JP5271257B2 - 二環式基でn置換されたジアミノ−1,3,5−トリアジン、その製造法、その組成物、並びに除草剤及び植物成長調節剤としてのその使用 - Google Patents
二環式基でn置換されたジアミノ−1,3,5−トリアジン、その製造法、その組成物、並びに除草剤及び植物成長調節剤としてのその使用 Download PDFInfo
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- JP5271257B2 JP5271257B2 JP2009504602A JP2009504602A JP5271257B2 JP 5271257 B2 JP5271257 B2 JP 5271257B2 JP 2009504602 A JP2009504602 A JP 2009504602A JP 2009504602 A JP2009504602 A JP 2009504602A JP 5271257 B2 JP5271257 B2 JP 5271257B2
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- 238000000034 method Methods 0.000 title claims description 44
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- 238000002360 preparation method Methods 0.000 title description 15
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- 125000002619 bicyclic group Chemical group 0.000 title description 2
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- -1 R 3 is H Chemical group 0.000 claims description 115
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 29
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 17
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 14
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 5
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 5
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- 239000001257 hydrogen Substances 0.000 claims description 4
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- 239000002168 alkylating agent Substances 0.000 claims description 3
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- 125000000524 functional group Chemical group 0.000 claims description 3
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- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 27
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- 229910052708 sodium Inorganic materials 0.000 description 15
- 239000011734 sodium Substances 0.000 description 15
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
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- 125000000217 alkyl group Chemical group 0.000 description 9
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- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
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- 235000011684 Sorghum saccharatum Nutrition 0.000 description 7
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- 150000001412 amines Chemical class 0.000 description 7
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
- 238000007796 conventional method Methods 0.000 description 6
- WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical compound NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 6
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- 125000004438 haloalkoxy group Chemical group 0.000 description 6
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- 239000000725 suspension Substances 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 5
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- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 4
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- 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 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 244000075850 Avena orientalis Species 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
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- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 4
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
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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 4
