JPWO2021153720A5 - - Google Patents
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- Publication number
- JPWO2021153720A5 JPWO2021153720A5 JP2021574142A JP2021574142A JPWO2021153720A5 JP WO2021153720 A5 JPWO2021153720 A5 JP WO2021153720A5 JP 2021574142 A JP2021574142 A JP 2021574142A JP 2021574142 A JP2021574142 A JP 2021574142A JP WO2021153720 A5 JPWO2021153720 A5 JP WO2021153720A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- polysubstituted
- substituted
- mono
- 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
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 84
- 125000003277 amino group Chemical group 0.000 claims 67
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 53
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 49
- -1 thiocarbamoyl group Chemical group 0.000 claims 26
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 24
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 23
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 23
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 22
- 125000004093 cyano group Chemical group *C#N 0.000 claims 19
- 125000005843 halogen group Chemical group 0.000 claims 16
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 15
- 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 15
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 14
- 241000607479 Yersinia pestis Species 0.000 claims 12
- 125000001072 heteroaryl group Chemical group 0.000 claims 12
- 229910052757 nitrogen Inorganic materials 0.000 claims 12
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 12
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 11
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 10
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 10
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 10
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 8
- 150000003839 salts Chemical class 0.000 claims 8
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 7
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 7
- 239000003795 chemical substances by application Substances 0.000 claims 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 7
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims 6
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 6
- 150000001408 amides Chemical class 0.000 claims 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 5
- 241000196324 Embryophyta Species 0.000 claims 5
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 4
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims 4
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims 4
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims 4
- 239000004480 active ingredient Substances 0.000 claims 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 125000004434 sulfur atom Chemical group 0.000 claims 4
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000001188 haloalkyl group Chemical group 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 2
- 125000006798 (C1-C6) haloalkylamino group Chemical group 0.000 claims 2
- 125000006772 (C1-C6) haloalkylsulfonyloxy group Chemical group 0.000 claims 2
- 150000001204 N-oxides Chemical class 0.000 claims 2
- 230000000895 acaricidal effect Effects 0.000 claims 2
- 239000000642 acaricide Substances 0.000 claims 2
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims 2
- 239000003905 agrochemical Substances 0.000 claims 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims 2
- 125000000676 alkoxyimino group Chemical group 0.000 claims 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 2
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 2
- 125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 claims 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 2
- 125000002393 azetidinyl group Chemical group 0.000 claims 2
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims 2
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims 2
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 239000002917 insecticide Substances 0.000 claims 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims 2
- 230000001069 nematicidal effect Effects 0.000 claims 2
- 239000005645 nematicide Substances 0.000 claims 2
- 239000002420 orchard Substances 0.000 claims 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 125000004043 oxo group Chemical group O=* 0.000 claims 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 2
- 125000003386 piperidinyl group Chemical group 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000005554 pyridyloxy group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 2
- 125000001425 triazolyl group Chemical group 0.000 claims 2
- SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical class NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000012872 agrochemical composition Substances 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 238000009395 breeding Methods 0.000 claims 1
- 230000001488 breeding effect Effects 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 238000005215 recombination Methods 0.000 claims 1
- 230000006798 recombination Effects 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2020014653 | 2020-01-31 | ||
