TW304946B - Pyrazol benzoyl derivatives - Google Patents
Pyrazol benzoyl derivatives Download PDFInfo
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- TW304946B TW304946B TW85102166A TW85102166A TW304946B TW 304946 B TW304946 B TW 304946B TW 85102166 A TW85102166 A TW 85102166A TW 85102166 A TW85102166 A TW 85102166A TW 304946 B TW304946 B TW 304946B
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- Prior art keywords
- so2ch3
- methyl
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- patent application
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- -1 unsaturated heterocyclic radical Chemical class 0.000 claims description 269
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 29
- 238000011049 filling Methods 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 11
- 238000005481 NMR spectroscopy Methods 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 230000002363 herbicidal effect Effects 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 150000003254 radicals Chemical class 0.000 claims description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 238000005160 1H NMR spectroscopy Methods 0.000 claims description 5
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 4
- 229910052757 nitrogen Chemical group 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 239000011593 sulfur Chemical group 0.000 claims description 3
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- CIISBYKBBMFLEZ-UHFFFAOYSA-N 1,2-oxazolidine Chemical compound C1CNOC1 CIISBYKBBMFLEZ-UHFFFAOYSA-N 0.000 claims 1
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 25
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- 238000012360 testing method Methods 0.000 description 10
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- 238000011282 treatment Methods 0.000 description 6
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 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
- JQMVGTOAKFLMOU-UHFFFAOYSA-N pentaoxane Chemical compound C1OOOOO1 JQMVGTOAKFLMOU-UHFFFAOYSA-N 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- DHHVAGZRUROJKS-UHFFFAOYSA-N phentermine Chemical compound CC(C)(N)CC1=CC=CC=C1 DHHVAGZRUROJKS-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical group 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 208000003383 pontocerebellar hypoplasia type 3 Diseases 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- XWRDGWGYYMWOFB-UHFFFAOYSA-N propane-1-sulfinamide Chemical compound CCCS(N)=O XWRDGWGYYMWOFB-UHFFFAOYSA-N 0.000 description 1
- LFILDSDQMSCNBV-UHFFFAOYSA-N propane-2-sulfinamide Chemical compound CC(C)S(N)=O LFILDSDQMSCNBV-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- 238000007347 radical substitution reaction Methods 0.000 description 1
- 229910052705 radium Inorganic materials 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 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
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
- 125000004354 sulfur functional group Chemical group 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- CESUXLKAADQNTB-UHFFFAOYSA-N tert-butanesulfinamide Chemical group CC(C)(C)S(N)=O CESUXLKAADQNTB-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000004149 thio group Chemical group *S* 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 210000003462 vein Anatomy 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
- 210000004916 vomit Anatomy 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 238000009333 weeding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/24—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms having sulfone or sulfonic acid radicals in the molecule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
A7 B7 1、發明説明(]) 本發明關於新穎具除草活性之吡唑苯甲醯基衍生物,製 错該等〃比峻苯甲醯基衍生物之方法,包含彼等之組合物, 及此等衍生物或包含彼等之組合物用以控制雜草之用途。 具除草活性之吡唑苯甲醯基衍生物業已揭示於文獻中, 例如,於歐洲專利352543。 然而’已知化合物之除草性質及其由作物植物之耐受度 並不全然令人滿意。 本發明之一目的在於發現具改良性質之新穎吡唑苯甲醯 基衍生物。 我們已發現此目的係由式I之吡唑苯甲醯基衍生物而達 成 (請先閱讀背面之·注意事項再填寫本頁)
L ,?τ 經濟部中央榡準局員工消費合作社印策 其中之取代基如下列: L,Μ爲氫,Cl_c6_ 烷基,c2-c6-烯基,c2_c6_ 炔基,Cl_ C4-烷氧基,對於此等基團可能爲未經取代或經一至五 個鹵原子或c!-c4-烷氧基取代,或爲鹵素,氰棊,硝 基,基團-(Y)n-S(0)mR7或基團-(Y)n-CO-R8 Z 爲5 -或6 -員飽和或未飽和雜環自由基,其具有一至三 個選自氧,硫與氮之雜原子,且其爲未經取代或經鹵 素,氰基,硝基,基團-CO-R8,CVCr烷基,Cl_c4-鹵烷基,c3-c8-環烷基,Crc4-烷氧基’ Cl-C4-鹵烷 -4- 本紙浪尺度適用中國國家標準(CNS ) Α4規格(210X297公釐〉 五 、發明説明( 2 A7 B7 經濟部中央標準局員工消費合作社印製 氧基,c!-c4-烷硫基,Cl_c4_齒烷硫基,二“Crf烷 胺基,經未經取代或經鹵素,氛基,硝基,Ci_cj·烷 基或C丨·<:4_鹵烷基取代之苯基,或經可於互變異構形 式中亦表現爲羥基之雙償氧取代,或其與所稠合之苯 環(其爲未經取代或經鹵素,氰基,硝基,烷基 或Ci-C4·鹵烷基取代)共同形成雙環系,或與所稠合之 竣環或所拥合之第二個雜環(其爲来經取代或經齒素, 氰基’硝基’ ci-c4-烷基,二-q-cv烷胺基,cvcv 故氧基,鹵烷氧基或Ci-cv鹵烷基取代)共同形 成雙環系, 爲0或NR9, 爲零或1, , 爲零^ 1或2, 爲C丨-C4-烷基,烷基或nr9r10 R8爲C^-GV燒基,c丨-C4-鹵坑基,Cj-C^-坡氧基或 nr9r10 R9爲氫或q-cv烷基, R10爲C丨-C4-烷基 Q 爲具式II之吡唑環 請 閲 讀 背 冬 意 事 項 再 本 頁 Yη m R7 R2 F OR3
II 訂 y 其中 -5 - 本紙張尺度適用中國國家標率(CNS ) A4規格(210X297公釐) 經濟部中央標率局員工消費合作社印裝 A7 B7 五、發明説明(3 ) R1 爲<^-(:4-烷基, R2爲氫或烷基且 R3爲氫,烷成基,苯戚基或烷基苯规基’而且 其係鍵聯於4 -位置上, 及式I化合物習用於農業上之殲類。 式I化合物係藉將式11 a之5 -雍基毗唑以式111之苯甲醯基 衍生物酿化(T = C1),並使所形成之?比吐酿進行重排反應以 給予具式Ic之化合物而獲得。
RS-TI N、N人 R1
Ila
於上式分子式中,τ爲齒素且L,Μ及Z係如前文所述者。 反應程序之第一步驟,名爲醯化作用,係以普遍已知之 方法完成,例如藉將式I I之苯甲醯基衍生物(T = C 1)於輔 助驗存在下加入5 -幾基p比唑11 a之溶液或懸浮液中。爲方 便起見,反應物與輔助鹼係以大約等莫耳之量使用。於某 些情況下可有利地使用稍過量之輔助鹼,例如1 2至1.5莫 -6 - 本紙張尺度適用巾國國家樣芈(CNS) M規格(210X297公楚 (請先閱讀背面之注意事項再填?ξ本頁)
0
