KR910004541A - 제초제 글루타람산 및 그 유도체 - Google Patents
제초제 글루타람산 및 그 유도체 Download PDFInfo
- Publication number
- KR910004541A KR910004541A KR1019900013703A KR900013703A KR910004541A KR 910004541 A KR910004541 A KR 910004541A KR 1019900013703 A KR1019900013703 A KR 1019900013703A KR 900013703 A KR900013703 A KR 900013703A KR 910004541 A KR910004541 A KR 910004541A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- hydrogen
- compound
- alkoxycarbonyl
- carboxy
- Prior art date
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- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 title claims 2
- 235000013922 glutamic acid Nutrition 0.000 title claims 2
- 239000004220 glutamic acid Substances 0.000 title claims 2
- 230000002363 herbicidal effect Effects 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 42
- 239000001257 hydrogen Substances 0.000 claims 33
- -1 carboxy, carboxy salt Chemical class 0.000 claims 27
- 150000001875 compounds Chemical class 0.000 claims 26
- 239000000460 chlorine Substances 0.000 claims 20
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 17
- 229910052731 fluorine Chemical group 0.000 claims 16
- 229910052736 halogen Chemical group 0.000 claims 16
- 150000002367 halogens Chemical group 0.000 claims 16
- 229910052801 chlorine Inorganic materials 0.000 claims 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 12
- 239000001301 oxygen Substances 0.000 claims 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 11
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 6
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 6
- 125000003302 alkenyloxy group Chemical group 0.000 claims 6
- 125000000304 alkynyl group Chemical group 0.000 claims 6
- 229910052794 bromium Inorganic materials 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 150000002431 hydrogen Chemical group 0.000 claims 5
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 claims 5
- 125000001424 substituent group Chemical group 0.000 claims 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 4
- 125000005133 alkynyloxy group Chemical group 0.000 claims 4
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- 125000005108 alkenylthio group Chemical group 0.000 claims 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 3
- 125000005109 alkynylthio group Chemical group 0.000 claims 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 239000011593 sulfur Substances 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 claims 2
- 125000006224 2-tetrahydrofuranylmethyl group Chemical group [H]C([H])(*)C1([H])OC([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 2
- 125000005236 alkanoylamino group Chemical group 0.000 claims 2
- 125000005452 alkenyloxyalkyl group Chemical group 0.000 claims 2
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000005336 allyloxy group Chemical group 0.000 claims 2
- 125000001589 carboacyl group Chemical group 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000011737 fluorine Chemical group 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000005394 methallyl group Chemical group 0.000 claims 2
- CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical compound CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 239000011591 potassium Substances 0.000 claims 2
- 229910052700 potassium Inorganic materials 0.000 claims 2
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 1
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005085 alkoxycarbonylalkoxy group Chemical group 0.000 claims 1
- 125000004849 alkoxymethyl group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 1
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 claims 1
- 125000005111 carboxyalkoxy group Chemical group 0.000 claims 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 1
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 125000004858 cycloalkoxyalkyl group Chemical group 0.000 claims 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims 1
- 125000005366 cycloalkylthio group Chemical group 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000005343 heterocyclic alkyl group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 claims 1
