KR950017984A - 치환된 페닐 에테르 - Google Patents
치환된 페닐 에테르 Download PDFInfo
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- KR950017984A KR950017984A KR1019940040745A KR19940040745A KR950017984A KR 950017984 A KR950017984 A KR 950017984A KR 1019940040745 A KR1019940040745 A KR 1019940040745A KR 19940040745 A KR19940040745 A KR 19940040745A KR 950017984 A KR950017984 A KR 950017984A
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- alkyl
- alkoxy
- alkylthio
- alkynyl
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- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 32
- 238000000034 method Methods 0.000 claims abstract 7
- 239000004480 active ingredient Substances 0.000 claims abstract 3
- -1 trifluoromethylphenyl Chemical group 0.000 claims 36
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 27
- 125000000217 alkyl group Chemical group 0.000 claims 18
- 229910052736 halogen Inorganic materials 0.000 claims 18
- 150000002367 halogens Chemical class 0.000 claims 18
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 15
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 14
- 125000001424 substituent group Chemical group 0.000 claims 13
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 12
- 229910052801 chlorine Inorganic materials 0.000 claims 12
- 239000000460 chlorine Substances 0.000 claims 12
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 10
- 229910052794 bromium Inorganic materials 0.000 claims 10
- 125000003545 alkoxy group Chemical group 0.000 claims 9
- 125000002541 furyl group Chemical group 0.000 claims 8
- 125000004076 pyridyl group Chemical group 0.000 claims 8
- 125000001188 haloalkyl group Chemical group 0.000 claims 7
- 125000006377 halopyridyl group Chemical group 0.000 claims 7
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 6
- 125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims 6
- 125000004438 haloalkoxy group Chemical group 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 5
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 4
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 4
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 3
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 3
- 241000607479 Yersinia pestis Species 0.000 claims 3
- 239000002671 adjuvant Substances 0.000 claims 3
- 125000003302 alkenyloxy group Chemical group 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000005530 alkylenedioxy group Chemical group 0.000 claims 3
- 125000000068 chlorophenyl group Chemical group 0.000 claims 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 3
- 239000012024 dehydrating agents Substances 0.000 claims 3
- 239000010977 jade Substances 0.000 claims 3
- 125000006730 (C2-C5) alkynyl group Chemical group 0.000 claims 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 2
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 2
- 239000003377 acid catalyst Substances 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 150000001345 alkine derivatives Chemical class 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 2
- 125000004969 haloethyl group Chemical group 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- 125000003944 tolyl group Chemical group 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 1
- 125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims 1
- 125000006378 chloropyridyl group Chemical group 0.000 claims 1
- 125000004188 dichlorophenyl group Chemical group 0.000 claims 1
- 125000004212 difluorophenyl group Chemical group 0.000 claims 1
- 125000001207 fluorophenyl group Chemical group 0.000 claims 1
- 230000012010 growth Effects 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 125000005291 haloalkenyloxy group Chemical group 0.000 claims 1
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000006372 monohalo methyl group Chemical group 0.000 claims 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000003839 salts Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
- A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
- A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
- A01N43/30—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/18—Radicals substituted by singly bound oxygen or sulfur atoms
- C07D317/22—Radicals substituted by singly bound oxygen or sulfur atoms etherified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/72—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 spiro-condensed with carbocyclic rings
Abstract
본 발명은 하기식(Ⅰ)의 화합물에 관한 것이다.