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- 125000006536 (C1-C2)alkoxy group Chemical group 0.000 description 3
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- 0 *N(*)C(NC#N)=N Chemical compound *N(*)C(NC#N)=N 0.000 description 3
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- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 3
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
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- 239000002798 polar solvent Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- BUCOQPHDYUOJSI-UHFFFAOYSA-N prohexadione Chemical compound CCC(=O)C1C(=O)CC(C(O)=O)CC1=O BUCOQPHDYUOJSI-UHFFFAOYSA-N 0.000 description 1
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 description 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
- OYJMHAFVOZPIOY-UHFFFAOYSA-N propan-2-yl 2-chloro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]benzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1 OYJMHAFVOZPIOY-UHFFFAOYSA-N 0.000 description 1
- FKLQIONHGSFYJY-UHFFFAOYSA-N propan-2-yl 5-[4-bromo-1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-2-chloro-4-fluorobenzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(C=2C(=C(N(C)N=2)C(F)(F)F)Br)=C1F FKLQIONHGSFYJY-UHFFFAOYSA-N 0.000 description 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 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
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- DVBARFVOVUTLAH-UHFFFAOYSA-N propyl 5,5-diphenyl-4h-1,2-oxazole-3-carboxylate Chemical compound C1C(C(=O)OCCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 DVBARFVOVUTLAH-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
- PHNUZKMIPFFYSO-UHFFFAOYSA-N propyzamide Chemical compound C#CC(C)(C)NC(=O)C1=CC(Cl)=CC(Cl)=C1 PHNUZKMIPFFYSO-UHFFFAOYSA-N 0.000 description 1
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- YXIIPOGUBVYZIW-UHFFFAOYSA-N pyraflufen Chemical compound ClC1=C(OC(F)F)N(C)N=C1C1=CC(OCC(O)=O)=C(Cl)C=C1F YXIIPOGUBVYZIW-UHFFFAOYSA-N 0.000 description 1
- APTZNLHMIGJTEW-UHFFFAOYSA-N pyraflufen-ethyl Chemical compound C1=C(Cl)C(OCC(=O)OCC)=CC(C=2C(=C(OC(F)F)N(C)N=2)Cl)=C1F APTZNLHMIGJTEW-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229960001404 quinidine Drugs 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- ABOOPXYCKNFDNJ-SNVBAGLBSA-N quizalofop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-SNVBAGLBSA-N 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000026267 regulation of growth Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 108091092562 ribozyme Proteins 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- QLMNCUHSDAGQGT-UHFFFAOYSA-N sintofen Chemical compound N1=C(C(O)=O)C(=O)C=2C(OCCOC)=CC=CC=2N1C1=CC=C(Cl)C=C1 QLMNCUHSDAGQGT-UHFFFAOYSA-N 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate 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
- RVULBHWZFCBODE-UHFFFAOYSA-M sodium;5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical compound [Na+].C1=C([N+]([O-])=O)C(C(=O)[O-])=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 RVULBHWZFCBODE-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- VACCAVUAMIDAGB-UHFFFAOYSA-N sulfamethizole Chemical compound S1C(C)=NN=C1NS(=O)(=O)C1=CC=C(N)C=C1 VACCAVUAMIDAGB-UHFFFAOYSA-N 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 150000003455 sulfinic acids Chemical class 0.000 description 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 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 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 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
