JP2016514139A - 4−アミノ−6−(4−置換フェニル)−ピコリネートおよび6−アミノ−2−(4−置換フェニル)−ピリミジン−4−カルボキシレートならびに除草剤としてのそれらの使用 - Google Patents
4−アミノ−6−(4−置換フェニル)−ピコリネートおよび6−アミノ−2−(4−置換フェニル)−ピリミジン−4−カルボキシレートならびに除草剤としてのそれらの使用 Download PDFInfo
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- JP2016514139A JP2016514139A JP2016501520A JP2016501520A JP2016514139A JP 2016514139 A JP2016514139 A JP 2016514139A JP 2016501520 A JP2016501520 A JP 2016501520A JP 2016501520 A JP2016501520 A JP 2016501520A JP 2016514139 A JP2016514139 A JP 2016514139A
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- -1 4-Amino-6- (4-substituted phenyl) -picolinates Chemical class 0.000 title claims abstract description 177
- 239000004009 herbicide Substances 0.000 title abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 128
- 238000000034 method Methods 0.000 claims abstract description 54
- 150000001875 compounds Chemical class 0.000 claims description 889
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 182
- 229910052739 hydrogen Inorganic materials 0.000 claims description 103
- 229910052736 halogen Inorganic materials 0.000 claims description 102
- 150000002367 halogens Chemical group 0.000 claims description 102
- 229920002554 vinyl polymer Polymers 0.000 claims description 99
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 93
- 229910052794 bromium Inorganic materials 0.000 claims description 54
- 229910052740 iodine Inorganic materials 0.000 claims description 52
- 229910052731 fluorine Inorganic materials 0.000 claims description 46
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 40
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 33
- 230000002363 herbicidal effect Effects 0.000 claims description 31
- 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 31
- 229910052801 chlorine Inorganic materials 0.000 claims description 29
- 239000001257 hydrogen Substances 0.000 claims description 29
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 25
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 25
- 150000003839 salts Chemical class 0.000 claims description 25
- 150000002431 hydrogen Chemical group 0.000 claims description 21
- 229920006395 saturated elastomer Polymers 0.000 claims description 21
- 150000001204 N-oxides Chemical class 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 12
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 6
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 6
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 6
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 6
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 5
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 5
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 5
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000005499 phosphonyl group Chemical group 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 309
- 239000000460 chlorine Substances 0.000 description 158
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 139
- 239000000243 solution Substances 0.000 description 123
- 235000019439 ethyl acetate Nutrition 0.000 description 117
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 114
- 239000007787 solid Substances 0.000 description 109
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 103
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 96
- 238000002360 preparation method Methods 0.000 description 95
- 239000011541 reaction mixture Substances 0.000 description 93
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 90
- 125000006017 1-propenyl group Chemical group 0.000 description 85
- 239000011734 sodium Substances 0.000 description 62
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 61
- 241000196324 Embryophyta Species 0.000 description 60
- 238000006243 chemical reaction Methods 0.000 description 52
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 52
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 50
- 239000012044 organic layer Substances 0.000 description 45
- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 39
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 36
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 35
- 238000003818 flash chromatography Methods 0.000 description 35
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 34
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 34
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 30
- 238000012360 testing method Methods 0.000 description 29
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 25
- 229910004298 SiO 2 Inorganic materials 0.000 description 24
- 239000003112 inhibitor Substances 0.000 description 24
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 23
- 239000003921 oil Substances 0.000 description 23
- 235000019198 oils Nutrition 0.000 description 23
- 239000000843 powder Substances 0.000 description 23
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 23
- 238000011282 treatment Methods 0.000 description 21
- SIOXPEMLGUPBBT-UHFFFAOYSA-M picolinate Chemical class [O-]C(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-M 0.000 description 20
- 239000002904 solvent Substances 0.000 description 20
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 19
- 238000003756 stirring Methods 0.000 description 19
- 150000002148 esters Chemical class 0.000 description 17
- 239000000741 silica gel Substances 0.000 description 17
- 229910002027 silica gel Inorganic materials 0.000 description 17
- 239000012074 organic phase Substances 0.000 description 16
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 16
- 238000002390 rotary evaporation Methods 0.000 description 16
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 15
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 14
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 14
- 239000012043 crude product Substances 0.000 description 14
- 239000000047 product Substances 0.000 description 14
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 13
- 239000012141 concentrate Substances 0.000 description 13
- 230000005484 gravity Effects 0.000 description 13
- 238000000746 purification Methods 0.000 description 13
- 239000011698 potassium fluoride Substances 0.000 description 12
- 235000003270 potassium fluoride Nutrition 0.000 description 12
- 239000002689 soil Substances 0.000 description 12
- 239000000284 extract Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000003586 protic polar solvent Substances 0.000 description 11
- 239000004094 surface-active agent Substances 0.000 description 11
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 10
