JP2019514848A - 除草剤 - Google Patents
除草剤 Download PDFInfo
- Publication number
- JP2019514848A JP2019514848A JP2018549833A JP2018549833A JP2019514848A JP 2019514848 A JP2019514848 A JP 2019514848A JP 2018549833 A JP2018549833 A JP 2018549833A JP 2018549833 A JP2018549833 A JP 2018549833A JP 2019514848 A JP2019514848 A JP 2019514848A
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- JP
- Japan
- Prior art keywords
- alkyl
- formula
- compound
- compounds
- pyridyl
- 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
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 25
- 239000004009 herbicide Substances 0.000 title claims description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 190
- 239000000203 mixture Substances 0.000 claims abstract description 73
- 241000196324 Embryophyta Species 0.000 claims abstract description 56
- 238000000034 method Methods 0.000 claims abstract description 39
- -1 phenoxy, pyridinyl Chemical group 0.000 claims description 55
- 229910052739 hydrogen Inorganic materials 0.000 claims description 40
- 239000001257 hydrogen Substances 0.000 claims description 30
- 229910052736 halogen Inorganic materials 0.000 claims description 22
- 150000002367 halogens Chemical class 0.000 claims description 22
- 125000003545 alkoxy group Chemical group 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 18
- 125000005842 heteroatom Chemical group 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 15
- 150000002431 hydrogen Chemical class 0.000 claims description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 13
- 238000009472 formulation Methods 0.000 claims description 12
- 125000004122 cyclic group Chemical group 0.000 claims description 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 125000001188 haloalkyl group Chemical group 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 9
- 238000009395 breeding Methods 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 239000000575 pesticide Substances 0.000 claims description 7
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 230000001488 breeding effect Effects 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000000335 thiazolyl group Chemical group 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 150000001204 N-oxides Chemical class 0.000 claims description 3
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
- 125000001544 thienyl group Chemical group 0.000 claims description 3
- 125000004001 thioalkyl group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 244000038559 crop plants Species 0.000 abstract description 6
- 238000002360 preparation method Methods 0.000 abstract description 5
- BWESROVQGZSBRX-UHFFFAOYSA-N pyrido[3,2-d]pyrimidine Chemical class C1=NC=NC2=CC=CN=C21 BWESROVQGZSBRX-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000543 intermediate Substances 0.000 abstract description 3
- 230000008635 plant growth Effects 0.000 abstract description 3
- 230000008569 process Effects 0.000 abstract description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 74
- 239000002904 solvent Substances 0.000 description 52
- 230000015572 biosynthetic process Effects 0.000 description 49
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 48
- 238000003786 synthesis reaction Methods 0.000 description 46
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 41
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 40
- 239000000243 solution Substances 0.000 description 36
- 235000019439 ethyl acetate Nutrition 0.000 description 34
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 33
- 238000006243 chemical reaction Methods 0.000 description 32
- YMWUJEATGCHHMB-UHFFFAOYSA-N dichloromethane Natural products ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 32
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 27
- 239000002585 base Substances 0.000 description 25
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 24
- 239000003480 eluent Substances 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 23