- 229960000278 theophylline Drugs 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical group CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- 150000003566 thiocarboxylic acids Chemical class 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
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical compound COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- DFFWZNDCNBOKDI-UHFFFAOYSA-N trinexapac Chemical compound O=C1CC(C(=O)O)CC(=O)C1=C(O)C1CC1 DFFWZNDCNBOKDI-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
- C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
R1及びR2は、各々独立して、H、(C1−C4)アルキル、(C1−C4)ハロアルキル、(C3−C4)アルケニル、(C3−C4)ハロアルケニル、(C3−C4)アルキニル、(C3−C4)ハロアルキニル、又はアシル基であり、
R3は、H、(C1−C6)アルキル、(C1−C6)アルコキシ、(C2−C6)アルケニル、(C2−C6)アルキニル、(C2−C6)アルケニルオキシ、又は(C2−C6)アルキニルオキシ、好ましくはH、(C1−C6)アルキル、又は(C1−C6)アルコキシであり、
R4、R5、R6、及びR7は、各々独立して、H、(C1−C4)アルキル、(C1−C3)ハロアルキル、ハロゲン、(C1−C3)アルコキシ、(C1−C3)ハロアルコキシ、CN、(C2−C6)アルケニル、(C2−C6)アルキニル、(C2−C6)アルケニルオキシ、又は(C2−C6)アルキニルオキシであるが、これらのうちの少なくとも一つは、(C1−C4)アルキル、(C1−C3)ハロアルキル、ハロゲン、(C1−C3)アルコキシ、(C1−C3)ハロアルコキシ、CN、(C2−C6)アルケニル、(C2−C6)アルキニル、(C2−C6)アルケニルオキシ、又は(C2−C6)アルキニルオキシであり、好ましくは、
R4、R5、R6、及びR7は、各々独立して、H、(C1−C4)アルキル、(C1−C3)ハロアルキル、ハロゲン、(C1−C3)アルコキシ、(C1−C3)ハロアルコキシ、又はCNであるが、これらのうちの少なくとも一つは(C1−C4)アルキル、(C1−C3)ハロアルキル、ハロゲン、(C1−C3)アルコキシ、(C1−C3)ハロアルコキシ、又はCNであり、
Aは、CH2、O、又は直接結合である]
に関する。
ハロゲンは、フッ素、塩素、臭素又はヨウ素を意味する。
リル、プロパルギル、CHO、−CO(C1−C3)アルキル、又は−CO(C1−C3)ハロアルキルであり、さらにより好ましくは、R1は、H、CHO、COCH3、COCH2Cl、COCH(CH3)Cl、又はCOCF3であり;最も好ましくはR1は、Hである。
R1がH、(C1−C4)アルキル、(C1−C4)ハロアルキル、(C3−C4)アルケニル、(C3−C4)アルキニル、又は1〜12個の炭素原子を有するアシル基であり、アシルが、好ましくは、CHO、−CO(C1−C6)アルキル、−CO(C1−C6)ハロアルキル、−CO2(C1−C6)アルキル、−SO2(C1−C6)アルキル、−CO2−フェニ
ル、又は−CO−フェニルであり、各フェニルが、非置換又はハロゲン、(C1−C2)アルキル、(C1−C2)ハロアルキル、(C1−C2)アルコキシ、(C1−C2)ハロアルコキシ、及びNO2からなる群から選択された一つ又はそれ以上の基により置換されており、
R2が、H、(C1−C4)アルキル、又は(C1−C4)ハロアルキル、好ましくはH又は(C1−C2)アルキル、より好ましくはHであり、
R3が、H、(C1−C3)アルキル、又は(C1−C3)アルコキシ、好ましくはH又は(C1−C3)アルキル、より好ましくはH、メチル、又はエチルであり;
R4、R5、R6、及びR7が、各々独立して、H、(C1−C3)アルキル、ハロゲン、又は(C1−C3)アルコキシであるが、これらのうちの少なくとも一つは、(C1−C3)アルキル、ハロゲン、又は(C1−C3)アルコキシであり、かつ
Aが、CH2、O、又は直接結合であり、好ましくはAがCH2又は直接結合、特に直接結合である、
化合物である。
R1が、H、(C1−C3)アルキル、(C1−C3)ハロアルキル、アリル、プロパルギル、CHO、−CO(C1−C3)アルキル、又は−CO(C1−C3)ハロアルキル、好ましくはH、CHO、COCH3、COCH2Cl、COCH(CH3)Cl、又はCOCF3、より好ましくはHであり、
R2が、H又は(C1−C2)アルキル、好ましくはHであり、
R3が、H、(C1−C3)アルキル、又は(C1−C3)アルコキシ、好ましくはH又は(C1−C3)アルキル、より好ましくはH、メチル、又はエチルであり、
R4、R5、R6、及びR7が、各々独立して、H、メチル、F、Cl、又はBr、好ましくはH、メチル、F、又はClであるが、これらのうちの少なくとも一つは、メチル、F、Cl、又はBr、好ましくはメチル、F、又はClであり、かつ
Aが、CH2、O、又は直接結合であり、好ましくはAがCH2又は直接結合、特に直接結合である、
化合物である。
R1が、H、(C1−C4)アルキル、(C1−C4)ハロアルキル、(C3−C4)アルケニル、(C3−C4)アルキニル、又は1〜12個の炭素原子を有するアシル基であり、アシルが、好ましくは、CHO、−CO(C1−C6)アルキル、−CO(C1−C6)ハロアルキル、−CO2(C1−C6)アルキル、−SO2(C1−C6)アルキル、−CO2−フェニル、又は−CO−フェニルであり、各フェニルが非置換又はハロゲン、(C1−C2)アルキル、(C1−C2)ハロアルキル、(C1−C2)アルコキシ、(C1−C2)ハロアルコキシ、及びNO2からなる群から選択された一つ又はそれ以上の基により置換されており、
R2が、H、(C1−C4)アルキル、又は(C1−C4)ハロアルキル、好ましくはH又は(C1−C2)アルキル、より好ましくはHであり、
R3がH、(C1−C3)アルキル、又は(C1−C3)アルコキシ、好ましくはH又は(C1−C3)アルキル、より好ましくはH、メチル、又はエチルであり、
R4、R5、及びR7が、各々独立して、H、(C1−C3)アルキル、ハロゲン、又は(C1−C3)アルコキシであり、R6が、(C1−C3)アルキル、ハロゲン、又は(C1−C3)アルコキシであり、かつ
Aが、CH2、O、又は直接結合であり、好ましくはAがCH2又は直接結合、特に直接結合である、
化合物である。
R1が、H、(C1−C3)アルキル、(C1−C3)ハロアルキル、アリル、プロパルギル、CHO、−CO(C1−C3)アルキル、又は−CO(C1−C3)ハロアルキル、好ましくはH、CHO、COCH3、COCH2Cl、COCH(CH3)Cl、又はCOCF3、より好ましくはHであり、
R2が、H又は(C1−C2)アルキル、好ましくはHであり、
R3が、H、(C1−C3)アルキル、又は(C1−C3)アルコキシ、好ましくはH又は(C1−C3)アルキル、より好ましくはH、メチル又はエチルであり、
R4、R5、及びR7が、各々独立して、H、メチル、F、Cl、又はBr、好ましくはH、メチル、F、又はClであり、
R6が、メチル、F、Cl、又はBr、好ましくはメチル、F、又はClであり、かつ
Aが、CH2、O、又は直接結合であり、好ましくはAがCH2又は直接結合、特に直接結合である、
化合物である。
R1がHであり、
R2がHであり、
R3が、H又は(C1−C3)アルキル、好ましくはH、メチル、又はエチルであり、
R4、R5、及びR7が、各々独立して、H、メチル、F、Cl、及びBr、好ましくはH、メチル、F、及びClからなる群から選択され、