- 239000007921 spray Substances 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 238000004458 analytical method Methods 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- 125000005843 halogen group Chemical group 0.000 description 9
- 239000011630 iodine Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 9
- 239000011550 stock solution Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 8
- 239000003999 initiator Substances 0.000 description 8
- 238000003973 irrigation Methods 0.000 description 8
- 230000002262 irrigation Effects 0.000 description 8
- 238000012544 monitoring process Methods 0.000 description 8
- 229910000027 potassium carbonate Inorganic materials 0.000 description 8
- 238000004007 reversed phase HPLC Methods 0.000 description 8
- 238000010898 silica gel chromatography Methods 0.000 description 8
- 239000010409 thin film Substances 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 7
- 238000006069 Suzuki reaction reaction Methods 0.000 description 7
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 7
- 239000012346 acetyl chloride Substances 0.000 description 7
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 125000004414 alkyl thio group Chemical group 0.000 description 7
- 125000000304 alkynyl group Chemical group 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 229910000029 sodium carbonate Inorganic materials 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 7
- 235000015112 vegetable and seed oil Nutrition 0.000 description 7
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 6
- OFOSNAUBFUBOPC-UHFFFAOYSA-N 2,6-dichloro-5-methoxypyrimidine-4-carbaldehyde Chemical compound COC1=C(Cl)N=C(Cl)N=C1C=O OFOSNAUBFUBOPC-UHFFFAOYSA-N 0.000 description 6
- 241000219318 Amaranthus Species 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 6
- QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- PBCJIPOGFJYBJE-UHFFFAOYSA-N acetonitrile;hydrate Chemical compound O.CC#N PBCJIPOGFJYBJE-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- UBOUJNVKCFPWEB-UHFFFAOYSA-N 2,4-dichloro-6-ethenyl-5-methoxypyrimidine Chemical compound COC1=C(Cl)N=C(Cl)N=C1C=C UBOUJNVKCFPWEB-UHFFFAOYSA-N 0.000 description 5
- MRWWWZLJWNIEEJ-UHFFFAOYSA-N 4,4,5,5-tetramethyl-2-propan-2-yloxy-1,3,2-dioxaborolane Chemical compound CC(C)OB1OC(C)(C)C(C)(C)O1 MRWWWZLJWNIEEJ-UHFFFAOYSA-N 0.000 description 5
- 108010068327 4-hydroxyphenylpyruvate dioxygenase Proteins 0.000 description 5
- 102100028626 4-hydroxyphenylpyruvate dioxygenase Human genes 0.000 description 5
- 108010000700 Acetolactate synthase Proteins 0.000 description 5
- 102000000452 Acetyl-CoA carboxylase Human genes 0.000 description 5
- 108010016219 Acetyl-CoA carboxylase Proteins 0.000 description 5
- 108010018763 Biotin carboxylase Proteins 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 240000007594 Oryza sativa Species 0.000 description 5
- 235000007164 Oryza sativa Nutrition 0.000 description 5
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 239000004927 clay Substances 0.000 description 5
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- 238000002451 electron ionisation mass spectrometry Methods 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- 230000012010 growth Effects 0.000 description 5
- WPKWCOJJOVQDPB-UHFFFAOYSA-N methyl 2,6-dichloro-5-methoxypyrimidine-4-carboxylate Chemical compound COC(=O)C1=NC(Cl)=NC(Cl)=C1OC WPKWCOJJOVQDPB-UHFFFAOYSA-N 0.000 description 5
- KQCXXSKPUFSCJR-UHFFFAOYSA-N methyl 4-amino-6-chloro-3-ethenyl-5-fluoropyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=C(F)C(N)=C1C=C KQCXXSKPUFSCJR-UHFFFAOYSA-N 0.000 description 5
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 235000009566 rice Nutrition 0.000 description 5
- 238000013207 serial dilution Methods 0.000 description 5
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 5
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 5
- 235000019345 sodium thiosulphate Nutrition 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- 230000000153 supplemental effect Effects 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 4
- SQHSJJGGWYIFCD-UHFFFAOYSA-N (e)-1-diazonio-1-dimethoxyphosphorylprop-1-en-2-olate Chemical compound COP(=O)(OC)C(\[N+]#N)=C(\C)[O-] SQHSJJGGWYIFCD-UHFFFAOYSA-N 0.000 description 4
- HZNVUJQVZSTENZ-UHFFFAOYSA-N 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O HZNVUJQVZSTENZ-UHFFFAOYSA-N 0.000 description 4
- RYOVMJCNDAAHAM-UHFFFAOYSA-N 4-amino-6-chloro-5-fluoropyridine-2-carboxylic acid Chemical compound NC1=CC(C(O)=O)=NC(Cl)=C1F RYOVMJCNDAAHAM-UHFFFAOYSA-N 0.000 description 4
- 244000036975 Ambrosia artemisiifolia Species 0.000 description 4
- 244000144725 Amygdalus communis Species 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 4
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
- 239000005562 Glyphosate Substances 0.000 description 4
- 244000100545 Lolium multiflorum Species 0.000 description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 4
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 description 4
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- CNMNDVDPXMGIDC-UHFFFAOYSA-N [2,5-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-trimethylsilane Chemical compound O1C(C)(C)C(C)(C)OB1C1=CC(F)=C([Si](C)(C)C)C=C1F CNMNDVDPXMGIDC-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000012267 brine Substances 0.000 description 4
- 235000011089 carbon dioxide Nutrition 0.000 description 4
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010828 elution Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 239000003337 fertilizer Substances 0.000 description 4
- 230000035784 germination Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 125000000262 haloalkenyl group Chemical group 0.000 description 4
- 125000004438 haloalkoxy group Chemical group 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910001507 metal halide Inorganic materials 0.000 description 4
- 150000005309 metal halides Chemical class 0.000 description 4
- FRMBCYILCYTPHY-UHFFFAOYSA-N methyl 4-amino-3,6-dichloropyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=CC(N)=C1Cl FRMBCYILCYTPHY-UHFFFAOYSA-N 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- 235000015097 nutrients Nutrition 0.000 description 4
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 4
- KXCAEQNNTZANTK-UHFFFAOYSA-N stannane Chemical compound [SnH4] KXCAEQNNTZANTK-UHFFFAOYSA-N 0.000 description 4
- 229910000080 stannane Inorganic materials 0.000 description 4
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- WETFWFAAKQWRCA-UHFFFAOYSA-N methyl 4-acetamido-6-(4-bromo-2,3-difluorophenyl)-3-chloropyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Br)=CC=2)F)=C1 WETFWFAAKQWRCA-UHFFFAOYSA-N 0.000 description 2
