JP2019510020A5 - - Google Patents
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- Publication number
- JP2019510020A5 JP2019510020A5 JP2018548442A JP2018548442A JP2019510020A5 JP 2019510020 A5 JP2019510020 A5 JP 2019510020A5 JP 2018548442 A JP2018548442 A JP 2018548442A JP 2018548442 A JP2018548442 A JP 2018548442A JP 2019510020 A5 JP2019510020 A5 JP 2019510020A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- radical
- alkylsulfonyl
- 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
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- -1 cycloheteroalkyl Chemical group 0.000 claims 128
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 108
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 73
- 150000003254 radicals Chemical class 0.000 claims 52
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 51
- 229910052736 halogen Inorganic materials 0.000 claims 47
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 39
- 150000002367 halogens Chemical class 0.000 claims 36
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 35
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 33
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 28
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 26
- 125000001424 substituent group Chemical group 0.000 claims 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 22
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 21
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 19
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 18
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 18
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 18
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 18
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 18
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 17
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 17
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 claims 16
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 16
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 16
- 125000005843 halogen group Chemical group 0.000 claims 16
- 125000001072 heteroaryl group Chemical group 0.000 claims 16
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 15
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 15
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 15
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims 14
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 14
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims 14
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims 14
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims 14
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000004076 pyridyl group Chemical group 0.000 claims 13
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical group C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims 12
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 12
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 12
- 125000003118 aryl group Chemical group 0.000 claims 12
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 11
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 10
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 9
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 9
- 125000005842 heteroatom Chemical group 0.000 claims 9
- 229910052760 oxygen Inorganic materials 0.000 claims 9
- 239000001301 oxygen Substances 0.000 claims 9
- 239000011593 sulfur Chemical group 0.000 claims 9
- 229910052717 sulfur Inorganic materials 0.000 claims 9
- 229930192474 thiophene Chemical group 0.000 claims 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 8
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 8
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical group C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims 8
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 8
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 claims 7
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 7
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims 6
- 125000005059 halophenyl group Chemical group 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 6
- 125000001624 naphthyl group Chemical group 0.000 claims 6
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 claims 5
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 5
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 5
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 5
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 5
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 5
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 5
- 150000003852 triazoles Chemical class 0.000 claims 5
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical group C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 claims 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 4
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 4
- 125000004404 heteroalkyl group Chemical group 0.000 claims 4
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 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
- 229920006395 saturated elastomer Polymers 0.000 claims 4
- 238000006467 substitution reaction Methods 0.000 claims 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 238000009472 formulation Methods 0.000 claims 3
- 125000004254 isoquinolin-1-yl group Chemical group [H]C1=C([H])C2=C([H])C([H])=C([H])C([H])=C2C(*)=N1 0.000 claims 3
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 150000002831 nitrogen free-radicals Chemical class 0.000 claims 3
- 125000004553 quinoxalin-5-yl group Chemical group N1=CC=NC2=C(C=CC=C12)* 0.000 claims 3
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 2
- 239000004606 Fillers/Extenders Substances 0.000 claims 2
- 239000003905 agrochemical Substances 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000004188 dichlorophenyl group Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 2
- 230000000361 pesticidal effect Effects 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims 1
- 150000002829 nitrogen Chemical class 0.000 claims 1
- 210000000056 organ Anatomy 0.000 claims 1
- 230000001850 reproductive effect Effects 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 238000011282 treatment Methods 0.000 claims 1
- FOAVHYBFDIDICF-UHFFFAOYSA-N CC1=CCCC#CC1c1nc(C(O)O)n[n]1C Chemical compound CC1=CCCC#CC1c1nc(C(O)O)n[n]1C FOAVHYBFDIDICF-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16160293 | 2016-03-15 | ||
| EP16160293.3 | 2016-03-15 | ||
| PCT/EP2017/055405 WO2017157735A1 (de) | 2016-03-15 | 2017-03-08 | Substituierte sulfonylamide zur bekämpfung tierischer schädlinge |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2019510020A JP2019510020A (ja) | 2019-04-11 |
| JP2019510020A5 true JP2019510020A5 (enExample) | 2020-04-16 |
Family
ID=55532175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018548442A Pending JP2019510020A (ja) | 2016-03-15 | 2017-03-08 | 害虫を防除するための置換スルホニルアミド類 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US20200288710A1 (enExample) |
| EP (1) | EP3429355B1 (enExample) |
| JP (1) | JP2019510020A (enExample) |
| KR (1) | KR20180125960A (enExample) |
| CN (1) | CN109152368A (enExample) |
| AR (1) | AR107877A1 (enExample) |
| AU (1) | AU2017233739A1 (enExample) |
| BR (1) | BR112018068638A2 (enExample) |
| CA (1) | CA3017547A1 (enExample) |
| CL (1) | CL2018002645A1 (enExample) |
| CO (1) | CO2018009677A2 (enExample) |
| ES (1) | ES2775782T3 (enExample) |
| IL (1) | IL261403A (enExample) |
| MX (1) | MX2018011214A (enExample) |
| PH (1) | PH12018501966A1 (enExample) |
| TW (1) | TW201808103A (enExample) |
| UY (1) | UY37153A (enExample) |
| WO (1) | WO2017157735A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201617064D0 (en) | 2016-10-07 | 2016-11-23 | Inhibox Limited And Latvian Institute Of Organic Synthesis The | Compounds and their therapeutic use |
| TW201822637A (zh) * | 2016-11-07 | 2018-07-01 | 德商拜耳廠股份有限公司 | 用於控制動物害蟲的經取代磺醯胺類 |
| CN109608415B (zh) * | 2019-01-21 | 2020-12-01 | 暨南大学 | 噻唑甲酰胺类化合物及其合成和应用 |
| KR20220098170A (ko) * | 2019-11-07 | 2022-07-11 | 바이엘 악티엔게젤샤프트 | 동물 해충 방제를 위한 치환된 술포닐 아미드 |
| US10894812B1 (en) | 2020-09-30 | 2021-01-19 | Alpine Roads, Inc. | Recombinant milk proteins |
| IL301396A (en) | 2020-09-30 | 2023-05-01 | Nobell Foods Inc | Recombinant milk proteins and food compositions comprising the same |
| US10947552B1 (en) | 2020-09-30 | 2021-03-16 | Alpine Roads, Inc. | Recombinant fusion proteins for producing milk proteins in plants |
| JP2025503242A (ja) | 2022-01-27 | 2025-01-30 | ピーアイ インダストリーズ リミテッド | １，２，３－トリアゾールカルボニルスルホニルアミド化合物及びその使用 |
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2017
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2018
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