http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2535674-C2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7c45f3f15395ecd80506aa6c37fe3cb5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d092c923de85138e77fa4744fa73949b |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P7-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06 |
| filingDate | 2009-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2014-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0788f578eeacc890b57fa024d3fb1e94 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e60776d98ecdc4e4a2a08df960c32300 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a46b176890269576e544b453ad81df3 |
| publicationDate | 2014-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2535674-C2 |
| titleOfInvention | Novel imine derivatives, methods of obtaining thereof and insecticides, containing thereof |
| abstract | FIELD: chemistry. n SUBSTANCE: group of inventions relates to an imine derivative, represented by formula , where "Ar" stands for pyridine, containing a chlorine atom on a ring or thiazole, which can contain the chlorine atom on a ring; "X" stands for a sulphur atom or CH 2 ; when "Y" represents COR 1 , "R 1 " stands for a hydrogen atom or a C 1 -C 5 alkyl group, halogenated methyl group, except trifluoromethyl group, halogenated C 2 -C 5 alkyl group, C 2 -C 5 alkenyl group, halogenated C 2 -C 5 alkenyl group, C 3 -C 5 alkinyl group, non-substituted or substituted with an atom of chlorine, fluorine, methyl group or acetamide phenyl group, non-substituted (C 6 ) aryl(C 1 -C 3 )alkyl group, (C 1 -C 4 )alkoxy (C 1 -C 5 )alkyl group, C 1 -C 3 alkoxycarbonyl group, (C 1 -C 3 ) alkylsulphonyl (C 1 -C 3 )alkyl group, (C 1 -C 3 )alkylthio (C 1 -C 3 )alkyl group, non-substituted or substituted with a methyl group or a fluorine atom C 3 -C 7 cycloalkyl group, cyano(C 1 -C 3 ) alkyl group, non-substituted phenoxy(C 1 -C 3 ) alkyl group, non-substituted pyridylmethyl group, non-substituted imidazolylmethyl group, furanyl group, morpholine group, adamantly group, isothiocyanate group or a heterocyclic ring selected from quinoline, indole, pyridine, pyrazine, pyridazine or tetrahydrofurane, substituted with one, two or five substituents, selected from chlorine, bromine, trifluoromethane or fluorine, and a non-substituted heterocyclic ring, selected from quinoline, indole, pyridine, pyrazine, pyridazine or tetrahydrofurane, when "Y" represents CONR 3 R 4 "R 3 " and "R 4 " stands for a hydrogen atom or C 1 -C 5 alkyl group, C 1 -C 3 alkoxygroup, non-substituted phenyl group, (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl group, C 1 -C 3 alkoxycarbonylmethyl group, non-substituted C 3 -C 7 cycloalkyl group, non-substituted benzenesulphonyl group; except the cases, when "R 3 " and "R 4 " simultaneously stand for hydrogen; when "Y" represents CONHCOR 5 , "R 5 " stands for a halogenated C 1 -C 5 alkyl group, non-substituted phenyl group; when "Y" represents CO 2 R 9 , "R 9 " stands for C 1 -C 7 alkyl group, halogenated C 1 -C 5 alkyl group, C 2 -C 5 alkenyl group, halogenated C 2 -C 5 alkenyl group, C 3 -C 5 alkinyl group, non-substituted or substituted with chlorine, fluorine or a nitro group naphthyl or a phenyl group, non-substituted (C 6 )aryl(C 1 -C 3 )alkyl group, (C 1 -C 3 )alkoxy (C 1 -C 3 ) alkyl group, (C 1 -C 3 )alkylthio (C 1 -C 3 )alkyl group, tri(C 1 -C 3 alkyl)silyl(C 1 -C 3 )alkyl group, non-substituted C 3 -C 7 cycloalkyl group, 3-6-membered non-substituted heterocycloalkyl group, containing an oxygen atom as the heteroatom, non-substituted or substituted with methoxygroup phenylmethyl group, non-substituted furanylmethyl group, non-substituted thienylmethyl group, non-substituted pyridylmethyl group, succinimide group. The group of inventions also relates to methods of obtaining imine derivative of formula (1) (versions). The compound by the invention can be obtained from compounds, selected from the group, consisting of compounds, represented by formulas ACO-B (5), ACOOCOA (6), ACOOH (7), D-N=C=O (8) or HCO 2 Et(10) in the interaction with the compound of formula . n EFFECT: imine derivative, used as an insecticide, possessing the prolonged effect and wide spectrum of action. n 5 cl, 22 tbl, 1 dwg |
| priorityDate | 2008-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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