- JTHRPOUXRHBNBA-UHFFFAOYSA-N methyl 4-acetamido-6-(4-bromo-2,5-difluorophenyl)-3-chloropyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=CC(Br)=C(F)C=2)F)=C1 JTHRPOUXRHBNBA-UHFFFAOYSA-N 0.000 description 2
- JPHQWZRJJOYJAC-UHFFFAOYSA-N methyl 4-acetamido-6-(4-bromo-3-fluorophenyl)-3-chloropyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(Br)=CC=2)=C1 JPHQWZRJJOYJAC-UHFFFAOYSA-N 0.000 description 2
- KIKNEFFJHGIUKZ-UHFFFAOYSA-N methyl 4-amino-3,6-dichloro-5-fluoropyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=C(F)C(N)=C1Cl KIKNEFFJHGIUKZ-UHFFFAOYSA-N 0.000 description 2
- HNVKGYSSRCIGCA-UHFFFAOYSA-N methyl 4-amino-3,6-dichloro-5-iodopyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=C(I)C(N)=C1Cl HNVKGYSSRCIGCA-UHFFFAOYSA-N 0.000 description 2
- NCHGKZMCULPZCI-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-fluoro-6-[4-(2-trimethylsilylethynyl)phenyl]pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(=CC=2)C#C[Si](C)(C)C)=C1F NCHGKZMCULPZCI-UHFFFAOYSA-N 0.000 description 2
- JZJQFGQWNFRFBA-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-methyl-6-[4-(2-trimethylsilylethynyl)phenyl]pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(=CC=2)C#C[Si](C)(C)C)=C1C JZJQFGQWNFRFBA-UHFFFAOYSA-N 0.000 description 2
- RFSNAISBBNPURU-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(2,3-difluoro-4-iodophenyl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(I)=CC=2)F)=C1 RFSNAISBBNPURU-UHFFFAOYSA-N 0.000 description 2
- HTGCDSKBLGRCPN-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(3-fluoro-4-formylphenyl)-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(C=O)=CC=2)=C1C HTGCDSKBLGRCPN-UHFFFAOYSA-N 0.000 description 2
- ZEFOCXXGHMNVEA-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(3-fluoro-4-iodophenyl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(I)=CC=2)=C1 ZEFOCXXGHMNVEA-UHFFFAOYSA-N 0.000 description 2
- PBDMUJHAYZEOJM-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(3-fluoro-4-trimethylsilylphenyl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(=CC=2)[Si](C)(C)C)=C1 PBDMUJHAYZEOJM-UHFFFAOYSA-N 0.000 description 2
- ORTBHEUCRUVIMT-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-cyano-2-fluorophenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=CC(=CC=2)C#N)F)=C1F ORTBHEUCRUVIMT-UHFFFAOYSA-N 0.000 description 2
- BJOJJHXDNOFITB-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-cyano-3-fluorophenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(C#N)=CC=2)=C1F BJOJJHXDNOFITB-UHFFFAOYSA-N 0.000 description 2
- DHRUSJRLJCUXBW-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-cyano-3-fluorophenyl)-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(C#N)=CC=2)=C1C DHRUSJRLJCUXBW-UHFFFAOYSA-N 0.000 description 2
- BOFQAQVPSDZUMV-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-ethynyl-3-fluorophenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(C#C)=CC=2)=C1F BOFQAQVPSDZUMV-UHFFFAOYSA-N 0.000 description 2
- KTQTWZHVIGALFO-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-ethynylphenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(=CC=2)C#C)=C1F KTQTWZHVIGALFO-UHFFFAOYSA-N 0.000 description 2
- LBBHGXSRQHIEET-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-[4-(difluoromethoxy)phenyl]-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(OC(F)F)=CC=2)=C1C LBBHGXSRQHIEET-UHFFFAOYSA-N 0.000 description 2
- UKWLCOPQJRFLSD-UHFFFAOYSA-N methyl 4-amino-3-ethenyl-5-fluoro-6-(4-formylphenyl)pyridine-2-carboxylate Chemical compound NC1=C(C=C)C(C(=O)OC)=NC(C=2C=CC(C=O)=CC=2)=C1F UKWLCOPQJRFLSD-UHFFFAOYSA-N 0.000 description 2
- MVDKCXGLDYCLLZ-UHFFFAOYSA-N methyl 4-amino-6-(4-bromo-2,3-difluorophenyl)-3-chloro-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Br)=CC=2)F)=C1F MVDKCXGLDYCLLZ-UHFFFAOYSA-N 0.000 description 2
- BFNZMSLWDVLSKY-UHFFFAOYSA-N methyl 4-amino-6-(4-bromo-2,3-difluorophenyl)-3-chloropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Br)=CC=2)F)=C1 BFNZMSLWDVLSKY-UHFFFAOYSA-N 0.000 description 2
- FTXUITVKEMXOGJ-UHFFFAOYSA-N methyl 4-amino-6-(4-bromo-2,5-difluorophenyl)-3-chloro-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=CC(Br)=C(F)C=2)F)=C1F FTXUITVKEMXOGJ-UHFFFAOYSA-N 0.000 description 2
- INSNBBAQFQYSTR-UHFFFAOYSA-N methyl 4-amino-6-(4-bromo-3-fluorophenyl)-3,5-dichloropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(Br)=CC=2)=C1Cl INSNBBAQFQYSTR-UHFFFAOYSA-N 0.000 description 2
- PAPKJMWZRCOVKA-UHFFFAOYSA-N methyl 4-amino-6-(4-bromo-3-fluorophenyl)-3-chloropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(Br)=CC=2)=C1 PAPKJMWZRCOVKA-UHFFFAOYSA-N 0.000 description 2
- IRKBBKUZUCFISI-UHFFFAOYSA-N methyl 4-amino-6-(4-bromophenyl)-3-chloro-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(Br)=CC=2)=C1F IRKBBKUZUCFISI-UHFFFAOYSA-N 0.000 description 2
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- JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 description 1
- LYPWWQLKWQNQKV-UHFFFAOYSA-N methyl 2-[5-ethyl-2-[[4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]phenoxy]methyl]phenoxy]propanoate Chemical compound COC(=O)C(C)OC1=CC(CC)=CC=C1COC1=CC=C(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)C=C1 LYPWWQLKWQNQKV-UHFFFAOYSA-N 0.000 description 1
- ZTYVMAQSHCZXLF-UHFFFAOYSA-N methyl 2-[[4,6-bis(difluoromethoxy)pyrimidin-2-yl]carbamoylsulfamoyl]benzoate Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC(F)F)=CC(OC(F)F)=N1 ZTYVMAQSHCZXLF-UHFFFAOYSA-N 0.000 description 1
- ZTURLTDPSGZVHQ-UHFFFAOYSA-N methyl 4-[bis[(2-methylpropan-2-yl)oxycarbonyl]amino]-3-chloro-6-(4-chloro-3-fluorophenyl)-5-fluoropyridine-2-carboxylate Chemical compound CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)C1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(Cl)=CC=2)=C1F ZTURLTDPSGZVHQ-UHFFFAOYSA-N 0.000 description 1
- GOFMPWFEKKZLEN-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-(2,5-difluoro-4-trimethylsilylphenyl)pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=CC(=C(F)C=2)[Si](C)(C)C)F)=C1 GOFMPWFEKKZLEN-UHFFFAOYSA-N 0.000 description 1
- KKYGRAZUDDLVHY-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-iodopyridine-2-carboxylate Chemical compound COC(=O)C1=NC(I)=CC(NC(C)=O)=C1Cl KKYGRAZUDDLVHY-UHFFFAOYSA-N 0.000 description 1
- URYYFLIQTVTPKE-UHFFFAOYSA-N methyl 4-acetamido-6-(4-amino-2,3,6-trifluorophenyl)-3-chloropyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(N)=CC=2F)F)=C1 URYYFLIQTVTPKE-UHFFFAOYSA-N 0.000 description 1
- JAGCWBGANJWMHB-UHFFFAOYSA-N methyl 4-acetamido-6-(4-bromophenyl)-3-chloropyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(Br)=CC=2)=C1 JAGCWBGANJWMHB-UHFFFAOYSA-N 0.000 description 1
