http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2042056-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-86 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-86 |
filingDate | 1970-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fc6051ddbc94918603d3b1607ebf33dc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40a8739b1573ccb040fe4529b87b60de |
publicationDate | 1972-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | DE-2042056-A1 |
titleOfInvention | New heterocyclic compounds |
abstract | Heterocyclic cpds. are formed by reacting quinone aldehydes (I) : (where R and R1 are H or lower alkyl and together opt. form part of 5- or 6-membered ring; and X, Y and Z are further substits. where X and Y together form part of an anellated (o-fussed) 5- or 6-membered carbocyclic ring) with hydrazine derivs. (II), having a free H2N-NH- gp., which do not have a reducing activity towards (I), in 1:1 mole ratio, pref. at 0-100 (10-30) degrees C, in weakly acid, neutral or pref. weakly alkaline medium, pref. using pyridine and/or alkyl pyridine catalyst, and opt. separating any isomeric linear aldehyde hydrazones formed at same time. |
priorityDate | 1970-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 80.