http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2013357-A1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-22 |
| filingDate | 1970-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1971-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DE-2013357-A1 |
| titleOfInvention | Iminocarboxylic acid derivs in prepn of s-triazines |
| abstract | Prepn. of s-triazine derivs. (III) with plant protective activity: (where X is R-O- or R1R2N-; n is 0 or 1; R3 and R4 are opt. substd. aliphatic, aromatic or heterocyclic gps.; R is haloalkyl or opt. substd. aryl which can be combined with heterocyclic gps.; R1, R2 are opt. substd. aliphatic, aromatic or heterocyclic gps. and R1 and R2 together with N can form a ring which can contain further heteroatoms), takes place by direct ring closure reaction of novel iminocarboxylic acid derivs. X-C(Hal)=N-CO-(COO)n-R3 (I) with amidines R4C(=NH)NH2 (II) at -30 to 100 degrees C, pref. at -10 to 60 degrees c, pref. in presence of a diluent, R3 and R4 being opt. substd. aliphatic, aromatic or heterocyclic gps. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012508223-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9427974-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5759956-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-695697-B2 |
| priorityDate | 1970-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 147.