- 240000008042 Zea mays Species 0.000 description 23
- 238000003818 flash chromatography Methods 0.000 description 23
- 239000007787 solid Substances 0.000 description 23
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
- 239000003054 catalyst Substances 0.000 description 21
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 20
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 20
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 18
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 18
- 235000005822 corn Nutrition 0.000 description 18
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 18
- 239000000047 product Substances 0.000 description 18
- 239000011541 reaction mixture Substances 0.000 description 18
- 239000000460 chlorine Substances 0.000 description 16
- 229910052740 iodine Inorganic materials 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 239000000377 silicon dioxide Substances 0.000 description 15
- 235000019441 ethanol Nutrition 0.000 description 14
- 239000004094 surface-active agent Substances 0.000 description 13
- 241000192043 Echinochloa Species 0.000 description 12
- 244000075850 Avena orientalis Species 0.000 description 11
- 241000611157 Brachiaria Species 0.000 description 11
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 11
- 244000062793 Sorghum vulgare Species 0.000 description 11
- 229910052801 chlorine Inorganic materials 0.000 description 11
- 239000000284 extract Substances 0.000 description 11
- 239000008187 granular material Substances 0.000 description 11
- 239000011734 sodium Substances 0.000 description 11
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 11
- 241000743985 Alopecurus Species 0.000 description 10
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 10
- 229910052794 bromium Inorganic materials 0.000 description 10
- 239000003153 chemical reaction reagent Substances 0.000 description 10
- NXQGGXCHGDYOHB-UHFFFAOYSA-L cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;dichloropalladium;iron(2+) Chemical compound [Fe+2].Cl[Pd]Cl.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NXQGGXCHGDYOHB-UHFFFAOYSA-L 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- 239000000741 silica gel Substances 0.000 description 10
- 229910002027 silica gel Inorganic materials 0.000 description 10
- 239000003643 water by type Substances 0.000 description 10
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 9
- 241000044408 Eriochloa Species 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 9
- 235000007320 Avena fatua Nutrition 0.000 description 8
- 240000004296 Lolium perenne Species 0.000 description 8
- 244000022203 blackseeded proso millet Species 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- 125000000623 heterocyclic group Chemical group 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- 239000004530 micro-emulsion Substances 0.000 description 8
- 241000743339 Agrostis Species 0.000 description 7
- 235000017896 Digitaria Nutrition 0.000 description 7
- 241001303487 Digitaria <clam> Species 0.000 description 7
- 241000857233 Rottboellia Species 0.000 description 7
- 241000207929 Scutellaria Species 0.000 description 7
- 235000005775 Setaria Nutrition 0.000 description 7
- 241000232088 Setaria <nematode> Species 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- 238000013459 approach Methods 0.000 description 7
- 238000006880 cross-coupling reaction Methods 0.000 description 7
- 239000003814 drug Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 235000005781 Avena Nutrition 0.000 description 6
- 241000209764 Avena fatua Species 0.000 description 6
- 241000209120 Cenchrus Species 0.000 description 6
- 244000058871 Echinochloa crus-galli Species 0.000 description 6
- 241000209215 Eleusine Species 0.000 description 6
- 235000007351 Eleusine Nutrition 0.000 description 6
- 241000209082 Lolium Species 0.000 description 6
- 235000011999 Panicum crusgalli Nutrition 0.000 description 6
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 6
