IL93623A - History of 2-Propenyl Transformed Nitric Trotocycles, Processes for Their Preparation, Fungicides Preparations Containing Them and Methods for Their Use - Google Patents

History of 2-Propenyl Transformed Nitric Trotocycles, Processes for Their Preparation, Fungicides Preparations Containing Them and Methods for Their Use

Info

Publication number: IL93623A
Authority: IL; Israel
Prior art keywords: compound; substituted; structural formula; accordance; phenyl
Prior art date: 1989-03-09

Application number

IL9362390A

Other languages

English (en)

Hebrew (he)

Other versions

IL93623A0 (en

Original Assignee

Uniroyal Chem Co Inc

Uniroyal Chemical Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1989-03-09

Filing date

1990-03-04

Publication date

1994-07-31

1990-03-04 Application filed by Uniroyal Chem Co Inc, Uniroyal Chemical Ltd filed Critical Uniroyal Chem Co Inc

1990-12-23 Publication of IL93623A0 publication Critical patent/IL93623A0/xx

1994-07-31 Publication of IL93623A publication Critical patent/IL93623A/en

Links

238000000034 method Methods 0.000 title claims abstract description 58
239000000203 mixture Substances 0.000 title claims abstract description 47
229910052757 nitrogen Inorganic materials 0.000 title claims abstract description 18
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title claims abstract description 16
230000000855 fungicidal effect Effects 0.000 title claims description 13
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 title claims description 10
125000000623 heterocyclic group Chemical group 0.000 title claims description 10
238000002360 preparation method Methods 0.000 title description 10
150000001875 compounds Chemical class 0.000 claims abstract description 143
241000233866 Fungi Species 0.000 claims abstract description 54
-1 phenoxy, substituted phenoxy, benzyl Chemical group 0.000 claims abstract description 31
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 20
125000000217 alkyl group Chemical group 0.000 claims abstract description 15
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 15
150000003839 salts Chemical class 0.000 claims abstract description 15
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 9
150000001412 amines Chemical class 0.000 claims abstract description 7
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 7
125000005843 halogen group Chemical group 0.000 claims abstract description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
239000002904 solvent Substances 0.000 claims description 18
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
239000002689 soil Substances 0.000 claims description 8
238000000576 coating method Methods 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 5
239000011248 coating agent Substances 0.000 claims description 5
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
239000007818 Grignard reagent Substances 0.000 claims description 4
150000004795 grignard reagents Chemical class 0.000 claims description 4
125000001041 indolyl group Chemical group 0.000 claims description 4
125000005956 isoquinolyl group Chemical group 0.000 claims description 4
125000005493 quinolyl group Chemical group 0.000 claims description 4
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
125000004076 pyridyl group Chemical group 0.000 claims description 3
239000000376 reactant Substances 0.000 claims description 3
229920006395 saturated elastomer Polymers 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
125000004434 sulfur atom Chemical group 0.000 claims description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
239000008096 xylene Substances 0.000 claims description 3
125000002785 azepinyl group Chemical group 0.000 claims description 2
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 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
150000002430 hydrocarbons Chemical class 0.000 claims description 2
239000012442 inert solvent Substances 0.000 claims description 2
125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 2
125000002757 morpholinyl group Chemical group 0.000 claims description 2
125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 2
125000000168 pyrrolyl group Chemical group 0.000 claims description 2
125000004568 thiomorpholinyl group Chemical group 0.000 claims description 2
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 claims 1
229940117389 dichlorobenzene Drugs 0.000 claims 1
238000006243 chemical reaction Methods 0.000 abstract description 6
230000015572 biosynthetic process Effects 0.000 abstract description 5
150000002391 heterocyclic compounds Chemical class 0.000 abstract description 5
125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 1
125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 50
201000010099 disease Diseases 0.000 description 26
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 26
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
239000000839 emulsion Substances 0.000 description 15
240000005979 Hordeum vulgare Species 0.000 description 14
238000012360 testing method Methods 0.000 description 14
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241000315044 Passalora arachidicola Species 0.000 description 10
238000009835 boiling Methods 0.000 description 10
230000009885 systemic effect Effects 0.000 description 10
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
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239000000243 solution Substances 0.000 description 9
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239000000417 fungicide Substances 0.000 description 8
239000007788 liquid Substances 0.000 description 8
239000000047 product Substances 0.000 description 8
241000213004 Alternaria solani Species 0.000 description 7
241000123650 Botrytis cinerea Species 0.000 description 7