Ic ΌΗ 經濟部中央標準局員工消費合作社印製 A7 _______Β7 五、發明説明(4 ) 耳當量。 適宜之輔助鹼爲例如第三級烷胺類,吡啶或鹼金屬碳酸 鹽類,而二氣甲烷,二乙基醚,甲苯或乙酸乙酯可用作爲 溶劑。於添加酸氣化物期間,有利地將反應混合物冷卻至 0-10°C,並然後將混合物於較高溫度(例如25-5CTC)下攪拌 ,直到反應終止。 逐漸造成係以習知方法完成,例如將反應混合物倒入水 中並使用二氣甲炊萃取。待有機相經乾燥並將溶劑去除後 ’粗5 -經基峨峻可未經進一步純化而用於重排反應中。5_ 經基峨吐之苯甲酸酯之製備實例可見於(例如)歐洲專利_A_ 282 944或美國專利 US 4 643 757。 爲方便起見,,給予式1£5化合物之5_羥基吡唑酯重排反應 係於20 °C至40 Ό下,於溶劑中及於輔助鹼存在下,並藉 助於作爲觸媒之氰基化合物而完成。可用溶劑之實例爲乙 恥,一氣甲烷,1,2 -二氣乙烷,乙酸乙酯或甲苯。較佳之 溶劑爲乙腈》適宜之輔助鹼爲第三級胺類,吡啶或畛金屬 碳酸鹽,其可以等莫耳量或至多四倍過量使用。較佳之輔 助驗爲以兩倍量使狀三6胺。通宜之觸媒純化物化合 物,如用量例如爲1至50(特別係5_5〇)莫耳百分比,以% 爽墓nb唑酯爲基準,之氰化鉀或丙酮氰醇。丙酮氰醇較佳 係以例如1 0莫耳百分率之量加入。 5-羥基吡唑苯甲酸酯重排作用之實例見於,例如,歐洲 專利-A-282 944或美國專利US 4 643 757 *,然其中僅所 用之觸媒爲存於二,号烷中之碳酸钟或碳酸納。而氛化卸或 ____________ -7- 本紙張尺度適用中)以驗(2ι〇㈣公酱).—-_— (請先閲讀背面之注意事項再填寫本頁) --° 經濟部中央標準局員工消費合作社印製 A7 —____ _ B7 五、發明説明(5 ) 丙酮氰醇與環己烷-1,3-二酮烯醇酯之類似重排作用結合之 用途業已揭示(US 4 695 673),從該文獻得知無用以説明 氰化物化合物於5-羥基吡唑Ο-醢基衍生物佛利斯重排作用 (Fries rearrangement)上之特別良好適用性。 逐漸造成係以習知方法完成,例如將反應混合物以稀無 機酸(如5 %強度鹽酸或硫酸)酸化,並將混合物用例如二 氣甲炊或乙酸乙酯萃取。對於純化,將萃取物以冰5 ·〖〇 〇/〇 強度鹼金屬碳酸鹽溶液萃取,終產物進入水相中。將具式 Ic之產物藉酸化水溶液而沉殿,或使用二氣甲坑再萃取, 乾燥接著再除去溶劑。 用作爲起始物之式II 5-經基P比峻爲已知,且可藉本身已 知之方法製備得(參見歐洲專利A-240 001及J. Prakt. Chem. 5J_1,382 (1973))。1,3-二甲基-5-經基p比峻爲市售可得之化 合物。 具式III之笨甲酸衍生物可依下列製備得: 苯甲醯基鹵化物,例如式III (T = C1)之氣化苯甲基,係以 本身已知之方法藉將式in (T = OH)之苯曱酸與硫醯氯反應 而製備得。式III (T = OH)之苯甲酸可以已知方法藉酸或鹼 水解之方式由相對應之式III = 烷氧基)酯類製備 得。 具式III之中間物可例如根據流程圖2及3以下文所述之途 徑合成得。 -8- -I-------广-- (請先S讀背面之注意事項再填寫本頁) 訂 本紙張尺度適财ϋ g) ( CNS ) A4規格(21〇 χ297公董) Α7 Β7 五、發明説明( 流程圈2
IV + Z-A1
III
V 經濟部中央標準局員工消費合作社印製 τ 爲Ci-C4•烷氧基, X 爲 C卜 Br,I,-S0(0)2CF3,-0S(0)2F A1 爲 Sn(C丨-C4-烷基)3,b(OH)2,ZnHal,而 Ha@ C1 或Br且 L,M,Z爲如上所定義。 根據此,芳基鹵素化合物或芳基磺酸酯IV可以本身已知 之方法,與雜芳基錫酸酯類(史泰勒偶合作用,Stille couplings),雜芳基硼化合物(鈴木偶合作用,Suzuki couplings)或雜芳基-鋅化合物(尼吉許反應,Negishi reaction) V(參見,例如,合成 19 87, 51-53,合成 1992, 413) 於把或鎳過渡金屬觸媒存在下,及於有或無鹼存在下反應 而得新穎之通式III化合物。 具式III之苯甲酸衍生物亦可藉將式VI之適宜經溴_或碘_ 取代之化合物 流程圖3
Br,I
VI
CO/TOH 觸媒
T
111/ - 9 - 本紙張尺反通用中國國家標準(CNS ) A4規格(2ΐ〇χ^^- (請先聞讀背面之a意事項再填巧本頁〕
五 發明説明(7 A7 B7 其中 Z1爲Z或CN, T 爲(^或仏-〜-烷氧基且 L與Μ爲如上所定義, 與一氧化碳及水於提高之壓力下,於鈀,鎳,鈷或錢過波 金屬觸媒及鹼存在下反應而獲得。 本發明範圍内較佳之苯甲醯基衍生物爲該等式IIIa化合 物 〇 Η
Ilia (请先閱讀背面之·江意事項存填寫本貫) 經濟部中央標準局員工消费合作社印製 其中Τ,L,Μ及Z爲如下所示: τ 爲氣’ 〇Η或CVC4-烷氧基, 爲 CrC6-烷基 ’ C2-C6-烯基 ’ C2-C6-炔基,(^-(:4-烷 氧基’烷硫基,q-cv鹵烷基,q-cv鹵坑氧 基,C^C:4 -鹵烷硫基,Cl_C4_烷颯基,鹵素,硝基或 氰基, 爲 Ci-Cf 炫* 基 ’ C2_Cg-稀基 ’ C2_C(5 -決基 ’ Ci_C4 -坡 氧基,Ci-cv烷硫基,Cl-c4-鹵烷基,Ci-cv·鹵烷氧 基’ Ci-C4_鹵燒硫基,C^-C4·燒艰基,面素,石肖基或 氰基且 爲如上所定義者。 其他較佳之苯甲醯基衍生物爲該等具式IIIb之化合物
L
Z -10 - 私紙張尺度適用中國國家標隼(CNS ) A4規格(21〇χ297公釐) 訂 A7 A7 經濟部中央標準局員工消費合作社印製 Β7 五、發明説明(8 )
其中T,L,Μ及Z係如下所示·· Τ 爲氣,〇^1或<:1-(:4-烷氧基, L,Μ 爲〇丨-(:6-烷基,C2-C6-烯基,C2-C6-炔基,c丨-C4-烷氧基’ q-CV烷硫基,q-CV鹵烷基,鹵 燒乳基’ Ci-C^-卣坑硫基’ C丨-C 4 -坑械基,卣素, 硝基或氣基,且 z 爲如上所定義者。 觸媒鎳,鈷,,铑及(尤其)鈀可以金屬形式或以習知鹽類 形式於已知價度下表現,如以鹵化合物形式如PdCl2, RI1CI3 . Ηβ ’以醋酸鹽形式如pd(〇Ac)2,氮化物形式及 類似物表現《亦可存在與第三級膦之金屬複合物,金屬坡 羰基,金屬羰基,例如C〇2(CO)8,Ni(co)4,與第三級膦 疋·金屬羰基複合物,如(PPh3)2Ni(c〇)2,或與第三級膦之 過渡金屬複合物。最後提及之具體實施例當使用鈀作爲觸 媒時爲特別較佳。膦配位子之性質變化廣泛。例如,其可 以下列分子式代表: ·、
/RU P T R12 · Rll\ / R13 \RU 或 RVP—(CH2)n—P\r14 其中n指數字1,2,3或4且自由基rH至Ri4爲低分子量烷 I紙張尺度適用----- _ 朱榇準(CNS ) Α4规^1107297公釐)--—~一 (請先閱請背面之注意事項再填寫本頁)
經濟部中央標準局員工消費合作社印製 A7 _______B7 五、發明説明(9 ) 基’如crcv烷基,芳基,Ci_C4_烷芳基,如苯甲基,苯 6基或芳氧基。芳基爲(例如)茬基,蒽基及(較佳地)經取 代或未經取代之苯基,而取代基可於廣泛範圍内變化,且 只要其對需要進行之羧基化反應爲惰性,該等取代基包含 所有情性C-有機自由基,如C〇〇H,COOM(其中Μ爲例如 鹼金屬’檢土金屬或銨鹽)’或藉氧鍵結之c·有機自由基 〇 騰複合物可以本身已知之方法,例如前文所提及之文獻 所述之方法製備得。例如,起始物可爲市售可得之金屬鹽 類’如 PdCl2 ’ 或 Pd(OCOCH3)2,並將膦如 p(c6H5)3, Ρ(正- C4H9)3, PCH3(C6H5)2或1,2-雙(二苯基膦基)乙坑加入。 以過渡金屬爲基準之膦含量習知爲〇至20(尤其係0.1至10) 莫耳當量,特別較佳地爲1至5莫耳當量。 過渡金屬之量並不嚴苛。當然,爲經濟之理由較佳使用 少量’例如0· 1至10莫耳。/〇,特別係1至5莫耳%(以起始物VI 爲基準)。 爲製備苯甲酸III (Τ = ΟΗ),使用一氧化碳及至少等莫耳 量水(以起始物VI爲基準)完成反應。該反應物水同時亦可 作用爲溶劑,即最大量並不嚴苛。 然而,視所使用之起始物及觸媒而定,亦可有利地使用 不同之惰性溶劑或於幾基化反應使用之鹼作爲取代反應物 之溶劑。 適宜之惰性溶劑爲習用於羧基化反應之溶劑,如烴類如 甲苯,二甲苯,己燒,戊炫^環己坑,謎類如甲基第三-丁 _ -12 - 本紙乐尺度通用中國國家標準(CNS ) ,Vt規格(210 Χ 297公釐) (請先閲讀背面之注意事項再填寫本頁)
A7 B7 經濟部中央榡準局員工消費合作社印製 五、發明説明( 基醚,四氫呋喃,二咩烷,二甲氧基乙烷,經取代之醯胺 如二甲基甲醯胺,過取代之脲如四- Ci_c4_烷基脲,或腈類 如苯甲腈或乙腈。 於方法之較佳具體實施例中’使用過量之其中一反應物 (特別係鹼),因而免除另外溶劑之需要。 適合該方法之鹼爲所有可與於反應期間所釋出之碘化氫 或溪化氫結合之惰性鹼。可提及之實例爲第三級胺如第三 -烷基胺(如三烷胺,如三乙胺),環胺類(如N -甲基六氫吡 咬或Ν,Ν1-二甲基六氫p比喑),p比咬,驗金屬碳酸鹽,驗金 屬碳故氫鹽’或四規1基_經取代之脲衍生物,如四 烷基脉(例如四甲基腺)。 驗之量並不嚴苛,習知係使用i至i 〇 (尤其係1至5 )莫耳 。若验係同時用作爲溶劑,通常其量係以使反應物溶解之 方式測量,且無需爲實施原因而造成不必要之高過量,因 而節省經費,能夠使用小的反應容器並確保反應物間之最 次接觸。 於反應期間,一氧化碳I力係以使c 〇達過量(以VI爲基 準)之方式調整。於室溫下一氧化碳壓力較佳爲1至25〇巴 ,特別係5至150巴C0。 通常,羧基化作用係於2 0至2 5 0 °C,特別係3 0至1 5 0 °C 下,連續或分批地完成。若該方法係分批地完成,爲方便 起見將一氧化碳連續注於反應混合物上以維持恆壓。 該等芳基齒素化合物VI(其仍不爲已知者)可立即藉適宜 已知合成方法之組合而得。 -13 - 私紙張尺度適用中國國家標準(CMS ) A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) ,4 -6 〇〇494ι A7 B7 五、發明説明 11 例如,南素化合物vi可藉山德邁爾反應由(依次)可藉將 適宜硝基化合物還原而合成得之相對應苯胺獲得(參見, 例如’於其中 Z1=CN之情形中:Liebigs Ann. Chem. 1980, 768-778)。又芳基溴化物%可藉適宜起始化合物之直接溴 化作用而獲得[參見’例如,M〇natsh_ Chem. 99,815-822 (1968)] » 流程圖4 0 Μ Τ
X L (請先閱讀背而之注意事項再填寫本頁)
IVa
IV
R15 IVb Ο
r16 、v5 n
0 IVd 經濟部中央標準局員工消費合作社印製
H5J 丁 爲cvc4-烷氧基,
x 爲 Cl,Br,I,-〇S(0)2CF3,-0S(0)2F L, M,Z爲如上所定義,
Rl5 爲氫,Ci-Cy烷基,crc4-齒烷基,c3-c8-環烷基 -14- 本紙張尺度適用中國國家標準(CNS) A4規格(2l0x 297公釐) 經濟部中央樣準局員工消費合作社印製 Α7 Β7 五、發明説明(12 ) ,未經取代或經取代之苯基或三甲矽烷基,且 R16 爲氫,CrC4-卤烷基,C3-C8-環烷基或爲未經取 代或經取代之苯基。 於鈀或鎳過渡金屬觸媒存在下及於有或無鹼存在下,芳 基甲基酮IVa可藉由文獻已知從芳基鹵素化合物或芳基磺 酸酯IV開始,將其與乙烯基烷基醚反應,接著進行水解作 用之方法而製備得[參見’例如,Tetrahedron Lett. 32, 1753-1756 (1991)]。 乙烯化芳族化合物I V b可以本身已知之方法,藉將芳基 鹵素化合物或芳基績酸g旨IV與經取代之乙炔,於把或線過 渡金屬觸媒存在下反應而製備得(例如雜環化合物, Heterocycles,24, 3 1-32 (1986))。爲方便起見其中 之衍生物I Vb係從矽坑基化合物(Ri5 = _si(CH3)3)獲得[j 〇rg. Chem. 46, 2280-2286 (1981)] 〇 芳基自素化合物或芳基磺酸酯Ϊ V與烯烴於鈀觸媒存在下 之希克反應(Heck, reaction)得到芳基烯類ivc(參見,例如 ’ Heck ’有機化學合成之钯試劑,學院出版,儉敦1985, 或合成 1993, 735-762)。 該等非已存在之苯甲醢基衍生物I v (參見,例如,c〇ii.
Czech. Chem· Commn. 40, 3009-3019 (1965)]可以簡便方法 由已知合成法之逍宜组合而獲得β 例如’磺酸酯IV (X=-〇s(〇)2CF3, -os(o)2f)可由相對應 盼類’其依序爲已知(參見,例如,EP 195247),或可藉 已知方法製備得(參見’例如,合成1993, 735 762),獲得 (請先閱讀背面之注意事項再填寫本頁) 、v5 本紙張尺家辟(CNS) Α·^( 21〇 -15- X 297公釐) 五、發明説明( 13 A7 B7 鹵素化合物IV (X=C1,Br或I)可,例如,從相對應苯胺類 藉山德邁爾反應獲得。 流程圖5 *
Ac20 〇
CN (請先閲讀背面之注意事項再填寫本頁) -5
IVi r\
IVk η
nh2 且 經濟部中央標準局負工消費合作社印製 A 爲 S,NH,或 NOH, T 爲<31-<34-烷氧基且L及M爲如上所定義。 異酞酸衍生物IVf可從醢類IVe藉已知方法製備得[參見J. March高等有機化學第3版,第629頁等,Wiley-Interscience 發行(1985)]。 肋IVg係有利地藉將醛類I V e與胲以本身已知方法獲得[ 16 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 五、發明説明 14 A7 B7 參見J.M一高等有機化學第3版,第齡_頁,·ey_
Interscience發行(1985)】。 肟1¥藉亦爲本身已知之方法轉化成腈類[參見J, March高等有機化學第3版,第931_932頁,则化⑽-science發行(1985)]。 料趁類,其爲作爲起始化合物所需且其爲非已知者) 可藉已知方法獲得。例如,其可由根據流程圖6之甲基化 合物VII合成得。 流程圖6 請 閱 讀 背 面 之 注 意 事 項 再 寫 本 頁 ▲
VII
CH2Br
