JP2020503277A5 - - Google Patents
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- JP2020503277A5 JP2020503277A5 JP2019529623A JP2019529623A JP2020503277A5 JP 2020503277 A5 JP2020503277 A5 JP 2020503277A5 JP 2019529623 A JP2019529623 A JP 2019529623A JP 2019529623 A JP2019529623 A JP 2019529623A JP 2020503277 A5 JP2020503277 A5 JP 2020503277A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- haloalkyl
- salt
- alkyl
- 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.)
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- 150000001875 compounds Chemical class 0.000 claims description 85
- 150000003839 salts Chemical class 0.000 claims description 30
- 125000001188 haloalkyl group Chemical group 0.000 claims description 25
- 229910052736 halogen Inorganic materials 0.000 claims description 24
- 150000002367 halogens Chemical class 0.000 claims description 23
- 125000004122 cyclic group Chemical group 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 19
- 125000003545 alkoxy group Chemical group 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 125000004434 sulfur atom Chemical group 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- 241000607479 Yersinia pestis Species 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 6
- 230000001850 reproductive effect Effects 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 101100025412 Arabidopsis thaliana XI-A gene Proteins 0.000 claims description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 150000003863 ammonium salts Chemical class 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004770 (C1-C4) haloalkylsulfanyl group Chemical group 0.000 claims description 2
- 125000004771 (C1-C4) haloalkylsulfinyl 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 compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 230000002140 halogenating effect Effects 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 230000000361 pesticidal effect Effects 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- -1 stereoisomers Chemical class 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 description 26
- 125000000217 alkyl group Chemical group 0.000 description 15
- 125000004438 haloalkoxy group Chemical group 0.000 description 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 1
- 125000004966 cyanoalkyl group Chemical group 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 description 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN201611041146 | 2016-12-01 | ||
| IN201611041146 | 2016-12-01 | ||
| IN201711010969 | 2017-03-28 | ||
| IN201711010969 | 2017-03-28 | ||
| PCT/EP2017/080295 WO2018099812A1 (en) | 2016-12-01 | 2017-11-24 | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020503277A JP2020503277A (ja) | 2020-01-30 |
| JP2020503277A5 true JP2020503277A5 (cg-RX-API-DMAC7.html) | 2021-01-07 |
| JP7282031B2 JP7282031B2 (ja) | 2023-05-26 |
Family
ID=60812015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019529623A Active JP7282031B2 (ja) | 2016-12-01 | 2017-11-24 | 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 (8)
| Country | Link |
|---|---|
| US (1) | US10961248B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3548466B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP7282031B2 (cg-RX-API-DMAC7.html) |
| CN (2) | CN117624038A (cg-RX-API-DMAC7.html) |
| DK (1) | DK3548466T3 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2910790T3 (cg-RX-API-DMAC7.html) |
| HU (1) | HUE058180T2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2018099812A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| CN113348169A (zh) | 2018-12-31 | 2021-09-03 | 先正达农作物保护股份公司 | 具有含硫取代基的杀有害生物活性的杂环衍生物 |
| BR112022005137A2 (pt) | 2019-09-20 | 2022-06-14 | Syngenta Crop Protection Ag | Derivados heterocíclicos com substituintes contendo enxofre e sulfoximina ativos em termos pesticidas |
| CN111223532B (zh) * | 2019-11-14 | 2023-06-20 | 腾讯科技(深圳)有限公司 | 确定目标化合物的反应物的方法、设备、装置、介质 |
| AU2021403544A1 (en) * | 2020-12-14 | 2023-06-29 | Basf Se | Sulfoximine pesticides |
| WO2022208370A1 (en) | 2021-03-31 | 2022-10-06 | Pi Industries Ltd. | Fused heterocyclic compounds and their use as pest control agents |
| AU2024235487A1 (en) | 2023-03-14 | 2025-09-25 | Syngenta Crop Protection Ag | Control of pests resistant to insecticides |
| TW202517614A (zh) | 2023-07-12 | 2025-05-01 | 瑞士商先正達農作物保護股份公司 | 2-(三氟甲基)吡啶-4-胺的合成 |
| WO2025177310A1 (en) | 2024-02-23 | 2025-08-28 | Pi Industries Ltd. | Fused heterocyclic compounds and its uses thereof |
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| US9949483B2 (en) | 2014-08-07 | 2018-04-24 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| CN107074846B (zh) | 2014-08-12 | 2020-05-19 | 先正达参股股份有限公司 | 具有含硫取代基的杀有害生物活性杂环衍生物 |
| JP6695326B2 (ja) | 2014-08-21 | 2020-05-20 | 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 |
| WO2016046071A1 (en) | 2014-09-25 | 2016-03-31 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| BR112017007510A2 (pt) | 2014-10-16 | 2018-06-19 | Syngenta Participations Ag | derivados heterocíclicos tetracíclicos com substituintes contendo enxofre ativos em termos pesticidas |
| CN107074865B (zh) * | 2014-11-07 | 2020-06-30 | 先正达参股股份有限公司 | 具有含硫取代基的杀有害生物活性多环衍生物 |
| WO2016091731A1 (en) | 2014-12-11 | 2016-06-16 | Syngenta Participations Ag | Pesticidally active tetracyclic derivatives with sulfur containing substituents |
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| CN108290884A (zh) | 2015-11-16 | 2018-07-17 | 先正达参股股份有限公司 | 具有含硫取代基的杀有害生物活性杂环衍生物 |
| EP3411373A1 (en) | 2016-02-05 | 2018-12-12 | Syngenta Participations AG | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
-
2017
- 2017-11-24 CN CN202311578234.XA patent/CN117624038A/zh active Pending
- 2017-11-24 WO PCT/EP2017/080295 patent/WO2018099812A1/en not_active Ceased
- 2017-11-24 JP JP2019529623A patent/JP7282031B2/ja active Active
- 2017-11-24 ES ES17821477T patent/ES2910790T3/es active Active
- 2017-11-24 DK DK17821477.1T patent/DK3548466T3/da active
- 2017-11-24 EP EP17821477.1A patent/EP3548466B1/en active Active
- 2017-11-24 HU HUE17821477A patent/HUE058180T2/hu unknown
- 2017-11-24 US US16/465,014 patent/US10961248B2/en active Active
- 2017-11-24 CN CN201780074390.9A patent/CN110023287B/zh not_active Expired - Fee Related