CN1036202A - 有机化合物或有关有机化合物的改进 - Google Patents
有机化合物或有关有机化合物的改进 Download PDFInfo
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- CN1036202A CN1036202A CN89101743A CN89101743A CN1036202A CN 1036202 A CN1036202 A CN 1036202A CN 89101743 A CN89101743 A CN 89101743A CN 89101743 A CN89101743 A CN 89101743A CN 1036202 A CN1036202 A CN 1036202A
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- alkyl
- compound
- phenyl
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- 150000002894 organic compounds Chemical class 0.000 title description 4
- 230000006872 improvement Effects 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 164
- 239000000203 mixture Substances 0.000 claims abstract description 26
- 241000196324 Embryophyta Species 0.000 claims abstract description 16
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 64
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 60
- 238000000034 method Methods 0.000 claims description 54
- -1 methylenedioxy group Chemical group 0.000 claims description 47
- 125000004432 carbon atom Chemical group C* 0.000 claims description 43
- 229910052799 carbon Inorganic materials 0.000 claims description 36
- 229910052736 halogen Inorganic materials 0.000 claims description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 150000002367 halogens Chemical class 0.000 claims description 30
- 238000006243 chemical reaction Methods 0.000 claims description 24
- 125000001072 heteroaryl group Chemical group 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 229910052801 chlorine Inorganic materials 0.000 claims description 16
- 150000002148 esters Chemical class 0.000 claims description 16
- 125000004076 pyridyl group Chemical group 0.000 claims description 16
- 125000001544 thienyl group Chemical group 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 15
- 150000003839 salts Chemical group 0.000 claims description 15
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 13
- 229910052717 sulfur Inorganic materials 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 11
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 8
- 125000002541 furyl group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 150000002430 hydrocarbons Chemical group 0.000 claims description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 5
- 230000032050 esterification Effects 0.000 claims description 5
- 238000005886 esterification reaction Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
- 125000001188 haloalkyl group Chemical group 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- 230000026030 halogenation Effects 0.000 claims description 2
- 238000005658 halogenation reaction Methods 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 230000008707 rearrangement Effects 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims 2
- 125000006164 6-membered heteroaryl group Chemical group 0.000 claims 2
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 125000006557 (C2-C5) alkylene group Chemical group 0.000 claims 1
- OOKZENRMTOTMNZ-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-(1-methyl-4-nitropyrazole-3-carbonyl)pyran-3-one Chemical compound CN1N=C(C(=C1)[N+](=O)[O-])C(=O)C=1C(C(OC(C1)(C)C)(C)C)=O OOKZENRMTOTMNZ-UHFFFAOYSA-N 0.000 claims 1
- WHCJTVRJFBFZCQ-UHFFFAOYSA-N 2-(1-methyl-4-nitropyrazole-3-carbonyl)cyclohexane-1,3-dione Chemical compound CN1N=C(C(=C1)[N+](=O)[O-])C(=O)C1C(CCCC1=O)=O WHCJTVRJFBFZCQ-UHFFFAOYSA-N 0.000 claims 1
- DPESGCDZEPKCBL-UHFFFAOYSA-N 2-(2-chloro-4-methylsulfonylbenzoyl)-5-(trifluoromethyl)cyclohexane-1,3-dione Chemical compound ClC1=C(C(=O)C2C(CC(CC2=O)C(F)(F)F)=O)C=CC(=C1)S(=O)(=O)C DPESGCDZEPKCBL-UHFFFAOYSA-N 0.000 claims 1
- VCFVEDUNKGXVDF-UHFFFAOYSA-N 2-(2-methyl-4-nitropyrazole-3-carbonyl)cyclohexane-1,3-dione Chemical compound CN1N=CC([N+]([O-])=O)=C1C(=O)C1C(=O)CCCC1=O VCFVEDUNKGXVDF-UHFFFAOYSA-N 0.000 claims 1