- 125000003884 phenylalkyl group Chemical group 0.000 claims 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/04—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
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- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A01N37/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides containing at least one oxygen or sulfur atom being directly attached to the same aromatic ring system
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- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/30—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the groups —CO—N< and, both being directly attached by their carbon atoms to the same carbon skeleton, e.g. H2N—NH—CO—C6H4—COOCH3; Thio-analogues thereof
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- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
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- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/48—Nitro-carboxylic acids; Derivatives thereof
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- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
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- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
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- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides
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- 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
- A01N43/04—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 one hetero atom
- A01N43/06—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 one hetero atom five-membered rings
- A01N43/08—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 one hetero atom five-membered rings with oxygen as the ring hetero atom
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- 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
- A01N43/04—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 one hetero atom
- A01N43/06—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 one hetero atom five-membered rings
- A01N43/12—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 one hetero atom five-membered rings condensed with a carbocyclic ring
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
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- A—HUMAN NECESSITIES
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- 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
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- 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
- A01N43/84—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/04—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C233/07—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
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Abstract
Description
Claims (28)
- 다음 일반식 I의 글루타람산 화합물상기 일반식 I에서, A는 히드록시메틸, 클로로메틸, 카르복시, 카르복시염(CO2 -M+, 여기서 M+는 농경학적으로 허용되는 염임), 알콕시 카보닐, 또는 알킬아미노카보닐이고 ; D는 CH 또는 N이고 ; n은 0 또는 1이고 ; R은 수소, (C1-C4)알킬, 1개 내지 9개의 할로겐 원자를 함유하는 할로(C1-C4)알킬 또는 페닐이고 ; R1은 수소, (C1-C2)알킬 또는 할로(C1-C2)알킬이고 ; R2는 수소 또는 (C1-C2)알킬이고 ; T는 수소 또는 불소이고 ; X는 수소 또는 할로겐이고 ; Y는 수소, 할로(C1-C3)알킬, (C1-C3)알킬, 시아노, 니트로, 할로겐, 페녹시 또는 페닐 티오이고 ; Z는 수소, 히드록시, 할로겐, 알콕시, 알케닐옥시, 알키닐옥시, 알킬티오, 알케닐티오, 알키닐티오, 카르복시알콕시, 카르복시알킬티오, 알콕시카보닐알콕시, 알콕시카보닐알킬티오, 시클로알콕시, 시클로알킬알콕시, 시클로알킬티오, 시클로알킬알킬디오, 헤테로고리알콕시, 포르밀, 알카노일, 알콕시카보닐, 알케닐옥시카보닐, 알키닐옥시카보닐, 시클로알콕시카보닐, 시클로알킬알콕시카보닐, 알콕시카보닐 알콕시카보닐, 알킬, 히드록시알킬, 알콕시알킬, 알케닐옥시알킬, 알키닐옥시알킬, 알킬티오알킬, 알케닐티오알킬, 알키닐티오알킬, 시클로알콕시알킬, 시클로알킬알콕시알킬, 시클로알킬티오알킬, 시클로알킬알킬티오알킬, 알콕시카보닐, 알콕시알킬, 페녹시알킬, 페닐티오알킬, 알킬아미노알킬, 헤테로고리, 옥시밀(-CH=NOH), 알킬옥시밀, 알케닐옥시밀, 알키닐오시밀, 알콕시카보닐알킬옥시밀, 알킬(알킬)옥시밀, 알케닐(알킬)옥시밀, 알키닐(알킬)옥시밀, 알콕시카보닐알킬(알킬)옥시밀, 알킬아미노, 모노알케닐아미노, 모노알키닐아미노, 알킬술포닐아미노 또는 알카노일아미노 이며 ; 또는 Y와 Z는 함께 다음 구조식의 이중고리를 형성하도록 페닐 고리에 연합되는 헤테로고리를 형성할 수 있으며 ;상기 구조식들에서, L은 산소 또는 황이고 ; R3은 수소 또는 알킬이며 ; R4는 수소, 알킬, 알케닐, 알키닐, 알콕시알킬, 알케닐옥시알킬, 알키닐옥시알킬, 알콕시카보닐알킬, 시클로알킬, 시클로알킬알킬, 페닐알킬, 알킬리오알킬, 알케닐티오알킬, 알키닐티오알킬, 헤테로고리알킬, 알킬아미노알킬, 알콕시카보닐 또는 알카노일임.X와 Z가 각각 수소 또는 할로겐이고, Y가 할로겐이며, D가 CH인 경우, R은 반드시 트리플루오로메틸(CF3)이고 ; Y가 수소이고, R이 트리플루오로메틸인 경우, R1과 R2는 수소이고 Z는 수소가 아니고 ; Y가 염소이고 Z가 산소에 의하여 페닐고리에 연결된 치환체인 경우, R은 수소가 아니고 ; Z가 아세트아미도인 경우, Y는 염소가 아니다.
