EA004941B1 - СОЕДИНЕНИЯ N-(5,7-ДИМЕТОКСИ[1,2,4]ТРИАЗОЛО [1,5-a]ПИРИМИДИН-2-ил) АРИЛСУЛЬФОНАМИДА И ИХ ИСПОЛЬЗОВАНИЕ В КАЧЕСТВЕ ГЕРБИЦИДОВ - Google Patents
СОЕДИНЕНИЯ N-(5,7-ДИМЕТОКСИ[1,2,4]ТРИАЗОЛО [1,5-a]ПИРИМИДИН-2-ил) АРИЛСУЛЬФОНАМИДА И ИХ ИСПОЛЬЗОВАНИЕ В КАЧЕСТВЕ ГЕРБИЦИДОВ Download PDFInfo
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- EA004941B1 EA004941B1 EA200200748A EA200200748A EA004941B1 EA 004941 B1 EA004941 B1 EA 004941B1 EA 200200748 A EA200200748 A EA 200200748A EA 200200748 A EA200200748 A EA 200200748A EA 004941 B1 EA004941 B1 EA 004941B1
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- EA
- Eurasian Patent Office
- Prior art keywords
- compound
- compounds
- alkyl
- hundred
- formula
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 97
- 239000004009 herbicide Substances 0.000 title description 26
- 239000000203 mixture Substances 0.000 claims abstract description 46
- -1 arylsulfonamide compound Chemical class 0.000 claims abstract description 35
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 24
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000002671 adjuvant Substances 0.000 claims abstract description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 8
- 150000003839 salts Chemical class 0.000 claims abstract description 8
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000000010 aprotic solvent Substances 0.000 claims abstract description 3
- 230000003197 catalytic effect Effects 0.000 claims abstract description 3
- 125000005843 halogen group Chemical group 0.000 claims abstract 8
- 229910052736 halogen Inorganic materials 0.000 claims description 11
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000004421 aryl sulphonamide group Chemical group 0.000 claims description 7
- 239000013256 coordination polymer Substances 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 9
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 5
- 238000002360 preparation method Methods 0.000 abstract description 5
- 125000003342 alkenyl group Chemical group 0.000 abstract description 4
- 125000000304 alkynyl group Chemical group 0.000 abstract description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract description 4
- 241000196324 Embryophyta Species 0.000 description 49
- 239000000843 powder Substances 0.000 description 21
- 238000012360 testing method Methods 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000007787 solid Substances 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- 230000006378 damage Effects 0.000 description 10
- 239000012141 concentrate Substances 0.000 description 9
- 239000011550 stock solution Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000000969 carrier Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000004927 clay Substances 0.000 description 6
- 238000007865 diluting Methods 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- 244000075850 Avena orientalis Species 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 239000000729 antidote Substances 0.000 description 5
- 150000001768 cations Chemical class 0.000 description 5
- 230000001276 controlling effect Effects 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- DWJMBQYORXLGAE-UHFFFAOYSA-N pyridine-2-sulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=N1 DWJMBQYORXLGAE-UHFFFAOYSA-N 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 229940075522 antidotes Drugs 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- LVFRCHIUUKWBLR-UHFFFAOYSA-N 4,6-dimethoxypyrimidin-2-amine Chemical compound COC1=CC(OC)=NC(N)=N1 LVFRCHIUUKWBLR-UHFFFAOYSA-N 0.000 description 3