- SYONNCMCFHWZMB-UHFFFAOYSA-N 2-(3,5-dichloropyridine-2-carbonyl)cyclohexane-1,3-dione Chemical compound ClC=1C(=NC=C(C1)Cl)C(=O)C1C(CCCC1=O)=O SYONNCMCFHWZMB-UHFFFAOYSA-N 0.000 claims 1
- KUTUJOZUNFHEQL-UHFFFAOYSA-N 2-(4-chloro-2-nitrobenzoyl)-4,4-dimethyl-5-(trifluoromethyl)cyclohexane-1,3-dione Chemical compound ClC1=CC(=C(C(=O)C2C(CC(C(C2=O)(C)C)C(F)(F)F)=O)C=C1)[N+](=O)[O-] KUTUJOZUNFHEQL-UHFFFAOYSA-N 0.000 claims 1
- LZMPUWLYWBQDKD-UHFFFAOYSA-N 2-(4-chloro-2-nitrobenzoyl)-4,6,6-trimethylcyclohex-4-ene-1,3-dione Chemical compound ClC1=CC(=C(C(=O)C2C(C(C=C(C2=O)C)(C)C)=O)C=C1)[N+](=O)[O-] LZMPUWLYWBQDKD-UHFFFAOYSA-N 0.000 claims 1
- OYFIKDIHZBKBAX-UHFFFAOYSA-N 2-(4-chloro-2-nitrobenzoyl)-4-methyl-5-(trifluoromethyl)cyclohexane-1,3-dione Chemical compound ClC1=CC(=C(C(=O)C2C(CC(C(C2=O)C)C(F)(F)F)=O)C=C1)[N+](=O)[O-] OYFIKDIHZBKBAX-UHFFFAOYSA-N 0.000 claims 1
- ASGKABVRXKRDBX-UHFFFAOYSA-N 2-(4-chloro-2-nitrobenzoyl)-4-phenylcyclohexane-1,3-dione Chemical compound [O-][N+](=O)C1=CC(Cl)=CC=C1C(=O)C1C(=O)C(C=2C=CC=CC=2)CCC1=O ASGKABVRXKRDBX-UHFFFAOYSA-N 0.000 claims 1
- LPFCVLBBMAFFOS-UHFFFAOYSA-N 2-(4-chloro-2-nitrobenzoyl)-5-(trifluoromethyl)cyclohexane-1,3-dione Chemical compound ClC1=CC(=C(C(=O)C2C(CC(CC2=O)C(F)(F)F)=O)C=C1)[N+](=O)[O-] LPFCVLBBMAFFOS-UHFFFAOYSA-N 0.000 claims 1
- MYNYFWLFSAIAHJ-UHFFFAOYSA-N 4,4,6,6-tetramethyl-2-(1-methyl-4-nitropyrazole-3-carbonyl)cyclohexane-1,3-dione Chemical compound CN1N=C(C(=C1)[N+](=O)[O-])C(=O)C1C(C(CC(C1=O)(C)C)(C)C)=O MYNYFWLFSAIAHJ-UHFFFAOYSA-N 0.000 claims 1
- VZHNIDFKKGGLMO-UHFFFAOYSA-N 4,4,6-trimethyl-2-(1-methyl-4-nitropyrazole-3-carbonyl)cyclohexane-1,3-dione Chemical compound CN1N=C(C(=C1)[N+](=O)[O-])C(=O)C1C(C(CC(C1=O)(C)C)C)=O VZHNIDFKKGGLMO-UHFFFAOYSA-N 0.000 claims 1
- QRRFZEDMEBSVER-UHFFFAOYSA-N 5-methyl-2-(1-methyl-4-nitropyrazole-3-carbonyl)cyclohexane-1,3-dione Chemical compound CN1N=C(C(=C1)[N+](=O)[O-])C(=O)C1C(CC(CC1=O)C)=O QRRFZEDMEBSVER-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- 150000001559 benzoic acids Chemical class 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 229920001577 copolymer Chemical group 0.000 claims 1
- 238000006266 etherification reaction Methods 0.000 claims 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 150000003413 spiro compounds Chemical class 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 abstract description 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 27
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 26
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
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- 239000002904 solvent Substances 0.000 description 9
- JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 8
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- VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
- MQRIUFVBEVFILS-UHFFFAOYSA-N n-methyl-1-naphthalen-1-ylmethanamine Chemical compound C1=CC=C2C(CNC)=CC=CC2=C1 MQRIUFVBEVFILS-UHFFFAOYSA-N 0.000 description 1
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- XCRBXWCUXJNEFX-UHFFFAOYSA-N peroxybenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1 XCRBXWCUXJNEFX-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
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- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
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- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
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- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
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- 239000011701 zinc Substances 0.000 description 1
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Classifications
-
- 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
