JP2017504624A5 - - Google Patents
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- Publication number
- JP2017504624A5 JP2017504624A5 JP2016546934A JP2016546934A JP2017504624A5 JP 2017504624 A5 JP2017504624 A5 JP 2017504624A5 JP 2016546934 A JP2016546934 A JP 2016546934A JP 2016546934 A JP2016546934 A JP 2016546934A JP 2017504624 A5 JP2017504624 A5 JP 2017504624A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- pyrimidine
- haloalkyl
- chloro
- independently
- 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
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- 229910052736 halogen Inorganic materials 0.000 claims 22
- 150000002367 halogens Chemical class 0.000 claims 22
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 21
- 150000001875 compounds Chemical class 0.000 claims 16
- 125000004093 cyano group Chemical group *C#N 0.000 claims 16
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 12
- -1 SO n R 2A Chemical group 0.000 claims 11
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 8
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 8
- 230000002363 herbicidal effect Effects 0.000 claims 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 8
- 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 8
- 125000001424 substituent group Chemical group 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 6
- 239000003112 inhibitor Substances 0.000 claims 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 4
- 150000001721 carbon Chemical group 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 239000003085 diluting agent Substances 0.000 claims 4
- 239000004009 herbicide Substances 0.000 claims 4
- 125000005842 heteroatom Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 108010068327 4-hydroxyphenylpyruvate dioxygenase Proteins 0.000 claims 3
- 102100028626 4-hydroxyphenylpyruvate dioxygenase Human genes 0.000 claims 3
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 3
- 239000004480 active ingredient Substances 0.000 claims 3
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 3
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims 2
- QUTYKIXIUDQOLK-PRJMDXOYSA-N 5-O-(1-carboxyvinyl)-3-phosphoshikimic acid Chemical compound O[C@H]1[C@H](OC(=C)C(O)=O)CC(C(O)=O)=C[C@H]1OP(O)(O)=O QUTYKIXIUDQOLK-PRJMDXOYSA-N 0.000 claims 2
- 239000005504 Dicamba Substances 0.000 claims 2
- 239000005562 Glyphosate Substances 0.000 claims 2
- 239000005578 Mesotrione Substances 0.000 claims 2
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 claims 2
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 claims 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 2
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims 2
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims 2
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims 2
- 229940097068 glyphosate Drugs 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 2
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000007787 solid Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 150000004669 very long chain fatty acids Chemical class 0.000 claims 2
