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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D-
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A23K1-16
filingDate 1973-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1975-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f70bf3a645e0c75b9f61a57e51ce4fd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c74f9017d567c81baf1b7ddbf024329
publicationDate 1975-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3900482-A
titleOfInvention 1-(pyridyl-thioalkyl)-2-alkyl-5-nitro-imidazoles
abstract 1-(PYRIDYL-THIOALKYL)-2-ALKYL-5-NITRO-IMIDAZOLES OF THE FORMULA IN WHICH R1 is hydrogen, methyl or ethyl, -(CH2)n- is an alkyl chain of 2 to 4 carbon atoms which may be branched and to which the pyridyl group is linked in 2-, 3- or 4-position via a sulfur atom, are prepared by reaction of 1-( omega -halogeno-alkyl)-2alkyl-5-nitro-imidazole with mercapto-pyridine in the presence of an acid-binding agent or by reaction of 2-alkyl-5-nitro-imidazole with omega -halogeno-alkyl-thio-pyridine in the presence of an acid-binding agent or with omega -hydroxy-alkyl-thio-pyridine in the presence of a condensation agent or with an aryl-sulfonyloxyalkyl-thio-pyridine. The products of the invention are suitable for the treatment of protozoal diseases.
priorityDate 1972-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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