JP2015502927A - 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用ｉｉｉ - Google Patents
置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用ｉｉｉ Download PDFInfo
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- JP2015502927A JP2015502927A JP2014541676A JP2014541676A JP2015502927A JP 2015502927 A JP2015502927 A JP 2015502927A JP 2014541676 A JP2014541676 A JP 2014541676A JP 2014541676 A JP2014541676 A JP 2014541676A JP 2015502927 A JP2015502927 A JP 2015502927A
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- alkyl
- alkoxy
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- haloalkyl
- halogen
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- 150000002244 furazanes Chemical class 0.000 title claims abstract description 6
- 239000004009 herbicide Substances 0.000 title description 19
- -1 1,2,5-oxadiazole compound Chemical class 0.000 claims abstract description 589
- 150000001875 compounds Chemical class 0.000 claims abstract description 457
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 189
- 150000002367 halogens Chemical class 0.000 claims abstract description 182
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 154
- 239000001257 hydrogen Substances 0.000 claims abstract description 134
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 118
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 111
- 239000000203 mixture Substances 0.000 claims abstract description 73
- 150000003839 salts Chemical class 0.000 claims abstract description 55
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 44
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims abstract description 40
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 39
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 39
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 36
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims abstract description 34
- 150000001204 N-oxides Chemical class 0.000 claims abstract description 22
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 13
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims abstract description 8
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims abstract description 7
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims abstract description 7
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims abstract description 5
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims abstract description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 109
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 78
- 229910052757 nitrogen Inorganic materials 0.000 claims description 76
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 64
- 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 description 63
- 229910052717 sulfur Inorganic materials 0.000 claims description 51
- 229910052760 oxygen Inorganic materials 0.000 claims description 50
- 229910052731 fluorine Inorganic materials 0.000 claims description 49
- 125000005842 heteroatom Chemical group 0.000 claims description 49
- 229910052801 chlorine Inorganic materials 0.000 claims description 48
- 229910004013 NO 2 Inorganic materials 0.000 claims description 43
- 229920006395 saturated elastomer Polymers 0.000 claims description 40
- 125000002950 monocyclic group Chemical group 0.000 claims description 37
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 26
- 125000002619 bicyclic group Chemical group 0.000 claims description 23
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 22
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 21
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 15
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 14
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 12
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 12
- 125000003971 isoxazolinyl group Chemical group 0.000 claims description 12
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 12
- 125000002837 carbocyclic group Chemical group 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 4
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 3
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 2
- 125000005879 dioxolanyl group Chemical group 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000002757 morpholinyl group Chemical group 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
