CN113292502A - 作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯 - Google Patents
作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯 Download PDFInfo
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- CN113292502A CN113292502A CN202110442807.0A CN202110442807A CN113292502A CN 113292502 A CN113292502 A CN 113292502A CN 202110442807 A CN202110442807 A CN 202110442807A CN 113292502 A CN113292502 A CN 113292502A
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- radical
- alkyl
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- chloro
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- 239000004009 herbicide Substances 0.000 title claims abstract description 28
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 title description 3
- NUILQFNJMVDDJG-UHFFFAOYSA-N 4-aminopyrimidine-2-carboxylic acid Chemical class NC1=CC=NC(C(O)=O)=N1 NUILQFNJMVDDJG-UHFFFAOYSA-N 0.000 title description 3
- 229960004979 fampridine Drugs 0.000 title description 3
- -1 2-substituted phenyl Chemical group 0.000 claims abstract description 236
- 238000000034 method Methods 0.000 claims abstract description 29
- 150000001875 compounds Chemical class 0.000 claims description 252
- 239000000203 mixture Substances 0.000 claims description 123
- 150000003254 radicals Chemical class 0.000 claims description 120
- 229910052736 halogen Inorganic materials 0.000 claims description 105
- 150000002367 halogens Chemical group 0.000 claims description 105
- 229910052801 chlorine Inorganic materials 0.000 claims description 92
- 229910052740 iodine Inorganic materials 0.000 claims description 88
- 229910052731 fluorine Inorganic materials 0.000 claims description 85
- 229910052794 bromium Inorganic materials 0.000 claims description 82
- 229910052739 hydrogen Inorganic materials 0.000 claims description 69
- 239000001257 hydrogen Substances 0.000 claims description 63
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 45
- 125000000304 alkynyl group Chemical group 0.000 claims description 41
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 38
- 230000002363 herbicidal effect Effects 0.000 claims description 37
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 37
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 32
- 125000001188 haloalkyl group Chemical group 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 30
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 30
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 28
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 26
- 150000003839 salts Chemical class 0.000 claims description 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 24
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 19
- 150000001204 N-oxides Chemical class 0.000 claims description 18
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 18
- 229920006395 saturated elastomer Polymers 0.000 claims description 17
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- 239000002671 adjuvant Substances 0.000 claims description 9
- 125000004414 alkyl thio group Chemical group 0.000 claims description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 6
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 5
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 claims description 5
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 5
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims description 4
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 4
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 3
- 125000006519 CCH3 Chemical group 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 150000002431 hydrogen Chemical group 0.000 claims 10
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 4
- 125000004076 pyridyl group Chemical group 0.000 abstract description 3
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 abstract description 2
- YPOXGDJGKBXRFP-UHFFFAOYSA-N pyrimidine-4-carboxylic acid Chemical class OC(=O)C1=CC=NC=N1 YPOXGDJGKBXRFP-UHFFFAOYSA-N 0.000 abstract 1
