=) |
| CA (1) | CA3017547A1 (https=) |
| CL (1) | CL2018002645A1 (https=) |
| CO (1) | CO2018009677A2 (https=) |
| ES (1) | ES2775782T3 (https=) |
| IL (1) | IL261403A (https=) |
| MX (1) | MX2018011214A (https=) |
| PH (1) | PH12018501966A1 (https=) |
| TW (1) | TW201808103A (https=) |
| UY (1) | UY37153A (https=) |
| WO (1) | WO2017157735A1 (https=) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201617064D0 (en) | 2016-10-07 | 2016-11-23 | Inhibox Limited And Latvian Institute Of Organic Synthesis The | Compounds and their therapeutic use |
| 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 |
| CN109608415B (zh) * | 2019-01-21 | 2020-12-01 | 暨南大学 | 噻唑甲酰胺类化合物及其合成和应用 |
| US20220380318A1 (en) * | 2019-11-07 | 2022-12-01 | Bayer Aktiengesellschaft | Substituted sulfonyl amides for controlling animal pests |
| US10894812B1 (en) | 2020-09-30 | 2021-01-19 | Alpine Roads, Inc. | Recombinant milk proteins |
| AU2021353004A1 (en) | 2020-09-30 | 2023-04-13 | Nobell Foods, Inc. | Recombinant milk proteins and food compositions comprising the same |
| US10947552B1 (en) | 2020-09-30 | 2021-03-16 | Alpine Roads, Inc. | Recombinant fusion proteins for producing milk proteins in plants |
| US20250129031A1 (en) | 2022-01-27 | 2025-04-24 | Pi Industries Ltd. | 1,2,3-triazole carbonyl sulfonylamide compounds and use thereof |
Family Cites Families (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4853383A (en) | 1975-03-03 | 1989-08-01 | Merck & Co., Inc. | β-blocking substituted imidazoles |
| DE4020052A1 (de) | 1990-06-23 | 1992-01-02 | Bayer Ag | Verfahren zur herstellung von 2-chlor-5-methyl-pyridin |
| US5300498A (en) | 1993-06-04 | 1994-04-05 | Hoechst-Roussel Pharmaceuticals Incorporated | 6-piperazinyl-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acids, esters, amides and related compounds |
| JPH08114887A (ja) * | 1994-10-17 | 1996-05-07 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
| US6020357A (en) | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
| US6288061B1 (en) | 1997-12-26 | 2001-09-11 | Welfide Corporation | Imidazole derivatives |
| US6492516B1 (en) | 1999-05-14 | 2002-12-10 | Merck & Co., Inc. | Compounds having cytokine inhibitory activity |
| UY27450A1 (es) | 2001-09-24 | 2003-04-30 | Bayer Corp | Preparación y uso de derivados de imidazol para el tratamiento de la obesidad |
| GB0213715D0 (en) | 2002-06-14 | 2002-07-24 | Syngenta Ltd | Chemical compounds |
| KR100693367B1 (ko) | 2002-06-27 | 2007-03-12 | 아스텔라스세이야쿠 가부시키가이샤 | 아미노알콜 유도체 |
| US7247628B2 (en) | 2002-12-12 | 2007-07-24 | Pfizer, Inc. | Cannabinoid receptor ligands and uses thereof |
| CN101012193A (zh) | 2003-01-02 | 2007-08-08 | 霍夫曼-拉罗奇有限公司 | 新cb 1受体反激动剂 |
| TWI312272B (en) | 2003-05-12 | 2009-07-21 | Sumitomo Chemical Co | Pyrimidine compound and pests controlling composition containing the same |
| US7232823B2 (en) | 2003-06-09 | 2007-06-19 | Pfizer, Inc. | Cannabinoid receptor ligands and uses thereof |
| WO2005099705A2 (en) | 2004-03-24 | 2005-10-27 | Bayer Pharmaceuticals Corporation | Preparation of imidazole derivatives and methods of use |