IVe 訂 經濟部中央樣準局員工消费合作社印袈 自由基Τ,Μ及L係如流程圖5中所定義。可將甲奉化合 物藉一般已知之方法,例如與!^•溴琥珀醯亞胺或13-二溪^ 5,5-二甲基反應而得到苯甲基溴化物νιπ。苯甲基溴化物 得到苯甲醛IVe之反應亦由文獻得知[參見,Synth c〇mmun 22? 1967-1971 (1992)] 〇 先驅物IVa至IVh適於合成雜環中間物ΠΙ。 例如,5-哼唑基[參照,例如,j雜環化學,28, 17_28 (1991)1或4-嘍唑基衍生物[參照,例如,Metzger,嘍唑類 於:雜環化合物之化學,卷34,第175頁等(〗976)]可從苯 -17- 本紙浪尺度適用中國國家標準(CNS ) A4規格(2丨OXM7公釐) S04946 A7 ____ B7 五、發明説明(15 ) ~ 乙酮IVa藉經鹵化之中間物iVd獲得。 乙炔IVb或烯類IVc適於合成4-異p塞唑基,5-異喳唑基, 4,5-二氫異p塞唑_4_基,4,5_二氫異p塞唑_5_基衍生物(參照, 例如’胡本-威爾 Houben-Weyl Methoden der organischen
Chemie[有機化學之方法],第4版,卷χ/3,第843等頁 (1965)]。 2·4吐基,1,2,4_嘮二唑-5-基或1,3,4-哼二唑-2-基衍生物 (參照,例如’ J·雜環化學’ 28, 17_28 (1991)]或2-吡咯基 衍生物[參照,例如,雜環類26, 3141-3151 (1987)]可例如 藉文獻已知之方法從苯甲酸IVf或從酸氣化物IVi(其可藉標 準方法由其獲得)製備得。 1,2,4-三唑-3-基衍生物可藉已知方法從笨甲骑IVh製備得 % [參照,例如,J. Chem. Soc. 3461-3464 (1954)] 〇 經濟部中央標準局負工消費合作社印製 苯甲腈IVh可藉中間物硫醯胺類,醯胺肟或脒類1¥111轉化 成l,2,4-p号二唑-3-基丨參照,例如’ j.雜環化學,28, 17-28 (1991)],2-p塞唑基,4,5-二氫嘍喳-2-基或 5,6-二氧-4H-】,3-p塞喷-2-基衍生物[參見,例如,胡本_威爾,Methoden der organischen Chemie[有機化學之方法],第4版,卷E5, 第1268等頁(l%5)]。此外,l,2,4_p塞二唑_5-基衍生物[參照 ,例如,J. Org. Chem. 45, 3750-3753 (1980)]或 1,3,4-噬二 嗤 _2-基衍生物[參照,例如,j. chem. Soc·,Perkin Trans. I 19 87-1991 (1982)】可藉文獻已知之方法由硫醯胺類IVm (A=S)獲得。 B IVg可以本身已知之方法藉中間物羥肟酸氣化物Ivk轉 ____ -18- 本紙張尺度適用t國國家標準(CNS )八4祕(2l〇x297公瘦) 經濟部中央標準局員工消費合作社印製 A7 ________Β7 五 '發明説明(16 ) 化成3-異哼唑基衍生物[參照,例如,胡本-威爾, Methoden der organischen Chemie[有機化學之方法],第 4版 ,卷乂/3,第843等頁(1965)]。 關於具通式I苯甲醯基衍生物之既定用途,以下列自由 基爲適宜之取代基: L與Μ爲氫,
CrC6-烷基,如甲基,乙基,丙基,1-甲基乙基,丁基, 1- 甲基丙基,2-甲基丙基,1,1-二甲基乙基,戊基,丨_甲基 丁基,2-甲基丁基,3-甲基丁基,1,1-二〒基丙基,1,2_二 甲基丙基,2,2-二甲基丙基,1-乙基丙基,己基,丨·曱基 戊基,2-〒基戊基,3-甲基戊基,4-甲基戊基,1,1_二甲基 丁基,1,2-二甲基丁基,1,3-二甲基丁基,2,2-二甲基丁基 ,2,3-二甲基丁基,3,3-二甲基丁基,1-乙基丁基,H2- 三甲基丙基,1,2,2-三甲基丙基,1-乙基-1-甲基丙基或【_ 乙基-2-甲基-丙基, 特別係甲基,乙基,1 -甲基乙基,1 -甲基丙基,2-甲基丙 基,1,1-二甲基乙基及1,1-二甲基丙基; -稀·基’如2 -丙稀基,2 -丁缔基’ 3 -丁缔基,1-甲基_ 2- 丙烯基,2-甲基-2-丙烯基,2-戊缔基,3-戊烯基,4-戊缔 基,3-甲基-2·丁烯基,1-甲基-2-丁烯基,2-甲基-2-丁缔基 ,:l-f基-3-丁烯基,2-甲基-4-丁烯基,3-甲基-3-丁晞基, 1,1-二甲基丙烯基,1,2-二甲基-2-丙烯基,1-乙基_2_丙 坤基’ 2 -己稀基’ 3 -己稀基,4 -己缔基,5 -己稀基,1-甲基_ 2-戊烯基,2-甲基-2-戊烯基,3-甲基-2-戊烯基,4-甲基-2- -19 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) " ---- (請先間讀背面之注意事項再4·寫本頁) -丨、私. -β
經濟部中央橾準局員工消費合作社印製 戊烯基,1-甲基-3-戊烯基,2-甲基-3-戊烯基,3-甲基-3-戊 晞基,4-甲基-3-戊烯基,1-甲基-4-戊烯基,2-甲基-4-戊缔 基,3-甲基-4-戊烯基,4-甲基-4-戊烯基,1,卜二甲基-2-丁 烯基,1,1-二甲基-3-丁烯基,1,2-二甲基-2-丁烯基,1,3_ 二甲基-3-丁晞基,2,2-二甲基-3-丁烯基,2,3-二甲基-2-丁 烯基,2,3-二甲基-3-丁晞基,1-乙基-2-丁烯基,1-乙基_3_ 丁晞基,2 -乙基-2-丁晞基,2 -乙基-3-丁烯基,1,1,2-三甲 基-2-丙晞基,1-乙基-1-甲基-2-丙埽基及乙基-2 -甲基-2-丙 缔基’ 特別係1-甲基-2-丙烯基,卜曱基-2-丁烯基,1,1-二甲基-2-丙締基及1,1-二甲基-2-丁埽基; C2_C6-炔基,如丙块基,2 -丁块基,3 -丁炔基,2 -戍块基, 3-戊炔基,4-戊炔基,1-甲基-3-丁炔基,2-甲基-3-丁炔基 ’ 1-甲基-2-丁炔基,1,1-二甲基-2-丙炔基,1-乙基-2-丙炔 基’ 2-己炔基,3_己炔基,4-己炔基,5-己炔基,1-甲基-2-戊炔基,1-甲基-3-戊炔基,1-甲基-4-戊炔基,3-甲基-4-戊 炔基,4-甲基-2-戊炔基,1,1-二曱基-2-丁炔基,1,1·二甲基 -3-丁炔基,1,2-二甲基_3_ 丁炔基,2,2·二甲基-3-丁炔基,1-乙基-2-丁炔基,1-乙基-3-丁炔基,2-乙基-3-丁炔基及1-乙 基曱基-2-丙块基; CrC4-烷氧基,如甲氧基,乙氧基,正-丙氧基,1-甲基乙 氧基,正-丁氧基,卜甲基丙氧基,2-甲基丙氧基及1,1-二甲 基-乙氧基, 特別係CrC3-烷氧基,如甲氧基,乙氧基及異-丙氧基, (請先閱讀背面之注意^-:?再填寫本頁 -裝 訂 線 -20- A7 B7 18 五、發明説明( 此等基固可能爲未經取代或如上所述經一至五個南素原子 (如氟’氣’溴及碘,較佳爲氟及氣)或crc4-烷氧基取代 Ο 上述所定義之基團-(Y)n_S(0)mR7爲,例如, C丨-C4-烷硫基,如甲硫基,乙硫基,正-丙硫基,1-甲基乙 硫基,正-丁硫基,1-甲基丙焱基,2-甲基丙硫基及1,1-二 甲基乙硫基,特別係甲硫基;
CrC4-烷亞磺醯基,如甲亞磺醯基,乙亞磺醯基,正-丙亞 磺釀基,1-甲基乙亞磺醯基,正-丁亞磺醯基,1-甲基丙亞 磺醯基,2-甲基丙亞磺醯基及1,1·二甲基乙亞磺醢基,特 別係甲亞磺醯基; C1-C4-坑績酿基’如甲殘随基,乙確酿基,正-丙靖酿基, % 1-甲基乙磺醯基,正-丁磺醯基,1-甲基丙磺醯基,2-甲基 丙磺醯基及1,1 -二甲基乙磺醯基,特別係甲磺醯基; crc4-烷氧碟酿基,如甲氧確醯基,乙氧績醯基,正-丙氧 磺醯基,1-甲基乙氧磺醯基,正-丁氧磺醯基,1-曱棊丙氧 碎釀基,2-f基丙氧續醯基及1,1-二甲基乙氧續醯基,特 別係甲氧磺醢基; N-C^-C4-坡胺確酿基,如N-甲胺確酿基,N-乙胺確酿基, N-正-丙胺續酿基’ N-1-曱基乙胺靖酿基,N·正-丁胺殘酿 基’ N-1-甲基丙胺績酿基,N-2 -甲基丙胺確酿基及N-l,i_ 二甲基乙胺磺醯基,特別係N-甲胺磺醯基; N-CrC4-坑胺亞續酿基,如N-甲胺亞績醯基,N-乙胺亞續 酿基,N-正-丙胺亞績酿基,N-1-甲基乙胺亞續酿基,义正 -21 - 本紙張尺度適用中國國家標準(CNS ) Α4^格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) 、11 經濟部中央標準局員工消费合作社印製 經濟部中央操準局貝工消費合作社印製 A7 B7 五、發明说明(19 ) -丁胺亞續醢基,N-甲基丙胺亞續醯基,N-2-甲基丙胺亞確 醯基及N-l,l-二甲基乙胺亞磧醯基,特別係N-甲胺亞續醯 基; 二-CrC4-烷胺磺醯基,如二甲胺磺醯基,二乙胺磺醯基, 二丙胺績醯基’二丁胺項酿基’ N-甲基-N-乙基胺續醯基, N-甲基-N-丙胺磺醯基,N-甲基-N-1-甲基乙胺磺醯基,N-甲 基-N-1,1-二f基-乙胺磺酿基,二-1-甲基乙胺磺醯基,N-乙 基-N-1-甲基乙胺磺醯基及N·乙基-N-l,l-二甲基乙胺磺醯基 ,特別係二甲胺磺釀基; 二-CrC4-烷胺亞磺醯基,如二甲胺亞磺醯基,二乙胺亞磺 醯基,二丙胺亞磺醯基,二丁胺亞磺醯基,N-甲基-N-乙 胺亞磺醯基,N-甲基-N-丙胺亞磺醯基,N-甲基-N-甲基乙 雩 胺亞磺醯基,N-甲基-N-l,l-二甲基乙胺亞磺醢基,二-1-甲 基-乙胺亞磺醯基,N-乙基-N-1-甲基乙胺亞磺醯基及N-乙 基-N-l,l-二甲基乙胺亞磺醯基;特別係二甲胺亞磺醯基; CpCr烷亞磺醯氧基,如甲亞磺醯氧基,乙亞磺醯$基, 正·丙亞磺釀氧基,正-丁亞磺醯氧基,1-甲基乙亞磺醯氧 基,1-甲基丙亞磺醯氧基,乙-甲基丙亞磺醯氧基及1,1-二 甲基乙亞磺醢氧基,特別係甲亞磺醯氧基;
Ci_C4-燒確酿氧基》如甲績酿氧基,乙靖酿乳基,正-丙績 醯氧基,1-甲基乙磺醯氧基,正-丁磺醯氧基,1-甲基丙磺 醯氧基,2-甲基丙磺醯氧基及i,i-二甲基乙磺醯氧基,特 別係甲磺醢氧基; crc4-烷亞磺醯胺基,如甲亞磺醯胺基,乙亞磺醯胺基, -22- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁) .—二衣· 訂 經濟部中央榡準局負工消費合作社印製 A7 ____B7_ 五、發明説明(2〇 ) 正-丙亞磺酿胺基,1-甲基乙亞磺醯胺基,正-丁亞磺醯胺 基,1-甲基丙亞磺醢胺基,2-甲基-丙亞磺醯胺基及1,卜二 甲基乙亞磺醢胺基,特別係甲亞磺醯胺基;
Cj-C4-燒績酿胺基,如甲績酿胺基’乙續酿胺基’正-丙續 醯胺基,1-T基乙磺醯胺基,2-f基丙磺醯胺基及1,1-二 甲基乙磺醯胺基,特別係甲磺醯胺基: N-CVq-烷亞磺醯基-N-甲胺基,如N-甲亞磺醢基-N_甲胺 基,N-乙亞磺醯基-N-甲胺基,N-正-丙亞磺醯基-N-甲胺基 ,N-1-甲基乙亞磺醢基-N-甲胺基,N-正-丁亞磺醢基-N-甲 胺基,N-1-甲丙亞磺醯基-N-甲胺基,N-2-甲基丙亞磺醯基 -N-甲胺基及N-l,l-二甲基乙亞磺醯基-N-甲胺基,特別係 N·甲亞磺醯基-N-甲胺基; N-CpC^-烷亞醯基-N-乙胺基,如N-甲亞磺醯基-N-乙基 ,Ν-乙亞磺醯基-Ν·乙胺基,Ν-正-丙亞磺醯基-Ν-乙胺基, Ν-1-甲基乙亞磺醯基-Ν-乙胺基,Ν-正-丁亞磺醯基-Ν-乙胺 基,Ν-1-甲基-丙亞磺醯基-Ν-乙胺基,Ν-2-甲基丙舜磺醯 基-Ν-乙胺基及N-l,l-二甲基乙亞磺醢基-Ν-乙胺基,特別 係Ν-甲亞磺醯基-Ν_乙胺基; N-CrC4-烷磺醯基-Ν-甲胺基,如Ν-甲磺醯基-Ν-甲胺基, N-乙磺醯基-N-甲胺基,N-正-丙磺醯基-N-f胺基,N-1-甲 基-乙磺醯基-N-甲胺基,N-正-丁磺醢基-N-甲胺基,N-1-甲基丙磺醯基-N-甲胺基,N-2-甲基丙磺醯基-N-甲胺基及 Ν-1,1·二f基乙磺醯基-N_甲胺基,特別係N-T磧醯基-N-甲胺基; -23 - 本紙張尺度逋用中國國家榡準(CNS ) A4規格(2丨Ο X 297公釐) (請先閲讀背面之注意事項再填艿本頁) i
、1T 經濟部中央標準局員工消費合作社印製 A7 B7 _ 五、發明説明(21 ) N-CrC4-燒磺醯基-N-乙胺基,如N-甲磺醯基-N-乙胺基, N-乙磺醯基-N-乙胺基,N-正-丙磺醯基-N-乙胺基,N-卜甲 基乙磺醯基-N-乙胺基,N-正-丁磺醯基-N-乙胺基,N-1-甲 基丙磺醯基-N-乙胺基,N-2-曱基丙磺醯基-N-乙胺基及N-1,1-二甲基乙磺醯基-N-乙胺基,特別係N-甲磺醢基-N-乙 胺基;
CrC4-鹵烷硫基,如氣甲硫基,二氣甲硫基,三氣甲硫基 ,氟甲硫基,二氟甲硫基,三氟甲硫基,氣氟甲硫基,氣 二氟甲硫基,1-氟乙硫基,2-氟乙硫基,2,2-二氟乙硫基 ’ 2,2,2·二氣乙硫基,2 -氣-2,2-二氣乙硫基’ 2,2-二氣-2-氣 乙硫基,2,2,2-三氟乙硫基及五氟乙硫基,特別係三氟乙 硫基。 上述所定義之基團-(Y)n-CO-R8爲,例如,
Ci-C4-烷羰基,如甲羰基,乙羰基,正-丙羰基,1-甲基乙 羰基,正丁羰基,1-曱基丙羰基,2-甲基丙羰基及1,1-二 甲基乙羰基,特別係甲羰基;