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 239000000443 aerosol Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000008878 coupling Effects 0.000 description 6
- 238000010168 coupling process Methods 0.000 description 6
- 238000005859 coupling reaction Methods 0.000 description 6
- 239000012043 crude product Substances 0.000 description 6
- MKRTXPORKIRPDG-UHFFFAOYSA-N diphenylphosphoryl azide Chemical compound C=1C=CC=CC=1P(=O)(N=[N+]=[N-])C1=CC=CC=C1 MKRTXPORKIRPDG-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N tert-butyl alcohol Substances CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
- 239000000080 wetting agent Substances 0.000 description 6
- PTYNWPNRVGRFHR-UHFFFAOYSA-N 1-[6-(5-fluoropyridin-3-yl)-2-(trifluoromethyl)pyridin-3-yl]pyrrolidine-2,5-dione Chemical compound FC=1C=C(C=NC=1)C1=CC=C(C(=N1)C(F)(F)F)N1C(CCC1=O)=O PTYNWPNRVGRFHR-UHFFFAOYSA-N 0.000 description 5
- QPKJRALYTKFVFI-UHFFFAOYSA-N 6-(5-fluoropyridin-3-yl)-2-(trifluoromethyl)pyridin-3-amine Chemical compound FC=1C=C(C=NC=1)C1=CC=C(C(=N1)C(F)(F)F)N QPKJRALYTKFVFI-UHFFFAOYSA-N 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 241001666377 Apera Species 0.000 description 5
- 241000209200 Bromus Species 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 5
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- YIDIKWDMBNAVKZ-UHFFFAOYSA-N N-[6-(5-fluoropyridin-3-yl)-2-(trifluoromethyl)pyridin-3-yl]pyridine-3-carboxamide Chemical compound FC=1C=C(C=NC=1)C1=CC=C(C(=N1)C(F)(F)F)NC(=O)C=1C=NC=CC=1 YIDIKWDMBNAVKZ-UHFFFAOYSA-N 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 5
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- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
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- 238000010992 reflux Methods 0.000 description 5
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- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- 240000006995 Abutilon theophrasti Species 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- 239000005562 Glyphosate Substances 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
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- XLYPOBOMKUKHQD-UHFFFAOYSA-N N-[6-(5-fluoropyridin-3-yl)-2-(trifluoromethyl)pyridin-3-yl]acetamide Chemical compound FC=1C=C(C=NC=1)C1=CC=C(C(=N1)C(F)(F)F)NC(C)=O XLYPOBOMKUKHQD-UHFFFAOYSA-N 0.000 description 4
- 241000069499 Ottochloa Species 0.000 description 4
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- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 240000006394 Sorghum bicolor Species 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
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- 239000000654 additive Substances 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- 239000012267 brine Substances 0.000 description 4
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- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachloro-phenol Natural products OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 4
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- 238000004704 ultra performance liquid chromatography Methods 0.000 description 4
- 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 3
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 3
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- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
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- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- 235000003990 Monochoria hastata Nutrition 0.000 description 3
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- 238000003971 tillage Methods 0.000 description 1
- 125000003944 tolyl group Chemical group 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
- 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
- 125000001425 triazolyl group Chemical group 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
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical class C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-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
