http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-042127-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e559abcd8f120b071dc1162360867ffa |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D217-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D217-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-74 |
| filingDate | 2003-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2005-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-042127-A1 |
| titleOfInvention | QUINOLINAS, ISOQUINOLINAS AND QUINAZOLIN- OXIALQUILAMIDAS AND ITS USES AS FUNGICIDES |
| abstract | Fungicidal compounds of the general formula (1), where one of X and Y is N or N-oxide and the other is CR or X and Y are both N; Z is H, halo, C1-6 alkyl optionally substituted with halo or C1-4 alkoxy, C3-6 cycloalkyl optionally substituted with halo or C2-4 alkoxy, alkenyl optionally substituted with halo, C2-4 alkynyl optionally substituted with halo, alkoxy C1-6 optionally substituted with halo or C1-4 alkoxy, C2-4 alkenyloxy optionally substituted with halo, C2-4 alkynyloxy optionally substituted with halo, cyano, nitro, C1-4 alkoxycarbonyl, -OSO2R ', S (O) nR' , -COR '', -CONR''R '' ', -CR' '= NOR', NR''R '' ', NR''COR', NR''CO2R ', where n is 0, 1 or 2; R 'is alkyl optionally substituted with halogen and R' 'and R' '' are independently H or C1-6 alkyl or, in the case of -CONR''R '' ', can be joined to form a ring of 5 or 6 members containing a single nitrogen atom, saturated carbon atoms and optionally a single oxygen atom; R is H, halo, C 1-8 alkyl, C 3-6 cycloalkyl, C 2-8 alkenyl, C 2-8 alkynyl, C 1-8 alkoxy, C 1-8 alkylthio, nitro, amino, mono- or di- (C 1-6 alkylamino) ), mono- or di-alkenylamino (C2-6), mono- or di-alkylamino (C2-6), formylamino, alkyl (formyl) amino, C1-4 alkylcarbonylamino, C1-4 alkoxycarbonylamino, (C1-4) alkyl (C 1-4 alkylcarbonyl) amino, cyano, formyl, C 1-4 alkylcarbonyl, C 1-4 alkoxycarbonyl, aminocarbonyl, mono- or di-C 1-6 alkylaminocarbonyl, carboxy, C 1-4 alkylcarbonyloxy, arylC 1-4 alkylcarbonyloxy, C 1-4 alkylsulfinyl, C 1-4 alkylsulfonyl or C 1-4 alkylsulfonyloxy; R1 is C1-4 alkyl, C2-4 alkenyl or C2-4 alkynyl where the alkyl, alkenyl and alkynyl groups are optionally substituted on their terminal carbon atom with one, two or three halogen atoms, with a cyano group, with a cyano group C1-4 alkylcarbonyl group, with a C1-4 alkoxycarbonyl or with a hydroxy group, or R1 is alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl or alkylsulfonylalkyl where the total amount of carbon atoms is 2 or 3, or R1 is a C1- alkoxy group 4 linear chain; R2 is H, 1-4 alkyl, C1-4 alkoxymethyl or benzyloxymethyl wherein the phenyl ring of the benzyl portion is optionally substituted with C1-4 alkoxy; R3 and R4 are independently H, C1-3 alkyl, C2-3 alkenyl or C2-3 alkynyl with the proviso that they are not both H and that when the two are not H the combined total amount of their carbon atoms does not exceeds 4, or R3 and R4 bind with the carbon atom to which they are attached to form a 3 or 4 membered carbocyclic ring optionally containing an O, S or N atom and which is optionally substituted with halo or C1- alkyl 4; and R5 is H, C1-4 alkyl or C3-6 cycloalkyl wherein the alkyl or cycloalkyl group is optionally substituted with halo, hydroxy, C1-6 alkoxy, cyano, C1-4 alkylcarbonyloxy, aminocarbonyloxy, mono-di-alkylaminocarbonyloxy (C1 -4), -S (O) C1-6alkyl, where n is 0, 1 or 2, triazolyl (for example 1,2,4-triazol-1-yl), tri (C1-4 alkylsilyloxy), phenoxy optionally substituted, optionally substituted thienyloxy, optionally substituted benzyloxy or optionally substituted thienylmethoxy, or R5 is optionally substituted phenyl, optionally substituted thienyl or optionally substituted benzyl, wherein the optionally substituted phenyl and thienyl rings of the values of R5 are optionally substituted with one, two or three substituents selected from halo, hydroxy, mercapto, C 1-4 alkyl, C 2-4 alkenyl, C 2-4 alkynyl, C 1-4 alkoxy, C 2-4 alkenyloxy, C 2-4 alkynyloxy, halo C 1-4 alkyl, halo- C1-4 alkoxy, C1-4 alkylthio, C1-4 halo alkylthio, C1-4 hydroxy alkyl, alkoxy (C1-4) -C1-4 alkyl, C3-6 cycloalkyl, C3-6 cycloalkyl-C1-4 alkyl, phenoxy, benzyloxy, benzoyloxy, cyano, isocyanate, thiocyanate, isothiocyanate, nitro, -NRmRn , -NHCORm, -NHCONRmRn, -CONRmRn, -SO2Rm, -OSO2Rm, -CORm, -CRm = NRn or -N = CRmRn, where Rm and Rn are independently hydrogen, C1-4 alkyl, halo-C1-alkyl 4, C1-4 alkoxy, halo C1-4 alkoxy, C1-4 alkylthio, C3-6 cycloalkyl, (C3-6) cycloalkyl (C1-4) alkyl, phenyl or benzyl, where the phenyl and benzyl groups are substituted optionally with halogen, C1-4 alkyl or C1-4 alkoxy. |
| priorityDate | 2002-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 47.