- JVRRFCJGMDGZNY-UHFFFAOYSA-N methyl 4-amino-3,6-dichloro-5-methylpyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=C(C)C(N)=C1Cl JVRRFCJGMDGZNY-UHFFFAOYSA-N 0.000 description 1
- KNPHDAGNWRUJQS-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-fluoro-6-trimethylstannylpyridine-2-carboxylate Chemical compound COC(=O)C1=NC([Sn](C)(C)C)=C(F)C(N)=C1Cl KNPHDAGNWRUJQS-UHFFFAOYSA-N 0.000 description 1
- KEAKTSIHENLLPO-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(2,3-difluoro-4-formylphenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(C=O)=CC=2)F)=C1F KEAKTSIHENLLPO-UHFFFAOYSA-N 0.000 description 1
- IDQBCURGVLNYCV-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(2,5-difluoro-4-iodophenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=CC(I)=C(F)C=2)F)=C1F IDQBCURGVLNYCV-UHFFFAOYSA-N 0.000 description 1
- PJCVRUXGHHZVMB-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(3-fluoro-4-trimethylsilylphenyl)-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(=CC=2)[Si](C)(C)C)=C1C PJCVRUXGHHZVMB-UHFFFAOYSA-N 0.000 description 1
- XQTZNXRUDWEMGM-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-chloro-3-fluorophenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(Cl)=CC=2)=C1F XQTZNXRUDWEMGM-UHFFFAOYSA-N 0.000 description 1
- OPOHGOGCTSUMMV-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-cyanophenyl)-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(=CC=2)C#N)=C1C OPOHGOGCTSUMMV-UHFFFAOYSA-N 0.000 description 1
- HYIDDAKQWJXMIL-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-ethynyl-3-fluorophenyl)-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(C#C)=CC=2)=C1C HYIDDAKQWJXMIL-UHFFFAOYSA-N 0.000 description 1
- RYRHEHYDDMZEEI-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-ethynylphenyl)-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(=CC=2)C#C)=C1C RYRHEHYDDMZEEI-UHFFFAOYSA-N 0.000 description 1
- YIQAOCODJHEVOS-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-[3-fluoro-4-(trifluoromethyl)phenyl]-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(=CC=2)C(F)(F)F)=C1C YIQAOCODJHEVOS-UHFFFAOYSA-N 0.000 description 1
- AWVGHQWCYFSYDK-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-[3-fluoro-4-(trifluoromethyl)phenyl]pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(=CC=2)C(F)(F)F)=C1 AWVGHQWCYFSYDK-UHFFFAOYSA-N 0.000 description 1
- OAOQRMAGHNANRT-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(OC(F)F)=CC=2)=C1F OAOQRMAGHNANRT-UHFFFAOYSA-N 0.000 description 1
- PZUMSDCIWAESCE-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-iodopyridine-2-carboxylate Chemical compound COC(=O)C1=NC(I)=CC(N)=C1Cl PZUMSDCIWAESCE-UHFFFAOYSA-N 0.000 description 1
- DHXPHFPOWYACCH-UHFFFAOYSA-N methyl 4-amino-3-ethenyl-5-fluoro-6-(4-iodophenyl)pyridine-2-carboxylate Chemical compound NC1=C(C=C)C(C(=O)OC)=NC(C=2C=CC(I)=CC=2)=C1F DHXPHFPOWYACCH-UHFFFAOYSA-N 0.000 description 1
- OCXWEKVDGGPQIQ-UHFFFAOYSA-N methyl 4-amino-3-ethenyl-6-(4-ethynylphenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(C=C)C(C(=O)OC)=NC(C=2C=CC(=CC=2)C#C)=C1F OCXWEKVDGGPQIQ-UHFFFAOYSA-N 0.000 description 1
- DJARJCVEIVICJW-UHFFFAOYSA-N methyl 4-amino-5-bromo-3-chloro-6-(2,5-difluoro-4-trimethylsilylphenyl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=CC(=C(F)C=2)[Si](C)(C)C)F)=C1Br DJARJCVEIVICJW-UHFFFAOYSA-N 0.000 description 1
- CBXHTAVWBUOLQX-UHFFFAOYSA-N methyl 4-amino-6-(4-aminophenyl)-3-ethenyl-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(C=C)C(C(=O)OC)=NC(C=2C=CC(N)=CC=2)=C1F CBXHTAVWBUOLQX-UHFFFAOYSA-N 0.000 description 1
- WMOVVJBSJGDBQH-UHFFFAOYSA-N methyl 4-amino-6-(4-bromo-3-fluorophenyl)-3-chloro-5-methylpyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=C(F)C(Br)=CC=2)=C1C WMOVVJBSJGDBQH-UHFFFAOYSA-N 0.000 description 1
- FCGPWQKPZOMANG-UHFFFAOYSA-N methyl 4-amino-6-(4-bromophenyl)-3-ethenyl-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(C=C)C(C(=O)OC)=NC(C=2C=CC(Br)=CC=2)=C1F FCGPWQKPZOMANG-UHFFFAOYSA-N 0.000 description 1
- XGFMRQLOXJEMLI-UHFFFAOYSA-N methyl 4-amino-6-[2,3-difluoro-4-(trifluoromethyl)phenyl]-3-ethenyl-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(C=C)C(C(=O)OC)=NC(C=2C(=C(F)C(=CC=2)C(F)(F)F)F)=C1F XGFMRQLOXJEMLI-UHFFFAOYSA-N 0.000 description 1
- MXSMNAYNNWXEQP-UHFFFAOYSA-N methyl 4-amino-6-bromo-3,5-difluoropyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Br)=C(F)C(N)=C1F MXSMNAYNNWXEQP-UHFFFAOYSA-N 0.000 description 1
- WUCUJDCRYGSBBL-UHFFFAOYSA-N methyl 4-amino-6-chloro-5-fluoro-3-iodopyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=C(F)C(N)=C1I WUCUJDCRYGSBBL-UHFFFAOYSA-N 0.000 description 1
- OHCUEIWJGFSBLH-UHFFFAOYSA-N methyl 4-amino-6-chloro-5-fluoro-3-methoxypyridine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=C(F)C(N)=C1OC OHCUEIWJGFSBLH-UHFFFAOYSA-N 0.000 description 1
- YEUYMEGMXJWEDE-UHFFFAOYSA-N methyl 6-amino-2,5-dichloropyrimidine-4-carboxylate Chemical compound COC(=O)C1=NC(Cl)=NC(N)=C1Cl YEUYMEGMXJWEDE-UHFFFAOYSA-N 0.000 description 1
- ZQHHCZXNYJZEBY-UHFFFAOYSA-N methyl 6-amino-2-(2,3-difluoro-4-formylphenyl)-5-methoxypyrimidine-4-carboxylate Chemical compound NC1=C(OC)C(C(=O)OC)=NC(C=2C(=C(F)C(C=O)=CC=2)F)=N1 ZQHHCZXNYJZEBY-UHFFFAOYSA-N 0.000 description 1
- PVNLGAXNNKRZFK-UHFFFAOYSA-N methyl 6-amino-2-(2,3-difluoro-4-iodophenyl)-5-methoxypyrimidine-4-carboxylate Chemical compound NC1=C(OC)C(C(=O)OC)=NC(C=2C(=C(F)C(I)=CC=2)F)=N1 PVNLGAXNNKRZFK-UHFFFAOYSA-N 0.000 description 1
- HQKGVWBHGFYNHQ-UHFFFAOYSA-N methyl 6-amino-2-(2,5-difluoro-4-trimethylsilylphenyl)-5-methoxypyrimidine-4-carboxylate Chemical compound NC1=C(OC)C(C(=O)OC)=NC(C=2C(=CC(=C(F)C=2)[Si](C)(C)C)F)=N1 HQKGVWBHGFYNHQ-UHFFFAOYSA-N 0.000 description 1
- HZTUJBORYGIYIQ-UHFFFAOYSA-N methyl 6-amino-2-(2-fluoro-4-formylphenyl)-5-methoxypyrimidine-4-carboxylate Chemical compound NC1=C(OC)C(C(=O)OC)=NC(C=2C(=CC(C=O)=CC=2)F)=N1 HZTUJBORYGIYIQ-UHFFFAOYSA-N 0.000 description 1
- YDHPNKFKYAKBET-UHFFFAOYSA-N methyl 6-amino-2-(2-fluoro-4-trimethylsilylphenyl)-5-methoxypyrimidine-4-carboxylate Chemical compound NC1=C(OC)C(C(=O)OC)=NC(C=2C(=CC(=CC=2)[Si](C)(C)C)F)=N1 YDHPNKFKYAKBET-UHFFFAOYSA-N 0.000 description 1
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- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
- CCRMAATUKBYMPA-UHFFFAOYSA-N trimethyltin Chemical compound C[Sn](C)C.C[Sn](C)C CCRMAATUKBYMPA-UHFFFAOYSA-N 0.000 description 1
- PIHCREFCPDWIPY-UHFFFAOYSA-N tris[2-(2,4-dichlorophenoxy)ethyl] phosphite Chemical compound ClC1=CC(Cl)=CC=C1OCCOP(OCCOC=1C(=CC(Cl)=CC=1)Cl)OCCOC1=CC=C(Cl)C=C1Cl PIHCREFCPDWIPY-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
