JP2019503342A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2019503342A5 JP2019503342A5 JP2018525468A JP2018525468A JP2019503342A5 JP 2019503342 A5 JP2019503342 A5 JP 2019503342A5 JP 2018525468 A JP2018525468 A JP 2018525468A JP 2018525468 A JP2018525468 A JP 2018525468A JP 2019503342 A5 JP2019503342 A5 JP 2019503342A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- haloalkyl
- cycloalkyl
- cyano
- 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.)
- Ceased
Links
- 125000000217 alkyl group Chemical group 0.000 claims description 122
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 82
- 125000001424 substituent group Chemical group 0.000 claims description 71
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 70
- 229910052736 halogen Inorganic materials 0.000 claims description 70
- 150000002367 halogens Chemical class 0.000 claims description 70
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 58
- 229910052739 hydrogen Inorganic materials 0.000 claims description 48
- 239000001257 hydrogen Substances 0.000 claims description 48
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 42
- 150000002431 hydrogen Chemical class 0.000 claims description 32
- 150000001875 compounds Chemical class 0.000 claims description 25
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 16
- -1 C 1 -C 6 alkoxy Chemical group 0.000 claims description 15
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 13
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 10
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 125000004770 (C1-C4) haloalkylsulfanyl group Chemical group 0.000 claims description 9
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 8
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 7
- 125000004076 pyridyl group Chemical group 0.000 claims description 7
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 241000607479 Yersinia pestis Species 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 239000001301 oxygen Chemical group 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 239000011593 sulfur Chemical group 0.000 claims description 6
- 125000004434 sulfur atom Chemical group 0.000 claims description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 4
- 125000004740 (C1-C6) haloalkylsulfanyl group Chemical group 0.000 claims description 4
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 4
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000001188 haloalkyl group Chemical group 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims description 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 239000012752 auxiliary agent Substances 0.000 claims description 2
- 125000006255 cyclopropyl carbonyl group Chemical group [H]C1([H])C([H])([H])C1([H])C(*)=O 0.000 claims description 2
- 125000002883 imidazolyl group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 description 25
- 125000004414 alkyl thio group Chemical group 0.000 description 9
- 125000003282 alkyl amino group Chemical group 0.000 description 5
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 5
- 0 CCc1pc(*)c(*(*)*)cc1** Chemical compound CCc1pc(*)c(*(*)*)cc1** 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 2
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 description 2
- 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 description 1
- 241001414900 Anopheles stephensi Species 0.000 description 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000005169 cycloalkylcarbonylamino group Chemical group 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 description 1