- AIAYSXFWIUNXRC-PHIMTYICSA-N (1r,5s)-3-[hydroxy-[2-(2-methoxyethoxymethyl)-6-(trifluoromethyl)pyridin-3-yl]methylidene]bicyclo[3.2.1]octane-2,4-dione Chemical compound COCCOCC1=NC(C(F)(F)F)=CC=C1C(O)=C1C(=O)[C@@H](C2)CC[C@@H]2C1=O AIAYSXFWIUNXRC-PHIMTYICSA-N 0.000 claims 1
- 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 claims 1
- KQTZTDYBTPDJOX-UHFFFAOYSA-N 2-bromo-5-[2-[5-(trifluoromethyl)pyrimidin-2-yl]oxyphenyl]-1,3-thiazole Chemical compound BrC=1SC(=CN1)C1=C(OC2=NC=C(C=N2)C(F)(F)F)C=CC=C1 KQTZTDYBTPDJOX-UHFFFAOYSA-N 0.000 claims 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 claims 1
- VSNKMVKVGZAYDJ-UHFFFAOYSA-N 3-[2-(5-bromopyrimidin-2-yl)oxyphenyl]-5-(difluoromethyl)-1,2-oxazole Chemical compound BrC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=NOC(=C1)C(F)F VSNKMVKVGZAYDJ-UHFFFAOYSA-N 0.000 claims 1
- RYGZAFCOAXZLKX-UHFFFAOYSA-N 3-[2-(5-chloropyrimidin-2-yl)oxy-6-(difluoromethoxy)phenyl]-5-(difluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)OC(F)F)C1=NOC(=C1)C(F)F RYGZAFCOAXZLKX-UHFFFAOYSA-N 0.000 claims 1
- YFONPKHXTHJVEX-UHFFFAOYSA-N 3-[2-(5-chloropyrimidin-2-yl)oxy-6-fluorophenyl]-5-(difluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C(=CC=C1)F)C1=NOC(=C1)C(F)F YFONPKHXTHJVEX-UHFFFAOYSA-N 0.000 claims 1
- QPSICHSPZUBPEQ-UHFFFAOYSA-N 3-[2-(5-chloropyrimidin-2-yl)oxy-6-fluorophenyl]-5-(trifluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C(=CC=C1)F)C1=NOC(=C1)C(F)(F)F QPSICHSPZUBPEQ-UHFFFAOYSA-N 0.000 claims 1
- VYYBZFUDXORZPD-UHFFFAOYSA-N 3-[2-(5-chloropyrimidin-2-yl)oxy-6-fluorophenyl]-5-cyclopropyl-1,2-oxazole Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)F)C1=NOC(=C1)C1CC1 VYYBZFUDXORZPD-UHFFFAOYSA-N 0.000 claims 1
- XKRNZOJMWSUCOP-UHFFFAOYSA-N 3-[2-(5-chloropyrimidin-2-yl)oxyphenyl]-5-(difluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=NOC(=C1)C(F)F XKRNZOJMWSUCOP-UHFFFAOYSA-N 0.000 claims 1
- FVBZRASHHMVMJR-UHFFFAOYSA-N 3-[2-(5-chloropyrimidin-2-yl)oxyphenyl]-5-(fluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=NOC(=C1)CF FVBZRASHHMVMJR-UHFFFAOYSA-N 0.000 claims 1
- MJBAXGVCHMNNBK-UHFFFAOYSA-N 3-[2-(5-chloropyrimidin-2-yl)oxyphenyl]-5-(trifluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=NOC(=C1)C(F)(F)F MJBAXGVCHMNNBK-UHFFFAOYSA-N 0.000 claims 1
- NHRSVXAHAWSPGT-UHFFFAOYSA-N 3-[2-bromo-6-(5-chloropyrimidin-2-yl)oxyphenyl]-5-(difluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Br)C1=NOC(=C1)C(F)F NHRSVXAHAWSPGT-UHFFFAOYSA-N 0.000 claims 1
- MMOLHDPOZXRQMM-UHFFFAOYSA-N 3-[2-bromo-6-(5-chloropyrimidin-2-yl)oxyphenyl]-5-(trifluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Br)C1=NOC(=C1)C(F)(F)F MMOLHDPOZXRQMM-UHFFFAOYSA-N 0.000 claims 1
- PHHJJLZMRYZEBR-UHFFFAOYSA-N 3-[2-chloro-6-(5-chloropyrimidin-2-yl)oxyphenyl]-5-(trifluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=NOC(=C1)C(F)(F)F PHHJJLZMRYZEBR-UHFFFAOYSA-N 0.000 claims 1
- JKDODGORIBNPHY-UHFFFAOYSA-N 3-bromo-5-[2-(5-chloropyrimidin-2-yl)oxyphenyl]-1,2-oxazole Chemical compound BrC1=NOC(=C1)C1=C(OC2=NC=C(C=N2)Cl)C=CC=C1 JKDODGORIBNPHY-UHFFFAOYSA-N 0.000 claims 1
- UFMSKAMNTPCISV-UHFFFAOYSA-N 4-[2-(5-bromopyrimidin-2-yl)oxyphenyl]-2-(trifluoromethyl)pyrimidine Chemical compound BrC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=NC(=NC=C1)C(F)(F)F UFMSKAMNTPCISV-UHFFFAOYSA-N 0.000 claims 1
