http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1742957-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H17-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-00
filingDate 2005-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_037da872be2a8dc7a18cf5eee8b2e3f5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e1e419800a974ef6df02b60387e65e7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f36e01e82a3bf2c168513a29dbd91f3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01b493ab025ca064453961d63531df1c
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d339a4957e441ca5c708eafd2cda6a7
publicationDate 2007-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1742957-B1
titleOfInvention Process for the preparation of telithromycin
abstract The present invention relates to the process for the preparation of compounds of formula (I) or its pharmaceutically acceptable salts Formula I The novel compounds (i) 10,11-Anhydro-2',4''-di-O-benzoyl-12-O-imidazolylcarbonyl-6-O-methylerythromycin A of formula (Xa) Formula (Xa) (ii) 2',4''-di-O-benzoyl-11-amino-11-N-[4-[4-(3-pyridyl)imidazol-1-yl]butyl]-11-deoxy-6-O-methylerythromycin A 11,12-cyclic carbamate of formula (XIa) Formula (XIa) (iii) 2'-O-benzoyl-11-amino-11-N-[4-[4-(3-pyridyl)imidazol-1-yl]butyl]-11-deoxy-5-O-desosaminyl-6-O-methylerythronolide A 11,12-cyclic carbamate of formula (XIIa) Formula (XIIa) (iv) 2'-benzoyl-11-amino-11-N-[4-[4-(3-pyridyl)imidazol-1-yl]butyl]-11-deoxy-5-O-desosaminyl-6-O-methylerythronolide A 11,12-cyclic carbamate of formula (XIIa) Formula (XIIa) and their use as intermediates in formation of compound of Formula I. Also the process of preparation of compound of formula (XIIIa). Formula (XIIIa)
priorityDate 2004-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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