http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-690466-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D335-16
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-723
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-203
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-747
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-743
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-17
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-67
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-65
filingDate 1951-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1953-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-690466-A
titleOfInvention Derivatives of thiaxanthone
abstract The invention comprises thiaxanthones of the formula: <FORM:0690466/IV (b)/1> where n is 2 or 3 and R and salts thereof, anp their production by condensing 1-chloro-4-methyl-thiaxanthone with a substituted piperazine of the formula: <FORM:0690466/IV (b)/2> The reactions may be effected in a high-boiling solvent, e.g. quinoline or phenol. Examples are given of the preparation of 1-ethyl-4-b -(41 - methyl - thiaxanthone - 11 - amino) - ethyl piperazine and 11-ethyl- and 11-butyl-4-g -(41-methyl - thiazanthone - 11 - amino) - propyl piperazine and their hydrochlorides. 1-chloro-4-methyl-thiazanthone is obtained by reacting thiosalicylic acid with p-chlorotoluene.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2859216-A
priorityDate 1950-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 32.