http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BG-51157-A3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-52 |
| filingDate | 1990-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4a2047c7ddeb04da5ccebd4b3e6ba4b |
| publicationDate | 1993-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | BG-51157-A3 |
| titleOfInvention | Process for the prepation of 2-anilinepyrimidine derivatives |
| abstract | The compounds are new and are applicable in agriculture as fungicides against fungal diseases on cultivated plants. They are highly active and have a broad spectrum of application. The compounds have the following general formula:<IMAGE>where R1 and R2, independently of each other, represent hydrogen or halogen, R3 represents C3-C6-cycloalkyl or a C3-C6-cycloalkyl radical, whose methyl or halogen are substituted with the same or different substitutes one time or three times, R4 represents halogen, thiocyano, -OR5, -SR5, -NR5R6, where R5 and R6 take many different values. The method runs as follows. A substituted phenylguanidine salt, respectively phenylguanidine, reacts with a substituted -ketoester and the produced substituted 2-phenylamino-4-hydroxypyrimidin is subject to acylation, carbonisation or carbamoilation or the OH group is substituted with halogen, whish is further substituted with one of the indicated R4 groups. |
| priorityDate | 1989-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 20.