R6がメチル、F、Cl、又はBr、好ましくはメチル、F、又はClであり、かつ
Aが、CH2、O、又は直接結合、好ましくはCH2又は直接結合、特に直接結合である、
化合物である。
である。
1. N原子
2. ベンゼン環における次のC原子
3. CHR3基の環C原子
4. 水素原子
を有することを条件として、カーン・インゴルド・プレローグ則(Cahn−Ingold−Prelog system)に従い主として(R)である(「(R)異性体」についての式(Ia)に示される結合の配向も参照されたい)。化合物(Ia)の立体化学配置は、ここでは一般的に(R)配置として示されているが、同じ立体化学構造を有する式(Ia)の特定の化合物が、カーン・インゴルド・プレローグの命名法に従う(S)配置に相当することにも留意すべきである。例えば、R3がアルコキシ基の場合、基CHR3は通常、ベンゼン環の隣接するC原子より上の順位を有することになる。従って、この式(Ia)で表されるアルコキシ置換型化合物の配置は通常、カーン・インゴルド・プレローグの立体化学命名法に従えば(S)配置である。しかし、一般式(Ia)及び以下で言及される他の光学的に活性な化合物の一般との関係では、これらの化合物は、式(Ia)について上述されたような置換基の一般的な順位を適用して、印を付けた1のC原子に関して「(R)配置」を表わす化合物である。しかし、式(Ia)又は他の光学的に活性な化合物の式の特定の化合物の完全な化学名が与えられる場合は、そうでないことが記されない限り、カーン・インゴルド・プレローグの命名法が厳密に適用され、このような式(Ia)の化合物は上で説明したように(S)配置を有する可能性がある。
もまた好ましい。(R)配置の定義は、示された式及び式(Ia)についてすでに言及した定義に従い定義される。
他の記号が式(I)において定義された通りであるか又は式(I)について好ましいものとして定義された通りである、
式(I)、(Ia)、(Ib)、又は(Ic)の化合物が好ましい。
R3がメチル又はエチルであり、
R4、R5、R6、及びR7が各々独立してH、メチル、Br、Cl、又はFであるがこれらのうちの少なくとも一つがメチル、Br、Cl、又はFであり、かつ
AがCH2、O、又は直接結合である、
式(Ib)及び(Ic)で表される化合物がより好ましい。
R3がメチル又はエチルであり、
R4、R5、及びR7が各々独立してH、メチル、Br、Cl、又はFであり、R6がメチル、Br、Cl、又はFであり、かつ
AがCH2、O、又は直接結合である、
式(Ia)及び(Ib)で表される化合物もまたより好ましい。
と、式(III)のビグアニジン化合物又はその酸付加塩
との反応により製造することができる。
が使用される。
と、式(V)又は(Va)のアミンのそれぞれ、又はその酸付加塩
の反応によっても製造され得る。
R1−L2 (VI) R2−L2 (VII)
(ここにおいて、L2は脱離基であり、一般的にはハロゲン、好ましくは塩素、臭素若しくはヨウ素、又はメチルスルホニルオキシ若しくは4−トルエンスルホニルオキシのような、アルキル−若しくはフェニル−スルホニルオキシ部分である)それぞれとの反応で製造することができる。使用する反応物質の量及び反応性並びに生成物の反応性に応じて、式(I)の化合物はモノ−又はジアルキル化の生成物である。反応は通常、テトラヒドロフラン、ジオキサン、アセトニトリル又はN,N−ジメチルホルムアミドのような不活性溶媒中で、温度は0℃から溶媒の還流温度、好ましくは20℃から100℃において行なわれる。
R1−L3 (VIII) R2−L3 (IX)
(ここにおいて、R1及びR2はそれぞれ式(I)において定義したアシル基であり、そしてL3は脱離基であり、一般的にはハロゲン、好ましくは塩素である)それぞれと、又はギ酸−無水酢酸のようなホルミル化剤との反応で製造することができる。塩基は、場合によりアシル化反応に使用され、一般的には、アルカリ金属水酸化物、アルカリ金属水素化物、アルカリ金属炭酸塩、アルカリ金属アルコキシド、アルカリ土類金属炭酸塩、又は第三級アミン、例えばトリエチルアミンのような有機塩基から選択される。使用する反応物質の量及び反応性に応じて、式(I)の化合物はモノ−又はジアシル化の生成物である。反応は、一般にテトラヒドロフラン、ジオキサン、アセトニトリル又はN,N−ジメチルホルムアミドのような不活性溶媒中で、温度は0℃から溶媒の還流温度、好ましくは20℃から100℃において行なわれる。
の還元的アミノ化、場合により不斉還元的アミノ化、又は例えば国際特許出願公開WO−A−97/031904に記載されるような既知の手順に従い、式(XII)の化合物
とアンモニア若しくはその塩の反応によって製造され得る。
以下の実施例において、量(百分率を含む)は、他に記載がない限り、質量基準である。溶媒の比率は、他に記載がない限り、容量基準である。
6−(ジフルオロメチル)−N−[(4R)−8−フルオロ−3,4−ジヒドロ−2H−クロメン−4−イル]−1,3,5−トリアジン−2,4−ジアミン(表2、化合物番号2.206)
メタノール中25%ナトリウムメトキシド(0.94g、0.99ml、0.0043mol)溶液を、アミノ−N−[{[(4R)−8−フルオロ−3,4−ジヒドロ−2H−クロメン−4−イル]−アミノ}(イミノ)メチル]イミノメタンアンモニウムクロリド(式(IIIa)のビグアニド)(0.5g、0.0017mol)のメタノール中撹拌懸濁液に加えた。次に、ジフルオロ酢酸エチル(0.65g、0.52ml、0.0052mol)を加えた。4時間後、混合物を濾過し、その濾液を蒸発させた。残留物を酢酸エチルに溶解し、洗浄し(水)、乾燥させ(硫酸ナトリウム)、蒸発させた。残留物を、溶離液として酢酸エチル:ヘプタン混合液(7:3)を用いて溶離するカラムクロマトグラフィにより精製し、6−(ジフルオロメチル)−N−[(4R)−8−フルオロ−3,4−ジヒドロ−2H−クロメン−4−イル]−1,3,5−トリアジン−2,4−ジアミン(泡状固形物、0.298g、純度約90%、収率50%)を得た。
6−(ジフルオロメチル)−N−[(1R,2S)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]−1,3,5−トリアジン−2,4−ジアミン(表3、化合物番号3.1)
メタノール中25%ナトリウムメトキシド(1.08g、1.14ml、0.0050mol)溶液を、(1R,2S)−1−(ビスグアニジノ)−2,6−ジメチルインダンモノヒドロクロリド(0.564g、0.0020mol)のメタノール中撹拌懸濁液に加えた。次に、ジフルオロ酢酸エチル(0.75g、0.0060mol)を加えた。4時間後、混合物を濾過し、その濾液を蒸発させた。残留物を酢酸エチルに溶解し、洗浄し(水)、乾燥させ(硫酸ナトリウム)、蒸発させた。残留物を、溶離液として酢酸エチル:ヘプタン混合液(7:3)を用いて溶離するカラムクロマトグラフィにより精製し、6−(ジフルオロメチル)−N−[(1R,2S)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]−1,3,5−トリアジン−2,4−ジアミン(0.491g、収率76%)、mp.132−134℃、旋光度(クロロホルム、c=1):+161.0°、純度95%(hplc,Chiralcel OD、250X4.6mm、溶離液n−ヘキサン:2−プロパノール90:10、rf 17.93分)を得た;得られた光学純度は少なくとも90%ee(ee%=鏡像異性体余剰%)であった。
N−(4−(ジフルオロメチル)−6−{[(1R,2S)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]−アミノ}−1,3,5−トリアジン−2−イル)プロパンアミド(表3、化合物番号3.109)