Ci-C4-烷氧羰基,如甲氧羰基,乙氧羰基,正-丙氧羰基, 1-甲基乙氧羰基,正-丁氧羰基,1-甲基丙氧羰基,2_甲基 丙氧羰基及1,1 -二甲基乙氧羰基,特別係甲氧羰基; N-CrC4_烷胺f醯基,如N-甲胺甲醯基,N-乙胺曱醯基, N-正-丙胺甲醯基,N-1-甲基乙胺甲醯基,Ν·正-丁胺甲醯 基,Ν-1-甲基丙胺甲酿基,ν-2-甲基丙胺甲酿基及N-l,l-二甲基乙胺甲醯基,特別係Ν-甲胺甲醯基; 二-Ci-C4_烷胺甲醯基’如二甲胺甲醯基,二乙胺甲醯基, _______ _24_ 本紙張尺度適家鱗(CNS )A4規格(21f297公瘦) -- (請先閱讀背面之注意事項再填寫本萸)
經濟部中央標準局員工消費合作社印製 A7 ______!L___ 五、發明説明(22 ) ,二丙胺甲醯基,二丁胺甲醢基,N-甲基-N-乙胺甲酿基 ,N-甲基-N-丙胺甲醢基,N-甲基-N-1-甲基乙胺甲醢基, N-甲基-1,1-二甲基乙胺甲醯基,二-1-甲基-乙胺甲醯基, N-乙基-N-1-甲基乙胺甲醯基及N-乙基-N-M-二甲基乙胺甲 醯基,特別係二T胺T醮基; 烷羰基氧基,如甲羰基氧基,乙羰基氧基,正-丙羰 基氧基,1-甲基乙羰基氧基,正-丁羰基氧基,1-甲基丙羰 基氧基,2-甲基丙羰基氧基及1,1-二甲基乙羰基氧基,特 別係甲羰基氧基;
Crc4-烷羰基胺基,如甲羰基胺基,乙羰基胺基,正-丙羰 基胺基,1-甲基乙羰基胺基,正-丁羰基胺基,1-甲基丙 羰基胺基,2 -甲基丙羰基胺基及1,卜二甲基乙羰基胺基, 特別係甲羰基胺基; N-CrC4-烷羰基-N-甲胺基,如N-甲羰基-N-甲胺基,N-乙 羰基-N-甲胺基,正-丙羰基-N-甲胺基,N小甲基乙羰基-N-甲胺基,N-正-丁羰基-N-甲胺基,N-1-甲基丙羰棊-N-甲 胺基’ N-2-甲基丙羰基-N-甲胺基及N-l,l-二甲基乙羰基_N_ 甲胺基,特別係N-甲羰基-N-甲胺基。 Z爲,例如, 具有一至三個選自氧,硫及氮之雜原子之飽和或未飽和5_ 或6-員雜環自由基,例如五-員雜芳自由基如2_攻喃基,3_ 呋喃基,2-喳吩基,3-〇塞吩基,2-吡咯基,3-吡咯基,3-異 吟哇基,4-異啐唑基,5-異噚唑基,3-異嘍唑基,4_異嘍 »坐基’ 5-異魂座基’ 3-ρ比啼基,4-说嗅基,5-峨嗤基,2-今 -25 - 本紙張尺度適财ϋ®家轉(CNS ) A4im( 21GX297公瘦)' --- (請先閱讀背面之注意事項再填'*Γ本頁j 訂 _B7 五、發明说明(23 ) 唑基,4-崎咭基,5-哼吐基,2-嘍唑基,4-嘧唑基,5-«*墓唑 基,2-咪唑基,4_咪唑基,i,2,4·气二唑-3-基,l,2,4-p号二 唑-5-基,U,4-崎二唑·2_基,丨,2,3-呤二唑-4-基,1,2,3-吟 二唑-5-基,丨,2,5_呤二唑 _3·基,i,2,4-噬二唑-3_基,1,2,4-〇塞二唑 _5-基,i,3,4_p塞二唑·2·基,l,2,3-p塞二唑·4-基, 1,2,3-〇塞二唑 _5_基,L2,5·嘍二唑·3_ 基,1,2,4-三唑-3-基, 1,3,4-三唑-2_基,1,2,3_三唑_4-基,1,2,3-三唑-5-基,1,2,4- 三唑-5-基,四唑_5_基,特別係2^塞唑基及3-異嘮唑基; 六-員雜芳自由基如2·吡啶基,3-吡啶基,4-吡啶基,3-嗒 喑基,4-嗒畊基,2-嘧啶基,4-嘧啶基,5_嘧啶基,2_吡畊 基,1,3,5-三嗜-2-基,1,2,4-三畊-5-基及ι,2,4-三畊-3-基, 1,2,4-三 51 井-6-基 ’ 1,2,4,5-四 $-3-基; 具有一至三個氮原子及/或一至二個氧或硫原予之飽和或 部分未飽和5-至6-員雜環,如2·四氫呋喃基,3_四氫吱喃 基,2-四氫11塞吩基,3·四氫ρ墓吩基,四氫硫喊喃-2-基,四 氩硫旅喃-3-基,四氫硫3瓜喃-4-基,1,3-二氫二ρ墓%基, 1,3,-二氩二噻β-4·基,丨,3-二氫-塞吩-2-基,ΐ,3-二氫》塞吩-4-基,5,6-二氫-4Η-1,3-ρ塞 11 井-2-基,1,3-氧二 ρ塞、,成-2-基, 經濟部中央標準局貝工消費合作社印製 1,3-氧-塞吩-2-基,1-吡咯啶基,2-吡咯啶基,3_吡咯啶基 ,3-異崎唑淀基,4-異号唑淀基,5-異气唑淀基,3-異'•塞 嗅淀基’ 4-異》塞峻淀基’ 5-異I»塞峻咬基,3-f比嗅淀基,4-比座攻基,5-吨吐症基,2-·*号峻症基,4-,号咬淀基,5-<*号 峻咬基,塞吐咬基,4-f塞吐淀基,5-p塞咬咬基,2-咪咬 攻基,4-咪峻症基,1,2,4-,号二峻虎-3-基,i,2,4-pf二咬症 _ -26 - 本紙張又度適用中國國家梯準(CMS ) A4規格(21 Οχ 297公釐)~~ ~ 經濟部中央標準局員工消費合作杜印製 A7 B7 五、發明説明(24 ) -5-基,1,2,4-嘧二唑啶-3-基,1,2,4-嘧二唑啶-5-基,1,3,4-号二咬症-2-基,1,3,4->·塞二4症-2 -基,1,3,4 -三吐岐-2 -基 ,2,3-二氫呋喃-2-基,2,3-二氫呋喃-3-基,2,4-二氫呋喃-2-基,2,4-二氫呋喃-3-基,2,3-二氫嘧吩_2_基,2,3-二氩嘧 吩-3-基,2,4-二氮p塞吩-2-基,2,4-二氮p塞吩-3-基’ 2,3-々匕 略**林-2 -基^ 2,3 - p比略- 3 -基’ 2,4 - ?比哈11林-3 -基’ 2,4 - p比洛 啉-3-基,2,3-異嘮唑啉-3-基,3,4-異呤唑啉-3-基,4,5-異 °号也#-3-基,2,3-異今峻》林-4-基,3,4-異1^峻'林-4-基, 4,5-異嘮唑啉-4-基,2,3-異哼唑啉-5-基,3,4-異哼唑啉-5-基,4,5-異哼唑啉-5-基,2,3-異嘧唑啉-3-基,3,4-異嘧唑啉 -3-基,4,5-異噻哇啉-3-基,2,3·異嘍唑啉-4·基,3,4-異嚓 吐淋-4-基,4,5 -異ρ塞峻ρ林-4-基,2,3 -異《•塞峡'#-5-基,3,4- 零 異嘧唑啉-5-基,4,5-異-塞唑啉-5-基,2,3-二氫吡唑-1-基, 2.3- 二氫吡唑-2-基,2,3-二氫毗唑-3-基,2,3-二氫吡唑-4-基,2,3-二氫吡唑-5-基,3,4-二氫吡唑-1-基,3,4-二氩毗 峻-4-基,3,4-二氫ρ比峻-3-基,3,4-二氫ρ比峻-5-基,4,^-二氩 峨吐-1-基,4,5-二氫ρ比唑-3-基,4,5-二氫?比峻-4-基,4,5-二氫吡唑-5-基,2,3-二氫嘮唑-2-基,2,3-二氫呤唑_3_基, 2.3- 二氫 4 咬-4-基,2,3-二氩 4 峻-5-基,4,5-二氫 4 峻-2-基,4,5-二氫噚唑-4-基,4,5-二氫哼唑-5-基,1,3-二哼戊 烷-2-基,1,3-二哼戊烷-4-基,1,3-二哼戊烷-5-基,1,4-二 ρ号烷-2 -基,2 -六氫峨淀基,3 -六氫ρ比淀基,4 -六氫?比淀基 ,3-四氫嗒ρ井基,4-四氫嗒畊基,2-四氩嘧啶基,4_四氫 口密咬基,5 -四氫°密咬基,2 -四氫卩比*1井基’ l,3,5-四氣-三t^井- -27- 本^^Ziϊi_?ϊΐ¾iT^T^S^ΰϊ'ό^^F_i (請先閱讀背面之注意事項再填艿本頁)
如如46 A7 ________B7_ 五、發明説明(迅) 2-基及1,2,4-四氫三畊-3-基,特別係2-四氫呋喃基,1,3-二 哼戊烷-2-基及1,3-二呤戊烷-2-基, 且其爲未經取代或經上述齒素(特別係氟或氣),氰基,硝 基, 基團-COR8,例如上述之燒幾基,上述之烷氧叛基,上述 之N-烷胺甲醯基,或上述之二烷胺甲醯基; 上述之CrC4-烷基,
Crc4-画统基,如氣甲基,二氟甲基,二氣甲基,三氟甲 基,三氣甲基,氣二氟甲基,1-氟乙基,2-氟乙基,2,2-一乱乙基’ 1,1,2,2 -四氟乙基,2,2,2 -三氟乙基,2 -氣_ 1,1,2-三氟乙基及五氟乙基,九氟丁基, 1,1-雙三氟甲基-2,2,2-三氟乙基,較佳爲二氟甲基,三氟 甲基,三氣甲基及氣二氟甲基; c3 -c8 -環烷基,如環丙基,環丁基,環戊基,環己基,環 庚基,環辛基,特別係環丙基及環己基; 上述之crc4-烷氧基, 經濟部中央標準局員工消費合作社印製
CrCr鹵烷氧基,如氣甲氧基,二氣甲氧基,三氣甲氧基 ,氟甲氧基,二氟甲氧基,三氟甲氧基,氣二氟曱氧基, 二氣氟甲氧基,1-氟乙氧基,2-氟乙氧基,2,2-二氟乙氧 基’ 1,1,2,2 -四氟乙乳基,2,2,2 -三氟乙氧基,2 -氣-1,1,2 · 三氟乙氧基及五氟乙氧基,特別係C丨-C3 -鹵烷氧基,如 2,2,2-三氟乙氧基及2-氣-2,2-二氟乙氧基; 上述之CpCj-坑硫基, 上述之crc4-卣烷硫基, -28 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -- 五 發明説明( A7 B7 — -一'1-C4·炊胺基’如二甲胺基,二乙胺基,二丙胺基,二 丁胺基’ Ν'甲基-N•乙胺基,N-甲基-N-丙胺基,N-甲基-N- 1:甲基乙胺基,Nm!小二甲基乙胺基,二]甲基乙 :基N乙基-Ν'1·甲基乙胺基及N-乙基-N-1,卜二甲基乙胺 基; 經取代或未經取代之苯基; 或經於互變異構形式中亦爲録之氧基取代,如嗓吐琳-4’5-二嗣.2_ 基,3_氧.31^,2,4_ 二❹基或 2·氧 _2h 嚏唑基。 ’ ’ 苯幷稍合之5.或6_貞雜芳自由基,例如,爲苯并咬喃 ,,苯幷嗓吩基,命朵基,苯幷,号峻基,苯幷異号吐基, 笨H坐基、苯幷異㈣基,苯幷㈣基叫丨吐基, 1,2,3-苯幷P塞二唑基,213_苯幷嘍二嗤基,苯幷三唑基 ’笨幷$二二峻基’七林基,異如林基,4«,峻如林 基’ 4㈣基或0基。具通式!特別較佳之化合物列於 下表1申。 (請先閱讀背面之注意事項再填寫本頁) i 、广衣--
.. - I - II 裡濟部中央栳準局員工消費合作杜印製 -29- 本紙法尺度適用中國國家標準(CNS ) A4規格(210X297公釐)
S04946 A7 B7 五、發明説明(27 ) 表1 :具結構式Id之化合物 〇 Μ
經濟部中央標準局員工消費合作社印製 R3 No. R1 R2 R3 L M z 1.1 ch3 ch3 H so2ch3 Cl 2-p塞吩基 1.2 ch3 ch3 H so2ch3 Cl 3-n塞吩基 1.3 ch3 ch3 H so2ch3 Cl 2-吱喃基 1.4 ch3 ch3 H so2ch3 Cl 3 -咬喃基 1.5 ch3 ch3 H so2ch3 Cl 3-甲基-異哼唑-5-基 1.6 ch3 ch3 H so2ch3 Cl 5-嘍唑基 1.7 ch3 cii3 H so2ch3 Cl 1.8 ch3 ch3 H so2ch3 Cl 2-埭唑基 1.9 ch3 ch3 H so2ch3 Cl 3-甲基-異4唑-5-基 1.10 ch3 ch3 H so2ch3 Cl t異喳唑基 1.11 ch3 ch3 H so2ch3 Cl 5-苯基唼唑-2-基 1.12 ch3 gh3 H so2ch3 Cl 2-*»比淀基 1.13 ch3 CII3 H s〇2ch3 Cl 3 - 〃比淀基 1.14 ch3 ch3 H s〇2ch3 Cl 4 - 〃比淀基 1.15 ch3 cii3 H so2ch3 Cl 1-甲基-2-峨咯基 1.16 ch3 ch3 H so2ch3 Cl 1-甲基-1,2,4-三唑-5-基 1.17 ch3 ch3 H so2ch3 Cl 2-苯幷唼唑基 1.18 ch3 ch3 H S〇2〇H3 Cl 2 - 奎淋基 1.19 ch3 Cl-13 H so2ch3 Cl 2-喳啉基 _ 1.20 ch3 ch3 H so2ch3 Cl 1-甲基苯幷咪唑-2-基 1.21 ch3 cii3 H so2ch3 Cl 2-哼唑基 1.22 ch3 CH3 H so2ch3 Cl Ί-苯基吡哇-5-基 1.23 ch3 CII3 H so2ch3 Cl 1-甲基吡唑-3-基 1.24 ch3 ch3 H so2ch3 Cl Ί-甲篡》比唑-5^Έ 1.25 ch3 ch3 H so2ch3 Cl 1,3-二Τ基吡唑-3-基 1.26 ch3 ch3 H so2ch3 Cl 1-苯基吡唑-3-基 1.27 ch3 cii3 H s〇2ch3 Cl 1,4-二甲基》比吐-5-基 1.28 ch3 ch3 H so2ch3 Cl 5-11等哇基 1.29 ch3 ch3 H s〇2ch3 Cl 1,3-二甲墓吡唑-4-基 1.30 ch3 ch3 H s〇2ch3 Cl 1,5-二甲基吡唑-4-基 1.31 ch3 ch3 H S〇2〇H3 Cl 1-甲基吡唑-4-基 1.32 ch3 ch3 H so2ch3 Cl 1,3-二甲基吡唑-5-基 1.33 ch3 CIi3 H so2ch3 Cl 4-甲墓4咬-2-基 ---------(i衣-- (請先閱讀背面之注意事項再填寫本頁) -δ .Τ -30 - 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) 五、發明説明(28) Μ Β7 經濟部中央標準局員工消費合作社印裝