- 238000001946 ultra-performance liquid chromatography-mass spectrometry Methods 0.000 description 1
- 241001478887 unidentified soil bacteria Species 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N43/74—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
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- Organic Chemistry (AREA)
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- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Description
X1はNまたはCR1であり;
R1は、水素、ハロゲン、シアノ、C1〜C6アルキル、C3〜C6シクロアルキル、C2〜C6アルケニル、C2〜C6アルキニル、C1〜C6アルコキシ、−C(O)OC1〜C6アルキル、−S(O)pC1〜C6アルキル、NR6R7、C1〜C6ハロアルコキシおよびC1〜C6ハロアルキルからなる群から選択され;
R2は、ハロゲン、シアノ、ニトロ、C1〜C6アルキル、C1〜C6ハロアルキル、C2〜C6アルケニル、C2〜C6アルキニル、C3〜C6シクロアルキル、−C(O)OC1〜C6アルキル、−S(O)p(C1〜C6アルキル)、C1〜C6アルコキシおよびC1〜C6ハロアルコキシからなる群から選択され;
R3は−C(O)R9であり;
R4は、水素、C1〜C6アルキル、C1〜C6ハロアルキル、C3〜C6アルケニル、C3〜C6アルキニル、CrアルコキシCsアルキル、−CrアルコキシCsハロアルキル、CrアルコキシCsチオアルキル、−C(O)R9および−(CRaRb)qR5からなる群から選択され;
各Raは独立して、水素またはC1〜C2アルキルであり;
各Rbは独立して、水素またはC1〜C2アルキルであり;
Rcは、水素またはC1〜C4アルキルであり;
R5は、−C(O)OC1〜C6アルキル、−C3〜C6シクロアルキル、シアノ、−NR6R7、−C(O)NRaRb、−S(O)p(R11)n、−アリールまたは−ヘテロアリールであり、前記アリールおよびヘテロアリールは、1〜3個の独立したR8で任意選択により置換されており;
R6およびR7は、水素およびC1〜C6アルキルからなる群から独立して選択され;
各R8は、ハロゲン、C1〜C6アルキルおよびC1〜C6アルコキシ−、C1〜C6ハロアルキル、C1〜C6ハロアルコキシ−、シアノおよびS(O)p(C1〜C6アルキル)からなる群から独立して選択され;
各R9は、水素、C1〜C6アルキル、CrアルコキシCsアルキル、C1〜C6ハロアルキル、CrアルコキシCsハロアルキル、C2〜C6アルケニル、C2〜C6アルキニルおよび−(CRaRb)qR10からなる群から独立して選択され;
または、R4およびR9は、これらが結合する原子と一緒になって、1〜3個のヘテロ原子を含有する5〜7員環系を形成し、ここで、少なくとも1個のヘテロ原子はNであり、ならびに、いずれかの追加のヘテロ原子は、S、OおよびNから独立して選択され;
R10は、−C(O)ORc、−OC(O)Rc、−C3〜C6シクロアルキルまたは−アリール、−アリールオキシ、−ヘテロアリール、−ヘテロアリールオキシまたは−ヘテロシクリル環であり、ここで、前記環は、1〜3個の独立したR8で任意選択により置換されており;
各nは独立して、0または1であり;
pは、0、1または2であり;
各qは独立して、0、1、2、3、4、5または6であり;
rは、1、2、3、4または5であり、sは、1、2、3、4または5であり、および、r+sの和は6以下であり;ならびに
R11はC1〜C6アルキルである)
が提供されている。
Ac=アセチル
app=明らか
BINAP=2,2’−ビス(ジフェニルホスフィノ)−1,1’−ビナフチル
br.=幅広
tBu=t−ブチル
t−BuOH=t−ブタノール
d=二重項
dd=二重の二重項
Dba=ジベンジリデンアセトン
DCM=ジクロロメタン
DMF=N,N−ジメチルホルムアミド
DMSO=ジメチルスルホキシド
DPPA=ジフェニルホスホリルアジド
Et3N=トリエチルアミン
Et2O=ジエチルエーテル
EtOAc=酢酸エチル
EtOH=エタノール
m=多重項
mCPBA=メタ−クロロ−過安息香酸
Me=メチル
MeOH=メタノール
Ms=メシレート
Ph=フェニル
q=四重項
RT=室温
s=一重項
t=三重項
Tf=トリフレート
TFA=トリフルオロ酢酸
THF=テトラヒドロフラン
TMS=テトラメチルシラン
tr=保持時間
置換基X1、R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、Ra、Rb、Rc、n、p、q、r、およびsの性質に応じて、式Iの化合物は、例えばS.A.Richards and J.C.Hollerton,Essential Practical NMR for Organic Chemistry,John Wiley and sons(2010)に記載されている異なる相互に変換可能な回転異性体形態で存在し得ることを当業者は理解するであろう。明確さのために、主な回転異性体形態に係る分光データのみが引用されている。
1H NMR(400MHz,CDCl3)δ8.28(1H,d),7.44(1H,dd),7.21(1H,d),4.43(2H,q),1.44(3H,t)
1H NMR(400MHz,CDCl3)δ8.09(d,1H),7.60(d,1H),4.43(q,2H),1.43(t,3H)
1H NMR(400MHz,CDCl3)δ8.12(1H,d),7.62(1H,d)
1H NMR(400MHz,CDCl3)δ8.64(d,1H),7.48(d,1H),6.89(br.s,1H),1.52(s,9H)
1H NMR(400MHz,CDCl3)δ9.02(dd,1H),8.79(d,1H),8.52(d,1H),8.12(m,1H),7.94(d,1H),7.01(br.s,1H),1.56(s,9H)
1H NMR(400MHz,CDCl3)δ8.93(m,1H),8.45(d,1H),8.12−8.00(m,1H),7.75(d 1H),7.21(d,1H),4.38(br.s,2H)
1H NMR(400MHz,CDCl3)δ9.07(br.s,1H),8.78(d,1H),8.52(1H,br.s),8.12(m,1H),7.92(d,1H),7.67(br.s,1H),2.58(m,1H),1.31(d,6H)
1H NMR(400MHz,CDCl3)δ9.03(d,1H),8.83(d,1H),8.54(d,1H),8.14(m,1H),7.95(d,1H),7.58(br.s,1H),2.30(s,3H)
1H NMR(400MHz,CD3OD,メジャー回転異性体)δ9.18(1H,s),8.57(1H,d),8.17(1H,m),8.12(1H,d),7.77(1H,d),3.18(3H,s),2.21(1H,m),1.12(3H,d),0.97(3H,d)
1H NMR(400MHz,CDCl3)δ9.08(s,1H),8.61(d,1H),8.18(m,1H),8.08(d,1H),7.72(d,1H),2.33(s,6H)
の合成
1H NMR(400MHz,CDCl3)δ7.25(d,1H),7.02(d,1H),4.27(br.s,2H)
1H NMR(400MHz,CDCl3)δ8.73(d,1H),7.58(br.s,1H),7.51(d,1H),2.67−2.54(m,1H),1.29および1.21(2 x d,6H)
1H NMR(400MHz,CDCl3)δ9.08(s,1H),8.89(d,1H),8.62(s,1H),8.38(s,1H),7.96(d,1H),7.68(br s,1H),2.69−2.59(m,1H),1.32(d,6H)
1H NMR(400MHz,CDCl3,メジャー回転異性体)δ9.07(s,1H),8.57(d,1H),8.20(br.d,1H),8.01(d,1H),7.76(d,1H),3.22(s,3H),1.33(s,9H)
1H NMR(400MHz,CDCl3)δ8.93(s,1H),8.42(d,1H),8.05(m,1H),7.82(d,1H),7.17(d,1H),4.72(br.s,1H),2.98(app.d,3H)
1H NMR(400MHz,CDCl3,メジャー回転異性体)δ9.15(s,1H),8.64(m,1H),8.39(m,1H),8.15(d,1H),7.86(d,1H),3.27(s,3H),2.00(2H,m),1.08(3H,t)
1H NMR(400MHz,CDCl3)δ8.18(br.d,1H),7.16(d,1H),6.26(br.d,1H),2.48(s,3H),1.52(s,9H).