- C07D231/12—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/45—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by at least one doubly—bound oxygen atom, not being part of a —CHO group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/55—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/56—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/57—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/58—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton the carbon skeleton being further substituted by halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/20—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/70—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/82—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/31—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
- C07C255/40—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by doubly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- Chemical & Material Sciences (AREA)
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- Pest Control & Pesticides (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pyrane Compounds (AREA)
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Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15069988A | 1988-02-01 | 1988-02-01 | |
| US150,699 | 1988-02-01 | ||
| US15842988A | 1988-02-22 | 1988-02-22 | |
| US158,429 | 1988-02-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1036202A true CN1036202A (zh) | 1989-10-11 |
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ID=26847934
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN89101743A Pending CN1036202A (zh) | 1988-02-01 | 1989-01-31 | 有机化合物或有关有机化合物的改进 |
Country Status (15)
| Country | Link |
|---|---|
| JP (1) | JPH021422A (ja) |
| KR (1) | KR890012938A (ja) |
| CN (1) | CN1036202A (ja) |
| AU (1) | AU2895589A (ja) |
| BR (1) | BR8900420A (ja) |
| DE (1) | DE3902818A1 (ja) |
| DK (1) | DK40989A (ja) |
| FR (1) | FR2626573A1 (ja) |
| GB (1) | GB2215333A (ja) |
| HU (1) | HUT50312A (ja) |
| IL (1) | IL89112A0 (ja) |
| IT (1) | IT1229560B (ja) |
| NL (1) | NL8900243A (ja) |
| PL (1) | PL277487A1 (ja) |
| PT (1) | PT89570B (ja) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106187866A (zh) * | 2016-07-12 | 2016-12-07 | 李为忠 | 吡啶酰基类化合物及其制备与应用 |
| WO2017075910A1 (zh) * | 2015-11-06 | 2017-05-11 | 青岛清原化合物有限公司 | 吡唑酮类化合物或其盐、制备方法、除草剂组合物及用途 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU616956B2 (en) * | 1988-04-18 | 1991-11-14 | Sandoz Ltd. | Substituted phenyl or pyrimidine bicyclodiones |
| ZA904951B (en) | 1989-07-04 | 1991-05-29 | Nippon Soda Co Limited | Substituted bicycloheptandione derivatives |
| ATE119146T1 (de) * | 1989-07-04 | 1995-03-15 | Nippon Soda Co | Substituierte bicycloheptadionderivate. |
| DE3924241A1 (de) * | 1989-07-21 | 1991-01-31 | Shell Int Research | Neue glyoxyl-cyclohexendione, verfahren zu ihrer herstellung, diese verbindungen enthaltende formulierungen und ihre verwendung |
| US5294598A (en) * | 1990-06-29 | 1994-03-15 | Nippon Soda Co., Ltd. | Herbicidal 3-substitutedbenzoyl-bicyclo[4,1,0]heptane-2, 4-dione derivatives |
| JPH04247052A (ja) * | 1991-01-31 | 1992-09-03 | Nippon Soda Co Ltd | ビシクロ〔4,1,0〕ヘプタン−2,4−ジオン誘導体、その製造法 |
| WO1993020037A1 (fr) * | 1992-03-27 | 1993-10-14 | Nippon Soda Co., Ltd. | Compose a base de cyclohexenone et production |
| EP0563817A3 (en) * | 1992-03-31 | 1993-11-03 | Hoechst Ag | Salts of 2-benzoyl-cyclohexane diones, selective herbicidal agents, process for their preparation and their use for combatting weeds |
| WO1994024099A1 (fr) * | 1993-04-19 | 1994-10-27 | Nippon Soda Co., Ltd. | Procede pour la production de benzene trisubstitue, et intermediaire |
| CA2257196A1 (en) * | 1996-06-06 | 1997-12-11 | Morris Padgett Rorer | Herbicidal pyridinyl and pyrazolylphenyl ketones |
| JP2002524554A (ja) | 1998-09-15 | 2002-08-06 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | 除草剤として有用なピリジンケトン |
| AR023071A1 (es) | 1998-12-23 | 2002-09-04 | Syngenta Participations Ag | Compuestos de piridincetona, compuestos intermediarios, composicion herbicida e inhibidora del crecimiento de plantas, metodo para controlar la vegetacion indeseada, metodo para inhibir el crecimiento de las plantas, y uso de la composicion para controlar el crecimiento indeseado de plantas. |