No. R1 R2 R3 L M z 1.34 ch3 ch3 H so2ch3 Cl 5-甲基硫》塞哇-2-基 1.35 ch3 ch3 H so2ch3 Cl 5-甲基硫》塞唑-2-基 1.36 ch3 ch3 H so2ch3 Cl 4-甲氧基-1-甲基吡唑-5-基 1.3 7 ch3 ch3 H so2ch3 Cl 3-環丙基異哼唑-5-基 1.38 ch3 ch3 H so2ch3 Cl 3-異丙基異哼唑-5-基 1.39 ch3 ch3 H so2ch3 Cl (3-甲基苯基)-"塞唑-2-基 1.40 ch3 ch3 H so2ch3 Cl 5-甲基《塞唑-2-基 1.41 ch3 ch3 H so2ch3 Cl 4-溴-2-4吩基 1.42 ch3 ch3 H so2ch3 Cl 5-甲基-2-»塞吩基 1.43 ch3 ch3 H so2ch3 Cl 4-甲基-2-»塞吩基 1.44 ch3 ch3 H so2ch3 Cl 4-甲基-塞唑-2-基 1.45 ch3 ch3 H so2ch3 Cl 4-氣》1:唑-2-基 1.46 ch3 CH-^ H s〇2ch3 Cl 4,5-二甲基嘍唑-2-基 - 1.47 ch3 ch3 H so2ch3 Cl 4-苯基嘍唑-2-基 1.48 ch3 ch3 H so2ch3 Cl 2-甲氧基嘍哇-5-基 1.49 ch3 ch3 H so2ch3 Cl 4-甲基-2-»比啶基 1.50 ch3 ch3 H so2ch3 Cl 6(2-甲氧基乙基)-2-吡啶基 1.51 ch3 ch3 H so2ch3 Cl 6-甲基硫基-2-说啶基 1.52 ch3 ch3 H so2ch3 Cl 6-甲氧基-3-吡啶基 1.53 ch3 QH3 H so2ch3 Cl 6-甲氧基-2-吡啶基 1.54 ch3 ch3 H so2ch3 Cl 6-甲基-2-吡啶基 1.55 ch3 ch3 H s〇2ch3 Cl 6-(2,2,2-三氟乙氧基)-2-毗 咬基 1.56 ch3 ch3 H so2ch3 Cl 6-(2,2,2-三氟乙氧基)-3-吡 淀基 1.57 ch3 ch3 H s〇2ch3 Cl 5-喊淀基 1.5 8 ch3 ch3 H so2ch3 Cl 6-二甲胺基-3-吡啶基 1.59 ch3 ch3 H so2ch3 Cl 1,2,4-嗖二唑-5-基 1.60 ch3 ch3 H so2ch3 Cl 3-乙氧羰基-1-甲基吡唑-5-基 1.61 CH^ ch3 H so2ch3 Cl 2 -甲硫基喊症-5 -基 1.62 ch3 ch3 H so2ch3 Cl 2 -痛淀基 1.63 ch3 ch3 H so2ch3 Cl 2-甲硫基嘧啶-4-基 1.64 ch3 ch3 H so2ch3 Cl 5-甲硫基-1,3,4-埭二唑-2-基 1.65 ch3 CI13 H so2ch3 Cl 5-甲氧基-1,3,4-4二唑-2-基 1.66 ci-i3 C1I3 H so2ch3 Cl 4,5-二羥基-塞唑-2-基 1.67 ch3 ch3 H so2ch3 Cl 5-甲基崎唑-2-基 1.68 ch3 ch3 H so2ch3 Cl 5-笨基呤唑-2-基 1.69 ch3 CH3 H so2ch3 Cl 2-甲基哼唑-5-基 1.70 ch3 ch3 H so2ch3 Cl 2-笨基哼唑-5-基 1.71 ch3 ch3 H 4 s〇2ch3 Cl 2-甲基-1,3,4-哼二唑-3-基 -31 - 本紙張尺度逋用中國國家標準(CMS ) Α4規格(210 X 297公釐) (請先閱讀背面之注意事項再填窍本頁) 袈. 訂
B 五、發明説明(29) 經濟部中央標準局員工消費合作社印製
No. R1 R2 R3 L M z 1.72 ch3 ch3 H s〇2ch3 Cl 5-甲基-1,2,4-哼二唑-5-基 1.73 ch3 ch3 H so2ch3 Cl 2-苯基-1,3,4-崎二唑-5-基 1.74 ch3 CIi3 H so2ch3 Cl 5-三氣甲基-1,2,4-崎二吐-3-基 1.75 ch3 ch3 H so2ch3 Cl 5-f^],2,4--咢二唑-3-墓~ 1.76 ch3 ch3 H so2ch3 Cl 5-苯基-1,2,4-哼唑-3-基 1.77 ch3 ch3 H so2ch3 Cl 5-苯基-異噚唑-3-基 1.78 ch3 CH3 H so2ch3 Cl 1-(4-氣苯基)-1,2,4-三唑-2-基 1.79 CHj ch3 H so2ch3 Cl 5-氰基-4,5-二氩-異哼唑-3-篡 1.80 ch3 ch3 H so2ch3 Cl 5,6-二氫-4H-1,3-嘍畊-2-基 1.81 ch3 ch3 H so2ch3 Cl 1,3-二氫"塞喊-2-基 1.82 ch3 ch3 H so2ch3 Cl 1,3-二哼戍烷-2-基 1.S3 ch3 ch3 H s〇2ch3 Cl 1,3-二氫》塞吩-2-基 1.84 ch3 ch3 H so2ch3 Cl 1,3-二呤烷-2-基 1.85 ch3 ch3 H so2ch3 Cl 1,3-氧二氫-塞戊-2-基 1.86 ch3 ch3 H so2ch3 Cl 1,2,4-三呔-1-基 1.87 ch3 ch3 H so2ch3 Cl 3- f 基-1,2,4-嘧二唑-5-基 1.88 ch3 ch3 H so2ch3 Cl 1,2,4-了塞二哇-5-墓 1.89 ch3 ch3 H so2ch3 Cl »墓唑啶-4,5-二酮-2-基 1.90 ch3 ch3 H so2ch3 Cl 3-氧-3-H-],2,4-二嘍唑-5-基 1.91 ch3 c,h3 H so2ch3 Cl 2-氧-2-Η-1,3,4-二嗒唑-5-基 1.92 ch3 H H so2ch3 Cl 3-»塞吩基 1.93 ch3 H H so2ch3 Cl 2-唆喃基 1.94 ch3 H H so2ch3 Cl 3-呋喃基 1.95 ch3 H H so2ch3 Cl 3-甲基異哼唑-5-基 1.96 CH3 H H so2ch3 Cl 5-嘧哇基 1.97 ch3 H H s〇2ch3 Cl 4--塞唑基 1.98 ch3 H H so2ch3 Cl : 1.99 ch3 H H so2ch3 c] 3-異哼唑基 1.100 ch3 H H so2ch3 Cl 2 - p比症基 1.101 ch3 H H so2ch3 Cl 3 - p比咬基 1.102 ch3 H H so2ch3 Cl 4-吡啶基 1.103 ch3 H H so2ch3 Cl 2-苯幷嘍吐基 1.104 ch3 H H so2ch3 Cl 2-»奎啉基 1.105 ch3 H H so2ch3 Cl 4-甲基哼唑-2-基 1.106 ch3 H H so2ch3 Cl 5-嘧咬基 1.107 c2h5 H H so2ch3 Cl 3-»裳喻基 1.108 c2h5 H H so2ch3 Cl 2-峡喃基 1.109 c2h5 H H so2ch3 Cl 3-吱喃基 1.110 c2h5 H H s〇2ch3 Cl 3-甲基異哼唑-5-基 (請先閱讀背面之注意事項再填寫本頁) .1:衣. 訂 -32 - 本紙張尺度適用中國.國家標準(CNS ) A4規格(210X 297公釐) 6 4 4 •VU 3 五、發明説明(3(3) 經濟部中央標準局®:工消費合作杜印製
No. R1 R2 RJ L M z 1.111 C2H5 H H so2ch3 Cl 5-»塞唑基 1.112 C2H5 H H so2ch3 Cl 4--塞唑基—. 1.113 C2H5 H H so2ch3 Cl 2--塞唑基 1.114 C2H5 H H so2ch3 Cl 3-異呤唑基 1.115 C2H5 H H so2ch3 Cl 2-吡啶基 1.116 C2H5 H H so2ch3 Cl 3 - »比 1.117 C2H5 H H so2ch3 Cl 4 - p比淀基 1.118 C2H5 H H S〇2〇H3 Cl 2-苯幷嘍唑基 1.119 C2H5 H H so2ch3 Cl 2-4琳基 1.120 c2h5 H H s〇2ch3 Cl 4-甲基崎唑-2-基 1.121 C2H5 H H so2ch3 Cl 5 - p密成基 1.122 c2h5 H H so2ch3 Cl 3-崦吩基 1.123 c2h5 H H so2ch3 Cl 2 -咬喃基 1.124 C2H5 H H so2ch3 a 3-»夫喃基 1.125 c2h5 H H so2ch3 Cl 3-甲基異哼吐-5-基 1.126 C2H5 H H so2ch3 Cl 5-»i哇基 1.127 C0H5 H H so2ch3 Cl 4-違哇基 1.128 C2H5 H H so2ch3 Cl 2 -違吐基 1.129 c2h5 H H so2ch3 Cl 3-異崎唑基 1.130 c2h5 H H so2ch3 Cl 2-0比淀墓 1.131 C2H5 H H so2ch3 Cl 3 - p比症基 1.132 C2H5 H H so2ch3 Cl 4-p比症基 1.133 C2H5 H H so2ch3 Cl 2-笨并嘍唑基 1.134 c2hs H H so2ch3 Me 2-ϊ*奎。沐基 1.135 H H so2ch3 Me 4-甲基崎唑-2-基 1.136 c2h5 ch3 H so2ch3 Me 5 -續淀基 1.137 ch3 ch3 H so2ch3 Me 3-嘍吩基 1.138 ch3 ch3 H s〇2ch3 Me 2-吱喃基 1.139 ch3 ch3 H so2ch3 Me 3 -咬喃基 1.140 ch3 ch3 H s〇2ch3 Me 3-甲基異哼哇-5-基 1.141 ch3 CH3 H so2ch3 Me 5-嘍唑基 1.142 ch3 ch3 H so2ch3 Me 4-碟唑基 1.143 ch3 C1I3 H so2ch3 Me 2-喵唑基 1.144 ch3 CH3 H S00CH3 Me 3-異噚唑基 1.145 ch3 ch3 H so2ch3 Me 2-吡啶基 1.146 ch3 ch3 H so2ch3 Me 3 - nb淀基 1.147 ch3 ch3 H SO0CH3 Me 4-吡啶基 1.148 ch3 ch3 H S02CH3 Me 2-笨幷嶁唑基 1.149 ch3 ch3 H so2ch3 ch3 2-口奎口沐基 1.150 ch3 ch3 H so2ch3 ch3 4-甲基哼吱-2-基 1.151 c.h3 ch3 H so2ch3 ch3 5 -[途咱:基 -33- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐〉 (請先間讀背面之注意事項再"寫本頁) " 、-0 五、發明説明(31 ) A7 B7 經濟部中央標準局員工消費合作社印製
No. R1 R2 R3 L M z 1.152 gh3 gh3 P-CH3 -c6h4 -S〇2 s〇2ch3 ch3 5-*塞吩基 1.153 gh3 ch3 P-CH3 -c6h4 -S〇2 so2ch3 gh3 2-呋喃基 1.154 ch3 p-ch3 °όΗ4 -S〇2 so2ch3 3-呋喃基 1.155 CH3 ch3 p-CH3 -c6H4 -S 〇 2 so2ch3 ch3 3-甲基異呤吱-5-基 1.156 gh3 ch3 p-ch3 -c6h4 -S〇2 so2ch3 ch3 5-嘆唑基 1.157 ch3 ch3 P-CH3 •C6H4 -so9 so2ch3 ch3 4-»塞哇基 1.158 ch3 ch3 P-CH3 -c6h4 -S02 i>U2CH3 ⑶3 2-嘆唑基 1.159 ch3 ^3~ p-ch3 -c6h4 -S〇2 so2ch3 ch3 3-具吟唑基 1.160 Ci-13 gh3 % P-CH3 -c6h4 -S 〇 2 so2ch3 CH3 2 - p比症基 1.161 ⑶3 ⑶3 p-ch3 -c6h4 -S〇2 so2ch3 ch3 3-吡啶基 1.162 ch3 ch3 P-CH3 -C6H,4 -S 〇 7 so2ch3 ch3 4 -峨淀基 1.163 uh3 "CTT^~ P-CH3~ •C6H4 -S〇2 su2ch3 ch3 2-笨幷》塞哇基 1.164 ch3 P-CH3 -c6h4 -SOo su2cjh3 ch3 2-嗤啉基 1.165 uh3 uh3 P-^H3 -c0h4 -S〇2 s〇2ch3 ch3 4-甲*呀唑-2-丞 1.166 ch3 ΤΓΗ3— p-c;h3 -c6h4 -S02 S02CH3 THTy 5-喷淀基 1.167 ch3 cf3 H S〇2CH3 Cl 2 - 塞吩基 1.168 ch3 cf3 H s〇2ch3 Cl 3 - *»塞吩基 1.169 ch3 cf3 H so2ch3 Cl 2 ·峡哧基 1.170 ch3 cf3 H so2ch3 Cl 3-峡嘀基 1.171 ch3 H so2ch3 Cl 3-甲基異吒呔-5-基 1.172 ch3 cf3 H so2ch3 Cl 5-喳哇基 -34- 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X 297公釐) ---------^-- (請先閱讀背面之注意事項再^寫本頁) 訂 Λνρ A7 B7 五、發明説明(32 )
