JP2017526678A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2017526678A5 JP2017526678A5 JP2017511237A JP2017511237A JP2017526678A5 JP 2017526678 A5 JP2017526678 A5 JP 2017526678A5 JP 2017511237 A JP2017511237 A JP 2017511237A JP 2017511237 A JP2017511237 A JP 2017511237A JP 2017526678 A5 JP2017526678 A5 JP 2017526678A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- oxazolyl
- alkylamino
- dihydro
- 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.)
- Granted
Links
- -1 C 1 -C 6 alkoxy Chemical group 0.000 claims description 56
- 229910052736 halogen Inorganic materials 0.000 claims description 38
- 150000002367 halogens Chemical group 0.000 claims description 38
- 150000001875 compounds Chemical class 0.000 claims description 34
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 24
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 24
- 125000005050 dihydrooxazolyl group Chemical group O1C(NC=C1)* 0.000 claims description 24
- 125000005879 dioxolanyl group Chemical group 0.000 claims description 24
- 125000002971 oxazolyl group Chemical group 0.000 claims description 24
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 24
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 24
- 125000004076 pyridyl group Chemical group 0.000 claims description 24
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 24
- 125000000335 thiazolyl group Chemical group 0.000 claims description 24
- 125000001424 substituent group Chemical group 0.000 claims description 22
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 21
- IGERFAHWSHDDHX-UHFFFAOYSA-N 1,3-dioxanyl Chemical group [CH]1OCCCO1 IGERFAHWSHDDHX-UHFFFAOYSA-N 0.000 claims description 20
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 18
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 16
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 16
- 125000004770 (C1-C4) haloalkylsulfanyl group Chemical group 0.000 claims description 14
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 14
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 12
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 12
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 10
- 125000003282 alkyl amino group Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 7
- 241000607479 Yersinia pestis Species 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 4
- 125000004122 cyclic 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 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
- 125000002496 methyl group Chemical group [H]C([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
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 229910052717 sulfur Chemical group 0.000 claims description 4
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 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 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000012752 auxiliary agent Substances 0.000 claims description 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 2
- 238000002405 diagnostic procedure Methods 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 125000002883 imidazolyl group Chemical group 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000004043 oxo group Chemical group O=* 0.000 claims description 2
- 239000001301 oxygen Chemical group 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 238000001356 surgical procedure Methods 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 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 description 33
- 125000003545 alkoxy group Chemical group 0.000 description 14
- 0 Cc1ccc(*)nc1 Chemical compound Cc1ccc(*)nc1 0.000 description 13
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 description 10
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 7
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 description 6
- XQQBUAPQHNYYRS-UHFFFAOYSA-N Cc1ccc[s]1 Chemical compound Cc1ccc[s]1 XQQBUAPQHNYYRS-UHFFFAOYSA-N 0.000 description 2
- ITQTTZVARXURQS-UHFFFAOYSA-N Cc1cccnc1 Chemical compound Cc1cccnc1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 241000256118 Aedes aegypti Species 0.000 description 1
- CNJQNAOCUYWMQQ-UHFFFAOYSA-N CC1=CNNC1 Chemical compound CC1=CNNC1 CNJQNAOCUYWMQQ-UHFFFAOYSA-N 0.000 description 1
- FNOKJRGVMILSFT-UHFFFAOYSA-N CN1N=CCC1 Chemical compound CN1N=CCC1 FNOKJRGVMILSFT-UHFFFAOYSA-N 0.000 description 1
