JP2016527208A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016527208A5 JP2016527208A5 JP2016522423A JP2016522423A JP2016527208A5 JP 2016527208 A5 JP2016527208 A5 JP 2016527208A5 JP 2016522423 A JP2016522423 A JP 2016522423A JP 2016522423 A JP2016522423 A JP 2016522423A JP 2016527208 A5 JP2016527208 A5 JP 2016527208A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- groups
- group
- ring
- 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
- 125000001424 substituent group Chemical group 0.000 claims 50
- 125000005842 heteroatom Chemical group 0.000 claims 46
- 229910052739 hydrogen Inorganic materials 0.000 claims 45
- 239000001257 hydrogen Substances 0.000 claims 44
- 150000001875 compounds Chemical class 0.000 claims 36
- 150000002431 hydrogen Chemical class 0.000 claims 35
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 31
- 125000000623 heterocyclic group Chemical group 0.000 claims 29
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 28
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 27
- 229910052760 oxygen Inorganic materials 0.000 claims 27
- 229920006395 saturated elastomer Polymers 0.000 claims 27
- 229910052717 sulfur Inorganic materials 0.000 claims 27
- -1 C 1 -C 6 -Alkyl Chemical group 0.000 claims 26
- 229910052736 halogen Inorganic materials 0.000 claims 24
- 150000002367 halogens Chemical class 0.000 claims 24
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 21
- 125000004093 cyano group Chemical group *C#N 0.000 claims 20
- 125000000753 cycloalkyl group Chemical group 0.000 claims 20
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 19
- 241000607479 Yersinia pestis Species 0.000 claims 16
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 16
- 125000001931 aliphatic group Chemical group 0.000 claims 15
- 229910052757 nitrogen Inorganic materials 0.000 claims 14
- 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 13
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 11
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 11
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 10
- 150000003839 salts Chemical class 0.000 claims 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 9
- 125000002723 alicyclic group Chemical group 0.000 claims 9
- 125000004438 haloalkoxy group Chemical group 0.000 claims 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 9
- 239000000463 material Substances 0.000 claims 8
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 7
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 7
- 125000004432 carbon atom Chemical group C* 0.000 claims 7
- 230000009545 invasion Effects 0.000 claims 7
- 125000006414 CCl Chemical group ClC* 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 6
- KWEDUNSJJZVRKR-UHFFFAOYSA-N carbononitridic azide Chemical compound [N-]=[N+]=NC#N KWEDUNSJJZVRKR-UHFFFAOYSA-N 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 125000000304 alkynyl group Chemical group 0.000 claims 5
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 4
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 4
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 4
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 4
- 241001465754 Metazoa Species 0.000 claims 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 125000000232 haloalkynyl group Chemical group 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- 125000004043 oxo group Chemical group O=* 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
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 125000004122 cyclic group Chemical group 0.000 claims 3
- 125000001188 haloalkyl group Chemical group 0.000 claims 3
- 208000015181 infectious disease Diseases 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 2
- 125000006416 CBr Chemical group BrC* 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 125000006413 ring segment Chemical group 0.000 claims 2
- 239000002689 soil Substances 0.000 claims 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- GUUULVAMQJLDSY-UHFFFAOYSA-N 4,5-dihydro-1,2-thiazole Chemical class C1CC=NS1 GUUULVAMQJLDSY-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 claims 1
- 125000004266 aziridin-1-yl group Chemical group [H]C1([H])N(*)C1([H])[H] 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 238000009395 breeding Methods 0.000 claims 1
- 230000001488 breeding effect Effects 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003925 fat Substances 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 150000002466 imines Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000004571 thiomorpholin-4-yl group Chemical group N1(CCSCC1)* 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361838370P | 2013-06-24 | 2013-06-24 | |
| US61/838,370 | 2013-06-24 | ||
| US201361896137P | 2013-10-28 | 2013-10-28 | |
| US61/896,137 | 2013-10-28 | ||
| PCT/EP2014/063106 WO2014206911A1 (en) | 2013-06-24 | 2014-06-23 | Isothiazoline compounds for combating invertebrate pests |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016527208A JP2016527208A (ja) | 2016-09-08 |
| JP2016527208A5 true JP2016527208A5 (enExample) | 2017-07-27 |
Family
