SI9200391B - Derivati fungicidov 2-imidazolin-5-onov in 2-imidazolin-5-tionov - Google Patents
Derivati fungicidov 2-imidazolin-5-onov in 2-imidazolin-5-tionov Download PDFInfo
- Publication number
- SI9200391B SI9200391B SI9200391A SI9200391A SI9200391B SI 9200391 B SI9200391 B SI 9200391B SI 9200391 A SI9200391 A SI 9200391A SI 9200391 A SI9200391 A SI 9200391A SI 9200391 B SI9200391 B SI 9200391B
- Authority
- SI
- Slovenia
- Prior art keywords
- carbon atoms
- group
- radical
- alkyl
- optionally substituted
- Prior art date
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- NXRIDTLKJCKPOG-UHFFFAOYSA-N 1,4-dihydroimidazole-5-thione Chemical class S=C1CN=CN1 NXRIDTLKJCKPOG-UHFFFAOYSA-N 0.000 title claims abstract 3
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 title claims abstract 3
- 230000000855 fungicidal effect Effects 0.000 title claims 3
- 150000001875 compounds Chemical class 0.000 claims abstract 36
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 14
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 13
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 8
- 238000002360 preparation method Methods 0.000 claims abstract 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract 4
- 125000005843 halogen group Chemical group 0.000 claims abstract 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 98
- -1 haloalkyl radical Chemical class 0.000 claims 78
- 125000000217 alkyl group Chemical group 0.000 claims 34
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 25
- 125000003342 alkenyl group Chemical group 0.000 claims 22
- 150000003254 radicals Chemical class 0.000 claims 18
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 17
- 125000001188 haloalkyl group Chemical group 0.000 claims 17
- 238000000034 method Methods 0.000 claims 16
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 15
- 125000000304 alkynyl group Chemical group 0.000 claims 14
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims 12
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 11
- 125000003710 aryl alkyl group Chemical group 0.000 claims 10
- 125000002252 acyl group Chemical group 0.000 claims 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 8
- 125000002541 furyl group Chemical group 0.000 claims 8
- 125000001624 naphthyl group Chemical group 0.000 claims 8
- 125000004076 pyridyl group Chemical group 0.000 claims 8
- 125000001544 thienyl group Chemical group 0.000 claims 8
- 239000002904 solvent Substances 0.000 claims 7
- 125000004414 alkyl thio group Chemical group 0.000 claims 6
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims 6
- 125000005164 aryl thioalkyl group Chemical group 0.000 claims 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 125000004995 haloalkylthio group Chemical group 0.000 claims 6
- 125000005956 isoquinolyl group Chemical group 0.000 claims 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 5
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000005493 quinolyl group Chemical group 0.000 claims 5
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 4
- 125000004429 atom Chemical group 0.000 claims 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 claims 3
- IPEWNTLWCRYSRY-UHFFFAOYSA-N [CH2]C1=CC=CO1 Chemical compound [CH2]C1=CC=CO1 IPEWNTLWCRYSRY-UHFFFAOYSA-N 0.000 claims 3
- 125000003302 alkenyloxy group Chemical group 0.000 claims 3
- 125000005108 alkenylthio group Chemical group 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000005256 alkoxyacyl group Chemical group 0.000 claims 3
- 125000005133 alkynyloxy group Chemical group 0.000 claims 3
- 125000003277 amino group Chemical group 0.000 claims 3
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims 3
- 125000005099 aryl alkyl carbonyl group Chemical group 0.000 claims 3
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 3
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 3
- 239000000460 chlorine Substances 0.000 claims 3
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims 3
- 125000005252 haloacyl group Chemical group 0.000 claims 3