- 제1항에 있어서, 일반식 I에서의 각 치환체들이 다음과 같은 글루타람산의 화합물. A는 CH2OH, CH2Cl, COOH, COO-M+(M+는 농경학적으로 허용되는 염임), (C1-C6)알콕시카보닐 또는 (C1-C6)알킬아미노카보닐이고 ; n은 0이고, D는 CH 또는 N이고 ; R은 H, (C1-C4)알킬, 할로(C1-C4)알킬 또는 페닐이고 ; R1은 H 또는 (C1-C2)알킬이고 ; R2는 H 또는 (C1-C2)알킬이고 ; T는 H 또는 F이고 ; X는 H 또는 할로겐이고 ; Y는 수소, 할로겐 CF3, OC6H5, 시아노 또는 NO2이고 ; Z는 수소, 할로겐, (C1-C6)알콕시, (C3-C6)알케닐옥시, 할로(C3-C6)알케닐옥시, (C3-C6)알키닐옥시, (C3-C6)알킬티오, (C3-C6)알케닐티오, (C3-C6)알키닐티오, 페닐(C1-C6)알콕시, 헤테로고리(C1-C6)알콕시, 페닐(C1-C6)알킬티오, 카르복시(C1-C6)알킬티오, (C1-C6)알콕시카보닐(C1-C6)알킬티오, (C1-C6)알카노일, (C1-C6)알콕시카보닐, (C1-C6)알킬, 히드록시(C1-C6)알킬, (C1-C6)알콕시(C1-C6)알킬, (C3-C6)알케닐옥시(C1-C6)알킬, (C3-C6)알키닐옥시(C1-C6)알킬, (C1-C6)알킬티오(C1-C6)알킬, (C1-C6)알콕시카보닐(C1-C6)알콕시(C1-C6)알킬, 페녹시(C1-C6)알킬, 페닐티오(C1-C6)알킬, 헤테로고리, 디(C1-C6)알킬아미노(C1-C6)알킬, 모노(C1-C6)알카노일아미노, 또는 디(C1-C6)알킬술포닐아미노이며 ; 또는 Y와 Z는 함께 다음 구조식의 이중 고리를 형성하도록 페닐 고리에 연합되는 헤테로고리를 형성할 수 있으며 ;상기 구조식들에서, L은 산소 또는 황이고 ; R3은 수소 또는 (C1-C3)알킬이고, R4는 수소, (C1-C6)알킬, (C3-C6)알케닐, 할로(C3-C6)알케닐, (C3-C6)알키닐, (C3-C6)시클로알킬(C1-C6)알킬, (C1-C6)알콕시(C1-C6)알킬, 페닐(C1-C6)알킬, 시아노(C1-C6)알킬, 헤테로고리(C1-C6)알킬, (C1-C6)알킬아미노(C1-C6)알킬, 또는 (C1-C6)알콕시카보닐(C1-C6)알킬임. X와 Z가 각각 수소 또는 할로겐이고, Y가 할로겐이며, D가 CH인 경우, R은 반드시 CF3이고 ; Y가 수소이고 R이 트리플루오로메틸(CF3)인 경우, R1과 R2는 수소이고 Z는 수소가 아니고 ; Y가 염소(C1)이고 Z가 산소에 의하여 페닐고리에 연결된 치환체인 경우, R은 수소가 아니며 ; Z가 아세트아미도인 경우, Y는 염소가 아니다.