ID=50981521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016522423A Pending JP2016527208A (ja) | 2013-06-24 | 2014-06-23 | 無脊椎有害生物を駆除するためのイソチアゾリン化合物 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP3013819B1 (enExample) |
| JP (1) | JP2016527208A (enExample) |
| CN (1) | CN105473582A (enExample) |
| BR (1) | BR112015032346A2 (enExample) |
| CA (1) | CA2916766C (enExample) |
| ES (1) | ES2688893T3 (enExample) |
| MX (1) | MX368592B (enExample) |
| WO (1) | WO2014206911A1 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9744542B2 (en) | 2013-07-29 | 2017-08-29 | Apeel Technology, Inc. | Agricultural skin grafting |
| CA2973974A1 (en) | 2015-01-16 | 2016-07-21 | Avista Pharma Solutions, Inc. | Antiparasitic compounds |
| JP7157531B2 (ja) | 2015-05-20 | 2022-10-20 | アピール テクノロジー，インコーポレイテッド | 植物抽出物組成物およびその調製方法 |
| EP4793326A2 (en) | 2015-09-16 | 2026-08-19 | Apeel Technology, Inc. | Method for forming a protective coating by applying fatty acid glyceride compounds to a surface |
| EP3386303B1 (en) | 2015-12-10 | 2020-03-11 | Apeel Technology, Inc. | Process for depolymerising cutin |
| TWI731928B (zh) | 2016-01-26 | 2021-07-01 | 美商ａＰＥＥＬ科技公司 | 製備及保存經消毒產品之方法 |
| WO2018094269A1 (en) | 2016-11-17 | 2018-05-24 | Apeel Technology, Inc. | Compositions formed from plant extracts and methods of preparation thereof |
| WO2018166855A1 (en) | 2017-03-16 | 2018-09-20 | Basf Se | Heterobicyclic substituted dihydroisoxazoles |
| EP3710453A1 (en) | 2017-11-16 | 2020-09-23 | Avista Pharma Solutions, Inc. | Single enantiomer antiparasitic compounds |
| TWI812673B (zh) | 2018-02-12 | 2023-08-21 | 美商富曼西公司 | 用於防治無脊椎害蟲之萘異噁唑啉化合物 |
| US12245605B2 (en) | 2018-09-05 | 2025-03-11 | Apeel Technology, Inc. | Compounds and formulations for protective coatings |
| EP4114181A1 (en) | 2020-03-04 | 2023-01-11 | Apeel Technology, Inc. | Coated agricultural products and corresponding methods |
| IL302360B2 (en) | 2020-10-30 | 2025-01-01 | Apeel Tech Inc | Preparations and methods of their preparation |
| US12408680B2 (en) | 2021-09-08 | 2025-09-09 | Apeel Technology, Inc. | Compounds and formulations for protective coatings |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0508140B1 (pt) * | 2004-03-05 | 2015-03-17 | Nissan Chemical Ind Ltd | Composto benzamida substituída por isoxazolina da fórmula (1); da fórmula (2) substituído por 3,5-bis (aril substituído); da fórmula (4) substituída por alquinibenzeno ou um sal do mesmo; "pesticida, agroquímico, inseticida, parasiticida contendo como ingrediente ativo um ou mais composto benzamida substituída por isoxazolina e sal do mesmo" |
| KR20120125332A (ko) * | 2010-02-01 | 2012-11-14 | 바스프 에스이 | 동물 해충을 퇴치하기 위한 치환된 케톤계 이속사졸린 화합물 및 유도체 |
| US9078444B2 (en) * | 2011-09-13 | 2015-07-14 | Syngenta Participations Ag | Isothiazoline derivatives as insecticidal compounds |
| US9732051B2 (en) * | 2011-12-23 | 2017-08-15 | Basf Se | Isothiazoline compounds for combating invertebrate pests |
-
2014
- 2014-06-23 WO PCT/EP2014/063106 patent/WO2014206911A1/en not_active Ceased
- 2014-06-23 CN CN201480043338.3A patent/CN105473582A/zh active Pending
- 2014-06-23 MX MX2015018015A patent/MX368592B/es active IP Right Grant
- 2014-06-23 ES ES14732176.4T patent/ES2688893T3/es active Active
- 2014-06-23 BR BR112015032346A patent/BR112015032346A2/pt not_active Application Discontinuation
- 2014-06-23 JP JP2016522423A patent/JP2016527208A/ja active Pending
- 2014-06-23 CA CA2916766A patent/CA2916766C/en active Active
- 2014-06-23 EP EP14732176.4A patent/EP3013819B1/en not_active Not-in-force
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2022528181A5 (enExample) | ||
| JP2017523997A5 (enExample) | ||
| JP2022525966A5 (enExample) | ||
| JP2022504273A5 (enExample) | ||
| RU2017125267A (ru) | Пестицидно активные гетероциклические производные с серосодержащими заместителями | |
| JP2016530226A5 (enExample) | ||
| RU2016142309A (ru) | Пестицидно активные гетероциклические производные с серосодержащими заместителями | |
| RU2016152470A (ru) | Применение замещенных оксадиазолов для борьбы с фитопатогенными грибами | |
| JP2018502912A5 (enExample) | ||
| JP2009526798A5 (enExample) | ||
| RU2018138748A (ru) | Замещенные оксадиазолы для борьбы с фитопатогенными грибами | |
| JP2017537882A5 (enExample) | ||
| JP2018509418A5 (enExample) | ||
| RU2016103149A (ru) | Пестицидно-активные би-или трициклические гетероциклы с серосодержащими заместителями | |
| RU2019139232A (ru) | Бициклические пестицидные соединения | |
| EA201400212A1 (ru) | N-тиоантраниламидные соединения и их применение в качестве пестицидов | |
| RU2016138118A (ru) | Азолины | |
| JP2022523434A5 (enExample) | ||
| RU2010107171A (ru) | Фунгицидные n-циклоалкилбензилтиокарбоксамиды или n-циклоалкилбензил-n, -замещенные амидиновые производные | |
| JP2018501226A5 (enExample) | ||
| JP2024532329A5 (enExample) | ||
| JP2016528201A5 (enExample) | ||
| IN2014CN01025A (enExample) | ||
| RU2013139313A (ru) | 6-амино-2-замещенные-5- винилсилилпиримидин-4-карбоновые кислоты и сложные эфиры и 4-амино-6-замещенные-3-винилсилилпиридин-пиколиновые кислоты и сложные эфиры как гербициды | |
| JP2017511378A5 (enExample) |