- MCTWTZJPVLRJOU-UHFFFAOYSA-N C[n]1cncc1 Chemical compound C[n]1cncc1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 1
- MWZDIEIXRBWPLG-UHFFFAOYSA-N C[n]1ncnc1 Chemical compound C[n]1ncnc1 MWZDIEIXRBWPLG-UHFFFAOYSA-N 0.000 description 1
- KJRRQXYWFQKJIP-UHFFFAOYSA-N Cc1c[o]cc1 Chemical compound Cc1c[o]cc1 KJRRQXYWFQKJIP-UHFFFAOYSA-N 0.000 description 1
- QENGPZGAWFQWCZ-UHFFFAOYSA-N Cc1c[s]cc1 Chemical compound Cc1c[s]cc1 QENGPZGAWFQWCZ-UHFFFAOYSA-N 0.000 description 1
- AIKUBOPKWKZULG-UHFFFAOYSA-N Cc1ccnnc1 Chemical compound Cc1ccnnc1 AIKUBOPKWKZULG-UHFFFAOYSA-N 0.000 description 1
- RLYUNPNLXMSXAX-UHFFFAOYSA-N Cc1cnc[s]1 Chemical compound Cc1cnc[s]1 RLYUNPNLXMSXAX-UHFFFAOYSA-N 0.000 description 1
- TWGNOYAGHYUFFR-UHFFFAOYSA-N Cc1cncnc1 Chemical compound Cc1cncnc1 TWGNOYAGHYUFFR-UHFFFAOYSA-N 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14182118.1 | 2014-08-25 | ||
| EP14182118 | 2014-08-25 | ||
| EP15159505 | 2015-03-17 | ||
| EP15159505.5 | 2015-03-17 | ||
| PCT/EP2015/068953 WO2016030229A1 (en) | 2014-08-25 | 2015-08-18 | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017526678A JP2017526678A (ja) | 2017-09-14 |
| JP2017526678A5 true JP2017526678A5 (enExample) | 2018-09-27 |
| JP6695861B2 JP6695861B2 (ja) | 2020-05-20 |
Family
ID=53872066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017511237A Expired - Fee Related JP6695861B2 (ja) | 2014-08-25 | 2015-08-18 | 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) | US9809587B2 (enExample) |
| EP (1) | EP3186249B1 (enExample) |
| JP (1) | JP6695861B2 (enExample) |
| CN (1) | CN106604922B (enExample) |
| BR (1) | BR112017003366B1 (enExample) |
| WO (1) | WO2016030229A1 (enExample) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6663907B2 (ja) * | 2014-07-08 | 2020-03-13 | シンジェンタ パーティシペーションズ アーゲー | 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 |
| BR112017003168B1 (pt) * | 2014-08-21 | 2021-03-02 | Syngenta Participations Ag | compostos derivados de heterocíclicos, composição pesticida, método para controle de pragas e método para a proteção de material de propagação de plantas do ataque por pragas |
| KR102551157B1 (ko) * | 2014-11-07 | 2023-07-03 | 신젠타 파티서페이션즈 아게 | 황 함유 치환기를 가지는 살충 활성 폴리사이클릭 유도체 |
| HRP20220345T1 (hr) * | 2016-02-26 | 2022-05-13 | Nihon Nohyaku Co., Ltd. | Kondenzirani heterociklički spoj na koji su vezani heterocikli i njegove soli, poljoprivredni/hortikulturalni insekticid koji sadrži spomenuti spoj, i metoda korištenja spomenutog insekticida |
| WO2017164108A1 (ja) * | 2016-03-25 | 2017-09-28 | 住友化学株式会社 | 複素環化合物 |
| EP3444245B1 (en) * | 2016-03-31 | 2022-02-23 | Sumitomo Chemical Company, Limited | Heterocyclic compound |
| BR112018070537B1 (pt) | 2016-04-06 | 2022-11-01 | Sumitomo Chemical Company, Limited | Composto heterocíclico, composição compreendendo o mesmo e seus usos |
| WO2018065292A1 (de) | 2016-10-06 | 2018-04-12 | Bayer Cropscience Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlings-bekämpfungsmittel |
| WO2018091389A1 (en) * | 2016-11-17 | 2018-05-24 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| US10934287B2 (en) * | 2017-03-23 | 2021-03-02 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and composition containing same |
| WO2018197315A1 (en) | 2017-04-25 | 2018-11-01 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| US10945435B2 (en) * | 2017-05-08 | 2021-03-16 | Syngenta Participations Ag | Imidazopyrimidine derivatives with sulfur containing phenyl and pyridyl substituents |
| TW201920146A (zh) | 2017-07-05 | 2019-06-01 | 瑞士商先正達合夥公司 | 具有含硫取代基之殺有害生物活性的雜環衍生物 |
| EP3649128A1 (en) | 2017-07-07 | 2020-05-13 | Syngenta Participations AG | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2019065568A1 (ja) * | 2017-09-26 | 2019-04-04 | 住友化学株式会社 | 複素環化合物及びそれを含有する有害節足動物防除剤 |
| CA3086303A1 (en) * | 2017-12-22 | 2019-06-27 | Sumitomo Chemical Company, Limited | Heterocyclic compound and harmful arthropod controlling agent containing same |
| CN111511741B (zh) * | 2017-12-22 | 2022-04-01 | 住友化学株式会社 | 杂环化合物和含有该杂环化合物的有害节肢动物防除剂 |
| US11407756B2 (en) | 2017-12-25 | 2022-08-09 | Sumitomo Chemical Company, Limited | Heterocyclic compounds and noxious arthropod control agent containing same |
