http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-417732-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-04
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filingDate 1973-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-417732-A1
titleOfInvention PROCEDURE FOR THE PREPARATION OF NEW AMINOETHANOLS.
abstract Procedure for the preparation of new aminoethanols of the general formula Ia **(See formula)** where R1 represents a chlorine atom and Hal represents a chlorine or bromine atom and n represents the numbers 0, 1 or 2, and of their acid addition salts physiologically compatible with organic or inorganic acids, characterized in that one or two protecting radicals from a compound of the general formula II **(See formula)** in which R1, Hal and n are as initially defined, Y means a protecting radical for an amino group and X means a protecting radical capable of being separated by hydrolysis, one of the radicals X or Y being able to also mean a hydrogen atom ; and a compound of the general formula Ia obtained according to the procedure is transformed, if desired, by reaction with an aldehyde of the general formula. R2 - CHO wherein R2 signifies a hydrogen atom, an alcoholic, alkenyl, aryl, aralcoyl, heteroaryl or heteroaralcoyl radical any, in its oxazolidine of the general formula Ib, **(See formula)** wherein R1, R2, Hal and n are as initially defined, and/or if desired in their salt by the addition of acid physiologically compatible with an organic or inorganic acid. (Machine-translation by Google Translate, not legally binding)
priorityDate 1972-04-22-04:00^^<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: 25.