- 235000007320 Avena fatua Nutrition 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 3
- WREOTYWODABZMH-DTZQCDIJSA-N [[(2r,3s,4r,5r)-3,4-dihydroxy-5-[2-oxo-4-(2-phenylethoxyamino)pyrimidin-1-yl]oxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]1N(C=C\1)C(=O)NC/1=N\OCCC1=CC=CC=C1 WREOTYWODABZMH-DTZQCDIJSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000007900 aqueous suspension Substances 0.000 description 3
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical group ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 3
- 229940125758 compound 15 Drugs 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000034994 death Effects 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- 230000000855 fungicidal effect Effects 0.000 description 3
- 239000000417 fungicide Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 229940124530 sulfonamide Drugs 0.000 description 3
- 150000003456 sulfonamides Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 2
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
- SJEIPAUSEWIHJI-UHFFFAOYSA-N 5,7-dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-amine Chemical compound N1=C(OC)C=C(OC)N2N=C(N)N=C21 SJEIPAUSEWIHJI-UHFFFAOYSA-N 0.000 description 2
- 240000001592 Amaranthus caudatus Species 0.000 description 2
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
- 206010021033 Hypomenorrhoea Diseases 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 240000006394 Sorghum bicolor Species 0.000 description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 150000008331 benzenesulfonamides Chemical class 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 244000038559 crop plants Species 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- ALVPFGSHPUPROW-UHFFFAOYSA-N dipropyl disulfide Chemical compound CCCSSCCC ALVPFGSHPUPROW-UHFFFAOYSA-N 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- BDTDECDAHYOJRO-UHFFFAOYSA-N ethyl n-(sulfanylidenemethylidene)carbamate Chemical compound CCOC(=O)N=C=S BDTDECDAHYOJRO-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 230000035784 germination Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000003973 irrigation Methods 0.000 description 2
- 230000002262 irrigation Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- JZGSGJCCWHTYHY-UHFFFAOYSA-N n-(5,7-dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)benzenesulfonamide Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1NS(=O)(=O)C1=CC=CC=C1 JZGSGJCCWHTYHY-UHFFFAOYSA-N 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 239000005416 organic matter Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- JQJOGAGLBDBMLU-UHFFFAOYSA-N pyridine-2-sulfonyl chloride Chemical group ClS(=O)(=O)C1=CC=CC=N1 JQJOGAGLBDBMLU-UHFFFAOYSA-N 0.000 description 2
- 150000003222 pyridines Chemical class 0.000 description 2
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 238000003828 vacuum filtration Methods 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 description 1
- 150000005589 1,3-dimethoxybenzenes Chemical class 0.000 description 1
- LQIAZOCLNBBZQK-UHFFFAOYSA-N 1-(1,2-Diphosphanylethyl)pyrrolidin-2-one Chemical compound PCC(P)N1CCCC1=O LQIAZOCLNBBZQK-UHFFFAOYSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- BCMYXYHEMGPZJN-UHFFFAOYSA-N 1-chloro-2-isocyanatoethane Chemical compound ClCCN=C=O BCMYXYHEMGPZJN-UHFFFAOYSA-N 0.000 description 1