6−(ジフルオロメチル)−N−[(1R,2S)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]−1,3,5−トリアジン−2,4−ジアミン(0.300g,0.0009mol)(実施例A2参照)のプロパン酸無水物(3ml)中撹拌懸濁液を120℃に60分間加熱にした。反応混合物を冷却した後に、溶離液として酢酸エチル:ヘプタン混合液(7:3)を用いて溶離するカラムクロマトグラフィにより精製し、N−(4−(ジフルオロメチル)−6−{[(1R,2S)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]−アミノ}−1,3,5−トリアジン−2−イル)プロパンアミド(0.145g、収率43%)、mp.66℃を得た。
N−[−4−(ジフルオロメチル)−6−{[(1R,WS)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]アミノ}−1,3,5−トリアジン−2−イル]ホルムアミド
6−(ジフルオロメチル)−N−[(1R,2S)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]−1,3,5−トリアジン−2,4−ジアミン(0.25g、0.0008Mol)とオルトギ酸トリエチル(1.46g、1.63ml、0.0098Mol)の無水酢酸(acetanhydride)(0.5g、0,46ml、0.0049Mol)中混合物を160℃に30分間加熱した(密栓バイアル、SmithSynthesizerマイクロウェーブシステム、Biotage,1725 Discovery Drive,Charlottesville,VA 22911,USAから入手可能)。反応混合物を冷却した後に、溶離液として酢酸エチル:ヘプタン混合液(7:3)を用いて溶離するカラムクロマトグラフィにより精製し、N−[−4−(ジフルオロメチル)−6−{[(1R,2S)−2,6−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル]アミノ}−1,3,5−トリアジン−2−イル]ホルムアミド(ろう状物、0.159g、純度約90%、収率50%)、mp.66°Cを得た。
Me = メチル
Et = エチル
n−Prop = n−プロピル
i−Prop = イソプロピル
n−Bu = n−ブチル
sec−Bu = sec−ブチル
i−Bu = イソブチル
t−Bu = tert−ブチル
− = Aの定義における直接結合
Cpd = 化合物番号。化合物番号は参照目的で付与したにすぎない。
Ref. = 表の最後尾に記されるデータに対する参照
光学純度 = 光学活性化合物は少なくとも90%ee
(ee%=鏡像異性体余剰%)の光学純度で得た。
化合物番号1.5: ろう状物質として得た
化合物番号1.205: ろう状物質として得た
化合物番号1.207: 固形物、融点214.6℃
化合物番号2.1: 固形物、融点181〜182℃
化合物番号2.2: ろう状物質として得た
化合物番号2.3: 固形物
化合物番号2.5: 固形物、融点101〜102℃
化合物番号2.25: 固形物
化合物番号2.139: ろう状物質として得た
化合物番号2.206: 固形物
化合物番号3.1: 固形物、融点132℃
化合物番号3.31: 固形物、融点112℃
化合物番号3.82: 固形物
化合物番号3.106: ろう状物質として得た
化合物番号3.109: 固形物、融点66℃
化合物番号3.112: ろう状物質として得た
化合物番号3.118: ろう状物質として得た
― 植物中で合成されるデンプンを改変する目的の農作植物の遺伝子工学的修飾(例えば、WO 92/11376,WO 92/14827,WO 91/19806)、
― 特定の除草剤、例えば、グルホシネート系(例えば、EP−A−0242236,EP−A−242246を参照)、又はグリホサート系(WO 92/00377)、又はスルホニルウレア系(EP−A−0257993,US−A−5013659)の除草剤に対して抵抗性を示すトランスジェニック農作植物
― トランスジェニック農作植物、例えば、バチルス ツリンギエンシス(Bacillus thuringiensis)毒素(Bt毒素)を産生する能力を獲得し、その結果として特定の有害生物に対して抵抗性となった棉(EP−A−0142924,EP−A−0193259)、
― 改変された脂肪酸スペクトルを有するトランスジェニック農作植物(WO 91/13972)。
ラム(proxulam)、キンクロラック、キンメラック、キノクラミン、キノホップ(quinofop)及びそのエステル誘導体、キザロホップ及びキザロホップ−P、及びそれらのエステル誘導体、例えば、キザロホップ−エチル及びキザロホップ−P−テフリル及び−エチル、レンリデュロン(renriduron)、リムスルフロン(DPX−E9636)、S−275、即ち、2−[4−クロロ−2−フルオロ−5−(2−プロピニルオキシ)フェニル]−4,5,6,7−テトラヒドロ−2H−インダゾール、セクブメトン、セトキシジム、シデュロン、シマジン、シメトリン、シントフェン(sintofen)、SN106279、即ち、2−[[7−[2−クロロ−4−(トリフルオロメチル)フェノキシ]−2−ナフタレニル]オキシ]プロパン酸及びそのメチルエステル、スルコトリオン、スルフェントラゾン(FMC−97285,F−6285)、スルファズロン(sulfazuron)、スルホメツロン(sulfometuron)(−メチル)、スルホサート(ICI−A0224)、スルホスルフロン、TCA、テブタム(GCP−5544)、テブチウロン、テクナセン(tecnacene)、テンボトリオン、テフリルトリオン、テプラロキシジム、ターバシル、テルブカルブ、テルブクロール(terbuchlor)、テルブメトン、テルブチラジン、テルブトリン、TFH450、即ち、N,N−ジエチル−3−[(2−エチル−6−メチルフェニル)スルホニル]−1H−1,2,4−トリアゾール−1−カルボキサミド、テニルクロール(NSK−850)、チアフルアミド(thiafluamide)、チアザフルロン、チアゾピル(Mon−13200)、チジアジミン(thidiazimin)(SN−24085)、チジアズロン、チジアズロン、チエンカルバゾン、チフェンスルフロン(−メチル)、チオベンカルブ、Ti 35、チオカルバジル、トプラメゾン、トラルコキシジム、トリアレート(tri−allate)、トリアスルフロン、トリアジフラム、トリアゾフェナミド(triazofenamide)、トリベヌロン(−メチル)、2,3,6−トリクロロ安息香酸(2,3,6−TBA)、トリクロピル、トリジファン、トリエタジン、トリフロキシスルフロン(−ナトリウム)、トリフロキシスルフロン、トリフルラリン、トリフルスルフロン及びそのエステル(例えばメチルエステル、DPX−66037)、トリメツロン(trimeturon)、トリネキサパック、トリトスルフロン、チトデフ(tsitodef)、ウニコナゾール、バーナレート(vernolate)、WL110547、即ち、5−フェノキシ−1−[3−(トリフルオロメチル)フェニル]−1H−テトラゾール、UBH−509、D−489、LS 82−556、KPP−300、NC−324、NC−330、KH−218、DPX−N8189、SC−0774、DOWCO−535、DK−8910、V−53482、PP−600、MBH−001、KIH−9201、ET−751、KIH−6127、KIH−2023、KIH−485、及びKIH5996。
b) ジクロロフェニルピラゾールカルボン酸誘導体、好ましくは1−(2,4−ジクロロフェニル)−5−メチルピラゾール−3−カルボン酸エチル(S1−2)、1−(2,4−ジクロロフェニル)−5−イソプロピルピラゾール−3−カルボン酸エチル(S1−3)、1−(2,4−ジクロロフェニル)−5−(1,1−ジメチルエチル)ピラゾール−3−カルボン酸エチル(S1−4)、1−(2,4−ジクロロフェニル)−5−フェニルピラゾール−3−カルボン酸エチル(S1−5)のような化合物、並びにEP−A−333 131及びEP−A−269 806に記載されているような関連化合物;
c) トリアゾールカルボン酸タイプの化合物、好ましくは、フェンクロラゾール(及びそのエチルエステル)、即ち、1−(2,4−ジクロロフェニル)−5−トリクロロメチルー(1H)−1,2,4−トリアゾール−3−カルボン酸エチル(S1−6)のような化合物、及び関連化合物(EP−A−174 562及びEP−A−346 620参照);