241000223221 Fusarium oxysporum Species 0.000 description 7
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238000011081 inoculation Methods 0.000 description 7
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PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
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235000011152 sodium sulphate Nutrition 0.000 description 4
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101150041968 CDC13 gene Proteins 0.000 description 3
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OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
230000018109 developmental process Effects 0.000 description 3
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238000002844 melting Methods 0.000 description 3
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239000000843 powder Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
NOKIROATSCVWNY-UHFFFAOYSA-N 1-[2-(chloromethyl)prop-2-enyl]-4-phenylbenzene Chemical compound C1=CC(CC(=C)CCl)=CC=C1C1=CC=CC=C1 NOKIROATSCVWNY-UHFFFAOYSA-N 0.000 description 2
PEXNGRHUXFJLIS-UHFFFAOYSA-N 1-tert-butyl-4-[2-(chloromethyl)prop-2-enyl]benzene Chemical compound CC(C)(C)C1=CC=C(CC(=C)CCl)C=C1 PEXNGRHUXFJLIS-UHFFFAOYSA-N 0.000 description 2
IDWRJRPUIXRFRX-UHFFFAOYSA-N 3,5-dimethylpiperidine Chemical compound CC1CNCC(C)C1 IDWRJRPUIXRFRX-UHFFFAOYSA-N 0.000 description 2
QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical group N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 2
235000017060 Arachis glabrata Nutrition 0.000 description 2
235000010777 Arachis hypogaea Nutrition 0.000 description 2
235000018262 Arachis monticola Nutrition 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
241001157813 Cercospora Species 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
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DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
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JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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238000001914 filtration Methods 0.000 description 2
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239000007789 gas Substances 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
230000003902 lesion Effects 0.000 description 2
239000011707 mineral Substances 0.000 description 2
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239000003960 organic solvent Substances 0.000 description 2
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230000002829 reductive effect Effects 0.000 description 2
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238000006467 substitution reaction Methods 0.000 description 2
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238000009736 wetting Methods 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
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XHCAGOVGSDHHNP-UHFFFAOYSA-N 1-bromo-4-tert-butylbenzene Chemical compound CC(C)(C)C1=CC=C(Br)C=C1 XHCAGOVGSDHHNP-UHFFFAOYSA-N 0.000 description 1
HNVIQLPOGUDBSU-UHFFFAOYSA-N 2,6-dimethylmorpholine Chemical compound CC1CNCC(C)O1 HNVIQLPOGUDBSU-UHFFFAOYSA-N 0.000 description 1
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JEGMWWXJUXDNJN-UHFFFAOYSA-N 3-methylpiperidine Chemical compound CC1CCCNC1 JEGMWWXJUXDNJN-UHFFFAOYSA-N 0.000 description 1
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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
- C07D295/02—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 containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—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 containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
- C07D295/03—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 containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to acyclic carbon 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
- C07D295/02—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 containing only hydrogen and carbon atoms in addition to the ring hetero elements
- 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
- A01N43/36—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
- A01N43/38—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 condensed with carbocyclic 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
- A01N43/34—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
- A01N43/34—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
- A01N43/42—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 condensed with carbocyclic 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/06—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with radicals, containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
- C07D215/06—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms having only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to the ring nitrogen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- 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
- C07D295/06—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 halogen atoms or nitro radicals
- 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
- C07D295/06—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 halogen atoms or nitro radicals
- C07D295/073—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 halogen atoms or nitro radicals with the ring nitrogen atoms and the substituents separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
- 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
- C07D295/096—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 separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Indole Compounds (AREA)
Other In-Based Heterocyclic Compounds (AREA)
Hydrogenated Pyridines (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Pyrrole Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

