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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-22
filingDate 1992-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bb88c2d757339866eceac9f69b8721f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efd339e9576ed96f617c5732d3c414a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d265a8376b3af219ae69f967069da793
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5ba58c84ab6f6bb3358198de5c27f4f
publicationDate 1994-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2694753-A1
titleOfInvention Methods of specific synthesis of new aminothioethers by substitution of hydroxylated sites on mono or polyhydroxylated molecules, products obtained by these methods and their applications.
abstract Specific synthesis processes of aminothioethers and their salts of general formula: (CF DRAWING IN BOPI) in which, R1, R2 and R3 are generally hydrocarbon groups, saturated or not, branched or not and in which the precursor Sub-OH of the Sub group is a mono or polyhydroxylated molecule, cyclic or not, allowing the selective activation of a hydroxylated site to lead to the Sub-Y intermediate which receives, according to the two methods described, the R2 R3 N-R1 graft - S-. The new derivatives obtained can be used as medicaments, in particular as immunostimulants, immunoregulators, radioprotectants, or else for bacterial, viral, fungicidal, inflammatory and autoimmune diseases.
priorityDate 1992-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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