- 제2항에 있어서, 일반식 I에서의 각 치환체들이 다음과 같은 화합물.A는 CO2H, (C1-C6)알콕시카보닐 또는 CO2 -M+이고 ; D는 CH 또는 X가 H인 경우에는 N이고 ; n은 O이고 ; R은 (C1-C4)알킬 또는 할로(C1-C4)알킬이고 ; R1은 H 또는 (C1-C2)알킬이고 ; R2는 H이고 ; X는 수소 또는 할로겐이고 ; Y는 수소 또는 할로겐이고 ; T는 H 또는 F이고 ; Z는 H, (C1-C6)알콕시, (C1-C6)알케닐옥시, 할로(C3-C6)알케닐옥시, (C3-C6)알키닐옥시, (C1-C6)알킬티오, (C3-C6)알케닐티오, (C3-C6)알키닐티오, 페닐(C1-C6)알콕시, 헤테로고리(C1-C6)알콕시, 페닐(C1-C6)알킬티오, 카르복시(C1-C6)알킬티오, 또는 (C1-C6)알콕시카보닐(C1-C6)알킬티오임.
- 제3항에 있어서, A는 카르복시, (C1-C6)알콕시카보닐 또는 CO2 -M+이고 ; D는 CH이고 ; n은 0이고 ; R은 CH3, CF3, CHF2또는 CF2CF3이고 ; R1은 H이고 ; X는 Cl 또는 F이고 ; Y는 Br, F 또는 Cl이고 ; T는 H이고 ; Z는 (C1-C6)알콕시, (C3-C6)알케닐옥시 또는 (C3-C6)알키닐옥시인 것을 특징으로 하는 화합물.
- 제4항에 있어서, A는 카르복시, 에톡시카보닐, 메톡시카보닐, 이소프로필옥시카보닐, 에토민카르복실레이트, 이소프로필 암모늄카르복실레이트 또는 칼륨 카르복실레이트이고 ; X는 F이고 ; Y는 Br 또는 Cl이고 ; Z는 프로파길옥시, 알릴옥시, n-프로필옥시, 이소프로필옥시, 에톡시 또는 메톡시인 것을 특징으로 하는 화합물.
- 제5항에 있어서, A는 카르복시이고 ; R은 CF3이고 ; Y는 Cl이고 ; Z는 프로파길옥시, 이소프로파길옥시, n-프로필옥시, 에톡시, 메톡시 또는 알릴옥시인 것을 특징으로 하는 화합물.
- 제5항에 있어서, R은 CH3이고 ; A는 COOH이고 ; Y는 Cl 또는 Br이며 ; Z는 프로파길옥시인 것을 특징으로 하는 화합물.
- 제5항에 있어서, R은 CF2CF3이고 ; A는 COOH이며 ; Z는 프로파길옥시인 것을 특징으로 하는 화합물.
- 제5항에 있어서, R은 CF3이고 ; Y는 Cl이고 ; Z는 프로파길옥시이며 ; A는 카르복시, 에톡시카보닐, 메톡시카보닐, 이소프로필옥시카보닐, 에토민카르복실레이트, 이소프로필암모늄 카르복실레이트 또는 칼륨카르복실레이트인 것을 특징으로 하는 화합물.
- 제5항에 있어서, R은 CHF2이고 ; Y는 Cl이고 ; Z는 프로파길옥시이며 ; A는 카르복시인 것을 특징으로 하는 화합물.
- 제5항에 있어서, R은 CF3이고 ; Y는 Cl이고 ; Z는 이소프로필옥시이며 ; A는 카르복시 또는 메톡시 카보닐인 것을 특징으로 하는 화합물.
- 제2항에 있어서, A는 카르복시이고 ; D는 CH 또는 X가 H인 경우에는 N이고 ; n은 0이고 ; R은 (C1-C4)알킬 또는 할로(C1-C4)알킬이고 ; R1은 H 또는 (C1-C2)알킬이고 ; R2는 H이고 ; X는 H 또는 할로겐이고 ; Y는 H 또는 할로겐이고 ; T는 H 또는 F이며 ; Z는 (C1-C6)알콕시카보닐인 것을 특징으로 하는 화합물, 및 농경학적으로 허용되는 그 염.
