http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-755446-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9d757a010abaaa7cd45b5a33e46ca149
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-14
filingDate 1954-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3545b6964216e4a95b92c8afa308ea28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_316149088c2dabf6fa8d0352dd565b65
publicationDate 1956-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-755446-A
titleOfInvention Improvements in or relating to heterocyclic compounds
abstract The invention comprises compounds of the general formula <FORM:0755446/IV(a)/1> wherein R is an alkyl or aralkyl group and R1 and R2 are the same or different and are each hydrogen, halogen or alkoxy, and salts and quaternary salts thereof; and their preparation by condensation of 2,6-diamino-3-nitroso-pyridine with a suitably substituted O-acyl indoxyl in solution or suspension in a solvent in an inert atmosphere in the presence of an acid binding condensing agent such as sodium carbonate, sodium bicarbonate, a sodium alkoxide or piperidine followed if desired by treatment with an acid or quaternizing agent. Examples describe the preparation of (1) compounds of the above general formula in which R1 and R2 are hydrogen and R is methyl, ethyl, propyl, amyl and benzyl; and the methosulphate, hydrochloride and acetate of the compound in which R is methyl; (2) 31 - amino - 6 - bromo - 9 - methyl-1,4,9,41 - tetra - aza - 2,3 - 61, 51 - benzofluorene, the corresponding 6-chloro compound and its ethane sulphonate, (3) 31-amino-6,7-dimethoxy-9 - methyl - 1,4,9,41 - tetra - aza - 2,3 - 61, 51-benzofluorene; and (4) 31-amino-6,8-dichloro-9 - methyl - 1,4,9,41 - tetra - aza - 2,3 - 61, 51-benzofluorene. According to the Provisional Specification, R1 and R2 in the general formula above may additionally represent nitro or amino groups.
priorityDate 1954-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394834
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448098817
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903349
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393636
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID99676
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558919
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID175
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID516892
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419557048
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8082
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3717105
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393736
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407907393
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453034310
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10340
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393346
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415804754
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393705
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458427722

Total number of triples: 34.