| JP2020014653 | 2020-01-31 | ||
| PCT/JP2021/003204 WO2021153720A1 (ja) | 2020-01-31 | 2021-01-29 | ３－アルコキシ安息香酸アミド誘導体及び有害生物防除剤 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2021153720A1 JPWO2021153720A1 (https=) | 2021-08-05 |
| JPWO2021153720A5 true JPWO2021153720A5 (https=) | 2022-12-09 |
| JP7308989B2 JP7308989B2 (ja) | 2023-07-14 |
Family
ID=77079131
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021574142A Active JP7308989B2 (ja) | 2020-01-31 | 2021-01-29 | ３－アルコキシ安息香酸アミド誘導体及び有害生物防除剤 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20230110603A1 (https=) |
| EP (1) | EP4098650B1 (https=) |
| JP (1) | JP7308989B2 (https=) |
| KR (2) | KR102638962B1 (https=) |
| CN (1) | CN115052856B (https=) |
| AU (1) | AU2021214350C1 (https=) |
| BR (1) | BR112022015176B1 (https=) |
| ES (1) | ES3063746T3 (https=) |
| IL (1) | IL295328B2 (https=) |
| MX (1) | MX2022009417A (https=) |
| TW (1) | TWI837454B (https=) |
| WO (1) | WO2021153720A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR129265A1 (es) | 2022-05-12 | 2024-08-07 | Syngenta Crop Protection Ag | Compuestos de alcoxi-heteroaril-carboxamida o tioamida |
| CN114989032B (zh) * | 2022-06-14 | 2024-04-12 | 安徽大学 | 一种酰亚胺类衍生物的合成方法 |
| WO2024033374A1 (en) | 2022-08-11 | 2024-02-15 | Syngenta Crop Protection Ag | Novel arylcarboxamide or arylthioamide compounds |
| CN115791716B (zh) * | 2022-09-19 | 2023-07-21 | 河北科技大学 | 一种蛋白核小球藻荧光检测扑灭通生物毒性的方法 |
| WO2024089216A1 (en) | 2022-10-27 | 2024-05-02 | Syngenta Crop Protection Ag | Novel sulfur-containing heteroaryl carboxamide compounds |
| JP2026500298A (ja) | 2022-12-15 | 2026-01-06 | 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 | 殺有害生物剤として有用である新規な二環式カルボキサミド化合物 |
| AR131541A1 (es) | 2023-01-07 | 2025-04-09 | Syngenta Crop Protection Ag | Compuestos de carboxamida novedosos |
| WO2025032129A1 (en) * | 2023-08-08 | 2025-02-13 | Syngenta Crop Protection Ag | Novel aminoindane and aminotetraline compounds |
| WO2025104032A1 (en) * | 2023-11-14 | 2025-05-22 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2025109114A1 (en) * | 2023-11-24 | 2025-05-30 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| PY2501648A (es) | 2024-01-12 | 2025-10-31 | Syngenta Crop Protection Ag | Nuevos compuestos de carboxamida |
| WO2025149637A1 (en) | 2024-01-12 | 2025-07-17 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2026008750A1 (en) | 2024-07-05 | 2026-01-08 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3996280A (en) * | 1973-04-09 | 1976-12-07 | Riker Laboratories, Inc. | Polyfluoroalkoxy-substituted aromatic carboxylic amides and hydrozides |
| GB1494117A (en) * | 1974-11-02 | 1977-12-07 | Bayer Ag | Process for the preparation of acid amides |
| JPS5826747B2 (ja) * | 1975-05-10 | 1983-06-04 | カブシキガイシヤ パ−マケム アジア | ２ ２’− ジチオビスベンツアミドカゴウブツノセイホウ |
| WO1994005153A1 (en) | 1992-09-09 | 1994-03-17 | E.I. Du Pont De Nemours And Company | Herbicidal benzene compounds |
| JPH0848662A (ja) * | 1994-08-05 | 1996-02-20 | Fujirebio Inc | ２−オキシベンズアミド誘導体 |
| SE9904505D0 (sv) | 1999-12-09 | 1999-12-09 | Astra Pharma Prod | Novel compounds |
| WO2002092584A1 (en) | 2001-05-14 | 2002-11-21 | Nihon Nohyaku Co., Ltd. | Thiadiazole derivatives, pesticides for agricultural and horticultural use and usage thereof |
| DE10320782A1 (de) * | 2003-05-09 | 2004-11-25 | Bayer Cropscience Ag | Substituierte Oxyarene |
| EP1730103B1 (en) * | 2004-03-23 | 2010-05-26 | Pfizer Limited | Formamide derivatives useful as adrenoceptor |
| DE102004062542A1 (de) * | 2004-12-24 | 2006-07-06 | Bayer Cropscience Ag | Substituierte Oxyarene |
| US7381487B2 (en) | 2004-12-27 | 2008-06-03 | Fuelcell Energy, Inc. | In-situ removal of electrolyte from gas oxidizer |
| DK2903440T3 (en) * | 2012-10-02 | 2017-12-11 | Bayer Cropscience Ag | THETEROCYCLIC COMPOUNDS AS PESTICIDES |
| RU2684396C2 (ru) | 2014-10-29 | 2019-04-09 | Донг-А Ст Ко., Лтд. | Новые соединения пиридопиримидинона для модулирования каталитической активности гистонлизиндеметилаз (KDMS) |
| WO2019099703A1 (en) * | 2017-11-16 | 2019-05-23 | Sidecar Therapeutics, Inc. | Apoptosis signal-regulating kinase 1 (ask 1) inhibitor compounds |
-
2021
- 2021-01-29 TW TW110103526A patent/TWI837454B/zh active
- 2021-01-29 US US17/796,592 patent/US20230110603A1/en active Pending
- 2021-01-29 MX MX2022009417A patent/MX2022009417A/es unknown
- 2021-01-29 AU AU2021214350A patent/AU2021214350C1/en active Active
- 2021-01-29 WO PCT/JP2021/003204 patent/WO2021153720A1/ja not_active Ceased
- 2021-01-29 EP EP21748308.0A patent/EP4098650B1/en active Active
- 2021-01-29 JP JP2021574142A patent/JP7308989B2/ja active Active
- 2021-01-29 CN CN202180012114.6A patent/CN115052856B/zh active Active
- 2021-01-29 KR KR1020227026158A patent/KR102638962B1/ko active Active
- 2021-01-29 ES ES21748308T patent/ES3063746T3/es active Active
- 2021-01-29 KR KR1020247005391A patent/KR20240028543A/ko active Pending
- 2021-01-29 BR BR112022015176-4A patent/BR112022015176B1/pt active IP Right Grant
- 2021-01-29 IL IL295328A patent/IL295328B2/en unknown
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