- 125000004438 haloalkoxy group Chemical group 0.000 claims 3
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims 3
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims 3
- 125000004193 piperazinyl group Chemical group 0.000 claims 3
- 125000005400 pyridylcarbonyl group Chemical group N1=C(C=CC=C1)C(=O)* 0.000 claims 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 3
- 239000011593 sulfur Substances 0.000 claims 3
- 125000004434 sulfur atom Chemical group 0.000 claims 3
- 125000005301 thienylmethyl group Chemical group [H]C1=C([H])C([H])=C(S1)C([H])([H])* 0.000 claims 3
- KKFDJZZADQONDE-UHFFFAOYSA-N (hydridonitrato)hydroxidocarbon(.) Chemical compound O[C]=N KKFDJZZADQONDE-UHFFFAOYSA-N 0.000 claims 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 2
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims 2
- 239000003849 aromatic solvent Substances 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 150000005840 aryl radicals Chemical class 0.000 claims 2
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims 2
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 claims 2
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 229910052740 iodine Chemical group 0.000 claims 2
- 238000007254 oxidation reaction Methods 0.000 claims 2
- 125000005188 oxoalkyl group Chemical group 0.000 claims 2
- 150000002978 peroxides Chemical class 0.000 claims 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 2
- SCCCIUGOOQLDGW-UHFFFAOYSA-N 1,1-dicyclohexylurea Chemical group C1CCCCC1N(C(=O)N)C1CCCCC1 SCCCIUGOOQLDGW-UHFFFAOYSA-N 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical group C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- AZZPAAYLMUOGNP-UHFFFAOYSA-N 2-methylsulfanyl-1,4-dihydroimidazol-5-one Chemical class CSC1=NC(=O)CN1 AZZPAAYLMUOGNP-UHFFFAOYSA-N 0.000 claims 1
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 claims 1
- 208000031888 Mycoses Diseases 0.000 claims 1
- SPTHOEKISABNFX-UHFFFAOYSA-N OC(=S)S=N Chemical compound OC(=S)S=N SPTHOEKISABNFX-UHFFFAOYSA-N 0.000 claims 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000011149 active material Substances 0.000 claims 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims 1
- 150000004703 alkoxides Chemical class 0.000 claims 1
- 238000005804 alkylation reaction Methods 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000003435 aroyl group Chemical group 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 150000004292 cyclic ethers Chemical class 0.000 claims 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims 1
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 150000002540 isothiocyanates Chemical class 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 229910052987 metal hydride Inorganic materials 0.000 claims 1
- 150000004681 metal hydrides Chemical class 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 150000004965 peroxy acids Chemical class 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
Classifications
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
- C07C331/16—Isothiocyanates
- C07C331/18—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms
- C07C331/20—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/14—Dithiocarbamic acids; Derivatives thereof
- C07C333/18—Esters of dithiocarbamic acids
- C07C333/20—Esters of dithiocarbamic acids having nitrogen atoms of dithiocarbamate groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
- C07D233/84—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
- C07D233/86—Oxygen and sulfur atoms, e.g. thiohydantoin
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (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)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9116200A FR2685328B1 (fr) | 1991-12-20 | 1991-12-20 | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SI9200391A SI9200391A (en) | 1993-06-30 |
| SI9200391B true SI9200391B (sl) | 2002-02-28 |
Family
ID=9420553
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI9200391A SI9200391B (sl) | 1991-12-20 | 1992-12-16 | Derivati fungicidov 2-imidazolin-5-onov in 2-imidazolin-5-tionov |
