http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003502403-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-33 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-57 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-34 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-57 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-33 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
| filingDate | 2000-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2003-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2003502403-A |
| titleOfInvention | New intermediate |
| abstract | (57) [Summary]nThe following formula (I):nEmbedded imagen 中 where R 0 Are, independently of one another, halogen, C 1 -C 6 Alkyl, C Two -C 6 Alkenyl, C Two -C 6 Alkynyl, C 1 -C 6 Haloalkyl, cyano-C 1 -C 6 Alkyl, C Two -C 6 Haloalkenyl, cyano-C Two -C 6 Alkenyl, C Two -C 6 Haloalkynyl, cyano-C Two -C 6 Alkynyl, hydroxy, hydroxy-C 1 -C 6 Alkyl, C 1 -C 6 Alkoxy, nitro, amino, C 1 -C 6 Alkylamino, di (C 1 -C 6 Alkyl) amino, C 1 -C 6 Alkylcarbonylamino, C 1 -C 6 Alkylsulfonylamino, C 1 -C 6 Alkylaminosulfonyl, C 1 -C 6 Alkylcarbonyl, C 1 -C 6 Alkylcarbonyl-C 1 -C 6 Alkyl, C 1 -C 6 Alkoxycarbonyl-C 1 -C 6 Alkyl, C 1 -C 6 Alkylcarbonyl-C Two -C 6 Alkenyl, C 1 -C 6 Alkoxycarbonyl, C 1 -C 6 Alkoxycarbonyl-C Two -C 6 Alkenyl, C 1 -C 6 Alkylcarbonyl-C Two -C 6 Alkynyl, C 1 -C 6 Alkoxycarbonyl-C Two -C 6 An alkynyl, cyano, carboxyl, phenyl or aromatic ring containing one or two heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the latter two aromatic rings are 1 -C Three Alkyl, C 1 -C Three Haloalkyl, C 1 -C Three Alkoxy, C 1 -C Three May be substituted by haloalkoxy, halogen, cyano or nitro; or R 0 Is an adjacent substituent R 1 , R Two , And R Three And is interrupted by one or two heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and / or 1 -C Four Saturated or unsaturated C which can be substituted by alkyl Three -C 6 Forming a hydrocarbon bridge; R 1 , R Two , And R Three Are, independently of one another, hydrogen, halogen, C 1 -C 6 Alkyl, C Two -C 6 -Alkenyl, C Two -C 6 Alkynyl, C Three -C 6 Cycloalkyl, C 1 -C 6 Haloalkyl, C Two -C 6 Haloalkenyl, C 1 -C 6 Alkoxy-carbonyl-C Two -C 6 Alkenyl, C 1 -C 6 Alkylcarbonyl-C Two -C 6 Alkenyl, cyano-C Two -C 6 Alkenyl, nitro-C Two -C 6 -Alkenyl, C Two -C 6 Haloalkynyl, C 1 -C 6 Alkoxycarbonyl-C Two -C 6 Alkynyl, C 1 -C 6 Alkylcarbonyl-C Two -C 6 -Alkyl, cyano-C Two -C 6 Alkynyl, nitro-C Two -C 6 Alkynyl, C Three -C 6 Halocycloalkyl, hydroxy-C 1 -C 6 Alkyl, C 1 -C 6 Alkoxy-C 1 -C 6 Alkyl, C 1 -C 6 Alkylthio-C 1 -C 6 Alkyl, cyano, C 1 -C Four Alkylcarbonyl, C 1 -C 6 -Alkoxycarbonyl, hydroxy, C 1 -C Ten Alkoxy, C Three -C 6 Alkenyloxy, C Three -C 6 Alkynyloxy, C 1 -C 6 Haloalkoxy, C Three -C 6 Haloalkenyloxy, C 1 -C 6 Alkoxy-C 1 -C 6 Alkoxy, mercapto, C 1 -C 6 Alkylthio, C 1 -C 6 Haloalkylthio, C 1 -C 6 Alkylsulfinyl, C 1 -C 6 Alkylsulfonyl, nitro, amino, C 1 -C 6 Alkylamino, di (C 1 -C 6 Alkyl) amino or phenoxy wherein the phenyl ring is C 1 -C Three Alkyl, C 1 -C Three Haloalkyl, C 1 -C Three -Alkoxy, C 1 -C Three Substituted by haloalkoxy, halogen, cyano or nitro; R Two Can be phenyl, naphthyl or a 5- or 6-membered aromatic ring which can contain one or two heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the phenyl ring The naphthyl ring system and the 5- or 6-membered aromatic ring are halogen, C Three -C 8 Can be substituted by cycloalkyl, hydroxy, mercapto, amino, cyano, nitro or formyl; and / or the phenyl ring, the