- DQCVMPBZXNIIGP-UHFFFAOYSA-N 5-[2-(5-bromopyrimidin-2-yl)oxy-6-fluorophenyl]-3-(difluoromethyl)-1,2-oxazole Chemical compound BrC=1C=NC(=NC1)OC1=C(C(=CC=C1)F)C1=CC(=NO1)C(F)F DQCVMPBZXNIIGP-UHFFFAOYSA-N 0.000 claims 1
- HVHPKAKZOCCFRX-UHFFFAOYSA-N 5-[2-(5-chloropyrimidin-2-yl)oxy-6-fluorophenyl]-3-(difluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C(=CC=C1)F)C1=CC(=NO1)C(F)F HVHPKAKZOCCFRX-UHFFFAOYSA-N 0.000 claims 1
- ASJSTDCPPXZJAQ-UHFFFAOYSA-N 5-[2-(5-chloropyrimidin-2-yl)oxyphenyl]-3-(difluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=CC(=NO1)C(F)F ASJSTDCPPXZJAQ-UHFFFAOYSA-N 0.000 claims 1
- CCPDZEMJVLHFFJ-UHFFFAOYSA-N 5-[2-(5-chloropyrimidin-2-yl)oxyphenyl]-3-(trifluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=CC(=NO1)C(F)(F)F CCPDZEMJVLHFFJ-UHFFFAOYSA-N 0.000 claims 1
- SOZRVJLJEGLPGH-UHFFFAOYSA-N 5-[2-chloro-6-(5-chloropyrimidin-2-yl)oxyphenyl]-3-(difluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=CC(=NO1)C(F)F SOZRVJLJEGLPGH-UHFFFAOYSA-N 0.000 claims 1
- XMZWACJDWGRJAZ-UHFFFAOYSA-N 5-[2-chloro-6-(5-chloropyrimidin-2-yl)oxyphenyl]-3-(trifluoromethyl)-1,2-oxazole Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=CC(=NO1)C(F)(F)F XMZWACJDWGRJAZ-UHFFFAOYSA-N 0.000 claims 1
- QTNHRGJECGBVIF-UHFFFAOYSA-N 5-chloro-2-[2-(5-chloropyridin-2-yl)phenoxy]pyrimidine Chemical compound ClC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=NC=C(C=C1)Cl QTNHRGJECGBVIF-UHFFFAOYSA-N 0.000 claims 1
- NCICYJPUVSWACW-UHFFFAOYSA-N 5-chloro-2-[2-[5-(trifluoromethyl)pyridin-2-yl]phenoxy]pyrimidine Chemical compound ClC=1C=NC(=NC1)OC1=C(C=CC=C1)C1=NC=C(C=C1)C(F)(F)F NCICYJPUVSWACW-UHFFFAOYSA-N 0.000 claims 1
- QXQHRVNRLDGAIC-UHFFFAOYSA-N 5-chloro-2-[3-chloro-2-(5-chloropyridin-2-yl)phenoxy]pyrimidine Chemical compound ClC=1C=NC(=NC1)OC1=C(C(=CC=C1)Cl)C1=NC=C(C=C1)Cl QXQHRVNRLDGAIC-UHFFFAOYSA-N 0.000 claims 1
- SKULPEWKXKSUNZ-UHFFFAOYSA-N 5-chloro-2-[4-methyl-2-[2-(trifluoromethyl)pyridin-4-yl]phenoxy]pyrimidine Chemical compound ClC=1C=NC(=NC1)OC1=C(C=C(C=C1)C)C1=CC(=NC=C1)C(F)(F)F SKULPEWKXKSUNZ-UHFFFAOYSA-N 0.000 claims 1
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims 1
- 108010000700 Acetolactate synthase Proteins 0.000 claims 1
- 229930192334 Auxin Natural products 0.000 claims 1
- 239000005476 Bentazone Substances 0.000 claims 1
- ZDQNUSTWYFSPLP-UHFFFAOYSA-N BrC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=CC(=NO1)C(F)(F)F Chemical compound BrC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=CC(=NO1)C(F)(F)F ZDQNUSTWYFSPLP-UHFFFAOYSA-N 0.000 claims 1
- CUDJYYKZWCKPCS-UHFFFAOYSA-N BrC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=CC(=NO1)C(F)F Chemical compound BrC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=CC(=NO1)C(F)F CUDJYYKZWCKPCS-UHFFFAOYSA-N 0.000 claims 1
- 239000005489 Bromoxynil Substances 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000005492 Carfentrazone-ethyl Substances 0.000 claims 1
- KRMJFJLNGUGGHW-UHFFFAOYSA-N ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Br)C1=CC(=NO1)C(F)F Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Br)C1=CC(=NO1)C(F)F KRMJFJLNGUGGHW-UHFFFAOYSA-N 0.000 claims 1