상기식에서, R1,R2,R3,R4,R5및 R6은 제1항에서 정의된 바와 같고 농화학적 활성 성분으로서 사용될 수 있으며 공지된 방법으로 제조될 수 있다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (18)
- 하기식(Ⅰ)의 화합물;상기식에서, R1는 치환 또는 비치환된 C1-C8알킬, 치환 또는 비치환된 C3-C8시클로알킬, 치환 또는 비치환된 C2-C8알켄일, 치환 또는 비치환된 C2-C8알킨일, 치환 또는 비치환된 C1-C8알콕시, 치환 또는 비치환된 C3-C8시클로알콕시, 치환 또는 비치환된 C2-C8알켄일옥시, 치환 또는 비치환된 C2-C8알킨일옥시 또는 치환 또는 비치환된 C1-C8알킬티오이고; R2는 염소, 브롬, 메틸 또는 모노할로메틸이며; R3는 H, 할로겐 또는 메틸이고; R4는 H 또는 메틸이며; R5는 H, C1-C8알킬, C3-C6시클로알킬, C2-C5알켄일, C2-C5알킨일, C1-C3알콕시-C1-C3알킬, C1-C4시아노알킬, C1-C6할로알킬, C2-C5할로알켄일, C2-C3할로알킨일, C1-C3알콕시카르보닐, 트리플루오로메틸페닐, 벤질 또는 치환된 벤질이고, 이 치환제는 C1-C3알킬, C1-C3알콕시 및 할로겐으로 이루어진 군으로부터 선정되며; R6는 H, C1-C6알킬, C3-C6시클로알킬, C2-C5알켄일, C2-C4알킨일, C1-C4알콕시, 페닐, 치환된 페닐이고, 치환체는 C1-C3알킬, C1-C3알콕시, C1-C3할로알킬, C1-C3할로알콕시, C1-C3알킬렌디옥시 및 할로겐으로 이루어진 군으로부터 선정되며; 피리딜, 할로피리딜, 푸릴, 티엔일이거나, 또는 R5및 R6는 함께 직쇄 C3-C5알킬렌이다.
- 제1항에 있어서, R1이 C1-C8알킬, C3-C8시클로알킬, C2-C8알켄일, C2-C8알킨일, C1-C8알콕시, C3-C8시클로알콕시, C2-C8알콕시-C1-C4알킬, C1-C8알콕시-C2-C4알콕시-C1-C4알킬, C1-C8알콕시-C2-C4알콕시, C4-C8시클로알콕시-C1-C3알킬, C3-C8알켄일옥시, C3-C8알켄일옥시-C1-C3알킬, C3-C8알킨일옥시, C3-C8알킨일옥시-C1-C3알킬, C3-C8할로알킬, C3-C8할로알켄일, C3-C8할로알킨일, C3-C8할로알콕시, C3-C8할로알콕시-C1-C3알킬, C3-C8할로알켄일옥시, C3-C8할로알켄일옥시-C1-C3알킬, C3-C8할로알킨일옥시-C1-C3알킬, C3-C8알킬티오, C3-C8알킬티오-C1-C3알킬, C2-C8알킬티오-C2-C3알콕시, C2-C8알킬티오-C2-C3알콕시-C1-C4알킬, C2-C8알킬티오-C2-C3알킬티오, C2-C8알킬티오-C2-C3알킬티오-C1-C4알킬, C2-C8알콕시-C2-C3알킬티오 또는 C2-C8알콕시-C2-C3알킬티오-C1-C4알킬이고; R2가 염소, 브롬 또는 메틸이며; R3가 H, 할로겐 또는 메틸이고; R4가 H 또는 메틸이며; R5가 H, C1-C8알킬, C3-C6시클로알킬, C2-C4알켄일, C2-C3알킨일, C1-C3알콕시-C1-C3알킬, C2-C4시아노알킬, C2-C6할로알킬, C2-C5할로알켄일, C2-C3할로알킨일, C1-C3알콕시카르보닐, 트리플루오로메틸페닐, 벤질 또는 치환된 벤질이고, 치환체는 C1-C3알킬, C1-C3알콕시 및 염소로 이루어진 군으로부터 선정되며; R6가 H, C1-C6알킬, C3-C6시클로알킬, C2-C5알켄일, C2-C4알킨일, C1-C4알콕시, 페닐, 치환된 페닐이고, 치환체는 C1-C2알킬, C1-C2알콕시, C1-C2할로알킬, C1-C2할로알콕시, C1-C3알킬렌디옥시 및 할로겐으로 이루어진 군으로부터 선정되며; 피리딜, 할로피리딜, 푸릴이거나, 또는 R5및 R6가 함께 C3-C5알킬렌인 일반식(Ⅰ)의 화합물.