No. R1 R2 R3 L — M z ~ 1.1 73 ch3 CF 3 H SO?.CH^ Cl 4--袁唑基 --- 1.174 ch3 cf3 H so2ch3 Cl 2-嘎唑基 1.175 ch3 H S〇2CH3· — Cl 1.176 ch3 CF 3 H so2ch3 Cl 3-異〃号咬基 ~~ 1.177 ch3 cf3 H so2ch3 Cl 5 -苯基p塞岐-2-在 1.178 ch3 cf3 H S"〇2CHr Cl 2-吡啶基 -— 1.179 ch3 cf3 H so2ch^~ Cl 3-吡啶基 — 1.180 ch3 cf3 H so2ch3 — rcl 4 - 比咬基 1.181 ch3 cf3 H so2ch3 Cl 曱基-2-吡咯基 1.182 ch3 cf3 μΗ nS09CH^ Cl 卜甲墓-1,2,4-三唑 1. 183 CH^ cf3 H so〇chV Cl 2 -未并I*本吐▲ 1.184 ch3 cf3 H SO2CH3 Cl 2-4淋基 1.185 ch3 Cl·. 3 H so2ch3 Cl 2-·1奎>林基 "" 1.18ο ch3 cf3 H so2ch3 Cl 1-甲基苯幷咪嗖-2-基-- 1.187 CH3 CF3 H so2ch3 Cl 2-吁唑基 1.188 ch3 CF3 H so2ch3 Cl 5-»号唑基 (諳先閲請背面之注意事項再填寫本頁) 袈. 經濟部中央標準局員工消費合作社印製 化合物I及其养業上可使用鹽類適合作爲除草劑,二者 皆以異構物混合物及純異構物之形式存在◊包含I之除萆 組合物在未開發土地上控制植物非常有效,特別係於高施 用率下。其作用對抗作物中’如小麥,稻米,玉米,大豆 及棉花中之濶葉雜草與禾木雜草,且不明顯損害作物植物 。此功效於低施用率下尤其顯著。 斟酌施用方法之多樣性,化合物I或包含彼等之组合物 可另使用於許多其他作物中,以消除不希望之植物。適宜 作物之實例如下: 玉E,鳳梨,落花生,石刀柏,甜菜,砂糖菜菔’芥菜 ,蕓苔’九茱蔓菁’山茶’紅花,山核桃,檸檬,柑橘, 咖(Coffea Caneph〇ra,c〇ffea liberica),胡瓜,行儀芝, 胡蘿蔔,油掠,白花蛇莓,黃大豆,草绵(G〇ssypiUm -35 - .訂· 本紙乐尺度適财_家縣(CNS) M規格(21QX297公疫 經濟部中央標準局員工消費合作杜印製 A7 B7 五、發明説明(33 ) arboreum,G_ herbaceum,G. vitifolium),向日葵,巴西護 謨樹’大麥,忍布,甘藉,胡挑,兵豆,亞麻,紅茄’蘋 果屬’木薯,紫直稽,连藏屬,煙草(Nicotianarustica), 阿列布’稻米,菜豆,針樅,松樹,醋栗,蓖麻,甘蔗, 黑麥’馬鈐薯’高梁(s. vulgare),可可樹,紅和蘭翹搖, 小麥,Triticum durum,蠶豆,葡萄,玉蜀黍。 此外,化合物I亦可用於已藉育種之方式(包括使用遺傳 工程方法)使其對除草劑作用具耐受性之作物。 除草組合物或活性成份可於緊急情況前或緊急情況後施 用。若活性成份較不被特定作物植物忍受,則可使用其中 除草组合物係經噴霧之施用技術(藉助於喷霧設備),以使 其儘可能於活1成份達不希望植物(其生長於下方)之葉, 或裸露之土壤表面(珞標’停車場空地)時少與過敏性作物 植物之葉接觸。 化合物I或包含彼等之除草組合物可(例如)以立即可喷霧 水溶液,粉末,懸浮液,及高濃縮水性,油性或其他懸浮 液或分散液’乳液,油分散液,膏劑,撒粉,撒佈物質或 顆粒藉噴霧,噴灑,撒粉,撒佈或灌澆之方式使用。使用 形式依所欲達之目的而定;任何情況下,應確保根據本發 明之活性成份達最佳可能之分佈。 適宜之惰性添加劑爲礦物油(具中至高沸點之)餾份,如 煤油或柴油,其他爲煤洛油及植物或動物來源之油類,脂 族,環族及芳族烴類,例如石蠟,四氫莕,烷基化茶或其 衍生物’炊基化笨或其折生物’甲醇,乙醇,丙醇,丁醢 _ - 36- 本紙張又&用中國國家標準(CNS ) A4規格(210x177^ (請先閱讀背面之注意事項再續寫本頁) 訂 A7 發明説明( ,環己醇,環己酮或強極性溶劑如N_甲基吡咯啶酮或水。 水性使用形式可藉添加水而從乳液濃縮物,懸浮液,膏 劑,可濕性粉末或水-可分散顆粒製備得。爲製備乳液, 青劑或油分散液,可使用濕化劑,膠黏劑,分散劑或乳化 劑將物質(本身或已溶於油或溶劑中)均質化於水中。另外 ’可製備得由活性物質,濕化劑,膠黏劑,分散劑及可能 地溶劑或油組成之濃縮物,且此等濃縮物適合以水稀釋。 k宜之界面活性物質(佐劑)爲芳績酸之檢金屬鹽類,驗 土金屬鹽類或胺鹽,如木質_,紛·,茶_及二丁基苯績酸 疋鹽,及脂㈣之鹼金屬鹽,驗土金屬鹽❹鹽,坑靖酸 鹽及炊基芳橫酸鹽’坑基’月桂基謎與脂肪酵硫酸醋,及 硫酸化十六-十,七與十八醇及脂肪醇乙二醇鍵之鹽類,磺 奴化茶及其衍生物與之縮合產物,I或料酸與盼及 甲膝之縮合產物,聚氧乙料基_,乙氧基化之異辛基 ,辛基或壬基酚,烷苯基聚乙二蜉醚,三丁 醇醚,烷芳基聚醚醇類,異十二醇^ · 一 井丁 —蜉脂肪醇/環氧乙烷縮 :物’乙氧基化之萬麻油,聚氧乙缔坡基醇或聚氧丙晞烷 基瞇’月桂醇聚乙二鮮醚乙酸醋’山梨醇 硫酸鹽廢液或甲基纖維素。 木質素亞 粉末,撒体物質與撒粉可藉將活性物質 載 混合或研磨而製備得。 极戰隨/、π ,顆粒,如包被顆粒,浸潰顆粒與均質顆粒,可藉使 风份與固體載體結合而製備得。固體栽體爲礦物: 石,砂石凝膠’秒酸鹽,滑石,高嶺土,石灰石,石灰, _____ -37- 本纸張尺度適财關家縣(CNS ) Α4^ 请 先 閱 背 面 之 注 意 事 項 填 本 η 裝 訂 經濟部中央樣準局舅工消費合作社印裝 A7 B7 起濟部中央標準局員工消费合作社印製 五、發明説明() 白要’膠塊黏土,黃土,黏土,白雲石,矽藻土,硫酸鈣 ,硫酸鎂,氧化鎂,經研磨之聚合物,肥料如硫酸銨,磷 酸銨,硝酸銨與尿素,植物產物如穀類碎粉,經研磨之樹 皮’木屑與經研磨之椰殼,纖維素粉末或其他固體載體。 活性成份I於立即使用製劑中之濃度可於廣泛範圍内變化 。通常,該等調配物包含0 00i至98%(以重量計),較佳爲 0_01至95%(以重量計)之活性成份。活性成份係以9〇%至 100%(較佳爲95%至1〇〇〇/0)(NMR光譜)之純度使用。 根據本發明之化合物I可例如依如下調配: I將20份(以重量計)化合物No. 1.28溶於由80份(以重量 计)烷基化苯’ 10份(以重量計)8至1〇莫耳環氧乙烷與1 莫耳油酸N-,單乙醇醯胺得之加成產物,3份(以重量計 )40莫耳?衣乳乙燒與1莫耳蓖麻油得之加成產物组成之 混合物中。將溶液倒入1〇〇,〇〇〇份(以重量計)水中,並 使其充份均勻分佈於其中而得包含〇 〇2%(以重量計)活 性成份之水性分散液。 Π將20份(以重量計)化合物No丨28溶於由40份(以重量 計)環己酮,30份(以重量計)異丁醇,20份(以重量計)7 莫耳環氧乙烷與1莫耳辛基酚之加成產物及1〇份(以重 量計)4〇莫耳環氧乙烷與1莫耳蓖麻油得之加成產物组 成之處合物中。將溶液倒入100,000份(以重量計)水中 ’並使其充份均勻分佈於其中,而得包含〇 〇2%(以重 量計)活性成份之水性分散液。 III將20份(以重量計)活性成份N〇 i 28溶於由25份(以重 一.裝— (讀先閱讀背面之注意事項再填寫本頁) *-°
本紙張尺度顧巾_家標rG X 297公釐 A7 _____B7 五、發明説明--- 量計)環己酮,65份(以重量計)沸點爲i 28〇至28〇乇之 礦物油餾份及1〇份(以重量計)4〇莫耳環氧乙烷與1〇英 耳蓖麻油之加成產物組成之混合物中。將溶 ΜΟ,ΟΟΟ份(以重量計)水中,並使其充份均勾分佈於其 中,而得包含0.02%(以重量計)活性成份之水性分散液 〇 IV將20份(以重量計)活性成份\0丨28充份與3份(以重量 計)二異丁基莕-α-磺酸之鈉鹽,17份(以重量計)由亞 硫酸廢液得之木質磺酸鈉鹽及60份(以重量計)粉狀矽 石凝膠充份混合,並將混合物置於鍤碎機中研磨。將 混合物均勻分佈於20,〇〇〇份(以重量計)水中,而得包 含0.1%(以亨量計)活性成份之喷霧混合物。 \將3伤(以重量叶)活性成份No. 1.28與97份(以重量計) 細分之高嶺土混合。此得到包含3〇/。(以重量計)活性成 份之撒粉。 VI將20份(以重量計)活性成份N〇. 1.28緊密地與2价(以重 量计)十二基苯確酸舞鹽,8份(以重量計)脂防醇聚乙 二醇謎’ 2份(以重量計)酚/尿素/甲醛縮合物之鈉鹽及 68份(以重量計)石蠟礦物油混合。此得到安定之油性 分散液。 VII將1份(以重量計)化合物ν〇· 1_28溶於由70份(以重量計) 環己酮’ 20份(以重量計)乙氧基化異辛基酚及丨〇份(以 重量計)乙氧基化蓖麻油組成之混合物中。此得到安定 之乳液濃縮物。 -39- 本紙張又度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本页) -so 經濟部中央標準局負工消費合作社印裝 A7 B7 經濟部中央標準局員工消費合作社印製 五、發明説明(37 ) νΠΙ將1份(以重量計)化合物No. 1.28溶於由80份(以重量計) 環己明及20份(以重量計)蓖麻油/環氧乙烷縮合物 (Emulphor EL.)组成之混合物中。此得到安定之乳液濃 縮物。 爲拓寬作用範圍及達到相乘功效,吡唑苯甲醯基衍生物 I可與多數代表性其他組具除草或植物生長調節活性成分 混合,且该混合物可共同施用。適於混合物之組成實例爲 一 u井類’ 4 Η - 3,1 -笨幷〃号f井衍生物,苯幷邊二喷酮,2,6 _二 碑基苯胺,N-苯基胺甲酸酯,硫胺甲酸酯,鹵羧酸,尿。密 啶,苯幷呋喃衍生物,於2_位置上接有例如羧基或胺甲醯 亞胺基之環己-1,3 ·二酮衍生物,《奎琳羧酸衍生物,咪嗤淋 酮,確酿胺類,,磺醯脲類,芳氧基-與雜芳氧基苯氧丙酸 及其鹽類,酯類與醯胺類,以及其他。 此外,亦可有利地以與甚至多種作物保護組合物,例如 與控制害蟲或植物病原性眞菌或細菌之組合物所成之混合 物形式施用化合物1(獨自或與其他除草劑組合)^亦有興 趣者在於可與用以中和營養及痕量元素缺乏症之無機鹽溶 液之互混性。亦可能添加無植物毒性之油及油滚縮物。 活性成份之施用率爲0.001至30(較佳爲〇〇1至1〇)公斤/ 公故活性成份(a.i·),視所欲達之目的,季節,標的植物及 生長階段而定。 用途實施例 式I成峻苯甲酿基衍生物之除草作用係以溫室實驗證明 -40 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁) 裝 A7 -. ' . B*7 五、發明説明(38 ) 所使用之培養容器爲含有具約3 〇%腐植土作爲受質之壤 土砂之塑膠花盆。測試植物分別依各種類播種。 對於緊急情況前處理,將懸浮於或乳化於水中之活性成 知,直接於播種後使用細密分体喷嘴施用。溫和地將容器 灌溉以促進萌芽及生長,並接著以透明塑膠籠覆蓋直到植 物生長開始。此以籠覆蓋使測試植物均一萌芽,除非此受 到活性成份希望地影響。 對於緊急情況後處理,首先使測試植物生長到3至丨5公 分之高度,視其生長形式而定,然後僅以已懸浮於或乳化 承水中之活性成份處理。測試植物係直接播種且生長於相 同容器中,或其係分開育菌並於處理前幾天再移植到實驗 容器中。 % 視種類而定,將植物保持於10_25。〇或2〇_35。(:下。測試 期爲2至4週。此期間,照護植物,並評估其對個別處理之 反應。 評估係使用0至100分進行^ 100意指無植物之緊急情況 發生或至少於空氣中之部份完全毁滅,而0意指盔^金, 或正常生長。 " (請先閱讀背面之注意事項再填寫本頁) 裝. 訂
經濟部中央標準局員工消资合作社印II 浪 纸 準 一標 家 國 國 中 用 適 規 釐 公 3υ494β A7 B7 五、發明説明 表2 -當於溫室中緊急情況後使用時之除草活性
實施例編號 1.28 施用率 (a. i·/公故之公斤數) 0.125 0.0625 測試植物 受損害% ZEAMX ‘ 10 0 CHEAL 95 95 SINAL 90 90 表3 -當於溫室中緊急情況後使用時之除草活性 4-水-- ( (請先閱讀背面之注意事項再填窍本頁)
,1T C1 0
經濟部中央標準局員工消費合作杜印製
A 實施例編號 1.98 施用丰 (a.i./公故之公斤數) 0.125 0.0625 測試植物 受損害% ZEAMX 15 10 ECHCG 100 100 SETFA 98 90 CHEAL 98 98 SINAL 100 95 -42- 本紙張尺度適用中國國家標準(CNS ) Α4規格(210 X 297公釐) 經濟部中央梯準局員工消費合作.杜印繁 A7 _______ B7_ 五、發明説明(40 ) 製備實施例 A)起始物之製備 I 2-氣-3-甲醯基-4-甲磺醯基苯甲酸甲酯 a. 於286克(2.14莫耳)三氣化鋁存於420毫升1,2-二氣乙 烷之懸浮液中,逐滴於15-20°C下加入157克(2莫耳) 乙酿氣溶於420毫升1,2 -二氣乙燒之溶液。接著將 3 46克(2莫耳)2-氣-6-甲基硫甲苯溶於1升i,2-二氣乙 烷之溶液逐滴加入。連續攪拌1 2小時,並將反應混 合物倒入含3升冰與1升濃HC1之混合物中。使用二氣 甲烷萃取混合物,並將有機相以水萃洗,使用硫酸 鈉乾燥並濃縮。將殘餘物於眞空中蒸餾。 此得到25,6克(60%理論値)2-氣-3-甲基-4-甲硫基乙醯 苯酮,m.p. : 46°C b. 將163克(0.76莫耳)2-氣-3 -甲基-4-甲破基乙醯苯網溶 於1·5升冰醋酸中’將18.6克鎢酸鈉加入,再伴隨冷 卻將173.3克30%強度之過氧化氳溶液逐滴加八。持 續樓掉2天並將混合物接著以水稀釋。將已沉殿之固 體以抽氣濾出,以水沖洗並乾燥。 此得到164克(88%理論値)之2-氣-3-甲基-4-甲磺醯基 乙酿苯酮,m.p. : liO-iiiX;。 C.將82克(0.33莫耳)2-氣-3-T基-4-甲讀酿基乙酿苯_ 溶於700毫升二呤烷中,並於室溫下以1升12 5%強度 之次氣酸鈉溶液處理《接著於8〇 t:下持續攪拌1小時 。待冷卻後’形成二相,其♦將下層相以水稀釋並 -43- 本紙張尺度適用中國國家標準(CNS ) A4規格(21 Ox297公缝) (請先閱讀背面之注意事項再填寫本頁) 装. 訂