- 125000004193 piperazinyl group Chemical group 0.000 claims description 2
- 125000003386 piperidinyl group Chemical group 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 abstract description 9
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 156
- 239000000460 chlorine Substances 0.000 description 73
- 241000196324 Embryophyta Species 0.000 description 65
- 125000005869 (methoxyethoxy)methanyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])OC([H])([H])* 0.000 description 54
- 125000004432 carbon atom Chemical group C* 0.000 description 43
- YUCFVHQCAFKDQG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH] YUCFVHQCAFKDQG-UHFFFAOYSA-N 0.000 description 34
- 230000002363 herbicidal effect Effects 0.000 description 34
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 33
- 229910052794 bromium Inorganic materials 0.000 description 31
- 238000000034 method Methods 0.000 description 31
- 150000002148 esters Chemical group 0.000 description 27
- 244000038559 crop plants Species 0.000 description 25
- 239000003053 toxin Substances 0.000 description 24
- 231100000765 toxin Toxicity 0.000 description 24
- 108700012359 toxins Proteins 0.000 description 24
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- 125000001424 substituent group Chemical group 0.000 description 18
- 238000009472 formulation Methods 0.000 description 17
- 239000003112 inhibitor Substances 0.000 description 17
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 16
- 108090000623 proteins and genes Proteins 0.000 description 16
- 239000011737 fluorine Substances 0.000 description 15
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 14
- 239000000049 pigment Substances 0.000 description 14
- 150000003254 radicals Chemical class 0.000 description 14
- 102000004169 proteins and genes Human genes 0.000 description 13
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 12
- 240000008042 Zea mays Species 0.000 description 12
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 12
- 238000006467 substitution reaction Methods 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 11
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 11
- 239000002253 acid Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 235000005822 corn Nutrition 0.000 description 11
- 239000008187 granular material Substances 0.000 description 11
- 125000004284 isoxazol-3-yl group Chemical group [H]C1=C([H])C(*)=NO1 0.000 description 11
- 125000001072 heteroaryl group Chemical group 0.000 description 10
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 10
- 238000011282 treatment Methods 0.000 description 10
- 229920000742 Cotton Polymers 0.000 description 9
- 241000219146 Gossypium Species 0.000 description 9
- 239000002671 adjuvant Substances 0.000 description 9
- 239000003905 agrochemical Substances 0.000 description 9
- 238000010790 dilution Methods 0.000 description 9
- 239000012895 dilution Substances 0.000 description 9
- 239000002270 dispersing agent Substances 0.000 description 9
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 125000006345 2,2,2-trifluoroethoxymethyl group Chemical group [H]C([H])(*)OC([H])([H])C(F)(F)F 0.000 description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 6
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 6
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 6
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 6
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000005562 Glyphosate Substances 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
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- 239000004480 active ingredient Substances 0.000 description 6
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- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 6
- 230000035784 germination Effects 0.000 description 6
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- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 5
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- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 1
- 125000004300 thiazolidin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])SC1([H])* 0.000 description 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 description 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 description 1