- 제1항에 있어서, R1이 C3-C8알킬, C3-C8시클로알킬, C3-C8알켄일, C3-C8알킨일, C3-C8알콕시, C3-C8시클로알콕시, C2-C8알콕시-C1-C4알킬, C1-C8알콕시-C2-C4알콕시-C1-C4알킬, C1-C8알콕시-C2-C4알콕시, C4-C8시클로알콕시-C1-C3알킬, C3-C8알켄일옥시-C1-C3알킬, C3-C8알켄일옥시, C3-C8알킨일옥시-C1-C3알킬, C3-C8할로알킬, C3-C8할로알켄일, C3-C8할로알킨일, C3-C8할로알콕시, C3-C8할로알콕시-C1-C3알킬, C3-C8할로알켄일옥시-C1-C3알킬, C3-C8할로알킨일옥시, C3-C8할로알킨일옥시-C1-C3알킬, C3-C8알킬티오, C3-C8알킬티오-C1-C3알킬, C2-C8알킬티오-C2-C3알콕시, C2-C8알킬티오-C2-C3알콕시-C1-C4알킬, C2-C8알킬티오-C2-C3알킬티오-C1-C4알킬, C2-C8알콕시-C2-C3알킬티오-C1-C4알킬이고; R2가 염소, 브롬 또는 메틸이며; R3가 H, 할로겐 또는 메틸이고; R4가 H 또는 메틸이며; R5가 H, C1-C8알킬, C3-C6시클로알킬, C2-C5알켄일, C2-C5알킨일, C1-C3알콕시-C1-C3알킬, C2-C4시아노알킬, C2-C6할로알킬, C2-C6할로알켄일, C2-C3할로알킨일, C1-C3알콕시카르보닐, 트리플루오로메틸페닐, 벤질 또는 치환된 벤질이고, 치환체는 C1-C3알킬, C1-C3알콕시 및 할로겐으로 이루어진 군으로부터 선정되며; R6가 H, C1-C6알킬, C3-C6시클로알킬, C2-C5알켄일, C2-C4알킨일, C1-C4알콕시, 페닐, 피환된 페닐이고, 치환체는 C1-C3알킬, C1-C3알콕시, C1-C3할로알킬, C1-C3할로알콕시, C1-C3알킬렌디옥시 및 할로겐으로 이루어진 군으로부터 선정되며; 피리딜, 할로피리딜, 푸릴이거나 또는 R5및 R6가 함께 직쇄 C3-C5알킬렌인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 C3-C6알킬, C3-C6시클로알킬, C3-C6알켄일, C3-C6알킨일, C3-C6알콕시, C3-C6시클로알콕시, C2-C6알콕시-C1-C4알킬, C1-C6알콕시-C2-C4알콕시, C4-C6시클로알콕시-C1-C3알킬, C3-C6알켄일옥시, C3-C6알켄일옥시-C1-C3알킬, C3-C6알킨일옥시, C3-C6알킨일옥시, C3-C6알킨일옥시-C1-C3알킬, C3-C6할로알킬, C3-C6할로알켄일, C3-C6할로알콕시, C3-C6할로알콕시-C1-C3알킬, C3-C6할로알켄일옥시, C3-C6할로알켄일옥시-C1-C3알킬, C3-C6할로알킨일옥시, C3-C6할로알킨일옥시-C1-C3알킬, C3-C6알킬티오, C3-C6알킬티오-C1-C3알킬, C2-C6알킬티오-C2-C3알콕시, 또는 C2-C6알킬티오-C2-C3알킬티오이고; R2가 염소, 브롬 또는 메틸이며; R3가 H, 할로겐 또는 메틸이고; R4가 H 또는 메틸이며; R5가 H, C1-C8알킬, C3-C6시클로알킬, C2-C4알켄일, C2-C3알킨일, C1-C3알콕시-C1-C3알킬, C2-C4시아노알킬, C2-C6할로알킬, C2-C5할로알켄일, C2-C3할로알킨일, C1-C3알콕시카르보닐, 트리플루오로메틸페닐, 벤질 또는 치환된 벤질이고, 치환체는 C1-C3알킬, C1-C3알콕시 및 할로겐으로 이루어진 군으로부터 선정되며; R6가 H, C1-C6알킬, C3-C6시클로알킬, C2-C5알켄일, C2-C4알킨일, C1-C4알콕시, 페닐, 치환된 페닐이고, 치환체는 C1-C3알킬, C1-C3알콕시, C1-C3할로알킬, C1-C3할로알콕시, C1-C3알킬렌디옥시 및 할로겐으로 이루어진 군으로부터 선정되며; 피리딜, 할로피리딜, 푸릴이거나 또는 R5및 R6가 함께 직쇄 C3-C5알킬렌인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 