http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050032683-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-38
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-38
filingDate 2003-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_024c9c94ed62c0ebb315070dc3dddb07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d17a277112d3b5dfd1569eb0ccb2194
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publicationDate 2005-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20050032683-A
titleOfInvention A process for preparing erdosteine
abstract The present invention relates to a generic name Erdosteine, ie, [(2-oxo-3-tetrahydrothienylcarbamoyl) -methylthio] acetic acid of the formula (I), used as a therapeutic agent for acute and chronic respiratory diseases. A method for preparing the compound, wherein D, L-homocysteine thiolactone hydrochloride of the following formula (II) is reacted with chloroacetyl chloride of the formula (III) to form 3-chloroacetamido-2-oxo- of the following formula (IV) A method for producing erthostein, comprising the steps of preparing tetrahydrothiophene, and reacting a compound of formula (IV) with thioglyconic acid of formula (V) to produce erdostein of formula (I) , The reaction of all the steps is characterized in that by reacting the reactants of each step in a two-phase solution consisting of a basic aqueous solution and an organic solvent for 2 to 3 hours at a temperature of -10 ~ 20 ℃.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20220148616-A
priorityDate 2003-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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