- 제12항에 있어서, A는 카르복시이고 ; D는 CH이고 ; R은 CH3, CF3또는 CHF2이고 ; R1항에 있어서,은 H이고 ; X는 Cl 또는 F이고 ; Y는 Br, F 또는 Cl이고 ; T는 H이며 ; Z는 (C1-C6)알콕시카보닐인 것을 특징으로 하는 화합물.
- 제13항에 있어서, R은 CF3이고 ; X는 F이고 ; Y는 Cl 또는 Br이고 ; Z는 이소프로필옥시카보닐인 것을 특징으로 하는 화합물.
- 제13항에 있어서, R은 CHF2또는 CH3이고 ; X는 F이고 ; Y는 Cl이며 ; Z는 이소프로필옥시카보닐인 것을 특징으로 하는 화합물.
- 제2항에 있어서, A는 카르복시이고 ; D는 CH 또는, X가 H인 경우에는 N이고 ; n은 0이고 ; R은 (C1-C4)알킬 또는 할로(C1-C4)알킬이고 ; R1은 H 또는 (C1-C2)알킬이고 ; R2는 H이고 ; X는 H 또는 할로겐이고 ; Y는 H 또는 할로겐이고 ; T는 H 또는 F이며 ; Z는 (C1-C6)알콕시(C1-C6)알킬, (C3-C6)알케닐옥시(C1-C6)알킬 또는 (C3-C6)알키닐(C1-C6)알킬인 것을 특징으로 하는 화합물 및 농경학적으로 허용되는 그 염.
- 제16항에 있어서, A는 카르복시이고 ; D는 CH이고 ; n은 0이고 ; R은 CF3이고 ; R1은 H이고 ; X는 Cl 또는 F이고 ; Y는 Br, F 또는 Cl이고 ; T는 H이며 ; Z는 (C1-C6)알콕시(C1-C6)알킬, (C3-C6)알케닐옥시(C1-C6)알킬 또는 (C3-C6)알킬닐옥시(C1-C6)알킬인 것을 특징으로 하는 화합물.
- 제17항에 있어서, X는 F이고 ; Y는 Cl이며 ; Z는 이소프로필옥시메틸 또는 1-메틸프로파길옥시메틸인 것을 특징으로 하는 화합물.
- 제2항에 있어서, Y와 Z가 함께 하기 구조식의 헤테로고리를 형성하며 각 치환체가 다음과 같은 화합물.A는 COOH, (C1-C6)알콕시카보닐 또는 COO-M+이고 ; D는 CH이고 ; n은 0이고 ; L은 산소 또는 황이고 ; X는 수소 또는 불소이고 ; R은 (C1-C4)알킬 또는 할로(C1-C4)알킬이고 ; R1은 H 또는 (C1-C2)알킬이고 ; R2는 수소이고 ; R3은 수소 또는 (C1-C3)알킬이며 ; R4는 수소, (C1-C6)알킬, (C3-C6)알케닐, 할로(C3-C6)알케닐, (C3-C6)알키닐, (C3-C6)시클로알킬(C1-C6)알킬, (C1-C6)알콕시(C1-C6)알킬, 페닐(C1-C6)알킬, 시아노(C1-C6)알킬, 헤테로고리(C1-C6)알킬, (C1-C6)알킬아미노(C1-C6)알킬 또는 (C1-C6)알콕시카보닐(C1-C6)알킬임.
- 제19항에 있어서, 다음 일반식을 갖는 화합물.상기 일반식에서, A는 카르복시, COO-M+또는 (C1-C6)알콕시카보닐이고 ; X는 H 또는 F이고 ; L은 0 또는 S이고 ; R은 CH3, CF2H 또는 CF3이고 ; R3은 H 또는 (C1-C3)알킬이며 ; R4는 (C1-C6)알킬, (C3-C6)알케닐, 할로(C3-C6)알케닐, (C3-C6)알키닐, (C3-C6)시클로알킬(C1-C6)알킬, (C1-C6)알콕시메틸, 시아노(C1-C6)알킬, 푸라닐(C1-C6)알킬 또는 페닐(C1-C6)알킬임.