- 125000000232 haloalkynyl group Chemical group 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN3735DE2015 | 2015-11-16 | ||
| IN3735/DEL/2015 | 2015-11-16 | ||
| IN201611028887 | 2016-08-24 | ||
| IN201611028887 | 2016-08-24 | ||
| PCT/EP2016/076493 WO2017084879A1 (en) | 2015-11-16 | 2016-11-03 | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2019503342A JP2019503342A (ja) | 2019-02-07 |
| JP2019503342A5 true JP2019503342A5 (https=) | 2019-12-12 |
Family
ID=57233455
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018525468A Ceased JP2019503342A (ja) | 2015-11-16 | 2016-11-03 | 硫黄含有置換基を有する殺有害生物的に活性な複素環式誘導体 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US10730872B2 (https=) |
| EP (1) | EP3377489B1 (https=) |
| JP (1) | JP2019503342A (https=) |
| CN (1) | CN108290884A (https=) |
| BR (1) | BR112018009852A2 (https=) |
| WO (1) | WO2017084879A1 (https=) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3523299B1 (de) * | 2016-10-06 | 2021-04-14 | Bayer CropScience Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlings-bekämpfungsmittel |
| WO2018077565A1 (en) * | 2016-10-27 | 2018-05-03 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur and hydroxylamine substituents |
| DK3548466T3 (da) | 2016-12-01 | 2022-04-19 | Syngenta Participations Ag | Fremgangsmåde til fremstilling af et mellemprodukt af pesticidaktive heterocykliske derivater med svovlindeholdende substituenter |
| US10894792B2 (en) * | 2017-05-02 | 2021-01-19 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| KR102635481B1 (ko) * | 2017-09-18 | 2024-02-07 | 신젠타 파티서페이션즈 아게 | 황 함유 치환기를 갖는 살충 활성 헤테로사이클릭 유도체 |
| WO2019076778A1 (en) | 2017-10-16 | 2019-04-25 | Syngenta Participations Ag | HETEROCYCLIC DERIVATIVES HAVING PESTICIDAL ACTIVITY HAVING SUBSTITUENTS CONTAINING SULFUR AND SULFONIMIDAMIDES |
| CN111741958A (zh) | 2018-02-21 | 2020-10-02 | 拜耳公司 | 作为害虫防治剂的稠合双环杂环衍生物 |
| KR20200131268A (ko) | 2018-03-12 | 2020-11-23 | 바이엘 악티엔게젤샤프트 | 해충 방제제로서의 융합된 비시클릭 헤테로시클릭 유도체 |
| WO2019229088A1 (en) * | 2018-05-30 | 2019-12-05 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2019229089A1 (en) | 2018-05-31 | 2019-12-05 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| CA3102190A1 (en) | 2018-06-06 | 2019-12-12 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfoximine containing substituents |
| AR115495A1 (es) * | 2018-06-06 | 2021-01-27 | Syngenta Crop Protection Ag | Derivados heterocíclicos con sustituyentes que contienen azufre activos como plaguicidas |
| TW202035404A (zh) | 2018-10-24 | 2020-10-01 | 瑞士商先正達農作物保護公司 | 具有含亞碸亞胺的取代基之殺有害生物活性雜環衍生物 |
| AR119140A1 (es) | 2019-06-13 | 2021-11-24 | Pi Industries Ltd | Compuestos heterocíclicos fusionados y su uso como agentes de control de plagas |
| WO2020254530A1 (en) | 2019-06-18 | 2020-12-24 | Syngenta Crop Protection Ag | 7-sulfonyl-n-(1,3,4-thiadiazol-2-yl)-quinoxaline-6-carboxamide derivatives and the respective -benzimidazole-5-, -imidazo[4,5-b]pyridine-5-, -3h-furo[3,2b]pyridine-5-, -quinoline-2-, and -naphthalene-2-carboxamide derivatives as pesticides |
| CN110407744A (zh) * | 2019-08-13 | 2019-11-05 | 上海毕得医药科技有限公司 | 一种1-(4-氨基吡啶-2-基)乙酮的合成方法 |
| JP7581336B2 (ja) | 2019-09-20 | 2024-11-12 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 硫黄及びスルホキシミン含有置換基を有する殺有害生物的に活性な複素環式誘導体 |
| CN112824402B (zh) * | 2019-11-21 | 2023-02-28 | 浙江省化工研究院有限公司 | 一类苯并咪唑类衍生物、其制备方法及应用 |
| TW202134214A (zh) * | 2020-03-04 | 2021-09-16 | 瑞士商先正達農作物保護公司 | 用於製備具有3-含硫取代基的5-氯-吡啶-2-甲酸醯胺以及甲酸鹽之方法 |
| BR112022021895A2 (pt) | 2020-04-30 | 2023-01-24 | Syngenta Crop Protection Ag | Derivados heterocíclicos com substituintes contendo enxofre ativos em termos pesticidas |