Country Status (32)
| Country | Link |
|---|---|
| EP (1) | EP0551048B1 (cs) |
| JP (1) | JP3462516B2 (cs) |
| KR (1) | KR100263576B1 (cs) |
| CN (1) | CN1035594C (cs) |
| AP (1) | AP405A (cs) |
| AT (1) | ATE221878T1 (cs) |
| AU (2) | AU651021B2 (cs) |
| BR (1) | BR9204699A (cs) |
| CA (1) | CA2085192C (cs) |
| CZ (1) | CZ287207B6 (cs) |
| DE (1) | DE69232719T2 (cs) |
| DK (1) | DK0551048T3 (cs) |
| EC (1) | ECSP920893A (cs) |
| EG (1) | EG19910A (cs) |
| ES (1) | ES2176186T3 (cs) |
| FI (1) | FI119732B (cs) |
| FR (1) | FR2685328B1 (cs) |
| HR (1) | HRP921456B1 (cs) |
| HU (1) | HU215384B (cs) |
| IL (2) | IL104091A (cs) |
| MA (1) | MA22747A1 (cs) |
| MX (1) | MX9207383A (cs) |
| MY (1) | MY110823A (cs) |
| NZ (1) | NZ245489A (cs) |
| PL (1) | PL170819B1 (cs) |
| PT (1) | PT551048E (cs) |
| RU (1) | RU2111207C1 (cs) |
| SI (1) | SI9200391B (cs) |
| SK (1) | SK283470B6 (cs) |
| TW (1) | TW267928B (cs) |
| YU (1) | YU49164B (cs) |
| ZA (1) | ZA929772B (cs) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3931907A1 (de) * | 1989-09-25 | 1991-04-04 | Henkel Kgaa | Waessriges lackoverspray-schutzcoating fuer spritzkabinen sowie verfahren zu dessen herstellung |
| FR2706455B1 (fr) * | 1993-06-18 | 1995-08-04 | Rhone Poulenc Agrochimie | Dérivés optiquement actifs de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| US6002016A (en) * | 1991-12-20 | 1999-12-14 | Rhone-Poulenc Agrochimie | Fungicidal 2-imidazolin-5-ones and 2-imidazoline-5-thiones |
| FR2706456B1 (fr) * | 1993-06-18 | 1996-06-28 | Rhone Poulenc Agrochimie | Dérivés optiquement actifs de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| FR2685328B1 (fr) * | 1991-12-20 | 1995-12-01 | Rhone Poulenc Agrochimie | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| FR2698359B1 (fr) * | 1992-11-25 | 1995-10-27 | Rhone Poulenc Agrochimie | Derives de 2-alkoxy 2-imidazoline-5-ones fongicides. |
| DE69329027T2 (de) * | 1992-05-22 | 2001-03-22 | E.I. Du Pont De Nemours And Co., Wilmington | Fungizide imidazolinone |
| US6008370A (en) * | 1992-11-25 | 1999-12-28 | Rhone-Poulenc Agrochimie | Fungicidal-2-alkoxy/haloalkoxy-1-(mono- or disubstituted)amino-4,4-disubstituted-2-imidazolin-5-ones |
| FR2716192B1 (fr) * | 1994-02-17 | 1996-04-12 | Rhone Poulenc Agrochimie | Dérivés de 2-imidazoline-5-ones fongicides. |
| AU1892495A (en) * | 1994-03-09 | 1995-09-25 | Rhone-Poulenc Agrochimie | Pesticide substituted 2-imidazolinones |
| FR2721022B1 (fr) * | 1994-06-10 | 1996-07-19 | Rhone Poulenc Agrochimie | Dérivés de 5-imino 2-imidazolines fongicides. |
| FR2722499B1 (fr) * | 1994-07-13 | 1996-08-23 | Rhone Poulenc Agrochimie | Nouveaux derives de 2-imidazoline-5-ones fongicides |
| FR2722652B1 (fr) * | 1994-07-22 | 1997-12-19 | Rhone Poulenc Agrochimie | Composition fongicide comprenant une 2-imidazoline-5-one |
| JPH09183725A (ja) * | 1995-09-01 | 1997-07-15 | Pfizer Inc | ガン治療用治療剤 |
| FR2751327A1 (fr) | 1996-07-22 | 1998-01-23 | Rhone Poulenc Agrochimie | Intermediaires pour la preparation de 2-imidazoline-5-ones |
| UA61064C2 (uk) * | 1997-12-02 | 2003-11-17 | Рон-Пуленк Агро | Синергічна фунгіцидна композиція, що містить 2-інідазолін-5-он та спосіб боротьби з фітопатогенними грибками культур |
| UA70327C2 (uk) | 1998-06-08 | 2004-10-15 | Баєр Акціенгезельшафт | Спосіб боротьби з фітопатогенними хворобами сільськогосподарських рослин та фунгіцидна композиція |
| FR2783401B1 (fr) * | 1998-09-21 | 2000-10-20 | Rhone Poulenc Agrochimie | Nouvelles compositions fongicides |
| EP1092712A1 (en) * | 1999-10-13 | 2001-04-18 | E.I. Du Pont De Nemours And Company | Process for preparing fungicidal oxazolidinones and imidazolinones |
| CA2697544C (en) | 2002-04-24 | 2012-06-19 | Basf Aktiengesellschaft | Use of defined alcohol alkoxylates as adjuvants in the agrotechnical field |
| CN101863835B (zh) * | 2010-06-29 | 2012-10-10 | 渤海大学 | S-取代-5,5-二苯基-2-硫代海因衍生物的合成方法 |
| CN103081915A (zh) * | 2011-11-07 | 2013-05-08 | 深圳诺普信农化股份有限公司 | 一种杀菌组合物 |