| US6673938B1 (en) | 1998-12-23 | 2004-01-06 | Syngenta Participations Ag | Substituted pyridine herbicides |
| GB9911792D0 (en) * | 1999-05-20 | 1999-07-21 | Zeneca Ltd | Herbicides |
| GT200100103A (es) | 2000-06-09 | 2002-02-21 | Nuevos herbicidas | |
| KR20040029410A (ko) | 2001-08-08 | 2004-04-06 | 바스프 악티엔게젤샤프트 | 벤조일시클로헥세논 유도체 |
| EP2394995B1 (en) | 2009-02-03 | 2014-01-15 | Kumiai Chemical Industry CO., LTD. | Ring-fused 2-pyridone derivatives and herbicides |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4350705A (en) * | 1979-03-31 | 1982-09-21 | Eisai Co., Ltd. | Cyclohexane derivatives, process for preparation thereof and medicines containing these cyclohexane derivatives |
| PH21446A (en) * | 1983-09-16 | 1987-10-20 | Stauffer Chemical Co | Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones |
| EP0137963B1 (en) * | 1983-09-16 | 1988-09-28 | Stauffer Chemical Company | Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones |
| IL77350A (en) * | 1984-12-20 | 1991-01-31 | Stauffer Chemical Co | Production of acylated diketonic compounds |
| IL77349A (en) * | 1984-12-20 | 1990-07-12 | Stauffer Chemical Co | 2-(2'-nitrobenzoyl)-1,3-cyclohexanediones,their preparation and their use as herbicides |
| IL77348A (en) * | 1984-12-20 | 1991-05-12 | Stauffer Chemical Co | 2-(2'-substituted benzoyl)-1,3-cyclohexanediones,their preparation and their use as herbicides |
| TR22585A (tr) * | 1984-12-20 | 1987-12-07 | Stauffer Chemical Co | Bazi 2-(2'-alkilbenzoil)-1,3-sikloheksandion'lar |
-
1989
- 1989-01-20 HU HU89232A patent/HUT50312A/hu unknown
- 1989-01-30 FR FR8901257A patent/FR2626573A1/fr not_active Withdrawn
- 1989-01-30 DK DK040989A patent/DK40989A/da not_active Application Discontinuation
- 1989-01-30 PT PT89570A patent/PT89570B/pt not_active IP Right Cessation
- 1989-01-30 GB GB8902016A patent/GB2215333A/en not_active Withdrawn
- 1989-01-30 IL IL89112A patent/IL89112A0/xx unknown
- 1989-01-31 IT IT8947598A patent/IT1229560B/it active
- 1989-01-31 AU AU28955/89A patent/AU2895589A/en not_active Abandoned
- 1989-01-31 JP JP1022460A patent/JPH021422A/ja active Pending
- 1989-01-31 PL PL27748789A patent/PL277487A1/xx unknown
- 1989-01-31 CN CN89101743A patent/CN1036202A/zh active Pending
- 1989-01-31 KR KR1019890001047A patent/KR890012938A/ko not_active Withdrawn
- 1989-01-31 BR BR898900420A patent/BR8900420A/pt not_active IP Right Cessation
- 1989-01-31 DE DE3902818A patent/DE3902818A1/de not_active Withdrawn
- 1989-02-01 NL NL8900243A patent/NL8900243A/nl not_active Application Discontinuation
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017075910A1 (zh) * | 2015-11-06 | 2017-05-11 | 青岛清原化合物有限公司 | 吡唑酮类化合物或其盐、制备方法、除草剂组合物及用途 |
| US11076594B2 (en) | 2015-11-06 | 2021-08-03 | Qingdao Kingagroot Chemical Compounds Co., Ltd. | Pyrazolone compound or salt thereof, preparation method therefor, herbicide composition and use thereof |
| CN106187866A (zh) * | 2016-07-12 | 2016-12-07 | 李为忠 | 吡啶酰基类化合物及其制备与应用 |
| CN106187866B (zh) * | 2016-07-12 | 2019-04-16 | 李为忠 | 吡啶酰基类化合物及其制备与应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH021422A (ja) | 1990-01-05 |
| FR2626573A1 (fr) | 1989-08-04 |
| IL89112A0 (en) | 1989-08-15 |
| GB8902016D0 (en) | 1989-03-22 |
| DE3902818A1 (de) | 1989-08-10 |
| IT1229560B (it) | 1991-09-04 |
| PL277487A1 (en) | 1989-10-16 |
| DK40989D0 (da) | 1989-01-30 |
| HUT50312A (en) | 1990-01-29 |
| DK40989A (da) | 1989-08-02 |
| NL8900243A (nl) | 1989-09-01 |
| KR890012938A (ko) | 1989-09-20 |
| PT89570B (pt) | 1994-05-31 |
| GB2215333A (en) | 1989-09-20 |
| IT8947598A0 (it) | 1989-01-31 |
| BR8900420A (pt) | 1989-09-26 |
| AU2895589A (en) | 1989-08-03 |
| PT89570A (pt) | 1989-10-04 |
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