- MKYRMMMSZSVIGD-UHFFFAOYSA-N thieno[3,2-c]pyridine Chemical compound N1=CC=C2SC=CC2=C1 MKYRMMMSZSVIGD-UHFFFAOYSA-N 0.000 description 1
- 125000004275 thietan-2-yl group Chemical group [H]C1([H])SC([H])(*)C1([H])[H] 0.000 description 1
- 125000006300 thietan-3-yl group Chemical group [H]C1([H])SC([H])([H])C1([H])* 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000004569 thiomorpholin-2-yl group Chemical group N1CC(SCC1)* 0.000 description 1
- 125000004570 thiomorpholin-3-yl group Chemical group N1C(CSCC1)* 0.000 description 1
- 125000004571 thiomorpholin-4-yl group Chemical group N1(CCSCC1)* 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- AZHZOGYUMMIAOF-UHFFFAOYSA-N trifludimoxazin Chemical compound O=C1N(C)C(=S)N(C)C(=O)N1C(C(=C1)F)=CC2=C1OC(F)(F)C(=O)N2CC#C AZHZOGYUMMIAOF-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 150000004669 very long chain fatty acids Chemical class 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161561324P | 2011-11-18 | 2011-11-18 | |
| US61/561,324 | 2011-11-18 | ||
| PCT/EP2012/072810 WO2013072450A1 (en) | 2011-11-18 | 2012-11-16 | Substituted 1,2,5-oxadiazole compounds and their use as herbicides iii |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2015502927A true JP2015502927A (ja) | 2015-01-29 |
Family
ID=47189941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014541676A Pending JP2015502927A (ja) | 2011-11-18 | 2012-11-16 | 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用ｉｉｉ |
Country Status (15)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9736924B2 (en) | 2013-02-26 | 2017-08-15 | Tatsuta Electric Wire & Cable Co., Ltd. | Reinforcing member for flexible printed wiring board, flexible printed wiring board, and shield printed wiring board |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112013023603A2 (pt) * | 2011-03-15 | 2016-08-02 | Bayer Ip Gmbh | n-(1,2,5-oxadiazol-3-il)piridinacarboxamidas e seu emprego como herbicidas |
| JP5960170B2 (ja) * | 2011-03-15 | 2016-08-02 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | 除草剤薬害軽減剤組成物 |
| AR088886A1 (es) | 2011-11-16 | 2014-07-16 | Basf Se | Compuestos de 1,2,5-oxadiazol sustituido y su uso como herbicidas ii |
| WO2014184014A1 (en) * | 2013-05-15 | 2014-11-20 | Basf Se | N-(1,2,5-oxadiazol-3-yl)carboxamide compounds and their use as herbicides |
| CN105229005B (zh) | 2013-05-31 | 2018-01-02 | 日产化学工业株式会社 | 杂环酰胺化合物 |
| WO2015052152A1 (en) * | 2013-10-10 | 2015-04-16 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
| WO2015052178A1 (en) * | 2013-10-10 | 2015-04-16 | Basf Se | 1,2,5-oxadiazole compounds and their use as herbicides |
| AR101230A1 (es) * | 2014-07-28 | 2016-11-30 | Bayer Cropscience Ag | Amidas del ácido arilcarboxílico bicíclicas y su uso como herbicidas |
| WO2017042259A1 (en) | 2015-09-11 | 2017-03-16 | Bayer Cropscience Aktiengesellschaft | Hppd variants and methods of use |
| BR112019018175A2 (pt) | 2017-03-07 | 2020-04-07 | BASF Agricultural Solutions Seed US LLC | molécula, célula, planta, sementes, polipeptídeos recombinantes, método para produzir um polipeptídeo, planta, método para controlar ervas, uso do ácido nucleico e produto de utilidade |
| CN112624989B (zh) * | 2019-10-08 | 2024-01-26 | 沈阳中化农药化工研发有限公司 | 一种酰胺类化合物及其应用 |
| DK4132915T3 (da) * | 2020-04-07 | 2024-02-19 | Bayer Ag | Substituerede isophtalsyrediamider |
| US11772496B2 (en) | 2020-08-26 | 2023-10-03 | Anusheel Nahar | Regenerative braking system of an automobile and a method to operate |
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| JPH05117255A (ja) * | 1991-10-25 | 1993-05-14 | Nippon Soda Co Ltd | オキサジアゾール及びチアジアゾール誘導体、その製法 |
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| AU5920601A (en) | 2000-04-28 | 2001-11-12 | American Cyanamid Co | Use of the maize x112 mutant ahas 2 gene and imidazolinone herbicides for selection of transgenic monocots, maize, rice and wheat plants resistant to the imidazolinone herbicides |
| GEP20063931B (en) | 2000-05-04 | 2006-10-10 | Basf Aktiengescellschaft | Uracil substituted phenyl sulfamoyl carboxamides |