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 129
- 239000011541 reaction mixture Substances 0.000 description 123
- 239000000243 solution Substances 0.000 description 113
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 112
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 105
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 105
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 104
- 238000002360 preparation method Methods 0.000 description 99
- 235000019439 ethyl acetate Nutrition 0.000 description 83
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 78
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 72
- 239000007787 solid Substances 0.000 description 72
- 241000196324 Embryophyta Species 0.000 description 65
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 59
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- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 54
- 238000006243 chemical reaction Methods 0.000 description 54
- 238000005160 1H NMR spectroscopy Methods 0.000 description 52
- 239000012044 organic layer Substances 0.000 description 47
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 47
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 46
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 44
- 238000001914 filtration Methods 0.000 description 43
- 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 41
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 38
- 238000003818 flash chromatography Methods 0.000 description 38
- 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 33
- 239000003921 oil Substances 0.000 description 33
- 235000019198 oils Nutrition 0.000 description 33
- 239000005582 Metosulam Substances 0.000 description 32
- VGHPMIFEKOFHHQ-UHFFFAOYSA-N Metosulam Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl VGHPMIFEKOFHHQ-UHFFFAOYSA-N 0.000 description 32
- 238000001035 drying Methods 0.000 description 32
- 238000004293 19F NMR spectroscopy Methods 0.000 description 31
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 29
- 238000012360 testing method Methods 0.000 description 29
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 29
- 238000000119 electrospray ionisation mass spectrum Methods 0.000 description 28
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 26
- CSNNHWWHGAXBCP-UHFFFAOYSA-L magnesium sulphate Substances [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 24
- 238000003756 stirring Methods 0.000 description 24
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 22
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 22
- 241000234653 Cyperus Species 0.000 description 21
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 21
- 239000003112 inhibitor Substances 0.000 description 21
- 238000000746 purification Methods 0.000 description 20
- 239000011734 sodium Substances 0.000 description 20
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 19
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 19
- 235000011089 carbon dioxide Nutrition 0.000 description 19
- 150000002148 esters Chemical class 0.000 description 19
- 239000000047 product Substances 0.000 description 19
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- 238000002451 electron ionisation mass spectrometry Methods 0.000 description 18
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 17
- 239000006013 carbendazim Substances 0.000 description 17
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 17
- 239000002904 solvent Substances 0.000 description 17
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 16
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- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 description 15
- 239000012074 organic phase Substances 0.000 description 15
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 14
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- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 13
- 239000011698 potassium fluoride Substances 0.000 description 13