- HQWPMWBXIZSEJM-UHFFFAOYSA-N ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=NOC(=C1)C(F)F Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)Cl)C1=NOC(=C1)C(F)F HQWPMWBXIZSEJM-UHFFFAOYSA-N 0.000 claims 1
- LNMQUKUXISPCBA-UHFFFAOYSA-N ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)F)C1=CC(=NO1)C(F)(F)F Chemical compound ClC=1C=NC(=NC=1)OC1=C(C(=CC=C1)F)C1=CC(=NO1)C(F)(F)F LNMQUKUXISPCBA-UHFFFAOYSA-N 0.000 claims 1
- 239000005529 Florasulam Substances 0.000 claims 1
- QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 claims 1
- 239000005561 Glufosinate Substances 0.000 claims 1
- 239000005571 Isoxaflutole Substances 0.000 claims 1
- 239000005574 MCPA Substances 0.000 claims 1
- 239000005584 Metsulfuron-methyl Substances 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 239000005586 Nicosulfuron Substances 0.000 claims 1
- 108010060806 Photosystem II Protein Complex Proteins 0.000 claims 1
- 239000005616 Rimsulfuron Substances 0.000 claims 1
- 239000005620 Tembotrione Substances 0.000 claims 1
- 239000005623 Thifensulfuron-methyl Substances 0.000 claims 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims 1
- 239000005626 Tribenuron Substances 0.000 claims 1
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims 1
- 239000002363 auxin Substances 0.000 claims 1
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims 1
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims 1
- WGLYADVYCJUFAY-UHFFFAOYSA-N cloran Chemical compound C12CC3C(=O)OC(=O)C3CC2C2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl WGLYADVYCJUFAY-UHFFFAOYSA-N 0.000 claims 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 1
- JLYFCTQDENRSOL-VIFPVBQESA-N dimethenamid-P Chemical compound COC[C@H](C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-VIFPVBQESA-N 0.000 claims 1
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 claims 1
- FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 claims 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 claims 1
- 229940088649 isoxaflutole Drugs 0.000 claims 1
- RSMUVYRMZCOLBH-UHFFFAOYSA-N metsulfuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 RSMUVYRMZCOLBH-UHFFFAOYSA-N 0.000 claims 1
- 230000003278 mimic effect Effects 0.000 claims 1
- RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 claims 1
- OLZQTUCTGLHFTQ-UHFFFAOYSA-N octan-2-yl 2-(4-amino-3,5-dichloro-6-fluoropyridin-2-yl)oxyacetate Chemical group CCCCCCC(C)OC(=O)COC1=NC(F)=C(Cl)C(N)=C1Cl OLZQTUCTGLHFTQ-UHFFFAOYSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 claims 1
- GNHDVXLWBQYPJE-UHFFFAOYSA-N saflufenacil Chemical compound C1=C(Cl)C(C(=O)NS(=O)(=O)N(C)C(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1F GNHDVXLWBQYPJE-UHFFFAOYSA-N 0.000 claims 1
- 230000001568 sexual effect Effects 0.000 claims 1
- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 claims 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 claims 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 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461928129P | 2014-01-16 | 2014-01-16 | |
| US61/928,129 | 2014-01-16 | ||
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| RU2735278C2 (ru) * | 2015-03-18 | 2020-10-29 | ЭфЭмСи Корпорейшн | Замещенные производные пиримидинилокси-пиридина в качестве гербицидов |