- 235000020234 walnut Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene 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
- C07D213/06—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 containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/04—Oxygen or sulfur attached to an aliphatic side-chain of a carbocyclic ring system
-
- 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
-
- 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
- C07D213/79—Acids; Esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- 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
- C07D213/73—Unsubstituted amino or imino radicals
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- 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
本出願は、2013年3月15日に出願された米国特許出願第13/840,233号の利益を主張し、この全体を参照により本明細書に組み込む。
Xは、NまたはCYであり;ここで、Yは水素、ハロゲン、C1〜C3アルキル、C1〜C3ハロアルキル、C1〜C3アルコキシ、C1〜C3ハロアルコキシ、C1〜C3アルキルチオまたはC1〜C3ハロアルキルチオであり;
R1はOR1’であり、ここで、R1’はH、C1〜C8アルキルまたはC7〜C10アリールアルキルであり;
R2は、ハロゲン、C1〜C4アルキル、C1〜C4ハロアルキル、C2〜C4アルケニル、C2〜C4ハロアルケニル、C2〜C4アルキニル、C2〜C4ハロアルキニル、C1〜C4アルコキシ、C1〜C4ハロアルコキシ、C1〜C4アルキルチオ、C1〜C4ハロアルキルチオ、アミノ、C1〜C4アルキルアミノ、C2〜C4ハロアルキルアミノ、ホルミル、(C1〜C3アルキル)カルボニル、(C1〜C3ハロアルキル)カルボニル、シアノ、または式−CR17=CR18−SiR19R20R21の基であり、ここでR17は、水素、FまたはClであり;R18は水素、F、Cl、C1〜C4アルキルまたはC1〜C4ハロアルキルであり;R19、R20およびR21は、各々独立して、C1〜C10アルキル、C3〜C6シクロアルキル、C1〜C10ハロアルキル、C3〜C6ハロシクロアルキル、フェニル、置換フェニル、C1〜C10アルコキシまたはOHであり;
R3およびR4は、各々独立して、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ハロアルケニル、C3〜C6アルキニル、ヒドロキシ、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、ホルミル、(C1〜C3アルキル)カルボニル、(C1〜C3ハロアルキル)カルボニル、(C1〜C6アルコキシ)カルボニル、(C1〜C6アルキル)カルバミル、C1〜C6アルキルスルホニル、トリ(C1〜C6アルキル)シリル、ジ(C1〜C6アルキル)ホスホニル、であるか、またはR3およびR4は、それらが結合している窒素原子と一緒に、5員もしくは6員の飽和環を形成するか、またはR3およびR4は一緒になって、=CR3’R4’を表し、ここで、R3’およびR4’は、各々独立して、水素、C1〜C6アルキル、C3〜C6アルケニル、C3〜C6アルキニル、C1〜C6アルコキシもしくはC1〜C6アルキルアミノであり、またはR3’およびR4’は、それらが結合している炭素原子と一緒に、5員もしくは6員の飽和環を形成し;
Arは、Ar1、Ar2、Ar3、Ar4、Ar5またはAr6であり:
X1は、H、F、Br、I、エチニル、ハロエチニル、CF2H、OCF2H、OCF3、CN、CONH2、CO2H、CO2CH3またはNO2であり;
X2は、H、F、Cl、Br、I、エチニル、ハロエチニル、CH3、CFH2、CF2H、CF3、OCF2H、OCF3、CN、CONH2、CO2HまたはNO2であり;
X3は、H、F、Br、I、エチニル、ハロエチニル、CH3、CFH2、CF2H、CF3、OCF2H、OCF3、CN、CONH2、CO2HまたはNO2であり;
ここで、
a)Arが、
ただし、
i)XがNである場合、R2はClまたはビニルではなく;
ii)R2がClであり、XがCHである場合、X1はH、F、OCF3またはCNではなく;
iii)R2がOCH3であり、XがCFである場合、X1はF、I、CNまたはエチニルではなく;
iv)XがCClである場合、X1はHではなく;
b)Arが、
ただし、
i)XがNである場合、R2はClではなく;
ii)R2がOCH3またはビニルであり、XがNである場合、X2はClではなく;
iii)R2がClであり、XがCHである場合、X2はClではなく;
iv)R2がOCH3であり、XがCFである場合、X2はCl、Br、IまたはCF3ではなく;
c)Arが、
ただし、
i)XがNである場合、R2はClではなく;
ii)R2がOCH3であり、XがNである場合、X3はCH3ではなく;
iii)R2がClであり、XがCHである場合、X3はH、FまたはCH3ではなく;
iv)R2がOCH3であり、XがCFである場合、X3はBrまたはIではなく;
d)Arが、
ただし、
i)XがNである場合、R2はClではなく;
ii)R2がOCH3またはビニルであり、XがNである場合、X2はClではなく;
iii)R2がClであり、XがCHである場合、X2はFではなく;
iv)R2がOCH3であり、XがCFである場合、X2はCl、Br、IまたはCF3ではなく;
e)Arが、
ただし、
i)R2がClであり、XがNである場合、X3はCH3ではなく;
ii)XがCFであり、R2がOCH3である場合、X3はBrまたはIではなく;
f)Arが、
またはそのN−オキシドもしくは農業的に許容される塩である。
本明細書で使用される場合、除草剤および除草活性成分は、適切な量で施用される場合に望ましくない植生を防除する化合物を意味する。
R13R14R15R16N+
式中、R13、R14、R15およびR16は各々、水素またはC1〜C12アルキル、C3〜C12アルケニルもしくはC3〜C12アルキニルを独立して表し、これらの各々は、ヒドロキシ基、C1〜C4アルコキシ基、C1〜C4アルキルチオ基またはフェニル基などの1個または複数の置換基によって任意選択により置換されているが、ただし、R13、R14、R15およびR16は、立体適合性である。追加として、任意の2つのR13、R14、R15およびR16は一緒に、1個から12個の炭素原子および最大2個までの酸素原子または硫黄原子を含有する脂肪族二官能性部分を表し得る。式(I)の化合物の塩は、水酸化ナトリウムなどの金属水酸化物、アンモニア、トリメチルアミン、ジエタノールアミン、2−メチル−チオプロピルアミン、ビスアリルアミン、2−ブトキシエチルアミン、モルホリン、シクロドデシルアミンもしくはベンジルアミンなどのアミン、または水酸化テトラメチルアンモニウムもしくは水酸化コリンなどの水酸化テトラアルキルアンモニウムを用いる式(I)の化合物の処理によって調製することができる。式(I)の化合物のアミン塩は、式(I)の化合物の有用な形態または誘導体であり、なぜならば、それらは水溶性であり、望ましい水性ベースの除草組成物の調製に役立つからである。
本明細書で使用される場合、「アルコキシ」は、Rが上記で定義されている通りのアルキルである式R−O−の基を指す。別段に特定されていない限り、RがC1〜C8アルキル基であるアルコキシ基が意図される。例としては、以下に限定されないが、メトキシ、エトキシ、プロポキシ、1−メチル−エトキシ、ブトキシ、1−メチル−プロポキシ、2−メチル−プロポキシ、1,1−ジメチル−エトキシ、ペントキシ、1−メチル−ブチルオキシ、2−メチル−ブトキシ、3−メチル−ブトキシ、2,2−ジ−メチル−プロポキシ、1−エチル−プロポキシ、ヘキソキシ、1,1−ジメチル−プロポキシ、1,2−ジメチル−プロポキシ、1−メチル−ペントキシ、2−メチル−ペントキシ、3−メチル−ペントキシ、4−メチル−ペノキシ、1,1−ジメチル−ブトキシ、1,2−ジメチル−ブトキシ、1,3−ジメチル−ブトキシ、2,2−ジメチル−ブトキシ、2,3−ジメチル−ブトキシ、3,3−ジメチル−ブトキシ、1−エチル−ブトキシ、2−エチルブトキシ、1,1,2−トリメチル−プロポキシ、1,2,2−トリメチル−プロポキシ、1−エチル−1−メチル−プロポキシ、および1−エチル−2−メチル−プロポキシが挙げられる。
化合物
本明細書において提供されるのは、本明細書において(例えば、上記の要約において)定義されている通りの式(I)の化合物、ならびにそのN−オキシドおよび農業的に許容される塩である。
Arは、Ar1、Ar2、Ar3、Ar4、Ar5およびAr6からなる群から選択され;
R1は、R1’がHまたはC1〜C8アルキルであるOR1’であり;
R2は、ハロゲン、C2〜C4アルケニル、C2〜C4ハロアルケニル、C1〜C4アルコキシ、C1〜C4ハロアルコキシ、C1〜C4アルキルチオまたはC1〜C4ハロアルキルチオであり;
R3およびR4は、各々独立して、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ハロアルケニル、C3〜C6アルキニル、ホルミル、(C1〜C3アルキル)カルボニル、(C1〜C3ハロアルキル)カルボニル、(C1〜C6アルコキシ)カルボニル、(C1〜C6アルキル)カルバミル、トリ(C1〜C6アルキル)シリルであるか、またはR3およびR4は、一緒になって、R3’およびR4’が各々独立して水素、C1〜C6アルキル、C3〜C6アルケニル、C3〜C6アルキニル、C1〜C6アルコキシまたはC1〜C6アルキルアミノである=CR3’R4’を表し;
Xは、NまたはCYであり、ここでYは、水素、ハロゲン、C1〜C3アルキル、C1〜C3ハロアルキル、C1〜C3アルコキシ、C1〜C3ハロアルコキシ、C1〜C3アルコキシ、C1〜C3アルキルチオまたはC1〜C3ハロアルキルチオである。
またはそのN−オキシドもしくは農業的に許容される塩が本明細書において提供される。
i)XがNである場合、R2はClまたはビニルではなく;
ii)R2がClであり、XがCHである場合、X1はH、F、OCF3またはCNではなく;
iii)R2が合OCH3であり、XがCFである場合、X1はF、I、CNまたはエチニルではなく;
iv)XがCClである場合、X1はHではない。
i)XがNである場合、R2はClではなく;
ii)R2がOCH3またはビニルであり、XがNである場合、X2はClではなく;
iii)R2がClであり、XがCHである場合、X2はClではなく;
iv)R2がOCH3であり、XがCFである場合、X2はCl、Br、IまたはCF3ではない。
i)XがNである場合、R2はClではなく;
ii)R2がOCH3であり、XがNである場合、X3はCH3ではなく;
iii)R2がClであり、XがCHである場合、X3はH、FまたはCH3ではなく;
iv)R2がOCH3であり、XがCFである場合、X3はBrまたはIではない。
i)XがNである場合、R2はClではなく;
ii)R2がOCH3またはビニルであり、XがNである場合、X2はClではなく;
iii)R2がClであり、XがCHである場合、X2はFではなく;
iv)R2がOCH3であり、XがCFである場合、X2はCl、Br、IまたはCF3ではない。
i)R2がClであり、XがNである場合、X3はCH3ではなく;
ii)XがCFであり、R2がOCH3である場合、X3はBrまたはIではない。
該化合物を調製する方法
式(I)の化合物を合成するための例証的な手順を下記に提供する。
組成物および方法
一部の実施形態において、本明細書において提供される化合物は、少なくとも1種の農業的に許容されるアジュバントまたは担体と一緒に化合物の除草有効量を含有する混合物中に用いられる。例証的なアジュバントまたは担体としては、例えば作物の存在下で選択的雑草防除のための組成物を施用する際に用いられる濃度で、貴重な作物に対して植物毒性もしくは有意に植物毒性ではない、および/または本明細書において提供される化合物または他の組成物成分と化学的に反応しないもしくは有意に反応しないものが挙げられる。こうした混合物は、雑草もしくはそれらの場所への直接施用のために設計することができるか、または施用の前に追加の担体およびアジュバントで希釈される濃縮物もしくは処方物であってよい。それらは、例えば粉剤、顆粒、水分散性顆粒もしくは水和剤などの固体、または乳剤、溶液、エマルジョンもしくは懸濁液などの液体であってよい。それらは、プレミックスとしても提供され得るか、またはタンク混合もされ得る。
概論:フッ素スペクトルをBruker DRX400分光計上にて376MHzで獲得した。該スペクトルを外部標準としてトリクロロフルオロメタン(CFCl3)に対する参照とし、プロトンデカップリングを用いて典型的に行った。
[実施例1]
メチル4−アミノ−3,6−ジクロロピコリネート(ヘッドA)の調製
[実施例2]
メチル4−アミノ−3,6−ジクロロ−5−フルオロピコリネート(ヘッドB)の調製
[実施例3]
2,6−ジクロロ−5−メトキシ−4−ビニルピリミジンの調製
[実施例4]
2,6−ジクロロ−5−メトキシ−ピリミジン−4−カルバルデヒドの調製
[実施例5]
メチル2,6−ジクロロ−5−メトキシ−ピリミジン−4−カルボキシレートの調製
[実施例6]
メチル6−アミノ−2−クロロ−5−メトキシ−ピリミジン−4−カルボキシレート(ヘッドC)の調製
[実施例7]
メチル4−アミノ−3,6−ジクロロ−5−ヨードピコリネートの調製
[実施例8]
メチル4−アミノ−3,6−ジクロロ−5−メチルピコリネート(ヘッドD)の調製
[実施例9]
メチル6−アミノ−2,5−ジクロロピリミジン−4−カルボキシレート(ヘッドE)の調製
[実施例10]
メチル4−アミノ−6−クロロ−5−フルオロ−3−メトキシピコリネート(ヘッドF)の調製
[実施例11]
メチル4−アミノ−6−クロロ−5−フルオロ−3−ビニルピコリネート(ヘッドG)の調製
[実施例12]
メチル4−アミノ−3,5,6−トリクロロピコリネート(ヘッドH)の調製
[実施例13]
メチル4−アミノ−6−ブロモ−3−クロロ−5−フルオロピコリネート(ヘッドI)の調製
[実施例14]
メチル4−アミノ−3−クロロ−5−フルオロ−6−(トリメチルスタンニル)ピコリネート(ヘッドJ)の調製
[実施例15]
メチル4−アセトアミド−3−クロロ−6−(トリメチルスタンニル)−ピコリネート(ヘッドK)の調製
[実施例16]