C4-C6알킬, C4-C6시클로알킬, C3-C6알켄일, C3-C5알킨일, C4-C8알콕시, C5-C6시클로알콕시, C2-C4알콕시-C1-C4알킬, C1-C3알콕시-C2-C4알콕시, C5-C6시클로알콕시-C1-C2알킬, C4-C6알켄일옥시, C3-C5알켄일옥시-C1-C3알킬, C3-C5알킨일옥시, C3-C5알킨일옥시, C3-C6알킨일옥시-C1-C3알킬, C3-C5할로알킬, C3-C5할로알켄일, C3-C5할로알콕시, C3-C5할로알콕시-C1-C3알킬, C3-C4할로알켄일옥시, C3-C4할로알켄일옥시-C1-C3알킬, C3-C4할로알킨일옥시, C3-C4할로알킨일옥시-C1-C2알킬, C3-C5알킬티오, C3-C5알킬티오-C1-C3알킬, C2-C4알킬티오-C2-C3알콕시, 또는 C2-C4알킬티오-C2-C3알킬티오이고; R2가 염소, 브롬 또는 메틸이며; R3가 H, 할로겐 또는 메틸이고; R4가 H 또는 메틸이며; R5가 H, C1-C8알킬, C3-C6시클로알킬, C2-C4알켄일, C2-C3알킨일, 메톡시에틸, 시아노메틸, 할로에틸, 할로비닐, 할로아세틸렌일, 트리플루오로메틸페닐, 벤질 또는 치환된 벤질이고, 치환체는 메틸, 메톡시 및 염소로 이루어진 군으로부터 선정되며; R6가 H, C1-C3알킬, C3-C6시클로알킬, C2-C3알켄일, C2-C3알킨일, C1-C3알콕시, 페닐, 치환된 페닐이고, 치환체는 C1-C2알킬, C1-C2알콕시, C1-C2할로알킬, C1-C2할로알콕시, C1-C2알킬렌디옥시 및 할로겐으로 이루어진 군으로부터 선정되며; 피리딜, 할로피리딜, 푸릴이거나 또는 R5및 R6가 함께 직쇄 C3-C5알킬렌인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 C4-C6알킬, 시클로헥실, C4-C5알킨일, C4-C5알콕시, C5-C6시클로알콕시, C2-C4알콕시-C1-C4알킬, C1-C3알콕시에톡시, C5-C6시클로알콕시메틸, C4-C6알켄일옥시, C3-C5알켄일옥시메탈, C3-C5알킨일옥시, C3-C4알킨일옥시, C3-C4할로알콕시, C3할로알켄일옥시, C3할로알케닐옥시메틸, C3할로알킨일옥시, C3할로알킨일옥시메탈, C4알킬티오메틸, C2-C3알킬티오에톡시 또는 C2-C3알킬티오티오에틸티오이고; R2가 염소, 브롬 또는 메틸이며; R3가 H, 할로겐 또는 메틸이고; R4가 H 또는 메틸이며; R5가 H, C1-C8알킬, C3-C6시클로알킬, C2-C4알켄일, C2-C3알킨일, 메톡시에틸, 시아노메틸, 할로에틸, 할로비닐, 할로아세틸렌일, 트리플루오로메틸페닐, 벤질 또는 치환된 벤질이고, 치환체는 메틸, 메톡시 및 염소로 이루어진 군으로부터 선정되며; R6가 H, C1-C3알킬, C3-C6시클로알킬, C2-C3알켄일, C2-C3알킨일, C1-C3알콕시, 페닐, 치환된 페닐이고, 치환체는 C1-C2알킬, C1-C2알콕시, C1-C2할로알킬, C1-C2할로알콕시, C1-C2알킬렌디옥시 및 할로겐으로 이루어진 군으로부터 선정되며; 피리딜, 할로피리딜, 푸릴이거나 또는 R5및 R6가 함께 C3-C5알킬렌인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 C4-C6알킬, 시클로헥실, C4-C5알킨일, C4-C5알콕시, C5-C6시클로알콕시, C2-C4알콕시-C1-C4알킬, C1-C3알콕시에톡시, C5-C6시클로알콕시메틸, C4-C6알켄일옥시, C3-C5알켄일옥시메탈, C3-C5알킨일옥시, C3-C4할로알콕시, C3할로알켄일옥시, C3할로알켄일옥시메틸, C3할로알킨일옥시, C3할로알킨일옥시메탈, C4알킬티오, C4알킬티오메틸, C2-C3알킬티오에톡시 또는 C2-C3알킬티오티오에틸티오이고; R2가 염소, 브롬 또는 메틸이며; R3가 H, 할로겐 또는 메틸이고; R4가 H 또는 메틸이며; R5가 H, C1-C8알킬, 시클로프로필, C2-C4알켄일, C2-C3알킨일, 메톡시에틸, 시아노메틸, 플로오로에틸, 클로로에틸, 플로오로비닐, 클로로비닐, 브로모비닐, 