http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1319959-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_01dc8a8a3ae90ebd3658b65c494e2a4d |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D293-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-84 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D293-12 |
filingDate | 1969-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1973-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-1319959-A |
titleOfInvention | Method for the preparation of 2-alkyl substituted thiazoles and selenazoles |
abstract | 1319959 Fused thiazoles and selenazoles AGFA-GEVAERT 27 Oct 1970 [3 Nov 1969] 53824/69 Heading C2C 2 - Alkyl - benzothiazoles, naphthothiazoles, benzoselenazoles and naphthoselenazoles, the benzenoid rings optionally having further substituents, are prepared by catalytic hydrogenation of a bis-2-nitro-or-amino-phenyl or naphthyl-disulphide or diselenide in the presence of an alkane carboxylic acid anhydride using as catalyst a rhenium sulphide, followed if desired by hydrolysis of any carboxylic ester or amide groups formed by acylation during the reaction. Bis - 2 - nitrophenyl and 2 - nitro naphthyl disulphides, optionally having further substituents, are prepared by reaction of sodium disulphide with a 2-nitroaryl chloride. Bis-2-nitrophenyl-selenides, optionally having further substituents, are prepared by reaction of a 2-nitrophenylselenocyanide with potassium hydroxide. Bis-2-aminophenyl-disulphide is prepared by reaction of o-nitro-chlorobenzene with sodium disulphide, followed by reaction with hydrogen peroxide. |
priorityDate | 1969-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.