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- 239000000741 silica gel Substances 0.000 description 13
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- VEKIYFGCEAJDDT-UHFFFAOYSA-N 2-pyridin-3-ylpyridine Chemical compound N1=CC=CC=C1C1=CC=CN=C1 VEKIYFGCEAJDDT-UHFFFAOYSA-N 0.000 description 12
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- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
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- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
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- 230000001678 irradiating effect Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
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- 150000002632 lipids Chemical class 0.000 description 1
- DBTNVRCCIDISMV-UHFFFAOYSA-L lithium;magnesium;propane;dichloride Chemical compound [Li+].[Mg+2].[Cl-].[Cl-].C[CH-]C DBTNVRCCIDISMV-UHFFFAOYSA-L 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- HAWPXGHAZFHHAD-UHFFFAOYSA-N mechlorethamine Chemical compound ClCCN(C)CCCl HAWPXGHAZFHHAD-UHFFFAOYSA-N 0.000 description 1
- 229960004961 mechlorethamine Drugs 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 description 1
- MEBQXILRKZHVCX-UHFFFAOYSA-N methidathion Chemical compound COC1=NN(CSP(=S)(OC)OC)C(=O)S1 MEBQXILRKZHVCX-UHFFFAOYSA-N 0.000 description 1
- ZLVYVRPDAZFSGR-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-(2,6-dichloropyridin-3-yl)pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=NC(Cl)=CC=2)Cl)=C1 ZLVYVRPDAZFSGR-UHFFFAOYSA-N 0.000 description 1
- WGKRAPJRDJPSFC-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-(3-fluoro-4-iodo-2-methylphenyl)pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(I)=CC=2)C)=C1 WGKRAPJRDJPSFC-UHFFFAOYSA-N 0.000 description 1
- AGQQROCGXPSWHN-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-(4-chloro-2-ethenyl-3-fluorophenyl)pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2)C=C)=C1 AGQQROCGXPSWHN-UHFFFAOYSA-N 0.000 description 1
- CBPJENHYKRKZCQ-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-(4-chloro-3,6-difluoro-2-methoxyphenyl)pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2F)OC)=C1 CBPJENHYKRKZCQ-UHFFFAOYSA-N 0.000 description 1
- USMMTCBQCPXCDN-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-[4-[dimethyl(phenyl)silyl]-3-fluoro-2-methylphenyl]pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(=CC=2)[Si](C)(C)C=2C=CC=CC=2)C)=C1 USMMTCBQCPXCDN-UHFFFAOYSA-N 0.000 description 1
- NWHGSXJBEWJOCT-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-[4-chloro-2-(difluoromethyl)-3-fluorophenyl]pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2)C(F)F)=C1 NWHGSXJBEWJOCT-UHFFFAOYSA-N 0.000 description 1
- VHKCGDNLSOCZGN-UHFFFAOYSA-N methyl 4-acetamido-3-chloro-6-[4-chloro-3-fluoro-2-(hydroxymethyl)phenyl]pyridine-2-carboxylate Chemical compound CC(=O)NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2)CO)=C1 VHKCGDNLSOCZGN-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
- 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
- VKZZGBQGFWXJSR-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-fluoro-6-(2-fluoro-6-methylpyridin-3-yl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=NC(C)=CC=2)F)=C1F VKZZGBQGFWXJSR-UHFFFAOYSA-N 0.000 description 1
- SUBCFTQVBFSLBA-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-fluoro-6-(3-fluoro-2-methoxyphenyl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C=CC=2)OC)=C1F SUBCFTQVBFSLBA-UHFFFAOYSA-N 0.000 description 1
- QYXZOLDSKUOOJB-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-fluoro-6-(6-iodopyridin-3-yl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=NC(I)=CC=2)=C1F QYXZOLDSKUOOJB-UHFFFAOYSA-N 0.000 description 1
- MCEFZGSSSFCYJC-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-fluoro-6-[2-fluoro-6-(trifluoromethyl)pyridin-3-yl]pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=NC(=CC=2)C(F)(F)F)F)=C1F MCEFZGSSSFCYJC-UHFFFAOYSA-N 0.000 description 1