| GB0414438D0 (en) | 2004-06-28 | 2004-07-28 | Syngenta Participations Ag | Chemical compounds |
| JP4970950B2 (ja) | 2004-10-20 | 2012-07-11 | クミアイ化学工業株式会社 | ３−トリアゾリルフェニルスルフィド誘導体及びそれを有効成分として含有する殺虫・殺ダニ・殺線虫剤 |
| GB0508472D0 (en) | 2005-04-26 | 2005-06-01 | Glaxo Group Ltd | Compounds |
| MY141762A (en) | 2005-10-06 | 2010-06-30 | Nippon Soda Co | Cross-linked cyclic amine compounds and agents for pest control |
| WO2007045096A1 (en) | 2005-10-21 | 2007-04-26 | University Of Saskatchewan | Oligoheteroaromatic luminiscent assemblies as high-affinity dna sequence-directed ligands |
| US20090042926A1 (en) | 2005-12-20 | 2009-02-12 | Jason Imbriglio | Niacin Receptor Agonists, Compositions Containing Such Compounds and Methods of Treatment |
| GB0606774D0 (en) | 2006-04-03 | 2006-05-10 | Novartis Ag | Organic compounds |
| US20070287734A1 (en) | 2006-06-09 | 2007-12-13 | Auspex Pharmaceuticals, Inc. | Preparation and utility of substituted pyrazole compounds with cannabinoid receptor activity |
| WO2008085302A1 (en) | 2006-12-20 | 2008-07-17 | Merck & Co., Inc. | Imidazopyridine analogs as cb2 receptor modulators, useful in the treatment of pain, respiratory and non-respiratory diseases |
| WO2008084218A1 (en) | 2007-01-12 | 2008-07-17 | Boehringer Ingelheim International Gmbh | Benzazole derivatives for the treatment of inflammations |
| US7547690B2 (en) | 2007-03-14 | 2009-06-16 | Bristol-Myers Squibb Company | Compounds for the treatment of Hepatitis C |
| CA2693138A1 (en) | 2007-07-16 | 2009-01-22 | Wyeth Llc | Aminoalkylazole derivatives as histamine-3 antagonists |
| EP2196459B1 (en) | 2007-09-28 | 2016-11-02 | Takeda Pharmaceutical Company Limited | 5-membered heterocyclic compound |
| JP5416710B2 (ja) | 2007-11-20 | 2014-02-12 | ブリストル−マイヤーズ スクイブ カンパニー | シクロプロピル縮合インドロベンズアゼピンｈｃｖｎｓ５ｂ阻害剤 |
| EP2092824A1 (de) | 2008-02-25 | 2009-08-26 | Bayer CropScience AG | Heterocyclyl-Pyrimidine |
| JP5268461B2 (ja) | 2008-07-14 | 2013-08-21 | Ｍｅｉｊｉ Ｓｅｉｋａファルマ株式会社 | Ｐｆ１３６４物質、その製造方法、生産菌株、及び、それを有効成分とする農園芸用殺虫剤 |
| CN101337940B (zh) | 2008-08-12 | 2012-05-02 | 国家农药创制工程技术研究中心 | 具杀虫活性的含氮杂环二氯烯丙醚类化合物 |
| CN101337937B (zh) | 2008-08-12 | 2010-12-22 | 国家农药创制工程技术研究中心 | 具有杀虫活性的n-苯基-5-取代氨基吡唑类化合物 |
| JP2010070514A (ja) * | 2008-09-19 | 2010-04-02 | Toray Ind Inc | ピラゾール誘導体及びその医薬用途 |
| CN101715774A (zh) | 2008-10-09 | 2010-06-02 | 浙江化工科技集团有限公司 | 一个具有杀虫活性化合物制备及用途 |
| EP2184273A1 (de) | 2008-11-05 | 2010-05-12 | Bayer CropScience AG | Halogen-substituierte Verbindungen als Pestizide |
| GB0820344D0 (en) | 2008-11-06 | 2008-12-17 | Syngenta Ltd | Herbicidal compositions |
| TWI482771B (zh) | 2009-05-04 | 2015-05-01 | Du Pont | 磺醯胺殺線蟲劑 |
| WO2011078360A1 (ja) | 2009-12-24 | 2011-06-30 | 武田薬品工業株式会社 | アミド化合物 |
| WO2011085575A1 (zh) | 2010-01-15 | 2011-07-21 | 江苏省农药研究所股份有限公司 | 邻杂环甲酰苯胺类化合物及其合成方法和应用 |
| US8557980B2 (en) | 2010-02-18 | 2013-10-15 | The Board Of Trustees Of The University Of Illinois | Methods for forming protected organoboronic acids |
| US9162981B2 (en) | 2010-03-23 | 2015-10-20 | The Johns Hopkins University | Compositions and methods for treatment of neurodegenerative disease |