- XHONYVFDZSPELQ-UHFFFAOYSA-N 1-methoxy-3-(trifluoromethyl)benzene Chemical compound COC1=CC=CC(C(F)(F)F)=C1 XHONYVFDZSPELQ-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- PQODWTNHDKDHIW-UHFFFAOYSA-N 2,3-dichlorobenzenesulfonyl chloride Chemical compound ClC1=CC=CC(S(Cl)(=O)=O)=C1Cl PQODWTNHDKDHIW-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- BFBKUYFMLNOLOQ-UHFFFAOYSA-N 2-butoxyethanamine Chemical compound CCCCOCCN BFBKUYFMLNOLOQ-UHFFFAOYSA-N 0.000 description 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 description 1
- 125000004791 2-fluoroethoxy group Chemical group FCCO* 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- BYGXVIBRFSQTPY-UHFFFAOYSA-N 2-methoxy-4-(trifluoromethyl)pyridine Chemical compound COC1=CC(C(F)(F)F)=CC=N1 BYGXVIBRFSQTPY-UHFFFAOYSA-N 0.000 description 1
- DMKFWTCEKLNOKK-UHFFFAOYSA-N 2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonyl chloride Chemical compound COC1=NC=CC(C(F)(F)F)=C1S(Cl)(=O)=O DMKFWTCEKLNOKK-UHFFFAOYSA-N 0.000 description 1
- BJYNYQGJTZULJI-UHFFFAOYSA-N 2-methoxy-5-methylbenzenesulfonyl chloride Chemical compound COC1=CC=C(C)C=C1S(Cl)(=O)=O BJYNYQGJTZULJI-UHFFFAOYSA-N 0.000 description 1
- NBZJAHPYJUXLQC-UHFFFAOYSA-N 2-methoxy-6-(trifluoromethyl)benzenesulfonyl chloride Chemical compound COC1=CC=CC(C(F)(F)F)=C1S(Cl)(=O)=O NBZJAHPYJUXLQC-UHFFFAOYSA-N 0.000 description 1
- NDYYWMXJZWHRLZ-UHFFFAOYSA-N 2-methoxyethyl carbonochloridate Chemical compound COCCOC(Cl)=O NDYYWMXJZWHRLZ-UHFFFAOYSA-N 0.000 description 1
- NGBMMSDIZNGAOK-UHFFFAOYSA-N 2h-triazolo[4,5-d]pyrimidine-5-sulfonamide Chemical class NS(=O)(=O)C1=NC=C2NN=NC2=N1 NGBMMSDIZNGAOK-UHFFFAOYSA-N 0.000 description 1
- 150000003929 3-aminopyridines Chemical class 0.000 description 1
- MCNQUWLLXZZZAC-UHFFFAOYSA-N 4-cyano-1-(2,4-dichlorophenyl)-5-(4-methoxyphenyl)-n-piperidin-1-ylpyrazole-3-carboxamide Chemical compound C1=CC(OC)=CC=C1C1=C(C#N)C(C(=O)NN2CCCCC2)=NN1C1=CC=C(Cl)C=C1Cl MCNQUWLLXZZZAC-UHFFFAOYSA-N 0.000 description 1
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 1
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 1
- 108010000700 Acetolactate synthase Proteins 0.000 description 1
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 description 1
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- NKFLEFWUYAUDJV-UHFFFAOYSA-N pyridine-3-sulfonamide Chemical compound NS(=O)(=O)C1=CC=CN=C1 NKFLEFWUYAUDJV-UHFFFAOYSA-N 0.000 description 1
- CDRNYKLYADJTMN-UHFFFAOYSA-N pyridine-3-sulfonyl chloride Chemical class ClS(=O)(=O)C1=CC=CN=C1 CDRNYKLYADJTMN-UHFFFAOYSA-N 0.000 description 1
- FFWJHVGUAKWTKW-UHFFFAOYSA-N pyridine-3-thiol Chemical compound SC1=CC=CN=C1 FFWJHVGUAKWTKW-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 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
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- PNQBEPDZQUOCNY-UHFFFAOYSA-N trifluoroacetyl chloride Chemical compound FC(F)(F)C(Cl)=O PNQBEPDZQUOCNY-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24583600P | 2000-11-03 | 2000-11-03 | |
| PCT/US2001/046150 WO2002036595A2 (en) | 2000-11-03 | 2001-11-02 | N-(5,7-DIMETHOXY[1,2,4]TRIAZOLO[1,5-a]PYRIMIDIN-2-YL) ARYLSULFONAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200200748A1 EA200200748A1 (ru) | 2002-12-26 |
| EA004941B1 true EA004941B1 (ru) | 2004-10-28 |