IL9362390A 1989-03-09 1990-03-04 History of 2-Propenyl Transformed Nitric Trotocycles, Processes for Their Preparation, Fungicides Preparations Containing Them and Methods for Their Use IL93623A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/321,028 US4950671A (en)	1989-03-09	1989-03-09	Substituted 2-propenyl derivatives of pyridine

Publications (2)

Publication Number	Publication Date
IL93623A0 IL93623A0 (en)	1990-12-23
IL93623A true IL93623A (en)	1994-07-31

Family

ID=23248865

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9362390A IL93623A (en)	1989-03-09	1990-03-04	History of 2-Propenyl Transformed Nitric Trotocycles, Processes for Their Preparation, Fungicides Preparations Containing Them and Methods for Their Use

Country Status (16)

Country	Link
US (1)	US4950671A (de)
EP (1)	EP0462148B1 (de)
JP (1)	JPH0688967B2 (de)
KR (1)	KR920701186A (de)
CN (1)	CN1026046C (de)
AT (1)	ATE106396T1 (de)
AU (1)	AU629619B2 (de)
BR (1)	BR9007118A (de)
CA (1)	CA2050352C (de)
DE (1)	DE69009466T2 (de)
DK (1)	DK0462148T3 (de)
ES (1)	ES2056451T3 (de)
FI (1)	FI95243C (de)
HU (1)	HU206693B (de)
IL (1)	IL93623A (de)
WO (1)	WO1990010627A1 (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5384315A (en) *	1994-02-14	1995-01-24	Uniroyal Chemical Company, Inc.	Thiophene substituted cycloamines, compositions and use
US5580544A (en) *	1995-03-29	1996-12-03	Uniroyal Chemical Company, Inc.	Paste formulation useful for seed treatment and foliar treatment of plants
US5719103A (en) *	1996-05-02	1998-02-17	Uniroyal Chemical Company, Inc.	Powder formulation useful for seed treatment and foliar treatment of plants
US7081436B2 (en)	2001-01-26	2006-07-25	General Electric Company	Paste formulation for seed treatment of plants
US20070293548A1 (en) *	2006-03-31	2007-12-20	Wang Eric Y	Inhibitors of semicarbazide-sensitive amine oxidase (SSAO) and VAP-1 mediated adhesion useful for treatment and prevention of diseases
MX2010002650A (es)	2007-09-14	2010-03-30	Du Pont	Metodo de desinfeccion de semilla liquido para desinfectar cantidades pequeñas de semilla.

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AT354187B (de) *	1976-11-22	1979-12-27	Hoffmann La Roche	Fungizides mittel
DE2830127A1 (de) *	1978-07-08	1980-01-17	Basf Ag	N-arylpropyl-substituierte cyclische amine
FI874121A7 (fi) *	1986-09-24	1988-03-25	Sumitomo Chemical Co	Heterocykliska foereningar, och deras framstaellning och anvaendning.

1989
- 1989-03-09 US US07/321,028 patent/US4950671A/en not_active Expired - Lifetime
1990
- 1990-02-27 KR KR1019910701049A patent/KR920701186A/ko not_active Ceased
- 1990-02-27 ES ES90904130T patent/ES2056451T3/es not_active Expired - Lifetime
- 1990-02-27 JP JP2504341A patent/JPH0688967B2/ja not_active Expired - Fee Related
- 1990-02-27 DK DK90904130.3T patent/DK0462148T3/da active
- 1990-02-27 HU HU902279A patent/HU206693B/hu not_active IP Right Cessation
- 1990-02-27 EP EP90904130A patent/EP0462148B1/de not_active Expired - Lifetime
- 1990-02-27 DE DE69009466T patent/DE69009466T2/de not_active Expired - Fee Related
- 1990-02-27 AU AU51931/90A patent/AU629619B2/en not_active Ceased
- 1990-02-27 AT AT90904130T patent/ATE106396T1/de active
- 1990-02-27 WO PCT/US1990/000735 patent/WO1990010627A1/en not_active Ceased
- 1990-02-27 BR BR909007118A patent/BR9007118A/pt not_active IP Right Cessation
- 1990-02-27 CA CA002050352A patent/CA2050352C/en not_active Expired - Fee Related
- 1990-03-03 CN CN90101224A patent/CN1026046C/zh not_active Expired - Fee Related
- 1990-03-04 IL IL9362390A patent/IL93623A/en unknown
1991
- 1991-09-06 FI FI914224A patent/FI95243C/fi active