1H NMR(400MHz,CDCl3)δ6.89(d,1H),6.81(d,1H),3.59(br.s,2H),2.29(s,3H).
1H NMR(400MHz,CDCl3)δ8.27(d,1H),7.19(d,1H,6.93(br.s,1H),2.61−2.54(m,1H),2.49(s,3H),1.29(d,6H).
1H NMR(400MHz,CDCl3)δ9.30(s,2H),9.22(s,1H),8.50(d,1H),7.63(d,1H),7.08(br.s,1H),2.68−2.58(m,1H),2.62(s,3H),1.32(d,6H).
1H NMR(400MHz,CDCl3)δ9.03(s,1H),8.58(s,1H),8.15(d,1H),7.98(d,1H),7.92(d,1H).
1H NMR(400MHz,CDCl3)δ9.16(s,1H),9.10−9.00(m,2H),8.91−8.87(m,1H),8.56(d,1H),8.48(br.s,1H),8.25−8.20(m,1H),8.20−8.13(m,1H),8.07(d,1H),7.56−7.50(m,1H).
1H NMR(400MHz,CDCl3)δ9.03(s,1H),8.57(s,1H),8.17(d,1H),8.04(d,1H),7.80(d,1H),3.66−3.53(m,2H),2.17−2.53(m,2H),2.11−1.90(m,4H).
1H NMR(400MHz,CDCl3)9.46(s,2H),9.28(s,1H),8.05(d,1H),7.78(d,1H),3.15−2.87(m,4H).
1H NMR(400MHz,CD3OD)δ8.95(d,1H),8.43(d,1H),8.18−8.09(m,1H),7.93(d,1H),7.35(d,1H)
1H NMR(400MHz,CDCl3)δ9.12(br.s,1H),9.02(s,1H),9.00(d,1H),8.55(d,1H),8.09(m,1H),8.00(d,1H),4.13(s,2H),3.60(s,3H)
1H NMR(400MHz,CDCl3)δ9.08(t,1H),8.60(d,1H),8.21(m,1H),8.11(d,1H),7.77(d,1H),2.52(m,1H),2.40(s,3H),1.14(t,3H).
1H NMR(400MHz,CD3OD)9.14(dd,1H),8.55(d,1H),8.32−8.24(m,3H),2.75(m,2H),2.70(m,2H).
1H NMR(400MHz,CDCl3)δ9.48(s,1H),9.27(s,2H),9.09(t,1H),9.00(d,1H),8.59(d,1H),8.33(br.s,1H),8.25−8.17(m,1H),8.10(d,1H).