Family
ID=22928273
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200200748A EA004941B1 (ru) | 2000-11-03 | 2001-11-02 | СОЕДИНЕНИЯ N-(5,7-ДИМЕТОКСИ[1,2,4]ТРИАЗОЛО [1,5-a]ПИРИМИДИН-2-ил) АРИЛСУЛЬФОНАМИДА И ИХ ИСПОЛЬЗОВАНИЕ В КАЧЕСТВЕ ГЕРБИЦИДОВ |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US6559101B2 (enExample) |
| EP (1) | EP1242425B1 (enExample) |
| JP (1) | JP3911236B2 (enExample) |
| KR (1) | KR100467128B1 (enExample) |
| CN (1) | CN1262552C (enExample) |
| AR (1) | AR035209A1 (enExample) |
| AT (1) | ATE260917T1 (enExample) |
| AU (1) | AU780115B2 (enExample) |
| BG (1) | BG65806B1 (enExample) |
| BR (1) | BRPI0107403B8 (enExample) |
| CA (1) | CA2395050C (enExample) |
| CZ (1) | CZ300942B6 (enExample) |
| DE (2) | DE122009000008I2 (enExample) |
| DK (1) | DK1242425T3 (enExample) |
| EA (1) | EA004941B1 (enExample) |
| ES (1) | ES2213124T3 (enExample) |
| FR (1) | FR09C0056I2 (enExample) |
| HU (1) | HU227229B1 (enExample) |
| IL (2) | IL150493A0 (enExample) |
| MX (1) | MX226072B (enExample) |
| NL (1) | NL350045I1 (enExample) |
| PL (1) | PL208906B1 (enExample) |
| PT (1) | PT1242425E (enExample) |
| RO (1) | RO121339B1 (enExample) |
| SK (1) | SK286484B6 (enExample) |
| TR (1) | TR200400746T4 (enExample) |
| UA (1) | UA66952C2 (enExample) |
| WO (1) | WO2002036595A2 (enExample) |
| ZA (1) | ZA200205097B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2762732C1 (ru) * | 2021-04-27 | 2021-12-22 | Акционерное общество Фирма "Август" | Новое производное 1,2,4-триазоло[1,5-с]пиримидин-2-сульфонамида и его применение в качестве гербицида |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE407559T1 (de) * | 2003-03-13 | 2008-09-15 | Basf Se | Herbizide mischungen auf 3-phenyluracil-grundlage |
| EP1605760A2 (en) * | 2003-03-13 | 2005-12-21 | Basf Aktiengesellschaft | Synergistically acting herbicidal mixtures |
| EA200501354A1 (ru) * | 2003-03-13 | 2006-02-24 | Басф Акциенгезельшафт | Гербицидные смеси синергического действия |
| ES2295960T3 (es) * | 2003-12-23 | 2008-04-16 | Dow Agrosciences Llc | Proceso para la preparacion de triazolopirimidinas. |
| JP4929155B2 (ja) * | 2004-03-26 | 2012-05-09 | ダウ アグロサイエンシィズ エルエルシー | Ｎ−（［１，２，４］トリアゾロピリミジン−２−イル）アリールスルホンアミドの改善された調製方法 |
| ES2413629T3 (es) * | 2004-04-01 | 2013-07-17 | Basf Agrochemical Products, B.V. | Mezclas herbicidas de acción sinérgica |
| CN1300142C (zh) * | 2004-05-11 | 2007-02-14 | 南开大学 | 磺酰胺类化合物及其制备方法和用途 |
| UA90757C2 (ru) | 2005-10-12 | 2010-05-25 | Басф Се | Гербицидная композиция, способ борьбы с нежелательной растительностью и способ защиты посевов от фитотоксичного действия 3-фенилурацилов |
| WO2008013904A1 (en) * | 2006-07-26 | 2008-01-31 | Dow Agrosciences Llc | Herbicidal compositions |
| RU2325390C1 (ru) * | 2007-01-29 | 2008-05-27 | Государственное образовательное учреждение высшего профессионального образования "Южно-Российский государственный технический университет (Новочеркасский политехнический институт)" | СПОСОБ ПОЛУЧЕНИЯ 2-СУЛЬФОНИЛАМИНО-1,2,4,-ТРИАЗОЛО[1,5-a] ПИРИМИДИНОВ |
| CN100500666C (zh) * | 2007-02-14 | 2009-06-17 | 浙江工业大学 | 一种三唑并嘧啶磺酸酯类化合物及其制备方法和应用 |
| DE102008033252A1 (de) | 2007-07-18 | 2009-01-22 | Fleissner Gmbh | Vorrichtung zur Herstellung von Textilien aus synthetischen, schmelzgezogenen Filamenten |
| EP2052606A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| DE102008037620A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Crop Science Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