| EP2558458B1 (de) * | 2010-04-16 | 2017-09-06 | Bayer Intellectual Property GmbH | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
| WO2011149874A2 (en) | 2010-05-26 | 2011-12-01 | Schering Corporation | N-phenyl imidazole carboxamide inhibitors of 3-phosphoinositide-dependent protein kinase-1 |
| PH12013500237A1 (en) | 2010-08-31 | 2013-03-11 | Mitsui Chemicals Crop & Life Solutions Inc | Pest control agent |
| CN101967139B (zh) | 2010-09-14 | 2013-06-05 | 中化蓝天集团有限公司 | 一种含一氟甲氧基吡唑的邻甲酰氨基苯甲酰胺类化合物、其合成方法及应用 |
| CN103188934B (zh) | 2010-10-18 | 2015-08-26 | 纳幕尔杜邦公司 | 磺酰胺杀线虫剂 |
| TWI515187B (zh) | 2010-12-16 | 2016-01-01 | 健生科學愛爾蘭無限公司 | 作為呼吸道融合病毒抗病毒劑之吲哚類 |
| US20120238599A1 (en) | 2011-03-17 | 2012-09-20 | Chemizon, A Division Of Optomagic Co., Ltd. | Heterocyclic compounds as mek inhibitors |
| EP2540163A1 (en) * | 2011-06-30 | 2013-01-02 | Bayer CropScience AG | Nematocide N-cyclopropyl-sulfonylamide derivatives |
| WO2013050317A1 (en) | 2011-10-03 | 2013-04-11 | Syngenta Limited | Polymorphs of an isoxazoline derivative |
| TWI577286B (zh) | 2011-10-13 | 2017-04-11 | 杜邦股份有限公司 | 殺線蟲磺醯胺之固體形態 |
| CN102391261A (zh) | 2011-10-14 | 2012-03-28 | 上海交通大学 | 一种n-取代噁二嗪类化合物及其制备方法和应用 |
| ES2638144T3 (es) | 2011-12-21 | 2017-10-18 | Bayer Intellectual Property Gmbh | Bencilpirazoles sustituidos |
| CN104202981B (zh) | 2012-03-30 | 2018-01-30 | 巴斯夫欧洲公司 | 防治动物害虫的n‑取代的吡啶亚基化合物和衍生物 |
| EP2647626A1 (en) | 2012-04-03 | 2013-10-09 | Syngenta Participations AG. | 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides |
| US9282739B2 (en) | 2012-04-27 | 2016-03-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| CN104822266B (zh) | 2012-04-27 | 2017-12-05 | 陶氏益农公司 | 杀虫组合物和与其相关的方法 |
| JO3215B1 (ar) | 2012-08-09 | 2018-03-08 | Phenex Pharmaceuticals Ag | حلقات غير متجانسة بها 5 ذرات تحتوي على النيتروجين بها استبدال بكربوكساميد أو سلفوناميد كمعدلات لمستقبل نووي غير محمي RORy |
| UA117359C2 (uk) * | 2012-11-14 | 2018-07-25 | Тейдзін Фарма Лімітед | Похідне піридину |
| TWI605045B (zh) | 2013-01-14 | 2017-11-11 | 杜邦股份有限公司 | 殺線蟲磺醯胺之製備 |
| WO2014115077A1 (en) | 2013-01-22 | 2014-07-31 | Novartis Ag | Substituted purinone compounds |
| CN103232431B (zh) | 2013-01-25 | 2014-11-05 | 青岛科技大学 | 一种二卤代吡唑酰胺类化合物及其应用 |
| CN103109816B (zh) | 2013-01-25 | 2014-09-10 | 青岛科技大学 | 硫代苯甲酰胺类化合物及其应用 |
| US20140275503A1 (en) | 2013-03-13 | 2014-09-18 | Dow Agrosciences Llc | Process for the preparation of certain triaryl rhamnose carbamates |
| WO2014146246A1 (en) | 2013-03-19 | 2014-09-25 | Merck Sharp & Dohme Corp. | Cycloalkyl nitrile pyrazolo pyridones as janus kinase inhibitors |
| CN105555136A (zh) | 2013-07-17 | 2016-05-04 | 拜耳作物科学股份公司 | 具有杀线虫性能的杂环磺酰氨基(硫代)羰基衍生物 |
| CN105578885B (zh) | 2013-07-23 | 2018-06-26 | 拜耳作物科学股份公司 | 作为杀线虫剂的咪唑并噻(二)唑磺酰胺 |
| JP2016533385A (ja) | 2013-08-22 | 2016-10-27 | エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ | アルキニルアルコール及び使用方法 |
| CN103524422B (zh) | 2013-10-11 | 2015-05-27 | 中国农业科学院植物保护研究所 | 苯并咪唑衍生物及其制备方法和用途 |
| 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 |