d) 5−ベンジル−若しくは5−フェニル−2−イソオキサゾリン−3−カルボン酸タイプ、若しくは5,5−ジフェニル−2−イソオキサゾリン−3−カルボン酸タイプの化合物、好ましくは、5−(2,4−ジクロロベンジル)−2−イソオキサゾリン−3−カルボン酸エチル(S1−7)、又は5−フェニル−2−イソオキサゾリン−3−カルボン酸エチル(S1−8)のような化合物、及びWO 91/08202に記載されているような関連化合物、又はWO−A−95/07897で公開された国際特許出願に記載されているような、5,5−ジフェニル−2−イソオキサゾリンカルボン酸エチル(S1−9)(「イソキサジフェン−エチル」)、又は5,5−ジフェニル−2−イソオキサゾリンカルボン酸n−プロピル(S1−10)若しくは5−(4−フルオロフェニル)−5−フェニル−2−イソオキサゾリン−3−カルボン酸エチル(S1−11);
(5−クロロ−8−キノリンオキシ)酢酸1,3−ジメチルブタ−1−イル(S2−2)、
(5−クロロ−8−キノリンオキシ)酢酸4−アリルオキシブチル(S2−3)、
(5−クロロ−8−キノリンオキシ)酢酸1−アリルオキシプロパ−2−イル(S2−4)、
(5−クロロ−8−キノリンオキシ)酢酸エチル(S2−5)、
(5−クロロ−8−キノリンオキシ)酢酸メチル(S2−6)、
(5−クロロ−8−キノリンオキシ)酢酸アリル(S2−7)、
(5−クロロ−8−キノリンオキシ)酢酸2−(2−プロピリデンイミノオキシ)−1−エチル(S2−8)、
(5−クロロ−8−キノリンオキシ)酢酸2−オキソプロパ−1−イル(S2−9)、
及びEP−A−86 750、EP−A−94 349及びEP−A−191 736若しくはEP−A−0 492 366に記載されている関連化合物;
f) (5−クロロ−8−キノリンオキシ)マロン酸タイプの化合物、好ましくは(5−クロロ−8−キノリンオキシ)マロン酸ジエチル、(5−クロロ−8−キノリンオキシ)マロン酸ジアリル、(5−クロロ−8−キノリンオキシ)マロン酸メチルエチルのような化合物、及びEP−A−0 582 198に記載されているような関連化合物;
g) 例えば、2,4−ジクロロフェノキシ酢酸(及びそのエステル)(2,4−D)、4−クロロ−2−メチルフェノキシプロピオン酸エステル(メコプロップ)、MCPA、又は、3,6−ジクロロ−2−メトキシ安息香酸(及びそのエステル)(ジカンバ)のような、フェノキシ酢酸若しくはフェノキシプロピオン酸誘導体タイプ又は芳香族カルボン酸タイプの有効物質;
h) 例えば、「フェンクロリム」(PM)(=4,6−ジクロロ−2−フェニルピリミジン)のような、イネの土壌作用性薬害軽減剤として用いられ、またイネの播種後に用いられるプレチラクロールの薬害軽減剤としても知られているピリミジンタイプの有効物質;
「R−29148」(=3−ジクロロアセチル−2,2,5−トリメチル−1,3−オキサゾリジン、Stauffer社製品)、
「ベノキサコール」(PM)(=4−ジクロロアセチル−3,4−ジヒドロ−3−メチル−2H−1,4−ベンゾオキサジン)、
「PPG−1292」(=N−アリル−N−[(1,3−ジオキソラン−2−イル)メチル]ジクロロアセトアミド、PPG Industries社製品)、
「DK−24」(=N−アリル−N−[(アリルアミノカルボニル)メチル]ジクロロアセトアミド、Sagro−Chem社製品)、
「AD−67」又は「MON4660」(=3−ジクロロアセチル−1−オキサ−3−アザスピロ[4,5]デカン、それぞれ、Nitrokemia及びMonsanto社製品)、
「ジクロノン」又は「BAS145138」又は「LAB145138」(=3−ジクロロアセチル−2,5,5−トリメチル−1,3−ジアザビシクロ[4.3.0]ノナン、BASF社製品)、及び
「フリラゾール」又は「MON13900」(PM参照)(=(RS)−3−ジクロロアセチル−5−(2−フリル)−2,2−ジメチルオキサゾリジン)、のような、出芽前薬害軽減剤(土壌作用性薬害軽減剤)としてしばしば用いられるジクロロアセトアミドタイプの有効物質;
k) 例えば、モロコシ及びキビのためのメトラクロール損傷に対する種子処理薬害軽減剤として知られている「オキサベトリニル」(PM)(=(Z)−1,3−ジオキソラン−2−イルメトキシイミノ(フェニル)−アセトニトリル)、モロコシ及びキビのためのメトラクロール損傷に対する種子粉衣薬害軽減剤として知られている「フルキソフェニム(fluxofenim)」(PM)(=1−(4−クロロフェニル)−2,2,2−トリフルオロ−1−エタノン O−(1,3−ジオキソラン−2−イルメチル)オキシム、及び
モロコシ及びキビのためのメトラクロール損傷に対する種子処理薬害軽減剤製品として知られている「シオメトリニル(cyometrinil)」又は「CGA−43089」(PM)(=(Z)−シアノメトキシ−イミノ(フェニル)アセトニトリル)のような、種子処理製品として知られているオキシイミノ化合物タイプの有効物質;
l) 例えば、モロコシ及びキビのためのアラクロール及びメトラクロールの損傷に対する種子処理薬害軽減剤として知られている「フルラゾール(flurazole)」(PM)(=2−クロロ−4−トリフルオロメチル−1,3−チアゾール−5−カルボン酸ベンジル)のような種子処理製品として知られている、チアゾールカルボン酸エステルタイプの有効物質;
m) 例えば、トウモロコシのためのチオカルバメート除草剤の損傷に対する種子処理薬害軽減剤として知られている「ナフタル酸無水物」(PM)(=1,8−ナフタレンジカルボン酸無水物)のような種子処理製品として知られている、ナフタレンジカルボン酸誘導体タイプの有効物質;
n) 例えば、トウモロコシのためのイミダゾリノンによる損傷に対する薬害軽減剤として知られている「CL304415」(CAS登録番号31541−57−8)(=2−(4−カルボキシクロマン−4−イル)酢酸、American Cyanamid社製品)、のようなクロマン酢酸誘導体タイプの有効物質;
イネのための除草剤イマゾスルフロンの損傷に対する薬害軽減剤として知られている、「ダイムロン(daimuron)」又は「SK23」(PM)(=1−(1−メチル−1−フェニルエチル)−3−p−トリル尿素)、
イネのための数種類の除草剤による損傷に対する薬害軽減剤として知られている「クミルロン(cumyluron)」=「JC−940」(=3−(2−クロロフェニルメチル)−1−(1−メチル−1−フェニル−エチル)尿素、JP−A−60087254参照、
イネのための数種類の除草剤による損傷に対する薬害軽減剤として知られている、「メトキシフェノン(methoxyphenone)」又は「NK049」(=3,3’−ジメチル−4−メトキシベンゾフェノン)、
イネのための数種類の除草剤による損傷に対する薬害軽減剤として知られている「CSB」(=1−ブロモ−4−(クロロメチルスルホニル)ベンゼン)(CAS登録番号54091−06−4,Kumiai社製品)、のような、有害植物に対する除草活性に加えて、イネのような農作植物との関連において薬害軽減活性を示す有効物質;
a) 粉剤は、式(I)の化合物の10重量部と不活性物質としてのタルクの90重量部とを混合し、そしてその混合物をハンマーミルで粉砕して得た。
b) 水中に容易に分散可能な水和剤は、式(I)の化合物の25重量部、不活性物質として石英含有カオリンの64重量部、リグノスルホン酸カリウムの10重量部、及び湿展剤及び分散剤としてオレオイルメチルタウリン酸ナトリウムの1重量部を混合し、そしてその混合物をピン付きデイスクミルで粉砕して得た。
c) 水中に容易に分散可能な分散製剤は、式(I)の化合物の20重量部、アルキルフェノールポリグリコールエーテル(Triton(登録商標) X 207)の6重量部、イソトリデカノールポリグリコールエーテル(8 EO)の3重量部、及びパラフィン系鉱油(沸点範囲は、例えば約255から277℃以上)の71重量部を混合し、そしてその混合物をボールミルで、5ミクロン以下の微粉末になるまで粉砕して得た。
d) 乳剤は、式(I)の化合物の15重量部、溶媒としてシクロヘキサノンの75重量部、及び乳化剤としてオキシエチル化ノニルフェノールの10重量部より得た。