| US8143395B2 (en) | 2010-05-25 | 2012-03-27 | Dow Agrosciences Llc | Process for the preparation of 5-substituted-8-alkoxy[1,2,4]triazolo[1,5-c]pyrimidin-2-amines |
| NZ608906A (en) * | 2010-10-12 | 2015-05-29 | Dow Agrosciences Llc | Growth inhibition of perennial forage grasses with pyroxsulam |
| NO2627183T3 (enExample) | 2010-10-15 | 2018-03-03 | ||
| US9930891B2 (en) | 2011-03-16 | 2018-04-03 | Dow Agrosciences Llc | Synergistic herbicidal composition containing penoxsulam and pyroxsulam |
| US9370183B2 (en) | 2011-05-04 | 2016-06-21 | Bayer Intellectual Property Gmbh | Use of ALS inhibitor herbicides for control of unwanted vegetation in ALS inhibitor herbicide tolerant Brassica, such as B. napus, plants |
| CN102326567B (zh) * | 2011-10-21 | 2014-04-16 | 联保作物科技有限公司 | 一种小麦田除草组合物及其制剂 |
| RS57806B2 (sr) | 2012-12-13 | 2022-07-29 | Bayer Cropscience Ag | Upotreba als inhibitora herbicida za kontrolu neželjene vegetacije kod beta vulgaris biljaka tolerantnih na als inhibitore herbicida |
| SI2934114T1 (sl) * | 2012-12-21 | 2019-02-28 | Dow Agrosciences Llc | Temperaturno stabilni klokvintocet meksilni vodni sestavki |
| CN103222468A (zh) * | 2013-04-22 | 2013-07-31 | 山东滨农科技有限公司 | 含有吡草醚和啶磺草胺的除草剂组合物 |
| CN103329911B (zh) * | 2013-06-25 | 2015-04-01 | 山东滨农科技有限公司 | 一种含有氯酯磺草胺和甲氧咪草烟的除草组合物 |
| CN103749488A (zh) * | 2013-12-26 | 2014-04-30 | 广东中迅农科股份有限公司 | 一种含有二氯吡啶酸和啶磺草胺的除草组合物 |
| CN103975933A (zh) * | 2014-04-08 | 2014-08-13 | 广东中迅农科股份有限公司 | 一种含有唑嘧磺草胺和啶磺草胺的除草组合物 |
| CN103960257A (zh) * | 2014-04-08 | 2014-08-06 | 广东中迅农科股份有限公司 | 一种含有辛酰溴苯腈和啶磺草胺的除草组合物 |
| CN104430452A (zh) * | 2014-11-26 | 2015-03-25 | 广东中迅农科股份有限公司 | 一种含有甲基碘磺隆钠盐和啶磺草胺的除草组合物 |
| CN104430449B (zh) * | 2014-11-26 | 2017-10-17 | 广东中迅农科股份有限公司 | 一种含有酰嘧磺隆和啶磺草胺的除草组合物 |
| CN104488920A (zh) * | 2014-12-03 | 2015-04-08 | 广东中迅农科股份有限公司 | 小麦田除草剂 |
| CN107406450B (zh) | 2015-03-10 | 2019-06-04 | 泸州东方农化有限公司 | 一种制备高纯度磺胺化合物的方法及其中间体 |
| CN104910165A (zh) * | 2015-06-02 | 2015-09-16 | 安徽兴东化工有限公司 | 一种2-氨基-5,7-二甲氧基-三嗪并嘧啶的制备方法 |
| CN105399746B (zh) * | 2015-12-28 | 2017-11-07 | 黑龙江凯奥科技开发有限公司 | 三唑并嘧啶磺酰胺化合物、含有该化合物的组合物及其应用 |
| NZ744230A (en) * | 2016-01-19 | 2022-01-28 | Corteva Agriscience Llc | Cloquintocet salts for safening pyroxsulam compositions |
| CN113227052B (zh) | 2018-12-27 | 2025-05-06 | 科迪华农业科技有限责任公司 | 磺酰胺除草剂方法中间体的制备 |
| US12077505B2 (en) | 2018-12-27 | 2024-09-03 | Corteva Agriscience Llc | Preparation of sulfonamide herbicide process intermediates |
| WO2020188571A1 (en) | 2019-03-19 | 2020-09-24 | Adama Agan Ltd. | Crystalline forms of n-(5,7-dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide |
| WO2021101927A1 (en) | 2019-11-18 | 2021-05-27 | Vanderbilt University | Wdr5-myc inhibitors |
| CN111217817B (zh) * | 2020-02-26 | 2022-06-10 | 山东潍坊润丰化工股份有限公司 | 一种三唑并嘧啶类除草剂的制备方法 |
| CN118201483A (zh) | 2021-10-15 | 2024-06-14 | 科沃施种子欧洲股份两合公司 | ALS抑制剂除草剂耐受的甜菜(Beta Vulgaris)突变体 |
| WO2024023035A1 (en) | 2022-07-25 | 2024-02-01 | Syngenta Crop Protection Ag | Herbicidal compositions |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4822404A (en) | 1984-01-26 | 1989-04-18 | The Dow Chemical Company | Sulfonamides derived from substituted 2-amino-1,2,4-triazolo (1,5-a) pyrimidines and compositions and methods of controlling undesired vegetation |
| US4638075A (en) | 1985-01-14 | 1987-01-20 | The Dow Chemical Company | Herbicidal sulfonamides |
