http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1067082-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-425
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-10
filingDate 1977-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1979-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a5759c28dd2bfb6fddaddf9e8c7d21a
publicationDate 1979-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1067082-A
titleOfInvention 6-(m-aminophenyl)-2,3,5,6-tetrahydroimidazo (2.1-6) thiazole (m-aminotetramisole) compounds
abstract ABSTRACT OF THE DISCLOSURE Novel optically-active derivatives of 6-(m-aminophenyl)-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole(m-aminotetramisole], which are useful anthelmintic agents, are disclosed, and also a process for the preparation thereof which comprises acylating the d1- or 1- form of 6-(m-aminophenyl)-2,3,5,6-tetrahydroimidazo-[2,1-b]thiazole(m-aminotetramisole) with a halonicotinic acid or a functional equivalent thereof.
priorityDate 1976-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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