JP2017537916A5 - - Google Patents
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- JP2017537916A5 JP2017537916A5 JP2017529090A JP2017529090A JP2017537916A5 JP 2017537916 A5 JP2017537916 A5 JP 2017537916A5 JP 2017529090 A JP2017529090 A JP 2017529090A JP 2017529090 A JP2017529090 A JP 2017529090A JP 2017537916 A5 JP2017537916 A5 JP 2017537916A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- group
- radical
- optionally substituted
- alkoxy
- 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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- 150000003254 radicals Chemical class 0.000 claims 136
- 125000000217 alkyl group Chemical group 0.000 claims 129
- -1 al Kill Chemical group 0.000 claims 90
- 125000003545 alkoxy group Chemical group 0.000 claims 66
- 229910052736 halogen Inorganic materials 0.000 claims 61
- 150000002367 halogens Chemical class 0.000 claims 61
- 229910052739 hydrogen Inorganic materials 0.000 claims 61
- 239000001257 hydrogen Substances 0.000 claims 61
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 60
- 125000000753 cycloalkyl group Chemical group 0.000 claims 59
- 125000001188 haloalkyl group Chemical group 0.000 claims 48
- 229910052760 oxygen Inorganic materials 0.000 claims 44
- 125000000304 alkynyl group Chemical group 0.000 claims 43
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 42
- 239000001301 oxygen Substances 0.000 claims 42
- 229910052757 nitrogen Inorganic materials 0.000 claims 40
- 229910052717 sulfur Chemical group 0.000 claims 39
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 37
- 239000011593 sulfur Chemical group 0.000 claims 37
- 125000003342 alkenyl group Chemical group 0.000 claims 36
- 150000002431 hydrogen Chemical class 0.000 claims 36
- 125000004438 haloalkoxy group Chemical group 0.000 claims 32
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 31
- 125000004093 cyano group Chemical group *C#N 0.000 claims 29
- 125000005842 heteroatom Chemical group 0.000 claims 28
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 27
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 25
- 125000002619 bicyclic group Chemical group 0.000 claims 25
- 229910052799 carbon Inorganic materials 0.000 claims 25
- 125000004432 carbon atom Chemical group C* 0.000 claims 25
- 125000004414 alkyl thio group Chemical group 0.000 claims 23
- 125000001072 heteroaryl group Chemical group 0.000 claims 22
- 125000004430 oxygen atom Chemical group O* 0.000 claims 21
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 20
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 19
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 17
- 125000003118 aryl group Chemical group 0.000 claims 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 17
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 16
- 229920006395 saturated elastomer Polymers 0.000 claims 16
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 claims 15
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 15
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 14
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims 14
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 14
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 12
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 11
- 125000003282 alkyl amino group Chemical group 0.000 claims 10
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims 10
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 10
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 10
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 9
- 125000003302 alkenyloxy group Chemical group 0.000 claims 8
- 125000003277 amino group Chemical group 0.000 claims 8
- 125000004663 dialkyl amino group Chemical group 0.000 claims 8
- 125000004995 haloalkylthio group Chemical group 0.000 claims 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 8
- 125000003107 substituted aryl group Chemical group 0.000 claims 8
- 125000005133 alkynyloxy group Chemical group 0.000 claims 7
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 claims 7
- 125000005108 alkenylthio group Chemical group 0.000 claims 6
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 6
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 6
- 125000005553 heteroaryloxy group Chemical group 0.000 claims 6