- 제20항에 있어서, 다음 일반식을 갖는 화합물.상기 일반식에서, A는 카르복시이고 ; L은 산소이고 ; X는 H 또는 F이고 ; R은 CF3또는 CHF2이고 ; R3은 메틸이며 ; R4는 프로파길임.
- 제20항에 있어서, A는 카르복시 또는 알콕시카보닐이고 ; L은 산소이고 ; X는 H 또는 F이고 ; R은 CF3또는 CHF2이고 ; R3은 수소이고 ; R4는 프로파길, 에틸, 알릴, 2-메틸알릴, 2-클로로알릴, 시클로프로필메틸, n-프로필, 이소프로필, 이소부틸, 2-테트라하이드로푸라닐메틸, 시아노메틸, 에톡시메틸, 메톡시메틸 또는 2-부테닐인 것을 특징으로 하는 화합물.
- 제22항에 있어서, A는 카르복시이고 ; L은 산소이고 ; X는 수소이고 ; R은 CF3이고 ; R3은 수소이며 ; R4는 프로파길, 알릴 또는 메톡시메틸인 것을 특징으로 하는 화합물.
- 제22항에 있어서, A는 카르복시이고 ; L은 산소이고 ; X는 F이고 ; R은 CF3이고 ; R3은 수소이며 ; R4는 프로파길, 에틸, 알릴, 2-메틸알릴, 2-클로로알릴, n-프로필, 이소프로필, 이소부틸, 시클로프로필메틸, 시아노메틸, 2-테트라하이드로푸라닐메틸, 메톡시메틸, 에톡시메틸 또는 2-부테닐인 것을 특징으로 하는 화합물.
- 제22항에 있어서, A는 메톡시카보닐 또는 이소프로필옥시카보닐 이고 ; L은 산소이고 ; X는 F이고 ; R은 CF3이고 ; R4는 H이며 ; R4는 알릴인 것을 특징으로 하는 화합물.
- 제22항에 있어서, A는 COO-NM4 +또는 COO-K+이고 ; L은 산소이고 ; X는 F이고 R3은 H이며 ; R4는 알릴인 것을 특징으로 하는 화합물.
- 제22항에 있어서, A는 COOH이고 ; R은 CHF2이고 ; L은 산소이고 ; X는 F이고 ; R3은 H이며 ; R4는 프로파길인 것을 특징으로 하는 화합물.
- 제20항에 있어서, 다음 일반식을 갖는 화합물.상기 일반식에서, A는 COOH이고 ; X는 H 또는 F이며 ; R4는 프로파길임.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40126889A | 1989-08-31 | 1989-08-31 | |
US401268 | 1989-08-31 | ||
US563779 | 1990-08-09 | ||
US07/563,779 US5238908A (en) | 1989-08-31 | 1990-08-09 | Herbicidal glutaramic acids and derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910004541A true KR910004541A (ko) | 1991-03-28 |
Family
ID=27017367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900013703A KR910004541A (ko) | 1989-08-31 | 1990-08-31 | 제초제 글루타람산 및 그 유도체 |
Country Status (21)
Country | Link |
---|---|
US (1) | US5238908A (ko) |
EP (1) | EP0415641B1 (ko) |
JP (1) | JPH03173855A (ko) |
KR (1) | KR910004541A (ko) |
CN (1) | CN1049770A (ko) |
AR (1) | AR246247A1 (ko) |
AT (1) | ATE100441T1 (ko) |
AU (1) | AU638739B2 (ko) |
BR (1) | BR9004332A (ko) |
CA (1) | CA2023495A1 (ko) |
DE (1) | DE69006142T2 (ko) |
DK (1) | DK0415641T3 (ko) |
EG (1) | EG19278A (ko) |
ES (1) | ES2062389T3 (ko) |
FI (1) | FI904283A0 (ko) |
HU (1) | HUT54459A (ko) |
IE (1) | IE64662B1 (ko) |
IL (1) | IL95530A (ko) |
NO (1) | NO903759L (ko) |
NZ (1) | NZ235091A (ko) |
PT (1) | PT95172B (ko) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991004027A1 (en) * | 1989-09-15 | 1991-04-04 | Pfizer Inc. | New n-aryl and n-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme a: cholesterol acyl transferase (acat) |
EP0600089A4 (en) * | 1992-02-26 | 1994-07-06 | Central Glass Co Ltd | N-acyl-n-phenyltetrahydrophthalamic acid derivative, production thereof, and herbicide containing the same as active ingredient. |