| EP2622961A1 (en) | 2012-02-02 | 2013-08-07 | Bayer CropScience AG | Acive compound combinations |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2329276A1 (fr) * | 1975-10-29 | 1977-05-27 | Roussel Uclaf | Nouvelles imidazolidines substituees, procede de preparation, application comme medicament et compositions les renfermant |
| DE3305203A1 (de) * | 1983-02-16 | 1984-08-16 | Bayer Ag, 5090 Leverkusen | N-sulfenylierte hydantoine, ein verfahren zu ihrer herstellung und ihre verwendung als mikrobizide |
| DE3340595A1 (de) * | 1983-11-10 | 1985-05-23 | Hoechst Ag, 6230 Frankfurt | Imidazolinone, verfahren zu ihrer herstellung und ihre verwendung im pflanzenschutz |
| DE3634887A1 (de) * | 1986-10-14 | 1988-04-21 | Bayer Ag | 2-(5-oxo-2-imidazolin-2-yl)-pyridin-derivate |
| JPH02502721A (ja) * | 1987-03-20 | 1990-08-30 | イー・アイ・デユポン・デ・ニモアス・アンド・カンパニー | 殺菌・殺カビ性アミノトリアゾール及びアミノイミダゾール |
| WO1990012791A1 (en) * | 1989-04-21 | 1990-11-01 | E.I. Du Pont De Nemours And Company | Fungicidal oxazolidinones |
| IE910913A1 (en) * | 1990-03-20 | 1991-09-25 | Sanofi Sa | N-substituted heterocyclic derivates, their preparation¹and pharmaceutical compositions containing them |
| FR2671348B1 (fr) * | 1991-01-09 | 1993-03-26 | Roussel Uclaf | Nouvelles phenylimidazolidines, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant. |
| FR2706456B1 (fr) * | 1993-06-18 | 1996-06-28 | Rhone Poulenc Agrochimie | Dérivés optiquement actifs de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| FR2685328B1 (fr) * | 1991-12-20 | 1995-12-01 | Rhone Poulenc Agrochimie | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| DE69329027T2 (de) * | 1992-05-22 | 2001-03-22 | E.I. Du Pont De Nemours And Co., Wilmington | Fungizide imidazolinone |
-
1991
- 1991-12-20 FR FR9116200A patent/FR2685328B1/fr not_active Expired - Lifetime
-
1992
- 1992-02-17 EG EG78692A patent/EG19910A/xx active
- 1992-12-11 CA CA002085192A patent/CA2085192C/fr not_active Expired - Lifetime
- 1992-12-14 IL IL104091A patent/IL104091A/en not_active IP Right Cessation
- 1992-12-16 EC EC1992000893A patent/ECSP920893A/es unknown
- 1992-12-16 PT PT92420461T patent/PT551048E/pt unknown
- 1992-12-16 ES ES92420461T patent/ES2176186T3/es not_active Expired - Lifetime
- 1992-12-16 MY MYPI92002315A patent/MY110823A/en unknown
- 1992-12-16 DE DE69232719T patent/DE69232719T2/de not_active Expired - Lifetime
- 1992-12-16 NZ NZ245489A patent/NZ245489A/en unknown
- 1992-12-16 AT AT92420461T patent/ATE221878T1/de active
- 1992-12-16 SI SI9200391A patent/SI9200391B/sl unknown
- 1992-12-16 MA MA23037A patent/MA22747A1/fr unknown
- 1992-12-16 EP EP92420461A patent/EP0551048B1/fr not_active Expired - Lifetime
- 1992-12-16 DK DK92420461T patent/DK0551048T3/da active
- 1992-12-17 ZA ZA929772A patent/ZA929772B/xx unknown
- 1992-12-17 MX MX9207383A patent/MX9207383A/es unknown
- 1992-12-18 YU YU109092A patent/YU49164B/sh unknown
- 1992-12-18 SK SK3753-92A patent/SK283470B6/sk not_active IP Right Cessation
- 1992-12-18 AU AU30310/92A patent/AU651021B2/en not_active Ceased
- 1992-12-18 PL PL92297064A patent/PL170819B1/pl unknown
- 1992-12-18 TW TW081110177A patent/TW267928B/zh active
- 1992-12-18 BR BR9204699A patent/BR9204699A/pt not_active IP Right Cessation
- 1992-12-18 CZ CS19923753A patent/CZ287207B6/cs not_active IP Right Cessation
- 1992-12-18 FI FI925763A patent/FI119732B/fi not_active IP Right Cessation
- 1992-12-18 HU HUP9204030A patent/HU215384B/hu not_active IP Right Cessation
- 1992-12-18 RU RU92016214A patent/RU2111207C1/ru active
- 1992-12-19 KR KR1019920024827A patent/KR100263576B1/ko not_active Expired - Lifetime
- 1992-12-21 AP APAP/P/1992/000466A patent/AP405A/en active
- 1992-12-21 CN CN92115091A patent/CN1035594C/zh not_active Expired - Lifetime
- 1992-12-21 JP JP35634492A patent/JP3462516B2/ja not_active Expired - Fee Related
- 1992-12-22 HR HR921456A patent/HRP921456B1/xx not_active IP Right Cessation
-
1994
- 1994-10-07 AU AU74499/94A patent/AU671389B2/en not_active Ceased
-
1997
- 1997-08-04 IL IL12146597A patent/IL121465A0/xx not_active IP Right Cessation
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Owner name: BAYER S.A.S.; FR Effective date: 20100708 |