メチル4−アセトアミド−3,6−ジクロロピコリネート(ヘッドL)の調製
[実施例17]
メチル4−アミノ−3−クロロ−6−ヨードピコリネート(ヘッドM)の調製
[実施例18]
メチル4−アセトアミド−3−クロロ−6−ヨードピコリネート(ヘッドN)の調製
[実施例19]
メチル4−アミノ−6−ブロモ−3,5−ジフルオロピコリネート(ヘッドO)の調製
[実施例20]
メチル6−アミノ−2−クロロ−5−ビニルピリミジン−4−カルボキシレート(ヘッドP)の調製
[実施例22]
(4−ブロモ−2−フルオロフェニル)トリメチルシランの調製
[実施例23]
(2−フルオロ−4−(4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン−2−イル)フェニル)トリメチルシランの調製
実施例23に開示した手順に従って、以下の化合物を作製した:
2−(4−(ジフルオロメチル)フェニル)−4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン
2−(4−(ジフルオロメチル)−3−フルオロフェニル)−4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン
[実施例24]
(2,3−ジフルオロ−4−(4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン−2−イル)フェニル)トリメチルシランの調製
[実施例25]
(3−フルオロ−4−(4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン−2−イル)フェニル)トリメチルシランの調製
[実施例26]
2,3,5−トリフルオロ−4−ヨードアニリンの調製
[実施例27]
4−ブロモ−1−(ジフルオロメトキシ)−2−フルオロベンゼンの調製
1−ブロモ−4−(ジフルオロメトキシ)−2−フルオロベンゼン
1−ブロモ−4−(ジフルオロメトキシ)−2,3−ジフルオロベンゼン
[実施例28]
2−(4−(ジフルオロメトキシ)−3−フルオロフェニル)−4,4,5,5−テトラメチル−1,3,2−ジオキサボロランの調製
2−(4−(ジフルオロメトキシ)−2−フルオロフェニル)−4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン
2−(4−(ジフルオロメトキシ)−2,3−ジフルオロフェニル)−4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン
[実施例29]
1,4−ジフルオロ−2−ヨード−5−(トリフルオロメチル)ベンゼンの調製
[実施例30]
2−(2,5−ジフルオロ−4−(トリフルオロメチル)フェニル)−4,4,5,5−テトラメチル−1,3,2−ジオキサボロランの調製
[実施例31]
4−ブロモ−2,5−ジフルオロベンズアルデヒドの調製
[実施例32]
(E)−4−ブロモ−2,5−ジフルオロベンズアルデヒドオキシムの調製
[実施例33]
4−ブロモ−2,5−ジフルオロベンゾニトリルの調製
[実施例34]
1−ブロモ−4−(ジフルオロメチル)−2,5−ジフルオロベンゼンの調製
[実施例35]
1−ブロモ−4−(ジフルオロメトキシ)−2,5−ジフルオロベンゼンの調製
[実施例36]
ボロン酸合成の一般的手順
(4−(ジフルオロメトキシ)−2,5−ジフルオロフェニル)ボロン酸
(4−(ジフルオロメチル)−2,5−ジフルオロフェニル)ボロン酸
[実施例37]
ボロン酸合成の一般的手順(方法A)
(2,5−ジフルオロ−4−メチルフェニル)ボロン酸
[実施例38]
ボロン酸合成の一般的手順(方法B)
(4−シアノ−2,5−ジフルオロフェニル)ボロン酸
[実施例39]
メチル4−アミノ−3−クロロ−6−(3−フルオロ−4−(トリメチルシリル)フェニル)ピコリネートの調製
メチル4−アミノ−3,5−ジクロロ−6−(3−フルオロ−4−(トリメチルシリル)フェニル)ピコリネート
メチル6−アミノ−2−(3−フルオロ−4−(トリメチルシリル)フェニル)−5−メトキシピリミジン−4−カルボキシレート
メチル4−アセトアミド−3−クロロ−6−(3−フルオロ−4−(トリメチルシリル)フェニル)ピコリネート
メチル4−アミノ−3−クロロ−6−(4−シアノ−2−フルオロフェニル)−5−フルオロピコリネート(化合物44)
メチル6−アミノ−2−(3−フルオロ−4−(トリフルオロメチル)フェニル)−5−ビニルピリミジン−4−カルボキシレート(化合物137)
メチル6−アミノ−2−(4−シアノ−2−フルオロフェニル)−5−ビニルピリミジン−4−カルボキシレート(化合物98)
メチル6−アミノ−2−(4−アミノフェニル)−5−ビニルピリミジン−4−カルボキシレート
メチル6−アミノ−2−(2,3,4−トリフルオロフェニル)−5−ビニルピリミジン−4−カルボキシレート(化合物197)
[実施例40]
メチル4−アミノ−3−クロロ−6−(3−フルオロ−4−(トリフルオロメチル)フェニル)ピコリネート(化合物29)の調製
メチル4−アミノ−3−クロロ−6−(4−シアノフェニル)−5−メチルピコリネート(化合物83)
メチル4−アミノ−3−クロロ−6−(4−(ジフルオロメトキシ)フェニル)−5−メチルピコリネート(化合物111)
メチル4−アミノ−3−クロロ−5−メチル−6−(4−(トリメチルシリル)フェニル)ピコリネート
メチル4−アミノ−3−クロロ−6−(3−フルオロ−4−(トリメチルシリル)フェニル)−5−メチルピコリネート
メチル4−アミノ−3−クロロ−6−(4−シアノ−3−フルオロフェニル)−5−メチルピコリネート(化合物155)
メチル4−アミノ−3−クロロ−6−(3−フルオロ−4−ホルミルフェニル)−5−メチルピコリネート
メチル4−アミノ−3−クロロ−5−フルオロ−6−(2,4,5−トリフルオロフェニル)ピコリネート(化合物200)
[実施例41]
メチル4−アミノ−3−クロロ−5−フルオロ−6−(4−ニトロフェニル)ピコリネート(化合物95)の調製
メチル4−アセトアミド−3−クロロ−6−(2,3−ジフルオロ−4−(トリフルオロメチル)フェニル)ピコリネート
[実施例42]
メチル4−アミノ−3−クロロ−6−(4−シアノ−3−フルオロフェニル)−5−フルオロピコリネート(化合物135)の調製
[実施例43]
メチル4−アミノ−3−クロロ−5−フルオロ−6−(4−(メトキシカルボニル)フェニル)ピコリネート(化合物190)の調製
[実施例44]
メチル4−アミノ−6−(4−ブロモ−2,3−ジフルオロフェニル)−3−クロロピコリネート(化合物114)の調製
ステップ2:メチル4−アセトアミド−6−(4−ブロモ−2,3−ジフルオロフェニル)−3−クロロピコリネート(0.515g、1.227mmol)をメタノール(20mL)に懸濁し、塩化アセチル(1.559mL、21.93mmol)を滴下添加した。反応混合物を室温で終夜撹拌し、真空下に濃縮した。残留物を酢酸エチルと5%重炭酸ナトリウム水溶液との間で分配した。有機相をシリカゲル上に濃縮し、フラッシュクロマトグラフィー(SiO2;ヘキサン中5〜60%酢酸エチルで溶出)により精製して、標題化合物を白色固体として得た(0.231g、55.8%)。
[実施例45]
メチル4−アミノ−3−クロロ−6−(2,3−ジフルオロ−4−(トリメチルシリル)フェニル)−5−フルオロピコリネートの調製
[実施例46]
メチル6−アミノ−2−(3−フルオロ−4−(トリフルオロメチル)フェニル)−5−メトキシピリミジン−4−カルボキシレート(化合物26)の調製
[実施例47]
メチル4−アミノ−3−クロロ−5−フルオロ−6−(4−(トリメチルシリル)フェニル)ピコリネートの調製
メチル4−アミノ−3−クロロ−5−フルオロ−6−(2−フルオロ−4−ホルミルフェニル)ピコリネート
メチル6−アミノ−2−(2−フルオロ−4−ホルミルフェニル)−5−メトキシピリミジン−4−カルボキシレート
メチル4−アミノ−3−クロロ−6−(2,3−ジフルオロ−4−ホルミルフェニル)−5−フルオロピコリネート
メチル6−アミノ−2−(2,3−ジフルオロ−4−ホルミルフェニル)−5−メトキシピリミジン−4−カルボキシレート
メチル6−アミノ−2−(4−ホルミルフェニル)−5−メトキシピリミジン−4−カルボキシレート
メチル4−アミノ−3,5−ジクロロ−6−(4−ホルミルフェニル)ピコリネート
[実施例48]
メチル4−アミノ−3−クロロ−5−フルオロ−6−(3−フルオロ−4−(トリメチルシリル)フェニル)ピコリネートの調製
メチル4−アミノ−3−クロロ−6−(2,3−ジフルオロ−4−(トリメチルシリル)フェニル)−5−フルオロピコリネート
メチル4−アミノ−3−クロロ−5−フルオロ−6−(2−フルオロ−4−(トリメチルシリル)フェニル)ピコリネート
メチル6−アミノ−2−(2−フルオロ−4−(トリメチルシリル)フェニル)−5−メトキシピリミジン−4−カルボキシレート
メチル4−アセトアミド−3−クロロ−6−(2,3−ジフルオロ−4−(トリメチルシリル)フェニル)ピコリネート
メチル6−アミノ−5−メトキシ−2−(4−(トリメチルシリル)フェニル)ピリミジン−4−カルボキシレート
メチル4−アセトアミド−3−クロロ−6−(4−(トリメチルシリル)フェニル)ピコリネート
[実施例49]
メチル4−アセトアミド−6−(4−アミノ−2,3,6−トリフルオロフェニル)−3−クロロピコリネートの調製
[実施例50]
メチル4−アミノ−3−クロロ−6−(2,5−ジフルオロ−4−(トリメチルシリル)フェニル)−5−フルオロピコリネートの調製
[実施例51]
メチル4−アミノ−3−クロロ−6−(2,5−ジフルオロ−4−(トリメチルシリル)フェニル)ピコリネートの調製
[実施例52]
メチル4−アセトアミド−3−クロロ−6−(2,5−ジフルオロ−4−(トリメチルシリル)フェニル)ピコリネートの調製
[実施例53]
メチル6−アミノ−2−(2,5−ジフルオロ−4−(トリメチルシリル)フェニル)−5−メトキシピリミジン−4−カルボキシレートの調製
[実施例54]
メチル4−アミノ−6−(2,3−ジフルオロ−4−(トリフルオロメチル)フェニル)−5−フルオロ−3−ビニルピコリネート(化合物53)の調製
[実施例55]
メチル4−アミノ−6−(4−アミノフェニル)−5−フルオロ−3−ビニルピコリネートの調製
[実施例56]
メチル6−アミノ−2−(4−(ジフルオロメトキシ)フェニル)−5−メトキシピリミジン−4−カルボキシレート(化合物106)の調製
[実施例57]
メチル4−アミノ−6−(4−シアノフェニル)−5−フルオロ−3−ビニルピコリネート(化合物107)の調製
[実施例58]
メチル4−アミノ−5−フルオロ−6−(4−ホルミルフェニル)−3−ビニルピコリネートの調製
[実施例59]
メチル4−アミノ−3−クロロ−6−(2,5−ジフルオロ−4−(トリフルオロメチル)フェニル)ピコリネート(化合物70)の調製
[実施例60]
メチル6−アミノ−2−(2,5−ジフルオロ−4−(トリフルオロメチル)フェニル)−5−メトキシピリミジン−4−カルボキシレート(化合物148)の調製
[実施例61]
メチル6−アミノ−2−(2,3−ジフルオロ−4−(トリメチルシリル)フェニル)−5−メトキシピリミジン−4−カルボキシレートの調製
メチル4−アミノ−3,5−ジクロロ−6−(4−(トリメチルシリル)フェニル)ピコリネート(ヘッドHを利用して調製した)
メチル4−アミノ−3−クロロ−6−(2−フルオロ−4−(トリメチルシリル)フェニル)ピコリネート(ヘッドAを利用して調製した)
メチル4−アミノ−3,5−ジクロロ−6−(2−フルオロ−4−(トリメチルシリル)フェニル)ピコリネート(ヘッドHを利用して調製した)
[実施例62]
鈴木カップリングの一般的手順(方法A)
ヘッドA、ヘッドBまたはヘッドC(1.0当量)、ボロン酸(1.0当量)、Na2CO3(2.0当量)およびPd(PPh3)4(0.1当量)の1:1トルエン:エタノール(20容量)溶液に、密封管中15分間アルゴンを吹き込んだ。次いで反応混合物を密封管中110℃で18時間加熱した。冷却した反応混合物を水で希釈し、酢酸エチルで抽出した。(注意:水層は以下に記載した通りに単離したカルボン酸生成物を含有していた)。有機抽出物を水で洗浄し、飽和ブライン溶液で洗浄し、乾燥(Na2SO4)し、濾過し、減圧下に蒸発乾固した。粗生成物を分取TLCにより精製して、純粋なエステルを得た。水層を1.5N HClを用いてpH2に酸性化し、酢酸エチルで抽出した。有機抽出物を飽和ブライン溶液で洗浄し、乾燥(Na2SO4)し、濾過し、減圧下に蒸発乾固した。粗生成物を分取TLCにより精製して、純粋なカルボン酸誘導体を得た。
[実施例63]
鈴木カップリングの一般的手順(方法B)
ヘッドA、ヘッドBまたはヘッドC(0.8当量)、ボロン酸(1.0当量)、NaHCO3(2M溶液、1.0当量)およびPd(PPh3)4(0.1当量)の乾燥ジオキサン(20容量)溶液に、密封管中15分間アルゴンを吹き込んだ。密封管を80℃で18時間加熱した。冷却した反応混合物を水で希釈し、酢酸エチルで抽出した。有機抽出物を水で洗浄し、飽和ブライン溶液で洗浄し、乾燥(Na2SO4)し、濾過し、減圧下に蒸発乾固した。粗生成物をフラッシュクロマトグラフィー(SiO2;ヘキサン中5〜40%酢酸エチルで溶出)により精製して、純粋な化合物を得た
[実施例64]
メチル4−アミノ−3−クロロ−6−(3−フルオロ−4−ヨードフェニル)ピコリネート(化合物66)の調製
実施例64に開示した手順に従って、以下の化合物を作製した:
メチル4−アミノ−3,5−ジクロロ−6−(3−フルオロ−4−ヨードフェニル)ピコリネート(化合物13)
メチル6−アミノ−2−(3−フルオロ−4−ヨードフェニル)−5−メトキシピリミジン−4−カルボキシレート(化合物27)
[実施例65]
メチル4−アミノ−3−クロロ−6−(4−ヨードフェニル)−5−メチルピコリネート(化合物136)の調製
メチル4−アミノ−3−クロロ−6−(3−フルオロ−4−ヨードフェニル)−5−メチルピコリネート(化合物79)
[実施例66]
メチル4−アミノ−6−(4−ヨードフェニル)−3−クロロ−5−フルオロピコリネート(化合物118)の調製
メチル4−アセトアミド−3−クロロ−6−(2,3−ジフルオロ−4−ヨードフェニル)ピコリネート
メチル4−アセトアミド−3−クロロ−6−(4−ヨードフェニル)ピコリネート
[実施例67]
メチル4−アミノ−3−クロロ−6−(2,5−ジフルオロ−4−ヨードフェニル)−5−フルオロピコリネート(化合物55)の調製
メチル4−アセトアミド−3−クロロ−6−(2,5−ジフルオロ−4−ヨードフェニル)ピコリネート
[実施例68]
メチル6−アミノ−2−(2,3−ジフルオロ−4−ヨードフェニル)−5−メトキシピリミジン−4−カルボキシレート(化合物24)の調製
[実施例69]
メチル4−アセトアミド−6−(4−ブロモ−3−フルオロフェニル)−3−クロロピコリネートの調製
メチル4−アミノ−6−(4−ブロモ−3−フルオロフェニル)−3,5−ジクロロピコリネート(化合物73)