JPH08151364A (ja) * | 1994-02-18 | 1996-06-11 | Nissan Chem Ind Ltd | 含窒素環状化合物および除草剤 |
US5518993A (en) * | 1994-08-12 | 1996-05-21 | Buckman Laboratories International, Inc. | Pesticidal compositions containing ethoxylated fatty amines for increasing the effectiveness of endothal and salts thereof |
EP2537829B1 (de) | 2002-10-30 | 2016-03-02 | Basf Se | Aminobenzoylsulfonsäureamide und deren Herstellung |
EA200801432A1 (ru) * | 2005-12-01 | 2008-12-30 | Басф Се | Способ получения сульфонамидов |
DE102005057681A1 (de) * | 2005-12-01 | 2007-06-06 | Basf Ag | Verfahren zur Herstellung fluorierter m-Nitro-Benzoesäurechloride |
AR068849A1 (es) * | 2007-10-12 | 2009-12-09 | Basf Se | Procedimiento para la preparacion de diamidas de acido sulfonico |
CN103755658B (zh) * | 2014-01-28 | 2016-06-01 | 迈克斯(如东)化工有限公司 | 苯并内酰胺化合物及其合成方法和应用 |
CN103880771B (zh) * | 2014-04-03 | 2016-03-16 | 北京颖泰嘉和生物科技股份有限公司 | 6-氨基-7-氟-4-丙炔基-1,4-苯并恶嗪-3(4h)-酮的制备方法 |
CN109748799A (zh) * | 2018-12-18 | 2019-05-14 | 内蒙古世杰化工有限公司 | 一种合成2-(5-氟-1,5二硝基苯氧)乙酸酯的方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH1237A (de) * | 1889-07-23 | 1889-10-26 | Joseph Irish | Stickmaschine |
CH3869A (de) * | 1891-08-25 | 1892-01-15 | Gottfried Meyer | Vorrichtung, um Eisenbahnzüge auf freier Bahn von den Stationen aus anzuhalten |
US3754031A (en) * | 1971-03-18 | 1973-08-21 | Ciba Geigy Corp | N,n'-bis(3,5-di-t-butyl-4-hydroxyphenyl) adipamide |
US4469885A (en) * | 1983-05-09 | 1984-09-04 | G. D. Searle & Co. | Halogenated protease inhibitors |
US4489010A (en) * | 1983-12-30 | 1984-12-18 | Stauffer Chemical Company | Meta-anilide and meta-anilide urea and urea salt herbicidal compounds and methods of use |
US4509975A (en) * | 1983-12-30 | 1985-04-09 | Stauffer Chemical Company | Meta-anilide and meta-anilide urea herbicidal compounds and methods of use |
US4557756A (en) * | 1983-12-30 | 1985-12-10 | Stauffer Chemical Company | Meta-anilide and meta-anilide urea herbicidal compounds and methods of use |
DE3614355A1 (de) * | 1986-04-28 | 1987-10-29 | Hoechst Ag | Neue benzothiazinon-derivate, verfahren zu ihrer herstellung , sie enthaltende arzneimittel und deren verwendung |
WO1989004821A1 (en) * | 1987-11-25 | 1989-06-01 | Pfizer Inc. | N-(biphenylmethyl)-3-hydroxyglutaramic acid and derivatives as hypocholesterolemic agents |
EP0391847A1 (de) * | 1989-04-04 | 1990-10-10 | Ciba-Geigy Ag | 1-Phenyl-piperidin-2,4-dione mit herbizider Wirkung |
