HU212751B - Fungicidal composition - Google Patents
Fungicidal composition Download PDFInfo
- Publication number
- HU212751B HU212751B HU91822A HU82291A HU212751B HU 212751 B HU212751 B HU 212751B HU 91822 A HU91822 A HU 91822A HU 82291 A HU82291 A HU 82291A HU 212751 B HU212751 B HU 212751B
- Authority
- HU
- Hungary
- Prior art keywords
- formula
- phenyl
- active ingredient
- methyl
- oxa
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 25
- 230000000855 fungicidal effect Effects 0.000 title claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 38
- -1 1-methyl-2,2-dichlorocyclopropyl Chemical group 0.000 claims description 22
- 239000004480 active ingredient Substances 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 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 description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- HNVIQLPOGUDBSU-UHFFFAOYSA-N 2,6-dimethylmorpholine Chemical compound CC1CNCC(C)O1 HNVIQLPOGUDBSU-UHFFFAOYSA-N 0.000 claims 1
- PLYTVAFAKDFFKM-UHFFFAOYSA-N 3,4-dimethylmorpholine Chemical compound CC1COCCN1C PLYTVAFAKDFFKM-UHFFFAOYSA-N 0.000 claims 1
- NJTZHGRSMSHOJI-UHFFFAOYSA-N 4-[2-[3-[(2,2-dichloro-1-methylcyclopropyl)methoxy]phenoxy]propyl]-2,6-dimethylmorpholine Chemical group C=1C=CC(OCC2(C)C(C2)(Cl)Cl)=CC=1OC(C)CN1CC(C)OC(C)C1 NJTZHGRSMSHOJI-UHFFFAOYSA-N 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000005554 pyridyloxy group Chemical group 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 15
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- 238000005481 NMR spectroscopy Methods 0.000 description 2
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000520648 Pyrenophora teres Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 150000001728 carbonyl compounds Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
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- WYFDDFHVCHDXIG-UHFFFAOYSA-N 4-[1-(2,6-dimethylmorpholin-4-yl)propan-2-yloxy]phenol Chemical compound C=1C=C(O)C=CC=1OC(C)CN1CC(C)OC(C)C1 WYFDDFHVCHDXIG-UHFFFAOYSA-N 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
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- 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
- C07D213/60—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 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
- C07D213/643—2-Phenoxypyridines; Derivatives thereof
-
- 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
- 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
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered 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
- A01N43/72—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
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
- C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
- C07C217/18—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted
- C07C217/20—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted by halogen atoms, by trihalomethyl, nitro or nitroso groups, or by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/104—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/108—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- Chemical & Material Sciences (AREA)
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- Wood Science & Technology (AREA)
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Claims (11)
- SZABADALMI IGÉNYPONTOK1. Fungicid készítmény, azzal jellemezve, hogy hatóanyagként 0,1-95 tömeg% mennyiségben valamely (I) általános képletű N-(fenoxi-alkil)-morfolin-származékot vagy mezőgazdaságilag alkalmazható sóját tartalmazza - az (I) általános képletbenR1 hidrogénatomot vagy 1-3 szénatomos alkilcsoportot jelent;n értéke 0 vagy 1;Y jelentése (VI) általános képletű csoport vagy halogénatommal, 1-4 szénatomos alkil- és/vagy 1-2 szénatomos halogén-alkil-csoporttal legfeljebb háromszorosan szubsztituált piridil- vagy 3-6 szénatomos cikloalkilcsoport, és a (VI) általános képletben C, D és E egymástól függetlenül hidrogénatomot vagy 1-4 szénatomos alkil- vagy fenilcsoportot jelentenek; ésRn, Rni és R,v 1-4 szénatomos alkilcsoportot jelentenek.
- 2. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként olyan (I) általános képletű vegyületet tartalmaz, amelynek képletében Y jelentése ciklohexil-, ciklopropil-, ciklopentil-, ciklobutil-, 1metil-2,2-diklór-ciklopropil-, trimetíl-szilil-, terc-butildimetil-szilil- vagy dimetil-fenil-szilil-csoport.
- 3. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-{3-[4-(trimetil-szilil-metoxi)-fenil]-2-metil-3oxa-propil}-2,6-dimetil-morfolint tartalmaz.