| WO2019138018A1 (en) | 2018-01-15 | 2019-07-18 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| MX2020013188A (es) | 2018-06-06 | 2021-02-26 | Syngenta Crop Protection Ag | Derivados heterociclicos activos como plaguicidas con sustituyentes que contienen sulfoximina. |
| WO2020116296A1 (ja) | 2018-12-07 | 2020-06-11 | ユニマテック株式会社 | 含フッ素ピリミジン化合物およびその製造方法 |
| BR112021012991A2 (pt) | 2018-12-31 | 2021-09-14 | Syngenta Crop Protection Ag | Derivados heterocíclicos pesticidamente ativos com substituintes contendo enxofre |
| 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 |
| WO2021009311A1 (en) | 2019-07-17 | 2021-01-21 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| PH12022550582A1 (en) * | 2019-09-12 | 2023-03-27 | Nihon Nohyaku Co Ltd | Agricultural and horticultural pesticide having as active component condensed heterocyclic compound having substituted cyclopropane oxadiazole group or salt thereof; ectoparasite or endoparasite control agent for animals; and use method thereof |
| BR112022010313A2 (pt) | 2019-11-27 | 2022-08-16 | Syngenta Crop Protection Ag | Processo para a preparação de ácidos 5-cloro-piridina-2-carboxílicos e carboxilatos com substituintes contendo 3-enxofre |
| AR121344A1 (es) * | 2020-02-18 | 2022-05-11 | Pi Industries Ltd | Compuestos heterocíclicos fusionados y su uso como agentes para el control de plagas |
| 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 |
| JP7471407B2 (ja) | 2020-05-19 | 2024-04-19 | ユニマテック株式会社 | 含フッ素ピリミジン化合物および含フッ素ピリミジノン化合物 |
| WO2023036934A1 (en) * | 2021-09-13 | 2023-03-16 | Boehringer Ingelheim Vetmedica Gmbh | Cyclopropyl-(hetero)aryl-substituted ethylsulphonylpyridine derivatives |
| CN116081837B (zh) * | 2021-10-31 | 2025-04-01 | 中国石油化工股份有限公司 | 利用均相催化湿式氧化处理乙烯碱渣废水的方法 |
| US12522580B2 (en) | 2021-11-12 | 2026-01-13 | Unimatec Co., Ltd. | Fluorine-containing pyrimidine compounds, harmful fungus control agent, and method for producing fluorine-containing pyrimidine compounds |
| WO2024175558A1 (en) | 2023-02-23 | 2024-08-29 | Boehringer Ingelheim Vetmedica Gmbh | Cyclopropyl-(hetero)aryl-substituted ethyl-sulfone/sulfoximine-pyridine n-oxide derivatives |
| UY40647A (es) | 2023-02-23 | 2024-08-15 | Boehringer Ingelheim Vetmedica Gmbh | Derivados de etilsulfona/sulfoximina-piridina sustituidos con tetrazol |
| WO2024189139A1 (en) | 2023-03-14 | 2024-09-19 | Syngenta Crop Protection Ag | Control of pests resistant to insecticides |
| WO2026138640A1 (zh) * | 2024-12-27 | 2026-07-02 | 青岛清原化合物有限公司 | 一种稠杂环化合物及其制备方法、杀虫组合物和应用 |
| EP4782441A1 (en) | 2025-01-28 | 2026-07-29 | Boehringer Ingelheim Vetmedica GmbH | Spirocycle-substituted ethylsulfone / sulfoximine-pyridine derivatives |
| EP4782446A1 (en) | 2025-01-28 | 2026-07-29 | Boehringer Ingelheim Vetmedica GmbH | Bridged carbocycle- and heterocycle substituted ethylsulfone / sulfoximine-pyridine derivatives |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW201234965A (en) * | 2010-12-24 | 2012-09-01 | Sumitomo Chemical Co | 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 |
| EP2857397B1 (en) * | 2012-05-30 | 2020-04-08 | Sumitomo Chemical Company Limited | Fused heterocyclic compound |
| WO2013180193A1 (ja) * | 2012-05-31 | 2013-12-05 | 住友化学株式会社 | 縮合複素環化合物 |
| WO2013191113A1 (ja) * | 2012-06-18 | 2013-12-27 | 住友化学株式会社 | 縮合複素環化合物 |
| 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 |
| JP6663907B2 (ja) * | 2014-07-08 | 2020-03-13 | シンジェンタ パーティシペーションズ アーゲー | 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 |
| BR112017003168B1 (pt) * | 2014-08-21 | 2021-03-02 | Syngenta Participations Ag | compostos derivados de heterocíclicos, composição pesticida, método para controle de pragas e método para a proteção de material de propagação de plantas do ataque por pragas |
| KR102551157B1 (ko) * | 2014-11-07 | 2023-07-03 | 신젠타 파티서페이션즈 아게 | 황 함유 치환기를 가지는 살충 활성 폴리사이클릭 유도체 |
-
2015
- 2015-08-18 CN CN201580045561.6A patent/CN106604922B/zh not_active Expired - Fee Related
- 2015-08-18 WO PCT/EP2015/068953 patent/WO2016030229A1/en not_active Ceased
- 2015-08-18 JP JP2017511237A patent/JP6695861B2/ja not_active Expired - Fee Related
- 2015-08-18 US US15/505,758 patent/US9809587B2/en not_active Expired - Fee Related
- 2015-08-18 EP EP15750763.3A patent/EP3186249B1/en not_active Not-in-force
- 2015-08-18 BR BR112017003366-6A patent/BR112017003366B1/pt not_active IP Right Cessation