AU7745991A (en) * | 1990-04-11 | 1991-10-30 | Warner-Lambert Company | Amide ester acat inhibitors |
-
1990
- 1990-08-09 US US07/563,779 patent/US5238908A/en not_active Expired - Fee Related
- 1990-08-17 CA CA002023495A patent/CA2023495A1/en not_active Abandoned
- 1990-08-22 DE DE69006142T patent/DE69006142T2/de not_active Expired - Fee Related
- 1990-08-22 ES ES90309222T patent/ES2062389T3/es not_active Expired - Lifetime
- 1990-08-22 DK DK90309222.9T patent/DK0415641T3/da active
- 1990-08-22 AT AT90309222T patent/ATE100441T1/de not_active IP Right Cessation
- 1990-08-22 EP EP90309222A patent/EP0415641B1/en not_active Expired - Lifetime
- 1990-08-27 AR AR90317691A patent/AR246247A1/es active
- 1990-08-28 NO NO90903759A patent/NO903759L/no unknown
- 1990-08-29 NZ NZ235091A patent/NZ235091A/en unknown
- 1990-08-30 AU AU62019/90A patent/AU638739B2/en not_active Ceased
- 1990-08-30 IL IL9553090A patent/IL95530A/en not_active IP Right Cessation
- 1990-08-30 EG EG51390A patent/EG19278A/xx active
- 1990-08-30 FI FI904283A patent/FI904283A0/fi not_active Application Discontinuation
- 1990-08-30 IE IE314990A patent/IE64662B1/en not_active IP Right Cessation
- 1990-08-30 HU HU905702A patent/HUT54459A/hu unknown
- 1990-08-31 JP JP2230446A patent/JPH03173855A/ja active Pending
- 1990-08-31 KR KR1019900013703A patent/KR910004541A/ko active IP Right Grant
- 1990-08-31 CN CN90107105A patent/CN1049770A/zh active Pending
- 1990-08-31 BR BR909004332A patent/BR9004332A/pt not_active Application Discontinuation
- 1990-08-31 PT PT95172A patent/PT95172B/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP0415641A1 (en) | 1991-03-06 |
NO903759D0 (no) | 1990-08-28 |
BR9004332A (pt) | 1991-09-03 |
NO903759L (no) | 1991-03-01 |
IE64662B1 (en) | 1995-08-23 |
CN1049770A (zh) | 1991-03-13 |
AU638739B2 (en) | 1993-07-08 |
IE903149A1 (en) | 1991-03-13 |
PT95172A (pt) | 1991-05-22 |
DK0415641T3 (da) | 1994-02-28 |
JPH03173855A (ja) | 1991-07-29 |
AR246247A1 (es) | 1994-07-29 |
CA2023495A1 (en) | 1991-03-01 |
DE69006142T2 (de) | 1994-06-09 |
ATE100441T1 (de) | 1994-02-15 |
IL95530A0 (en) | 1991-06-30 |
AU6201990A (en) | 1991-03-07 |
EP0415641B1 (en) | 1994-01-19 |
US5238908A (en) | 1993-08-24 |
NZ235091A (en) | 1993-05-26 |
EG19278A (en) | 1994-08-30 |
ES2062389T3 (es) | 1994-12-16 |
PT95172B (pt) | 1997-06-30 |
HUT54459A (en) | 1991-03-28 |
FI904283A0 (fi) | 1990-08-30 |
IL95530A (en) | 1994-08-26 |
DE69006142D1 (de) | 1994-03-03 |
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