JP2010531318A5 - - Google Patents
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- Publication number
- JP2010531318A5 JP2010531318A5 JP2010513755A JP2010513755A JP2010531318A5 JP 2010531318 A5 JP2010531318 A5 JP 2010531318A5 JP 2010513755 A JP2010513755 A JP 2010513755A JP 2010513755 A JP2010513755 A JP 2010513755A JP 2010531318 A5 JP2010531318 A5 JP 2010531318A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- haloalkyl
- alkoxy
- halogen
- 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
Links
- 125000000217 alkyl group Chemical group 0.000 claims 175
- 125000003545 alkoxy group Chemical group 0.000 claims 55
- 125000001188 haloalkyl group Chemical group 0.000 claims 53
- 229910052736 halogen Chemical group 0.000 claims 53
- 150000002367 halogens Chemical group 0.000 claims 53
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 48
- 125000004093 cyano group Chemical group *C#N 0.000 claims 46
- 125000004438 haloalkoxy group Chemical group 0.000 claims 46
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 36
- 125000001072 heteroaryl group Chemical group 0.000 claims 34
- -1 C2Cyclopropyl Chemical group 0.000 claims 27
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 23
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 23
- 125000004414 alkyl thio group Chemical group 0.000 claims 23
- 125000000753 cycloalkyl group Chemical group 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 14
- 125000003282 alkyl amino group Chemical group 0.000 claims 13
- 239000001257 hydrogen Substances 0.000 claims 13
- 229910052717 sulfur Inorganic materials 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 11
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 9
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 9
- 125000004663 dialkyl amino group Chemical group 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000000304 alkynyl group Chemical group 0.000 claims 8
- 125000005240 diheteroarylamino group Chemical group 0.000 claims 8
- 125000000262 haloalkenyl group Chemical group 0.000 claims 8
- 125000005241 heteroarylamino group Chemical group 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 8
- 239000001301 oxygen Substances 0.000 claims 7
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 6
- 125000003302 alkenyloxy group Chemical group 0.000 claims 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 6
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 6
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 6
- 125000005133 alkynyloxy group Chemical group 0.000 claims 6
- 125000004103 aminoalkyl group Chemical group 0.000 claims 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 6
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 6
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 6
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 6
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 6
- 125000004971 nitroalkyl group Chemical group 0.000 claims 6
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 6
- 229920006395 saturated elastomer Polymers 0.000 claims 6
- 125000004434 sulfur atom Chemical group 0.000 claims 6
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 230000002363 herbicidal effect Effects 0.000 claims 3
- 239000004009 herbicide Substances 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 239000011593 sulfur Substances 0.000 claims 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 2
- 150000001340 alkali metals Chemical class 0.000 claims 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000003566 oxetanyl group Chemical group 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 1
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- 244000025254 Cannabis sativa Species 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000005400 pyridylcarbonyl group Chemical group N1=C(C=CC=C1)C(=O)* 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000004306 triazinyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0712653.5 | 2007-06-28 | ||
| GBGB0712653.5A GB0712653D0 (en) | 2007-06-28 | 2007-06-28 | Novel herbicides |
| PCT/EP2008/005197 WO2009000533A1 (en) | 2007-06-28 | 2008-06-26 | Novel herbicides |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013198942A Division JP2014040439A (ja) | 2007-06-28 | 2013-09-25 | 新規除草剤 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010531318A JP2010531318A (ja) | 2010-09-24 |
| JP2010531318A5 true JP2010531318A5 (enExample) | 2011-08-11 |
| JP5426542B2 JP5426542B2 (ja) | 2014-02-26 |
Family
ID=38420951
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010513755A Expired - Fee Related JP5426542B2 (ja) | 2007-06-28 | 2008-06-26 | 新規除草剤 |
| JP2013198942A Pending JP2014040439A (ja) | 2007-06-28 | 2013-09-25 | 新規除草剤 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013198942A Pending JP2014040439A (ja) | 2007-06-28 | 2013-09-25 | 新規除草剤 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US8956999B2 (enExample) |
| EP (2) | EP2527333A1 (enExample) |
| JP (2) | JP5426542B2 (enExample) |
| KR (1) | KR20100046161A (enExample) |
| CN (1) | CN101778834B (enExample) |
| AP (1) | AP2009005084A0 (enExample) |
| AR (1) | AR067144A1 (enExample) |
| AU (1) | AU2008267371B2 (enExample) |
| CA (1) | CA2690176A1 (enExample) |
| CL (1) | CL2008001901A1 (enExample) |