.. - 1 -I I- I 經濟部中央標準局員工消費合作杜印製 A7 B7 五、發明説明(41 ) 使之成爲弱酸。將已沉澱之固體以水沖洗並乾燥。 此得到60克(73%理論値)之2-氣-3-甲基-4-甲磺醢基 苯甲酸,m.p. : 230-231°C。 d. 將1〇〇克(〇.4莫耳)2-氣-3-甲基-4-甲磺醯基苯甲酸溶 於1升甲醇中,並於迴流溫度下將HC1通入5小時。接 著將混合物濃縮。 此得到88.5克(84%理論値)2-氣-3-甲基-4-甲磺醯基苯 甲酸甲酯,m.p. : 107-108°C。 e. 將82克(0.31莫耳)2-氣-3-甲基-4-甲磺酿基苯甲酸甲 酯溶於2升四氣甲烷中,並以56克(0.31莫耳)N-溴琥 珀醯亞胺(每次少量)伴隨曝光處理。將反應混合物 過濾,將濾液濃縮並將殘餘物吸收於200毫升甲基第 % 三-丁基醚令。將此溶液以石油醚處理,並將已沉澱 之固體以抽氣濾出且乾燥。 此得74.5克(70%理論値)3-溴甲基-2·氣-4-甲磺醯基苯 甲酸甲酿,m.p. : 74-75°C。 f. 將41克(0.12莫耳)3-溴甲基-2-氣-4-f磺醯基苯甲酸 甲酯溶於250毫升乙腈之溶液以42.1克(0.36莫耳)N-甲基嗎福啉N-氧化物處理。將此批於室溫下持續攪 拌12小時,接著濃縮,並將殘餘物吸收於乙酸乙酯 中。溶液以水萃取,乾燥(使用硫酸鈉)並濃縮。 此得到31.2克(94%理論値)2-氣-3-甲醯基-4-甲磺醯基 苯甲酸甲酯,m.p. : 98-105°C。 2. 2-氱-4-甲磺醯基-3-(三氟甲磺醢基)氧基苯甲酸甲酯 -44 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公董) (請先閱讀背面之注意事項再填寫本頁) 丨東· 、\έ 經濟部中央標準局員工消費合作社印製 A7 ___—_ B7 五、發明説明(42 ) a. 將1〇1克(0.41莫耳)2-氣-3-羥基-4-甲磺醯基苯甲酸溶 於1.3升甲醇中,並於迴流下將HC1氣體通入4小時。 將溶液濃縮’並將殘餘物吸收於二氣〒坑中,且使 用K2 C〇3溶液萃取。將水相使用稀鹽酸調整到pH 7 ,並以二氣甲烷萃洗。然後將混合物酸化至pH 1並 使用二氣甲烷萃取產物。 此得到76.2克(7 1%理論値)2-氣-3-羥基-4-甲磺醯基苯 甲酸甲酯》 b. 將76克(0.29莫耳)2-氣-3-¾基-4-甲續醯基笨甲酸甲 酯與68克吡啶溶於700毫升二氣甲烷之溶液,於-20 °C下以89克(0.32莫耳)三氟甲磺酸酐處理。於室溫下 將該溶液持續攪拌12小時,再將溶液以二氣甲烷稀 % 釋並用水萃取。將有機相通過硫酸鎂乾燥並濃縮。 此得到94克(820/。理論値)2-氣-4-甲磺醯基-3-(三氟甲 磺醯基)氧基苯甲酸甲酯,m.p. : 69°C。 B)中間物之製備 1. 3-(3-異丙基異,号唑-5-基)-4-甲磺醯基苯甲酸甲酯 a.將存於200毫升二乙胺中之30克(102毫莫耳)3-溴-4-甲磺醯基苯甲酸甲酯,90毫克二氣化鈀與240毫克三 苯基膦以及60毫升二甲基甲醯胺,以10克(102毫莫 耳)(三甲基矽烷基)乙炔及18〇毫克碘化銅(I)處理, 並將混合物於40°C下攪拌4.5小時。然後再於室溫下 持續攪拌12小時。將反應混合物過濾,將濾液濃縮 並將殘餘物通過使用甲苯爲溶析劑之矽石凝膠進行 (請先閱讀背面之注意事項再填寫本頁) .丨.4衣· 、11 -45-
經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(43 ) 層析® 此得到17.3克(55%理論値)4-甲績醯基-3_(三甲基矽 烷基)乙炔基苯甲酸甲酯,呈油。 b. 將25克4-甲磺醯基-3-(三甲基矽烷基)乙炔基苯甲酸 甲酯共同與100毫升甲醇及0.9克碳酸鉀於室溫下攪 拌18小時。接著將固體以抽氣濾除,並將濾液滚縮 且使用乙酸乙酯/水萃取。有機相通過硫酸鎂乾燥並 濃縮》 此得到15克(79%理論値)4-甲磺醯基-3-乙炔基笨甲酸 甲醋,m.p. : 95-98°C 〇 c. 將13.5克(57毫莫耳)4-甲基磺醯基-3-乙炔基苯甲酸甲 酯溶於50,毫升二氣甲烷中,將5.2克(60毫莫耳)異丁 醛肟加入,再將41克12.5%強度之次氣酸鈉溶液加入 。接著將混合物於室溫下持續攪拌24小時。接著將 反應批份用二氣甲烷/水萃取,將有機相濃縮,並將 殘餘物通過使用甲苯/乙酸乙酯爲溶析劑之矽;凝膠 進行層析。 此得到8_8克(48%理論値)3-(3-異丙基異哼唑-5-基)-4-甲磺醯基苯甲酸甲酯,m.p. : 102-104°C。 2. 2-氣-3-(異哼唑-3-基)-4-甲磺醯基笨甲酸曱酯 a.將15克(54毫莫耳)2-氣-3-甲醯基-4-甲磺酿基苯甲酸 甲酯(Ex. A.I.)及4.2克(60毫莫耳)氫氣化胲與300毫 升甲醇共攪拌,並將3.18克(30毫莫耳)碳酸鈉溶於80 毫升水之溶液逐滴加入。將反應混合物於室溫下攪 46- 各紙張尺度通用中國國家標皁(CNS ) A4規格(210x 297公釐 (請先閱讀背面之注意事項再填寫本頁)
五、發明説明 44 A7 B7 經濟部中央標準局貝工消費合作社印製 拌過夜,接著將甲醇蒸餾去除,並使用乙醚/水萃取 。將醚相使用硫酸鈉乾燥並濃縮。 此得到14.4克(91 %理論値)2-氣-3-羥亞胺基甲基-4-甲 磺醯基苯甲酸甲酯,m.p. : 126-128°C。 b.將5.3克(18毫莫耳)2-氣-3-羥基亞胺基甲基-4-甲磺醯 基苯甲酸甲酯溶於50毫升二氣甲烷中,並於〇-5°C下 將乙炔通入30分鐘。接著將刮勺尖端量之醋酸鈉加 入,並於10°C下將15毫升10%強度之次氣酸鈉溶液 逐滴加入,同時再通入更多乙块〇待添加終止後, 於10°C下將乙炔通入15分鐘,接著持績攪拌12小時 。然後使相分離,並將有機相以水萃洗,用硫酸鈉 乾燥並濃縮》 % 此得到4.8克(84%理論値)2 -氣-3-(異吟嗅-3-基)-4-甲 磺醢基苯甲酸甲酯,m.p. : 145-147°C。 3· 2-氣-3-(p塞唑-2-基)-4-甲磺醯基苯f酸甲酯 於固有壓力下將33克(88毫莫耳)2-(三丁基錫坑基)·嘍唑 ,17.5克(44毫莫耳)2-氯-4-甲磺醯基-3-(三氟甲磺醯基) 氧基苯甲酸甲3旨(£父_八.2.),5.8克氣化11,1克四個(三 苯基膦)鈀-(〇),一刮勺尖端量之2,6-二-第三-丁基-4-甲 基盼及200毫升1,4-二1^故置於熱壓器中於140下搜拌 3小時》於冷卻後,將反應混合物通過一層矽石凝膠過 遽’以甲基第三-丁基鍵沖洗並濃縮。將殘餘物通過使 用曱笨/乙酸乙酯爲溶析劑之矽石凝膠進行層析。 此得到9.1克(62.6%理論値)2-氣-3-(喳唑-2-基)-4- f磺醯 -47 - -·种衣— { (請先閱讀背面之注意事項再填寫本頁) -a Μ 本紙張尺度通财關家轉(⑽)A4規格 7^0X297 公釐) 3υ4θ46 Α7 Β7 五、發明説明( 45 基苯甲酸甲酯,m.p : 135 l38»e。 4. 2-氣-3-(气唑-5-基)·4_甲續酿基苯甲酸甲酯 將25克(0.09莫耳)2-氣_3_甲醯基_4_甲磺醯基苯甲酸甲酯 (Εχ· Α·1·) ’ 17·6克(〇.〇9莫耳)芴磺醯基亞甲基異氰化物 及6.2克(〇·045莫耳)細粉碎之碳酸鉀於迴流溫度下與450 毫升甲醇攪拌5小時。接著將溶劑去除,殘餘物吸收於 乙酸乙酯中並用水萃取。將乙酸乙酯相用硫酸鈉乾燥並 濃縮。 此得到24_ 7克(87%理論値)2_氣-3-0塞唑-5-基)-4-甲磺醢 基苯甲駿甲酯,1H nMR (CDC13) ^ : 8.24 (d, 1H), 8.15 (s, 1H), 8.01 (d, 1H), 7.40 (s, 1H), 4.0 (s, 3H), 2.96 (Sj 3H)摯 J 列示於下表之中間物係類似地獲得: 表4 〇 Μ
,ζ Ilia (請先閱讀背面之注意事項再填寫本頁) 4衣. 、v6 經濟部中央標準局負工消费合作社印裝
No. Τ L Μ Z 物理數據 M.p. t°C] or NMR 4.L 甲氡基 —S02Me Cl 夫喃基 1H NMR (CDC13) 6: 8.24 (d,lH),7.82 (d,lH), 7.64 (m,2H),6.55 (s,lH) 3.99 (s,3H),2.80 (s,3H) 4·2 甲氡基 -S〇2He Η 2-塞唑基 95-98 4 · 3 乙氧基 -S02Et Cl 2-埭唑基 XH NMR (CDCI3) δ: 8.18 (d,lH),7.97 (m,2H), 7.71 (d,lH)),4.47 (q,2H) 3.36 (q,2H),1.42 (t,3H), 1.24 (t,3H) 4.4 ΟΗ -S02CHj Cl 2-»塞吱基 288-290 -48 - 本紙張尺度適用中國國家標準(CNS ) a4規格(210X297公釐) A7 B7 五、發明説明(46 ) 經濟部中央標準局員工消費合作社印製
No. Τ L H z 物理數據 K-p, [°C] or !H NKR 4,5 OH -so2ch3 Cl 2-塞吩基 177-180 4.6 OH -so2ch3 ch3 2-·*塞吩基 175-178 4,7 OH -so2ch3 ch3 2-呋喃基 167-171 4,8 甲氣基 -so2ch3 ch3 2-"塞吩基 91-95 4.9 OH -so2ch3 H 2-咬味基 219-223 4.10 甲氡基 -so2ch3 ch3 2-咬味基 103-106 4.11 OH -so2ch3 H 2-»塞咬基 222-224 4.12 甲氧基 -so2ch3 Cl 3-吳哼唑基 lE NMR (CDCI3): 8.62 (1H); 8,18 (1H); 8·00 (1H); 6.58 (1H); 3·98 (3H); 3,22 (3H) 4.13 甲氣基 -so2ch3 Cl 5-笨基咩唑-2-基 115-118 4.14 r氧基 -so2ch3 Cl 5-,号也基 lE NMR (CDCI3) ϊ 8.76 (1H); 8.22 (1H); 8.10 (1H); 7.63 <1H); 4.04 (3H); 3.08 (3H) 4.15 甲氧基 "S02CH3 % Cl 5-環丙基異 -号唑基 NMR (CDCI3): 8.20 (1H); 7,95 (1H); 6·12 (1H); 3.98 (3H); 3,22 (3H); 2.15 (1H); 1.03-1.09 (4H) 4.16 甲氡基 -so2ch3 Cl 4,5-二氩異 •号哇-3-基 lE -NMR (CDCI3): 8.12 (1H); 7.98 (1H); 4.60 (2H); 3.98 (3H); 3·42 (2H)? 3.25 (3H) 4.17 甲氧基 -so2ch3 Cl 5」甲基-1,14-,号二嗖-3-基 102-105 4.18 甲氧墓 -so2CH3 Cl 4,5-二氯-吒哇-2-基 1H NMR (CDCI3): 8.08 (1H)? 7,98 (1H); 4·57 (2H)? 4.12 (2H); 3.98 (3H); 3-29 (3H) 4·19 OH -so2ch3 Cl 3-呋喃基 NMR (CDCI3): 8.29 (1H); 8.02 (1H); 7.67 (2H); 6,59 (1H); 2.83 (3H) 4·20 甲氡基 -so2ch3 Cl 3-"塞吩基 XH NMR (CDCI3): 8.23 (1H); 7.84 (1H); 7.49 (2H); 7.13 (1H); 3.98 (3H); 2.62 (3H) 4.21 OH -so2ch3 H 3-吹喃基 200-202 4.22 OH -so2ch3 Cl 5-甲基笨基 «塞唑-2-基 200-204 -49- (請先閱讀背面之注意事項再填"本頁) 裝 、-°
A 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 五、發明説明 47 C)終產物之製備 1. A7 B7 經濟部中央標準局員工消費合作社印衷 U-—甲基-4_[2-氣-4-甲磺醯基-3-卜号_ < _ # π , 、了唑·5·基)苯甲醯 IJ-5-羥基-吡唑(實施例128) a·將1.22克(1〇.9毫莫耳)1,3-二甲基<5.、甘 ,,^ 恭5~羥基吡唑及 ^克U0.9毫莫耳)三乙胺溶於75毫升乙腊中,並 於〇C下以3.5克(10_9毫莫耳)2•氣+甲確酿基-> ^号唑-5-基)-苯甲醯氣存於50毫升乙腈處理。於〇 c下持續攪拌1小時,接著於室溫下將4 45克(44 毫莫耳)三乙胺及(^丨克^二毫莫耳)乙醯氰醇逐 滴加入。將溶液於室溫下攪拌12小時。爲逐漸 疋成’首先將混*合物稀鹽酸處理,並用曱基第 二-丁,基醚萃取。然後將該醚相用5 %強度之碳酸 卸溶液萃取。待水相以鹽酸酸化後,將產物用 乙酸乙酯從永相萃取出。乙酸乙酯相用硫酸鈉 乾燥並濃縮。 此得到1.2克粗產物,其藉管柱層析術純化_。 此得到0.4克(27%理論値)之i,3_二甲基-4-[2-氣- 甲橫酿基-3-(吟唑-5-基)-苯甲醯基】-5-經基-p比 唑,m.p. : 236-241Ό。 列示於下表之化合物以相似之方法渡得: -50- 本紙張尺度適用中國國家標準(CNS ) A4规格(210X297公釐) (請先閱讀背面之注意事項再填??本頁) 装· 訂 ·" 〇u4U46 A7 B7 五、發明説明(43 ) 表5