- ZXVVUHPWARFKNR-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-fluoro-6-[2-methoxy-6-(trifluoromethyl)pyridin-3-yl]pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=NC(=CC=2)C(F)(F)F)OC)=C1F ZXVVUHPWARFKNR-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
- GGPLNHFKKLUESD-UHFFFAOYSA-N methyl 4-amino-3-chloro-5-methyl-6-[6-(trifluoromethyl)pyridin-3-yl]pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=NC(=CC=2)C(F)(F)F)=C1C GGPLNHFKKLUESD-UHFFFAOYSA-N 0.000 description 1
- HUECTYOQUGETHX-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(2-chloro-6-methoxypyridin-3-yl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=NC(OC)=CC=2)Cl)=C1F HUECTYOQUGETHX-UHFFFAOYSA-N 0.000 description 1
- IRQBZEOKRQNWSM-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-chloro-3-fluoro-2-methoxyphenyl)-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2)OC)=C1F IRQBZEOKRQNWSM-UHFFFAOYSA-N 0.000 description 1
- CKSAOUSGXKLVKZ-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(4-chloro-3-fluoro-2-methoxyphenyl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2)OC)=C1 CKSAOUSGXKLVKZ-UHFFFAOYSA-N 0.000 description 1
- XEDFVALLFDKIAC-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-(6-chloro-2-fluoropyridin-3-yl)pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=NC(Cl)=CC=2)F)=C1 XEDFVALLFDKIAC-UHFFFAOYSA-N 0.000 description 1
- HNVFNNGGDMTNQL-UHFFFAOYSA-N methyl 4-amino-3-chloro-6-[4-chloro-2-(difluoromethyl)-3-methoxyphenyl]pyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(OC)C(Cl)=CC=2)C(F)F)=C1 HNVFNNGGDMTNQL-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
- ISRHUXRUAAUHML-UHFFFAOYSA-N methyl 4-amino-3-ethenyl-5-fluoro-6-[6-(trifluoromethyl)pyridin-3-yl]pyridine-2-carboxylate Chemical compound NC1=C(C=C)C(C(=O)OC)=NC(C=2C=NC(=CC=2)C(F)(F)F)=C1F ISRHUXRUAAUHML-UHFFFAOYSA-N 0.000 description 1
- PVGFYNMPHYBJPU-UHFFFAOYSA-N methyl 4-amino-6-(6-bromopyridin-3-yl)-3-chloro-5-fluoropyridine-2-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=NC(Br)=CC=2)=C1F PVGFYNMPHYBJPU-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
- WXUNXXKSYBUHMK-UHFFFAOYSA-N methyl 4-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate;methyl 5-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate Chemical compound COC(=O)C1=CC=C(C)C=C1C1=NC(C)(C(C)C)C(=O)N1.COC(=O)C1=CC(C)=CC=C1C1=NC(C)(C(C)C)C(=O)N1 WXUNXXKSYBUHMK-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
- SNMRBJFJRSFPKZ-UHFFFAOYSA-N methyl 6-amino-2-(2,4-dichloro-3-fluorophenyl)-5-methoxypyrimidine-4-carboxylate Chemical compound NC1=C(OC)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2)Cl)=N1 SNMRBJFJRSFPKZ-UHFFFAOYSA-N 0.000 description 1
- MNTJRDCMMMZBQJ-UHFFFAOYSA-N methyl 6-amino-2-(4-chloro-3-fluoro-2-methoxyphenyl)-5-methoxypyrimidine-4-carboxylate Chemical compound NC1=C(OC)C(C(=O)OC)=NC(C=2C(=C(F)C(Cl)=CC=2)OC)=N1 MNTJRDCMMMZBQJ-UHFFFAOYSA-N 0.000 description 1
- QWOGPGBREMPNFZ-UHFFFAOYSA-N methyl 6-amino-2-chloro-5-ethenylpyrimidine-4-carboxylate Chemical compound COC(=O)C1=NC(Cl)=NC(N)=C1C=C QWOGPGBREMPNFZ-UHFFFAOYSA-N 0.000 description 1
- DMWHRXIYJRVEPS-UHFFFAOYSA-N methyl 6-amino-5-chloro-2-[6-(trifluoromethyl)pyridin-3-yl]pyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=NC(=CC=2)C(F)(F)F)=N1 DMWHRXIYJRVEPS-UHFFFAOYSA-N 0.000 description 1
- MYURAHUSYDVWQA-UHFFFAOYSA-N methyl n'-(4-chlorophenyl)-n,n-dimethylcarbamimidate Chemical compound COC(N(C)C)=NC1=CC=C(Cl)C=C1 MYURAHUSYDVWQA-UHFFFAOYSA-N 0.000 description 1
- LFDDUUFFHPNIPZ-UHFFFAOYSA-N methyl n-[4-[[2-(4-chloro-2-methylphenoxy)acetyl]amino]phenyl]sulfonylcarbamate Chemical compound C1=CC(S(=O)(=O)NC(=O)OC)=CC=C1NC(=O)COC1=CC=C(Cl)C=C1C LFDDUUFFHPNIPZ-UHFFFAOYSA-N 0.000 description 1
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- VCCPBPXMXHHRLN-UHFFFAOYSA-N methylsulfinylmethane;propan-2-one Chemical compound CC(C)=O.CS(C)=O VCCPBPXMXHHRLN-UHFFFAOYSA-N 0.000 description 1
- 229960002939 metizoline Drugs 0.000 description 1
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- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 description 1