| CO (1) | CO6241077A2 (enExample) |
| EA (1) | EA020695B1 (enExample) |
| EC (1) | ECSP099827A (enExample) |
| ES (1) | ES2444706T3 (enExample) |
| GB (1) | GB0712653D0 (enExample) |
| HN (1) | HN2009003466A (enExample) |
| MA (1) | MA31526B1 (enExample) |
| MX (1) | MX2009013500A (enExample) |
| PL (1) | PL2173727T3 (enExample) |
| TN (1) | TN2009000536A1 (enExample) |
| TW (1) | TW200918510A (enExample) |
| WO (1) | WO2009000533A1 (enExample) |
| ZA (1) | ZA200908821B (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0714981D0 (en) | 2007-08-01 | 2007-09-12 | Syngenta Ltd | Novel herbicides |
| GB0900641D0 (en) | 2009-01-15 | 2009-02-25 | Syngenta Ltd | Novel herbicides |
| GB0901086D0 (en) | 2009-01-22 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| GB0901834D0 (en) | 2009-02-04 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| GB0901835D0 (en) | 2009-02-04 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| JP5795581B2 (ja) | 2009-07-31 | 2015-10-14 | シンジェンタ リミテッド | 除草活性を有するヘテロアリール置換環状ジオンまたはその誘導体 |
| CA2855948C (en) * | 2011-08-11 | 2020-07-28 | Bayer Cropscience Ag | 1,2,4-triazolyl-substituted keto-enols |
| CN111217767B (zh) * | 2020-01-19 | 2021-10-12 | 广东药科大学 | 一种通过Cu(I)催化的多组分环化反应制备官能化噻唑杂环化合物的方法及应用 |
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| PT67818A (en) | 1977-03-28 | 1978-04-01 | Union Carbide Corp | Process for the synthesis of biocidal 2-aryl-1,3-cycloalkanedionas and their enol esters |
| US4422870A (en) | 1977-03-28 | 1983-12-27 | Union Carbide Corporation | Biocidal 2-aryl-1, 3-cyclohexanedione enol ester compounds |
| US4175135A (en) | 1978-07-18 | 1979-11-20 | Union Carbide Corporation | Method of controlling acarina ectoparasites on warmblooded animals by orally administering to the animal an ectoparasitically effective amount of a 2-aryl-1,3-cyclohexanedione compound, and alkali metal salts, ammonium salts and enol esters thereof |
| US4436666A (en) | 1978-09-22 | 1984-03-13 | Union Carbide Corporation | Biocidal enol derivatives of 2-aryl-1,3-cycloalkanedione compounds |
| US4526723A (en) | 1978-09-27 | 1985-07-02 | Union Carbide Corporation | Biocidal enol esters of non-ortho substituted 2-aryl-1-3-cycloalkanedione compounds |
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| DE10331675A1 (de) | 2003-07-14 | 2005-02-10 | Bayer Cropscience Ag | Hetarylsubstituierte Pyrazolidindion-Derivate |
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| GB0704652D0 (en) | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0704653D0 (en) | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0710223D0 (en) | 2007-05-29 | 2007-07-11 | Syngenta Ltd | Novel Herbicides |
| GB0714981D0 (en) | 2007-08-01 | 2007-09-12 | Syngenta Ltd | Novel herbicides |
| GB0717082D0 (en) | 2007-09-03 | 2007-10-10 | Syngenta Ltd | Novel herbicides |
| US8895761B2 (en) | 2007-12-13 | 2014-11-25 | Syngenta Limited | 4-phenylpyrane-3,5-diones, 4-phenylthiopyrane-3,5-diones and 2-phenylcyclohexane-1,3,5-triones as herbicides |
| CL2008003785A1 (es) * | 2007-12-21 | 2009-10-09 | Du Pont | Compuestos derivados de piridazina; composiciones herbicidas que comprenden a dichos compuestos; y método para controlar el crecimiento de la vegetación indeseada. |
| WO2009150095A1 (en) * | 2008-06-12 | 2009-12-17 | Syngenta Participations Ag | Pesticidal compositions containing a pyrandione or a thiopyrandione or a cyclohexanetrione derivative |
-
2007
- 2007-06-28 GB GBGB0712653.5A patent/GB0712653D0/en not_active Ceased
-
2008
- 2008-06-24 AR ARP080102705A patent/AR067144A1/es unknown
- 2008-06-26 EP EP12170624A patent/EP2527333A1/en not_active Withdrawn
- 2008-06-26 TW TW097123871A patent/TW200918510A/zh unknown
- 2008-06-26 US US12/666,405 patent/US8956999B2/en not_active Expired - Fee Related
- 2008-06-26 CA CA2690176A patent/CA2690176A1/en not_active Abandoned
- 2008-06-26 MX MX2009013500A patent/MX2009013500A/es not_active Application Discontinuation
- 2008-06-26 AU AU2008267371A patent/AU2008267371B2/en not_active Ceased
- 2008-06-26 WO PCT/EP2008/005197 patent/WO2009000533A1/en not_active Ceased
- 2008-06-26 CL CL200801901A patent/CL2008001901A1/es unknown
- 2008-06-26 KR KR1020107002077A patent/KR20100046161A/ko not_active Ceased
- 2008-06-26 EA EA201000069A patent/EA020695B1/ru not_active IP Right Cessation
- 2008-06-26 CN CN2008800255713A patent/CN101778834B/zh not_active Expired - Fee Related
- 2008-06-26 JP JP2010513755A patent/JP5426542B2/ja not_active Expired - Fee Related
- 2008-06-26 EP EP08784557.4A patent/EP2173727B1/en not_active Not-in-force
- 2008-06-26 AP AP2009005084A patent/AP2009005084A0/en unknown
- 2008-06-26 ES ES08784557.4T patent/ES2444706T3/es active Active
- 2008-06-26 PL PL08784557T patent/PL2173727T3/pl unknown
-
2009
- 2009-12-10 ZA ZA200908821A patent/ZA200908821B/xx unknown
- 2009-12-22 CO CO09146293A patent/CO6241077A2/es not_active Application Discontinuation
- 2009-12-22 TN TNP2009000536A patent/TN2009000536A1/fr unknown
- 2009-12-22 HN HN2009003466A patent/HN2009003466A/es unknown
- 2009-12-23 EC EC2009009827A patent/ECSP099827A/es unknown
-
2010
- 2010-01-18 MA MA32524A patent/MA31526B1/fr unknown
-
2013
- 2013-09-25 JP JP2013198942A patent/JP2014040439A/ja active Pending
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