- 4. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-{3-(3-(2-(4,6-diklór-piridil)-oxi)-fenil]-2-metil3-oxa-propil}-2,6-dimetil-morfolint tartalmaz.
- 5. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-{3-(3-(2,2-diklór-1 -metil-ciklopropil-metoxi)-fenil]-2-metil-3-oxa-propil)-2,6-dimetil-morfolint tartalmaz.
- 6. Az 1. igénypont szerinti készítmény, azzal jellemezve. hogy hatóanyagként az (I) általános képlet alá eső 4- {3-[3-/5-(trifluor-metil)-2-piridil-oxi/-fenil]-2metil-3-oxa-propil}-2,6-dimetil-morfolint tartalmaz.
- 7. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-{3-[3-/3-klór-5-(trifluor-metil)-piridil-oxi/-fenil]-2-metil-3-oxa-propil)-2,6-dimetil-morfolint tartalmaz.
- 8. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-{3-[4-(dimetil-fenil-szilil-metoxi)-fenil]-2-metil3-oxa-propil)-2,6-dimetil-morfolint tartalmaz.
- 9. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-{3-[3-(dimetil-fenil-szilil-metoxi)-fenil]-2-metil3-oxa-propil}-2,6-dimetil-morfolint tartalmaz.
- 10. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-(3-(3-/1 -(trimetil-szilil)-etoxi/-fenil]-2-metil-3oxa-propil }-2,6-dimetil-morfolint tartalmaz.HU 212 751 Β
- 11. Az 1. igénypont szerinti készítmény, azzal jellemezve, hogy hatóanyagként az (I) általános képlet alá eső 4-{3-[4-/l-(trimetil-szilil)-etoxi/-fenil]-2-metil-3 oxa-propil}-2,6-dimetil-morfolint tartalmaz.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT19653A IT1240598B (it) | 1990-03-13 | 1990-03-13 | Derivati amminici ad azione antifungina |
Publications (2)
Publication Number | Publication Date |
---|---|
HUT56482A HUT56482A (en) | 1991-09-30 |
HU212751B true HU212751B (en) | 1996-10-28 |
Family
ID=11160100
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU91822A HU212751B (en) | 1990-03-13 | 1991-03-13 | Fungicidal composition |
Country Status (18)
Country | Link |
---|---|
US (1) | US5385892A (hu) |
EP (1) | EP0446873B1 (hu) |
JP (1) | JPH05310652A (hu) |
KR (1) | KR100193159B1 (hu) |
AT (1) | ATE128963T1 (hu) |
AU (1) | AU637204B2 (hu) |
BR (1) | BR9100971A (hu) |
CA (1) | CA2038076A1 (hu) |
DE (1) | DE69113659T2 (hu) |
DK (1) | DK0446873T3 (hu) |
ES (1) | ES2078369T3 (hu) |
GR (1) | GR3017838T3 (hu) |
HU (1) | HU212751B (hu) |
IL (1) | IL97499A (hu) |
IT (1) | IT1240598B (hu) |
NO (1) | NO179835C (hu) |
RU (1) | RU2038353C1 (hu) |
ZA (1) | ZA911850B (hu) |
Families Citing this family (2)
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JP2007500703A (ja) * | 2003-07-28 | 2007-01-18 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ベンズイミダゾール、ベンズチアゾールおよびベンゾキサゾール誘導体およびlta4hモジュレーターとしてのそれらの使用 |
CL2008000468A1 (es) * | 2007-02-14 | 2008-08-22 | Janssen Pharmaceutica Nv | Uso de compuestos derivados de heterociclos, inhibidores de leucotrina a4 hidrolasa (lta4h), utiles para tratar o prevenir la dermatitis, acne, infarto al miocardio, dolor, picazon, gingivitis, cancer, artritis, entre otras. |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
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DE167035C (hu) * | ||||
DE1670635A1 (de) * | 1967-09-06 | 1970-08-06 | Eisai Co Ltd | o-(ss-Morpholinoaethoxy) diphenylaether |
