http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-769749-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_19aaaa9f91b7bf94ef9bdd9425970c0c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03C1-83
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C1-83
filingDate 1955-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1957-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-769749-A
titleOfInvention Improvements in or relating to the manufacture of coloured photographic layers
abstract 4 : 41 - Dimethoxy - diphenyl - pyridinemethane is prepared by adding a mixture of acetic acid and conc. sulphuric acid to a cooled mixture of pyridine-4-aldehyde and anisole. The product is heated in acetic acid with PbO2 to give 4 : 41 - dimethoxy - diphenyl - pyridinecarbinol. The leuco base and carbinol are similarly prepared using benzothiazole-2-aldehyde and benzselenazole-2-aldehyde. 10 - Methyl - phenothiazine - 5 - dioxide is prepared by refluxing 10-methyl-phenothiazine with H2O2 in acetic acid.ALSO:The preparations of certain dyes which fall within the following formula are described:- <FORM:0769749/IV(b)/1> wherein A is a nitrogen and/or sulphurcontaining heterocyclic nucleus, B and B1 are alkoxy or substituted amino groups or B1 may be hydrogen, R and R1 are hydrogen or R1 is carboxy and X is an anion such as chloride. Those wherein A is the residue of a phenothiazine, N-acetylphenothiazine, N-methyl-phenothiazine, N-methyl-phenothiazine-5-dioxide and carbazole nucleus, are prepared by reacting the heterocyclic compound (AH) with the appropriately substituted benzophenone, such as p-dimethylamino-o1-carboxy-; p-p1-dimethoxy-; 4-methoxy-; p-dimethylamino- and 4-dimethylamino-41-methoxy-benzophenones in the presence of POCL3 or PCl5 + P2O5. Those wherein A is te residue of a pyridine or phenothiazine nucleus and B and B1 are the same are prepared by melting the 4:41-dimethoxy-diphenyl-pyridine-(or phenothiazine)-carbinol with benzoic acid and adding 2-chloro-5-aminobenzoic acid, or mono-ethanolamine, or p-aminophenol, or p-amino-salicylic acid wherein the amino group reacts with both the methoxy groups of the carbinol. The dyes wherein A is benzthiazole or benzselenazole and B and B1 are methoxy (R and R1=H) are prepared by reacting the heterocyclic 2-aldehyde, with anisol in acetic acid and sulphuric acid, oxidizing the leuco-base with PbO2 and treating the carbinol formed with HCl. Thiophene-malachite green (A=thiophene) is referred to.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0611807-A1
priorityDate 1954-04-28-04:00^^<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/SID419535738
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1118
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425413332
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID136087
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13389
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7519
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID74200
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456375171
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7108
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412584819
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID176
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID37879
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415831349
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID700
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423046428
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID887
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419525513
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419483691
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903350
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419545267
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411932836
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID243
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414392184
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409451045
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547992
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID947
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID403
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415752906
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8108
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420319568
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71015
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556970
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID241608
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393787
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1049
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7222
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397365
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID312
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415748593
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22795595
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559517
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421096511
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527948
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419851891
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8030
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4649
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419484158

Total number of triples: 60.