| CN112876366B (zh) * | 2021-01-21 | 2022-10-04 | 中国科学院昆明植物研究所 | 一种帚状异酯素、其制备方法和应用，以及药物组合物 |
| CN113912592B (zh) * | 2021-11-03 | 2023-03-10 | 西北农林科技大学 | 一种和厚朴酚并二氢呋喃酯类衍生物、制备方法及其应用 |
| CN114752535A (zh) * | 2022-05-16 | 2022-07-15 | 北京昊峰节能环保科技有限公司 | 一种总石油烃污染地下水生物修复剂及其制备方法与应用 |
| EP4680028A1 (en) | 2023-03-14 | 2026-01-21 | Syngenta Crop Protection AG | Control of pests resistant to insecticides |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3224512A1 (de) * | 1982-07-01 | 1984-01-05 | Dr. Karl Thomae Gmbh, 7950 Biberach | Neue imidazolderivate, ihre herstellung und diese verbindungen enthaltende arzneimittel |
| TW274551B (https=) * | 1991-04-16 | 1996-04-21 | Takeda Pharm Industry Co Ltd | |
| US5814651A (en) * | 1992-12-02 | 1998-09-29 | Pfizer Inc. | Catechol diethers as selective PDEIV inhibitors |
| WO2012086848A1 (en) * | 2010-12-24 | 2012-06-28 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use for pest control thereof |
| TWI545119B (zh) * | 2011-08-04 | 2016-08-11 | 住友化學股份有限公司 | 稠合雜環化合物及其在病蟲害防制上之用途 |
| EP2862853B1 (en) * | 2012-06-18 | 2020-01-22 | Sumitomo Chemical Co., Ltd | Fused heterocyclic compound |
| EP2864326A1 (en) * | 2012-06-22 | 2015-04-29 | E. I. Du Pont de Nemours and Company | Fungicidal heterocyclic compounds |
| TWI614242B (zh) * | 2013-01-31 | 2018-02-11 | 住友化學股份有限公司 | 有害生物防治組成物及有害生物之防治方法 |
| BR112015020204B1 (pt) * | 2013-02-28 | 2020-10-27 | Sumitomo Chemical Company, Limited | composto heterocíclico fundido, agente de controle de peste e método para controlar peste |
| WO2015000715A1 (en) | 2013-07-02 | 2015-01-08 | Syngenta Participations Ag | Pesticidally active bi- or tricyclic heterocycles with sulfur containing substituents |
| US10005775B2 (en) * | 2014-08-12 | 2018-06-26 | Syngenta Participations, Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| WO2016058928A1 (en) | 2014-10-14 | 2016-04-21 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| CA2994604A1 (en) * | 2015-08-07 | 2017-02-16 | Bayer Cropscience Aktiengesellschaft | 2-(het)aryl-substituted condensed heterocyclic derivatives as pest control agents |
-
2016
- 2016-11-03 US US15/775,582 patent/US10730872B2/en not_active Expired - Fee Related
- 2016-11-03 CN CN201680066815.7A patent/CN108290884A/zh active Pending
- 2016-11-03 BR BR112018009852A patent/BR112018009852A2/pt not_active Application Discontinuation
- 2016-11-03 WO PCT/EP2016/076493 patent/WO2017084879A1/en not_active Ceased
- 2016-11-03 JP JP2018525468A patent/JP2019503342A/ja not_active Ceased
- 2016-11-03 EP EP16790995.1A patent/EP3377489B1/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2019503342A5 (https=) | ||
| JP2017537882A5 (https=) | ||
| JP2018509418A5 (https=) | ||
| JP2017523997A5 (https=) | ||
| JP2018501226A5 (https=) | ||
| JP2018524336A5 (https=) | ||
| JP2018509379A5 (https=) | ||
| JP2017526678A5 (https=) | ||
| JP2017526667A5 (https=) | ||
| JP2018502912A5 (https=) | ||
| JP2018513190A5 (https=) | ||
| JP2017523167A5 (https=) | ||
| JP2018509417A5 (https=) | ||
| JP2018502148A5 (https=) | ||
| JP2018524337A5 (https=) | ||
| JP2017531616A5 (https=) | ||
| JP2020502115A5 (https=) | ||
| JP2016528201A5 (https=) | ||
| JP2020500170A5 (https=) | ||
| RU2017125267A (ru) | Пестицидно активные гетероциклические производные с серосодержащими заместителями | |
| JP2017512835A5 (https=) | ||
| JP2017537874A5 (https=) | ||
| RU2017103953A (ru) | Пестицидно активные гетероциклические производные с серосодержащими заместителями | |
| JP2019513739A5 (https=) | ||
| RU2013141413A (ru) | Производные изоксазолина для борьбы с беспозвоночными паразитами |