No. R1 R2 R3 L M z M.p. [°C] or *Η NMR 5.1 ch3 cf3 H so2ch3 Cl 5-崎哇基 183-190 5.2 ch3 ch3 H so2ch3 Cl 5-哼唑基 236-241 5.3 ch3 ch3 H so2ch3 Cl 3-異今哇基 117-130 5.4 ch3 ch3 % H so2ch3 Cl 4,5-二氫異号 唑-3-基 125-130 5.5 C2H5 H H so2ch3 Cl 4,5-二氫異哼 唑-3-基 61-65 5.6 C2H5 H H s〇2ch3 Cl 3-異哼唑基 175-178 5.7 ch3 ch3 H so2ch3 Cl 2-0塞哇基 125 5.8 ch3 ch3 H so2ch3 Cl 2-4吩基 90 5.9 ch3 H H so2ch3 Cl 2-«塞哇基 Ί% 5.10 C2H5 H H so2ch3 Cl 2-p塞唑基 191-194 <裝— i (請先閱讀背面之注意事項再填寫本頁) 、-» - 經濟部中央標準局負工消費合作社印製 -51 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐)
Claims (1)
- 赛8^设#^:專利申請案 中文申請專利範圍修正本(85年11月) 年 U一種具式la吡唑苯甲醯基衍生物Ο Μ其中之取代基如下列: L,Μ爲氫’ Ci-C6_烷基,鹵素,硝基或基團-S(0)mR7, 2 爲5員飽和或未飽和雜環自由基,其具有一至三個選 自氧’硫與氮之雜原子,且其爲未經取代或經c i -C4 -烷基取代, m 爲零,1或2, R 爲Ci-C4.燒基, Q 爲具式11之?比唆環 R2 --------> ,冬-----,—訂 (請先閣讀背面之注意事項再填寫本頁)經濟部中央標準局負工消費合作社印製 其中 Rl爲Cl-C4-烷基, R2爲氫或C1_C4-烷基且 RJ爲氫’ CKc4-烷颯基或苯颯基,而且 其係鍵聯於4 -位置上, 或式I化合物習用於農業上之鹽類。 2 ·根據申請專利範圍第1項之具式][a之吡唑-4 _基苯甲醯基 ( CNS j ( 210Χ297/>^:) >、申請專利範圍 " 公告本 Αί Βί ---- ______力其中匕爲ΑΑΊ風基,南素或硝基’且Μ爲氫 』1 c6 虎基’ CrC4_^基’或由素而〇及ζ爲如申 請專利範圍第1項中所定義者。 才艮據申請專利範圍P項之式㈣七4_基苯甲酿基衍生 L其中自由基爲氫,甲基,甲硫H甲 基或硝基。 —種製備根據中請專利範圍第^之式㈣七4_基笨甲 醯基衍生物之方法,其包含將式Ila之吡唑 R2 請 先 讀 背 ιδ '意 事 項 寫 本 頁 裝 NI R1 0H Ila 與式III之笨甲醯基衍生物反應 TIII 訂 經 濟 部t 央 標 準 局 員 工 消 費 合 η 印 製 其中τ爲卣素且L,Μ及Ζ爲如申請專利範圍第丨項所定義 〇 5 . 一種除草組合物,其包含至少一種如申請專利範圍第!項 之式I a咐嗅-4 -基苯甲醯基衍生物及習用之惰性添加劑。 6 · —種控制不希望植物之方法,其包含使具除草活性量之如 申請專利範圍第1項之式la吡唑_4_基苯甲醯基衍生物作 用於植物或其環境上。 -2- 本紙乐尺度適用中國國家榡準(CNS )八4規.格(21〇χ297公釐) 13帽46 第八五一〇二一六六號專利申請案 中文補充説明書(八十五年十一月) ΜNo. R1 R2 R3 M 2 FP[':C]或 'H-NMR 5". C2Hs H H so2ch3 Cl 3-異哼唑基 175-178 «TMi c2h5 H H so2ch3 H 3-呋喃基 140-143 C2H5 H H Ci Cl 3-異咩唑基 157-159 -r.w V c2h5 H H N〇2 Cl 3-異呤唑基 130-181 C2H5 H H so2ch3 H 3-異丁基-異B号哇-5-基 123-124 C ch3 H H s〇2ch3 Cl 3_異呤唑棊 195-200 •ΧΆ C2H5 H H Cl Cl 5-今咬基 TH-NMR (CDC:3) δ: S,72 (bs. 1H): 8,11 (s, 1H);7,59 - 7,25 (m, 3H); 4.10 (q, 2H), 1,47 ft. Γ.以 c2h5 H H s〇2ch3 H 2-»塞唑基 1H-_R (CDCI3) S: 3,43 (djH); 8,12 (m, 2H); 7,99 (d, 1H); 7,76 (s. :H); 7,59 (d, 1H}; 4.11 (q, 2H): 3,58 (s, 3H): 1,49 (t. •CM C2H5 H H Cl sch3 2-0塞唑基 126-130 正,C3H7 H H so2ch3 Cl 2-t> j吐基 182-184 正H H so2ch3 Cl 2-4唑基 126-128 r. zz 異丁基 H H s〇2ch3 C( 2-噹唑基 177 r. is c2h5 H H so2ch3 Cl 2-·»号峻基 206-207 ch3 H H so2ch3 Cl 2-D号唑基_ 208*212 -c. is c2h5 H H H ch3 4-第三丁基-1H-NMR (CDC丨3) δ: ρ塞吐-2-基 7,7S (m, 2H); 7:53 - 7,31 (m, 3H); 6,99 (S, 1H); 4,TO (q, 2H); 2,56 (s. 3H); 1.48 (t, 3H); 1,39 (s, 9H) R2 R3M 修正, 補充I ASS21 S.03 23 2 FP[°CJ bzw. H-NMR CH3 Η C2H5 Η -4^. l£ ,— ·» _ c2h5 Η 4 · 13 c2h5 Η M H CH3 SO2C5H5 S02CH3 C! so2ch3 so2ch3 Cl S02n-C3H7 S02CH3 C! 4_ 第三丁基-104-106 p塞吐-2-基 2-p塞嗅基 π 2-嘍唑基 175· 180 2-·1 塞唑基 140-142 .·α ζ^ IT riE ;
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19506572 | 1995-02-24 | ||
| PCT/EP1996/000635 WO1996026206A1 (de) | 1995-02-24 | 1996-02-14 | Pyrazol-4-yl-benzoylderivate und ihre verwendung als herbizide |
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| TW85102166A TW304946B (en) | 1995-02-24 | 1996-02-26 | Pyrazol benzoyl derivatives |
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| DE102011080016A1 (de) | 2011-07-28 | 2012-10-25 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Strobilurin-Fungizide als Safener |
| DE102011080007A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Conazole- und Triazol-Fungizide als Safener |
| DE102011080010A1 (de) | 2011-07-28 | 2012-10-25 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Anilid- und Thiazol-Fungizide als Safener |
| DE102011079991A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Crop Science Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Nicotinoid-Insektizide als Safener |
| DE102011080004A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Carbamat-Fungizide als Safener |
| DE102011080001A1 (de) | 2011-07-28 | 2012-10-25 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Carbamat-Insektizide als Safener |
| DE102011079997A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Corpscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Pyrazol-Insektizide als Safener |
| CN103717076B (zh) | 2011-08-10 | 2016-04-13 | 拜耳知识产权股份有限公司 | 含有特定特特拉姆酸衍生物的活性化合物组合物 |
| EP2908639A1 (en) | 2012-10-19 | 2015-08-26 | Bayer Cropscience AG | Active compound combinations comprising carboxamide derivatives |
| CN107311980B (zh) * | 2015-11-06 | 2019-04-19 | 青岛清原化合物有限公司 | 一种吡唑酮类化合物或其盐、中间体 |
| CN105399674B (zh) * | 2015-12-31 | 2017-02-15 | 青岛清原化合物有限公司 | 吡唑类化合物或其盐、制备方法、除草剂组合物及用途 |
| CN107629035B (zh) * | 2017-10-24 | 2021-11-16 | 青岛清原化合物有限公司 | 一种吡唑酮类化合物或其盐、除草剂组合物及用途 |
| CN107629046B (zh) * | 2017-10-24 | 2021-07-06 | 青岛清原化合物有限公司 | 吡唑酮类化合物或其盐、除草剂组合物及用途 |
| WO2020152200A1 (en) | 2019-01-25 | 2020-07-30 | Basf Se | Process for preparation of heteroarylketones |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4643757A (en) | 1985-05-20 | 1987-02-17 | Nissan Chemical Industries, Ltd. | Herbicidal 4-benzoyl-1-methyl-5-hydroxypyrazoles |
| US4695673A (en) | 1985-11-20 | 1987-09-22 | Stauffer Chemical Company | Process for the production of acylated 1,3-dicarbonyl compounds |
| IL85659A (en) * | 1987-03-17 | 1992-03-29 | Nissan Chemical Ind Ltd | 4-benzoylpyrazole derivatives,method for their preparation and herbicidal compositions containing them |
| US4986845A (en) | 1988-07-15 | 1991-01-22 | Nissan Chemical Industries Ltd. | Pyrazole derivatives and herbicides containing them |
| DE3925502A1 (de) * | 1989-07-28 | 1991-01-31 | Schering Ag | Substituierte 4-heteroaroylpyrazole, verfahren zur herstellung dieser verbindungen und ihre verwendung als mittel mit herbizider wirkung |
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