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 125000005880 oxathiolanyl group Chemical group 0.000 claims 6
- 125000003884 phenylalkyl group Chemical group 0.000 claims 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims 6
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 5
- 125000005843 halogen group Chemical group 0.000 claims 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 4
- 125000004946 alkenylalkyl group Chemical group 0.000 claims 4
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims 4
- 125000005055 alkyl alkoxy group Chemical group 0.000 claims 4
- 125000004465 cycloalkenyloxy group Chemical group 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims 4
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims 4
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims 4
- 125000005367 heteroarylalkylthio group Chemical group 0.000 claims 4
- 125000005368 heteroarylthio group Chemical group 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000002757 morpholinyl group Chemical group 0.000 claims 4
- DNNMCYZOLVTTCF-UHFFFAOYSA-N 3-(oxathiepan-3-yloxy)oxathiepane Chemical compound C1CCC(OC2CCCCOS2)SOC1 DNNMCYZOLVTTCF-UHFFFAOYSA-N 0.000 claims 3
- IIKUBFGKDMSATI-UHFFFAOYSA-N 3-(oxathiolan-3-yloxy)oxathiolane Chemical compound S1OCCC1OC1SOCC1 IIKUBFGKDMSATI-UHFFFAOYSA-N 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 3
- 241001024304 Mino Species 0.000 claims 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 3
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims 3
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 3
- 125000005050 dihydrooxazolyl group Chemical group O1C(NC=C1)* 0.000 claims 3
- 125000000532 dioxanyl group Chemical group 0.000 claims 3
- 125000005879 dioxolanyl group Chemical group 0.000 claims 3
- 125000005883 dithianyl group Chemical group 0.000 claims 3
- 125000005411 dithiolanyl group Chemical group S1SC(CC1)* 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- 239000011737 fluorine Substances 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 125000004992 haloalkylamino group Chemical group 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 3
- 125000005968 oxazolinyl group Chemical group 0.000 claims 3
- 125000002971 oxazolyl group Chemical group 0.000 claims 3
- 229910052700 potassium Inorganic materials 0.000 claims 3
- 239000011591 potassium Substances 0.000 claims 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 125000004963 sulfonylalkyl group Chemical group 0.000 claims 3
- 125000005247 tetrazinyl group Chemical group N1=NN=NC(=C1)* 0.000 claims 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- 125000004306 triazinyl group Chemical group 0.000 claims 3
- 125000001425 triazolyl group Chemical group 0.000 claims 3
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 claims 2
- SWQJWGBHPSUNSM-UHFFFAOYSA-N 3-(oxathiocan-3-yloxy)oxathiocane Chemical compound C1CCCCOSC1OC1SOCCCCC1 SWQJWGBHPSUNSM-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 2
- DAGYVIDJCUSBGI-UHFFFAOYSA-N C1CCOSC1OC1SOCCC1 Chemical compound C1CCOSC1OC1SOCCC1 DAGYVIDJCUSBGI-UHFFFAOYSA-N 0.000 claims 2
- 241000162682 Heterogen Species 0.000 claims 2
- 241001553014 Myrsine salicina Species 0.000 claims 2
- 229910001413 alkali metal ion Inorganic materials 0.000 claims 2
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims 2
- 125000006323 alkenyl amino group Chemical group 0.000 claims 2
- 125000005193 alkenylcarbonyloxy group Chemical group 0.000 claims 2
- 125000004702 alkoxy alkyl carbonyl group Chemical group 0.000 claims 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims 2
- 125000004666 alkoxyiminoalkyl group Chemical group 0.000 claims 2
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 claims 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 2
- 125000004686 alkyl sulfanyl alkyl group Chemical group 0.000 claims 2
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 2
- 125000006319 alkynyl amino group Chemical group 0.000 claims 2
- 125000005088 alkynylcarbonylamino group Chemical group 0.000 claims 2
- 125000005109 alkynylthio group Chemical group 0.000 claims 2
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 150000001768 cations Chemical group 0.000 claims 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 2
- 125000005169 cycloalkylcarbonylamino group Chemical group 0.000 claims 2
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims 2