- KGMBZDZHRAFLBY-UHFFFAOYSA-N n-(butoxymethyl)-n-(2-tert-butyl-6-methylphenyl)-2-chloroacetamide Chemical compound CCCCOCN(C(=O)CCl)C1=C(C)C=CC=C1C(C)(C)C KGMBZDZHRAFLBY-UHFFFAOYSA-N 0.000 description 1
- YGBMCLDVRUGXOV-UHFFFAOYSA-N n-[6-[6-chloro-5-[(4-fluorophenyl)sulfonylamino]pyridin-3-yl]-1,3-benzothiazol-2-yl]acetamide Chemical compound C1=C2SC(NC(=O)C)=NC2=CC=C1C(C=1)=CN=C(Cl)C=1NS(=O)(=O)C1=CC=C(F)C=C1 YGBMCLDVRUGXOV-UHFFFAOYSA-N 0.000 description 1
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- 239000001301 oxygen Substances 0.000 description 1
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- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
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- 239000003209 petroleum derivative Substances 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
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- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
- RJQUHEYNLDNJLN-UHFFFAOYSA-N picloram-methyl Chemical compound COC(=O)C1=NC(Cl)=C(Cl)C(N)=C1Cl RJQUHEYNLDNJLN-UHFFFAOYSA-N 0.000 description 1
- 235000020233 pistachio Nutrition 0.000 description 1
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- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
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- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- 229960003910 promethazine Drugs 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940010310 propylene glycol dioleate Drugs 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
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- 239000008262 pumice Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
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- 125000005554 pyridyloxy group Chemical group 0.000 description 1
- DEIKMOQTJBGGAX-DJKKODMXSA-N pyriminobac Chemical compound CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(O)=O DEIKMOQTJBGGAX-DJKKODMXSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 description 1
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 1
- 235000009736 ragweed Nutrition 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- FDBYIYFVSAHJLY-UHFFFAOYSA-N resmetirom Chemical compound N1C(=O)C(C(C)C)=CC(OC=2C(=CC(=CC=2Cl)N2C(NC(=O)C(C#N)=N2)=O)Cl)=N1 FDBYIYFVSAHJLY-UHFFFAOYSA-N 0.000 description 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 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229940115128 sebex Drugs 0.000 description 1
- 229940000207 selenious acid Drugs 0.000 description 1
- MCAHWIHFGHIESP-UHFFFAOYSA-N selenous acid Chemical compound O[Se](O)=O MCAHWIHFGHIESP-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- MRTAVLDNYYEJHK-UHFFFAOYSA-M sodium;2-chloro-2,2-difluoroacetate Chemical compound [Na+].[O-]C(=O)C(F)(F)Cl MRTAVLDNYYEJHK-UHFFFAOYSA-M 0.000 description 1
- NZYOAGBNMCVQIV-UHFFFAOYSA-N sodium;chloro-(4-methylphenyl)sulfonylazanide;trihydrate Chemical compound O.O.O.[Na+].CC1=CC=C(S(=O)(=O)[N-]Cl)C=C1 NZYOAGBNMCVQIV-UHFFFAOYSA-N 0.000 description 1
- VMSRVIHUFHQIAL-UHFFFAOYSA-M sodium;n,n-dimethylcarbamodithioate Chemical compound [Na+].CN(C)C([S-])=S VMSRVIHUFHQIAL-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 1
- 229960004306 sulfadiazine Drugs 0.000 description 1
- CCEKAJIANROZEO-UHFFFAOYSA-N sulfluramid Chemical compound CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CCEKAJIANROZEO-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- YHSXJEYVXPPZAC-UHFFFAOYSA-N tributyl-[6-(trifluoromethyl)pyridin-3-yl]stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=C(C(F)(F)F)N=C1 YHSXJEYVXPPZAC-UHFFFAOYSA-N 0.000 description 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical class OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- 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
- 229910052905 tridymite Inorganic materials 0.000 description 1
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-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