naphthyl ring system, and the 5- or 6-membered aromatic ring are 1 -C 6 Alkyl, C 1 -C 6 Alkoxy, hydroxy-C 1 -C 6 Alkyl, C 1 -C 6 Alkoxy-C 1 -C 6 Alkyl, C 1 -C 6 Alkoxy-C 1 -C 6 Alkoxy, C 1 -C 6 Alkylcarbonyl, C 1 -C 6 Alkylthio, C 1 -C 6 Alkylsulfinyl, C 1 -C 6 Alkylsulfonyl, mono-C 1 -C 6 Alkylamino, di (C 1 -C 6 Alkyl) amino, C 1 -C 6 Alkylcarbonylamino, C 1 -C 6 Alkylcarbonyl- (C 1 -C 6 Alkyl) amino, C Two -C 6 Alkenyl, C Three -C 6 Alkenyloxy, hydroxy-C Three -C 6 Alkenyl, C 1 -C 6 Alkoxy-C Two -C 6 -Alkenyl, C 1 -C 6 Alkoxy-C Three -C 6 Alkenyloxy, C Two -C 6 Alkenylcarbonyl, C Two -C 6 Alkenylthio, C Two -C 6 Alkenylsulfinyl, C Two -C 6 Alkenylsulfonyl, mono- or di- (C Two -C 6 Alkenyl) amino, C 1 -C 6 Alkyl (C Three -C 6 Alkenyl) -amino, C Two -C 6 Alkenylcarbonylamino, C Two -C 6 Alkenylcarbonyl (C 1 -C 6 Alkyl) amino, C Two -C 6 Alkynyl, C Three -C 6 Alkynyloxy, hydroxy-C Three -C 6 Alkynyl, C 1 -C 6 Alkoxy-C Three -C 6 Alkynyl, C 1 -C 6 Alkoxy-C Four -C 6 Alkynyloxy, C Two -C 6 Alkynylcarbonyl, C Two -C 6 Alkynylthio, C Two -C 6 Alkynylsulfinyl, C Two -C 6 Alkynylsulfonyl, mono- or di- (C Three -C 6 Alkynyl) amino, C 1 -C 6 Alkyl (C Three -C 6 Alkynyl) amino, C Two -C 6 Alkynylcarbonylamino or C Two -C 6 Alkynylcarbonyl (C 1 -C 6 Alkyl) amino; and / or the phenyl ring, the naphthyl ring system, and the 5- or 6-membered aromatic ring system are halo-substituted C 1 -C 6 Alkyl, C 1 -C 6 Alkoxy, hydroxy-C 1 -C 6 Alkyl, C 1 -C 6 Alkoxy-C 1 -C 6 Alkyl, C 1 -C 6 Alkoxy-C 1 -C 6 Alkoxy, C 1 -C 6 Alkylcarbonyl, C 1 -C 6 Alkylthio, C 1 -C 6 Alkylsulfinyl, C 1 -C 6 Alkylsulfonyl, mono-C 1 -C 6 Alkylamino, di (C 1 -C 6 Alkyl) amino, C 1 -C 6 Alkylcarbonylamino, C 1 -C 6 Alkylcarbonyl (C 1 -C 6 Alkyl) amino, C Two -C 6 Alkenyl, C Three -C 6 Alkenyloxy, hydroxy-C Three -C 6 Alkenyl, C 1 -C 6 Alkoxy-C Two -C 6 Alkenyl, C 1 -C 6 Alkoxy-C Three -C 6 Alkenyloxy, C Two -C 6 Alkenylcarbonyl, C Two -C 6 Alkenylthio, C Two -C 6 Alkenylsulfinyl, C Two -C 6 Alkenylsulfonyl, mono- or di- (C Two -C 6 Alkenyl) amino, C 1 -C 6 -Alkyl (C Three -C 6 Alkenyl) amino, C Two -C 6 Alkenylcarbonylamino, C Two -C 6 Alkenylcarbonyl (C 1 -C 6 -Alkyl) amino, C Two -C 6 Alkynyl, C Three -C 6 Alkynyloxy, hydroxy-C Three -C 6 Alkynyl, C 1 -C 6 Alkoxy-C Three -C 6 Alkynyl, C 1 -C 6 Alkoxy-C Four -C 6 Alkynyloxy, C Two -C 6 Alkynylcarbonyl, C Two -C 6 Alkynylthio, C Two -C 6 Alkynylsulfinyl, C Two -C 6 Alkynylsulfonyl, mono- or di- (C Three -C 6 Alkynyl) amino, C 1 -C 6 Alkyl (C Three -C 6 Alkynyl) amino, C Two -C 6 Alkynylcarbonylamino or C Two -C 6 Alkynylcarbonyl (C 1 -C 6 And / or the phenyl ring, the naphthyl ring system, and the 5- or 6-membered aromatic ring are of the formula COOR 50 , CONR 51 , SO Two NR 53 R 54 Or SO Two OR 55 Where R is 50 , R 51 , R 52 , R 53 , R 54 , And R 55 Are, independently of one another, C 1 -C 6 Alkyl, C Two -C 6 Alkenyl or C Three -C 6 Alkynyl or halo-, hydroxy-, alkoxy-, mercapto-, amino-, cyano-, nitro-, alkylthio-, alkylsulfinyl- or alkylsulfonyl-substituted C 1 -C 6 Alkyl, C Two -C 6 Alkenyl or C Three -C 6 Alkynyl; and n is 0, 1 or 2. Compounds represented by｝ are suitable as intermediates in the production of herbicides. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008529986-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012167122-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-7046050-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019521165-A |
| priorityDate | 1999-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 240.