e) 顆粒水和剤は、
式(I)の化合物 75重量部、
リグノスルホン酸カルシウム 10重量部、
ラウリル硫酸ナトリウム 5重量部、
ポリビニルアルコール 3重量部、及び
カオリン 7重量部、
を混合し、その混合物をピン付デイスクミルで粉砕し、そしてその粉末を流動床で造粒液としての水に噴霧することにより造粒して得た。
f) 別法による顆粒水和剤は、
式(I)で表わされる化合物 25重量部、
2,2’−ジナフチルメタン−6,6’−ジスルホン酸ナトリウム 5重量部、
オレオイルメチルタウリン酸ナトリウム 2重量部、
ポリビニルアルコール 1重量部、
炭酸カルシウム 17重量部、及び
水 50重量部、
をコロイドミルで均質化し、及び予粉砕し、続いてその混合物をビーズミルで粉砕し、シングルサブスタンスノズルを用いた噴射塔中で得られた懸濁液を噴霧乾燥することにより得た。
生物学的実施例1:雑草に対する出芽前効力
単子葉及び双子葉の雑草植物の種子又は根茎部分を、プラスチック製ポットの砂壌土中に置いて土壌をかけた。その後、水和剤又は乳剤の形態に製剤化された本発明の化合物を、それぞれ水性懸濁液又はエマルションとして、ヘクタール当たり水600から800リットル(換算)の施用割合で、種々の薬量で覆土の表面に施用した。
単子葉及び双子葉の雑草植物の種子又は根茎部分を、プラスチックポットの砂壌土中に置いて土壌をかけ、そして良好な生育条件下で、温室で生育させた。播種3週間後、試験植物の第三葉期に処理をした。水和剤又は乳剤に製剤化された本発明の化合物を、植物の緑色部分に、種々の薬量でヘクタール当たり水600〜800リットル(換算)の施用割合で散布した。試験植物を最適生育条件下で温室中に3〜4週間静置した後、製剤の効力を目視で評点し、無処理対照と比較した。本発明の、上記表1〜4の化合物番号:1.5、1.205、2.1、2.2、2.3、2.5、2.206、3.1、3.31、3.82、3.106、3.109、及び3.112は、ヘクタール当たりの有効成分2kg又はそれ未満の施用割合において、シロガラシ(Sinapis alba)、イヌビエ(Echinochloa crus−galli)、ネズミムギ(Lolium multiforum)、ハコベ(Stellaria media)、コゴメガヤツリ(Cyperus iria)、アオゲイトウ(Amaranthus retroflexus)、エノコログサ(Setaria viridis)、エンバク(Avena sativa)、ヒメオドリコソウ(Lamium purpureum)、イヌカミツレ(Matricaria inodora)、ヒナゲシ(Papaver rhoeas)、オオイヌノフグリ(Veronica persica)、サンシキスミレ(Viola trocolor)、ホウキギ類(Kochia spp)及びシロザ(Chenopodium album)のような有害植物に対して極めて優れた出芽後防除活性を示した。
更なる圃場試験においては、雑草が自然に発生する条件下で、プランテーション作物を生育させ、そして本発明の式(I)の物質を、種々の薬量で散布した。施用後、様々な間隔を置いて活性を目視で評点した結果、本発明の化合物、例えば上記表1〜4に係る化合物番号:1.5、1.205、2.1、2.2、2.3、2.5、2.206、3.1、3.31、3.82、3.106、3.109、及び3.112は、例えば油ヤシ、ココヤシ、インドゴム、柑橘類、パイナップル類、棉、コーヒー、カカオのようなプランテーション作物及びブドウ栽培に対して、有効物質の高い割合においても影響を与えないことが見い出された。式(I)の試験化合物は、先行技術の化合物と比較しても、より改善された度合いの選択性を示し、そしてそれ故に、プランテーション作物における望ましくない植生を防除するのに適するものである。
Claims (16)
- 式(I)
R1及びR2は、各々独立して、H、(C1−C4)アルキル、(C1−C4)ハロアルキル、(C3−C4)アルケニル、(C3−C4)ハロアルケニル、(C3−C4)アルキニル、(C3−C4)ハロアルキニル、又はアシル基であり、
R3は、H、(C1−C6)アルキル、(C1−C6)アルコキシ、(C2−C6)アルケニル、(C2−C6)アルキニル、(C2−C6)アルケニルオキシ、又は(C2−C6)アルキニルオキシ、好ましくはH、(C1−C6)アルケニル、又は(C1−C6)アルコキシであり、
R4、R5、R6、及びR7は、各々独立して、H、(C1−C4)アルキル、(C1−C3)ハロアルキル、ハロゲン、(C1−C3)アルコキシ、(C1−C3)ハロアルコキシ、CN、(C2−C6)アルケニル、(C2−C6)アルキニル、(C2−C6)アルケニルオキシ、又は(C2−C6)アルキニルオキシであるが、これらのうちの少なくとも一つは、(C1−C4)アルキル、(C1−C3)ハロアルキル、ハロゲン、(C1−C3)アルコキシ、(C1−C3)ハロアルコキシ、CN、(C2−C6)アルケニル、(C2−C6)アルキニル、(C2−C6)アルケニルオキシ、又は(C2−C6)アルキニルオキシであり、かつ、
Aは、CH2、O、又は直接結合である]
の化合物又はその塩〔但し、下記の化合物
及び
を除く〕。 - R1が、H、(C1−C4)アルキル、(C1−C4)ハロアルキル、(C3−C4)アルケニル、(C3−C4)アルキニル、又は1〜12個の炭素原子を有するアシル基であり、
R2が、H、(C1−C4)アルキル、又は(C1−C4)ハロアルキルであり、
R3が、H、(C1−C3)アルキル、又は(C1−C3)アルコキシであり、
R4、R5、R6、及びR7が、各々独立して、H、(C1−C3)アルキル、ハロゲン、又は(C1−C3)アルコキシであり、かつこれらのうちの少なくとも一つが、(C1−C3)アルキル、ハロゲン、又は(C1−C3)アルコキシであり、かつ
Aが、CH2又は直接結合である
ことを特徴とする、請求項1に記載の化合物。 - R1が、H、(C1−C3)アルキル、(C1−C3)ハロアルキル、アリル、プロパルギル、CHO、−CO(C1−C3)アルキル、又は−CO(C1−C3)ハロアルキルであり、
R2が、H、(C1−C2)アルキルであり、
R3が、H、メチル、又はエチルであり、
R4、R5、及びR7が、各々独立して、H、メチル、F、Cl、又はBrであり、
R6が、メチル、F、Cl、又はBrであり、かつ
Aが、CH2又は直接結合である
ことを特徴とする、請求項1又は2に記載の化合物。 - R1及びR2は各々Hであり、
R3はメチル又はエチルであり、
R4、R5、及びR7は、各々独立して、H、メチル、Br、Cl、又はFであり、
R6はメチル、Br、Cl、又はFであり、かつ
AはCH2、O、又は直接結合である
ことを特徴とする、請求項4〜6のいずれかに記載の化合物。 - 製造しようとする式(I)の化合物におけるR1若しくはR2基の一方、若しくは各々が、(C1−C4)アルキル、(C1−C4)ハロアルキル、(C3−C4)アルケニル、(C3−C4)ハロアルケニル、(C3−C4)アルキニル、又は(C3−C4)ハロアルキニルである場合、式(I’)
の化合物を、式(VI)若しくは(VII)
R1−L2 (VI) R2−L2 (VII)
(式中、R 1 、R 2 は式(I)の化合物において定義した通りであり、L2は脱離基である)
のアルキル化剤とそれぞれ反応させて、式(I)の化合物若しくはその塩をモノアルキル化若しくはジアルキル化の生成物として得る、
ことを特徴とする、請求項1に記載の式(I)の化合物又はその塩の製造方法。 - 製造しようとする式(I)の化合物のR1若しくはR2基の一方、若しくは各々がアシル基である場合、式(I’)
の化合物を式(VIII)若しくは(IX)
R1−L3 (VIII) R2−L3 (IX)
(式中、R 1 、R 2 は式(I)の化合物において定義した通りであり、L 3 は脱離基である)
のアシル化剤とそれぞれ反応させることによって、式(I)の化合物若しくはその塩をモノアシル化若しくはジアシル化の生成物として得る、