本発明の化合物を、以下の方法の1つまたは複数を用いて特性決定した。
本明細書に含まれているNMRスペクトルは、Bruker SMARTプローブを備える400MHz Bruker AVANCE III HD、または、Bruker Prodigyプローブを備える500MHz Bruker AVANCE IIIで記録した。化学シフトは、TMSまたは残存溶剤シグナルの内部標準を伴ってTMSの低磁場側にppmで表記されている。以下の多重度がピークの記載に用いられる:s=一重項、d=二重項、t=三重項、dd=二重の二重項、m=多重項。さらに、br.が幅広いシグナルの記載に用いられ、app.が明らかな多重度の記載に用いられる。
本明細書に含まれているLCMSデータは、クロマトグラムに記録されたピーク分子イオン[MH+]および保持時間(tr)からなる。以下の機器、方法および条件を用いてLCMSデータを得た。
計装:Sample Manager FTN、H−Class QSM、Column Manager、2xColumn Manager Aux、発光ダイオードアレイ(波長範囲(nm):210〜400、Waters HSS T3 C18カラム(カラム長30mm、カラム内径2.1mm、粒径1.8ミクロン)を備えるELSDおよびSQD2と共にサンプルオーガナイザを用いるWaters Acquity UPLC−MS。
計装:(a)Waters SQD2シングル四重極型MS検出器、発光ダイオードアレイ検出器(吸光波長:254nm、10pts/秒、時定数:0.2000秒)、荷電エアロゾル検出器(コロナ)およびWaters CTC 2770自動サンプラーユニット(インジェクション体積:2マイクロリットル、シール洗浄1分間)を備えるWaters Acquity UPLCシステム;または(b)Waters QDaシングル四重極型MS検出器、発光ダイオードアレイ検出器(吸光波長:254nm、10pts/秒、時定数:0.2000秒)、荷電エアロゾル検出器(コロナ)およびWaters CTC 2770自動サンプラーユニット(インジェクション体積:2マイクロリットル、シール洗浄1分間)を備えるWaters Acquity UPLCシステム。
Phenomenex ’Kinetex C18 100A’カラム(50mm×4.6mm、粒径2.6ミクロン)、
流量:313K(摂氏40度)で2mL/分、
勾配(溶剤A:H2O+0.1%ギ酸;溶剤B:アセトニトリル+0.1%ギ酸):
計装:(a)Waters SQD2シングル四重極型MS検出器、発光ダイオードアレイ検出器(吸光波長:254nm、10pts/秒、時定数:0.2000秒)、荷電エアロゾル検出器(コロナ)およびWaters CTC 2770自動サンプラーユニット(インジェクション体積:2マイクロリットル、シール洗浄1分間)を備えるWaters Acquity UPLCシステム;または(b)Waters QDaシングル四重極型MS検出器、発光ダイオードアレイ検出器(吸光波長:254nm、10pts/秒、時定数:0.2000秒)、荷電エアロゾル検出器(コロナ)およびWaters CTC 2770自動サンプラーユニット(インジェクション体積:2マイクロリットル、シール洗浄1分間)を備えるWaters Acquity UPLCシステム。
Phenomenex ’Kinetex C18 100A’カラム(50mm×4.6mm、粒径2.6ミクロン)、
流量:313K(摂氏40度)で2mL/分、
勾配(溶剤A:H2O+0.1%ギ酸;溶剤B:アセトニトリル+0.1%ギ酸):
B1 発芽前除草活性
ポット中の標準的な土壌中に多様なテスト種の種子を播種した:パンコムギ(Triticum aestivium)(TRZAW)、アベナファツア(Avena fatua)(AVEFA)、アロペクルスミオスロイデス(Alopecurus myosuroides)(ALOMY)、イヌビエ(Echinochloa crus−galli)(ECHCG)、ホソムギ(Lolium perenne)(LOLPE)、トウモロコシ(Zea mays)(ZEAMX)、イチビ(Abutilon theophrasti)(ABUTH)、アオゲイトウ(Amaranthus retroflexus)(AMARE)およびアキノエノコログサ(Setaria faberi)(SETFA)。温室において制御された条件下(24/16℃、昼/夜;14時間の明かり;65%湿度)で1日栽培した後(発芽前)、この植物に、0.5%Tween 20(ポリオキシエチレンソルビタンモノラウレート、CAS RN 9005−64−5)を含有するアセトン/水(50:50)溶液中における技術的活性処方成分の配合物に基づく噴霧水溶液を噴霧した。次いで、テスト植物を温室中において制御された条件下(24/16℃、昼/夜;14時間の明かり;65%湿度)で成長させ、1日に2回水をかけた。13日後にテストを評価した(5=植物に対する全損;0=植物に対する損傷は無し)。結果を表B1aおよびB1bに示す。