Also Published As

Publication number	Publication date
CA2050352A1 (en)	1990-09-10
CN1045391A (zh)	1990-09-19
AU5193190A (en)	1990-10-09
ES2056451T3 (es)	1994-10-01
DE69009466D1 (en)	1994-07-07
DK0462148T3 (da)	1994-09-19
IL93623A0 (en)	1990-12-23
ATE106396T1 (de)	1994-06-15
HU206693B (en)	1992-12-28
DE69009466T2 (de)	1994-09-29
FI95243C (fi)	1996-01-10
HU902279D0 (en)	1991-12-30
US4950671A (en)	1990-08-21
JPH04500212A (ja)	1992-01-16
AU629619B2 (en)	1992-10-08
JPH0688967B2 (ja)	1994-11-09
HUT58710A (en)	1992-03-30
EP0462148B1 (de)	1994-06-01
FI95243B (fi)	1995-09-29
KR920701186A (ko)	1992-08-11
CA2050352C (en)	2000-02-22
CN1026046C (zh)	1994-10-05
EP0462148A1 (de)	1991-12-27
WO1990010627A1 (en)	1990-09-20
BR9007118A (pt)	1991-12-17
FI914224A0 (fi)	1991-09-06

Legal Events

Date	Code	Title	Description
1996-06-18	KB	Patent renewed
2000-08-13	KB	Patent renewed

Publication	Publication Date	Title
RU2017735C1 (ru)	1994-08-15	Способ получения производных 2-анилинопиримидина или их кислотно-аддитивных солей
EP0462148B1 (de)	1994-06-01	Substituierte 2-propenyl-derivate von stickstoff-heterocyclen
EP0548285B1 (de)	1995-10-18	3,3-bis[alkylthio]-2-pyridylacrylsäurederivate als fungizide
IE861879L (en)	1987-01-25	1 - dimethyl carbamoyl-3-substituted¹-5-substituted-1h-1,2,4- triazoles
US4496559A (en)	1985-01-29	2-Selenopyridine-N-oxide derivatives and their use as fungicides and bactericides
US5384315A (en)	1995-01-24	Thiophene substituted cycloamines, compositions and use
US5071862A (en)	1991-12-10	2-(3-oxypyridinyl)-1,3-dioxolane and dioxane compounds, compositions containing same and process for controlling fungi using same
US4966910A (en)	1990-10-30	Fungicidal oxathiin azoles
US5006153A (en)	1991-04-09	Azole derivatives of naphthalenone oxime ethers
EP0494227B1 (de)	1994-10-12	Fungizide 3-imino-1,4-oxathiine
EP0351979A2 (de)	1990-01-24	Azolderivate von Naphthalenonoximethern
EP0663904A1 (de)	1995-07-26	Fungizide substituierte azolderivate
US5145982A (en)	1992-09-08	Fungicidal oxathin azoles
JPS6026109B2 (ja)	1985-06-21	新規１−アシルオキシ−１−フエニル−２−アゾリル−エタンまたはその塩、その製造方法およびそれを活性成分として含有する殺菌剤若しくは殺線虫剤組成物
US4943311A (en)	1990-07-24	Azole derivatives of spiroheterocycles
US5081143A (en)	1992-01-14	Fungicidal oxathiin azoles
JPH04187677A (ja)	1992-07-06	シンノリン誘導体および農園芸用殺菌剤