ことを特徴とする、請求項1に記載の式(I)の化合物又はその塩の製造方法。 - 製造しようとする式(I)の化合物のR1若しくはR2基の一方が(C1−C4)アルキル、(C1−C4)ハロアルキル、(C3−C4)アルケニル、(C3−C4)ハロアルケニル、(C3−C4)アルキニル、若しくは(C3−C4)ハロアルキニルであり、他方がアシル基である場合、式(I’)
の化合物を、式(VI)若しくは(VII)
R 1 −L 2 (VI) R 2 −L 2 (VII)
(式中、R 1 、R 2 は式(I)の化合物において定義した通りであり、L 2 は脱離基である)
のアルキル化剤とそれぞれ反応させ、その後に式(VIII)若しくは(IX)
R 1 −L 3 (VIII) R 2 −L 3 (IX)
(式中、R 1 、R 2 は式(I)の化合物において定義した通りであり、L 3 は脱離基である)
のアシル化剤とそれぞれ反応させて、式(I)の化合物若しくはその塩を得る、
ことを特徴とする、請求項1に記載の式(I)の化合物又はその塩の製造方法。 - 請求項1〜7のいずれかに記載の一つ又はそれ以上の式(I)の化合物又はそれらの塩、及び作物防疫に適用可能な製剤補助剤を含む除草又は植物成長調節組成物。
- 有効量の請求項1〜7のいずれかに記載の一つ又はそれ以上の式(I)の化合物又はそれらの塩を、植物の部位に施用することを含む有害植物の防除又は植物成長の調節方法。
- 除草剤又は植物成長調節剤としての請求項1〜7のいずれかに記載の式(I)の化合物又はその塩の使用。
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TW (1) | TWI401253B (ja) |
WO (1) | WO2007115695A1 (ja) |
ZA (1) | ZA200807617B (ja) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
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EP2147600A1 (en) * | 2008-07-21 | 2010-01-27 | Bayer CropScience AG | Method for weed control in lawn |
US8921270B2 (en) | 2011-11-08 | 2014-12-30 | Amvac Chemical Corporation | Method for pre-emergent weed control using triazine-based herbicide |
KR20180052652A (ko) * | 2015-09-11 | 2018-05-18 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 비구아나이드 염 및 s-트리아진의 제조 방법 |
WO2017220467A1 (de) * | 2016-06-24 | 2017-12-28 | Bayer Cropscience Aktiengesellschaft | 3-amino-1,2,4-triazinderivate und deren verwendung zur bekämpfung unerwünschten pflanzenwachstums |
CN110672753B (zh) * | 2019-11-04 | 2022-05-20 | 青海省农林科学院 | 一种氟咯草酮异构体的拆分和检测方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1988002368A1 (en) * | 1986-09-30 | 1988-04-07 | Idemitsu Kosan Company Limited | Triazine derivative, production thereof, and herbicide containing same as effective ingredient |
DE19522137A1 (de) * | 1995-06-19 | 1997-01-02 | Hoechst Schering Agrevo Gmbh | 2-Amino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
CN1207735A (zh) * | 1995-11-27 | 1999-02-10 | 出光兴产株式会社 | 三嗪衍生物 |
DE19604191A1 (de) * | 1996-02-06 | 1997-08-07 | Hoechst Schering Agrevo Gmbh | 2,4-Diamino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
DE19607450A1 (de) * | 1996-02-28 | 1997-09-04 | Hoechst Schering Agrevo Gmbh | 2-Amino-4-bicycloamino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
JP2001151612A (ja) * | 1999-09-09 | 2001-06-05 | Nippon Bayer Agrochem Co Ltd | 除草性1,3,5−トリアジン類 |
CA2515116C (en) * | 2003-02-05 | 2014-01-21 | Bayer Cropscience Gmbh | Amino-1,3,5-triazines n-substituted with chiral bicyclic radicals, process for their preparation, compositions thereof, and their use as herbicides and plant growth regulators |
MX2007009783A (es) * | 2005-02-17 | 2007-08-22 | Wyeth Corp | Derivados de indol, benzotiofeno, benzofurano e indeno cicloalquilfusionados. |
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Also Published As
Publication number | Publication date |
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TWI401253B (zh) | 2013-07-11 |
BRPI0710667A2 (pt) | 2011-08-16 |
JP2009533363A (ja) | 2009-09-17 |
EP2007738A1 (en) | 2008-12-31 |
EP2007738B1 (en) | 2014-02-26 |
US20070238617A1 (en) | 2007-10-11 |
AU2007236251B2 (en) | 2012-12-20 |
MX2008013172A (es) | 2008-10-21 |
CN101421254B (zh) | 2012-08-22 |
CN101421254A (zh) | 2009-04-29 |
TW200815419A (en) | 2008-04-01 |
MY154933A (en) | 2015-08-31 |
AU2007236251A1 (en) | 2007-10-18 |
CA2649021A1 (en) | 2007-10-18 |
DE102006016885A1 (de) | 2007-10-18 |
WO2007115695A1 (en) | 2007-10-18 |
AR060383A1 (es) | 2008-06-11 |
KR20080108529A (ko) | 2008-12-15 |
ZA200807617B (en) | 2009-07-29 |
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