http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-369438-B

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filingDate 2013-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6fb5b867fa07ede6fc7ee908744ee3f
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publicationDate 2019-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-369438-B
titleOfInvention IMIDAZOLINES 8-HEXYLOXIFENIL-2-IMIDAZOLINA, 8-NONYLOXIFENIL-2-IMID AZOLINA, 7-HEXYLOXIFENIL-2-IMIDAZOLINA AND 7-NONYLOXIFENIL-2-IMIDAZO LINA AND ITS PROCESS OF OBTAINING.
abstract The present invention relates to the compounds 7-HEXYLOXIFENIL-2-IMIDAZOLINA AND 7-NONYLOXIPENIL-2-IMIDAZOLINA, and the process to obtain them. These compounds are obtained through a two-step process: an alkylation of the 3-hydroxybenzaldehyde with the corresponding alkyl halide obtaining 81% isolated yield and a cyclization using ethylenediamine, potassium carbonate, triethylamine, iodine and t-butanol, obtaining quantitative yield . The two compounds 7-HEXYLOXIFENIL-2-IMI DAZOLINA AND 7-NONYLOXIFENIL-2- IMIDAZOLINA, have in vitro activity against Trypanosoma cruzi, the compounds have been evaluated on blood trypomastigotes of the NINOA and INC-5 strains and in the latter they present activity practically the same as the clinical drugs Nifurtimox and Benznidazole at concentrations of 19.2 and 38.4 µM. The compounds 7-HEXYLOXIFENIL-2-IMIDAZOLINA AND 7-NONYLOXIFENIL-2-IMIDAZOLINA, due to their chemical characteristics can give rise to molecular gels, which are formed by means of nanoparticles.
priorityDate 2013-01-25-04:00^^<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: 36.