요오드아세틸렌일, 트리플루오로메틸페닐, 벤질, 톨릴, 아니실 또는 클로로페닐이고; R6가 H, C1-C3알킬, C3-C6시클로알킬, C2-C3알켄일, C2-C3알킨일, C1-C3알콕시, 페닐, 치환된 페닐이고, 치환체는 C1-C2알킬, C1-C2알콕시, C1-C2할로알킬, C1-C2할로알콕시, C1-C2알킬렌디옥시 및 할로겐으로 이루어진 군으로부터 선정되고; 피리딜, 할로피리딜, 푸릴이거나 또는 R5및 R6가 함께 C3-C5알킬렌인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 C4-C6알킬, 시클로헥실, C4-C5알킨일, C4-C5알콕시, C5-C6시클로알콕시, C2-C4알콕시-C1-C4알킬, C1-C3알콕시에톡시, C5-C6시클로알콕시메틸, C4-C6알켄일옥시, C3-C5알켄일옥시메탈, C3-C5알킨일옥시, C3-C4할로알콕시, C3할로알켄일옥시, C3할로알켄일옥시메틸, C3할로알킨일옥시, C3할로알킨일옥시메탈, C4알킬티오, C4알킬티오메틸, C2-C3알킬티오에톡시 또는 C2-C3알킬티오티오에틸티오이고; R2가 염소, 브롬 또는 메틸이며; R3가 H, 할로겐 또는 메틸이고; R4가 H 또는 메틸이며; R5가 H, C1-C8알킬, 시클로프로필, C2-C4알켄일, C2-C3알킨일, 메톡시에틸, 시아노메틸, 플로오로에틸, 클로로에틸, 플로오로비닐, 클로로비닐, 브로모비닐, 요오드아세틸렌일, 트리플루오로메틸페닐, 벤질, 톨릴, 아니실 또는 클로로페닐이고; R6가 H, C1-C3알킬, C3-C6시클로알킬, 비닐, 아세틸렌일, C1-C2알콕시, 페닐, 4-톨릴, 4-에틸페닐, 아니실, 트리플루오로메틸페닐, 메틸렌디옥시페닐, 플루오로페닐, 디플루오로페닐, 클로로페닐, 디클로로페닐, 피리딜, 클로로피리딜, 푸릴이거나 또는 R5및 R6가 함께 C3-C5알킬렌인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 2차 부톡시 또는 이소부톡시이고; R2가 염소 또는 브롬이며; R3이 H 또는 브롬이고; R4및 R6가 H이며; R5가 에틸 또는 프로필인 일반식(Ⅰ)의 화합물.
- a) 필요하면, 산 촉매 또는 탈수제의 존재하에 공지되었거나 또는 상응하는 공지화합물과 유사하게 제조할수 있고, R5및 R6가 일반식(Ⅰ)에 정의된 바와 같은 하기식(Ⅲ)의 화합물, 또는 공지되었거나 또는 상응하는 공지 화합물과 유사하게 제조할수 있고 R5및 R6가 일반식(Ⅰ)에 정의된 바와 같으며 알킬이 메틸 또는 에틸인 하기식(Ⅳ)의 화합물과, 공지되었거나 또는 상응하는 공지 화합물과 유사하게 제조할 수 있고, R1,R2,R3및 R4가 일반식(Ⅰ)에 정의된 바와 같은, 유리 형태 또는 염 형태의 하기식(Ⅱ)의 화합물을 반응시키는 단계, 또는 b)필요하면, 산 촉매 또는 탈수제의 존재하에 일반식(Ⅲ)의 화합물과 공지되었거나 또는 상응하는 공기 화합물과 유사하게 제조할 수 있고, R1,R2,R3및 R4가 일반식(Ⅰ)에 대해 정의 된 바와 같은 하기식(Ⅴ)의 화합물을 반응시키는 단계, 또는 c)필요하면, 염기 또는 탈수제의 존재하에, 공지되었거나, 또는 상응하는 공기 화합물과 유사하게 제조할 수 있고 R4, R5및 R6이 일반식(I)에 대해 정의된 바와 같으며 X가 이탈기인 하기식(Ⅶ)의 화합물과 공지되었거나 또는 상응하는 공지 화합물과 유사하게 제조할 수 있고, R1,R2및 R3이 일반식(Ⅰ)에 대해 정의된 바와 같은 하기식(Ⅵ)의 화합물을 반응시키고, 또/또는, 원하면, 이 공정 또는 상이한 경로에 의해 얻을 수 있는 일반식(I)의 화합물을 일반식(I)의 상이한 화합물로 전환시키고, 또/또는 이 공정에 따라 얻을 수 있는 이성질체 혼합물을 분리시켜서 원하는 이성질체를 단리시키는 단계를 포함하는 제1항에 따른 화합물(I)의 제조방법;
- 활성 성분으로서, 제1항에 따른 일반식(I)의 화합물 1이상 및 필요하면, 1이상의 보조제를 포함하는 살충제.