| WO2015058028A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| WO2015162452A1 (en) * | 2014-04-23 | 2015-10-29 | Piramal Enterprises Limited | Substituted pyrazole compounds as cb1 receptor antagonists and uses thereof |
| CN106661022B (zh) | 2014-05-08 | 2018-05-04 | 拜耳作物科学股份公司 | 作为杀线虫剂的吡唑并吡啶磺酰胺 |
| GB201417094D0 (en) | 2014-09-26 | 2014-11-12 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
-
2017
- 2017-03-08 CN CN201780029972.5A patent/CN109152368A/zh active Pending
- 2017-03-08 KR KR1020187026374A patent/KR20180125960A/ko not_active Withdrawn
- 2017-03-08 CA CA3017547A patent/CA3017547A1/en not_active Abandoned
- 2017-03-08 BR BR112018068638A patent/BR112018068638A2/pt not_active Application Discontinuation
- 2017-03-08 US US16/084,159 patent/US20200288710A1/en not_active Abandoned
- 2017-03-08 ES ES17708548T patent/ES2775782T3/es active Active
- 2017-03-08 WO PCT/EP2017/055405 patent/WO2017157735A1/de not_active Ceased
- 2017-03-08 JP JP2018548442A patent/JP2019510020A/ja active Pending
- 2017-03-08 AU AU2017233739A patent/AU2017233739A1/en not_active Abandoned
- 2017-03-08 MX MX2018011214A patent/MX2018011214A/es unknown
- 2017-03-08 EP EP17708548.7A patent/EP3429355B1/de active Active
- 2017-03-13 TW TW106108115A patent/TW201808103A/zh unknown
- 2017-03-15 AR ARP170100636A patent/AR107877A1/es unknown
- 2017-03-15 UY UY0001037153A patent/UY37153A/es not_active Application Discontinuation
-
2018
- 2018-08-27 IL IL261403A patent/IL261403A/en unknown
- 2018-09-12 PH PH12018501966A patent/PH12018501966A1/en unknown
- 2018-09-14 CL CL2018002645A patent/CL2018002645A1/es unknown
- 2018-09-14 CO CONC2018/0009677A patent/CO2018009677A2/es unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2019510020A5 (https=) | ||
| JP2018509391A5 (https=) | ||
| JP2017537882A5 (https=) | ||
| JP2018502912A5 (https=) | ||
| JP2018509418A5 (https=) | ||
| JP2019503342A5 (https=) | ||
| RU2010111359A (ru) | Пиразольные соединения для борьбы с беспозвоночными вредителями | |
| JP2018513190A5 (https=) | ||
| JP2016528201A5 (https=) | ||
| JP2018536639A5 (https=) | ||
| JP2018516904A5 (https=) | ||
| RU2009141185A (ru) | Инсектицидные производные арилизоксазолина | |
| JP2017523167A5 (https=) | ||
| JP2015535834A5 (https=) | ||
| RU2010107171A (ru) | Фунгицидные n-циклоалкилбензилтиокарбоксамиды или n-циклоалкилбензил-n, -замещенные амидиновые производные | |
| JP2013501720A5 (https=) | ||
| JP2018501226A5 (https=) | ||
| UA98652C2 (uk) | Похідна n-циклоалкілкарбоксаміду, фунгіцидна композиція та спосіб боротьби із фітопатогенними грибами сільськогосподарських культур | |
| JP2005516038A5 (https=) | ||
| JP2007537172A5 (https=) | ||
| RU2017134776A (ru) | Арилзамещенные бициклические соединения в качестве гербицидов | |
| JP2011503103A5 (https=) | ||
| JPWO2019225663A5 (https=) | ||
| BRPI0718929A2 (pt) | Agente de tratamento de solo ou agente de tratamento de semente compreendendo compostos de quinolina ou sais destes como ingrediente ativo, ou método para a prevenção de doenças de planta mediante o seu uso. | |
| JP2019504050A5 (https=) |