http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-926335-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2dbb2d7ecbd600cf89fbdd230f4a466c |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-22 |
filingDate | 1959-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d34cbe17bfe9156575c1cb05ae6d8658 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03187e73d2a3f631a91a5ca00d7c5c27 |
publicationDate | 1963-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-926335-A |
titleOfInvention | Improvements in azocines |
abstract | The invention comprises dibenz[bg]tetrahydroazocine, which can be obtained by the cyclisation of 1,3-di-o-aminophenylpropane or one of its salts, e.g. the diphosphate. 2,2-dinitro-chalcone in methanol is reacted with potassium borohydride to give 1,3-di-o-nitrophenyl-3-hydroxyprop-1-ene, which is hydrogenated to 1,3-di-o-aminophenylpropan-1-ol. Treatment of the alcohol with acetic anhydride gives the acetyl derivative, from which 1,3-di-o-acetylaminophenyl-1-chloropropane is obtained with thionyl chloride. Hydrogenation gives 1,3-di-o-acetylaminophenylpropane from which 1,3-di-o-aminophenylpropane is obtained by hydrolysis. According to the Provisional Specification the azocine can be obtained by cyclisation of a compound in which one of the ortho groups is halogen. |
priorityDate | 1959-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 29.