ポット中の標準的な土壌中に多様なテスト種の種子を播種した:パンコムギ(Triticum aestivium)(TRZAW)、アベナファツア(Avena fatua)(AVEFA)、アロペクルスミオスロイデス(Alopecurus myosuroides)(ALOMY)、イヌビエ(Echinochloa crus−galli)(ECHCG)、ホソムギ(Lolium perenne)(LOLPE)、トウモロコシ(Zea mays)(ZEAMX)、イチビ(Abutilon theophrasti)(ABUTH)、アオゲイトウ(Amaranthus retroflexus)(AMARE)およびアキノエノコログサ(Setaria faberi)(SETFA)。温室において制御された条件下(24/16℃、昼/夜;14時間の明かり;65%湿度)で8日間栽培した後(発芽後)、この植物に、0.5%Tween 20(ポリオキシエチレンソルビタンモノラウレート、CAS RN 9005−64−5)を含有するアセトン/水(50:50)溶液中における技術的活性処方成分の配合物に基づく噴霧水溶液を噴霧した。次いで、テスト植物を温室中において制御された条件下(24/16℃、昼/夜;14時間の明かり;65%湿度)で成長させ、1日に2回水をかけた。13日後にテストを評価した(5=植物に対する全損;0=植物に対する損傷は無し)。結果を表B2aおよびB2bに示す。
Claims (15)
- 式(I)の化合物
X1はNまたはCR1であり;
R1は、水素、ハロゲン、シアノ、C1〜C6アルキル、C3〜C6シクロアルキル、C2〜C6アルケニル、C2〜C6アルキニル、C1〜C6アルコキシ、−C(O)OC1〜C6アルキル、−S(O)pC1〜C6アルキル、NR6R7、C1〜C6ハロアルコキシおよびC1〜C6ハロアルキルからなる群から選択され;
R2は、ハロゲン、シアノ、ニトロ、C1〜C6アルキル、C1〜C6ハロアルキル、C2〜C6アルケニル、C2〜C6アルキニル、C3〜C6シクロアルキル、−C(O)OC1〜C6アルキル、−S(O)p(C1〜C6アルキル)、C1〜C6アルコキシおよびC1〜C6ハロアルコキシからなる群から選択され;
R3は−C(O)R9であり;
R4は、水素、C1〜C6アルキル、C1〜C6ハロアルキル、C3〜C6アルケニル、C3〜C6アルキニル、CrアルコキシCsアルキル、−CrアルコキシCsハロアルキル、CrアルコキシCsチオアルキル、−C(O)R9および−(CRaRb)qR5からなる群から選択され;
各Raは独立して、水素またはC1〜C2アルキルであり;
各Rbは独立して、水素またはC1〜C2アルキルであり;
Rcは、水素またはC1〜C4アルキルであり;
R5は、−C(O)OC1〜C6アルキル、−C3〜C6シクロアルキル、シアノ、−NR6R7、−C(O)NRaRb、−S(O)p(R11)n、−アリールまたは−ヘテロアリールであり、前記アリールおよびヘテロアリールは、1〜3個の独立したR8で任意選択により置換されており;
R6およびR7は、水素およびC1〜C6アルキルからなる群から独立して選択され;
各R8は、ハロゲン、C1〜C6アルキルおよびC1〜C6アルコキシ−、C1〜C6ハロアルキル、C1〜C6ハロアルコキシ−、シアノおよびS(O)p(C1〜C6アルキル)からなる群から独立して選択され;
各R9は、水素、C1〜C6アルキル、CrアルコキシCsアルキル、C1〜C6ハロアルキル、CrアルコキシCsハロアルキル、C2〜C6アルケニル、C2〜C6アルキニルおよび−(CRaRb)qR10からなる群から独立して選択され;
または、R4およびR9は、これらが結合する原子と一緒になって、1〜3個のヘテロ原子を含有する5〜7員環系を形成し、ここで、少なくとも1個のヘテロ原子はNであり、ならびに、いずれかの追加のヘテロ原子は、S、OおよびNから独立して選択され;
R10は、−C(O)ORc、−OC(O)Rc、−C3〜C6シクロアルキルまたは−アリール、−アリールオキシ、−ヘテロアリール、−ヘテロアリールオキシまたは−ヘテロシクリル環であり、ここで、前記環は、1〜3個の独立したR8で任意選択により置換されており;
各nは独立して、0または1であり;
pは、0、1または2であり;
各qは独立して、0、1、2、3、4、5または6であり;
rは、1、2、3、4、または5であり;
sは、1、2、3、4または5であり、および、r+sの和は6以下であり;ならびに、
R11はC1〜C6アルキルである)。 - X1がNである、請求項1に記載の式(I)の化合物。
- X1がCR1であり、および、R1がハロゲンまたはシアノである、請求項1に記載の式(I)の化合物。
- R2が、ハロゲン、シアノ、C1〜C6アルキルまたはC1〜C6ハロアルキルである、請求項1〜3のいずれか一項に記載の式(I)の化合物。
- R3において、R9が、C1〜C6アルキル、C1〜C3ハロアルキル、C1〜C3アルコキシC1〜C3アルキルまたは−(CRaRb)qR10である、請求項1〜4のいずれか一項に記載の式(I)の化合物。