メチル6−アミノ−2−(4−ブロモ−3−フルオロフェニル)−5−メトキシピリミジン−4−カルボキシレート(化合物171)
[実施例70]
メチル4−アミノ−6−(4−ブロモフェニル)−3−クロロ−5−メチルピコリネート(化合物81)の調製
メチル4−アミノ−6−(4−ブロモ−3−フルオロフェニル)−3−クロロ−5−メチルピコリネート(化合物112)
[実施例71]
メチル4−アミノ−6−(4−ブロモ−2,3−ジフルオロフェニル)−3−クロロ−5−フルオロピコリネート(化合物109)の調製
[実施例72]
メチル4−アミノ−6−(4−ブロモフェニル)−3−クロロ−5−フルオロピコリネート(化合物138)の調製
メチル4−アセトアミド−6−(4−ブロモフェニル)−3−クロロピコリネート
[実施例73]
メチル4−アミノ−6−(4−ブロモ−2,5−ジフルオロフェニル)−3−クロロ−5−フルオロピコリネート(化合物51)の調製
メチル4−アセトアミド−6−(4−ブロモ−2,5−ジフルオロフェニル)−3−クロロピコリネート
[実施例74]
メチル6−アミノ−2−(4−ブロモ−2,3−ジフルオロフェニル)−5−メトキシピリミジン−4−カルボキシレート(化合物122)の調製
[実施例75]
メチル4−アミノ−6−(4−ブロモ−3−フルオロフェニル)−3−クロロピコリネート(化合物115)の調製
[実施例76]
メチル4−アミノ−3−クロロ−6−(2,3−ジフルオロ−4−ヨードフェニル)ピコリネート(化合物129)の調製
[実施例77]
メチル4−アミノ−6−(4−ブロモ−2,5−ジフルオロフェニル)−3−クロロピコリネート(化合物127)の調製
[実施例78]
メチル4−(N−アセチルアセトアミド)−3−クロロ−6−(2,5−ジフルオロ−4−(トリメチルシリル)フェニル)ピコリネートの調製
[実施例79]
メチル4−アミノ−6−(4−ブロモフェニル)−5−フルオロ−3−ビニルピコリネート(化合物57)の調製
メチル4−アセトアミド−6−(4−ブロモ−2,3,6−トリフルオロフェニル)−3−クロロピコリネート
[実施例80]
メチル6−アミノ−2−(4−ヨードフェニル)−5−ビニルピリミジン−4−カルボキシレート(化合物164)の調製
[実施例81]
メチル4−アミノ−5−フルオロ−6−(4−ヨードフェニル)−3−ビニルピコリネート(化合物139)の調製
メチル4−アセトアミド−3−クロロ−6−(2,3,6−トリフルオロ−4−ヨードフェニル)ピコリネート
[実施例82]
メチル4−アミノ−3−クロロ−5−メチル−6−(4−((トリメチルシリル)エチニル)フェニル)ピコリネートの調製
[実施例83]
メチル4−アミノ−3−クロロ−6−(4−エチニルフェニル)−5−メチルピコリネート(化合物40)の調製
[実施例84]
メチル4−アミノ−3−クロロ−5−フルオロ−6−(4−((トリメチルシリル)エチニル)フェニル)ピコリネートの調製
[実施例85]
メチル4−アミノ−3−クロロ−6−(4−エチニルフェニル)−5−フルオロピコリネート(化合物7)の調製
[実施例86]
メチル4−アミノ−3−クロロ−6−(4−エチニル−3−フルオロフェニル)−5−フルオロピコリネート(化合物133)の調製
[実施例87]
メチル4−アミノ−3−クロロ−6−(4−エチニル−3−フルオロフェニル)−5−メチルピコリネート(化合物151)の調製
[実施例88]
メチル4−アミノ−6−(4−エチニルフェニル)−5−フルオロ−3−ビニルピコリネート(化合物60)の調製
[実施例89]
メチル4−((tert−ブトキシカルボニル)アミノ)−3−クロロ−6−(4−クロロ−3−フルオロフェニル)−5−フルオロピコリネートの調製
ステップ2:メチル4−(ビス(tert−ブトキシカルボニル)アミノ)−3−クロロ−6−(4−クロロ−3−フルオロフェニル)−5−フルオロピコリネート(2.1g、3.94mmol)をジクロロエタン(20mL)に溶解し、トリフルオロ酢酸(0.598mL、7.76mmol)を室温で加えた。反応混合物を室温で終夜撹拌し、次いで真空下に濃縮した。生成物をフラッシュクロマトグラフィー(SiO2;ジクロロメタン中2〜20%酢酸エチルで溶出)により精製して、標題化合物を白色固体として得た(1.64g、98%):1H NMR (300MHz, CDCl3)δ7.80 (dd, J=22.0, 8.5Hz, 2H), 7.50 (dd, J=8.3, 7.6Hz, 1H), 6.51 (s, 1H), 4.02 (s, 3H), 1.56 (s, 9H);ESIMSm/z431([M−H]−)。
[実施例90]
メチル4−アミノ−6−(4−クロロ−3−フルオロフェニル)−5−フルオロ−3−ビニルピコリネート(化合物215)の調製
ステップ2:メチル4−(tert−ブトキシカルボニルアミノ)−6−(4−クロロ−3−フルオロフェニル)−5−フルオロ−3−ビニルピコリネート(0.966g、2.274mmol)をジクロロエタン(11mL)に溶解し、トリフルオロ酢酸(3.50mL、45.5mmol)を加えた。室温で4時間後、反応混合物を真空下に濃縮し、次いで更にジクロロエタンで更に2回共蒸発させた。残留物をフラッシュクロマトグラフィー(SiO2;ヘキサン中7〜60%酢酸エチルで溶出)により精製して、標題化合物を白色固体として得た(0.705g、95%)。
[実施例91]
メチル4−アミノ−5−ブロモ−3−クロロ−6−(2,5−ジフルオロ−4−(トリメチルシリル)フェニル)ピコリネートの調製
[実施例92]
4−アミノ−3−クロロ−6−(3−フルオロ−4−ヨードフェニル)ピコリン酸(化合物77)の調製
4−アミノ−3,5−ジクロロ−6−(3−フルオロ−4−ヨードフェニル)ピコリン酸(化合物145)
6−アミノ−2−(3−フルオロ−4−ヨードフェニル)−5−メトキシピリミジン−4−カルボン酸(化合物37)
4−アミノ−6−(4−ブロモ−3−フルオロフェニル)−3−クロロピコリン酸(化合物110)
4−アミノ−6−(4−ブロモ−3−フルオロフェニル)−3,5−ジクロロピコリン酸(化合物43)
6−アミノ−2−(4−ブロモ−3−フルオロフェニル)−5−メトキシピリミジン−4−カルボン酸(化合物113)
6−アミノ−2−(4−シアノ−2−フルオロフェニル)−5−ビニルピリミジン−4−カルボン酸(化合物5)
6−アミノ−2−(3−フルオロ−4−(トリフルオロメチル)フェニル)−5−ビニルピリミジン−4−カルボン酸(化合物32)
6−アミノ−2−(2,3,4−トリフルオロフェニル)−5−ビニルピリミジン−4−カルボン酸(化合物191)
[実施例93]
4−アミノ−3−クロロ−6−(4−シアノ−2−フルオロフェニル)−5−フルオロピコリン酸(化合物65)の調製
6−アミノ−2−(4−ヨードフェニル)−5−ビニルピリミジン−4−カルボン酸(化合物123)
[実施例94]
4−アミノ−3−クロロ−6−(3−フルオロ−4−(トリフルオロメチル)フェニル)−5−メチルピコリン酸(化合物161)の調製
4−アミノ−3−クロロ−6−(4−(ジフルオロメトキシ)フェニル)−5−メチルピコリン酸(化合物94)
4−アミノ−6−(4−ブロモフェニル)−3−クロロ−5−メチルピコリン酸(化合物78)
4−アミノ−3−クロロ−6−(4−ヨードフェニル)−5−メチルピコリン酸(化合物116)
4−アミノ−3−クロロ−6−(3−フルオロ−4−ヨードフェニル)−5−メチルピコリン酸(化合物87)
4−アミノ−3−クロロ−6−(4−エチニル−3−フルオロフェニル)−5−メチルピコリン酸(化合物6)
[実施例95]
4−アミノ−3−クロロ−5−フルオロ−6−(4−ニトロフェニル)ピコリン酸(化合物31)の調製
[実施例96]
4−アミノ−3−クロロ−6−(2,3−ジフルオロ−4−(トリフルオロメチル)フェニル)ピコリン酸(化合物172)の調製
[実施例97]
4−アミノ−3−クロロ−5−フルオロ−6−(4−ヨードフェニル)ピコリン酸(化合物45)の調製
[実施例98]
4−アミノ−3−クロロ−6−(2,3−ジフルオロ−4−ヨードフェニル)−5−フルオロピコリン酸(化合物141)の調製
[実施例99]
4−アミノ−6−(4−ブロモ−2,3,6−トリフルオロフェニル)−3−クロロピコリン酸(化合物162)の調製
[実施例100]
4−アミノ−6−(4−ブロモ−2,5−ジフルオロフェニル)−3−クロロ−5−フルオロピコリン酸(化合物42)の調製
[実施例101]
4−アミノ−3−クロロ−6−(4−(ジフルオロメトキシ)−3−フルオロフェニル)−5−フルオロピコリン酸(化合物92)の調製
0が活性なしを表し、100が完全な植物死滅を表す、0から100のスケールで視覚的に除草評価をした。該データをTable Aに示されている通りに呈示する。
出芽後試験I:試験種の種子を市販供給元から得て、土壌のない媒体ミックス(Metro−Mix360(登録商標)、Sun Gro Horticulture)を含有する13センチメートル(cm)の直径−円形ポットに植え付けた。出芽後処理物を施用より8〜12日(d)前に植え付け、24〜29℃で16時間(h)光周期を提供するために補足的な光供給源が備えられている温室内で培養した。全てのポットを表面灌漑した。
出芽前試験I:砂壌土を含有する円形プラスチックポット(5インチの直径)に、試験種の種子を植え付けた。植え付けた後、化合物施用より16時間前に全てのポットを地下灌漑した。
出芽後試験II:64平方センチメートルの表面積を有するプラスチックポット内の、6.0から6.8のpHおよび約30パーセントの有機物含有量を典型的に有するSun Gro Metro−Mix(登録商標)360植え付け用混合物中に、所望の試験植物種の種子または小堅果を植え付けた。良好な発芽および健康な植物を確実にすることが必要とされた場合、殺真菌剤処理および/または他の化学的もしくは物理的処理を適用した。日中は約23〜29℃および夜間は22〜28℃で維持するおよそ15時間の明期を用いる温室内で、7〜21日間、該植物を成長させた。栄養素および水を定期的に添加し、必要に応じてオーバーヘッド金属ハロゲン化物1000ワットランプを用いて補足の照明を提供した。該植物が第1または第2の本葉段階に達した時、それらを試験に用いた。
出芽後試験III.103.2平方センチメートルs(cm2)の表面積を有するプラスチックポット内の、6.0から6.8のpHおよび約30パーセントの有機物含有量を典型的に有するSun Gro MetroMix(登録商標)306植え付け用混合物中に、所望の試験植物種の種子を植え付けた。良好な発芽および健康な植物を確実にすることが必要とされた場合に、殺真菌剤処理および/または他の化学的もしくは物理的処理を適用した。日中は約18℃および夜間は17℃で維持されるおよそ14時間の明期を用いる温室内で7〜36日間、該植物を成長させた。栄養素および水を定期的に添加し、必要に応じてオーバーヘッド金属ハロゲン化物1000ワットランプを用いて補足の照明を提供した。該植物が第2または第3の本葉段階に達した時、それらを試験に用いた。
出芽前試験III.砂壌土を含有する四角のプラスチックポット(10cmの幅)に、試験種の種子を植え付けた。植え付けた後、化合物施用より16時間前に、全てのポットを地下灌漑した。
ローム土壌(43パーセント汚泥、19パーセント粘土、および38パーセント砂、約8.1のpHおよび約1.5パーセントの有機物含有量)および川砂を80対20比で混合することによって調製された土壌マトリックスに、所望の試験植物種の種子または小堅果を植え付けた。139.7cm2の表面積を有するプラスチックポットに土壌マトリックスを含有させた。良好な発芽および健康な植物を確実にすることが必要とされた場合に、殺真菌剤処理および/または他の化学的もしくは物理的処理を適用した。日中は約29℃および夜間は26℃で維持されるおよそ14時間の明期を用いる温室内で10〜17日間、植物を成長させた。栄養素および水を定期的に添加し、必要に応じてオーバーヘッド金属ハロゲン化物1000ワットランプを用いて補足の照明を提供した。植物が第2または第3の本葉段階に達した時、それらを試験に用いた。
Claims (36)
- 式(I)の化合物:
[式中、
Xは、NまたはCYであり;ここで、Yは水素、ハロゲン、C1〜C3アルキル、C1〜C3ハロアルキル、C1〜C3アルコキシ、C1〜C3ハロアルコキシ、C1〜C3アルキルチオまたはC1〜C3ハロアルキルチオであり;
R1はOR1’であり、ここで、R1’はH、C1〜C8アルキルまたはC7〜C10アリールアルキルであり;
R2は、ハロゲン、C1〜C4アルキル、C1〜C4ハロアルキル、C2〜C4アルケニル、C2〜C4ハロアルケニル、C2〜C4アルキニル、C2〜C4ハロアルキニル、C1〜C4アルコキシ、C1〜C4ハロアルコキシ、C1〜C4アルキルチオ、C1〜C4ハロアルキルチオ、アミノ、C1〜C4アルキルアミノ、C2〜C4ハロアルキルアミノ、ホルミル、(C1〜C3アルキル)カルボニル、(C1〜C3ハロアルキル)カルボニル、シアノ、または式−CR17=CR18−SiR19R20R21の基であり、ここで、R17は、水素、FまたはClであり;R18は水素、F、Cl、C1〜C4アルキルまたはC1〜C4ハロアルキルであり;R19、R20およびR21は、各々独立して、C1〜C10アルキル、C3〜C6シクロアルキル、C1〜C10ハロアルキル、C3〜C6ハロシクロアルキル、フェニル、置換フェニル、C1〜C10アルコキシまたはOHであり;
R3およびR4は、各々独立して、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ハロアルケニル、C3〜C6アルキニル、ヒドロキシ、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、ホルミル、(C1〜C3アルキル)カルボニル、(C1〜C3ハロアルキル)カルボニル、(C1〜C6アルコキシ)カルボニル、(C1〜C6アルキル)カルバミル、C1〜C6アルキルスルホニル、トリ(C1〜C6アルキル)シリル、ジ(C1〜C6アルキル)ホスホニル、であるか、またはR3およびR4は、それらが結合している窒素原子と一緒に、5員もしくは6員の飽和環を形成するか、またはR3およびR4は一緒になって、=CR3’R4’を表し、ここで、R3’およびR4’は、各々独立して、水素、C1〜C6アルキル、C3〜C6アルケニル、C3〜C6アルキニル、C1〜C6アルコキシもしくはC1〜C6アルキルアミノであり、またはR3’およびR4’は、それらが結合している炭素原子と一緒に、5員もしくは6員の飽和環を形成し;
Arは、Ar1、Ar2、Ar3、Ar4、Ar5またはAr6であり:
式中、
X1は、H、F、Br、I、エチニル、ハロエチニル、CF2H、OCF2H、OCF3、CN、CONH2、CO2H、CO2CH3またはNO2であり;
X2は、H、F、Cl、Br、I、エチニル、ハロエチニル、CH3、CFH2、CF2H、CF3、OCF2H、OCF3、CN、CONH2、CO2HまたはNO2であり;
X3は、H、F、Br、I、エチニル、ハロエチニル、CH3、CFH2、CF2H、CF3、OCF2H、OCF3、CN、CONH2、CO2HまたはNO2であり;
ここで、