US3988475A (en) * | 1974-02-05 | 1976-10-26 | Istituto Luso Farmaco D'italia S.R.L. | Phenoxyalkylamines |
CA1086733A (en) * | 1976-12-06 | 1980-09-30 | Ryoji Kikumoto | Pharmaceutically active 2-substituted-1-(omega- aminoalkoxy) benzenes |
GB2078217B (en) * | 1980-06-14 | 1984-01-11 | Beecham Group Ltd | Phenolic ethers their preparation and use |
US4393061A (en) * | 1982-06-21 | 1983-07-12 | Stiefel Laboratories, Inc. | Anesthetic-antipruritic morpholine compounds, compositions and use |
DE3410070A1 (de) * | 1984-03-20 | 1985-10-03 | Hoechst Ag, 6230 Frankfurt | 1-(2-aryl-1,3-dioxolan-2-ylmethyl)-azole, ihre salze, verfahren zu ihrer herstellung, sie enthaltende zubereitungen und ihre verwendung |
DK368687A (da) * | 1986-11-21 | 1988-05-22 | Cheminova As | Aminoalkylerede hydroxyforbindelser og deres anvendelse som fungicider |
-
1990
- 1990-03-13 IT IT19653A patent/IT1240598B/it active IP Right Grant
-
1991
- 1991-03-11 IL IL9749991A patent/IL97499A/en not_active IP Right Cessation
- 1991-03-11 AU AU72794/91A patent/AU637204B2/en not_active Ceased
- 1991-03-12 AT AT91103764T patent/ATE128963T1/de not_active IP Right Cessation
- 1991-03-12 DE DE69113659T patent/DE69113659T2/de not_active Expired - Fee Related
- 1991-03-12 CA CA002038076A patent/CA2038076A1/en not_active Abandoned
- 1991-03-12 ES ES91103764T patent/ES2078369T3/es not_active Expired - Lifetime
- 1991-03-12 EP EP91103764A patent/EP0446873B1/en not_active Expired - Lifetime
- 1991-03-12 BR BR919100971A patent/BR9100971A/pt not_active Application Discontinuation
- 1991-03-12 DK DK91103764.6T patent/DK0446873T3/da active
- 1991-03-12 NO NO910965A patent/NO179835C/no unknown
- 1991-03-12 RU SU914894899A patent/RU2038353C1/ru active
- 1991-03-13 ZA ZA911850A patent/ZA911850B/xx unknown
- 1991-03-13 JP JP3073837A patent/JPH05310652A/ja active Pending
- 1991-03-13 HU HU91822A patent/HU212751B/hu not_active IP Right Cessation
- 1991-03-13 KR KR1019910004009A patent/KR100193159B1/ko not_active IP Right Cessation
-
1993
- 1993-01-04 US US08/001,919 patent/US5385892A/en not_active Expired - Fee Related
-
1995
- 1995-10-24 GR GR950402936T patent/GR3017838T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
IL97499A (en) | 1994-11-11 |
NO910965L (no) | 1991-09-16 |
JPH05310652A (ja) | 1993-11-22 |
ES2078369T3 (es) | 1995-12-16 |
ATE128963T1 (de) | 1995-10-15 |
AU637204B2 (en) | 1993-05-20 |
NO179835C (no) | 1996-12-27 |
ZA911850B (en) | 1991-12-24 |
IT9019653A0 (it) | 1990-03-13 |
IL97499A0 (en) | 1992-06-21 |
EP0446873B1 (en) | 1995-10-11 |
HUT56482A (en) | 1991-09-30 |
IT9019653A1 (it) | 1991-09-13 |
DE69113659T2 (de) | 1996-04-04 |
IT1240598B (it) | 1993-12-17 |
KR100193159B1 (ko) | 1999-06-15 |
EP0446873A1 (en) | 1991-09-18 |
CA2038076A1 (en) | 1991-09-14 |
NO910965D0 (no) | 1991-03-12 |
RU2038353C1 (ru) | 1995-06-27 |
BR9100971A (pt) | 1991-11-05 |
DK0446873T3 (da) | 1996-02-19 |
DE69113659D1 (de) | 1995-11-16 |
KR910016729A (ko) | 1991-11-05 |
US5385892A (en) | 1995-01-31 |
NO179835B (no) | 1996-09-16 |
GR3017838T3 (en) | 1996-01-31 |
AU7279491A (en) | 1991-09-19 |
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