| TWI713530B (zh) * | 2015-06-05 | 2020-12-21 | 美商艾佛艾姆希公司 | 作為除草劑之嘧啶氧基苯衍生物 |
| BR112018000687B1 (pt) | 2015-07-13 | 2021-05-04 | Fmc Corporation | composto, composições herbicidas, misturas herbicidas e métodos para o controle do crescimento de vegetação indesejada |
| BR112018008467A2 (pt) * | 2015-10-28 | 2018-11-06 | Syngenta Participations Ag | derivados de oxadiazol microbiocidas |
| TW201904947A (zh) | 2017-05-02 | 2019-02-01 | 美商富曼西公司 | 作為除草劑的嘧啶氧基苯稠合化合物 |
| AR114169A1 (es) * | 2017-12-22 | 2020-07-29 | Bayer Cropscience Ag | Hidroxiisoxazolinas y derivados de estos |
| US20210002232A1 (en) * | 2018-03-09 | 2021-01-07 | Pi Industries Ltd. | Heterocyclic compounds as fungicides |
| WO2020002089A1 (de) | 2018-06-25 | 2020-01-02 | Bayer Aktiengesellschaft | Substituierte 2-heteroaryloxypyridine sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| CN108997325B (zh) * | 2018-07-06 | 2020-08-04 | 浙江工业大学 | 一种芳基联噻唑类化合物和应用 |
| GB201818013D0 (en) | 2018-11-05 | 2018-12-19 | Syngenta Participations Ag | Improvements in or relating to organic compunds |
| CN111217762B (zh) * | 2018-11-23 | 2021-08-20 | 华中师范大学 | 多卤代5-(2-羟基苯基)异噁唑类化合物及其制备方法和应用 |
| EP3670505A1 (de) * | 2018-12-18 | 2020-06-24 | Bayer AG | Substituierte pyridinyloxybenzole sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| CA3125948A1 (en) * | 2019-01-09 | 2020-07-16 | Upl Ltd | Herbicidal combination |
| AR118951A1 (es) * | 2019-05-20 | 2021-11-10 | Syngenta Crop Protection Ag | Composiciones y métodos para el control de malezas |
| WO2021028419A1 (de) | 2019-08-13 | 2021-02-18 | Bayer Aktiengesellschaft | Substituierte 3-(2-heteroaryloxyphenyl)isoxazoline sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| WO2021028421A1 (de) | 2019-08-13 | 2021-02-18 | Bayer Aktiengesellschaft | Substituierte 5-(2-heteroaryloxyphenyl)isoxazoline sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| GB201915043D0 (en) * | 2019-10-17 | 2019-12-04 | Syngenta Crop Protection Ag | Improvements in or relating to organic compounds |
| GB201916676D0 (en) | 2019-11-15 | 2020-01-01 | Syngenta Crop Protection Ag | Improvements in or relating to organic compounds |
| AR120598A1 (es) | 2019-12-02 | 2022-02-23 | Fmc Corp | Proceso para la síntesis de un 2-(5-isoxazolil)-fenol |
| TW202130623A (zh) * | 2019-12-02 | 2021-08-16 | 美商富曼西公司 | 用於合成2-硫烷嘧啶的製程 |
| GB202005175D0 (en) * | 2020-04-08 | 2020-05-20 | Syngenta Crop Protection Ag | Improvements in or relating to organic compounds |
| US20230303549A1 (en) * | 2020-06-30 | 2023-09-28 | Bayer Aktiengesellschaft | Substituted heteroaryloxypyridines, the salts thereof and their use as herbicidal agents |
| GB202016569D0 (en) * | 2020-10-19 | 2020-12-02 | Syngenta Crop Protection Ag | Herbicidal compositions |
| GB202114863D0 (en) * | 2021-10-18 | 2021-12-01 | Syngenta Crop Protection Ag | Improvements in or relating to organic compounds |
| WO2023208866A1 (en) | 2022-04-25 | 2023-11-02 | Syngenta Crop Protection Ag | Herbicidal compositions |
| WO2023222834A1 (en) | 2022-05-20 | 2023-11-23 | Syngenta Crop Protection Ag | Herbicidal compositions |
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