- 125000005366 cycloalkylthio group Chemical group 0.000 claims 2
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 claims 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000006776 haloalkenylcarbonyl group Chemical group 0.000 claims 2
- 125000000232 haloalkynyl group Chemical group 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000004354 sulfur functional group Chemical group 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 241000790917 Dioxys <bee> Species 0.000 claims 1
- 241000607479 Yersinia pestis Species 0.000 claims 1
- YKOWBJJOJNGCAD-SHYZEUOFSA-N [(2r,3s,5r)-3-hydroxy-5-[4-(hydroxyamino)-2-oxopyrimidin-1-yl]oxolan-2-yl]methyl dihydrogen phosphate Chemical compound O=C1N=C(NO)C=CN1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)C1 YKOWBJJOJNGCAD-SHYZEUOFSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 125000005002 aryl methyl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical group C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 claims 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- 0 Cc1c(*)[o]cc1 Chemical compound Cc1c(*)[o]cc1 0.000 description 17
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14195941 | 2014-12-02 | ||
| EP14195941.1 | 2014-12-02 | ||
| PCT/EP2015/078059 WO2016087371A1 (de) | 2014-12-02 | 2015-11-30 | Bicyclische verbindungen als schädlingsbekämpfungsmittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017537916A JP2017537916A (ja) | 2017-12-21 |
| JP2017537916A5 true JP2017537916A5 (enExample) | 2019-01-17 |
Family
ID=52002807
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017529090A Pending JP2017537916A (ja) | 2014-12-02 | 2015-11-30 | 有害生物防除剤としての二環式化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20170325459A1 (enExample) |
| EP (1) | EP3227283A1 (enExample) |
| JP (1) | JP2017537916A (enExample) |
| CN (1) | CN107207490A (enExample) |
| BR (1) | BR112017011661A2 (enExample) |
| WO (1) | WO2016087371A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI652014B (zh) | 2013-09-13 | 2019-03-01 | 美商艾佛艾姆希公司 | 雜環取代之雙環唑殺蟲劑 |
| KR102536024B1 (ko) | 2015-03-12 | 2023-05-24 | 에프엠씨 코포레이션 | 헤테로환-치환 이환 아졸 살충제 |
| JP6857614B2 (ja) | 2015-04-09 | 2021-04-14 | エフ エム シー コーポレーションＦｍｃ Ｃｏｒｐｏｒａｔｉｏｎ | 二環式ピラゾール殺有害生物剤 |
| CN109963860A (zh) * | 2016-09-19 | 2019-07-02 | 拜耳作物科学股份公司 | 吡唑并[1,5-a]吡啶衍生物及其作为农药的用途 |
| US20220324899A1 (en) * | 2019-08-14 | 2022-10-13 | Metro International Biotech, Llc | Compounds and compositions for differential modulation of nicotinamide adenine dinucleotide |
| GB202102088D0 (en) * | 2021-02-15 | 2021-03-31 | Mironid Ltd | Compounds and their use as pde4 activators |
| UY41082A (es) | 2024-03-28 | 2025-08-29 | Pi Industries Ltd | Compuestos bicíclicos condensados y su uso como agentes de control de plagas |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1019748A (en) * | 1972-06-02 | 1977-10-25 | Venkatachala L. Narayanan | Isothiocyanobenzoxazoles |
| US3985755A (en) * | 1972-06-02 | 1976-10-12 | E. R. Squibb & Sons, Inc. | Pyridine containing isothiocyanobenzoxazoles |
| US3985885A (en) * | 1975-09-19 | 1976-10-12 | E. R. Squibb & Sons, Inc. | Isothiocyanobenzothiazoles |
| PE20010830A1 (es) * | 2000-01-28 | 2001-09-06 | Syngenta Ltd | Derivados de azol insecticidas o fungicidas y composiciones que los comprenden |
| TW201018678A (en) * | 2006-01-27 | 2010-05-16 | Astrazeneca Ab | Novel heteroaryl substituted benzothiazoles |
| JP5369854B2 (ja) * | 2008-04-21 | 2013-12-18 | 住友化学株式会社 | 有害節足動物防除組成物および縮合複素環化合物 |
| WO2013106254A1 (en) * | 2012-01-11 | 2013-07-18 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| WO2014028931A2 (en) * | 2012-08-17 | 2014-02-20 | Brandeis University | Compounds and methods for treating mammalian gastrointestinal microbial infections |
| TWI652014B (zh) * | 2013-09-13 | 2019-03-01 | 美商艾佛艾姆希公司 | 雜環取代之雙環唑殺蟲劑 |
-
2015
- 2015-11-30 CN CN201580075180.2A patent/CN107207490A/zh active Pending
- 2015-11-30 BR BR112017011661-8A patent/BR112017011661A2/pt not_active Application Discontinuation
- 2015-11-30 EP EP15801853.1A patent/EP3227283A1/de not_active Withdrawn
- 2015-11-30 JP JP2017529090A patent/JP2017537916A/ja active Pending
- 2015-11-30 US US15/529,801 patent/US20170325459A1/en not_active Abandoned
- 2015-11-30 WO PCT/EP2015/078059 patent/WO2016087371A1/de not_active Ceased
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