- R10が、−C(O)ORc、−OC(O)Rc、シクロプロピル、シクロブチル、シクロペンチル、シクロヘキシル、または、フェニル、フェノキシ、ピリジニル、ピリミジニル、チアゾリルおよびチオフェニルから選択される環系であり、ここで、前記環系が、1〜3個の独立したR8で任意選択により置換されている、請求項5に記載の式(I)の化合物。
- R4が、水素、C1〜C4アルキル、C3〜C6アルケニル、CrアルコキシCsアルキル、CrアルキルチオCsアルキル、C3〜C6アルキニル、C1〜C3ハロアルキル、CrアルコキシCsハロアルキル、−C(O)R9および−(CRaRb)qR5からなる群から選択される、請求項1〜6のいずれか一項に記載の式(I)の化合物。
- R4が−C(O)R9であり、および、前記R9が、C1〜C3アルキル、C2〜C4アルケニルまたは−(CRaRb)qR10である、請求項7に記載の式(I)の化合物。
- R4が−(CRaRb)qR5であり、ならびに、R4において:
qが、1、2、または3であり;
RaおよびRbが独立して、水素、メチルまたはエチルであり;ならびに、
R5が、−C(O)NRaRb、−NR6R7、シアノ、−C3〜C6シクロアルキル、−アリールまたは−ヘテロアリールであり、ここで、前記アリールおよびヘテロアリールが、1〜3個の独立したR8で任意選択により置換されている、請求項7に記載の式(I)の化合物。 - R4およびR9が、これらが結合する原子と一緒になって、1〜3個のヘテロ原子を含有する5〜7員環系を形成し、ここで、少なくとも1個のヘテロ原子がNであり、ならびに、いずれかの追加のヘテロ原子がS、OおよびNから独立して選択される、請求項1〜4のいずれか一項に記載の式(I)の化合物。
- 請求項1〜10のいずれか一項に記載の式(I)の化合物、および、農学的に許容可能な配合助剤を含む除草組成物。
- 少なくとも1種の追加の殺有害生物剤をさらに含む、請求項11に記載の除草組成物。
- 前記追加の殺有害生物剤が除草剤または除草剤毒性緩和剤である、請求項12に記載の除草組成物。
- 繁殖地における雑草の防除方法であって、雑草防除量の請求項1〜10のいずれか一項に記載の化合物、または、雑草防除量の請求項11〜14のいずれか一項に記載の組成物を、前記繁殖地に適用するステップを含む防除方法。
- 除草剤としての、請求項1〜10のいずれか一項に定義されている式(I)の化合物の使用。
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GB201604970D0 (en) | 2016-05-04 |
UY37162A (es) | 2017-10-31 |
KR102423205B1 (ko) | 2022-07-19 |
CN108884069B (zh) | 2021-04-27 |
PL3433245T3 (pl) | 2022-08-01 |
WO2017162524A1 (en) | 2017-09-28 |
RU2762575C2 (ru) | 2021-12-21 |
UA124061C2 (uk) | 2021-07-14 |
EP3868749A1 (en) | 2021-08-25 |
MY197968A (en) | 2023-07-25 |
AR107953A1 (es) | 2018-07-04 |
ES2921649T3 (es) | 2022-08-30 |
BR112018069394B1 (pt) | 2022-08-02 |
CA3016207A1 (en) | 2017-09-28 |
RU2018136229A (ru) | 2020-04-23 |
BR112018069394A2 (pt) | 2019-01-22 |
RU2018136229A3 (ja) | 2020-04-30 |
AU2017239002B2 (en) | 2021-07-29 |
US20190330179A1 (en) | 2019-10-31 |
US11230538B2 (en) | 2022-01-25 |
DK3433245T3 (da) | 2022-07-11 |
HUE059462T2 (hu) | 2022-11-28 |
JP7171437B2 (ja) | 2022-11-15 |
KR20180128004A (ko) | 2018-11-30 |
EP3433245A1 (en) | 2019-01-30 |
ZA201805795B (en) | 2019-06-26 |
CN108884069A (zh) | 2018-11-23 |
BR122022000691B1 (pt) | 2023-02-23 |
RS63363B1 (sr) | 2022-07-29 |
US20210130319A1 (en) | 2021-05-06 |
EP3433245B1 (en) | 2022-04-27 |
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