| WO2002015701A2 (en) | 2000-08-25 | 2002-02-28 | Syngenta Participations Ag | Bacillus thuringiensis crystal protein hybrids |
| RU2004106631A (ru) | 2001-08-09 | 2005-05-10 | Нортвест Плант Бридинг Компани (Us) | Растения пшеницы с повышенной устойчивостью к имидозалиновым гербицидам |
| BRPI0211809B1 (pt) | 2001-08-09 | 2019-04-24 | University Of Saskatchewan | Método para o controle de ervas daninhas nas vizinhanças de uma planta de trigo ou triticale, método para modificar a tolerância de uma planta de trigo ou triticale a um herbicida de imidazolinona e método de produção de uma planta de trigo ou triticale transgênica tendo resistência aumentada a um herbicida de imidazolinona |
| RU2337532C2 (ru) | 2001-08-09 | 2008-11-10 | Юниверсити Оф Саскачеван | Растения пшеницы с повышенной устойчивостью к имидазолиноновым гербицидам |
| US7230167B2 (en) | 2001-08-31 | 2007-06-12 | Syngenta Participations Ag | Modified Cry3A toxins and nucleic acid sequences coding therefor |
| AU2002361696A1 (en) | 2001-12-17 | 2003-06-30 | Syngenta Participations Ag | Novel corn event |
| US7829762B2 (en) | 2002-07-10 | 2010-11-09 | Department Of Agriculture | Wheat plants having increased resistance to imidazolinone herbicides |
| UA92716C2 (uk) | 2003-05-28 | 2010-12-10 | Басф Акциенгезелльшафт | Рослини пшениці з підвищеною толерантністю до імідазолінонових гербіцидів |
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| CN101212967A (zh) * | 2005-05-10 | 2008-07-02 | 因塞特公司 | 吲哚胺2,3-双加氧酶调节剂及其用法 |
| GB0625598D0 (en) | 2006-12-21 | 2007-01-31 | Syngenta Ltd | Novel herbicides |
| GB0805318D0 (en) | 2008-03-20 | 2008-04-30 | Syngenta Ltd | Herbicidal compounds |
| RU2554349C9 (ru) * | 2009-09-25 | 2016-11-27 | Байер Интеллектуэль Проперти Гмбх | N-(1,2,5-оксадиазол-3-ил)бензамиды и их применение в качестве гербицидов |
| JP5960170B2 (ja) * | 2011-03-15 | 2016-08-02 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | 除草剤薬害軽減剤組成物 |
| BR112013023603A2 (pt) * | 2011-03-15 | 2016-08-02 | Bayer Ip Gmbh | n-(1,2,5-oxadiazol-3-il)piridinacarboxamidas e seu emprego como herbicidas |
-
2012
- 2012-11-16 EP EP12787442.8A patent/EP2780340A1/en not_active Withdrawn
- 2012-11-16 US US14/357,899 patent/US20140309115A1/en not_active Abandoned
- 2012-11-16 AR ARP120104330A patent/AR090397A1/es not_active Application Discontinuation
- 2012-11-16 IN IN3480CHN2014 patent/IN2014CN03480A/en unknown
- 2012-11-16 KR KR1020147016744A patent/KR20140107280A/ko not_active Withdrawn
- 2012-11-16 BR BR112014011685A patent/BR112014011685A2/pt not_active IP Right Cessation
- 2012-11-16 JP JP2014541676A patent/JP2015502927A/ja active Pending
- 2012-11-16 CN CN201280067028.6A patent/CN104039780A/zh active Pending
- 2012-11-16 WO PCT/EP2012/072810 patent/WO2013072450A1/en not_active Ceased
- 2012-11-16 CA CA2854100A patent/CA2854100A1/en not_active Abandoned
- 2012-11-16 AU AU2012338748A patent/AU2012338748A1/en not_active Abandoned
-
2014
- 2014-05-05 IL IL232468A patent/IL232468A0/en unknown
- 2014-05-09 CO CO14100202A patent/CO6950501A2/es not_active Application Discontinuation
- 2014-05-12 CR CR20140218A patent/CR20140218A/es unknown
- 2014-06-13 ZA ZA2014/04331A patent/ZA201404331B/en unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9736924B2 (en) | 2013-02-26 | 2017-08-15 | Tatsuta Electric Wire & Cable Co., Ltd. | Reinforcing member for flexible printed wiring board, flexible printed wiring board, and shield printed wiring board |
| US9867280B2 (en) | 2013-02-26 | 2018-01-09 | Tatsuta Electric Wire And Cable Co., Ltd. | Reinforcing member for flexible printed wiring board flexible printed wiring board, and shield printed wiring board |
Also Published As
| Publication number | Publication date |
|---|---|
| IL232468A0 (en) | 2014-06-30 |
| CR20140218A (es) | 2014-06-19 |
| IN2014CN03480A (cg-RX-API-DMAC7.html) | 2015-07-03 |
| CA2854100A1 (en) | 2013-05-23 |
| CN104039780A (zh) | 2014-09-10 |
| BR112014011685A2 (pt) | 2017-05-30 |
| ZA201404331B (en) | 2016-10-26 |
| WO2013072450A1 (en) | 2013-05-23 |
| AR090397A1 (es) | 2014-11-12 |
| EP2780340A1 (en) | 2014-09-24 |
| US20140309115A1 (en) | 2014-10-16 |
| AU2012338748A1 (en) | 2014-06-05 |
| KR20140107280A (ko) | 2014-09-04 |
| CO6950501A2 (es) | 2014-05-20 |
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