- 보조제와 활성성분을 치밀하게 혼합 및/또는 분쇄하는 것을 포함하는, 제11항에 따른 1이상의 보조제 함유 조성물의 제조 방법.
- 제11항에 따른 조성물의 제조를 위한, 일반식(I)의 제1항에 따른 화합물의용도.
- 해충 방제를 위한 제11항에 따른 조성물의 용도.
- 식물 증식 물질 보호를 위한 제14항에 따른 용도.
- 해충 또는 이들의 환경에 제11항에 따른 조성물을 도포하는 것을 포함하는 해충방제 방법.
- 증식 물질 또는 증식 물질이 심어져 있는 위치에 처리하는 것을 포함하는, 식물 증식 물질 보호를 위한 제17항에 따른 방법.
- 제17항에 기재되어 있는 방법에 따라 처리된 식물 증식 물질.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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US (1) | US5663379A (ko) |
EP (1) | EP0661281B1 (ko) |
JP (1) | JPH07206610A (ko) |
KR (1) | KR950017984A (ko) |
AU (1) | AU687928B2 (ko) |
BR (1) | BR9405307A (ko) |
CA (1) | CA2139208A1 (ko) |
DE (1) | DE59408689D1 (ko) |
ES (1) | ES2138653T3 (ko) |
GR (1) | GR3031996T3 (ko) |
ZA (1) | ZA9410388B (ko) |
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DE19846008A1 (de) * | 1998-10-06 | 2000-04-13 | Bayer Ag | Phenylessigsäure-heterocyclylamide |
FR2839296A1 (fr) | 2002-07-17 | 2003-11-07 | Tetra Laval Holdings & Finance | Recipient pourvu d'un goulot et equipe d'un bouchon pourvu d'une jupe interne |
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US4590282A (en) * | 1984-09-24 | 1986-05-20 | Sandoz Ltd. | Pest control agents |
ES2040375T3 (es) * | 1987-01-19 | 1993-10-16 | Ciba-Geigy Ag | Dioxolonderivados substituidos. |
TW231257B (ko) * | 1992-03-02 | 1994-10-01 | Ciba Geigy |
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1994
- 1994-12-19 ES ES94810734T patent/ES2138653T3/es not_active Expired - Lifetime
- 1994-12-19 EP EP94810734A patent/EP0661281B1/de not_active Expired - Lifetime
- 1994-12-19 DE DE59408689T patent/DE59408689D1/de not_active Expired - Fee Related
- 1994-12-22 AU AU81675/94A patent/AU687928B2/en not_active Ceased
- 1994-12-28 JP JP6340297A patent/JPH07206610A/ja active Pending
- 1994-12-28 CA CA002139208A patent/CA2139208A1/en not_active Abandoned
- 1994-12-29 ZA ZA9410388A patent/ZA9410388B/xx unknown
- 1994-12-29 KR KR1019940040745A patent/KR950017984A/ko not_active Application Discontinuation
- 1994-12-29 BR BR9405307A patent/BR9405307A/pt not_active IP Right Cessation
- 1994-12-29 US US08/366,128 patent/US5663379A/en not_active Expired - Fee Related
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US5663379A (en) | 1997-09-02 |
AU687928B2 (en) | 1998-03-05 |
ZA9410388B (en) | 1995-01-01 |
ES2138653T3 (es) | 2000-01-16 |
CA2139208A1 (en) | 1995-07-01 |
GR3031996T3 (en) | 2000-03-31 |
BR9405307A (pt) | 1995-09-19 |
DE59408689D1 (de) | 1999-10-07 |
JPH07206610A (ja) | 1995-08-08 |
EP0661281A1 (de) | 1995-07-05 |
AU8167594A (en) | 1995-07-06 |
EP0661281B1 (de) | 1999-09-01 |
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