| US5010195A (en) | 1988-05-25 | 1991-04-23 | The Dow Chemical Company | Herbicidal alkoxy-1,2,4-triazolo(1,5-c)primidine-2-sulfonamides |
| DE3539386A1 (de) * | 1985-11-04 | 1987-05-14 | Schering Ag | N-(s-triazolo(1,5-a)pyrimidin-2-yl)-2-alkoxy-benzolsulfonamide, verfahren zur herstellung dieser verbindungen sowie diese enthaltende mittel mit herbizider und pflanzenwachstumsregulierender wirkung |
| US4685958A (en) | 1986-05-06 | 1987-08-11 | The Dow Chemical Company | Sulfonamides derived from substituted 2-amino-1,2,4-triazolo[1,5-a]-1,3,5-triazines and compositions and methods of controlling undesired vegetation |
| US5571775A (en) | 1994-07-11 | 1996-11-05 | Dowelanco | N-aryl[1,2,4]triazolo[1,5-a]pyridine-2-sulfonamide herbicides |
| CN1159297C (zh) | 1996-09-24 | 2004-07-28 | 道农业科学公司 | N-([1,2,4]三唑并吖嗪基)苯磺酰胺和吡啶磺酰胺化合物和它们作为除草剂的用途 |
-
2001
- 2001-11-02 PT PT01992711T patent/PT1242425E/pt unknown
- 2001-11-02 RO ROA200200944A patent/RO121339B1/ro unknown
- 2001-11-02 EP EP01992711A patent/EP1242425B1/en not_active Expired - Lifetime
- 2001-11-02 CZ CZ20022327A patent/CZ300942B6/cs not_active IP Right Cessation
- 2001-11-02 DK DK01992711T patent/DK1242425T3/da active
- 2001-11-02 EA EA200200748A patent/EA004941B1/ru not_active IP Right Cessation
- 2001-11-02 IL IL15049301A patent/IL150493A0/xx unknown
- 2001-11-02 DE DE122009000008C patent/DE122009000008I2/de active Active
- 2001-11-02 DE DE60102215T patent/DE60102215T2/de not_active Expired - Lifetime
- 2001-11-02 TR TR2004/00746T patent/TR200400746T4/xx unknown
- 2001-11-02 SK SK914-2002A patent/SK286484B6/sk not_active IP Right Cessation
- 2001-11-02 UA UA2002086437A patent/UA66952C2/uk unknown
- 2001-11-02 AT AT01992711T patent/ATE260917T1/de active
- 2001-11-02 AR ARP010105142A patent/AR035209A1/es active IP Right Grant
- 2001-11-02 CN CNB018034438A patent/CN1262552C/zh not_active Expired - Lifetime
- 2001-11-02 US US10/000,935 patent/US6559101B2/en not_active Expired - Lifetime
- 2001-11-02 JP JP2002539353A patent/JP3911236B2/ja not_active Expired - Lifetime
- 2001-11-02 KR KR10-2002-7008656A patent/KR100467128B1/ko not_active Expired - Lifetime
- 2001-11-02 AU AU27180/02A patent/AU780115B2/en not_active Expired
- 2001-11-02 PL PL362927A patent/PL208906B1/pl unknown
- 2001-11-02 CA CA002395050A patent/CA2395050C/en not_active Expired - Lifetime
- 2001-11-02 MX MXPA02006640 patent/MX226072B/es active IP Right Grant
- 2001-11-02 WO PCT/US2001/046150 patent/WO2002036595A2/en not_active Ceased
- 2001-11-02 BR BRPI0107403A patent/BRPI0107403B8/pt not_active IP Right Cessation
- 2001-11-02 HU HU0204346A patent/HU227229B1/hu active Protection Beyond IP Right Term
- 2001-11-02 ES ES01992711T patent/ES2213124T3/es not_active Expired - Lifetime
-
2002
- 2002-06-25 ZA ZA200205097A patent/ZA200205097B/xx unknown
- 2002-06-30 IL IL150493A patent/IL150493A/en unknown
- 2002-07-03 BG BG106900A patent/BG65806B1/bg unknown
-
2009
- 2009-11-04 FR FR09C0056C patent/FR09C0056I2/fr active Active
-
2010
- 2010-01-26 NL NL350045C patent/NL350045I1/nl unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2762732C1 (ru) * | 2021-04-27 | 2021-12-22 | Акционерное общество Фирма "Август" | Новое производное 1,2,4-триазоло[1,5-с]пиримидин-2-сульфонамида и его применение в качестве гербицида |
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| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
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