- FNKGPXOPDRYAAQ-UHFFFAOYSA-K trisodium;3-bis(3-sulfonatophenyl)phosphanylbenzenesulfonate;hydrate Chemical compound O.[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC(P(C=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=C(C=CC=2)S([O-])(=O)=O)=C1 FNKGPXOPDRYAAQ-UHFFFAOYSA-K 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
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 235000005765 wild carrot Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—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
Landscapes
- 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)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361791892P | 2013-03-15 | 2013-03-15 | |
| US61/791,892 | 2013-03-15 | ||
| CN201480026863.4A CN105208859A (zh) | 2013-03-15 | 2014-03-12 | 作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201480026863.4A Division CN105208859A (zh) | 2013-03-15 | 2014-03-12 | 作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN113292502A true CN113292502A (zh) | 2021-08-24 |
Family
ID=51529785
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110442807.0A Pending CN113292502A (zh) | 2013-03-15 | 2014-03-12 | 作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯 |
| CN201480026863.4A Pending CN105208859A (zh) | 2013-03-15 | 2014-03-12 | 作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201480026863.4A Pending CN105208859A (zh) | 2013-03-15 | 2014-03-12 | 作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10765114B2 (https=) |
| EP (1) | EP2967057B1 (https=) |
| JP (3) | JP2016514138A (https=) |
| CN (2) | CN113292502A (https=) |
| AR (1) | AR095303A1 (https=) |
| BR (1) | BR102014006211B8 (https=) |
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| WO (1) | WO2014150809A1 (https=) |
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| CN119707787A (zh) * | 2024-12-24 | 2025-03-28 | 陕西师范大学 | 一种光连续流动合成4-烷基吡啶类化合物的方法 |
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| US20170280718A1 (en) * | 2014-09-10 | 2017-10-05 | The Regents Of The University Of California | Herbicidal and fungicidal compositions and their uses |
| GB201604969D0 (en) | 2016-03-23 | 2016-05-04 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| GB201604970D0 (en) | 2016-03-23 | 2016-05-04 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| US10087164B2 (en) * | 2016-05-19 | 2018-10-02 | Dow Agrosciences Llc | Synthesis of 6-aryl-4-aminopicolinates and 2-aryl-6-aminopyrimidine-4-carboxylates by direct Suzuki coupling |
| WO2018004223A1 (ko) | 2016-06-27 | 2018-01-04 | (주)목우연구소 | 이속사졸린 고리를 포함하는 피리딘계 화합물 및 제초제로서의 이의 용도 |
| EP3487848B1 (en) * | 2016-07-25 | 2020-09-30 | Basf Se | Herbicidal pyrimidine compounds |
| JP6681314B2 (ja) * | 2016-10-31 | 2020-04-15 | 日機装株式会社 | 水処理装置および水処理方法 |
| GB201715324D0 (en) * | 2017-09-22 | 2017-11-08 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| GB201715323D0 (en) * | 2017-09-22 | 2017-11-08 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| CN109704961A (zh) * | 2019-02-16 | 2019-05-03 | 安徽华胜医药科技有限公司 | 一种2-溴-2-(2-氟-3-甲氧基苯基)乙酸乙酯的合成方法 |
| CN110885290A (zh) * | 2019-12-16 | 2020-03-17 | 阿里生物新材料（常州）有限公司 | 一种3-氟-2-甲基-4-三氟甲基苯胺盐酸盐的合成方法 |
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| CN119707787A (zh) * | 2024-12-24 | 2025-03-28 | 陕西师范大学 | 一种光连续流动合成4-烷基吡啶类化合物的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| PL2967057T3 (pl) | 2019-05-31 |
| JP2016514138A (ja) | 2016-05-19 |
| ES2712103T3 (es) | 2019-05-09 |
| US20140274703A1 (en) | 2014-09-18 |
| EP2967057A1 (en) | 2016-01-20 |
| BR102014006211A2 (pt) | 2016-08-02 |
| AR095303A1 (es) | 2015-10-07 |
| US10765114B2 (en) | 2020-09-08 |
| CN105208859A (zh) | 2015-12-30 |
| UY35475A (es) | 2014-10-31 |
| JP6757374B2 (ja) | 2020-09-16 |
| EP2967057B1 (en) | 2018-11-21 |
| WO2014150809A1 (en) | 2014-09-25 |
| HUE041698T2 (hu) | 2019-05-28 |
| JP2018199686A (ja) | 2018-12-20 |
| BR102014006211B1 (pt) | 2020-02-04 |
| EP2967057A4 (en) | 2017-03-01 |
| BR102014006211B8 (pt) | 2022-08-23 |
| JP2019073516A (ja) | 2019-05-16 |
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