a)Arが、
である場合、XはN、CH、CF、CClまたはCCH3であり;
ただし、
v)XがNである場合、R2はClまたはビニルではなく;
vi)R2がClであり、XがCHである場合、X1はH、F、OCF3またはCNではなく;
vii)R2がOCH3であり、XがCFである場合、X1はF、I、CNまたはエチニルではなく;
viii)XがCClである場合、X1はHではなく;
b)Arが、
である場合、XはN、CH、CF、CClまたはCCH3であり;
ただし、
v)XがNである場合、R2はClではなく;
vi)R2がOCH3またはビニルであり、XがNである場合、X2はClではなく;
vii)R2がClであり、XがCHである場合、X2はClではなく;
viii)R2がOCH3であり、XがCFである場合、X2はCl、Br、IまたはCF3ではなく;
c)Arが、
である場合、XはN、CHまたはCFであり;
ただし、
v)XがNである場合、R2はClではなく;
vi)R2がOCH3であり、XがNである場合、X3はCH3ではなく;
vii)R2がClであり、XがCHである場合、X3はH、FまたはCH3ではなく;
viii)R2がOCH3であり、XがCFである場合、X3はBrまたはIではなく;
d)Arが、
である場合、XはN、CHまたはCFであり;
ただし、
v)XがNである場合、R2はClではなく;
vi)R2がOCH3またはビニルであり、XがNである場合、X2はClではなく;
vii)R2がClであり、XがCHである場合、X2はFではなく;
viii)R2がOCH3であり、XがCFである場合、X2はCl、Br、IまたはCF3ではなく;
e)Arが、
である場合、XはN、CHまたはCFであり;
ただし、
iii)R2がClであり、XがNである場合、X3はCH3ではなく;
iv)XがCFであり、R2がOCH3である場合、X3はBrまたはIではなく;
f)Arが、
である場合、XはN、CHまたはCFである]
またはそのN−オキシドもしくは農業的に許容される塩。 - ArがAr1である、請求項1に記載の化合物。
- ArがAr2である、請求項1に記載の化合物。
- ArがAr3である、請求項1に記載の化合物。
- ArがAr4である、請求項1に記載の化合物。
- ArがAr5である、請求項1に記載の化合物。
- ArがAr6である、請求項1に記載の化合物。
- R1がOR1’である、請求項1に記載の化合物。
- R1’がHまたはC1〜C8アルキルである、請求項8に記載の化合物。
- R1’がHまたはメチルである、請求項9に記載の化合物。
- XがNである、請求項1に記載の化合物。
- XがCYである、請求項1に記載の化合物。
- Yが水素、ハロゲン、C1〜C3アルキル、C1〜C3ハロアルキル、C1〜C3アルコキシ、C1〜C3ハロアルコキシ、C1〜C3アルコキシ、C1〜C3アルキルチオまたはC1〜C3ハロアルキルチオである、請求項12に記載の化合物。
- YがH、F、ClまたはCH3である、請求項13に記載の化合物。
- R2がハロゲン、C2〜C4アルケニル、C2〜C4ハロアルケニル、C1〜C4アルコキシ、C1〜C4ハロアルコキシ、C1〜C4アルキルチオまたはC1〜C4ハロアルキルチオである、請求項1に記載の化合物。
- R2がハロゲン、C2〜C4アルケニル、C2〜C4ハロアルケニルまたはC1〜C4アルコキシである、請求項15に記載の化合物。
- R2がCl、OCH3またはビニルである、請求項16に記載の化合物。
- R3およびR4が、各々独立して、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ハロアルケニル、C3〜C6アルキニル、ホルミル、(C1〜C3アルキル)カルボニル、(C1〜C3ハロアルキル)カルボニル、(C1〜C6アルコキシ)カルボニル、(C1〜C6アルキル)カルバミル、トリ(C1〜C6アルキル)シリルであるか、またはR3およびR4が一緒になって、=CR3’R4’を表し、ここでR3’およびR4’が、各々独立して、水素、C1〜C6アルキル、C3〜C6アルケニル、C3〜C6アルキニル、C1〜C6アルコキシまたはC1〜C6アルキルアミノである、請求項1に記載の化合物。
- R3およびR4が水素である、請求項18に記載の化合物。
- X1がH、F、Br、I、エチニル、CF2H、OCF2H、OCF3、CN、CONH2、CO2CH3またはNO2である、請求項1に記載の化合物。
- X1がH、F、Br、I、エチニル、CF2H、OCF2H、OCF3、CN、CONH2、CO2CH3またはNO2である、請求項2に記載の化合物。
- X2がH、Cl、Br、I、エチニル、CH3、CF2H、CF3、OCF2HまたはCNである、請求項1に記載の化合物。
- X2がH、Cl、Br、I、エチニル、CH3、CF2H、CF3、OCF2HまたはCNである、請求項3に記載の化合物。
- X3がH、Br、I、エチニル、OCF2H、CNまたはNO2である、請求項1に記載の化合物。
- X3がH、Br、I、エチニル、OCF2H、CNまたはNO2である、請求項4に記載の化合物。
- X2がH、F、Br、I、エチニル、CH3、CF3、OCF2HまたはCNである、請求項1に記載の化合物。
- X2がH、F、Br、I、エチニル、CH3、CF3、OCF2HまたはCNである、請求項5に記載の化合物。
- X3がH、F、Br、I、CH3、CF2H、CF3、OCF2HまたはCNである、請求項1に記載の化合物。
- X3がH、F、Br、I、CH3、CF2H、CF3、OCF2HまたはCNである、請求項6に記載の化合物。
- X2がBrまたはIである、請求項1に記載の化合物。
- X2がBrまたはIである、請求項7に記載の化合物。
- 化合物が、
である、請求項1に記載の化合物またはそのN−オキシドもしくは農業的に許容される塩。 - 請求項1に記載の化合物またはそのN−オキシドもしくは農業的に許容される塩と、農業的に許容されるアジュバントまたは担体とを含む除草組成物。
- 少なくとも1種の追加の除草化合物をさらに含む、請求項33に記載の組成物。
- 毒性緩和剤をさらに含む、請求項33または34に記載の組成物。
- 請求項1に記載の化合物または請求項33に記載の組成物を施用することを含む、望ましくない植生を防除するための方法。
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US13/840,233 | 2013-03-15 | ||
US13/840,233 US9113629B2 (en) | 2013-03-15 | 2013-03-15 | 4-amino-6-(4-substituted-phenyl)-picolinates and 6-amino-2-(4-substituted-phenyl)-pyrimidine-4-carboxylates and their use as herbicides |
PCT/US2014/024388 WO2014150850A1 (en) | 2013-03-15 | 2014-03-12 | 4-amino-6-(4-substituted-phenyl)-picolinates and 6-amino-2-(4-substituted-phenyl)-pyrimidine-4-carboxylates and their use as herbicides |
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JP2018076745A Pending JP2018127480A (ja) | 2013-03-15 | 2018-04-12 | 4−アミノ−6−(4−置換フェニル)−ピコリネートおよび6−アミノ−2−(4−置換フェニル)−ピリミジン−4−カルボキシレートならびに除草剤としてのそれらの使用 |
JP2020022143A Pending JP2020097614A (ja) | 2013-03-15 | 2020-02-13 | 4−アミノ−6−(4−置換フェニル)−ピコリネートおよび6−アミノ−2−(4−置換フェニル)−ピリミジン−4−カルボキシレートならびに除草剤としてのそれらの使用 |
JP2022052676A Pending JP2022088515A (ja) | 2013-03-15 | 2022-03-29 | 4-アミノ-6-(4-置換フェニル)-ピコリネートおよび6-アミノ-2-(4-置換フェニル)-ピリミジン-4-カルボキシレートならびに除草剤としてのそれらの使用 |
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JP2020022143A Pending JP2020097614A (ja) | 2013-03-15 | 2020-02-13 | 4−アミノ−6−(4−置換フェニル)−ピコリネートおよび6−アミノ−2−(4−置換フェニル)−ピリミジン−4−カルボキシレートならびに除草剤としてのそれらの使用 |
JP2022052676A Pending JP2022088515A (ja) | 2013-03-15 | 2022-03-29 | 4-アミノ-6-(4-置換フェニル)-ピコリネートおよび6-アミノ-2-(4-置換フェニル)-ピリミジン-4-カルボキシレートならびに除草剤としてのそれらの使用 |
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US (1) | US9113629B2 (ja) |
EP (2) | EP2967069B1 (ja) |
JP (4) | JP6527502B2 (ja) |
KR (2) | KR102272777B1 (ja) |
CN (2) | CN108689924B (ja) |
AP (1) | AP2015008772A0 (ja) |
AR (2) | AR095449A1 (ja) |
AU (3) | AU2014235571C1 (ja) |
BR (2) | BR122019021766B8 (ja) |
CA (2) | CA2902347C (ja) |
CL (1) | CL2015002665A1 (ja) |
CR (1) | CR20150521A (ja) |
DK (1) | DK2967069T3 (ja) |
ES (2) | ES2706504T3 (ja) |
HR (1) | HRP20182056T1 (ja) |
HU (1) | HUE063201T2 (ja) |
IL (1) | IL240854A (ja) |
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PH (1) | PH12015502146A1 (ja) |
PL (2) | PL2967069T3 (ja) |
PT (1) | PT2967069T (ja) |
RS (1) | RS58151B1 (ja) |
RU (2) | RU2652132C2 (ja) |
SI (1) | SI2967069T1 (ja) |
UA (2) | UA118189C2 (ja) |
UY (1) | UY35477A (ja) |
WO (1) | WO2014150850A1 (ja) |
ZA (1) | ZA201507330B (ja) |
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TWI689251B (zh) | 2014-09-15 | 2020-04-01 | 美商陶氏農業科學公司 | 源自於施用吡啶羧酸除草劑與合成生長素除草劑及/或生長素轉運抑制劑的協同性雜草控制 |
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JP7113762B2 (ja) * | 2016-05-19 | 2022-08-05 | コルテバ アグリサイエンス エルエルシー | 直接的な鈴木カップリングによる6-アリール-4-アミノピコリネートおよび2-アリール-6-アミノピリミジン-4-カルボキシレートの合成 |
CA3028949C (en) | 2016-06-27 | 2020-10-27 | Korea Research Institute Of Chemical Technology | Pyridine-based compound including isoxazoline ring and use thereof as herbicide |
CN109400526B (zh) * | 2018-12-27 | 2020-10-16 | 青岛清原化合物有限公司 | 吡啶氧基硫酯衍生物及其制备方法、除草组合物和应用 |
CN112110852B (zh) * | 2019-06-20 | 2022-04-26 | 青岛清原化合物有限公司 | 取代的吡啶甲酸吡啶亚甲基酯衍生物及其制备方法、除草组合物和应用 |
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CN113548982B (zh) * | 2021-09-03 | 2022-05-06 | 上海三牧化工技术有限公司 | 一种4-氰基-2-氟苄醇的制备方法 |
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JP2010538013A (ja) * | 2007-08-30 | 2010-12-09 | ダウ アグロサイエンシィズ エルエルシー | 2−(置換フェニル)−6−アミノ−5−アルコキシ、チオアルコキシ、およびアミノアルキル−4−ピリミジンカルボキシラート、ならびに除草剤としてのそれらの使用 |
JP2010540652A (ja) * | 2007-10-02 | 2010-12-24 | ダウ アグロサイエンシィズ エルエルシー | 2−置換−6−アミノ−5−アルキル、アルケニル又はアルキニル−4−ピリミジンカルボン酸及び6−置換−4−アミノ−3−アルキル、アルケニル又はアルキニルピコリン酸並びに除草剤としてのそれらの使用 |
WO2010092339A1 (en) * | 2009-02-13 | 2010-08-19 | Syngenta Limited | Pyrimidine derivatives and their use as herbicides |
WO2010125332A1 (en) * | 2009-05-01 | 2010-11-04 | Syngenta Limited | Method of controlling undesired vegetation |
WO2013003740A1 (en) * | 2011-06-30 | 2013-01-03 | Dow Agrosciences Llc | 3-alkoxy, thioalkyl and amino-4-amino-6-(substituted)picolinates and their use as herbicides |
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